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  • 8/13/2019 Neonatal Resuscitation in the Delivery Room

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    Neonatal resuscitation in the delivery roomAuthorCaraciolo J Fernandes, MDSection EditorLeonard E Weisman, MDDeputy EditorMelanie S Kim, MDDisclosures

    All topics are updated as new evidence becomes available and ourpeer review processiscomplete.Literature review current through:Nov 2013. | This topic last updated:ago 26, 2013.

    INTRODUCTIONThe successful transition from intrauterine to extrauterine life is dependent

    upon significant physiologic changes that occur at birth. In almost all infants (90 percent), these

    changes are successfully completed at delivery without requiring any special assistance. However,

    about 10 percent of infants will need some intervention, and 1 percent will require extensive

    resuscitative measures at birth [1].

    The indications and principles of neonatal resuscitation will be reviewed here. The physiological

    changes that occur in the transition from intrauterine to extrauterine life are discussed separately.

    (See"Physiologic transition from intrauterine to extrauterine life".)

    ANTICIPATION OF RESUSCITATION NEEDBeing prepared is the first and most important

    step in delivering effective neonatal resuscitation [1]. Neonates requiring resuscitation are inevitably

    born in locations where resuscitation is uncommon because most newborns are healthy and do not

    require additional special assistance. In these settings, the need for resuscitation is not anticipated

    in most infants who require resuscitation [2]. As a result, at every birthing location, personnel who

    are adequately trained in neonatal resuscitation should be readily available to perform neonatal

    resuscitation whether or not problems are anticipated.

    In all instances, at least one healthcare provider is assigned primary responsibility for the newborn

    infant. This person should have the necessary skills to evaluate the infant, and, if required, toinitiate resuscitation procedures such as positive pressure ventilation and chest compressions. In

    addition, either this person or another who is immediately available should have the requisite

    knowledge and skills to carry out a complete neonatal resuscitation including endotracheal

    intubation and administration of medications.

    Equipment needed for resuscitation should be available at every delivery area (table 1), and

    routinely checked to ensure the equipment is functioning properly [3].

    TrainingThe neonatal resuscitation program (NRP) was developed by the American Academy

    of Pediatrics (AAP) and American Heart Association (AHA) as a training program aimed at teaching

    the principles and skills of neonatal resuscitation [3]. Studies have demonstrated that NRP training

    improves the correct sequencing and timing of the resuscitative steps and procedures by healthcareproviders [2], provider knowledge and comfort in performing neonatal resuscitation [4], and five-

    minute Apgar scores [5].

    By 2005, the NRP had trained two million health care providers in the United States and was a

    model for similar neonatal resuscitation programs in over 100 countries [6]. The NRP has been

    updated five times since its inception. The most recent version is based upon the 2010 AHA, AAP,

    and International Liaison Committee on Resuscitation (ILCOR) neonatal resuscitative guidelines [1].

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    In our institution, all healthcare providers who care for newborn infants (clinicians, nurses, neonatal

    nurse practitioners, and respiratory therapists) are required to be NRP trained. It is recommended

    that all delivery room personnel complete the NRP in an effort to improve their individual and group

    performance in neonatal resuscitation.

    High-risk deliveryInfants who are more likely to require resuscitation can be identified by the

    presence of one or more of the following risk factors (table 2)[3,7]:

    Maternal conditionsAdvanced or very young maternal age, maternal diabetes mellitus or

    hypertension, maternal substance abuse, or previous history of stillbirth, fetal loss, or early

    neonatal death.

    Fetal conditionsPrematurity, postmaturity, congenital anomalies, or multiple gestations.

    Antepartum complicationsPlacental anomalies (eg, placenta previa), or presence of

    either oligohydramnios or polyhydramnios.

    Delivery complicationsTransverse lie or breech presentation, chorioamnionitis, foul-

    smelling or meconium-stained amniotic fluid, antenatal asphyxia with abnormal fetal heart

    rate pattern, maternal administration of a narcotic within four hours of birth, or delivery that

    requires instrumentation (eg, forceps, vacuum, or cesarean delivery).

    Individuals fully skilled in neonatal resuscitation should be present to care for the high-risk infant. If

    time permits, the team should meet with the parents and discuss the anticipated problems and

    plans for care of the infant, and address parental concerns to the best of their ability.

    Necessary equipment should be assembled prior to the birth of at-risk newborns as follows [3]:

    The radiant warmer is turned on and is heating.

    The oxygen source is open with adequate flow through the tubing.

    The suctioning apparatus is tested and is functioning properly.

    The laryngoscope is functional with a bright light.

    Testing of resuscitation bag and mask demonstrates an adequate seal and generation of

    pressure.

    In high-risk deliveries of multiple gestations, each infant will require a full complement of personnel

    and equipment.

    Preterm infantsPreterm infants pose a greater challenge than term infants because they are

    more likely to require resuscitation and develop complications from the resuscitative process. If a

    preterm birth can be anticipated and time permits, it is preferable to transfer the mother prior to

    delivery to a perinatal center that has fully trained staff with expertise and experience in the care of

    these infants [8,9].

