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History and Physical Examination in the Newborn History 1) identify disabling diseases that are amenable to prompt preventive actions or tx (e.g.respiratory distress syndrome) 2) Anticipate conditions that may be of later importance (gonococcal conjunctivitis) 3) Uncover possible causative factors that may explain pathologic conditions (screening for inborn errors of metabolism) Perinatal history • Includes demographic and social data • Past medical illnesses in the family • Previous maternal reproductive problems • labor and delivery • Maternal drug intake/ exposure to roentgen • Maternal smoking / alcoholic beverage intake PHYSICAL EXAMINATION • Initial examination - to detect abnormalities - to establish a baseline for subsequent examination • At 24 hours of life • Upon discharge Physical Examination • Pulse rate ( N: 120-160 bpm when awake, 70-80 when asleep) • Respiratory rate (30-60 breaths/min) • Temperature • Weight (2.5 -4.5 kg), length (45-55 cm), head circumference (32-37 cm), CC (32-34 cm), AC • Dimensions of any visible or palpable structural abnormality • General appearance - Physical activity, skin color, obvious congenital abnormalities - Unusual posture, muscle tone - Edema (skin of the fingers & toes lacks the normal fine wrinkles when filled w/ fluid) Physical Examination • Pulse rate ( N: 120-160 bpm when awake, 70-80 when asleep) • Respiratory rate (30-60 breaths/min) • Temperature • Weight, length, head circumference (32-37 cm) • Dimensions of any visible or palpable structural abnormality • General appearance - Physical activity, skin color, obvious congenital abnormalities - Unusual posture - Edema (skin of the fingers & toes lacks the normal fine wrinkles when filled w/ fluid) • Skin - Vasomotor instability & peripheral circulatory sluggishness- deep redness or purple lividity in a crying infant; - Mottling – lacy red pattern; in healthy infants, cold stress, hypovolemia or sepsis. Cutis marmorata- persistent mottling (Down syn, tri 13 or 18) - Cyanosis, icterus, pallor, plethora (ruddy red appearance seen in polycythemia) • Harlequin color change – division of the body fr the forehead to the pubis into red and pale halves; transient & harmless - Mongolian spots – slate blue, well demarcated areas of pigmentation over the buttocks, back & other parts;most common birthmark; tend to disappear w/in the first year - Lanugo – fine, soft, immature hair in premature infants - Post-term infants – peeling, parchment-like skin - Erythema toxicum – small, white, occasionally vesiculopustular papules on an erythematous base that develop 1-3 days after birth; benign rash - Pustular melanosis – benign lesion predominantly seen in black neonates; vesiculopustular eruption - Vernix caseosa – greasy white substance that covers the skin until the 38th wk of gestation; provides a moisture barrier Head - General shape of the head - Micro or macrocephaly - Large fontanelles- hypothyroidism, trisomy 13,18,21 syndromes - Small fontanelles – hyperthyroidism, microcephaly, or craniosynostosis Common Forms of head trauma in the NB: 1. Caput succadanuem – after prolonged labor secondary to accumulation of blood or serum above the periosteum; poorly demarcated soft tissue swelling that crosses the sutures lines, w/ accompanying pitting edema & overlying petechiae, ecchymoses & purpura; resolves w/in days 2. Cephalhematoma – secondary to rupture of bld vessels; well demarcated, fluctuant swelling that does not cross suture lines, no overlying skin discoloration; resolves w/in 2 wks-3mos 3. Molding – temporary asymmetry of the skull resulting fr the birth process; normal head shape regained w/in 1 wk • Neck - Palpate SCM for hematoma & thyroid for enlargement - Neck masses FACE • General shape & appearance: dysmorphic features may imply congenital syndromes (wide set eyes/hypertelorism, low set ears, epicanthal folds, microphthalmos, long philtrum, asymmetry) • Facial nerve injury – apparent on 1st or 2nd day of life • Asymmetry: 7th nerve palsy, hypoplasia of depressor ms, abN fetal posture • Symmetric palsy: hypoplasia of the 7th nerve nucleus or Mobius syndrome EARS • Shape, size, position, canal, extraneous tags or pits • Tympanic membrane: dull gray • Imaginary horizontal line from the inner and outer canthus of the eye peprendicular to vertical axis of the head • Low set: helix is below the line • Preauricular tags or papillomas – benign, common; if pedunculated, may be ligated at the base (leading to dry gangrene & sloughing) • Deformities of the pinnae • Hairy ears – diabetic mothers EYES • STRUCTURE, ROR • Doll’s eye maneuver (labyrinthine and neck reflexes) • Conjunctival and retinal hemorrhages (2-4 wks) • Pupillary reflex – 28-30 wks AOG • Cat’s eye reflex (white pupil) – lens, vitreous or fundus abN • White pupil reflex/ leucokoria – Cataract, tumor, chorioretinitis, retinopathy of prematurity, persistent hyperplastic primary vitreous • Iris – colobomas & heterochromia • Cornea > 1cm, photophobia, tearing – congenital glaucoma NOSE • Shape, size, patency (catheter), swelling over the nasolacrimal duct, size of philtrum, definition of nasolabial folds • Assymetry: facial compression and molding MOUTH • Rest & crying • Mandible, maxilla fit • Tongue, buccal surface, palate, back of mouth • Gums & hard palate – palpate for masses or submucous defects • Ranula, Epstein pearls, mucocele, natal teeth, macroglossia (Beckwith’s syndrome) CHEST • RATE – full minute in resting; N term – 3040/min • OBSERVE – if assymetric: tension pneumothorax - tachypnea, retractions, grunting on expiration: respiratory distress - minimal retractions N (compliant chest walls), abdominal breathing • BREATH SOUNDS – ® axilla - more tubular than vesicular - auscultate extrathoracic airways, transmitted well through the chest (possible obstruction) - Pneumothorax/atelectasis: unequal or absent - Diaphragmatic hernia: absent BS w/ bowel sounds CHEST • PECTUS EXCAVATUM – not significant • CLAVICLES – hypoplastic, absent or fractured - clavicular fractures: most common, decreased or absent movement, pain or tenderness on movement, deformity, discoloration, crepitus - tx: minimize pain/discomfort • BREASTS – usually 1 cm in diameter (M/F) at term - enlarged (3-4 cm) due to maternal estrogen - supernumarary nipples - witch’s milk HEART • Heart rate, rhythm, quality of heart sounds, active precordial activity, murmurs • Goal: rule out cardiac disease or determine if sxs are cardiac in origin • N HR: 120 to 160 - stimulate, if no increased activity, do ECG and serum electrolyte studies • Murmurs – if + after 12 hrs, significant ABDOMEN • OBSERVE – omphalocoele, gastroschisis, scaphoid (diaphragmatic hernia) • AUSCULTATE – Nly hypoactive • PALPATE – distention, tenderness, masses - liver: 1-2 cm below costal margins - spleen tip: below the costal margin Hepatomegaly – CHF, hepatitis, sepsis Splenomegaly – CMV, rubella, sepsis Kidney – Nly palpable, esp R - kidney size increased in RVT, polycystic kidney dse, hydronephrosis UMBILICUS • Bleeding, infection, granuloma, abN communication with intra-abdominal organs • Redness, discharge, edema at base: patent urachus or omphalitis • N: 2 arteries, 1 vein; if only 2 vessels: renal or genetic problems • Cord: translucent; if greenish yellow: meconium staining (fetal distress) GENITALIA • MALE – dorsal hood, epispadias, hypospadias, chordee - penis (> 2cm) w/ phimosis, meatus, testes in the scrotum, hernias - small penis: decreased androgen effect / growth hormone action in the 2nd & 3rd tri. - hydrocele: common, usually resolve: 1 yr GENITALIA • FEMALE – size and location of labia, clitoris, meatus, vaginal opening, relation of posterior fourchette to the anus - redundant hymenal tissue, imperforate hymen - discharge: common, blood-tinged due to maternal estrogen withdrawal - clitoris prominent • Ambiguous genitalia – medical emergency - determine pituitary and adrenal integrity ANUS • Meconium passage – usually 1st 12 hrs after birth - within 48 hours after birth • Imperforate anus – gentle insertion of finger or rectal tube, x-ray • Rectovaginal fistula, neurocutaneous sinus EXTREMITIES • PULSES – both UE and LE (coarctation of the aorta) • EFFECTS OF FETAL POSTURE – to explain cause and usual transitory nature (ie. Breech) • ACTIVITY – spontaneous or stimulated; to rule out fracture or nerve injury • HANDS & FEET – polydactyly, syndactyly, ab(N) dermatoglyphic patterns (Simian crease) • HIPS – rule out congenital dislocation (Barlow, Ortolani) TRUNK AND SPINE • GROSS DEFECTS • abN pigmentation, hairy patches – underlying vertebral anomaly • Sacral or pilonidal dimple – meningocele, etc. NEUROLOGIC EXAMINATION • IN UTERO MUSCULOSKELETAL DISEASES: limited fetal motion, ssx independent of specific disease • Arthrogryposis • Other manifestations: breech, polyhydramnios, failure to breath at birth, pulmonary hypoplasia, dislocated hips, undescended testes, thin ribs, clubfoot • State, spontaneous ms activity, tone, cranial nerves APGAR 0 1 2 Appearance (color) Blue, pale Pink body, blue extremities Pink Pulse rate - <100 >100 Grimace None Grimace Cough or sneeze Activity Limp Some flexion Active motion Respiratory rate - Slow, irregular Good, crying Thank you!