Peds: Prenatal/Newborn Assessment/Screening Flashcards

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1
Q

Assessment of Prenatal History

A
  • *course of prenatal care;
  • *xenobiotic used during gestational period;
  • *health problems during pregnancy;
    • intrauterine fetal health problems;
  • *mother’s perception of pregancy
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2
Q

Assessment of Perinatal History

A
  • *delivery process (vaginal vs c-section, planned vs emergent, induced, analgesia/anesthesia);
  • *complications during delivery (meconium, placenta previa/abruption, forceps/vacuum);
  • *birth size/wt (low < 2,500 g, very low < 1,500 g, extremely low < 1,000 g);
  • *assessment of wt for gestational (average 10th - 90th percentile, large > 90th percentile, small < 10th percentile);
  • *APGAR socres (5 areas= appearance, pulse, grimace, activity, & respiration = 0, 1, 2 pts possible with max score noted at 1 min & 5 min after birth = total max 10 pts)
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3
Q

Assessment of Postnatal History

A
  • *hospital course;
  • *maternal problems (bleeding, infection, dehydration, breastfeeding, anesthesia response, fever, depression);
  • *infant problems (ABO/RH incompatibilities, hyperbilirubinemia, Hip dysplasia, murmurs, Talipes equinovarus congenita (club feet), & genetic syndromes
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4
Q

Newborn Physical Examination:

  • average weight, length, head circumference
  • gestational age
A
  • *weight, length, head circumference:
  • —average length 20-21 inches;
  • —average wt 7 lbs (3.1 kg);
  • —average head circumference 13-14 in (33-35 cm);
  • – note ethnic differences in height;
  • *assessment of gestational age:
  • –37-41 weeks full term - best outcomes;
  • –prior to 37 weeks premature;
  • –after 41 weeks post term
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5
Q

Newborn Physical Examination
IUGR = Intrauterine Growth Retardation:
- Small Gestational Age (SGA)

A
  • SGA = small gestational age**
  • **33% of SGA infants = SYMMETRIC
  • – head circumference, weight, & length are < 10th percentile;
  • *due to long term compromise to fetus as in genetic disorders, intrauterine infection, inborn metabolism errors, & environment- drugs, smoking, or radiation;
  • **55% of SGA infants = ASYMMETRIC
  • — head circumference & length are normal but weight is < 10th percentile;
  • *due to extra fetal compromise occurring > 24 weeks; from chronic HTN, pre-eclampsia, renal disease, cyanotic heart disease, hemoglobinopathies, abruptio placentae, high altitudes (mountains), multiple gestation
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6
Q

Newborn Physical Examination:

LGA or Large Gestational Age

A
  • *weight > 90th percentile; may be due to-
  • *Beckwith-Wiedemann syndrome: congenital growth disorder which causes hemihypertrophy, large organs, & other symptoms;
  • *Hydrops Fetalis: fatal condition of which abnormal accumulation of fluid is noted in 2 or more fetal body areas;
  • *maternal diabetes;
  • *large mother
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7
Q

Newborn Physical Examination:
Dubowitz/Ballard Exam for Gestational Age
- part 1: physical maturity assessment

A
  • *physical maturity assessment–
  • *2 hours of birth with pts (-2 to +5) given for six criteria:
  • *skin texture (sticky, smooth, peeling);
  • *lanugo (soft, downy hair- absent on immature infants, present on mature infants, and disappears with post maturity);
  • *plantar creases (sole of feet ranging from absent to covering entire feet);
  • *breasts (thickness & size of breast tissue);
  • *eyes/ears, & genitals (male- presence/appearance of smooth to wrinkled scrotum; female- size/appearance of clitoris/labia)
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8
Q

Newborn Physical Examination:
Dubowitz/Ballard Exam for Gestational Age
- part 2: neuromuscular maturity assessment

A
  • *neuromuscular maturity assessment–
  • *24 hrs of birth with pts given for six criteria:
  • *posture- how arms/legs held (good tones/flex);
  • *square window- how baby’s hand flexes toward wrist (90 degree angle flex- premies, flex to forearm- term);
  • *arm recoil- how far arm’s spring back to flex position;
  • *popliteal angle;- how far knees extend;
  • *scarf’s sign- how far elbows cross chest (no cross midline- term; line of elbow cross midline- premie);
  • *heel to ear- how close feet move to ears;
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9
Q

Newborn Physical Examination:
Dubowitz/Ballard Exam for Gestational Age
- part 3: gestational age determination based upon sum of scores

A
  • *low scores indicate immaturity;

* *high scores indicate mature or post mature infant

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10
Q

The Dubowitz/Ballard Exam for Gestational Age has ____ parts.