    The following factors make the preterm infant more likely to require resuscitation and to be more

    susceptible to sequelae [3]:

    HypothermiaThe risk of heat loss leading to hypothermia is increased in infants with a

    large body surface area to mass, thin skin, and decreased subcutaneous fat. The smaller

    the infant, the more difficult it is to prevent hypothermia. (See'Provide warmth'below.)

    Inadequate ventilationImmature lungs may be deficient in surfactant, and therefore

    difficult to inflate and ventilate. Immature respiratory drive and weak respiratory muscles

    increase the likelihood of apnea and inadequate respiratory effort. The greater the degree

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    of prematurity, the more likely the infant will require intubation and positive pressure

    support. (See'Next steps'below.)

    InfectionMaternal infection is associated with premature delivery, and offspring of

    infected mothers are at risk for antenatal infection. Premature infants also have immature

    immune systems, which increases the risk of acquiring postnatal infection.

    (See"Pathogenesis of spontaneous preterm birth", section on 'Bacteria'.)

    Organ damageImmature tissues and capillaries (eg, retina or germinal matrix) are more

    vulnerable to injury resulting in complications (eg, retinopathy of prematurity and intracranial

    hemorrhage, respectively). (See"Clinical manifestations and diagnosis of intraventricular

    hemorrhage in the newborn"and"Retinopathy of prematurity", section on 'Risk factors'.)

    Reduced antioxidant functionImmature antioxidant defense systems may be unable to

    counteract the effects of free radicals. Free radicals and reactive oxygen species are

    speculated to contribute to many of the morbidities of prematurity (eg, bronchopulmonary

    dysplasia and necrotizing enterocolitis) [10]. The very preterm infant may be particularly

    susceptible to oxidant injury from the use of excess supplemental oxygen in the delivery

    room [11]. (See"Pathogenesis and clinical features of bronchopulmonary dysplasia",

    section on 'Oxygen toxicity'and"Pathology and pathogenesis of necrotizing enterocolitis in

    newborns".)

    Additional resources and personnel should be present when a preterm birth is anticipated. These

    include:

    Equipment to keep the infant warm. In infants less than 28 weeks gestation, the use of

    polyethylene bags and wraps have been used to maintain body temperature. (See"Short-

    term complications of the premature infant", section on 'Hypothermia'.)

    Personnel skilled in intubation are especially important for the extremely low birth weight

    infant (birth weight

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    If there is no chance of survival, resuscitation should not be initiated. (See'Withholding

    resuscitation'below.)

    When a good outcome is considered very unlikely, the parents should be given the choice

    of whether resuscitation should be initiated, and clinicians should respect their preference.

    If a good outcome is considered reasonably likely, clinicians should initiate resuscitation

    and, together with the parents, continually reevaluate whether intensive care should be

    continued. (See'Postresuscitation'below.)

    OVERVIEW OF RESUSCITATIVE STEPSAlthough there is increasing emphasis to incorporate

    the highest quality of evidence (ie, randomized clinical trials) into the American Heart

    Association (AHA)/American Academy of Pediatrics (AAP) and International Liaison Committee on

    Resuscitation (ILCOR) neonatal resuscitative guidelines [1], this is not always possible.

    Randomized trials are difficult to perform in the delivery room because of difficulties in obtaining

    consent before resuscitation, difficulty in blinding care providers regarding intervention, and the

    relatively uncommon occurrence of a poor neonatal outcome to measure the effectiveness of an

    intervention. As a result, many of the guideline recommendations are based upon extensive clinical

    experience [1].

    The following discussion and our own practice are in compliance with the

    2010 AHA/AAP/ILCOR guidelines for neonatal resuscitative care [1,13,14].

    The 2010 AHA/AAP/ILCOR guidelines include a rapid assessment of the neonate's clinical status

    based on the following questions:

    Is the infant full-term?

    Is the infant breathing or crying?

    Does the infant have good muscle tone?

    If the answer to all three questions is yes, the newborn does not need resuscitation, should not be

    separated from the mother, and is managed by routine neonatal care. (See"Overview of the routinemanagement of the healthy newborn infant".)

    The basic steps ("ABCDs") in resuscitation in any age group still apply in the newborn period.

    However, there are aspects of neonatal resuscitation that are unique and lead to differences in the

    initial resuscitative steps. (See'Initial steps'below.)

    The 2010 AHA/AAP/ILCOR guidelines recommend the following approach (algorithm 1)[1,3]:

    Initial steps (provide warmth, clear Airway if necessary, dry, and stimulate)

    Breathing (ventilation)

    Chest compressions

    Administration of Drugs, such asepinephrineand/or volume expansion

    The decision to progress from one step to the next is determined by the time-dependent response

    of the infant to the applied resuscitative effort based upon his/her respirations and heart rate

    (algorithm 1). A time allocation of 30 seconds is given to apply the resuscitative procedure,

    evaluate, and decide whether to proceed to the next intervention. Monitoring of oxygen saturation

    by using pulse oximetry should be performed in infants who are gasping, apneic, have labored

    breathing, have persistent cyanosis, or have a heart rate less than 100 beats per minute (bpm). No

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    further resuscitative actions are required if the infant responds with adequate spontaneous

    respirations and a heart rate above 100 beats per minute. (See'Pulse oximetry'below.)

