bahan referat postterm pregnancy

53
Postterm Pregnancy Author: Aaron B Caughey, MD, PhD, MPH; Chief Editor: David Chelmow Updated: Oct 22, 2013 Postterm pregnancy is defined as a pregnancy that extends to 42 0/7 weeks and beyond. [1] The reported frequency of postterm pregnancy is approximately 3-12%. [1, 2] However, the actual biologic variation is likely less since the most frequent cause of a postterm pregnancy diagnosis is inaccurate dating. [3, 4, 5, 6] Risk factors for actual postterm pregnancy include primiparity, prior postterm pregnancy, male gender of the fetus, and genetic factors. [7, 8, 9, 2, 1, 10] Laursen et al studied monozygotic and dizygotic twins and their subsequent development of prolonged pregnancies. They found that maternal but not paternal genetic factors influenced the rate of postterm pregnancies and accounted for the etiology in as many as 30% of these pregnancies. [11] A more recently described risk factor is obesity, which appears to increase the risk of pregnancies progressing beyond 41 or 42 weeks of gestation. [12, 13, 14] Although the last menstrual period (LMP) has been traditionally used to calculate the estimated due date (EDD), many inaccuracies exist using this method in women who have irregular cycles, have been on recent hormonal birth control, or who have first trimester bleeding. In particular, women are more likely to be oligo-ovulatory than polyovulatory, so cycles longer than 28 days are not uncommonly seen. [4] If such a cycle is 35 days instead of 28 days, a second trimester ultrasound will not be powerful enough to redate the pregnancy. Thus, not only the LMP date, but the regularity and length of cycles must be taken into account when estimating gestational age. Ultrasonographic dating early in pregnancy can improve the reliability of the EDD; however, it is necessary to understand the margin of error reported at various times during each trimester. A calculated gestational age by composite biometry from a sonogram must be considered an estimate and must take into account the range of possibilities. Estimation range varies. For example, crown-rump length (CRL) is 3-5 days, ultrasonography performed at 12-20 weeks of gestation is 7-10 days, at 20- 30 weeks is 2 weeks, and after 30 weeks is 3 weeks. Thus, a pregnancy that is 35 weeks by a 31-week ultrasound could actually be anywhere from 32 weeks to 38 weeks (35 wk +/-3 wk). If the calculated ultrasonographic gestational age varies from the LMP more than the respective range of error, it is used instead to establish the final EDD. The importance of determining by what method a pregnancy is dated cannot be overemphasized because this may have significant consequences if the physician delivers a so-called term pregnancy that is not or observes a so-called term pregnancy that is very postterm. When determining a management plan for an impending postterm pregnancy (>40 wk of gestation but < 42 wk), the 3 options are (1) elective induction of labor, (2) expectant management of the pregnancy, or (3) antenatal testing.

Upload: alyssa-diandra

Post on 27-Jan-2016

224 views

Category:

Documents


1 download

DESCRIPTION

kukukuku

TRANSCRIPT

Page 1: Bahan Referat Postterm Pregnancy

Postterm Pregnancy Author: Aaron B Caughey, MD, PhD, MPH; Chief Editor: David ChelmowUpdated: Oct 22, 2013

Postterm pregnancy is defined as a pregnancy that extends to 42 0/7 weeks and beyond.[1] The reported frequency of postterm pregnancy is approximately 3-12%.[1, 2] However, the actual biologic variation is likely less since the most frequent cause of a postterm pregnancy diagnosis is inaccurate dating.[3, 4, 5, 6] Risk factors for actual postterm pregnancy include primiparity, prior postterm pregnancy, male gender of the fetus, and genetic factors.[7, 8, 9, 2, 1, 10]

Laursen et al studied monozygotic and dizygotic twins and their subsequent development of prolonged pregnancies. They found that maternal but not paternal genetic factors influenced the rate of postterm pregnancies and accounted for the etiology in as many as 30% of these pregnancies.[11] A more recently described risk factor is obesity, which appears to increase the risk of pregnancies progressing beyond 41 or 42 weeks of gestation.[12, 13, 14]

Although the last menstrual period (LMP) has been traditionally used to calculate the estimated due date (EDD), many inaccuracies exist using this method in women who have irregular cycles, have been on recent hormonal birth control, or who have first trimester bleeding. In particular, women are more likely to be oligo-ovulatory than polyovulatory, so cycles longer than 28 days are not uncommonly seen.[4] If such a cycle is 35 days instead of 28 days, a second trimester ultrasound will not be powerful enough to redate the pregnancy. Thus, not only the LMP date, but the regularity and length of cycles must be taken into account when estimating gestational age.

Ultrasonographic dating early in pregnancy can improve the reliability of the EDD; however, it is necessary to understand the margin of error reported at various times during each trimester. A calculated gestational age by composite biometry from a sonogram must be considered an estimate and must take into account the range of possibilities.

Estimation range varies. For example, crown-rump length (CRL) is 3-5 days, ultrasonography performed at 12-20 weeks of gestation is 7-10 days, at 20-30 weeks is 2 weeks, and after 30 weeks is 3 weeks. Thus, a pregnancy that is 35 weeks by a 31-week ultrasound could actually be anywhere from 32 weeks to 38 weeks (35 wk +/-3 wk). If the calculated ultrasonographic gestational age varies from the LMP more than the respective range of error, it is used instead to establish the final EDD. The importance of determining by what method a pregnancy is dated cannot be overemphasized because this may have significant consequences if the physician delivers a so-called term pregnancy that is not or observes a so-called term pregnancy that is very postterm.

When determining a management plan for an impending postterm pregnancy (>40 wk of gestation but < 42 wk), the 3 options are (1) elective induction of labor, (2) expectant management of the pregnancy, or (3) antenatal testing. Each of these 3 options may be used at any particular time during this 2-week period.

Note that if the pregnancy is at risk for an adverse outcome from an underlying condition, either maternal or fetal, inducing labor may proceed without documented lung maturity. Also, an elective induction of labor may proceed at or after 39 weeks of gestation in the absence of documented lung maturity provided that 36 weeks have elapsed since documentation of a positive human chorionic gonadotropin (+hCG) test finding, 20 weeks of fetal heart tones have been established by a fetoscope or 30 weeks by a Doppler examination, or 39 weeks' gestation have been established by a CRL or by an ultrasound performed before 20 weeks of gestation consistent with dates by the patient's LMP.

Perinatal outcomes in postterm pregnancies

Recent studies have shown that the risks to the fetus[15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27] and to the mother[24, 28, 29,

30, 31, 32, 33, 34] of continuing the pregnancy beyond the estimated date of delivery is greater than originally appreciated.

Risks have traditionally been underestimated for 2 reasons. First, earlier studies were published before the routine use of obstetric ultrasonography and, as a result, likely included many pregnancies that were not truly postterm. As noted above, such a misclassification bias would artificially lower the

Page 2: Bahan Referat Postterm Pregnancy

complication rates of pregnancies designated postterm and increase the complication rates in those designated term, resulting in a diminution in the difference between term and postterm pregnancies.

The second issue relates to the definition of stillbirth rates. Traditionally, stillbirth rates were calculated using all pregnancies delivered at a given gestational age as the denominator. However, once a fetus is delivered, it is no longer at risk of intrauterine fetal demise, and use of this denominator has traditionally underestimated the risk of stillbirth. The appropriate denominator is not all deliveries at a given gestational age, but ongoing (undelivered) pregnancies.[19, 20, 34] In one retrospective study of more than 170,000 singleton births, for example, Hilder et al demonstrated that the stillbirth rate increased 6-fold (from 0.35-2.12 per 1,000 pregnancies) when the denominator was changed from all deliveries to ongoing (undelivered) pregnancies.[17]

Fetal and neonatal risks

Antepartum stillbirths account for more perinatal deaths than either complications of prematurity or sudden infant death syndrome.[18] Perinatal mortality (defined as stillbirths plus early neonatal deaths) at 42 weeks of gestation is twice that at 40 weeks (4-7 vs 2-3 per 1,000 deliveries, respectively) and increases 4-fold at 43 weeks and 5- to 7-fold at 44 weeks.[16, 17, 18] These data also demonstrate that, when calculated per 1000 ongoing pregnancies, fetal and neonatal mortality rates increase sharply after 40 weeks.[17]

Cotzias et al calculated the risk of stillbirth in ongoing pregnancies for each gestational age from 35-43 weeks.[18] The risk of stillbirth was 1 in 926 ongoing pregnancies at 40 weeks’ gestation, 1 in 826 at 41 weeks, 1 in 769 at 42 weeks, and 1 in 633 at 43 weeks. Uteroplacental insufficiency, asphyxia (with and without meconium), intrauterine infection, and anencephaly all contribute to excess perinatal deaths, although postterm anencephaly is essentially nonexistent with modern obstetrical care.[35]

A number of key morbidities are greater in infants born to postterm pregnancies as well as pregnancies that progress to and beyond 41 0/7 weeks gestation including meconium and meconium aspiration, neonatal acidemia, low Apgar scores, macrosomia, and, in turn, birth injury. For example, since postterm infants are larger than term infants, with a higher incidence of fetal macrosomia (defined as estimated fetal weight ≥ 4,500 g)[36] , they are, in turn, at greater risk for other complications.[37, 38] Such complications associated with fetal macrosomia include prolonged labor, cephalopelvic disproportion, and shoulder dystocia with resultant risks of orthopedic or neurologic injury.

Approximately 20% of postterm fetuses have fetal dysmaturity (postmaturity) syndrome, which describes infants with characteristics of chronic intrauterine growth restriction from uteroplacental insufficiency.[39] These pregnancies are at increased risk of umbilical cord compression from oligohydramnios, nonreassuring fetal antepartum or intrapartum assessment, intrauterine passage of meconium, and short-term neonatal complications (such as hypoglycemia, seizures, and respiratory insufficiency).

Meconium aspiration syndrome refers to respiratory compromise with tachypnea, cyanosis, and reduced pulmonary compliance in newborns exposed to meconium in utero and is seen in higher rates in postterm neonates.[40] Indeed, the 4-fold decrease in the incidence of the meconium aspiration syndrome in the United States from 1990-1998 has been attributed primarily to a reduction in the postterm delivery rate[22] with very little contribution from conventional interventions designed to protect the lungs from the chemical pneumonitis caused by chronic meconium exposure, such as amnioinfusion[41, 42] or routine nasopharyngeal suctioning of meconium-stained neonates.[43]

Postterm pregnancy is also an independent risk factor for neonatal encephalopathy[44] and for death in the first year of life.[17, 18]

While much of the work above has been conducted in postterm pregnancies. Some of the fetal risks such as presence of meconium, increased risk of neonatal acidemia, and even stillbirth have been described as being greater at 41 weeks of gestation and even at 40 weeks of gestation as compared with 39 weeks’ gestation.[23, 24] For example, in one study, the rates of meconium and neonatal acidemia both increased throughout term pregnancies beyond 38 weeks of gestation. In addition to stillbirth being increased prior to 42 weeks of gestation, one study found that the risk of neonatal mortality also increases beyond 41 weeks of gestation.[45]Thus, 42 weeks does not represent a threshold below which risk is uniformly distributed. Indeed, neonatal morbidity (including meconium

Page 3: Bahan Referat Postterm Pregnancy

aspiration syndrome, birth injury, and neonatal acidemia) appears to be the lowest at around 38 weeks and increase in a continuous fashion thereafter.[46]

While preterm delivery is a well-established risk factor for cerebral palsy, a recent study suggested that delivery at 42 weeks or later is also associated with increased risk (RR 1.4, 95% CI, 1.2-1.6 when compared with delivery at 40 weeks’ gestation).[47]

Maternal risks and mode of delivery

The maternal risks of postterm pregnancy are often underappreciated. These include an increase in labor dystocia (9-12% vs 2-7% at term), an increase in severe perineal injury (3rd and 4th degree perineal lacerations) related to macrosomia (3.3% vs 2.6% at term) and operative vaginal delivery, and a doubling in the rate of cesarean delivery (14% vs 7% at term).[19, 28, 29, 30] The latter is associated with higher risks of complications such as endometritis, hemorrhage, and thromboembolic disease.[29,

48]

In addition to the medical risks, the emotional impact (anxiety and frustration) of carrying a pregnancy 1-2 weeks beyond the estimated due date should not be underestimated. In a randomized, controlled trial of women at 41 weeks of gestation, women who were induced would desire the same management 74% of the time, whereas women with serial antenatal monitoring only desired the same management 38% of the time.[49]

Similar to neonatal outcomes, maternal morbidity also increases in term pregnancies prior to 42 weeks of gestation. Such complications as chorioamnionitis, severe perineal lacerations, cesarean delivery rates, postpartum hemorrhage, and endomyometritis all increase progressively after 39 weeks of gestation.[24, 31, 32, 33, 22]

Timing of DeliveryThe first decision that must be made when managing an impending postterm pregnancy is whether to deliver. In certain cases (eg, nonreassuring surveillance, oligohydramnios, growth restriction, certain maternal diseases), the decision is straightforward. In these high-risk situations, the time at which the risks of remaining pregnant begin to outweigh the risks of delivery may come at an earlier gestational age (eg, 39 weeks of gestation). However, frequently several options can be considered when determining a course of action in the low-risk pregnancy. The certainty of gestational age, cervical examination findings, estimated fetal weight, patient preference, and past obstetric history must all be considered when mapping a course of action.

The main argument against a policy of routine induction of labor at 41 0/7 to 41 6/7 weeks has been that induction increases the rate of cesarean delivery without decreasing maternal and/or neonatal morbidity. Some of the studies that failed to show a reduction in fetal/neonatal morbidity were diluted by poorly dated pregnancies that were not necessarily postterm. In addition, the potential for increasing the risk for cesarean delivery with a failed induction is far less likely in the era of safe and effective cervical ripening agents.

To date, more than 10 studies have been published of elective induction of labor, many of them at 41 weeks of gestation.[50, 35, 51, 52, 53, 54] The preponderance of the evidence from these studies, including meta-analyses, find that not only is rate of cesarean delivery not increased in women who were randomized to routine induction of labor, but also more cesarean deliveries were performed in the noninduction groups, and the most frequent indication was fetal distress. Even with multiple studies, very few neonatal differences have been demonstrated. However, the reduction in meconium is statistically significant and the rate of neonatal mortality is lower.

In summary, routine induction at 41 weeks of gestation does not increase the cesarean delivery rate and may decrease it without negatively affecting perinatal morbidity or mortality. In fact, both the woman and the neonate benefit from a policy of routine induction of labor in well-dated, low-risk pregnancies at 41 weeks' gestation. Because it is associated with a lower rate of adverse outcomes, including shoulder dystocia and meconium aspiration syndrome, this policy may also prove to be more cost-effective.[55]

A policy of routine induction at 40 weeks' has few benefits, and there are multiple reasons not to allow a pregnancy to progress beyond 42 weeks.

Page 4: Bahan Referat Postterm Pregnancy

Prior to 41 weeks of gestation, the evidence becomes more scant with only 3 small, non-US, randomized, controlled trials comparing elective induction of labor to expectant management of pregnancy.[53] However, elective induction of labor is increasingly being used as a management strategy.[56, 57] While this management may be reasonable in a practice that allows 48 hours or more for the management of the latent phase and the first stage of labor overall, in a setting where induction of labor is called a failure after 18-24 hours, it will likely further increase the cesarean delivery rate.

Prevention of Postterm PregnancyAs noted above, the most decisive way to prevent postterm pregnancy is induction of labor prior to 42 weeks’ gestation. However, since complications rise during 40 and 41 weeks' gestation and both clinicians and patients are concerned about the risks of induction of labor, it is perceivably better for women to go into spontaneous labor at 39 weeks of gestation on their own. Several minimally invasive interventions have been recommended to encourage the onset of labor at term and prevent postterm pregnancy, including membrane stripping, unprotected coitus, and acupuncture.

