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Academy · Prevention · Pediatrics

Newborn

Preventive visit

A high-yield reference for birth hospitalization and the first check.

Verify newborn history, examination, universal screening, prophylaxis, feeding, discharge counseling, and individualized pathways without opening a full guideline document.

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Clinician quick view

Newborn visit — verify in 20–30 seconds.

Birth hospitalization plus first-week follow-up at 3–5 days. Routine and individualized care are separated deliberately.

01

History

Prenatal/birth course; maternal blood type, HBsAg, HIV, STI and GBS results; medications/exposures; family history; feeding, elimination, sleep, safety and support.

02

Measure / examine

Weight, length, head circumference and WHO trajectory; vitals; complete newborn examination including red reflex, pulses, hips, cord, jaundice, tone and reflex symmetry.

03

Development / function

Surveil symmetric movement, primitive reflexes, sound response, brief fixation, state regulation, feeding cues and consolability. No routine formal developmental screen.

04

Universal screening

Bloodspot 24–48 h; hearing before discharge/by 1 mo; CCHD ≥24 h or before early discharge; TcB/TSB 24–48 h or before early discharge.

05

Immunization / prophylaxis

HepB by weight and maternal HBsAg pathway; RSV by season and maternal vaccination; IM vitamin K; erythromycin eye ointment.

06

Feeding / growth

Observed feeding before discharge and at 3–5 d; 8–12 feeds/24 h; assess output. Evaluate >7% loss by day 3–5 or >10% at any time.

07

Preventive counseling

Jaundice, fever/illness, ABC safe sleep, rear-facing car seat, cord care, hand hygiene, sick contacts and result follow-up.

08

Lifestyle counseling

Breast milk or iron-fortified formula, supervised awake tummy time, bonding/support, smoke-free care and avoidance of impaired caregiving.

09

Risk-based / individualized

Prematurity/<2,000 g, HBsAg positive/unknown, Rh-/type O, G6PD risk, substance exposure, home birth, abnormal screen, congenital anomaly, RSV history/season, vitamin K refusal and elective circumcision.

10

Follow-up

Confirm 3–5-day visit for weight, bilirubin and feeding reassessment; establish medical home and closed-loop screening-result follow-up.

Medical prevention

Examine, screen, immunize, provide prophylaxis, and identify illness early.

Lifestyle prevention

Support feeding, safe sleep, awake play, relationships, and exposure avoidance.

RoutineRisk-basedHistory / timing dependentGuideline difference

Detailed reference · History

Start with the pregnancy, delivery, and first feeds.

Prenatal & birth

  • Gestational age, delivery mode, ROM duration, maternal fever, meconium, Apgar scores
  • Birth weight, complications and resuscitation
  • Maternal blood/Rh, GBS, HIV, HBsAg, syphilis, gonorrhea and chlamydia results
  • Pregnancy medications and maternal RSV vaccination timing

Family & newborn health

  • Hemoglobinopathy, metabolic disorder, congenital heart disease, hearing loss
  • Sibling jaundice requiring treatment; G6PD deficiency
  • Current newborn concerns and 3–5-day follow-up plan

Feeding & elimination

  • Breast/bottle method, frequency, duration, latch and milk-transfer signs
  • Formula type, volume, preparation and storage
  • Urination in first 24 hours; wet diapers and stool transition

Sleep, behavior & safety

  • Sleep position, surface, location and caregiver plan
  • Alertness, consolability, tone, movement and feeding cues
  • Rear-facing car seat, smoke exposure, firearms, cord/circumcision care

Family / social environment

  • Bonding, caregiver adjustment, postpartum-depression symptoms
  • Supports, food/housing/transportation/financial needs
  • IPV, substance use, prior child loss or protective-services involvement when relevant

Age-specific modifiers

  • Home or birth-center birth and completion of hospital-based prevention
  • Maternal HBsAg, HIV and Rh status
  • Prenatal tobacco, alcohol, opioid, marijuana or other substance exposure

Detailed reference · Growth, examination & development

Confirm stability; establish the first trajectory.