    It is vital that each step be performed optimally because subsequent resuscitative efforts are

    dependent on the success of previous steps. Thus, more time should be spent if 30 seconds is not

    sufficient to effectively complete the components of an intervention. Inadequate attention to

    ensuring completeness and effectiveness of earlier steps will jeopardize the utility of subsequentactions and unnecessarily expose infants to more aggressive intervention when they only required

    the earlier steps of resuscitation.

    Apgar scores are not used to guide resuscitation but are useful as a measure of the newborn's

    overall status and response to resuscitation. When the five-minute Apgar score is less than seven,

    additional scores should be assigned every five minutes for up to 20 minutes. Apgar scores are not

    good predictors of outcome. Scores may be determined using the Apgar score calculator (calculator

    1).

    The following discussion will describe each resuscitative action in depth.

    INITIAL STEPSInitial care steps in the delivery room are started within a few seconds of birth

    and should be applied throughout resuscitation.

    Provide warmthHypothermia in the delivery room or immediate newborn period is

    independently associated with an increase in mortality [15,16]. Thus, maintaining body heat is the

    initial step in neonatal resuscitation. Hypothermia in the newborn increases oxygen consumption

    and metabolic demands, which can impair subsequent resuscitative efforts, especially in the

    asphyxiated or extremely low birth weight (ELBW) infant. Low birth weight and preterm infants are

    particularly prone to rapid loss of body heat because of their large body surface area relative to their

    mass, thin skin, and decreased subcutaneous fat.

    To minimize heat loss, the delivered infant is first placed in a warmed towel or blanket and then

    under a prewarmed radiant heat source, where he/she is dried with another warmed towel or

    blanket. The infant should remain uncovered to allow full visualization and permit the radiant heat toreach the patient. The radiant warmer also allows easy access to the infant for multiple members of

    the resuscitative team.

    As soon as possible after the infant is placed on the warmer, the temperature control of the warmer

    should be regulated by servo-control to avoid hyperthermia; the servocontrolled temperature of the

    warmer is set to maintain the infant's temperature at 36.5C, which is monitored by a temperature

    skin probe placed upon the infant's abdomen. Healthcare providers should understand how the

    warmer and temperature probe work, since a malfunctioning warmer and/or temperature probe may

    lead to inadvertent underheating or overheating of the infant.

    Although studies have not examined the effects of postnatal hyperthermia in the delivery room on

    neonatal outcome, there are data demonstrating that maternal fever is associated with neonatalrespiratory depression, neonatal encephalopathy, cerebral palsy, and increased mortality [17]. It is

    unclear whether hyperthermia directly contributes to morbidity or whether it is a marker for an

    underlying pathological process (eg, chorioamnionitis). Nevertheless, until further data are

    available, it is prudent to avoid neonatal hyperthermia, as well as hypothermia, in the delivery room.

    The following methods of warming infants are also used depending upon the condition of the

    neonate and the need for further resuscitative efforts:

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    Swaddling the infant after drying

    "Skin to skin" contact with mother and covering the infant with a blanket

    Use of polyurethane bags or wraps in infants with birth weights less than 1500 g

    Raise the environmental (room) temperature to 26C (78.8F)

    Warming pads

    In infants who require respiratory support, the use of humidified and heated air versus nonheated

    air decreases the rate of both mild (36 to 36.4C) and moderate hypothermia (

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    StimulationTactile stimulation of the newborn should be initiated promptly after birth, except in

    the case of the "nonvigorous" infant born with meconium-stained amniotic fluid who first requires

    endotracheal intubation. Drying and suctioning the infant, which is performed as part of the initial

    steps, may provide adequate stimulation. Safe, appropriate ways of providing additional stimulation

    include briefly slapping or flicking the soles of the feet, and rubbing the infant's back. More vigorous

    stimulation is not helpful and may cause injury. If, after one or two attempts of additional stimulation,

    the infant still remains apneic, positive pressure ventilation (PPV) should be initiated. (See'Positive

    pressure ventilation'below.)

    Given that most infants will be stimulated from the moment of birth, efforts at stimulating the infant

    should not be prolonged. The time elapsed from the baby's birth to placing the baby under the

    warmer, positioning, suctioning, and providing additional stimulation should be no more than 30

    seconds (algorithm 1)[3].

    Pulse oximetryThe 2010 AHA/AAP/ILCOR guidelines recommend the use of pulse oximetry to

    determine oxygen saturation (SpO2) in the following settings because oxyhemoglobin saturation

    may normally remain in the 70 to 80 percent range for several minutes following birth, which may

    result in the appearance of cyanosis, and the assessment of skin color is a poor indicator of

    oxyhemoglobin saturation during the immediate neonatal period [1]:

    When resuscitation is anticipated

    Positive pressure ventilation is used for more than a few breaths

    Persistent cyanosis

    Use of supplementary oxygen

    For these infants, the oximeter probe should be attached to a preductal location on the right upper

    extremity, usually the wrist or medial surface of the palm, as soon as possible.