Stripping or sweeping of the fetal membranes refers to digital separation of the membranes from the wall of the cervix and lower uterine segment. This technique, which likely acts by releasing endogenous prostaglandins from the cervix, requires the cervix to be sufficiently dilated to admit the practitioner’s finger. Although stripping of the membranes may be able to reduce the interval to spontaneous onset of labor, a reduction in operative vaginal delivery, cesarean delivery rates, or maternal or neonatal morbidity has not been consistently proven.[58, 59, 60]

Unprotected sexual intercourse causes uterine contractions through the action of prostaglandins in semen and potentially release of endogenous prostaglandins similar to stripping of the membranes. Indeed, prostaglandins were originally isolated from extract of prostate and seminal vesicle glands, hence their name. Despite some conflicting data, it appears that unprotected coitus may lead to the earlier onset of labor, reduction in postterm pregnancy rates, and less induction of labor.[61, 62, 63]

In a small randomized trial that attempted to address this question, women were randomized to a group advised to have coitus versus a control group that was not. In this study, the women advised to have coitus did so more often (60% vs 40%), the difference in the rate of spontaneous labor was not measurable in this underpowered study.[64] Similarly, the efficacy of acupuncture for induction of labor cannot be definitively assessed because of the paucity of trial data; this requires further examination.[65, 66]

Cervical Ripening and Intrapartum ManagementOnce the decision to deliver a patient has been made, the management of the labor induction depends on the clinical setting, and a brief review of cervical ripening agents and potential complications of induction of labor is appropriate. A comprehensive review of all available methods for cervical ripening, indications, contraindications, and dosing is beyond the scope of this article.

As many as 80% of patients who reach 42 weeks' gestation have an unfavorable cervical examination (ie, Bishop Score < 7). Many options are available for cervical ripening. The different preparations, indications, contraindications, and multiple dosing regimes of each require practitioners to familiarize themselves with several of the preparations.

Prostaglandin E2 gel and suppositories for vaginal application were used extensively until the late 1990s when many pharmacies stopped manufacturing them because of the advent of commercially available and less labor-intensive preparations. Currently available chemical preparations include prostaglandin E1 tablets for oral or vaginal use (misoprostol), prostaglandin E2 gel for intracervical application (dinoprostone cervical [Prepidil]), and a prostaglandin E2 vaginal insert (dinoprostone [Cervidil]). Cervidil contains 10 mg of dinoprostone and has a lower constant release of medication than Prepidil.[67] In addition, this vaginal insert device allows for easier removal in the event of uterine hyperstimulation.

Many studies have compared the efficacy and risks of various prostaglandin cervical ripening agents. Rozenburg et al performed a randomized trial comparing intravaginal misoprostol and dinoprostone vaginal insert in pregnancies at high risk of fetal distress. They found that both methods were equally safe for the induction of labor and misoprostol was actually more effective.[68]

Page 5: Bahan Referat Postterm Pregnancy

Another method for ripening the cervix is by mechanical dilation. These devices may act by a combination of mechanical forces and by causing release of endogenous prostaglandins. Foley balloon catheters placed in the cervix, extra-amniotic saline infusions, and laminaria have all been studied and have been shown to be effective.

Regardless of what method is chosen for cervical ripening, the practitioner must be aware of the potential hazards surrounding the use of these agents in the patient with a scarred uterus. In addition, the potential for uterine tachysystole and subsequent fetal distress requires that care be taken to avoid using too high a dose or too short a dosing interval in an attempt to get a patient delivered rapidly. Care should also be taken when using combinations of mechanical and pharmacologic methods of cervical ripening.

Once an induction of labor has begun, watch for the major potential complications associated with inductions beyond 41 weeks' gestation and have a plan for dealing with each. Complications include the presence of meconium, macrosomia, and fetal intolerance to labor.

The further the pregnancy progresses beyond 40 weeks, the more likely it is that significant amounts of meconium will be present. This is due to increased uteroplacental insufficiency, which leads to hypoxia in labor and activation of the vagal system. In addition, the presence of a smaller amount of amniotic fluid increases the relative concentration of meconium in utero.

Traditionally, saline amnioinfusion and aggressive nasopharyngeal and oropharyngeal suctioning at the perineum were used to decrease the risk of meconium aspiration syndrome. Recent studies contradict this standard practice. Fraser et al performed a prospective, randomized, multicenter study evaluating the risks and benefits of amnioinfusion for the prevention of meconium aspiration syndrome.[42] They concluded that in clinical settings, which have peripartum surveillance, amnioinfusion of thick meconium-stained amniotic fluid did not decrease the risk of moderate-to-severe meconium aspiration syndrome, perinatal death, or other serious neonatal disorders compared with expectant management. In addition, other recent studies have shown that deep suctioning of the airway at the perineum does not effectively prevent meconium aspiration syndrome, contrary to popular belief.

Fetal macrosomia can lead to maternal and fetal birth trauma and to arrest of both first- and second-stage labor. Because the risk of macrosomia increases throughout term and postterm pregnancies, one of the most important parts of the delivery plan is being prepared for shoulder dystocia in the event that this unpredictable, anxiety-provoking, and potentially dangerous condition arises. To prepare such an event, experienced clinicians should be present at the delivery, a stool/step next to the delivery bed should be placed to help with suprapubic pressure, and the maneuvers to reduce the shoulder dystocia should be reviewed.

Finally, intrapartum fetal surveillance in an attempt to document fetal intolerance to labor before it leads to acidosis is critical. Whether continuous fetal monitoring or intermittent auscultation is used, interpretation of the results by a well-trained clinician is of paramount importance. If the fetal heart rate tracing is equivocal, fetal scalp stimulation and/or fetal scalp blood sampling may provide the reassurance necessary to justify continuing the induction of labor. If the practitioner cannot find reassurance that the fetus is tolerating labor, cesarean delivery is recommended.

Antepartum Fetal SurveillanceAntepartum fetal surveillance is suggested in postterm pregnancies when delivery is not performed. Although no randomized prospective trials demonstrate a benefit of fetal monitoring, no proof exists that it negatively affects postterm pregnancies either. Despite a lack of evidence, antepartum fetal surveillance of postterm pregnancies has become an accepted standard of care despite a lack of consensus as to a specific regimen of surveillance to be offered.[1]

The perinatal mortality rate increases gradually throughout pregnancy, with the greatest risk affecting pregnancies continuing past 41 weeks. Therefore, although no evidence can prove that routine monitoring between 40 and 42 weeks improves perinatal outcome, ACOG states that it is reasonable to begin antepartum testing after 41 weeks' gestation.[1] In one study of this issue, Bochner et al demonstrated that initiating monitoring at 41 weeks of gestation led to lower rates of complications.[69]

Page 6: Bahan Referat Postterm Pregnancy

No single method of antenatal surveillance has been shown to be superior to any other. Options include a nonstress test, contraction stress test, full biophysical profile, modified biophysical profile (nonstress test and amniotic fluid index), or a combination of these modalities. Evaluation of the amniotic fluid level has been shown to be especially important because of demonstrated increased adverse pregnancy outcomes. Therefore, delivery should be implemented in the event of oligohydramnios with or without other nonreassuring tests. Doppler ultrasonography has been shown to provide no proven advantage for evaluating postdate or postterm pregnancies and should not be routinely used.

A modified biophysical profile has been shown to be as sensitive as a full biophysical profile. Boehm et al demonstrated that twice-weekly testing of patients at risk for fetal distress was superior to weekly testing, decreasing the rate of stillbirth from 6.1 per 1000 live births to 1.9 per 1000.

In summary, the use of a nonstress test and an amniotic fluid index 2 times per week for pregnancies continuing past 41 weeks is reasonable. In addition, if any indication during antepartum surveillance leads the practitioner to question the intrauterine environment, delivery should be expedited.

SummaryThe management of postterm pregnancies is complicated and fraught with complex issues. The decision of whether to induce labor or to proceed with expectant management with or without antepartum fetal surveillance is not taken lightly. Data support inducing labor at 41 weeks' gestation in an accurately dated, low-risk pregnancy, regardless of cervical examination findings. This strategy, although not without its critics, averts the need for antepartum fetal surveillance and does not increase the cesarean delivery rate; in fact, it may decrease the cesarean delivery rate.

ACOG Practice Bulletin. Clinical management guidelines for obstetricians-gynecologists. Number 55, September 2004 (replaces practice pattern number 6, October 1997). Management of Postterm Pregnancy.Obstet Gynecol. Sep 2004;104(3):639-46. [Medline].

Norwitz ER, Snegovskikh VV, Caughey AB. Prolonged pregnancy: when should we intervene?. Clin Obstet Gynecol. Jun 2007;50(2):547-57. [Medline].

Taipale P, Hiilesmaa V. Predicting delivery date by ultrasound and last menstrual period in early gestation.Obstet Gynecol. Feb 2001;97(2):189-94. [Medline].

Savitz DA, Terry JW Jr, Dole N, et al. Comparison of pregnancy dating by last menstrual period, ultrasound scanning, and their combination. Am J Obstet Gynecol. Dec 2002;187(6):1660-6. [Medline].

Bennett KA, Crane JM, O'shea P, et al. First trimester ultrasound screening is effective in reducing postterm labor induction rates: a randomized controlled trial. Am J Obstet Gynecol. Apr 2004;190(4):1077-81.[Medline].

Laughey AB, Nicholson JM, Washington AE. First versus Second Trimester Ultrasound: The Effect on Pregnancy Dating and Perinatal Outcomes. In Press, Am J Obstet Gynecol. 2008;[Medline].

Mogren I, Stenlund H, Hogberg U. Recurrence of prolonged pregnancy. Int J Epidemiol. Apr 1999;28(2):253-7. [Medline].

Olesen AW, Basso O, Olsen J. An estimate of the tendency to repeat postterm delivery. Epidemiology. Jul 1999;10(4):468-9. [Medline].

Divon MY, Ferber A, Nisell H, et al. Male gender predisposes to prolongation of pregnancy. Am J Obstet Gynecol. Oct 2002;187(4):1081-3. [Medline].

Oberg AS, Frisell T, Svensson AC, Iliadou AN. Maternal and fetal genetic contributions to postterm birth: familial clustering in a population-based sample of 475,429 Swedish births. Am J Epidemiol. Mar 15 2013;177(6):531-7. [Medline].

Laursen M, Bille C, Olesen AW, et al. Genetic influence on prolonged gestation: a population-based Danish twin study. Am J Obstet Gynecol. Feb 2004;190(2):489-94. [Medline].

Page 7: Bahan Referat Postterm Pregnancy

Hickey CA, Cliver SP, McNeal SF, et al. Low pregravid body mass index as a risk factor for preterm birth: variation by ethnic group. Obstet Gynecol. Feb 1997;89(2):206-12. [Medline].

Usha Kiran TS, Hemmadi S, Bethel J, et al. Outcome of pregnancy in a woman with an increased body mass index. BJOG. Jun 2005;112(6):768-72. [Medline].

Stotland NE, Washington AE, Caughey AB. Prepregnancy body mass index and the length of gestation at term. Am J Obstet Gynecol. Oct 2007;197(4):378.e1-5. [Medline].

Yudkin PL, Wood L, Redman CW. Risk of unexplained stillbirth at different gestational ages. Lancet. May 23 1987;1(8543):1192-4. [Medline].

Feldman GB. Prospective risk of stillbirth. Obstet Gynecol. Apr 1992;79(4):547-53. [Medline].

Hilder L, Costeloe K, Thilaganathan B. Prolonged pregnancy: evaluating gestation-specific risks of fetal and infant mortality. Br J Obstet Gynaecol. Feb 1998;105(2):169-73. [Medline].

Cotzias CS, Paterson-Brown S, Fisk NM. Prospective risk of unexplained stillbirth in singleton pregnancies at term: population based analysis. BMJ. Jul 31 1999;319(7205):287-8. [Medline].

Rand L, Robinson JN, Economy KE, et al. Post-term induction of labor revisited. Obstet Gynecol. Nov 2000;96(5 Pt 1):779-83. [Medline].

Smith GC. Life-table analysis of the risk of perinatal death at term and post term in singleton pregnancies.Am J Obstet Gynecol. Feb 2001;184(3):489-96. [Medline].

Froen JF, Arnestad M, Frey K, et al. Risk factors for sudden intrauterine unexplained death: epidemiologic characteristics of singleton cases in Oslo, Norway, 1986-1995. Am J Obstet Gynecol. Mar 2001;184(4):694-702. [Medline].

Yoder BA, Kirsch EA, Barth WH, et al. Changing obstetric practices associated with decreasing incidence of meconium aspiration syndrome. Obstet Gynecol. May 2002;99(5 Pt 1):731-9. [Medline].

Caughey AB, Washington AE, Laros RK Jr. Neonatal complications of term pregnancy: rates by gestational age increase in a continuous, not threshold, fashion. Am J Obstet Gynecol. Jan 2005;192(1):185-90.[Medline].

Caughey AB, Musci TJ. Complications of term pregnancies beyond 37 weeks of gestation. Obstet Gynecol. Jan 2004;103(1):57-62. [Medline].

Heimstad R, Romundstad PR, Salvesen KA. Induction of labour for post-term pregnancy and risk estimates for intrauterine and perinatal death. Acta Obstet Gynecol Scand. 2008;87(2):247-9. [Medline].

Herabutya Y, Prasertsawat PO, Tongyai T, Isarangura Na Ayudthya N. Prolonged pregnancy: the management dilemma. Int J Gynaecol Obstet. Apr 1992;37(4):253-8. [Medline].

Kahn B, Lumey LH, Zybert PA, Lorenz JM, Cleary-Goldman J, D'Alton ME, et al. Prospective risk of fetal death in singleton, twin, and triplet gestations: implications for practice. Obstet Gynecol. Oct 2003;102(4):685-92. [Medline].

Campbell MK, Ostbye T, Irgens LM. Post-term birth: risk factors and outcomes in a 10-year cohort of Norwegian births. Obstet Gynecol. Apr 1997;89(4):543-8. [Medline].

Alexander JM, McIntire DD, Leveno KJ. Forty weeks and beyond: pregnancy outcomes by week of gestation.Obstet Gynecol. Aug 2000;96(2):291-4. [Medline].

Treger M, Hallak M, Silberstein T, et al. Post-term pregnancy: should induction of labor be considered before 42 weeks?. J Matern Fetal Neonatal Med. Jan 2002;11(1):50-3. [Medline].

Caughey AB, Stotland NE, Washington AE, et al. Maternal and obstetric complications of pregnancy are associated with increasing gestational age at term. Am J Obstet Gynecol. Feb 2007;196(2):155.e1-6.[Medline].

Page 8: Bahan Referat Postterm Pregnancy

Heimstad R, Romundstad PR, Eik-Nes SH, et al. Outcomes of pregnancy beyond 37 weeks of gestation.Obstet Gynecol. Sep 2006;108(3 Pt 1):500-8. [Medline].

Caughey AB, Nicholson JM, Cheng YW, et al. Induction of labor and cesarean delivery by gestational age.Am J Obstet Gynecol. Sep 2006;195(3):700-5. [Medline].

Caughey AB, Stotland NE, Escobar GJ. What is the best measure of maternal complications of term pregnancy: ongoing pregnancies or pregnancies delivered?. Am J Obstet Gynecol. Oct 2003;189(4):1047-52.[Medline].

Hannah ME. Postterm pregnancy: should all women have labour induced? A review of the literature. Fetal and Maternal Medicine Review. 1993;5:3.

American College of Obstetricians and Gynecologists. Fetal Macrosomia. ACOG Practice Bulletin #22. ACOG. Washington, DC: 2000.

Spellacy WN, Miller S, Winegar A, et al. Macrosomia--maternal characteristics and infant complications.Obstet Gynecol. Aug 1985;66(2):158-61. [Medline].

Rosen MG, Dickinson JC. Management of post-term pregnancy. N Engl J Med. Jun 11 1992;326(24):1628-9.[Medline].

Shime J, Librach CL, Gare DJ, et al. The influence of prolonged pregnancy on infant development at one and two years of age: a prospective controlled study. Am J Obstet Gynecol. Feb 1986;154(2):341-5. [Medline].

Kabbur PM, Herson VC, Zaremba S, et al. Have the year 2000 neonatal resuscitation program guidelines changed the delivery room management or outcome of meconium-stained infants?. J Perinatol. Nov 2005;25(11):694-7. [Medline].

Hofmeyr GJ. Amnioinfusion for meconium-stained liquor in labour. Cochrane Database Syst Rev. 2002;CD000014. [Medline].

[Best Evidence] Fraser WD, Hofmeyr J, Lede R, Faron G, Alexander S, Goffinet F, et al. Amnioinfusion for the prevention of the meconium aspiration syndrome. N Engl J Med. Sep 1 2005;353(9):909-17. [Medline].

