problems in the newborn
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8/8/2019 Problems in the Newborn
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1. Hyperbilirubinemia2. Respiratory Distress3. Cleft Lip/Palate4. Hydrocephalus
5. Spina Bifida6. Down Syndrome7. Talipes Equinovarus8. Infant of a Diabetic Mom9. Infant of an HIV Positive Mom10. Infant of a Substance-Abusing Mom11. Phynylketonuria
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Definition:An excess bilirubin in the blood, maybe RTPhysiologic Jaundice or Pathologic Jaundice
Pathologic jaundice ² may lead to KernicterusCommon Cause: Rh Incompatibility
Management:A. Medical ² PhototherapyB. Surgical ² Exchange Transfusion
BT ́ Oµ, Rh (-) Blood is usedComplications: Hyper/Hypovolemia, infection,Arrhythmias, Air
embolism
Insert pic
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2 types:a. Respiratory Distress Syndrome (RDS)
- associated w/ preterm infants &surfactant deficiency
b. Transient tachypnea of the Newborn (TTN)- near term infants- results from failure to clear the airway oflung fluids & mucus or aspiration ofamniotic fluid- respiratory difficulties follows few hoursafter birth
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Medical Management:
- determine type of Respiratory Distress thenbegin tx
RDSa. Mild RDS ² increased, humidified O2 concentrationb. Mod RDS ² continuous positive airways pressurec. Severe RDS ² Mechanical Ventilator
TTN4 days treatment of Ambient O2 of 30-50% then
decreases
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Concern : Feeding
Special Considerations:1. Special Nipples & feeding devices
2. Held in upright position3. Frequent burping necessary4. Sleeping ² in side lying position
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Excess cerebrospinal fluid in thecerebral ventricles, causes the infant·shead to be enlarged
Interventions:Head CircumferenceMeasured daily
Fontanels checked if flator bulgingInfant·s position changedfrequently
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3 Types of Spina Bifida (Neural Tube Defects)1. Spina Bifida Occulta
- failure of the vertebral arch to close. There is adimple at the back which may have a tuft of hair.NO CARE required
2. Meningocele- saclike protrusion along the vertabral column filledw/ cerebrospinal fluid & meninges. Surgeryrequired, no long term effects
3. Myelomeningocele- saclike protrusion along the vertabral column filledw/ cerebrospinal fluid, meninges, nerve roots andspinal cord. Paralysis at some level after surgicalrepair
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Considerations:- Protrusion covered with sterile saline
dressing
- Care taken when changing position- Sac must be kept free from
contamination by urine and stool-
Head Circumference is measured andfontanels checked for bulging(hydrocephalus often develops)
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A chromosomal abnormality alsocalled Trisomy 21 resulting to severemental retardation
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AKA Clubfoot ² a congenital deformityin which the foot and ankle are twistedinward and cannot be moved to amidline position
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Transmission rate from mom ² infant = 28-35%Occur through:1. Placenta2. Maternal Blood
3. Secretions during labor and birth4. Breastmilk after birth
Every infant have HIV antibodies fromplacenta. By 8-15 mos, uninfected infantslost maternal antibodies
3-6 mos ² lymphoid insterstitial pneumonitis isa criterion for dx
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Infant is a substance abuser at birthWithdrawal symptoms seen after the
cord is cut usually within the first24-48H after birth or not until 4-5days of age.The severity of withdrawalsymptoms depends on the substancebeing abused and the time andamount of last dose
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Complications:Withdrawal
Respiratory DistressCongenital AnomaliesJaundiceBehaviour Problems
Growth Retardation
Management:Medical ² mgt of complicationsPharmacological ² Phenobarbital or tincture of
opium to control withdrawal symptomsDiazepam(Valium) ² to control seizures inROH-dependent infant
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- An inborn error of metabolism inwhich the infant has deficiency ofthe enzyme required to digest the
amono acid phenylalanine- Result to severe mental retardation
Test done after ingestion ofBreastmilk of formula within 24H