    The targeted SpO2levels for term infants born at sea level are as follows based on the time after

    delivery [1,20]:

    1 minute60 to 65 percent

    2 minutes65 to 70 percent

    3 minutes70 to 75 percent

    4 minutes75 to 80 percent

    5 minutes80 to 85 percent

    10 minutes85 to 95 percent

    Data on targeted levels for premature infants and term infants born at other altitudes are lacking,

    and the above levels are thought to be reasonable for these patients.

    NEXT STEPSThe initial steps delineated above are applied in every newborn delivery.

    Subsequent resuscitative care depends on the evaluation of the infant while performing these initial

    steps (algorithm 1). No further resuscitative actions are required if the infant responds with

    adequate spontaneous respirations (eg, sustained regular respirations) and a heart rate above 100

    beats per minute, and achieves targeted SpO2levels.

    Supplemental oxygenOver the last few decades, the standard practice of initial use of 100

    percent oxygen, whenever supplemental oxygen is needed, has been challenged, as increasing

    evidence has shown that hyperoxia due to oxygen supplementation may result in tissue and organ

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    injury [21-23]. Hyperoxia is thought to raise cellular oxygen contents, which leads to an increased

    generation of free oxygen radicals causing cellular and tissue injury [21-24].

    In addition, several studies including meta-analyses have shown improved survival and outcome in

    primarily term infants resuscitated with room air compared with those who received 100 percent

    oxygen.

    Two meta-analyses demonstrated a reduction in mortality in primarily term infants with the

    use of room air compared with 100 percent oxygen, and no difference in the risk of hypoxic

    ischemic encephalopathy or changes in neurodevelopmental outcome at 18 to 24 months

    of age [25,26].

    Two trials of asphyxiated term infants demonstrated that infants resuscitated in room air

    compared with those resuscitated with 100 percent oxygen more quickly achieved

    sustained respirations and had lower concentrations of markers or oxidative stress (ie,

    glutathione, superoxide dismutase, catalase, and glutathione peroxidase) [22,27].

    A retrospective population-based Swedish study compared the outcome of severely

    depressed infants (defined as a one-minute Apgar score less than four) who were

    resuscitated at one of four tertiary centers that used either 40 percent oxygen or 100percent oxygen during neonatal resuscitation. There were no differences in rates of

    neonatal death, hypoxic ischemic encephalopathy, or seizures between infants resuscitated

    with 40 percent oxygen and those who received 100 percent oxygen [28].

    Data are more limited in premature infants, but suggest that room air may be insufficient to achieve

    targeted oxygen levels and 100 percent oxygen results in excessive oxygen exposure [29]. As a

    result, in our practice, blended oxygen with concentration starting at 30 percent is used in the

    resuscitation of preterm infants below 30 weeks gestation, and oxygen concentration adjusted

    based on a predetermined SpO2target range. (See'Our approach'below.)

    In one observational study of preterm infants less than 30 weeks gestation, infants

    resuscitated with room air had median oxygen saturations of 31 and 54 percent at two and

    five minutes, and almost all of the infants required supplemental oxygen (91 of 106

    patients) [30]. In contrast, the median oxygen saturations of the 20 infants resuscitated with

    100 percent oxygen at two and five minutes were 84 and 95 percent.

    A small trial randomly assigned 42 premature infants (gestational age 28 weeks) who

    required resuscitation to initially receive either 30 percent oxygen, which was increased in a

    stepwise manner every 60 to 90 seconds by 10 percent if bradycardia (85 percent [31].

    There were no differences in mortality rate and the oxygen saturation values obtained by

    pulse oximeter from 1 to 20 minutes of life between the two groups. By five to seven

    minutes of life, the mean oxygen was 45 percent in both groups. In one small trial, preterm infants (24 to 28 weeks gestation) resuscitated with 30 percent

    oxygen, when compared with those resuscitated with 90 percent oxygen, needed fewer

    days of oxygen supplementation and mechanical ventilation, and had a lower incidence of

    bronchopulmonary dysplasia (15 versus 32 percent) [32].

    The following 2010 American Heart Association/American Academy

    of Pediatrics/International Liaison Committee on Resuscitation (AHA/AAP/ILCOR) guidelines reflect

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    the lack of data needed to establish evidence-based guidelines for a specific initial oxygen

    concentration for resuscitation [1]:

    Resuscitation should be initiated with blended oxygen. If blended oxygen is not available,

    room air should be used.

    The oxygen concentration should be adjusted to achieve targeted SpO2levels, which are

    monitored by pulse oximetry. (See'Pulse oximetry'above.)

    If the heart rate is below 60 bpm after 90 seconds of resuscitation, the oxygen

    concentration should be increased to 100 percent until recovery of a normal heart rate.