Vain NE, Szyld EG, Prudent LM, et al. Oropharyngeal and nasopharyngeal suctioning of meconium-stained neonates before delivery of their shoulders: multicentre, randomised controlled trial. Lancet. Aug 14-20 2004;364(9434):597-602. [Medline].

Badawi N, Kurinczuk JJ, Keogh JM, Alessandri LM, O'Sullivan F, Burton PR, et al. Antepartum risk factors for newborn encephalopathy: the Western Australian case-control study. BMJ. Dec 5 1998;317(7172):1549-53.[Medline].

[Best Evidence] Bruckner TA, Cheng YW, Caughey AB. Increased neonatal mortality among normal-weight births beyond 41 weeks of gestation in California. Am J Obstet Gynecol. Jul 16 2008;[Medline].

Nicholson JM, Kellar LC, Kellar GM. The impact of the interaction between increasing gestational age and obstetrical risk on birth outcomes: evidence of a varying optimal time of delivery. J Perinatol. Jul 2006;26(7):392-402. [Medline].

Moster D, Wilcox AJ, Vollset SE, Markestad T, Lie RT. Cerebral palsy among term and postterm births.JAMA. Sep 1 2010;304(9):976-82. [Medline].

Eden RD, Seifert LS, Winegar A, et al. Perinatal characteristics of uncomplicated postdate pregnancies.Obstet Gynecol. Mar 1987;69(3 Pt 1):296-9. [Medline].

Heimstad R, Romundstad PR, Hyett J, et al. Women's experiences and attitudes towards expectant management and induction of labor for post-term pregnancy. Acta Obstet Gynecol Scand. 2007;86(8):950-6.[Medline].

Page 9: Bahan Referat Postterm Pregnancy

Hannah ME, Hannah WJ, Hellmann J, Hewson S, Milner R, Willan A. Induction of labor as compared with serial antenatal monitoring in post-term pregnancy. A randomized controlled trial. The Canadian Multicenter Post-term Pregnancy Trial Group. N Engl J Med. Jun 11 1992;326(24):1587-92. [Medline].

NICHD. A clinical trial of induction of labor versus expectant management in postterm pregnancy. The National Institute of Child Health and Human Development Network of Maternal-Fetal Medicine Units. Am J Obstet Gynecol. Mar 1994;170(3):716-23. [Medline].

Knox GE, Huddleston JF, Flowers CE Jr. Management of prolonged pregnancy: results of a prospective randomized trial. Am J Obstet Gynecol. Jun 15 1979;134(4):376-84. [Medline].

[Best Evidence] Gülmezoglu AM, Crowther CA, Middleton P. Induction of labour for improving birth outcomes for women at or beyond term. Cochrane Database Syst Rev. Oct 18 2006;CD004945. [Medline].

Sanchez-Ramos L, Olivier F, Delke I, et al. Labor induction versus expectant management for postterm pregnancies: a systematic review with meta-analysis. Obstet Gynecol. Jun 2003;101(6):1312-8. [Medline].

Kaimal AJ, Little SE, Odibo AO, Stamilio DM, Grobman WA, Long EF, et al. Cost-effectiveness of elective induction of labor at 41 weeks in nulliparous women. Am J Obstet Gynecol. Feb 2011;204(2):137.e1-9.[Medline].

Caughey AB, Bishop JT. Maternal complications of pregnancy increase beyond 40 weeks of gestation in low-risk women. J Perinatol. Sep 2006;26(9):540-5. [Medline].

Menticoglou SM, Hall PF. Routine induction of labour at 41 weeks gestation: nonsensus consensus. BJOG. May 2002;109(5):485-91. [Medline].

[Best Evidence] de Miranda E, van der Bom JG, Bonsel GJ, et al. Membrane sweeping and prevention of post-term pregnancy in low-risk pregnancies: a randomised controlled trial. BJOG. Apr 2006;113(4):402-8.[Medline].

Boulvain M, Stan C, Irion O. Membrane sweeping for induction of labour. Cochrane Database Syst Rev. Jan 25 2005;CD000451. [Medline].

Kashanian M, Akbarian A, Baradaran H, et al. Effect of membrane sweeping at term pregnancy on duration of pregnancy and labor induction: a randomized trial. Gynecol Obstet Invest. 2006;62(1):41-4. [Medline].

Tan PC, Andi A, Azmi N, et al. Effect of coitus at term on length of gestation, induction of labor, and mode of delivery. Obstet Gynecol. Jul 2006;108(1):134-40. [Medline].

Schaffir J. Sexual intercourse at term and onset of labor. Obstet Gynecol. Jun 2006;107(6):1310-4. [Medline].

Kavanagh J, Kelly AJ, Thomas J. Sexual intercourse for cervical ripening and induction of labour. Cochrane Database Syst Rev. 2001;CD003093. [Medline].

[Best Evidence] Tan PC, Yow CM, Omar SZ. Effect of coital activity on onset of labor in women scheduled for labor induction: a randomized controlled trial. Obstet Gynecol. Oct 2007;110(4):820-6. [Medline].

Rabl M, Ahner R, Bitschnau M, et al. Acupuncture for cervical ripening and induction of labor at term--a randomized controlled trial. Wien Klin Wochenschr. Dec 17 2001;113(23-24):942-6. [Medline].

Smith CA, Crowther CA. Acupuncture for induction of labour. Cochrane Database Syst Rev. 2004;CD002962. [Medline].

Akay NÖ, Hizli D, Yilmaz SS, Yalvaç S, Kandemir O. Comparison of low-dose oxytocin and dinoprostone for labor induction in postterm pregnancies: a randomized controlled prospective study. Gynecol Obstet Invest. 2012;73(3):242-7. [Medline].

Page 10: Bahan Referat Postterm Pregnancy

Rozenberg P, Chevret S, Senat MV, et al. A randomized trial that compared intravaginal misoprostol and dinoprostone vaginal insert in pregnancies at high risk of fetal distress. Am J Obstet Gynecol. Jul 2004;191(1):247-53. [Medline].

Bochner CJ, Medearis AL, Davis J, et al. Antepartum predictors of fetal distress in postterm pregnancy. Am J Obstet Gynecol. Aug 1987;157(2):353-8. [Medline].

Alfirevic Z, Walkinshaw SA. Management of post-term pregnancy: to induce or not?. Br J Hosp Med. Sep 7-20 1994;52(5):218-21. [Medline].

American College of Obstetricians and Gynecologists. Antepartum fetal surveillance. ACOG Practice Bulletin #9. ACOG. Washington, DC: 1999.

Bochner CJ, Williams J 3rd, Castro L, et al. The efficacy of starting postterm antenatal testing at 41 weeks as compared with 42 weeks of gestational age. Am J Obstet Gynecol. Sep 1988;159(3):550-4. [Medline].

Clement D, Schifrin BS, Kates RB. Acute oligohydramnios in postdate pregnancy. Am J Obstet Gynecol. Oct 1987;157(4 Pt 1):884-6. [Medline].

Cotzias CS, Paterson-Brown S, Fisk NM. Prospective risk of unexplained stillbirth in singleton pregnancies at term: population based analysis. BMJ. Jul 31 1999;319(7205):287-8. [Medline].

Crowley P. Interventions for preventing or improving the outcome of delivery at or beyond term. Cochrane Database Syst Rev. 2000;CD000170. [Medline].

Crowley P, O'Herlihy C, Boylan P. The value of ultrasound measurement of amniotic fluid volume in the management of prolonged pregnancies. Br J Obstet Gynaecol. May 1984;91(5):444-8. [Medline].

Foong LC, Vanaja K, Tan G, et al. Membrane sweeping in conjunction with labor induction. Obstet Gynecol. Oct 2000;96(4):539-42. [Medline].

Gardosi J, Vanner T, Francis A. Gestational age and induction of labour for prolonged pregnancy. Br J Obstet Gynaecol. Jul 1997;104(7):792-7. [Medline].

Grant JM. Induction of labour confers benefits in prolonged pregnancy. Br J Obstet Gynaecol. Feb 1994;101(2):99-102. [Medline].

Guinn DA, Goepfert AR, Christine M, et al. Extra-amniotic saline, laminaria, or prostaglandin E(2) gel for labor induction with unfavorable cervix: a randomized controlled trial. Obstet Gynecol. Jul 2000;96(1):106-12.[Medline].

Harman JH Jr, Kim A. Current trends in cervical ripening and labor induction. Am Fam Physician. Aug 1999;60(2):477-84. [Medline].

Hashimoto B, Filly RA, Belden C, et al. Objective method of diagnosing oligohydramnios in postterm pregnancies. J Ultrasound Med. Feb 1987;6(2):81-4. [Medline].

Laursen M, Bille C, Olesen AW, et al. Genetic influence on prolonged gestation: a population-based Danish twin study. Am J Obstet Gynecol. Feb 2004;190(2):489-94. [Medline].

Martin JA, Hamilton BE, Sutton PD, et al. Births: final data for 2005. Natl Vital Stat Rep. Dec 5 2007;56(6):1-103. [Medline].

Morris JM, Thompson K, Smithey J, et al. The usefulness of ultrasound assessment of amniotic fluid in predicting adverse outcome in prolonged pregnancy: a prospective blinded observational study. BJOG. Nov 2003;110(11):989-94. [Medline].

Naeye RL. Causes of perinatal mortality excess in prolonged gestations. Am J Epidemiol. Nov 1978;108(5):429-33. [Medline].

Neilson JP. Ultrasound for fetal assessment in early pregnancy. Cochrane Database Syst Rev. 2000;CD000182. [Medline].

Page 11: Bahan Referat Postterm Pregnancy

Neilson JP. Ultrasound for fetal assessment in early pregnancy. Cochrane Database Syst Rev. 2000;CD000182. [Medline].

Nicholson JM, Kellar LC, Cronholm PF, et al. Active management of risk in pregnancy at term in an urban population: an association between a higher induction of labor rate and a lower cesarean delivery rate. Am J Obstet Gynecol. Nov 2004;191(5):1516-28. [Medline].

\Nicholson JM, Parry S, Caughey AB, et al. The impact of the active management of risk in pregnancy at term on birth outcomes: a randomized clinical trial. Am J Obstet Gynecol. May 2008;198(5):511.e1-15. [Medline].

Oz AU, Holub B, Mendilcioglu I, et al. Renal artery Doppler investigation of the etiology of oligohydramnios in postterm pregnancy. Obstet Gynecol. Oct 2002;100(4):715-8. [Medline].

Rozenberg P, Chevret S, Ville Y. [Comparison of pre-induction ultrasonographic cervical length and Bishop score in predicting risk of cesarean section after labor induction with prostaglandins]. Gynecol Obstet Fertil. Jan-Feb 2005;33(1-2):17-22. [Medline].

Saari-Kemppainen A, Karjalainen O, Ylöstalo P, et al. Ultrasound screening and perinatal mortality: controlled trial of systematic one-stage screening in pregnancy. The Helsinki Ultrasound Trial. Lancet. Aug 18 1990;336(8712):387-91. [Medline].

Seyb ST, Berka RJ, Socol ML, et al. Risk of cesarean delivery with elective induction of labor at term in nulliparous women. Obstet Gynecol. Oct 1999;94(4):600-7. [Medline].

Shaw K, Clark SL. Reliability of intrapartum fetal heart rate monitoring in the postterm fetus with meconium passage. Obstet Gynecol. Dec 1988;72(6):886-9. [Medline].

Shea KM, Wilcox AJ, Little RE. Postterm delivery: a challenge for epidemiologic research. Epidemiology. Mar 1998;9(2):199-204. [Medline].

Silver RM, Landon MB, Rouse DJ, et al. Maternal morbidity associated with multiple repeat cesarean deliveries. Obstet Gynecol. Jun 2006;107(6):1226-32. [Medline].

Stokes HJ, Roberts RV, Newnham JP. Doppler flow velocity waveform analysis in postdate pregnancies.Aust N Z J Obstet Gynaecol. Feb 1991;31(1):27- 30. [Medline].

Sullivan CA, Benton LW, Roach H,et al. Combining medical and mechanical methods of cervical ripening. Does it increase the likelihood of successful induction of labor?. J Reprod Med. Nov 1996;41(11):823-8.[Medline].

Usha Kiran TS, Hemmadi S, Bethel J, et al. Outcome of pregnancy in a woman with an increased body mass index. BJOG. Jun 2005;112(6):768-72. [Medline].

Vahratian A, Zhang J, Troendle JF, et al. Labor progression and risk of cesarean delivery in electively induced nulliparas. Obstet Gynecol. Apr 2005;105(4):698-704. [Medline].

Ventura SJ, Martin JA, Curtin SC, et al. Births: final data for 1998. Natl Vital Stat Rep. Mar 28 2000;48(3):1-100. [Medline]

Waldenstrom U, Axelsson O, Nilsson S, et al. Effects of routine one-stage ultrasound screening in pregnancy: a randomised controlled trial. Lancet. Sep 10 1988;2(8611):585-8. [Medline]

Xenakis EM, Piper JM, Conway DL, et al. Induction of labor in the nineties: conquering the unfavorable cervix. Obstet Gynecol. Aug 1997;90(2):235-9. [Medline].

Yeast JD, Jones A, Poskin M. Induction of labor and the relationship to cesarean delivery: A review of 7001 consecutive inductions. Am J Obstet Gynecol. Mar 1999;180(3 Pt 1):628-33.

Yoder BA, Gordon MC, Barth WH Jr. Late-preterm birth: does the changing obstetric paradigm alter the epidemiology of respiratory complications?. Obstet Gynecol. Apr 2008;111(4):814-22

http://emedicine.medscape.com/article/261369-overview#a30 post term pregnancy

Page 12: Bahan Referat Postterm Pregnancy

Post-term birth and the risk of behavioural and emotional problems in early childhood

1. Hanan El Marroun 1 ,2,*, 2. Mijke Zeegers 1 ,3, 3. Eric AP Steegers 4 , 4. Jan van der Ende 1 ,5. Jacqueline J Schenk 5 , 6. Albert Hofman 6 , 7. Vincent WV Jaddoe 2 ,6,7, 8. Frank C Verhulst 1  and9. Henning Tiemeier 1 ,6,8

+Author Affiliations1. 1Department of Child and Adolescent Psychiatry, Erasmus MC—Sophia,

Rotterdam, The Netherlands, 2The Generation R Study Group, Erasmus MC, Rotterdam, The Netherlands, 3Pallas Health Research and Consultancy, Rotterdam, The Netherlands, 4Department of Obstetrics and Gynecology, Erasmus MC, Rotterdam, The Netherlands, 5Department of Psychology, Erasmus University Rotterdam, The Netherlands, 6Department of Epidemiology, Erasmus MC, Rotterdam, The Netherlands, 7Department of Pediatrics, Erasmus MC, Rotterdam, The Netherlands and 8Department of Psychiatry, Erasmus MC, Rotterdam, The Netherlands

1. ↵ *Corresponding author. Department of Child and Adolescent Psychiatry, Erasmus MC—Sophia, P.O. Box 2060, 3000 CB Rotterdam, The Netherlands. Email:[email protected]

Accepted February 23, 2012. 

Next Section

Abstract

Background Post-term birth, defined as birth after pregnancy duration of 42 weeks, is associated with increased neonatal morbidity and mortality. The long-term consequences of post-term birth are unknown. We assessed the association of post-term birth with problem behaviour in early childhood.Methods The study was performed in a large population-based prospective cohort study in Rotterdam, The Netherlands. Pregnant mothers enrolled between 2001 and 2005. Of a cohort of 5145 children, 382 (7%) were born post-term, and 226 (4%) were born preterm. Parents completed a standardized and validated behavioural checklist (Child Behavior Checklist, CBCL/1.5–5) when their children were 1.5 and 3 years old. We examined the relation between gestational age (GA) at birth, based on early fetal ultrasound examination, and problem behaviour with regression analyses, adjusting for socio-economic and pregnancy-related confounders.Results A quadratic relationship between GA at birth and problem behaviour indicates that both preterm and post-term children have higher behavioural and emotional problem scores than the term born children. Compared with term born children, post-term born children had a higher risk for overall problem behaviour [odds ratio (OR) = 2.10, 95% confidence interval (CI) = 1.32–3.36] and were almost two and a half times as likely to have attention deficit / hyperactivity problem behaviour (OR = 2.44, 95% CI = 1.38–4.32).Conclusions Post-term birth was associated with more behavioural and emotional problems in early childhood, especially attention deficit / hyperactivity problem behaviour. When considering expectant management, this aspect of post-term pregnancy should be taken into account.

