Introduction to Newborn Care/Congenital infections Flashcards

(33 cards)

1
Q
  • All mothers have a blood type and antibody screen in pregnancy
  • only type O mothers have IgG antibody which crosses sthe placenta
  • this can lead to Incompatibility between mother and newborn
  • Present in 12% of all pregnancies but evidence of fetal sensitization (positive direct coombs) occurs in only 3-4%
A

ABO incompatibility

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2
Q

what should be focsed on during neonatal resusitation?

A
  • warm, dry, stimulate
  • provide positive pressure ventilation
  • more extensive resusitation as needed
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3
Q

what does the apgar score rate?

A
  • respiration, crying
  • reflexes, irritability
  • pulse, heart rate
  • skin color of body and extremities
  • muscle tone
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4
Q
  • Estimate gestational age of the baby based on neuromuscluar and physical exam characteristics on exam
  • use with estimates of gestational age based on LMP and prenatal ultrasound
  • helpful when there is no prenatal care
A

Ballard Score

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5
Q

what is analzyed during the growth assessment?

A
  • Length
  • head circumference
  • weight
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6
Q

what eye prophylaxis is given to prevent neonatal conjunctivitis

A

0.5% erythromycin ointment within 1 hour of birth

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7
Q

Classic onset

  • bleeding between 2 days- 1 wk in GI tract, skin, nose, umbilical stump, circ site

Late onset

  • Bleeding in infants 2 wks-6months
  • catastrophic brain and gut
  • decreased incidence with Vitamin K but not 0 (can be seen in newborns with malabsorption syndromes)
A

Vitamin K deficiency bleeding

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8
Q
  • Identifies asymptomatic congenital diseases that have improved outcomes with treatment
  • blood collected on all newborns between 24-48 hrs of life
  • 50 disorders are included on the NBS (state specific)
A

Neonatal Blood Screen

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9
Q
  • 1-3:1000 congenital hearing loss
  • diagnose before 3 months
  • provide services before 6 months
A

Hearing screen

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10
Q
  • pulse oximetry in right hand and either foot
  • pre and post ductal differential
  • any newborn with SpO2 < 95% or > 3% difference between pre and post ductal sat= positive screen
  • cyanotic blind spot
A

CCHD screen

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11
Q
  • incidence is high: 0.5% to 2.5% of fetuses and newborn infants (significant number asymptomatic)
  • clincial features in common but can be distinguished by history and physical findings
A

congential infections

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12
Q

with congenital infections TORCH should be considered. What does it stand for?

A
  • Toxoplasmosis
  • other (HIV, enterovirus, parvovirus, varicella, hepatitis, syphilis, zika)
  • Rubella
  • Cytomegalovirus
  • Herpes simplex
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13
Q
  • Parasitic infection
  • infection primarily acquired through eating raw or undercooked meat or exposure to cat stools
  • infected women generally asymptomatic
  • first trimester fetal infection more severe
  • third trimester fetal infection more common
A

Toxoplasmosis

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14
Q

what would an infection with toxoplasmosis look like?

A

many infants asymptomatic at birth but begin to show symptoms over time

  • Classic triad: Chorioenteritis, intracranial calcifications, hydrocephalus
  • Other signs: jaundice with HSM, fever, rash, petechiae, lymphadenopathy, pneumonitis, vomiting diarrhea, microcephaly
  • visual impairment, mental retardation, deafness
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15
Q

how do you diagnose and treat toxoplasmosis?

A

dx: toxoplasma-specific IgM
tx: treat pregnant women and symptomatic and asymptomatic infants- sulfadiazine and pyrimethamine (anti-malarial drug)

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16
Q
  • due to bacterium treponema pallidum
  • transmisson through transplacental infection of fetus
  • direct contact with lesions during or after delivery can also transmit spriochete
  • transplacental infection can occur throughout pregnany at any stage of maternal infection
17
Q

clinical symptoms of early congenital syphilis

A
  • intrauterine infection can cause stillbirth, hydrops or preterm birth
  • many asymptomatic at birth
  • rash: vesicular or bullous on face, diaper area, dark red copper spots on palms and soles
  • snuffles, and fissures in the lips
  • jaundice with HSM
  • Untreated infants, including those who are asymptomatic can develop late manifestations after 2 years
18
Q

who should be evaluated in terms of syphilis?

