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91 Cards in this Set
- Front
- Back
apgar score
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heart rate
respiration color tone reflex irritability |
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routine newborn care
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cleanse and rinse
bacterocidal agent to cord 1% silver nitrate or 0.5% erythromycin for eyes 1mg vitamin K IM |
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birth injuries
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subconjunctival hemorrhage
skull fracture brachial palsy clavicular fracture facial nerve palsy caput succedaneum cephalohematoma subcutaneous fat necrosis |
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subconjunctival hemorrhage
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from sudden increase in intrathoracic pressure passing through canal; resolves spontaneously
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skull fractures of newborn
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linear --> most common; no symptoms nor treatment needed
depressed --> elevate to prevent cortical injuries basilar --> fatal |
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brachial palsy
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Erb-Duchene --> C5-C6; no sholder abduction, external rotation or supination of arm
Klumpke --> C7/C8 +- T1; paralyzed hand +- Horner syndrome most will recover |
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clavicular fracture
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from shoulder dystocia in vertex position and arm in extension in breech; palpable callus within a week; immobilization
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facial nerve palsy
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from forceps or pressure during delivery; improves over week or neuroplasty
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caput succedaneum
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diffuse edematous swelling of scalp which crosses suture lines; spontaneously dissapears
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cephalohematoma
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diffuse edematous swelling of scalp which does not cross suture lines; spontaneously dissapears
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subcutaneous fat necrosis
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difficult labor/delivery, perinatal asphixia, prolonged hypothermia; hypocalcemia
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cutis marmorata
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lacy, reticulated vascular pattern over skin on most of the body; improves but may be associated with syndromes
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milia
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firm white papules, inclusion cyst and Epstein pearls on palate midlines; resolves
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salmon patch
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nevus simplex; pale pink vascular macules usually symmetric; facial ones dissapear
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mongolian spots
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blue to slate-gray macules on presacral, back or posterior thighs; improves; differentiate from child abuse
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erythema toxicum
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firm yellow-white papules/pustules with erythematous base; self-limited; differentiate from SSSS
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port-wine stain
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vascular malformation, permanent, unilateral; rule out Sturge-Weber; laser treatment
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hemangioma
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superficial --> bright red protuberant sharply demarcated; involutes in years
deep --> bluish hue firm cystic; may persist; check internal organs; laser therapy |
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neonatal acne
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erythematous papules on face from high maternal androgens; no treatment
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preauricular tags/pits
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may indicate hearing loss and GU anomalies
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nevus sebaceous
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area of alopecia with nodular orange skin; possible malignancy; remove before adolescence
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coloboma of iris
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cleft at six-o-clock position; most have other eye anomalies; CHARGE association
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aniridia
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hypoplasia of iris; associated with Wilms tumor
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brachial cleft cyst
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mass on lateral neck; infections are common; surgical removal
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thyroglosal duct cyst
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mass on neck midline; moves with swallowing
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congenital torticollis
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knotted-up sternocleidomastoid; treat with passive ROM exercises
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breast hypertrophy
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common; should be symmetric; otherwise may be absecess or mastitis
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suppernumerary nipples
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usually along mammary gland; associated with renal and cardiovascular anomalies
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Poland syndrome
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amastia, pectoralis muscle aplasia, rib deformities, webbed fingers, radial nerve aplasia
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pectus excavatum/carinatum
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usually benign; correction for cosmetic reasons
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diaphramagmatic hernia
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scaphoid abdomen and bowel sounds in chest
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omphalocele
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sac covered protrusion through umbilicus; associated with malformations and chromosome disorders
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umbilical hernia
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most close spontaneously; consider congenital hypothyroidism
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gastroschisis
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uncovered protrusion lateral to abdominal midline; may have intestinal atresia
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abdominal masses in newborn
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polycystic kidney disease, hydronephrosis, enlarged bladder
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hydrocele