Page 13: Bahan Referat Postterm Pregnancy

Key words

Post-term birth

 

preterm birth

 

behavioural and emotional problems

childhood

Previous Section Next Section

Introduction

Timely onset of labour is important for peri- and post-natal health. Both preterm (<37 weeks of gestation) and post-term birth (≥42 weeks of gestation) are associated with neonatal morbidity and mortality.1–3 Local management protocols with regard to elective caesarean delivery and labour induction affect the prevalence of post-term birth. Overall, labour induction before or at 42 weeks of gestation has increased,1 but post-term births still occur relatively frequently (up to 5–10%), even in industrialized countries.3,4 Accurate pregnancy dating is critical to the diagnosis of post-term births.3,4 Routine use of ultrasound to confirm pregnancy dating can decrease occurrence of post-term birth.5 Common risk factors for post-term birth include obesity, nulliparity and prior post-term birth and rare causes include placental sulphatase deficiency (an X-linked recessive disorder characterized by low estriol levels), fetal adrenal hypoplasia or insufficiency and trisomy 16 and 18.1,2,6,7

The long-term problems associated with preterm birth, such as increased incidence of cerebral palsy, sensory impairments and behavioural problems are well known.8 The studies investigating effects of post-term birth have focused on the risks during pregnancy and delivery.9 Post-term birth increased the risk of neonatal encephalopathy and death during the first year of life,5,10 but the long-term consequences are unclear. One of the few studies performed found that post-term born infants did not differ from controls at age 2 years regarding general intelligence, physical milestones and illnesses.11 However, a recent study using referral to a neurologist or psychologist as indicator of developmental problems found that 13% of children born post-term had a neurological or developmental disorder at the age of 5 years.12

In this population-based prospective study, we hypothesize that post-term birth is related to behavioural and emotional problems in preschool children. In order to examine the specificity of the association between post-term birth and problem behaviour, we examined specific behavioural and emotional problems including attention deficit / hyperactivity disorder problems (ADHD), affective problems and pervasive developmental problems.

Previous Section Next Section

Materials and methods

This study was embedded within the Generation R Study, a population-based cohort from fetal life onwards.13 Briefly, pregnant women who were resident in Rotterdam, The Netherlands, and whose delivery dates were between April 2002 and January 2006, were asked by their midwives and gynaecologists to participate. In the post-

Page 14: Bahan Referat Postterm Pregnancy

natal follow-up of the Generation R cohort, 7484 live born children and their prenatally recruited mothers participated. Post-natally, 38 children died. The remaining 7446 children were eligible for the study. Mothers of 477 children withdrew consent, and mothers of 410 children gave restricted consent (i.e. no participation in questionnaire studies). The remaining mothers of 6559 children gave full consent for post-natal follow-up. We excluded twin pregnancies, leaving 6422 children who could be contacted. Information on child behavioural and emotional problems at 18 and/or 36 months was available for 5145 children (response rate of 78%). Maternal report at both 18 and 36 months was available for 3840 children, 812 mothers reported at 18 months only and 493 mothers reported at 36 months only. The Medical Ethical Review Board of the Erasmus Medical Centre, Rotterdam approved the study protocol. All parents of participating children gave written informed consent.Ultrasound during the first visit determined gestational age (GA) to the nearest day, which will be expressed in our analyses in weeks. In total, 4132 women (80%) had their first ultrasound examination in early pregnancy (median 13.1 weeks, range 5.1–18.0), 868 women (17%) had it in mid-pregnancy (20.4 weeks, 18.1–25.0) and only 145 women (3%) had their first ultrasound examination in late pregnancy (30.2 weeks, 25.1–39.2). Crown–rump length was used for pregnancy dating until a GA of 12 weeks and 5 days (crown–rump length <65 mm), and biparietal diameter was used for pregnancy dating thereafter (GA from 12 weeks and 5 days onwards, biparietal diameter >23 mm). Methods for establishing GA and standard ultrasound planes for fetal measurements have been described previously.14 Inter- and intra-observer intra-class correlation coefficients were all >0.98.14

Preterm birth was defined as birth before 37 weeks gestation (N = 226) and post-term birth was defined as birth after ≥42 weeks gestation (N = 382). As an additional comparison group, we defined a group of children born before 35 weeks of gestation (N = 78) which is normally included in cohorts of preterm babies.The Child Behavior Checklist for toddlers (CBCL/1.5–5) was used to obtain standardized parental reports of children’s behavioural and emotional problems.15,16 The CBCL was a postal questionnaire and sent to be filled out by the mother when the child was 18 months old and again when the child was 36 months old. At 36 months of age, we also asked the father to fill out the CBCL. Each item (99 items in total) is scored on a three-point scale (0 = not true, 1 = somewhat or sometimes true and 2 = very true or often true), based on the child’s behaviour during the preceding 2 months. The sum of all problem items is the Total Problems score. There are five Diagnostic and Statistical Manual of Mental Disorders (DSM)-oriented scales: anxiety problems, affective problems, pervasive developmental problems, ADHD and oppositional defiant problems. It has been shown that these DSM-oriented scales provide accurate and supplementary information on clinical diagnoses.17 Also, good reliability and validity have been reported for the CBCL.16 We used the clinical cut-off scores (91st percentile for the Total Problems score and 98th percentile for the syndrome scales) to classify children as having behavioural problems in the clinical range.17 When parents filled out the questionnaire, they were not aware of our research question exploring the relation between post-term birth and behavioural problems, but parents generally are aware of the GA of their child and the risks associated with preterm birth. The maternal CBCL Total Problems ratings at 18 months and 36 months were correlated (r = 0.58, P < 0.001). Maternal and paternal CBCL Total Problems ratings at 36 months were correlated (r = 0.56, P < 0.001).Several covariates were considered in the analyses and were chosen based on the existing literature and effect estimate changes. Maternal weight and height were measured at intake. We used postal questionnaires to obtain information on mother’s parity, ethnicity and family income. Maternal ethnicity was defined according to the classification of Statistics Netherlands.18 Educational level was categorized into three levels: primary, secondary and higher education.19 Information

Page 15: Bahan Referat Postterm Pregnancy

about maternal smoking and alcohol use was obtained by questionnaires in each trimester. Based on these questionnaires, maternal smoking or drinking were categorized into ‘no’, ‘until pregnancy was known’ and ‘continued during pregnancy’ as described previously.20 The Brief Symptom Inventory (BSI) was used to assess maternal psychopathology in mid-pregnancy; the BSI is a validated self-report questionnaire, which defines a spectrum of psychiatric symptoms.21 Registries provided information on obstetric variables such as induction, birthweight, mode of delivery, umbilical artery pH and Apgar scores after 1 and 5 min. The post-natal questionnaire administered at age 6 and 12 months was used to gather information on breastfeeding and frequency of day care use.For descriptive analyses, children were categorized in three groups based on GA: (i) born after 37 weeks of gestation up to and including 41 weeks and 6 days (term, reference group); (ii) born after <37 weeks of gestation (preterm); and (iii) born after 42 + 0 weeks of gestation or more (post-term). Chi-square and t-tests were used to compare maternal and child characteristics. To test the associations between GA and behavioural problems, we used linear regression models with GA as a continuous variable. We used the generalized estimating equation (GEE) to analyse the relation of GA with the behavioural and emotional outcomes measured at different time points. GEE adjusts for auto-correlation within the same subject. We used an unstructured correlation matrix, and thus no assumptions were made about the correlations. The GEE procedure provides a more precise effect estimate and reduces the error derived from multiple comparisons (Type I error). A quadratic term was added to the linear regression models to test whether the associations between GA and behavioural problems were curvilinear. We conducted the primary analyses in all children, thus also including the children whose GA was assessed in the second and third trimester. This was done to reduce the risk of potential selection bias. Furthermore, we reran the analyses including only those children with a GA dating in early pregnancy (N = 4132), because GA dating by ultrasound is assumed to be more accurate in early pregnancy.5

Moreover, we performed linear regression analyses for maternal ratings at 18 and 36 months separately to assess whether the quadratic association between GA at birth and child total problems was present at both ages. We also performed the same linear regression analyses for paternal ratings at 36 months. The results of these analyses can be found in theSupplementary data, available at IJE online.Both linear and quadratic analyses were rerun after exclusion of the preterm children, to ascertain that the relationship between GA and behavioural problems was not solely driven by the preterm children. In addition, we restricted the analyses to the children born after 39 weeks of gestation. To check whether results were not unduly influenced by ethnicity, we reran analyses regarding the Total Problems score including only the indigenous Dutch children. Gender-specific estimates for the quadratic association between GA at birth and child behavioural problems are provided in the Supplementary Table S1, available as Supplementary data at IJE online.For logistic regression analyses, scales were dichotomized using the clinical cut-offs. We further explored the nature of the association between GA and behavioural problems with the GEE approach, and calculated the odds ratios (ORs) of clinical problem behaviour for pre- and post-term born children. We analysed only those scales on which >0.5% of the participants were classified as having clinical problems; these were the ADHD, affective problems and pervasive developmental problems scales.

Potential confounders were chosen based on the literature and effect estimate changes. Both linear and logistic regression models were adjusted for child gender, maternal age, education, ethnicity, psychopathology, smoking and drinking during pregnancy, family income and age of the child at the time of assessments of the CBCL. Maternal weight, height, parity, breastfeeding and day care did not change the effect estimates (<5%). Maternal age, psychopathology and age of the child

Page 16: Bahan Referat Postterm Pregnancy

were used as continuous variables. Maternal education, ethnicity, smoking, drinking and family income were used as categorical variables in the analyses.

Several post-hoc analyses were performed, including only post-term children without induction, without assisted extraction or no high birthweight (>4000 g) to test if effects were driven by these birth characteristics.

Not all variables were available for each participant, the mean proportion of missing values was 5.1% and these were imputed. Variables were centred and missing data were imputed with the mean or, for categorical variables, dummy variables were made. The association between GA at birth and child behaviour problems of the imputed and non-imputed data set were compared, and these associations were similar. Therefore, we only report results of analyses with the imputed data.

For the non-response analysis, we compared maternal and child characteristics of included participants with participants from whom we did not obtain behavioural data. Non-responders were lower educated (14.7% primary education vs 6.3%, P < 0.001), younger (maternal age 28.1 vs 31.2 years, P < 0.001), more likely to be non-Dutch (62.0 vs 35.4%, P < 0.001). Excluded infants had a lower birthweight (3313 vs 3431 g, P < 0.001) and were born after a shorter period of gestation (39.5 vs 39.8 weeks, P < 0.001), compared with included infants. The proportion of children born post-term was lower in the non-response group than in the response group (5.8 vs 6.9%, P < 0.001).Previous Section Next Section

Results

Table 1 compares demographic and birth characteristics of 5145 children of whom 4537 (88.2%) were born at term, 382 were born post-term (7.4%) and 226 were born preterm (4.4%).

View this table:

In this window  

In a new window

Table 1

Maternal and child characteristics in the study population

In Figure 1, the unadjusted associations between the Total Problems scale and GA at age 18 and 36 months are shown. The curves show a nadir of the Total Problems score in children born with a GA around 40 weeks, whereas the mean problem scores are higher in children who are born more preterm or more post-term. In addition, we present a scatterplot of the correlation between GA at birth and Total Problems score in theSupplementary data, available at IJE online.

View larger version:

In this page  

In a new window

Page 17: Bahan Referat Postterm Pregnancy

Download as PowerPoint Slide

Figure 1

The unadjusted association between GA at birth and total behavioural and emotional problem score

For continuous scores on the total problems, ADHD, affective problems scales and pervasive developmental problems, linear regression analyses showed a curvilinear relation between GA and behavioural problems, indicating that children with shorter or longer gestation had higher behavioural problem scores compared with children born at term (Table 2). After exclusion of the preterm born children, the curvilinear relations between GA and behavioural problems remained, showing that mean problem scores were higher in children with a longer GA [Total Problems score β GA2 = 0.34, 95% confidence interval (CI) = 0.14–0.54]. When we restricted the analyses to the children born after 39 weeks of gestation (n = 4115), we still observed a linear association between GA at birth and total child behavioural and emotional problems (data not shown).

View this table:

In this window  

In a new window

Table 2

Association between GA at birth and behavioural and emotional problem score (continuous)

Supplementary analyses demonstrated that results were similar when children with second or third trimester GA dating were excluded (Total Problems score β GA2 = 0.12, 95% CI = 0.06–0.18). Moreover, analyses on the Total Problems score were rerun in a smaller subset of Dutch children; the results were somewhat similar (β GA2 = 0.08, 95% CI = 0.01–0.12). In addition, there was no interaction between GA and the two time points of CBCL measurement indicating that effects remained stable over early childhood (data not shown).Separate linear regression analyses using the two maternal ratings each demonstrated that the quadratic association between GA at birth and child behavioural problems was present at 18 and 36 months (Supplementary Table S2, available as Supplementary data at IJE online). Analyses using the paternal ratings of child behavioural and emotional problems also demonstrated a quadratic relationship between GA at birth and child emotional and behavioural outcomes (Supplementary Table S3, available as Supplementary data at IJE online).Table 3 shows that post-term children were almost twice as likely as term born children to have clinical problem behaviour on the Total Problems scale and were more likely to have problems in the clinical range on the ADHD scale. Compared with term born children, post-term children did not have higher ORs on the affective problems or pervasive developmental problems scales.

View this table:

In this window  

In a new window

Table 3

Association between GA at birth and behavioural and emotional problems (clinical cut-off)

The preterm group showed considerably more behavioural or emotional problems compared with the term group; this group was more likely to develop problems on the Total Problems scale and the ADHD scale. With a more stringent cut-off for

Page 18: Bahan Referat Postterm Pregnancy

preterm birth (<35 weeks), we found that these children were more likely to have problems in the clinical range on the Total Problems scale, ADHD scale and the pervasive developmental problems scale.

In addition, some groups of children were excluded from the analyses. These exclusions did not change the results. The risk for developing total problems in children born post-term remained present after excluding children with induction (OR = 1.77, 95% CI = 1.01–3.10) or after excluding children >4000 g of birth weight (OR = 1.83, 95% CI = 1.06–3.15).

Previous Section Next Section

Discussion

Our study demonstrated that children born post-term were more likely than their term born peers to have emotional and behavioural problems at both 18 and 36 months after birth.

Post-term delivery and behavioural problems could be explained in several pathways. First, a larger baby typically has a higher risk for perinatal problems. Prolonged labour, cephalopelvic disproportion and shoulder dystocia are increased in post-term children.2 A perinatal lack of oxygen has been associated with behavioural problems.22 However, our results did not suggest increased fetal stress in the post-term children, as indicated by low Apgar score, low umbilical pH or meconium-stained amniotic fluid. We controlled for several birth characteristics. Moreover, exclusion of post-term children with induction and >4000 g of birth weight did not change results. A second explanation is uteroplacental insufficiency: a non-optimal ‘old’ placenta offers fewer nutrients and less oxygen than a full term fetus requires.1 The lack of nutrients and oxygen may predispose to abnormal fetal development and this may lead to abnormal emotional and behavioural development.23 In our study, we could not distinguish possible effects of uteroplacental insufficiency from perinatal problems. Thirdly, it is possible that a disturbance of the ‘placental clock’, which controls the length of pregnancy, is involved. A marker of this clock is the placental secretion of corticotrophin-releasing hormone (CRH), which is lower in women who deliver post-term than in women delivering at term.24 CRH is the principal regulator of the maternal and fetal hypothalamic–pituitary–adrenal (HPA) axis.25 It has been suggested that placental endocrine malfunctioning or maternal stress at critical times during fetal development may influence the fetal HPA axis, leading to neuroendocrine abnormalities that could increase the child’s vulnerability to emotional and behavioural problems later in life.26 Finally, the association between post-term birth and childhood behavioural problems could be explained by underlying causes of being born post-term. In other words, the cause for post-term could also be the cause for having behavioural problems, for example neurodevelopmental factors related to behavioural problems could be involved in the complex process of birth.This is a population-based study including many post-term children. We measured problem behaviour with the same validated instrument (CBCL/1.5–5) at two time points. As ultrasound gestational dating is thought to be superior to last menstrual period-based gestational dating,5we decided to use primarily ultrasound dating. Eighty percent of our sample was dated with ultrasound assessment in early pregnancy. However, some limitations must be discussed. Firstly, mothers were not formally blinded for the GA of their children and they might perceive more behavioural problems in post-term children. However, the notion that a post-term birth may signal at-risk babies is largely non-existent in the medical profession and absent in the public debate. Secondly, in the current study, we relied on the CBCL, as it was not feasible to obtain clinical diagnoses in such a large number of children. Moreover, these children were too young to be assessed by teachers or other informants, thus we had to rely on parental ratings that may be biased. Moreover,

Page 19: Bahan Referat Postterm Pregnancy

the CBCL is not a clinical instrument and cannot provide diagnoses, but addresses continuous traits in children. However, the DSM-oriented scales provide accurate information 17 and good reliability and validity have been reported.16

Finally, although we controlled for a large number of confounders, including maternal smoking, psychopathology and socio-economic characteristics, residual confounding, for example maternal malnutrition during pregnancy, cannot be ruled out.