    Our approachAt our institution, we currently utilize 21 percent oxygen for resuscitation of

    neonates >30 weeks gestation. For infants 30 weeks gestation, because of the increased risk of

    hyperoxia-related complications associated with prematurity [10], we initiate resuscitation with 30

    percent oxygen by use of a blender. In all infants, pulse oximetry guides further adjustments of the

    delivered supplemental oxygen in an effort to achieve and maintain the oxygen saturation based on

    target SpO2. (See'Pulse oximetry'above.)

    However, the optimal target SpO2levels in the delivery room are unknown in preterm infants [33].Target SpO2for premature infants is discussed in detail separately. (See"Oxygen monitoring and

    therapy in the newborn", section on 'Oxygen target levels'.)

    Positive pressure ventilationPositive pressure ventilation (PPV) is required in the following

    clinical settings after administering the initial steps of resuscitation:

    If the infant is gasping or apneic.

    If the heart rate is

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    opened at 35 to 40 cm H2O, oxygen concentrations fell to levels of 30 and 45 percent at

    flow rates 2L/min. With a 100 percent oxygen source and a reservoir, oxygen delivery is

    generally 90 to 100 percent oxygen. These findings are significant given the concern for

    potential oxygen toxicity and episodes of hyperoxia with high concentrations of delivered

    oxygen. They also demonstrate that pulse oximetry is required when supplemental oxygen

    and positive pressure ventilation are used. (See'Supplemental oxygen'above.)

    Flow-inflating bagThe flow-inflating bag (also referred to as an anesthesia bag) fills only

    when gas from a compressed source flows into it. It is technically more difficult to master

    than the self-inflating bag because a tight face-mask seal is needed for the bag to inflate;

    however, this feature may be considered an advantage because it assures an optimal face-

    mask seal is obtained, which is necessary for effective positive pressure ventilation.

    Because the flow-inflating bag does not have a pressure release valve, a pressure

    manometer should always be used to minimize the risk of overinflation resulting in

    pulmonary air leak. (See"Pulmonary air leak in the newborn".)

    T-piece resuscitatorThe T-piece resuscitator is similar to the flow-inflating bag, but with

    the addition of an adjustable flow-control valve, which more precisely controls the peak

    inflating pressure applied to the infant's lungs, decreasing the risk of pulmonary air leak

    complications. Like the flow-inflating bag, it requires a compressed gas source. In term infants and preterm infants with birth weights greater than 1500 g, laryngeal mask

    airway (LMA), which fits over the laryngeal inlet, has been found to be effective when BMV

    or endotracheal intubation is unsuccessful, or endotracheal intubation is not possible [35].

    The LMA is a soft mask with an inflatable cuff attached to a silicone rubber airway, which is

    inserted through the mouth by the clinician using his/her index finger to guide insertion

    along the hard palate "blindly" without the use of visualizing instruments. Following insertion

    and inflation of the cuff, the LMA covers the laryngeal opening and its rim conforms to the

    contours of the hypopharynx occluding the esophagus with a low-pressure seal. LMA

    should be considered only i f BMV is unsuccessful in providing adequate ventilation, and

    endotracheal intubation is unsuccessful or not feasible. [1,35-37].

    ProcedureThe following steps are required to effectively provide assisted positive pressure bag-

    mask ventilation (BMV):

    PositionThe infant should be positioned with the neck in a neutral to slightly extended

    position to ensure an open airway (figure 1). The clinician should stand at the head or side

    of the warmer to view the chest movement of the infant to assess whether ventilation is

    effectively delivered. (See'Airway'above.)

    SuctionThe nose and mouth should be suctioned as needed to clear any mucous to

    prevent aspiration prior to delivery of assisted breaths.

    SealAn airtight seal between the rim of the mask and the face is essential to achieve the

    positive pressure required to inflate the lungs. An appropriately sized mask is selected and

    positioned to cover the chin, mouth, and nose, but not the eyes of the infant. The mask is

    held on the face by positioning the hand of the clinician so that the little, ring, and middle

    fingers are spread over the mandible in the configuration of the letter "E" and the thumb and

    index are placed over the mask in the shape of the letter "C". The ring and fifth fingers lift

    the chin forward to maintain a patent airway. An airtight seal is formed by using light

    downward pressure on the rim of the mask and gently squeezing the mandible up towards

    the mask (picture 1).

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    Initial breathsThe initial administered breaths often require pressures of 30 to 40 cm H2O

    to inflate the lungs of the newly born term infant. In most preterm infants, an initial inflation

    pressure of 20 to 25 cm H2O is usually adequate. Adequacy of ventilation is demonstrated

    by improvement in heart rate. Chest wall movement should be assessed if heart rate does

    not improve. The infant should be ventilated at a rate of 40 to 60 times per minute to

    achieve a heart rate >100 bpm.

    When initiating ventilation, the care provider should try to avoid excess volume or pressure,

    which can result in volutrauma resulting in lung injury or pulmonary air leak, especially in

    the premature infant [38]. To minimize volutrauma, the positive pressure should be adjusted

    to deliver a tidal volume of 4 to 5 mL/kg. In addition, positive end-expiratory pressure

    (PEEP) of 4 to 5 cm H2O should be used to prevent atelectasis [38]. The self-inflating bag

    does not provide PEEP. (See"Prevention of bronchopulmonary dysplasia", section on

    'Noninvasive mechanical ventilation'and"Pulmonary air leak in the newborn".)