A

**physical maturity, neuromuscular maturity, & gestational age determination

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11
Q

Newborn Vital Signs

A
  • *FEVER = temperature > 100.4 degrees F (38 deg. C);
  • *PULSE 120-180 bpm;
  • *RESP 30-80 bpm;
  • *BLOOD PRESSURE < 112/74 mmHg
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12
Q

Newborn Skin: Common Variations

A
  • *typical skin changes - pallor, cyanosis, plethora (blotchy skin- polycythemia), jaundice, grey;
  • *milia- pinpoint white papules to face, disappears 3-4 wks (widespread distribution = genetic syndrome);
  • *miliaria- (R for red aka “prickly heat”)- obstructed sweat or eccrine gland ducts;
  • *erythema toxicum- most common, appears 2-5 days after birth, blotchy red spots with overlying white/yellow papules/pustules; disappears 14th day;
  • *Cafe au lait spots- subtle shade discoloration on either flank, may not present @ birth, size increase with age, more than 6 in child > 5 yrs suspect neurofibromatosis;
  • *Mongolian spots- benign, flat, congenital birthmark with wavy borders/irregular shape, commonly blue, last 3-5 days after birth, disappear @ puberty;
  • **Port wine stains- vascular birthmark of superficial deep dilated capillaries in skin, produce reddish/purplish discoloration, permament, associated to neuro (seizures) & ocular (glaucoma) disorders;
  • *Strawberry mark- “hemangiomas”- 2% babies, raised soft red lumps, common in prematurity, hypo/per-pigmented, shrink/fade after 6 mos of age
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13
Q

Newborn Neurological Exam:

Reflexes, LOC, Tones, & Posture

A
  • *LOC- alert;
  • *Posture- hips abducted/partially flexed, knees flexed, arms adducted, elbows flexed, fist clenched;
  • *Tone- head inline at least 3 sec;
  • *Reflexes- symmetrical;
  • *Primitive Newborn Reflexes- pacing/stepping (disappears 1-2 mos), rooting, sucking, moro, plantar grasp, tonic neck (disappear 3-4 mos); palmar grasp (disappear 3-6 mos), Babinski “toes fan”- (disappears 12 mos or walking)
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14
Q

Newborn Assessment of Head/Neck:

Head Variations

A
  • *Caput Succedaneum- fluid under skin, simple swelling, crosses suture lines, result of birth trauma, disappears 2-3 days; no tx required;
  • *Cephalohematoma- blood under periosteum (skull bone), does not cross midline, develops 24-48 hrs after birth, needs further evaluation;
  • *Bossing- protruding of various skull bones- noted in Rickets, , beta-thalessema (late), acromegaly, congenital syphillis, prematurity;
  • *Microcephaly- head circum smaller than 2 stand. dev, -small brain, fetal alcohol syndrome, chromo. abn, PKU
  • *Macrocephaly- head circum larger than 2 stand. dev, hydrocephalus;
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15
Q

Newborn Assessment of Head/Neck:

Eyes

A
  • *sclera is normally white and may appear bluish in premies;
  • *deep blue sclera- rule out osteogenesis imperfecta- prone to fxs;
  • *red reflex- normally ranges from pink, orange, & red in color on exam;
  • *red reflex- replaced by black spots (means no clear pathway from lens to retina);
  • *red reflex- replaced by whitish color (means retinoblastoma or congenital cataracts);
  • *Colobomas- (familial or spontaneous embryonic fissure defect- normally closes 5th wk gest)- mild forms affect iris, severe forms-choroid/optic nerve involved- suspect CNS defect ex. optic nerve hypoplasia;
  • *Heterochromia- mix/diff colors of the iris;
  • *Cloudy corner- sclerocornea, Peters anomaly, trauma, infection, dermoid tumor
  • *Salt/Pepper speckling (Brushfield spots of the iris)- assoc to Down syndrome
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16
Q