Management of prolonged pregnancy follows two approaches: proposing induction before 42 weeks of gestation or close monitoring of pregnancy after 41 weeks with selective induction in case of fetal distress or a favourable Bishop score.4 Pregnancy and perinatal care are criticized in The Netherlands, as perinatal mortality ranks as the third worst in Europe.27 Until mid-2008, a woman with a low-risk pregnancy at 42 weeks was referred to a gynaecologist for close monitoring only. The current revised policy requires a referral at 41 weeks. Although the rate of post-term births went down after introducing first trimester ultrasound dating of GA,5 post-term delivery remains common.4

In conclusion, post-term children have a considerably higher risk of clinically relevant problem behaviour. They are more than twice as likely as term born children to have clinical ADHD. Further research is needed to determine the causes of post-term birth to reduce post-term birth rates and to minimize long-term consequences. Also, longer follow-up is necessary to establish whether the relationship between post-term birth and behavioural problems will persist.

Previous Section Next Section

Supplementary Data

Supplementary Data are available at IJE online.Previous Section Next Section

Funding

The Sophia Children’s Hospital Fund (project number 553) and the WH Kröger Foundation. The first phase of the Generation R Study is made possible by financial support from the Erasmus Medical Centre, the Erasmus University and The Netherlands Organization for Health Research and Development (Zon MW, grant ZonMW Geestkracht 10.000.1003).

Previous Section Next Section

Acknowledgments

The Generation R Study is conducted by the Erasmus Medical Centre in close collaboration with the School of Law and Faculty of Social Sciences of the Erasmus University Rotterdam, the Municipal Health Service Rotterdam area, the Rotterdam Homecare Foundation and the Stichting Trombosedienst & Artsenlaboratorium Rijnmond (STAR), Rotterdam. We gratefully acknowledge the contribution of general practitioners, hospitals, midwives and pharmacies in Rotterdam. H.E.M. checked the references used in this article for accuracy and completeness. H.T. will act as guarantor for the article. Someone with an excellent mastery of the English language has carefully edited the article. This article represents original material and has not been published previously in whole or in part. In addition, no similar paper is in press or under review elsewhere.

Conflict of interest: F.C.V. is author and head of the Department of Child and Adolescent Psychiatry at Erasmus MC, which publishes the Achenbach System of Empirically Based Assessment (ASEBA) and from which he receives remuneration. All other authors report no conflicts of interest.

Page 20: Bahan Referat Postterm Pregnancy

KEY MESSAGES

GA at birth and behavioural and emotional problems in early childhood show a non-linear quadratic relation indicating that both preterm and post-term children are at higher risk for problems.

Children born post-term were twice as likely as their term-born peers to have ADHD in early childhood.

Our results suggest that children born post-term have a neurodevelopmental delay. However, further research is needed to demonstrate a causal relation.

Published by Oxford University Press on behalf of the International Epidemiological Association © The Author 2012; all rights reserved.Previous Section

 

References

1. ↵

 

1. Caughey AB, 2. Snegovskikh VV, 3. Norwitz ER

. Postterm pregnancy: how can we improve outcomes? Obstet Gynecol Surv 2008;63:715-24.

CrossRef Medline Google Scholar

2. ↵

 

1. Norwitz ER, 2. Snegovskikh VV, 3. Caughey AB

. Prolonged pregnancy: when should we intervene? Clin Obstet Gynecol 2007;50:547-57.

CrossRef Medline Google Scholar

3. ↵

 

1. Shea KM, 2. Wilcox AJ, 3. Little RE

. Postterm delivery: a challenge for epidemiologic research. Epidemiology 1998;9:199-204.

Medline Web of Science Google Scholar

4. ↵

 

1. Zeitlin J, 2. Blondel B, 3. Alexander S, 4. Breart G

. Variation in rates of postterm birth in Europe: reality or artefact? BJOG 2007;114:1097-103.

CrossRef Medline Google Scholar

5. ↵

 

Page 21: Bahan Referat Postterm Pregnancy

1. Savitz DA, 2. Terry JW Jr., 3. Dole N, 4. Thorp JM Jr., 5. Siega-Riz AM, 6. Herring AH

.Comparison of pregnancy dating by last menstrual period, ultrasound scanning, and their combination. Am J Obstet Gynecol 2002;187:1660-66.

CrossRef Medline Web of Science Google Scholar

6. ↵

 

1. Caughey AB, 2. Stotland NE, 3. Washington AE, 4. Escobar GJ

. Who is at risk for prolonged and postterm pregnancy? Am J Obstet Gynecol 2009;200:683.e1-e5.

CrossRef Medline Google Scholar

7. ↵

 

1. Roos N, 2. Sahlin L, 3. Ekman-Ordeberg G, 4. Kieler H, 5. Stephansson O

. Maternal risk factors for postterm pregnancy and cesarean delivery following labor induction.Acta Obstet Gynecol Scand 2010;89:1003-10.

CrossRef Medline Google Scholar

8. ↵

 

1. Allen MC. Preterm outcomes research: a critical component of neonatal intensive care. Ment Retard Dev Disabil Res Rev 2002;8:221-33.

CrossRef Medline Web of Science Google Scholar

9. ↵

 

1. Olesen AW, 2. Westergaard JG, 3. Olsen J

. Perinatal and maternal complications related to postterm delivery: a national register-based study, 1978–1993. Am J Obstet Gynecol 2003;189:222-27.

CrossRef Medline Web of Science Google Scholar

10. ↵

 

1. Mogren I, 2. Stenlund H, 3. Hogberg U

. Recurrence of prolonged pregnancy. Int J Epidemiol 1999;28:253-57.

Page 22: Bahan Referat Postterm Pregnancy

Abstract / FREE   Full Text

11. ↵

 

1. Shime J, 2. Librach CL, 3. Gare DJ, 4. Cook CJ

. The influence of prolonged pregnancy on infant development at one and two years of age: a prospective controlled study. Am J Obstet Gynecol 1986;154:341-45.

Medline Web of Science Google Scholar

12. ↵

 

1. Lindstrom K, 2. Fernell E, 3. Westgren M

. Developmental data in preschool children born after prolonged pregnancy. Acta Paediatr 2005;94:1192-97.

Medline Web of Science Google Scholar

13. ↵

 

1. Jaddoe VW, 2. van Duijn CM, 3. van der Heijden AJ, 4. et al

. The Generation R Study: design and cohort update 2010. Eur J Epidemiol 2010;25:823-41.

CrossRef Medline Web of Science Google Scholar

14. ↵

 

1. Verburg BO, 2. Mulder PG, 3. Hofman A, 4. Jaddoe VW, 5. Witteman JC, 6. Steegers EA

.Intra- and interobserver reproducibility study of early fetal growth parameters.Prenat Diagn 2008;28:323-31.

CrossRef Medline Web of Science Google Scholar

15. ↵

 

1. Reijneveld SA, 2. de Kleine MJ, 3. van Baar AL, 4. et al

. Behavioural and emotional problems in very preterm and very low birthweight infants at age 5 years. Arch Dis Child Fetal Neonatal Ed 2006;91:F423-28.

Abstract / FREE   Full Text

16. ↵

 

Page 23: Bahan Referat Postterm Pregnancy

1. Achenbach TM, 2. Rescorla LA

. Manual for the ASEBA Pre-School Forms and Profiles. Burlington, VT: Research Center for Children, Youth and Families, University of Vermont; 2000.

Google Scholar

17. ↵

 

1. Nakamura BJ, 2. Ebesutani C, 3. Bernstein A, 4. Chorpita BF

. A psychometric analysis of the child behavior checklist DSM-oriented scales. J Psychopathol Behav2009;31:178-89.

CrossRef Google Scholar

18. ↵

 

Statistics Nederland. Allochtonen in Nederland 2004. Heerlen: Voorburg;2004.

19. ↵

 

Statistics Nederland. Standaard onderwijsindeling 2003. Heerlen: Voorburg;2004.

20. ↵

 

1. Roza SJ, 2. Verburg BO, 3. Jaddoe VW, 4. et al

. Effects of maternal smoking in pregnancy on prenatal brain development: the Generation R Study. Eur J Neurosci2007;25:611-17.

CrossRef Medline Web of Science Google Scholar

21. ↵

 

1. Derogatis LR. Brief Symptom Inventory (BSI): Administration, Scoring and Procedures Manual. 3rd. Minneapolis, MN: National Computer Systems; 1993.

Google Scholar

22. ↵

 

1. van Handel M, 2. Swaab H, 3. de Vries LS, 4. Jongmans MJ

. Long-term cognitive and behavioral consequences of neonatal encephalopathy following perinatal asphyxia: a review. Eur J Pediatr 2007;166:645-54.

CrossRef Medline Web of Science Google Scholar

23. ↵

 

Page 24: Bahan Referat Postterm Pregnancy

1. Courchesne E, 2. Townsend J, 3. Chase C

. Neurodevelopmental principles guide research on developmental psychopathologies. In: Cicchetti D, Cohen DJ, editors.Developmental Psychopathology. New York: Wiley; 1995. p. 195-220.

Google Scholar

24. ↵

 

1. McLean M, 2. Bisits A, 3. Davies J, 4. Woods R, 5. Lowry P, 6. Smith R

. A placental clock controlling the length of human pregnancy. Nat Med 1995;1:460-63.

CrossRef Medline Web of Science Google Scholar

25. ↵

 

1. Smith R. Parturition. N Engl J Med 2007;356:271-83.

CrossRef Medline Web of Science Google Scholar

26. ↵

 

1. Austin MP, 2. Leader LR, 3. Reilly N

. Prenatal stress, the hypothalamic–pituitary–adrenal axis, and fetal and infant neurobehaviour. Early Hum Dev 2005;81:917-26.

CrossRef Medline Web of Science Google Scholar

27. Sheldon T. Perinatal mortality in Netherlands third worst in Europe. BMJ2008;337:a3118.

http://ije.oxfordjournals.org/content/early/2012/04/11/ije.dys043.full

Prolonged and post-term pregnancies: guidelines for clinical practice from the French College of Gynecologists and Obstetricians (CNGOF)Christophe Vayssière a b    , Jean-Baptiste Haumonte c , Anne Chantry d , Frédéric Coatleven e , Marie Pascal

Debord f , Conchita Gomez g , Camille Le Ray d h , Emmanuel Lopez i , Laurent J. Salomon j , Marie Victoire

Senat k , Loïc Sentilhes l , Aurelie Serry m , Norbert Winer n , Hélène Grandjean b , Eric Verspyck o and Damien

Subtil p

Page 25: Bahan Referat Postterm Pregnancy

European Journal of Obstetrics & Gynecology and Reproductive Biology, 1, 169, pages 10 - 16

Abstract

The duration of pregnancy varies between 40+0 and 41+3 weeks. Conventionally, and essentially arbitrarily, a

pregnancy is considered to be “prolonged” after 41+0 weeks, but the infant is not considered “post-term” until

42+0 weeks (Professional consensus). A term birth thus occurs during the period from 37+0 to 41+6 weeks.

In France, prolonged pregnancies (≥41+0weeks) involve 15–20% of pregnant women, and post-term pregnancies

(≥42+0 weeks) approximately 1%. The frequency of post-term pregnancies is very heterogeneous: in Europe and

the United States, it ranges from 0.5% to 10% according to country.

In prolonged pregnancies, the cesarean section rate—especially the emergency cesarean rate—is multiplied by

approximately 1.5 (grade B). From 370–6 to 430–6 weeks, the risk of perinatal mortality increases regularly, from

0.7‰ to 5.8‰.

Meconium aspiration syndrome is responsible for substantial morbidity and mortality, and its incidence increases

regularly between 38+0 and 42+6 weeks, from 0.24‰ to 1.42‰ (grade B). Similarly, the risks of neonatal acidosis

(grade B), 5-min Apgar scores less than 7 (grade B) and admissions to neonatal intensive care (grade B)

increase progressively between 38+0 and 42+6 weeks. These risks appear to double for post-term growth-

restricted newborns (grade C).

Ultrasound dating of the pregnancy makes it possible to reduce the risk that it will be incorrectly considered

prolonged and that labor will therefore be induced unnecessarily. To harmonize practices, if the crown-rump

length (CRL) is correctly measured (this measurement should be taken between 11+0 and 13+6 weeks, when CRL

should measure from 45 to 84 mm), ultrasound dating based on it should be used to determine the official date

pregnancy began, regardless of its difference from the date assumed by the patient or estimated based on the

date of the last menstrual period. This rule does not apply to pregnancies by IVF, for which the date pregnancy

began is defined by the date of oocyte retrieval (Professional consensus).

From 370–6 to 430–6 weeks, the risk of perinatal mortality increases regularly and there is no threshold at which a

clear increase in perinatal mortality becomes visible. Fetal monitoring by cardiotocography (CTG) that begins at

41+0 weeks would cover approximately 20% of women and reduce perinatal morbidity compared with monitoring

that begins at 42+0 weeks (grade C). The frequency recommended for this monitoring ranges between two and

three times a week (Professional consensus).

For ultrasonography assessment, measurement of the largest fluid pocket is recommended, because

measurement of the amniotic fluid index (that is, the sum of the four quadrants) is accompanied by more

diagnoses of oligohydramnios, inductions of labor, and cesareans for fetal distress without any improvement in

neonatal prognosis (grade A). The practice of assessing the Manning biophysical score increases the number of

diagnoses of oligohydramnios and fetal heart rage (FHR) abnormalities and generates an increase in the rates of

inductions and cesareans without improving neonatal prognosis. The use of this biophysical score in monitoring

prolonged pregnancies is therefore not recommended (grade B).

In the absence of a specific disorder, induction of labor can be proposed in patients between 41+0 and 42+6 weeks

(grade B). Nonetheless, the choice of prolongation beyond above 42+0 weeks appears to involve an increase in

fetal risk, which must be explained to the patient and balanced against the potential disadvantages of induction

(Professional consensus).

Stripping the membranes can reduce the duration of pregnancy by increasing the number of patients going into

labor spontaneously during the week afterward (grade B). Compared to an expectant approach, it does not

increase the cesarean section rate (grade A). It reduces recourse to induction by 41% at 41+0 weeks and by 72%

at 42+0 weeks (grade B), without increasing the risk of either membrane rupture or maternal or neonatal infection

(grade B).

Page 26: Bahan Referat Postterm Pregnancy

Used as a tampon or vaginal gel, prostaglandins E2 (PGE2) are an effective method of inducing labor (grade A).

They can be used to induce labor successfully, regardless of cervical ripeness (grade A). If misoprostol is

chosen, the lowest dose is to be preferred, starting with a vaginal dose of 25 μg every 3–6 h (grade A). For

misoprostol, more powerful studies remain necessary for better defining the doses, routes of administration,

tolerance and indications. Misoprostol at any dose is contraindicated in women with uterine scars (grade B).

Placement of an intracervical Foley catheter is an effective mechanical means of inducing labor, with less uterine

hyperstimulation than prostaglandins and no increase in the cesarean section rate (grade A). Nonetheless, as the

risk of infection might be increased, this technique requires more robust evaluation before entering general

practice (grade B).

In cases of meconium-stained amniotic fluid, pharyngeal aspiration before delivery of the shoulders is not

recommended (grade A). The team managing a post-term newborn with meconium-stained amniotic fluid at birth

must know how to perform intubation and, if the intubation is not helpful, endotracheal aspiration (grade C) and

ventilation with a mask. Routine endotracheal intubation of a vigorous newborn is not recommended (grade A).