    Next stepsFurther resuscitative efforts are based upon the heart rate response of the

    infant after the initial 30 seconds of BMV.

    If the heart rate is greater than 100 beats per minute (bpm) and spontaneous effectiverespiration has begun, BMV can be discontinued and free-flowing oxygen administered

    as needed, based on the target oxygen saturations for minutes after birth. The infant is

    observed closely (heart rate and SpO2) to determine whether his/her spontaneous

    respiratory effort is adequate without need for further intervention.

    If the heart rate is between 60 to 100 bpm, continue BMV ventilation and reevaluate

    after 30 seconds. Reevaluation includes the following sequence of M-Mask

    readjustment, R-Reposition the airway, S- Suction the mouth and nose, and O- Open

    the mouth slightly. If these maneuvers fail, consider increasing inflation pressure

    because failure of establishing effective positive pressure ventilation is an extremely

    common and potentially preventable cause of failed resuscitation.

    If the heart rate is below 60 bpm, immediately begin chest compression and reassessthat adequate positive pressure ventilation is being delivered. (See'Chest

    compressions'below.)

    CPAP or PEEPStudies in animals suggest the addition of continuous positive airway (CPAP) or

    end-expiratory pressure (PEEP) may be beneficial for adequate lung recruitment and reduce

    subsequent lung injury, especially in very premature animals [39,40].

    Data from observational studies and a single clinical trial appear to support the use of CPAP versus

    BMV in the initial resuscitation of preterm infants [41-44]. In a randomized controlled Dutch trial of

    207 preterm infants born at a gestational age less than 33 weeks, patients who required ventilatory

    support were randomized to a single pressure-controlled inflation of 10 seconds followed by CPAP

    delivered through a nasopharyngeal tube and T-piece resuscitator versus positive BMV [44]. Infants

    treated with single inflation/CPAP, when compared with those who received conventional BMV,were less likely to be intubated, receive more than one dose of surfactant, or develop

    bronchopulmonary dysplasia (BPD). However, further studies to confirm these findings are needed

    before CPAP verus BMV can be recommended for neonatal resuscitation.

    After BMV ventilation as the initial resuscitative intervention, CPAP rather than intubation and

    mechanical ventilation may be beneficial in the spontaneously vigorous preterm infants who require

    continued respiratory support or at risk for respiratory distress syndrome. (See"Prevention and

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    treatment of respiratory distress syndrome in preterm infants", section on 'Assisted ventilation

    techniques'.)

    In infants who require PPV, PEEP is likely to be beneficial, and should be used if suitable

    equipment is available [1].

    Endotracheal intubationEndotracheal (ET) intubation allows direct access to the upper trachea

    for suctioning (ie, meconium) or delivery of positive pressure ventilation (PPV). Intubation is a skill

    that must be learned and takes practice for one to become accomplished. While bag-mask

    ventilation (BMV) may suffice in most instances of neonatal resuscitation, there are instances when

    ET intubation may be preferred. Thus, when a high-risk delivery is anticipated, at least two

    individuals should be present for the birth to assist with resuscitation of the infant, and one should

    be skilled in ET intubation.

    ET intubation may be indicated if [1]:

    Tracheal suctioning for meconium is required

    BMV is ineffective or prolonged

    Chest compressions are being performed

    In addition to the above, ET intubation may be electively chosen in certain special circumstances,

    such as congenital diaphragmatic hernia, airway stabilization of the extremely low birth weight

    infant, and for administration of surfactant.

    All necessary supplies should be readied for intubation, including appropriate size ET tubes (ETT).

    The neonatal resuscitation program (NRP) guidelines use birth weight and gestational age to

    determine the appropriate ETT size (table 3). An alternate method for selection of ETT size is based

    upon the length of the infant [45]. However, its use has only been validated in one study. This

    approach cannot be recommended until further studies verify that it can accurately predict

    appropriate ETT size for neonates.

    Suction device should be available to remove secretions in the posterior oropharynx and

    laryngopharynx that may obstruct the view of the trachea and vocal cords.

    ProcedureTwo care providers are required for ET intubation, one to perform the procedure and

    the other to assist and monitor the status of the infant during the intubation. To minimize

    hypoxemia, time needed for intubation should be limited to 20 seconds, and free flowing oxygen is

    administered during the procedure.

    The following steps are required for successful intubation of the neonate:

    Initial stabilizationUnless contraindicated, the patient should be stabilized by BMV.

    PositioningThe infant is placed on his/her back with the head in the midline and the neck

    slightly extended.

    InsertionThe laryngoscope is held in the left hand of the clinician between the thumb and

    the first two or three fingers, with the blade pointing away from the clinician. The right hand

    stabilizes the head of the infant. The laryngoscope blade is inserted over the right side of

    the tongue pushing the tongue to the left and is advanced until the blade lies in the

    vallecula, just beyond the base of the tongue. The entire blade is lifted in the direction of the

    laryngoscope handle to allow visualization of the vocal cords. It is important not to twist the

    laryngoscope like a lever, the so-called "can opener" maneuver, as this can elevate the

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    vocal cords out of view and can damage the alveolar ridge. Once the vocal cords are

    visualized, an appropriate-sized ETT is inserted through them with the right hand until the

    vocal cord guide line (heavy black line near the tip of the tube) is at the level of the vocal

    cords.