Measurements

  • Birth and follow-up weight
  • Length
  • Head circumference
  • WHO charts, ages 0–24 months
  • Evaluate >7% loss by day 3–5 or >10% at any time

General / neurologic

Color, tone, activity, cry, gestational-age assessment; Moro, suck, grasp, rooting and movement symmetry.

Head / eyes / ears

Fontanelles, sutures, molding, cephalohematoma/caput; red reflex and pupils; ear position, pits and tags.

Heart / lungs

Murmur, femoral pulses, respiratory effort/rate, retractions and grunting; pulse oximetry under CCHD screening.

Abdomen / genitalia / hips

Cord vessels, organomegaly, hernia; testes, hypospadias or ambiguity; Ortolani and Barlow maneuvers.

Spine / skin

Sacral dimples, tufts or masses; jaundice, birthmarks, rashes and skin integrity. Visual inspection alone is insufficient for bilirubin risk.

Developmental surveillance

Symmetric movement, flexion, head turn, reflexes, sound response, brief fixation, state changes, consolability and feeding cues.

Developmental red flags

Persistent hypotonia or hypertonia, absent or asymmetric primitive reflexes, seizure-like activity, poor feeding or suck, lack of response to auditory stimuli, or dysmorphic features warrant evaluation. Formal developmental screening is not routine at the newborn visit.

Detailed reference · Recommended screening

Universal first. Risk-based only when the history supports it.

Dried-bloodspot screening

Routine

Universal at 24–48 hours; exact disorders vary by state.

Timing, method & qualifiers

Follow the state program. Abnormal results require immediate state-protocol follow-up and confirmatory testing. Verify the current RUSP and state-specific panel rather than relying on a fixed condition count.

HHS/ACHDNC, state programs, ACOG 2019

Newborn hearing screening

Routine

Before discharge; no later than 1 month. OAE or automated ABR.

Timing, method & qualifiers

USPSTF Grade B. The supplied EHDI goal is diagnosis by 3 months and intervention by 6 months. Family history may warrant heightened follow-up.

JCIH, AAP, USPSTF Grade B

CCHD screening

Routine

Pre- and post-ductal pulse oximetry at ≥24 hours, or before an earlier discharge.

Timing, method & qualifiers

AAP 2025 algorithm: ≥95% at both sites to pass, with one retest after an initial failed screen.

AAP 2025 CCHD clinical report; RUSP

Predischarge bilirubin

Routine

TcB or TSB at 24–48 hours, or before an earlier discharge.

Timing, method & qualifiers

AAP 2022 KAS 5. Confirm TcB with TSB when within 3 mg/dL of the phototherapy threshold or TcB ≥15 mg/dL. Determine follow-up from the difference between the measured value and phototherapy threshold, not the prior risk-zone nomogram alone.

AAP 2022 hyperbilirubinemia guideline; KAS 5 recommendation

Blood type / DAT

Risk-based

For maternal type O, Rh-negative, or unknown blood type.

Timing, method & qualifiers

Cord-blood DAT is specified when maternal blood is Rh-negative or type O; heighten jaundice surveillance. Exact primary guideline details were not supplied.

Primary guideline details unavailable in the reviewed evidence

G6PD testing

Risk-based

Consider for specified ancestry, particularly with severe or unexplained jaundice.

Timing, method & qualifiers

The reviewed guidance identifies males of African, Mediterranean, Middle Eastern, or Southeast Asian descent. Exact timing and primary recommendation details were unavailable.

Primary guideline details unavailable in the reviewed evidence

Toxicology testing

Risk-based

For suspected prenatal exposure based on history or clinical signs.

Timing, method & qualifiers

Urine or meconium methods are described. Maternal substance use also triggers NAS surveillance and may alter hospitalization and social-work involvement.

Primary guideline details unavailable in the reviewed evidence

Maternal postpartum depression

Check history

Surveil now; institutional birth-hospital screening varies. Formal AAP screening starts at 1 month.

Timing, method & qualifiers

AAP periodicity: 1, 2, 4, and 6 months. Many institutions screen before discharge, but no formal universal AAP birth-hospitalization time point was identified. EPDS or PHQ-9 may be used.