2. Definitions and conventions [6]

Depending on the method of calculation, genetic factors and some maternal characteristics, the duration of

gestation ranges from 280 to 290 days from the first day of the last menstrual period (for regular 28-day cycles).

This duration is generally expressed in France as weeks of amenorrhea, which corresponds to the English

expression “weeks of gestation”. The duration of pregnancy therefore varies between 40+0 and 41+3weeks.

Setting an official due date for women appears illusory, for these vary according to author, mode of calculation

and country. This generally does not present problems, however, for what is essential is that physicians explain

to their patients the date by which specific surveillance for “prolonged pregnancy” should start and the date at

which induction of labor might be envisioned.

Conventionally, and essentially arbitrarily, a pregnancy is considered to be “prolonged” after 41+0 weeks, but the

infant is not considered “post-term” until 42+0 weeks (professional consensus). A term birth thus occurs during the

period from 37+0 to 41+6 weeks (  Fig. 1   ). In view of the moderate, progressive increase in perinatal morbidity

during this period and beyond, the three days (at a maximum) that separate 41+0 weeks from 9 months do not

appear to produce a significant variation in perinatal complications, and this approximation between 41+0 weeks

and 9 months is acceptable (Professional consensus).

3. Frequency of prolonged and postterm pregnancies [7]

In France, prolonged pregnancies (≥41+0 weeks) involve 15–20% of pregnant women, and post-term pregnancies

(≥42+0 weeks) approximately 1%. This frequency of post-term pregnancies is very heterogeneous: in Europe and

the United States, it ranges from 0.5% to 10%, varying by and within countries (grade B). These variations

simultaneously reflect the diversity of the populations studied and the variations in obstetric practices between

countries: early pregnancy dating by ultrasound and increasingly frequent recourse to induction of labor have

jointly contributed to a progressive diminution in the incidence of prolonged and post-term pregnancies in most

countries (grade B).

4. Maternal complications of prolonged pregnancies [7]

In prolonged pregnancies, the cesarean section rate—especially the emergency cesarean rate—is multiplied by

approximately 1.5 (grade B). Nonetheless, the lack of precision in the studies prevents us from being able to

determine whether the increased cesarean risk is linked to the prolonged pregnancy or to policies that promote

induction of labor starting at some specific gestational age. Prolonged pregnancy is also accompanied by a

Page 27: Bahan Referat Postterm Pregnancy

moderate increase of the risk of third- and fourth-degree perineal lesions, postpartum hemorrhages,

chorioamnionitis and endometriosis (grade C).

5. Fetal and neonatal complications of prolonged pregnancies [8]

From 370–6 to 430–6 weeks, the risk of perinatal mortality increases regularly, from 0.7‰ to 5.8‰ (  Fig. 1   ). In

prolonged pregnancies, the fetus is at increased risk of oligohydramnios (grade C), fetal heart rate abnormalities

(grade A), and meconium-staining in utero (grade B).

The risk of in utero death has dropped considerably in recent decades (grade B). In 2001, its frequency was

estimated at 1.6‰ to 3.5‰ births in developed countries (grade B).

Meconium aspiration syndrome is responsible for substantial morbidity and mortality, and its incidence increases

regularly between 38+0 and 42+6 weeks, from 0.24‰ to 1.42‰ (grade B). Similarly, the risks of neonatal acidosis

(grade B), 5-min Apgar scores less than 7 (grade B) and admissions to neonatal intensive care (grade B)

increase progressively between 38+0 and 42+6 weeks. These risks appear to double for postterm growth-restricted

newborns (grade C). Post-term newborns have an increased risk of neurologic complications such as neonatal

convulsions (risk multiplied by 1.5) (grade B), anoxic-ischemic encephalopathy (grade C), cerebral motor

disorders (risk multiplied by 2.4) (grade B), psychomotor developmental disorders (risk multiplied by 2.2) (grade 

C) and childhood epilepsy (risk multiplied by 1.9) (grade B), but these complications cannot be directly attributed

to the post-term status. The absolute incidence of these risks nonetheless remains low.

Post-term newborns have a risk of macrosomia five times higher than that of term newborns (grade B), and

macrosomia (including in newborns of mothers without diabetes) increases the risk of hypoglycemia (grade B).

Although their prevalence remains low (less than 1%), post-term newborns are at increased risk of obstetric

injuries related to shoulder dystocia (grade B) and of bone fractures (grade C). Finally, postmaturity is a risk

factor for polycythemia (grade C), and the risk of neonatal sepsis increases by a factor of 1.3 in post-term

newborns (grade B).

6. Pregnancy dating [9]

Ultrasound dating of the pregnancy makes it possible to reduce the risk that it will be incorrectly considered

prolonged and that labor will therefore be induced unnecessarily (grade A). For spontaneous conceptions, it is

routinely recommended to use crown-rump length (CRL) measurement before 14 weeks to determine the date

pregnancy began and to calculate gestational age (grade C). Ideally, this measurement should be taken between

11+0 and 13+6 weeks (when CRL should measure from 45 to 84 mm).

To harmonize practices, if the CRL is correctly measured, the ultrasound dating based on it should be used to

determine the official date pregnancy began, regardless of its difference with the date assumed by the patient or

estimated based on the date of the last menstrual period. It should be explained to the patient that this

measurement provides the best determination of the theoretical ultrasound-determined date pregnancy began, to

serve as the reference for monitoring the pregnancy.

If the quality criteria for CRL measurement before 14 weeks are not met, the date pregnancy began should be

determined by the date of the last menstrual period and the usual duration of the patient's cycles. This rule does

not apply to pregnancies by IVF, for which the date pregnancy began is defined by the date of oocyte retrieval

(Professional consensus). Before any intervention for prolonged pregnancy, it should be verified that the best

indicators were used for dating the pregnancy: date of oocyte retrieval, CRL with its quality criteria, or date of last

menstrual period (Professional consensus).

Page 28: Bahan Referat Postterm Pregnancy

In the absence of a first trimester ultrasound and other information for dating the pregnancy (e.g., when the date

of the last menstrual period is unknown or cycles are irregular), ultrasound head measurements must be chosen

to estimate gestational age (head circumference or biparietal diameter before 18 weeks) (grade B). When

gestational age is still uncertain above 22 weeks, repeating the biometric measurements 15–20 days later makes

it possible to reassess the growth process and sometimes to estimate gestational age more accurately

(Professional consensus).

7. At what gestational age should monitoring begin and how often? [10]

From 370–6 to 430–6 weeks, the risk of perinatal mortality increases regularly and there is no threshold at which a

clear increase in perinatal mortality becomes visible. Beginning fetal monitoring at 40+0 weeks would require

close monitoring of nearly half of all pregnant women, and nothing indicates that such a policy would reduce

neonatal morbidity or mortality. On the other hand, fetal monitoring that begins at 41+0 weeks would cover

approximately 20% of women and reduce perinatal morbidity compared with monitoring that begins at 42+0 weeks

(grade C). The frequency recommended for this monitoring is 2–3 times a week (Professional consensus).7.1. Are there populations that should be particularly monitored? [10]

Fetal mortality among African–American women does not rise significantly at the end of pregnancy (grade B).

Nonetheless, no data justify modifying practices for prolonged pregnancies in this population.

The combination of fetal growth restriction and prolonged pregnancy is a risk factor for perinatal mortality (grade

C). Nonetheless, no specific data for this population allow us to define particular management for this situation.

8. What examinations are useful for monitoring prolonged pregnancies?8.1. Counting fetal movements? [11]

In prolonged pregnancies, the perceived diminution of fetal movements appears to be associated with an

increased risk of perinatal morbidity (grade C). Current data are nonetheless insufficient to show that asking

parents to count fetal movements in prolonged pregnancies yields any benefits (Professional consensus).

No method for counting these movements in this situation has been assessed.

Despite the sparse data available, it nonetheless appears sensible to recommend that patients consult their

obstetric professional when they perceive a reduction in these movements (Professional consensus). The

investigations to perform in this situation have not yet been clearly established (Professional consensus).8.2. Amnioscopy [11]

The diagnostic value of amnioscopy for predicting colored or meconium-stained amniotic fluid is mediocre (grade

C). No association has been demonstrated between colored amniotic fluid on amnioscopy and unfavorable

neonatal outcome in prolonged pregnancies (grade C). Amnioscopy is thus not useful in these cases

(Professional consensus).8.3. Visual or computerized analysis of fetal heart rate (FHR) [12]

Although visual analysis has not been associated with improved perinatal outcome in monitoring prolonged

pregnancies (grade B), recording FHR is the first-line examination for monitoring fetal well-being, and its

integration into monitoring protocols appears ineluctable (Professional consensus).

In computerized FHR analysis, a short-term variation equal to or greater than 4 ms may have a negative

predictive value near 100% for predicting fetal acidosis (grade B). Nonetheless, no study has demonstrated the

superiority of this type of analysis over visual FHR analysis in improving perinatal prognosis (grade B). Whether

or not the situation involves prolonged pregnancies, it is nonetheless a potential alternative to visual analysis,

Page 29: Bahan Referat Postterm Pregnancy

because it offers advantages in terms of organization and development of monitoring protocols, by reducing, in

particular, the duration and repetition of examinations (grade B). It may also be useful in the analysis of

suspicious tracings. The data for computerized FHR analysis, like those for visual analysis, remain insufficient to

demonstrate the value of its use in prolonged pregnancies (grade B).8.4. Oxytocin tests [12]

Oxytocin tests make it possible to reduce the false-negative rate of FHR recordings but the procedure is long and

has a false-positive rate of the order of 30%. Data are insufficient to recommend its use as a first- or second-line

tool for fetal monitoring in prolonged pregnancies (grade C).8.5. Ultrasound test for oligohydramnios [13]

In prolonged pregnancies, there is a significant association between oligohydramnios and the onset of FHR

abnormalities, meconium staining, and an increased cesarean section rate. The diagnostic value of

oligohydramnios in predicting unfavorable outcome is nonetheless only moderate (grade C).

For ultrasonography assessment, measurement of the largest fluid pocket is recommended, because

measurement of the amniotic fluid index (that is, the sum of the four quadrants) is accompanied by more

diagnoses of oligohydramnios, inductions of labor, and cesarean sections for fetal distress without any

improvement in neonatal prognosis (grade A).

In view of the risk of oligohydramnios and of increased morbidity and mortality after 41+0 weeks, it seems

reasonable to suggest prenatal ultrasound monitoring of the quantity of amniotic fluid (measurement of the

largest amniotic fluid pocket) starting at 41+0 weeks and thereafter twice a week (Professional consensus). In

cases of oligohydramnios, defined as less than 2 cm in the largest pocket, induction can be envisioned

(Professional consensus). In the absence of induction, monitoring must be reinforced (Professional consensus).8.6. Artery Doppler indexes [13]

Few studies have found a significant association between abnormal Doppler umbilical, cerebral or aortic indexes

and unfavorable outcome in pregnancies equal to or longer than 41+0 weeks. Because the diagnostic value of

these Doppler indexes is very low, their routine use for prolonged pregnancies is not recommended (grade C).8.7. The biophysical (Manning) score of fetal well-being [13]

The practice of assessing Manning biophysical scores increases the number of diagnoses of oligohydramnios

and FHR abnormalities and generates an increase in the rates of inductions and cesareans without improving

neonatal prognosis. The use of this biophysical score in monitoring prolonged pregnancies is therefore not

recommended (grade B).

9. At what point should delivery be induced? [14]

In the absence of a specific disorder, induction of labor can be proposed to patients between 41+0 and 42+6 weeks

(grade B). The moment of induction will be determined according to the mother's characteristics (local cervical

conditions, uterine scar, parity, body mass index, and age), her preference, and the organization of care in the

maternity unit (Professional consensus).

Nonetheless, the choice of prolongation beyond 42+0 weeks appears to involve an increase in fetal risk and must

therefore be explained to the patient and balanced against the potential disadvantages of induction (Professional

consensus). This comment is especially important in that the generalized use of CRL measurement during the

first trimester to estimate gestational age can increase the proportion of “true” post-term pregnancies compared

with the proportion in a similar population that includes inadequately dated pregnancies (Professional

consensus).

Page 30: Bahan Referat Postterm Pregnancy

10. How should delivery be induced? [15]10.1. Stripping the membranes [15]

Stripping (also called sweeping) the membranes can reduce the duration of pregnancy by increasing the number

of patients going into labor spontaneously during the week afterward (grade B). Compared to an expectant

approach, it does not increase the cesarean section rate (grade A). It reduces recourse to induction by 41% at

41+0 weeks and by 72% at 42+0 weeks (grade B), without increasing the risk of either membrane rupture or

maternal or neonatal infection (grade B). Its inconveniences (contractions, bleeding, and pain) must nonetheless

be clearly explained and accepted before it is practised. In view of these disadvantages, stripping the

membranes should not be performed during a routine examination without advance information and consent

(Professional consensus).10.2. Oxytocin [15]

Oxytocin administration is currently the reference method for induction of labor with a ripe cervix at 41 weeks and

later (grade A). When the cervix is unfavorable (Bishop score ≤5), oxytocin can still induce labor but is no longer

the agent of choice (grade A).10.3. E2 prostaglandins (dinoprostone) [15]

Used as a tampon or vaginal gel, prostaglandins E2 (PGE2) are an effective method of inducing labor (grade A).

They can be used to induce labor successfully, regardless of cervical ripeness (grade A). When cervical

conditions are unfavorable, PGE2 can reduce recourse to oxytocin and diminish the doses needed (grade A).

The use of PGE2 is associated with a risk of tachysystole that may be accompanied by abnormal FHR

(hyperstimulation syndrome) (grade A).10.4. E1 prostaglandins (misoprostol) [15]

Although misoprostol is not officially approved for prolonged pregnancies, it is an effective and uncomplicated

means of inducing labor, especially for a very unfavorable cervix (grade A). It is not yet clear whether vaginal or

oral administration is optimal, but the vaginal route has been assessed and chosen most often. A risk of

tachysystole with or without FHR modifications is clearly found in all studies with doses of 50 μg, but these do

not appear to increase the rates of either neonatal morbidity or cesarean delivery (grade A). The lowest doses

are to be preferred, starting with a vaginal dose of 25 μg every 3–6 h (grade A). The use of this substance

therefore requires an environment where appropriate obstetric monitoring is available in case of FHR

abnormalities. More powerful studies remain necessary for better defining the doses, routes of administration,

tolerance and indications. Misoprostol at any dose is contraindicated in women with uterine scars (grade B).10.5. Mechanical means [15]

Placement of an intracervical Foley catheter is an effective mechanical means of inducing labor, with less uterine

hyperstimulation than prostaglandins and no increase in the cesarean rate (grade A). Nonetheless, as the risk of

infection might be increased, this technique requires a more robust evaluation before entering general practice

(grade B).10.6. Other methods [15]

The current data do not show that acupuncture is effective for inducing labor either at term or in prolonged

pregnancies (grade C). Data concerning nipple stimulation and/or sexual activity are contradictory and insufficient

in this indication (grade C). Finally, the use of nitric oxide (NO) donors is under study.

10.7. Special case of the uterine scar

A uterine scar is a particular situation that exposes the woman and her fetus to the risk of uterine rupture, a risk

of the order of 0.5% in cases of spontaneous labor (grade A). This risk is increased, but moderately (0.7%), by

induction with oxytocin and multiplied by five for inductions by prostaglandins (2.45%) (grade A). It is therefore

logical to avoid non-medically indicated inductions in patients with uterine scars, to avoid prostaglandins, and to

Page 31: Bahan Referat Postterm Pregnancy

take the Bishop score into account for inductions with oxytocin. We note again that misoprostol is contraindicated

in women with uterine scars (grade B).

11. What management for the newborn? [16]

In cases of meconium-stained amniotic fluid, pharyngeal aspiration before delivery of the shoulders is not

recommended (grade A). The team managing a post-term newborn with meconium-stained amniotic fluid at birth

must know how to perform intubation and endotracheal aspiration (grade C) and ventilation with a mask, if the

intubation is not helpful. Routine endotracheal intubation of a vigorous newborn is not recommended (grade A).

Staff managing post-term newborns with perinatal asphyxia must know the initial steps to be taken in the delivery

room, know the indications for controlled hypothermia treatment (grade A) and have established a protocol for

transfer to the neonatal intensive care unit (NICU) (Professional consensus).

Systematic monitoring of blood glucose is recommended for macrosomic post-term newborns (Professional

consensus). Management of hypoglycemia in post-term newborns does not differ from that in other newborns.