    Some individuals prefer to use a stylet to provide rigidity and curvature to the tube; if a

    stylet is used, care should be taken that it does not protrude out of the tip of the tube, and

    when it is removed the tube is not inadvertently dislodged.

    Assessment of successful intubationSuccessful intubation following institution of PPV is

    associated with a prompt increase in heart rate. Other indicators of successful intubation

    include auscultation of audible breath sounds over both lung fields, vapor condensation

    inside the ETT during exhalation, and symmetrical chest movement; however, these

    findings have not been systematically studied in neonates. Chest radiography is needed to

    confirm that the ETT is correctly placed above the carina of the trachea.

    Exhaled carbon dioxide (CO2) detectors can be used to confirm ETT placement, especially

    in very low birth weight infants [46-49]. At our institution, we use CO2detectors to confirm

    ETT placement as endorsed by the 2010 guidelines [1]. Securing ETTIf the ETT is to be used for ventilation, it needs to be secured and taped. A

    simple calculation can be used to determine the depth of insertion (referred to as the 7-8-9

    or Tochen's rule). The distance measured in cm from the tip of the ETT to the lip of the

    infant is calculated as the infant's weight in kg plus "6". So for a 1 kg infant, the depth of

    insertion is 7 cm. This rule accurately places the tip of the ETT just above the midtracheal

    position in infants with birth weight (BW) 750 g. However, the Tochen's rule is not

    adequate for ETT placement in infants with BW

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    Resuscitation (AHA/AAP/ILCOR) guidelines in neonates because it generates higher systolic and

    coronary perfusion pressure [52-57].

    Chest compressions must always be accompanied by positive pressure ventilation (PPV). During

    neonatal resuscitation, the chest compression rate is 90 per minute accompanied by 30 ventilations

    per minute with one ventilation interposed after every third compression. Thus, the ventilation rate is

    reduced from the 40 to 60 breaths per minute used in the absence of chest compression to 30breaths in the presence of chest compression.

    After 30 seconds of chest compression and PPV, reassessment of the infant's heart rate, color, and

    respiratory rate should determine whether further interventions are required (eg, intubation or

    administration of medications).

    DRUGSDrugs are rarely required in neonatal resuscitation. Delivering adequate ventilation is

    the most important resuscitative step because the most common cause of bradycardia is

    inadequate lung inflation or profound hypoxemia.

    However, if the heart rate remains

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    Volume expansionIn the delivery room, neonatal hypovolemia requiring volume expansion is

    rarely needed. Hypovolemia may be suspected if there is ante- or intrapartum hemorrhage, which

    could be due to an umbilical cord accident, placenta previa, or trauma, or if there are clinical signs

    of hypovolemia seen despite an adequate heart rate, such as pallor, poor perfusion, and weak

    pulses.

    Because isotonic crystalloid solution is as effective as 5 percent albumin in restoring effectivecirculating volume in neonates [60-62], the current guidelines recommend a 10 mL/kg bolus of

    normal saline given over 5 to 10 minutes to correct hypovolemia. This dose can be repeated if

    necessary based upon the response to the initial bolus.

    Other acceptable solutions include Ringer's lactate or O Rh-negative blood. The latter may be

    preferable if severe blood loss and/or anemia is suspected or documented.

    NaloxoneIn the 2010 American Heart Association/International Liaison Committee on

    Resuscitation (AHA/ILCOR) guidelines, administration ofnaloxone,a narcotic antagonist,

    is notrecommended as part of initial resuscitation in the delivery room because data are lacking

    demonstrating its efficacy, and there remains uncertainty regarding its dosing, routes of

    administration, and safety [1,63]. Although, maternally administered opioids in the perinatal periodmay cause neonatal respiratory depression, attention to ventilation and oxygenation as described

    earlier is generally adequate for neonatal resuscitation.

    Sodium bicarbonateThere is insufficient evidence to determine whethersodium bicarbonateis

    beneficial or harmful in neonatal resuscitation [3,64,65]. Although theoretically sodium bicarbonate

    should be beneficial to correct acidosis, there is also evidence that sodium bicarbonate could

    adversely affect myocardial and cerebral function [66]. Given the uncertainty of benefit and the

    potential for adverse effects, we do not routinely recommend the use of sodium bicarbonate. This

    approach is consistent with the 2010 AHA/American Academy of Pediatrics(AAP)/ILCOR guidelines

    for neonatal resuscitative care, which do not include the use of sodium bicarbonate as a

    recommended or useful medication [1,13,14]. (See"Approach to the child with metabolic acidosis",

    section on 'Bicarbonate therapy in neonates'.)