AAP Periodicity Schedule; AAP 2025 MEB report; USPSTF 2016

Guideline difference

Universal predischarge bilirubin measurement

AAP 2022 recommends universal predischarge measurement under KAS 5. The reviewed USPSTF position is an I statement rather than a supporting universal recommendation. Preserve these positions separately.

Detailed reference · Immunization & medical prevention

Apply the weight, maternal-history, and seasonal pathways.

Hepatitis B — routine birth dose

Routine

Monovalent HepB within 24 hours for medically stable infants weighing ≥2,000 g.

Weight and maternal HBsAg pathways
  • <2,000 g: give at chronological age 1 month or hospital discharge, whichever comes first.
  • HBsAg positive: HepB + HBIG within 12 hours regardless of birth weight; post-vaccination serology at 9–12 months.
  • HBsAg unknown: HepB within 12 hours; determine status promptly; give HBIG if positive or not determined within 48 hours.

RSV monoclonal antibody

Check history

Nirsevimab or clesrovimab; AAP states no product preference.

Season and maternal-vaccine pathway
  • Born Oct–Mar: within 1 week, ideally during birth hospitalization.
  • Born Apr–Sep: shortly before RSV season, optimally Oct–Nov.
  • Generally not needed after maternal Abrysvo ≥14 days before delivery, except rare high-risk circumstances.
  • Needed if maternal vaccine was not given, unknown, in a prior pregnancy, or <14 days before delivery.

Intramuscular vitamin K

Routine

>1,500 g: vitamin K1 1 mg IM within 6 hours. ≤1,500 g: 0.3–0.5 mg/kg IM. Document refusal and bleeding-risk counseling. No safe U.S. oral alternative is identified in the AAP statement.

Ocular prophylaxis

Guideline difference

Erythromycin 0.5% ointment to both eyes within 24 hours; USPSTF Grade A and legally required in most U.S. states per the synthesis. It prevents gonococcal, not chlamydial, conjunctivitis. International recommendations differ.

Elective circumcision

Check history

Preference-sensitive, not universal. The AAP 2012 policy expired in 2017 and was not reaffirmed. Requires informed consent, sterile technique and adequate analgesia; contraindicated with hypospadias, ambiguous genitalia or medical instability.

Cord care & early detection

Routine

Keep the cord clean and dry. Identify anomalies, birth injury, jaundice, feeding problems, respiratory difficulty, abnormal tone/reflexes, or other illness; close the loop on every screening result.

DTaP, Hib, PCV, IPV, and rotavirus begin at 2 months rather than at birth in the reviewed schedule.

Detailed reference · Anticipatory guidance & lifestyle

Prepare the family for the first night home.

Medical and daily-life prevention meet in feeding assessment, safe sleep, early warning signs, and a confirmed follow-up plan.

Nutrition

Breast milk exclusively for about 6 months when breastfeeding; initiate within the first hour, use skin-to-skin and feed 8–12 times/24 h. Otherwise use iron-fortified formula with safe preparation. Observe breastfeeding before discharge and at 3–5 days.

Sleep

Supine every sleep; firm, flat, noninclined crib/bassinet with fitted sheet only; room-share without bed-sharing ≥6 months, ideally 12; no soft objects, overheating, head covering or home monitors for SIDS prevention.

Awake play

Begin supervised awake tummy time after discharge; increase toward 15–30 total min/day by 7 weeks (AAP Level A).

Relationships / emotional wellbeing

Promote skin-to-skin and bonding; assess caregiver stress, sleep deprivation, support and adjustment; normalize crying and discuss PURPLE Crying.

Exposure avoidance

No tobacco/nicotine in home or car (Level A). Avoid alcohol, marijuana, opioids and illicit drugs during breastfeeding or infant care; counsel against impaired caregiving.

Safety / when to seek care

Rear-facing car seat; not a sleep space outside travel. Rectal temperature ≥100.4°F (38°C) under 2 months is an emergency. Also address poor feeding, lethargy, breathing difficulty, persistent vomiting and reduced output.

