Every newborn deserves a careful health assessment to ensure a strong start to life. The newborn examination is a systematic evaluation performed by healthcare providers to assess a baby’s overall health, detect any congenital abnormalities, and identify conditions requiring immediate medical attention. This process involves specific assessments conducted at different time points-at birth, within 24 hours, and before discharge from the hospital.
Table of Contents
- When should newborn examinations be conducted?
- The Apgar score: assessing immediate wellbeing
- What does the Apgar score measure?
- Key parameters in newborn assessment
- Birth weight measurement
- Gestational age determination
- Vital signs monitoring
- Checking body orifices and patency
- Eyes
- Ears
- Nose
- Mouth
- Anal patency
- Genitourinary assessment
- Screening for congenital anomalies
- Physical examination findings
- Newborn screening tests
- Identifying respiratory difficulties
- Systematic head-to-toe examination
- Head and fontanelles
- Cardiovascular assessment
- Abdominal examination
- Musculoskeletal assessment
- Neurological evaluation
- Documentation and follow-up
When should newborn examinations be conducted?
Newborn examinations follow a structured timeline to ensure no health concern goes undetected. A thorough physical examination should be completed within 24 hours of birth, ideally with parents present so they can ask questions and receive guidance. However, the evaluation process actually begins much earlier.
The first assessment occurs immediately after birth-within the first few minutes of life. This initial examination focuses on the baby’s breathing, heart rate, and overall responsiveness. A follow-up detailed examination is then conducted within 24 to 48 hours. Finally, a discharge examination ensures the baby is stable and ready to go home. In some healthcare systems, the Newborn Infant Physical Examination must be performed within 72 hours of birth by a qualified practitioner.
The Apgar score: assessing immediate wellbeing
The Apgar score is one of the first standardized assessments performed on every newborn. This quick test is conducted at 1 minute and 5 minutes after birth. The 1-minute score indicates how well the baby tolerated the birthing process, while the 5-minute score shows how well the baby is adapting to life outside the womb.
What does the Apgar score measure?
The scoring system evaluates five key parameters, each rated from 0 to 2 points:
Appearance (skin colour): A score of 2 indicates a completely pink body; 1 means pink body with blue extremities; 0 indicates a pale or blue overall appearance.
Pulse (heart rate): This is considered the most important assessment. A heart rate above 100 beats per minute scores 2; below 100 scores 1; absent heartbeat scores 0.
Grimace (reflex irritability): Active crying or pulling away scores 2; grimacing scores 1; no response scores 0.
Activity (muscle tone): Active movement scores 2; some flexion scores 1; limp tone scores 0.
Respiration (breathing effort): Strong crying scores 2; slow or irregular breathing scores 1; absent breathing scores 0.
Scores of 7 to 10 are considered reassuring. Most healthy babies score 8 or 9, typically losing a point for blue hands and feet due to immature circulation. If the score remains below 7 at five minutes, assessments continue at 5-minute intervals until 20 minutes, or until the score improves.
Key parameters in newborn assessment
Birth weight measurement
Birth weight is an important marker of health. Full-term babies born between 37 and 41 weeks typically weigh around 3.2 kg (approximately 7 pounds). Healthcare providers weigh babies daily during the hospital stay to monitor growth and nutritional needs. Newborns commonly lose 8% to 10% of their birth weight in the first few days but usually regain it within two weeks.
Gestational age determination
Accurate gestational age assessment helps identify babies who may need special care. The Dubowitz/Ballard Examination evaluates physical and neuromuscular characteristics to estimate gestational age within 1-2 weeks. The physical maturity component examines skin texture, presence of lanugo (fine body hair), plantar creases, breast tissue development, and ear cartilage stiffness.
Vital signs monitoring
Normal vital parameters for newborns include:
Heart rate: 100 to 160 beats per minute (may slow during sleep)
Respiratory rate: 40 to 60 breaths per minute
Temperature: Stable body temperature between 36.1ยฐC and 37ยฐC
Blood pressure: Systolic 60-80 mmHg, diastolic 30-45 mmHg
Checking body orifices and patency
An essential part of the newborn examination involves verifying that all body openings (orifices) are present, properly formed, and patent (open). This systematic check helps identify structural abnormalities that may require intervention.
Eyes
Eyes should be examined for symmetry, position, and red light reflexes. The red reflex test, performed using an ophthalmoscope, screens for conditions like cataracts, glaucoma, and retinoblastoma. Eyelid swelling after birth is common and resolves within a few days.
Ears
The examiner checks for proper ear positioning-low-set or posteriorly rotated ears may indicate genetic abnormalities. External ear pits or tags should be noted, as they can sometimes be associated with hearing problems or kidney abnormalities.
Nose
Nasal patency is assessed to ensure the baby can breathe through each nostril. While nasal congestion is common in newborns, there should be no nostril flaring, which would indicate respiratory distress.
Mouth
The palate should be intact both visibly and by palpation, as submucosal clefts can occur. The tongue is checked for mobility-a restricted lingual frenulum (tongue-tie) may affect feeding. The examiner also looks for natal teeth or inclusion cysts (Epstein pearls) on the palate.