The initial clinical examination of macrosomic post-term newborns should routinely include checking for paralysis

of the brachial plexus and clavicle fractures (Professional consensus).

References [1]  C. Vayssiere. Prolonged pregnancy term and beyond–method and organization. Journal de Gynecologie,

Obstetrique et Biologie de la Reproduction. 2011;40:701-702

[2]  HAS. Les recommandations pour la pratique clinique. Base méthodologique pour la réalisation en France.

Available: http://www.has-sante.fr/portail/jcms/c_431294/les-recommandations-pour-la-pratique-clinique-base-

methodologique-pour-leur-realisation-en-france   .

[3]  ACOG Committee on Practice Bulletin-Obstetrics. ACOG Practice Bulletin. Clinical management guidelines

for obstetricians-gynecologists. Number 55, September 2004 (replaces practice pattern number 6, October

1997). Management of Postterm Pregnancy. Obstetrics and Gynecology. 2004;104:639-646

[4]  Clinical Practice Obstetrics Committee, Maternal Fetal Medicine Committee, M. Delaney, et al. Guidelines for

the Management of pregnancy at 41+0 to 42+0 weeks. Journal of Obstetrics and Gynaecology Canada.

2008;30:800-823

[5]  G. Mandruzzalo, Z. Alfirevic, F. Chervenak, et al. Guidelines for the management of postterm

pregnancy. Journal of Perinatal Medicine. 2010;38:111-119

[6]  C. Le Ray, O. Anselem. Definitions of expected date of delivery and postterm delivery. Journal de

Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:703-708

[7]  A. Chantry. Epidemiology of prolonged pregnancy: incidence and maternal morbidity. Journal de Gynecologie,

Obstetrique et Biologie de la Reproduction. 2011;40:709-716

[8]  A. Chantry, E. Lopez. Fetal and neonatal complications related to prolonged pregnancy. Journal de

Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:717-725

[9]  L.J. Salomon. How to date pregnancy?. Journal de Gynecologie, Obstetrique et Biologie de la Reproduction.

2011;40:726-733

[10]  J.B. Haumonte, C. d’Ercole. Prolonged pregnancy: when should surveillance be started and what should be

the frequency?. Journal de Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:734-746

[11]  M.P. Debord. To evaluate the role of fetal movement counting and amnioscopy in the management of

prolonged pregnancies. Journal de Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:767-773

[12]  F. Coatleven. Place of fetal heart rate monitoring and its computerized analysis during the surveillance of

prolonged pregnancy. Journal de Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:774-784

[13]  M.V. Senat. Management of postterm pregnancies: the role for AFI, biophysical score and Doppler. Journal

de Gynecologie, Obstetrique et Biologie de la Reproduction. 2011;40:785-795

[14]  L. Sentilhes, P.E. Bouet, M. Mezzadri, et al. Assessment of the benefit-harm balance depending on

gestational age to induce delivery for postterm pregnancies. Journal de Gynecologie, Obstetrique et Biologie de

la Reproduction. 2011;40:747-766

Page 32: Bahan Referat Postterm Pregnancy

[15]  N. Winer. Different methods for the induction of labour in posterm pregnancy. Journal de Gynecologie,

Obstetrique et Biologie de la Reproduction. 2011;40:796-811

[16]  E. Lopez. Management of postterm neonates. Journal de Gynecologie, Obstetrique et Biologie de la

Reproduction. 2011;40:812-817

Number 579, November 2013

The American College of Obstetricians and Gynecologists Committee on Obstetric Practice Society for Maternal-Fetal MedicineThis document reflects emerging clinical and scientific advances as of the date issued and is subject to change. The information should not be construed as dictating an exclusive course of treatment or procedure to be followed.

PDF Format

Definition of Term PregnancyABSTRACT: In the past, the period from 3 weeks before until 2 weeks after the estimated date of delivery was considered “term,” with the expectation that neonatal outcomes from deliveries in this interval were uniform and good. Increasingly, however, research has shown that neonatal outcomes, especially respiratory morbidity, vary depending on the timing of delivery within this 5-week gestational age range. To address this lack of uniformity, a work group was convened in late 2012, which recommended that the label “term” be replaced with the designations early term (37 0/7 weeks of gestation through 38 6/7 weeks of gestation), full term (39 0/7 weeks of gestation through 40 6/7 weeks of gestation), late term (41 0/7 weeks of gestation through 41 6/7 weeks of gestation), and postterm (42 0/7 weeks of gestation and beyond) to more accurately describe deliveries occurring at or beyond 37 0/7 weeks of gestation. The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine endorse and encourage the uniform use of the work group’s recommended new gestational age designations by all clinicians, researchers, and public health officials to facilitate data reporting, delivery of quality health care, and clinical research.

Opinion

Gestation in singleton pregnancies lasts an average of 40 weeks (280 days) from the first day of the last menstrual period to the estimated date of delivery. In the past, the period from 3 weeks before until 2 weeks after the estimated date of delivery was considered “term” (1), with the expectation that neonatal outcomes from deliveries in this interval were uniform and good. Increasingly, however, research has identified that neonatal outcomes, especially respiratory morbidity, vary depending on the timing of delivery even within this 5-week gestational age range. The frequency of adverse neonatal outcomes is lowest among uncomplicated pregnancies delivered between 39 0/7 weeks of gestation and 40 6/7 weeks of gestation (2, 3). For this reason, quality improvement projects have focused, for example, on eliminating nonmedically indicated deliveries at less than 39 0/7 weeks of gestation (4).In order to facilitate data reporting, delivery of quality health care, and clinical research, it is important that all clinicians, researchers, and public health officials use both uniform labels when describing deliveries in this period and a uniform approach to determining gestational age. To address the lack of uniformity in neonatal outcomes between 37 0/7 weeks of gestation and 42 0/7 weeks of gestation, a work group was convened in late 2012 to determine whether term pregnancy should be redefined (5). The work group included representatives from the Eunice Kennedy Shriver National Institute of Child Health and Human Development, the American College of Obstetricians and Gynecologists (the College), the Society for Maternal-Fetal Medicine (SMFM), and other professional societies and stakeholder organizations. The work group recommended that the label “term” be replaced by the designations early term, full term, late term, and postterm to more accurately describe deliveries occurring at or beyond 37 0/7 weeks of gestation (Box 1). The group

Page 33: Bahan Referat Postterm Pregnancy

recommended that the use of the label “term” to describe all deliveries between 37 0/7 weeks of gestation and 41 6/7 weeks of gestation should be discouraged. Details of the evidence and rationale that are the foundation of these recommendations can be found in published summaries of this conference (5).

Box 1. Recommended Classification of Deliveries From 37 Weeks of Gestation

Early term: 37 0/7 weeks through 38 6/7 weeksFull term: 39 0/7 weeks through 40 6/7 weeksLate term: 41 0/7 weeks through 41 6/7 weeksPostterm: 42 0/7 weeks and beyondData from Spong CY. Defining "term" pregnancy: recommendations from the Defining "Term" Pregnancy Workgroup. JAMA 2013;309:2445–6.

The College and SMFM endorse and encourage the uniform use of the work group’s recommended new gestational age designations by all clinicians, researchers, and public health officials to facilitate data reporting, delivery of quality health care, and clinical research.

Uniform definitions of term are predicated on a uniform method of determining gestational age. The work group provided a method for determination of gestational age (5) that, like other similar methods (6), focused on a hierarchy of clinical and ultrasonographic criteria. Individual methods may differ in the details of when and how ultrasonographic biometry should be used to change estimated date of delivery based on last menstrual period; however, it is not the purpose of this document to establish the priority of one method over another. The College and SMFM are working with other expert groups to establish evidence-based consensus on criteria for determining gestational age.

References

1. World Health Organization. ICD-10: International statistical classification of diseases and related health problems, 10th revision. Volume 2. 2nd ed. Geneva: WHO; 2004. Available at: http://www.who.int/classifications/icd/ICD-10_2nd_ed_volume2.pdf. Retrieved August 12, 2013. ⇦

2. Tita AT, Landon MB, Spong CY, Lai Y, Leveno KJ, Varner MW, et al. Timing of elective repeat cesarean delivery at term and neonatal outcomes. Eunice Kennedy Shriver NICHD Maternal-Fetal Medicine Units Network. N Engl J Med 2009;360:111–20. [PubMed] [Full Text] ⇦

3. Reddy UM, Bettegowda VR, Dias T, Yamada-Kushnir T, Ko CW, Willinger M. Term pregnancy: a period of heterogeneous risk for infant mortality. Obstet Gynecol 2011;117:1279–87. [PubMed] [Obstetrics & Gynecology] ⇦

4. Nonmedically indicated early-term deliveries. Committee Opinion No. 561. American College of Obstetricians and Gynecologists. Obstet Gynecol 2013;121:911–5. [PubMed] [Obstetrics & Gynecology] ⇦

5. Spong CY. Defining “term” pregnancy: recommendations from the Defining “Term” Pregnancy Workgroup. JAMA 2013;309:2445–6. [PubMed] [Full Text] ⇦

6. Ultrasonography in pregnancy. ACOG Practice Bulletin No. 101. American College of Obstetricians and Gynecologists. Obstet Gynecol 2009;113:451–61. [PubMed] [Obstetrics & Gynecology] ⇦

Copyright November 2013 by the American College of Obstetricians and Gynecologists, 409 12th Street, SW, PO Box 96920, Washington, DC 20090-6920. All rights reserved.

ISSN 1074-861X

Definition of term pregnancy. Committee Opinion No. 579. American College of Obstetricians and Gynecologists. Obstet Gynecol 2013;122:1139–40.

A comparison of orally administered misoprostol and membrane sweeping for labour induction in uncomplicated singleton post-term pregnancies

A O Adeniji, S E Akinola

Page 34: Bahan Referat Postterm Pregnancy

 

Department of Obstetrics and Gynaecology, Ladoke Akintola University of Technology Teaching

Hospital, Osogbo, Nigeria

A O Adeniji, MB BS, FWACS, FMCOG

S E Akinola, MB BS, FWACS, FRCOG

Corresponding author: A O Adeniji ([email protected]; [email protected])

Objectives. This study assessed the efficacy of the two outpatient processes of single-dose 50 µg oral misoprostol (OM) and membrane sweeping (MS) on the outcome of labour induction and the possibility of reducing the need for hospital admission for cervical ripening/labour induction in uncomplicated post-term singleton pregnancies at a tertiary health institution in south-western Nigeria.

Methods. A total of 100 patients were equally randomised into the two groups between April 2007 and March 2010. Primary outcome measures were delivery within 48 hours after the start of induction and route of delivery. Secondary outcome measures were time interval from induction to onset of labour (latency period), time interval from start of induction to delivery (duration of labour), need for oxytocin augmentation, labour complications, Apgar scores at 1 and 5 minutes, and need for neonatal intensive care unit (NICU) admission.

Results. Both groups were similar at the baseline with regard to age, parity and days beyond 40 weeks’ gestation. There was a significantly shorter induction to onset of labour (latency) interval in the OM group, with a mean of 17.0 hours compared with 31.9 hours in the MS group (p=0.005), with 82.0% of the patients in the OM group in spontaneous labour within the latency period of 18 hours as opposed to 32.6% of the MS group (p<0.005). Forty-two patients in the OM group and 40 in the MS group had a vaginal delivery (84.0% v. 87.0%, p=0.361), with 12 and 20 patients in the OM and MS groups, respectively, requiring oxytocin augmentation (p=0.023). The duration of labour was significantly shorter in the OM group, in which 78.6% of those who had a vaginal delivery achieved it within 9 hours, compared with 57.5% in the MS group (p=0.036). Overall, neonatal outcomes and need for NICU admission were similar and comparable in the two groups. On a preference scale, 43% of the women in the MS group felt positive about the intervention, compared with 92% of the women in the OM group.

Conclusion. The study demonstrated a shorter latency period, less need for oxytocin augmentation and shorter duration of labour in patients who received OM. The two induction agents were similar with regard to neonatal outcomes and need for NICU admission. Both showed good safety profiles for outpatient care, although further assessment of the safety profile with larger studies will be needed. More patients felt positive about the intervention in the OM group than in the MS group.

S Afr J OG 2013;19(1):4-7. DOI:10.7196/SAJOG.584

 

Post-term pregnancy is fairly common in obstetric practice and is the most common indication for induction of labour.1 , 2 , 3 , 4 Recent studies have shown that the risks to the fetus5 , 6 and to the mother7 , 8 of continuing pregnancy beyond the estimated date of delivery are greater than originally thought, and induction of labour remains an accepted means of achieving vaginal delivery. In some cases the status of the cervix is unfavourable for labour induction, the success of which depends to a large extent on

Page 35: Bahan Referat Postterm Pregnancy

the consistency, compliance and configuration of the cervix.9 Various methods of cervical ripening, from membrane sweeping (MS) and use of a transcervical Foley catheter to administration of prostaglandins (PG) and prostaglandin E1 (PGE1) analogue, are therefore used.

MS involves digital separation of the fetal membranes from the lower segment of the uterus. It is an established method of promoting the onset of labour without hospital admission, and is regularly applied to prevent pregnancies extending beyond term.10 , 11 This method causes an increase in local PG production,12 , 13 which results in ripening of the cervix and ultimately brings about spontaneous onset of labour. The results of trials on the effectiveness of MS have been inconsistent,3 , 8 , 11 possibly owing to methodological differences between studies. A Cochrane review suggested that routine use of MS between 38 and 40 weeks does not seem to produce clinically important benefits;11 however, it may be beneficial in women with post-term pregnancies.14 , 15

Misoprostol, a PGE1 analogue, has been reported to be an effective and affordable cervical ripening and medical induction agent. It can be used intravaginally or orally and has excellent shelf-life. These factors are immensely advantageous in low-resource tropical countries.2 ,4 However, the processes of cervical ripening and labour induction require admission to hospital, resulting in additional costs in terms of both human and material resources. Any safe and effective interventions that also cut costs are therefore desirable. This study explored the comparative efficacy and safety of the two outpatient techniques of single-dose 50 µg oral misoprostol (OM) and MS on the outcome of labour induction and their effects on reducing the need for hospital admission for cervical ripening/labour induction in uncomplicated post-term singleton pregnancies.

MethodsThis study was a prospective, randomised controlled trial of a single dose of 50 µg OM and MS in uncomplicated singleton post-term pregnancies. All patients recruited had had early ultrasound dating of their pregnancy, which was correlated with the expected delivery date to exclude wrong dates. The study was conducted between April 2007 and March 2010 at Ladoke Akintola University of Technology Teaching Hospital, Osogbo, Nigeria. Patients with singleton post-term pregnancies were recruited after giving informed consent. One hundred sealed opaque envelopes containing papers marked OM or MS (50 each) were placed in a box, thoroughly mixed and then numerically labelled. Computer-generated random numbers were used for patient allocation. Patients were allocated sequential numbers in order of recruitment, and the correspondingly numbered envelope was opened for randomisation. The institutional ethical review committee approved the study. Inclusion criteria were a singleton live fetus, post-term pregnancy from 40 weeks and 1 day to 40 weeks and 9 days, intact fetal membranes, Bishop’s score ≤5 and cephalic presentation. Exclusion criteria were post-term pregnancies of ≥40 weeks and 10 days, multiple pregnancies, grand multiparity, cephalopelvic disproportion, previous caesarean section or a uterine scar, fetal malpresentation, fetal distress, placenta praevia, antepartum haemorrhage, premature rupture of the membranes and medical disorders.

Study groups

One hundred patients, randomised to 50 in each group, were studied. The OM group received a single 50 µg misoprostol tablet orally on an outpatient basis, and the MS group had MS once only at the antenatal clinic. Patients with unyielding cervices preventing access into the cervical canal were termed ‘failed MS’. All patients in both

Page 36: Bahan Referat Postterm Pregnancy

groups who did not go into spontaneous labour after 48 hours were categorised as ‘failed labour induction’ and together with the women with post-term pregnancies of ≥40 weeks and 10 days managed according to our departmental protocol of cervical ripening and labour induction (transcervical Foley catheter or intravaginal misoprostol) to ensure delivery before 42 weeks’ gestation.