Before discharge

Confirm the 3–5-day appointment for feeding, weight, and bilirubin reassessment; review jaundice, output, safe sleep, car-seat use, cord/circumcision care, hand hygiene, sick contacts, and how results will be communicated.

Detailed reference · When routine care changes

Exceptions and evidence should be visible, not buried.

Prematurity / <2,000 g

Risk-based

Alter HepB timing; use weight-based vitamin K; increase surveillance for jaundice, feeding difficulty and apnea; use corrected developmental age.

Maternal HBsAg positive / unknown

Risk-based

Use the HepB/HBIG pathways above and post-vaccination serology when maternal HBsAg is positive.

Maternal Rh-negative / type O

Risk-based

Cord-blood DAT and heightened jaundice surveillance.

Substance exposure

Risk-based

NAS surveillance, possible prolonged hospitalization, toxicology when indicated and social-work involvement.

Home or birth-center birth

Risk-based

Ensure bloodspot, hearing, CCHD, vitamin K, ocular prophylaxis and HepB completion. The evidence does not specify which items require repeat verification, so no repeat interval is operationalized here.

Abnormal screen / anomaly

Risk-based

Immediate state-protocol follow-up and confirmatory testing; alter discharge and specialty planning when needed.

RSV history / season

Risk-based

Maternal vaccine product/timing, birth season and rare high-risk circumstances determine infant antibody use.

Preference-sensitive care

Risk-based

Document vitamin K refusal counseling. Treat elective circumcision as individualized and respect contraindications.

Evidence conflicts retained

Do not silently merge these recommendations.

Ocular prophylaxis

AAP/USPSTF support routine U.S. use; Canadian guidance recommends against routine use in the described context; European positions vary.

Elective circumcision

Expired AAP statement supports availability, not universal use; European societies are described as disagreeing.

Developmental screening

AAP surveillance now and formal screening later vs USPSTF insufficient evidence for universal screening of asymptomatic children.

Postpartum-depression timing

AAP formal time points begin at 1 month; many hospitals screen before discharge.

Vitamin K route

AAP recommends IM only in the U.S.; international multidose oral regimens are described but not fully sourced.

Bilirubin

AAP recommends universal predischarge measurement; the reviewed USPSTF position is an I statement.

Primary sources used on this page

S1 · American Academy of Pediatrics

Preventive Pediatric Health Care / Periodicity Schedule

2017; rolling updates

S2 · AAP / Bright Futures

Guidelines for Health Supervision, 4th edition

2017

S3 · American Academy of Pediatrics

Management of Hyperbilirubinemia in Newborns ≥35 Weeks

2022

S4 · American Academy of Pediatrics

Updated CCHD Screening Algorithm

2025

S5 · American Academy of Pediatrics

Vitamin K and the Newborn Infant

2022

S6 · American Academy of Pediatrics

Sleep-Related Infant Deaths: Updated Recommendations

2022

S7 · American Academy of Pediatrics

Breastfeeding and the Use of Human Milk

2022

S8 · CDC / ACIP

Child and Adolescent Immunization Schedule

2025; addendum 2025-07-02

S9 · American Academy of Pediatrics

Prevention of RSV Disease in Infants and Children

2025

S10 · U.S. Food and Drug Administration

Clesrovimab approval

2025-06-27

S13 · U.S. Preventive Services Task Force

Ocular Prophylaxis for Gonococcal Ophthalmia Neonatorum

Grade A

S15 · American College of Obstetricians and Gynecologists

Newborn Screening and the Role of the Obstetrician-Gynecologist

2019

S17 · U.S. Preventive Services Task Force

Newborn hearing screening recommendation

Grade B

Direct source URLs were unavailable in the reviewed evidence, so references are identified by organization, title, and date rather than linked. Current state newborn-screening panels must be verified locally.

References & review

This clinician reference was last reviewed August 10, 2026. It is educational and does not replace individualized clinical care.

Evidence reviewed includes guidance from the American Academy of Pediatrics and Bright Futures, CDC/ACIP, USPSTF, HHS/ACHDNC, JCIH, ACOG, and FDA. Where recommendations differ, those differences are identified explicitly.