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transitory; palpation and illumination of testes diffrentiated from inguinal hernia
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hypospadia
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urethral opening on ventral surface of penis
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epispadia
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urethral opening on dorsal surface
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undescended testes
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usually in inguinal canal; differentiate from retractile testes; if not descended by one year then surgical removal to avoid sterility and malignancy
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hernias in newborn
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usually inguinal and indirect; surgical treatment
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syndactyly
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fusion of fingers or toes; get x-ray first for surgical planning
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polydactyly
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> 5 fingers; no treatment needed if good blood supply
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newborn screening
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do before discharge or fourth day
more realiable after 48 hours examples: phenylketonuria, galactosemia, hypothyroidism |
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phenylketonuria
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phenylalanine hydroxylase deficiency with excess phe; mental retardation, vomiting, abnormal movements, fair hari skin blue eyes, normal at birth; treatment is phenylalanine restriction for life
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galactosemia
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G-1-P uridyltransferase deficiency; jaundice, hypoglycemia, catarracts, mental retardation, e. coli sepsis; restric lactose
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intrauterine growth restriction
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symmetric --> genetic syndromes, chromosomal abnormalities, congenital infections, teratogens
assymetric --> uteroplacental insufficiency due to maternal diseases; placental dysfunction |
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infants of diabetic mothers
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fetal hyperinsulinemia --> hypoglycemia
large for gestational age and plethoric hyperbilirubinemia tachypnea cardiomegaly - assymetric septal hypertrophy birth trauma - macrosomia polycythemia renal vein thrombosis |
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causes of respiratory distress in newborn
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respiratory distress syndrome
transient tachypnea of the newborn meconium aspiration diaphragmatic hernia |
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respiratory distress syndrome of newborn presentation
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due to surfactant deficiency in premature
tachypnea, nasal flaring, grunting hypoxemia, hypercabia and respiratory acidosis |
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respiratory distress syndrome of newborn diagnosis
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initial diagnostic test --> chest x-ray (ground glass appearance, atelectasis, air bronchograms)
most accurate test --> L/S ratio (done on amniotic fluid prior to birth) |
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respiratory distress syndrome of newborn treatment
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best initial treatment --> oxygen + nasal continuous positive airway pressure
most effective treatment --> exogenous surfactant administration prevention --> avoid prematurity with tocolysis antenatal betamethasone |
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transient tachypnea of newborn
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due to slow absorption of lung fluid with increased dead space
presents with tachypnea after birth do chest x-ray (air trapping, fluid in fissures, perihilar streaking improves within hours to days |
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meconium aspiration presentation
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meconium passes as result of fetal hypoxia and distress
severe respiratory distress hypoxemia barrel chest |
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meconium aspiration diagnosis
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chest x-ray --> patchy infiltrates, increased AP diameter, flattening of diaphragm
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meconium aspiration complications
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pneumothorax
aspiration pneumonitis pulmonary artery hypertension |
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meconium aspiration treatment and prevention
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treatment --> positive pressure ventilation, high frequency ventilation, nitric oxide, extracorporeal membrane oxygenation
prevention --> endotracheal intubation and airway suction of depressed infants with thick meconium |
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diaphragmatic hernia
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abdominal content into thorax causes pulmonary hypoplasia
respiratory distress scaphoid abdomen bowel sounds in chest bowel in chest seen in x-ray diagnosis --> prenatal ultrasound treatment --> immediate intubation and surgical correction |
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meconium plugs
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seen in IODM, Hirchsprung, cystic fibrosis, maternal drug abuse
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meconium ileus
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mostly in cystic fibrosis
abdominal distention, vomitting, perforation, no passage of meconium within 24-48 hours first test --> abdominal x-ray shows distention of bowel loops treatment --> high gastrografin enemas |
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tracheoesophageal fistula
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coughing choking or gagging with first feeding
respiratory distress aspiration pneumonia mostly proximal esophageal atresia and distal fistula with air in stomach |
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necrotizing enterocolitis
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transmural intestinal necrosis associated with prematurity
bloody stools, apnea, lethargy, abdominal distention pneumatosis intestinalis on abdominal x-ray is pathognomonic |
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Hirchsprung disease
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initial test --> barium enema shws megaacolon proximal to aganglionic segment
best test --> rectal biopsy shows absent ganglionic cells |
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duodenal atresia
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bilious vomiting from first feeding
abdominal x-ray shows double bubble sign surgical correction |
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kernicterus