    Ifsodium bicarbonateis used, it should be given only after adequate ventilation and circulation has

    been established to prevent increased CO2retention. Sodium bicarbonate is a caustic and

    hypertonic agent, and, if administered, it must be given through a large vein. Given the controversy

    over its use in neonatal resuscitation, no dose for sodium bicarbonate use has been established. If

    it is used, the usual dose is 1 or 2 mEq/kg, given at a rate no faster than 1 mEq/kg per minute.

    (See"Primary drugs in pediatric resuscitation", section on 'Sodium bicarbonate'.)

    FAILURE OF INITIAL RESUSCITATIONRarely, infants will not respond to the initial

    resuscitative efforts. The clinical team needs to review that all the resuscitative steps were fully and

    properly administered.

    If the infant fails to respond despite properly executed resuscitation, the following clinical approachmay help ascertain the cause:

    Failure to respond to positive pressure ventilation (PPV):

    Mechanical blockage (eg, meconium, mucus, choanal atresia, pharyngeal airway

    malformation [Robin sequence], or laryngeal web)

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    Impaired lung function (pneumothorax, pleural effusions, congenital diaphragmatic

    hernia, pulmonary hypoplasia, congenital pneumonia, or hyaline membrane disease)

    Central cyanosisCongenital heart disease

    Persistent bradycardiaHeart block

    ApneaBrain injury (hypoxic ischemic encephalopathy), congenital neuromuscular

    disorder, or respiratory depression from maternally administered opioids

    WITHHOLDING RESUSCITATIONWith antenatal screening, it is now possible to identify

    conditions associated with high neonatal mortality or poor outcome. In these settings, intensive

    therapy including neonatal resuscitation may result in prolongation of dying with significant pain and

    discomfort for the neonate or survival with unacceptable quality of life. Decisions regarding whether

    intervention should be initiated and to what degree are difficult and are made together by parents

    and care providers, guided by their understanding of the child's best interests.

    Our approach in deciding whether resuscitation should be initiated or withheld is consistent with the

    recommendations of the American Academy of Pediatrics (AAP) and includes the following [1,67].

    The decision not to initiate intensive therapy is made together by the parents and the

    healthcare team. Parents should be active participants in the decision-making process

    concerning the treatment of their child. Discussion, if possible, should occur prior to the

    birth of the infant.

    Noninitiation of resuscitation may be considered if early death is very likely and survival

    would be accompanied by unacceptably high morbidity. These clinical conditions include

    infants with gestational age

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    DISCONTINUING RESUSCITATIONResuscitation efforts may be discontinued if the neonate

    has demonstrated no signs of life (no heart beat or no respiratory effort for greater than 10 minutes)

    after 10 minutes of resuscitation [1,3], because outcome is associated with high early mortality and

    unacceptably high morbidity among the rare survivors [68-70].

    As previously discussed, if additional data obtained after resuscitation is started demonstrates that

    neonatal outcome is almost certain early death or unacceptably high morbidity, support can bediscontinued if agreed upon by the parents and healthcare team.

    POSTRESUSCITATIONInfants who required resuscitation are at risk of developing

    postresuscitative complications [71]. These include:

    Hypo- or hyperthermia

    Hypoglycemia (see"Neonatal hypoglycemia")

    Central nervous system (CNS) complications: apnea, seizures, or hypoxic ischemic

    encephalopathy (see"Clinical features, diagnosis, and treatment of neonatal

    encephalopathy")

    Pulmonary complications: Pulmonary hypertension, pneumonia, pulmonary air leaks, or

    transient tachypnea of the newborn (see"Overview of neonatal respiratory distress:Disorders of transition")

    Hypotension

    Electrolyte abnormalities: Hyponatremia or hypocalcemia

    Feeding difficulties: Ileus, gastrointestinal bleeding, or dysfunctional sucking or swallowing

    The longer and the greater the extent of resuscitation, the more likely that there will be subsequent

    and serious complications. Thus, infants who required resuscitation should be placed in a setting in

    which close monitoring and ongoing appropriate care can be provided.

    SUMMARY AND RECOMMENDATIONS

    Most infants successfully transfer from intrauterine to extrauterine life without any special

    assistance. However, about 10 percent of newborns will need some intervention, and 1

    percent will require extensive resuscitative measures at birth.

    Because the need for resuscitation is not anticipated in the majority of neonates, personnel

    who are adequately trained should be readily available to perform neonatal resuscitation at

    every birthing location, whether or not problems are anticipated. (See'Anticipation of

    resuscitation need'above.)

    Infants who are more likely to require resuscitation can be identified by maternal and

    neonatal risk factors, and the presence of antepartum and delivery room complications.

    Care providers skilled in neonatal resuscitation should be present and equipment should be

    prepared prior to the birth of the high-risk infant. (See'High-risk delivery'above.)

    Preterm infants are more likely to require resuscitation and develop complications fromresuscitation than term infants. If a preterm birth can be anticipated and time permits, it is

    preferable to transfer the mother prior to delivery to a perinatal center. (See'Preterm

    infants'above.)

    Resuscitation stepsWe suggest the following practices described in the 2010 American Heart

    Association, American Academy of Pediatrics, and International Liaison Committee on

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