Newborn Assessment of

Cardiovascular, Pulmonary, Gastrointestinal, & Genitourinary system

A
  • *Pulmonary/Chest- assess resp rate/pattern (normally abdominal breathers); retractions, stridor, grunting, breast enlargement;
  • *CV- assess cap refill, radio-femoral pulse delay- diff noted in upper/lower extremities (consider coarctation of aorta), pulse character, location/size of PMI (point of max impulse)- 3rd-4th intercostal space/lfet midclavicular line, murmurs- present in 85% newborns;
  • *Abdomen- flat abdomen is abnormal (should be slightly protruding), umb. cord (2 arteries/1 vein), color of umb cord, hernias, anal patency (noted by meconium passage);
  • *genitourinary- males -penis for urethral meatus (hypospadias- ventral side & epispadias- dorsal side); ability to retract foreskin, tests- 97% descended @ birth (occurs in 3rd trimester); females- discharge/small amount of bleeding may be noted (hormones)
17
Q

Newborn Assessment: Screening Principles

A
  • *screen for disorders of which symptoms may not present until irreversible damage occurred;
  • *disorders without cure;
  • *prevalence of disease in population;
  • *use simple screening method;
  • *use screening which has low false +/false - results;
  • *high benefit-to-cost ration (most cost effective);
  • *mechanism present for follow-up after dx;
  • *tests available for over 50 conditions;
  • *early identification of metabolic disorders is a goal;
  • *all 50 states require testing of: PKU, GALACTOSEMIA, SICKLE CELL, CONGENITAL HYPOTHYROIDISM
18
Q

Newborn Assessment: Screening Considerations

A
  • *re-screen is mandatory if newborn tested < 24 hrs of birth;
    • re-screen infants who appear asymptomatic;
  • *identify disease risk factors-
  • *vision screening- congenital cyanotic disease or structural anomalies;
  • *hearing screening-absent startle (moro) reflex, BSAER (brain stem auditory evoked response) test- no later than 3 mos and tx by 6 mos of age;
19
Q

Newborn Assessment of Head/Neck:

Hair Patterns & Growth

A
  • *color should match/uniform;
  • *distribution- uniform;
  • *white forelocks iwth other anomalies- assoc. to deafness & retardation (Waardenburg syndrome- group of familial conditions);
  • *more than 1 whorl (patch of hair growing in oppos direction of rest of hair)- possible poor brain growth;
  • *unruly hair with unusual facies, SGA, & microcephaly- assoc to Down syndrome
20
Q

Newborn Assessment of Head/Neck:

Fontanels

A
  • *anterior fontanel- largest (2-5 cm), closes by 18 mos;
  • *posterior fontanel- may not be palpable at birth, closes by 2-3 mos;
  • *Overriding sutures- normal and disappears as brain/head grows;
  • *wide fontanels- prematurity, IUGR, Down, hydrocephalus, & hypothyroidism
21
Q

Newborn Assessment of Head/Neck:

Ears, Nose, & Throat

A
  • *assess for symmetry, placement, pits, skin tags;
  • *Choanal atresia (narrowing/blockage of nasla airway by tissue at birth);
  • *Mouth/plalate- assess size/shape-
  • *Microstomia (small mouth)- trisomy 18 “Edwards” (high pitch cry, posturing, mult. defects, high mortality) and 21 “Down”;
  • *Macrostomia (large mouth)- mucopolysaccharidoses (lysosomal disorder- cannot break down sugar) and fetal alcohol syndrome;
  • *Cleft lip/palate- assess feeding/aspiration, freq. URI; teach- feeding position, may need sx repair;
  • *Tongue- macroglossia- hypothyroidism, Down (hypotonia), mucopolysaccharidoses;
  • *Teeth- Epstein pears- collect in gums over time (assoc with Miliria); Natal teeth
22
Q

Newborn Assessment of Musculoskeletal system

A
  • *scoliosis- lateral curvature of spine;
  • *kyphosis- curvature of thoracic spine;
  • *lordosis- curvature of lumbar spine;
  • *spinal defects- ex. meningomyeloceles (spina bifida);
  • *clavicle fx;
  • *fingers/creases;
  • *hip dsyplasia- hips flexed 90 degrees/knees together (check knee ht)- abduct and adduct while fingers @ greater trochanter-
  • **ORTOLANI click- heard/felt as dislocation reduced;
  • **BARLOW’S MANEUVER- feeling of slip as femoral head slps from acetabulum causing dislocation; also note fat pads (skin fold thickness @ hip)
23
Q

A newborn is considered ____ months of age.

A

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