A

evaluate infants and mothers with + treponemal test and:

  • untreated or inadequately treated syphilis
  • syphilis during pregnancy not treated with PCN
  • failure of antibody titers to decrease after treatment
  • syphilis treated < 1 month prior to delivery
19
Q
  • Transmission occurs from exposure to maternal blood during labor and delivery
  • transmission is as high as 90% in those exposed at birth without vaccination
  • more than 90% of infants who are infected perinataly will develop chronic infection
  • may have symptomatic infection with jaundice, lethargy, failure to thrive, abdominal distension and clay colored stools
A

Hep B infection

20
Q
  • risk of perinatal transmission 5-6%
  • spontaneous viral clearance is possible, 20% will clear virus by 2 years of age
  • most children with chronic infection are asymptomatic, although liver failure is possible
  • Breastfeeding is still possible, antibody testing at 18months will identify children with infection
21
Q
  • all pregnant women should be on antiretroviral drug regimens
  • timing of vertical transmission is uncertain
  • can be transmitted through breastfeeding
  • if the status is unknown birth parent should have the rapid test done during labor and delivery
  • can be transmitted through breastfeeding
  • prenatal and intrapartum zidovudine (AZT) reduces the rate of transmission
22
Q
  • IUGR
  • scarring skin lesions, dermatomal distribution
  • limb hypoplasia
  • ocular deficits: chorioretinitis, cataracts
  • CNS: seizures, mental retardation, microcephaly
  • mortality after birht 30% without VZIG
  • mother and infant should be isolated until mother’s vesicles have dried
  • pumped breast milk can be fed to infant as long as mother has no active lesions
A

congenital varicella syndrome

23
Q
  • extremely rare in US
  • all pregnant women screened for susceptibility
  • infection in first 20 weeks of pregnancy lead to structural fetal defects
  • infection in third trimester not associated with increased risk of fetal defects
24
Q

how does congenital rubella present?

A
  • can result in miscarriage or fetal date or CRS

classic congenital rubella syndrome (CRS)

  • CHD (PDA or branch pulmonary stenosis), myocarditis
  • eye defects: cataracts, glaucoma, microphtalmia
  • auditory: SNHL
  • neurologic: microcephaly, encephalitis, developmental disabilities
  • IUGR
  • jaundice with HSM
  • skin: thrombocytopenic purpura, blueberry muffin rash
  • language delay, strabismus, deafness, neonatal hepatitis

classic triad: cataract, cardiac abnormalities, deafness

25
* most common congenital infection * only 10% are symptomatic at birth * primary maternal or reactivation of latent infection can result- but symptomatic is more likely with primary maternal infection * PCR from amniotic fluid is the most sensitive test for fetal infection * transplacental passage of the virus, contact with secretions at the time of birth, ingestion of infected breast milk or tranfusion
CMV
26
Symptoms of CMV
* IUGR/SGA * Jaundice (direct hyperbilirubinemia) with HSM * thromobcytopenia (petechiae, purpura) * hearing loss (40% won't be detected within first month) * developmental delays (epilepsy, CP, visual impairment, can occur in later infancy and early childhood) * **asymptomatic infection- most with CMV will not have symptoms and no long-term sequelae** * microcephaly | **blueberry muffin rash just like rubella**
27
diagnosis and treatment of CMV
diagnosis * salivary CMV PCR with confirmatory urine * test for congenital infection in first 3 weeks of life. Later testing may identify acquired CMV infection Congenital CMV treatment * must start within the first month of life * oral valgancyclovir for 6 months * for life threatening- IV ganciclovir is used
28
* Transmission can occur in utero (5%), perinatally (85%) or postnatally (10%) * most newborns are delivered to women who have asymptomatic or unrecognized infections * contact with infected lower genital tract at time of delivery * ascending infection to the fetus even when membranes are apparently intact * post-natal infection * can be from type I or II but mostly from two
herpes simplex virus
29
* most devastating form of HSV infection * presents like sepsis, involves multiple organs including CNS-especially liver and lungs, respiratory and hepatic failure, DIC
Disseminated Disease
30
* Encephalitis: seizuers, lethargy, temperature instability * mortality 15%, morbidity 40-80%
CNS disease with or without SEM
31
* Herpetic lesions on skin, eye or mucous membrane * must have LP to exclude CNS involvement * 2/3rds with disseminated or CNS disease have skin lesions, may not be present at the time of onset of symptoms
Skin, Eye and Mucous Membrane (SEM) disease
32
* infection during pregnancy can lead to fetal death * half of pregnant women are immune to * fetal loss occurs in < 10% of non-immune women who become infected during 1st half of pregnancy * if infected before 20 weeks- fetal loss (11%) * if infected after 20 weeks- fetal loss < 1% * there are reports of third trimester maternal infection leading to hydrops fetalis and fetal death
Parvovirus 19
33
most frequent newborn rash 1. small erythematous macules or papules--> pustules on erythematous bases 3-5 days after birth. does not involve the palms or soles- individual lesions may spontaneously disappear 2. self-limted. usually resolves spntaneously in 1-2 weeks
erythema toxicum