To eliminate bias, attending obstetricians in the labour ward were blinded to the labour-inducing agents used in the study groups. Primary outcome measures were delivery within 48 hours after the start of induction and route of delivery. Secondary outcome measures were time interval from the start of induction to onset of labour (latency period), time interval from the start of induction to delivery (duration of labour), need for oxytocin augmentation, labour complications, Apgar scores at 1 and 5 minutes, and need for neonatal intensive care unit (NICU) admission.

Data were entered onto a pre-designed sheet and analysed with SPSS version 17. Mean (± standard deviation (SD)), independent t-test, Pearson’s chi-square (with Yates’ corrections as appropriate), confidence intervals (CIs) and relative risk (RR) were determined as necessary. The level of significance was set at 0.05.

ResultsA total of 100 patients (50 in each group) were recruited for the study; 4 in the MS group were categorised as ‘failed MS’. At baseline the two groups were similar with regard to mean age, parity and days beyond 40 weeks’ gestation (Table 1). Table 2 shows that the latency period was significantly shorter in the OM group than in the MS group, with a mean of 17.0 hours (CI 11.8 - 22.1) as opposed to 31.9 hours (CI 24.7 - 39.0) in the MS group (p=0.005). Eighty-two per cent of the patients in the OM group went into labour spontaneously within the latency period of 18 hours, as opposed to 32.6% in the MS group (p<0.005). Two patients in the OM group and 1 in the MS group went beyond the 48 hours time limit and were categorised as ‘failed induction’, but subsequently had a vaginal delivery after oxytocin augmentation of labour.

Table 1. Socio-demographic characteristics of study patients

Biodata OM group ( N =50) MS group ( N =50) p -value

Age (years), mean (±SD) 26.30 (±4.9) 25.38 (±5.1) 0.830

Parity, mean (±SD) 1.70 (±0.8) 1.32 (±0.9)

Nulliparous, n (%) 3 (6.0) 10 (20.0) 0.071

Multiparous, n (%) 47 (94.0) 40 (80.0)

Days beyond 40 weeks,

mean (±SD)

5.26 (±1.6) 5.00 (±1.7) 0.290

OM = oral misoprostol; MS = membrane sweeping.

Table 2. Comparison of the agents of induction with regard to latency period

Latency period (hours) OM group ( N =50) n (%)

MS group ( N =46) n (%)

p -value

<6 5 (10.0) 4 (8.7) <0.005

>6 - 12 18 (36.0) 4 (8.7)

Page 37: Bahan Referat Postterm Pregnancy

>12 - 18 18 (36.0) 7 (15.2)

>18 - 24 4 (8.0) 13 (28.3)

>24 - 48 3 (6.0) 17 (37.0)

>48 2 (4.0) 1 (2.2)

Forty-two patients in the OM group and 40 in the MS group had a vaginal delivery (84.0% v. 87.0%, p=0.361), with 12 and 20 patients, respectively, requiring oxytocin augmentation (p=0.023). Of the caesarean sections (8 in the OM group v. 6 in the MS group), 5 in the OM group were necessitated by presumed fetal distress, compared with 4 in the MS group (Table 3). The duration of labour was significantly shorter in the OM group, with 33/42 patients (78.6%) who had a vaginal delivery achieving it within 9 hours, compared with 23/40 (57.5%) in the MS group (Table 4).

Table 3. Comparison of events and outcomes of labour in the study groups

Labour events OM group ( N =50) n (%)

MS group ( N =46) n (%)

p -value (CI)

Oxytocin augmentation 0.02 (1.1 - 7.0)

Yes 12 (24.0) 20 (43.5)

No 38 (76.0) 26 (56.5)

Mode of delivery 0.36 (0.1 - 1.8)

Vaginal 42 (84.0) 40 (87.0)

Caesarean section 8 (16.0) 6 (13.0)

Table 4. Comparison of labour duration in the study groups

Duration of labour (hours) OM group ( N =42)

n (%)

MS group ( N =40)

n (%)

p -value

<6 1 (2.4) 4 (10.0) 0.036

>6 - 9 32 (76.2) 19 (47.5)

>9 - 10 8 (19.0) 12 (30.0)

>10 - 12 1 (2.4) 5 (12.5)

Overall, neonatal outcomes were similar and comparable in the two groups, with more babies in the OM group (6/50) than in the MS group (3/46) having moderate asphyxia at the first minute after birth. However, this was statistically insignificant. NICU admission rates were similar for the two groups. On a preference scale, 43% of the women in the MS group felt positive about the intervention, compared with 92% of the women in OM group who said that they would agree to use of the drug in another post-term pregnancy.

Page 38: Bahan Referat Postterm Pregnancy

Table 5. Neonatal outcomes in the study groups

Neonatal outcome factors OM group ( N =50)

MS group ( N =46)

p -value (CI)

Birth weight (g), mean (±SD) 3 123 (±328) 3 089 (±302)

Apgar score at 1 minute, mean (±SD)

7.7 (±1.0) 7.4 (±0.7) 0.150 (-0.1 - 0.6)

Apgar score at 1 minute <7, n (%)

6 (12.0) 3 (6.5) 0.358

Apgar score at 5 minutes, mean (±SD)

9.5 (±0.6) 9.478 (±0.4) 0.867 (-0.2 - 0.3)

Apgar score at 5 minutes <7 - - -

NICU admission, n (%) 2 (4.0) 2 (4.4) 0.930

DiscussionThis study randomised 100 patients, with established gestations beyond 40 weeks but less than 40 weeks and 10 days, into two groups receiving a single-dose 50 µg OM tablet or single MS on an outpatient basis. The intention was to compare the efficacy of these two methods for induction of labour, evaluate their possible impact on the number of post-term women requiring hospital admission for induction of labour at our institution, and compare fetomaternal safety profiles of the two methods. Various studies have shown individual benefits of MS as opposed to no sweeping,16 , 17 and of OM as opposed to intravaginal misoprostol or other labour-inducing agents.18 ,19 However, we did not find any study that compared MS with OM, especially in the outpatient context we adopted in this study. Outpatient management of post-term pregnancies will reduce the financial burden on families by eliminating the cost of hospital admission. It will also allow women to begin labour at home and only come into hospital for delivery, which is more like the natural process of labour and involves fewer interventions.

At baseline the two groups were similar with regard to age distribution and number of days beyond 40 weeks’ gestation. Although there were more nulliparous patients in the MS group, this was not statistically significant. Theoretically it has been argued that MS may be more effective in multiparous than nulliparous patients. This assumption has been disputed by de Miranda et al.16 and could not be substantiated by our study, although it is noteworthy that 4 patients in our nulliparous group could not have MS owing to inability to gain access to the cervical canal (failed MS), a technical challenge in this subset of patients that cannot be overlooked. Previous studies2 , 4 ,19 , 20 have demonstrated that intravaginal misoprostol was more effective at improving cervical effacement and consistency than cervical os dilatation, and also that misoprostol was a better agent for initiating labour than the transcervical Foley catheter.

Our findings suggest that both 50 µg OM and MS, administered on an outpatient basis, are safe and effective agents for inducing labour in uncomplicated post-term singleton pregnancies, with OM having the advantages of a shorter latency period, less need for oxytocin augmentation in labour and shorter duration of labour. Within 12 hours of initiation of the induction at the clinic, 46.0% of the patients in the OM group (23/50) reported back in labour, compared with 17.4% in the MS group (8/46). The proportion

Page 39: Bahan Referat Postterm Pregnancy

increased to 82.0% (41/50) by 18 hours in OM group, whereas it was 32.6% (15/46) in the MS group. The faster effect of induction in the OM group might be due to the reported rapid absorption of this agent after oral administration, peaking about 15 - 30 minutes after administration. We also reason that as misoprostol is a PGE1 analogue and undergoes rapid de-esterification to its active, free acid metabolites, its onset of action will be speedier than the local PG production via a cascade of synthetic processes that would be expected in MS.21 , 22 Studies on misoprostol have demonstrated less need for oxytocin augmentation than there was with MS, similar to our findings.2 , 23 Of our patients 24.0% in the OM group as opposed to 43.5% in the MS group required oxytocin augmentation (RR 0.5, CI 0.3 - 0.9). This further enhances acceptability of OM, as women perceive their labour as more ‘natural’ with less intervention.

The proportions of vaginal deliveries were similar in the two groups, (83.3% v. 86.7%, RR 0.1, CI 0.8 - 1.1). When duration of labour was compared, 78.6% of the OM group, but only 57.5% of the MS group achieved vaginal delivery within 9 hours of onset of labour (RR 1.2, CI 0.8 - 1.8). Neonatal outcomes in the two groups were similar and favourable, although the prevalence of moderate birth asphyxia was higher in the OM group. These episodes occurred in babies of relatively low birth weight and recovery was recorded by the Apgar score at 5 minutes. All admissions to the NICU in both groups were for observation only and the infants were discharged within 24 hours.

A major limitation of randomised trials like ours is that they are seldom large enough to study rare adverse effects. No harmful adverse effects of MS have been reported in previous studies.11 Reported adverse effects of misoprostol, such as vomiting, diarrhoea, tachysystole or hyperstimulation, were not recorded in this study, possibly because of the single low dose administered. However, 20% of the patients in the MS group reported that the procedure was uncomfortable and/or painful, similar to earlier reports,16 , 24 and 9% had minimal spotting after the procedure, which subsequently subsided. No case of rupture of the membranes or antepartum haemorrhage was recorded. On a preference scale, 43% of the women in the MS group felt positive about the intervention, compared with 92% of the women in the OM group who would agree to use of the drug in another post-term pregnancy.

ConclusionThis study showed a shorter latency period, less need for oxytocin augmentation and a shorter duration of labour in patients given single-dose OM compared with MS on an outpatient basis. The two induction agents were similar with regard to neonatal outcomes and need for NICU admission, but differences in outcomes cannot be excluded owing to the small numbers studied. Patient preference for the intervention was higher in the OM group than in the MS group.

Conflict of interest. We declare that we have no conflict of interest; no funding/grant was received for this study and there was no commercial relationship. We have full control of all primary data and agree to allow SAJOG to review our data if requested.

 

1. Harman JH, Kim A. Current trends in cervical ripening and labor induction. Am Fam

Physician 1999;60(2):477-483.

2. Adeniji OA, Oladokun A, Olayemi O, et al. Pre-induction cervical ripening: Transcervical

Foley catheter versus intravaginal misoprostol. J Obstet Gynaecol 2005;25(2):134-139.

[http://dx.doi.org/10.1080/01443610500040737]

3. Dare FO, Oboro VO. The role of membrane stripping in prevention of post-term

pregnancy: A randomised clinical trial in Ile-lfe, Nigeria. J Obstet Gynaecol

2002;22(3):283-286. [http://dx.doi.org/10.1080/01443610220130571]

Page 40: Bahan Referat Postterm Pregnancy

4. Ande AB, Ezeanochie CM, Olagbuji NB. Induction of labour in prolonged pregnancy with

unfavourable cervix: Comparison of sequential intracervical Foley catheter-intravaginal

misoprostol and intravaginal misoprostol. Arch Gynecol Obstet 2012;285(4):967-971.

[http://dx.dopi.org/10.1007/s00404-011-2094-4]

5. Caughey AB, Washington AE, Laros RK Jr. Neonatal complications of term pregnancy:

Rates by gestational age increase in a continuous, not threshold, fashion. Am J Obstet

Gynecol 2005;192(1):185-190. [http://dx.doi.org/10.1016/j.ajog.2004.06.068]

6. Heimstad R, Romundstad PR, Salvesen KA. Induction of labour for post-term pregnancy

and risk estimates for intrauterine and perinatal death. Acta Obstet Gynecol Scand

2008;87(2):247-249. [http://dx.doi.org/10.1080/00016340701743165]

7. Caughey AB, Stotland NE, Washington AE, et al. Maternal and obstetric complications of

pregnancy are associated with increasing gestational age at term. Am J Obstet Gynecol

2007;196(2):155.e1-155.e6. [http://dx.doi.org/10.1016/j.ajog.2006.08.040]

8. Heimstad R, Romundstad PR, Eik-Nes SH, et al. Outcomes of pregnancy beyond 37

weeks of gestation. Obstet Gynecol 2006;108(3 Pt 1):500-508.

[http://dx.doi.org/10.1097/01.AOG.0000227783.65800.0f]

9. Trofatter KF, Bowers D. Stanby RN, Gall A, Killam AP. Preinduction cervical ripening with

prostaglandin E2 gel. Am J Obstet Gynecol 1985;153:268-271.

10. Munro KJ, Johnson RW, Philips MH. Historical Review of British Obstetrics and

Gynaecology, 1800-1950. Edinburgh: Livingstone, 1954.

11. Boulvain M, Stan CM, Irion O. Membrane sweeping for induction of labour. Cochrane

Database of Systematic Reviews 2005, Issue 1. Art. No.: CD000451.

[http://dx.doi.org/10.1002/14651858.CD000451.pub2]

12. Mitchell MD, Flint AP, Bibby J, et al. Rapid increases in plasma prostaglandin

concentrations after vaginal examination and amniotomy. Br Med J 1977;2:1183-1185.

[http://dx.doi.org/10.1136/Fbmj.2.6096.1183]

13. Keirse MJ, Thiery M, Parewijck W, Mitchell MD. Chronic stimulation of uterine

prostaglandin synthesis during cervical ripening before the onset of labor. Prostaglandins

1983;25(5):671-682. [http://dx.doi.org/10.1016/0090-6980%2883%2990121-1]

14. el Torkey M, Grant JM. Sweeping of the membranes is an effective method of induction

of labour in prolonged pregnancy: A report of a randomized trial. Br J Obstet Gynaecol

1992;99(6):455-458. [http://dx.doi.org/10.1111/j.1471-0528.1992.tb13780.x]

15. Goldenberg M, Dulitzky M, Feldman B, Zolti M, Bider D. Stretching of the cervix and

stripping of the membranes at term: A randomised controlled study. Eur J Obstet Gynecol

Reprod Biol 1996;66(2):129-132. [http://dx.doi.org/10.1016/0301-2115%2896%2902405-

0]

16. de Miranda E, van der Bom J, Bonsel G, Bleker O, Rosendaal F. Membrane sweeping

and prevention of post-term pregnancy in low-risk pregnancies: A randomised controlled

trial. Br J Obstet Gynaecol 2006;113(4):402-408. [http://dx.doi.org/10.1111/j.1471-

0528.2006.00870.x]

17. Wong SF, Hui SK, Choi H, Ho LC. Does sweeping of membranes beyond 40 weeks

reduce the need for formal induction of labour? Br J Obstet Gynaecol 2002;109(6):632-

636. [http://dx.doi.org/10.1016/S1470-0328(028)01193-X]

18. Akter S, Chowdhury SB, Fatema N. A comparison of orally administered misoprostol

with vaginally administered misoprostol for cervical ripening and labour induction. Orion

Medical Journal 2010;33(1):710-713.

Page 41: Bahan Referat Postterm Pregnancy

19. How HY, Leaseburge L, Khoury JC, Siddiqi TA, Spinnato JA, Sibai BM. A comparision of

various routes and doses of misoprostol for cervical ripening and the induction of labour.

Am J Obstet Gynecol 2001;185(4):L911-915.

20. Adeniji AO, Olayemi O, Odukogbe AA. Intravaginal misoprostol versus transcervical

Foley catheter in pre-induction cervical ripening. Int J Gynaecol Obstet 2006;92(2):130-

132. [http://dx.doi.org/10.1016/j.ijgo.2005.10.010]

21. Tang OS, Schweer H, Seyberth HW, Lee SWH, Ho PC. Pharmacokinetics of different

routes of administration of misoprostol. Hum Reprod 2002;17(2):332-336.

[http://dx.doi.org/10.1093/humrep%2F17.2.332]

22. Brian C. Misoprostol: Pharmacokinetics and pharmacodynamics. HRB PhD Scholar

Health Services Research TCD/CWIUH/RCSI. 2010. http://www.medicine.tcd.ie/obstetrics-

gynaecology/assets/pdf/Brian-Cleary-Feb-2010.pdf (accessed 3 July 2012).

23. Alfirevic Z, Weeks A. Oral misoprostol for induction of labour. Cochrane Database of

Systematic Reviews 2006, Issue 2. Art. No.: CD001338.

[http://dx.doi.org/10.1002/14651858.CD001338.pub2]

24. Boulvain M, Fraser WD, Marcoux S, et al. Does sweeping of the membranes reduce

the need for formal induction of labour? A randomised controlled trial. Br J Obstet

Gynaecol 1998;105:34-40.