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unconjugated bilirubin in basal ganglia and brain stem nuclei
hypotonia seizures opisthotonos delayed motor skills choreoathetosis sensorineural hearing loss |
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physiologic Vs. pathologic jaundice
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physiologic --> 2-3 day of life, dissapears by 5th, peak bilirubin 10-12mg/dL, rate of rise <5mg/dL/day
pathologic --> appears in 1st 24 hours, variable dissapearance, unlimited bilirubin, rate of rise > 5mg/dL/day |
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jaundice work-up in newborn
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1) determine if it's physiologic or pathologic
2) determine if it's direct or indirect 3) if indirect --> Coombs test; if negative --> 4) determine hemoglobin levels |
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indirect hyperbilirubinemia, Coombs test +
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Rh/ABO incompatibility
thalassemia minor |
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indirect hyperbilirubinemia, Coombs test -, high hb
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polycythemia
twin-twin transfusion maternal-fetal transfusion delayed cord IUGR infant of diabetic mother |
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indirect hyperbilirubinemia, Coombs test -, low hb
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spherocytosis
eliptocytosis G6PD deficiency pyruvate kinase |
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direct hyperbilirubinemia causes
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sepsis
TORCH total parenteral nutrition hypothyroidism galactosemia tyrosinemia cystic fibrosis choledochal cyst |
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treatment of hyperbilirubinemia
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phototherapy (complications are loose stools, rash, overheating, dehydration, bronze baby)
if phototherapy is not enough --> double volume exchange transfusion |
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Crigler-Najjar type I
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glucoronyl transferase deficiency leads to unconjugated hyperbilirubinemia
rapid rise in indirect bilirubin >20mg/dL, no hemolysis, kernicterus Dx --> closed liver bipsy to measure glucoronyl transferase Tx --> intensive phototherapy and exchange transfusions |
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Crigler-Najjar type II
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partial glucoronyl transferase deficiency leads to unconjugated hyperbilirubinemia
milder than type I with no kernicterus Tx --> phenobarbital |
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Gilbert syndrome
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unconjugated hyperbilirubinemia
low glucoronyl transferase levels benign, no treatment necessary |
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Dubin-Johnson
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conjugated bilirubin cant get out of liver
mild disease detected in adolescence |
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Rotor syndrome
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conjugated bilirubin can't get out of liver
mild disease detected in adolescence |
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neonatal sepsis presentation
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irritability
poor feeding fever grunting bulging fontanel delayed capillary filling |
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neonatal sepsis risk factors
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prematurity
chorioamnionitis intrapartum fever maternal leukocytosis prolonged rupture of membranes |
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neonatal sepsis bugs
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group B strep
E. coli listeria |
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neonatal sepsis work-up and diagnosis
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CBC
blood culture urinalysis urine culture chest x-ray if meningitis is suspected --> lumbar puncture |
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neonatal sepsis treatment
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if no meningitis --> ampicillin + aminoglycoside
if meningitis --> ampicillin + 3rd gen ceph (except ceftriaxone) |
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TORCH
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Toxoplasmosis
Other Rubella Cytomegalovirus Herpes |
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toxoplasmosis congenital infection
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usually in cat feces or undercooked raw meat
chorioretinitis hydrocephalus generalized intracranial calcifications seizures visual impairments treat mother with spiramycin treat baby with sulfonamide for 6 months |
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congenital rubella
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blueberry muffin spots
PDA pulmonary artery stenosis cataracts congenital hearing loss |
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cytomegalovirus neonatal infection
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periventricular calcifications
microcephaly chorioretinitis sensorineural hearing loss |
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neonatal herpes
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disseminated --> pneumonia, shock, hepatitis
skin, eyes, mouth --> keratoconjunctivits CNS --> meningitis, lethargy, seizures outcomes --> deafness, blindness, microcephaly, seizures diagnosis --> PCR + Tzanck smear culture treatment acyclovir |
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congenital syphilis
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before 2 --> fever, anemia, rash, jaundice, anemia
after 2 --> Hutchinson teeth, Clutton joints, saber shins, saddle nose, osteochondritis, rhagades diagnosis --> radiographic bone changes, treponema in scrapings from lesions; most specific --> FTA-ABS treatment --> penicillin |
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TORCH work-up if suspected
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total cord IgM
urine CMV culture --> if negative, excludes CMV IgM --> toxoplasmosis, rubella maternal rubella status --> if positive, excludes it PCR --> for herpes |
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neonatal seizures causes
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hypoxic ischemic encephalopathy --> cerebral palsy
intraventricular hemorrhage --> preterm metabolic --> IODM, inborn errors of metabolism, DiGeorge infection --> TORCH, maternal fever, sepsis/meningitis |
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neonatal seizures work-up
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EEG --> may be normal
CBC, electrolytes, glucose if meningitis --> lumbar puncture if infection --> blood and urine cultures if preterm --> ultrasound of the head for intraventricular hemorrhage |
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neonatal seizures presentation
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chewing, tongue thrusting, apnea, staring, blinking, color changes, desaturation
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