Anal patency
The presence of a normally placed, patent anus must be confirmed to rule out imperforate anus, which requires surgical correction.
Genitourinary assessment
In male infants, the penis is examined for hypospadias or epispadias (abnormal urethral opening positions), and both testes should be palpable in the scrotum. In female infants, both labia majora and minora should be visible with normal hymenal tissue. White or mucoid discharge in female newborns is normal due to maternal hormone exposure.
Screening for congenital anomalies
Congenital disorders are structural or functional anomalies that occur during intrauterine life and can be identified prenatally, at birth, or sometimes later in infancy. Some anomalies are immediately visible, such as cleft lip or clubfoot, while others require specific testing for detection.
Physical examination findings
Many structural problems are detected through physical examination immediately after birth. The examiner looks for abnormalities including facial asymmetry, limb deformities, spinal defects, and skin markings. The head is inspected for proper shape and size, and fontanelles are palpated to assess their dimensions.
Newborn screening tests
Newborn screening identifies infants at increased risk for certain health conditions. This includes the heel prick blood test, which screens for metabolic disorders like phenylketonuria (PKU), congenital hypothyroidism, and galactosemia. Testing is usually done between 2 and 7 days of age using a few drops of blood from the baby’s heel.
Additional screening includes hearing tests to detect congenital deafness and pulse oximetry to identify critical congenital heart defects by measuring the baby’s oxygen levels.
Identifying respiratory difficulties
Respiratory assessment is crucial in newborn examination. Respirations should be counted over a full minute because breathing in neonates is irregular. The examiner looks for signs of respiratory distress, which include:
Grunting: A sound made during exhalation as the baby tries to keep air in the lungs
Nasal flaring: Widening of the nostrils during breathing
Retractions: Visible indrawing of the chest wall between ribs or below the ribcage
Tachypnea: Abnormally rapid breathing (above 60 breaths per minute)
Cyanosis: Bluish discolouration of the skin indicating low oxygen levels
The chest should appear symmetrical, and breath sounds should be equal on both sides. A scaphoid (sunken) abdomen may indicate diaphragmatic hernia, where abdominal contents have migrated into the chest cavity.
Systematic head-to-toe examination
Head and fontanelles
The head shape may be affected by the delivery process. In vertex (head-first) delivery, some moulding and scalp swelling (caput succedaneum) is common. Cephalhematoma-blood collection between the skull bone and its covering-may develop and gradually resolves over several months. Fontanelles (soft spots) are assessed for size; unusually large fontanelles may indicate hypothyroidism.
Cardiovascular assessment
A murmur heard in the first 24 hours is most commonly caused by a patent ductus arteriosus, which usually resolves within three days. Femoral pulses are compared with brachial pulses-weak or delayed femoral pulses may suggest aortic coarctation.
Abdominal examination
The abdomen should be round and symmetrical. The liver edge is normally palpable 1-2 cm below the right costal margin. The umbilical cord is checked-there should be two arteries and one vein. Umbilical hernias are common but rarely cause problems.
Musculoskeletal assessment
The spine is inspected for defects such as spina bifida. Hip examination using the Barlow and Ortolani manoeuvres screens for developmental dysplasia of the hip (DDH). Clavicles are palpated for fractures, which may occur during delivery.
Neurological evaluation
Newborn reflexes including the Moro (startle), sucking, rooting, and grasp reflexes are assessed. These primitive reflexes indicate a healthy peripheral nervous system. The baby’s muscle tone, alertness level, and limb movements are also evaluated.
Documentation and follow-up
The purpose of newborn examination includes screening for congenital abnormalities that will benefit from early intervention and making appropriate referrals for further tests or treatment. All findings should be carefully documented, and parents should receive education about warning signs requiring medical attention.
A second examination is typically performed at 6-8 weeks of age, usually by a general practitioner, to identify any abnormalities that develop or become apparent later. This follow-up ensures continuity of care and early detection of conditions not visible at birth.
What do you think? How important is parental involvement during the newborn examination process? Have you considered how early detection of health conditions can significantly improve outcomes for newborns and their families?
References
- https://www.merckmanuals.com/professional/pediatrics/care-of-newborns-and-infants/physical-examination-of-the-newborn
- https://geekymedics.com/newborn-baby-assessment/
- https://medlineplus.gov/ency/article/003402.htm
- https://www.ncbi.nlm.nih.gov/books/NBK470569/
- https://www.stanfordchildrens.org/en/topic/default?id=assessments-for-newborn-babies-90-P02336
- https://med.stanford.edu/newborns/clinical-rotations/students/students-newborn-exam.html
- https://www.who.int/news-room/fact-sheets/detail/birth-defects
- https://www.nichd.nih.gov/health/topics/congenital-anomalies/conditioninfo/diagnosed
- https://www.cdc.gov/birth-defects/diagnosis/screening-for-birth-defects.html
- https://www.stanfordchildrens.org/en/topic/default?id=overview-of-newborn-screening-for-birth-defects-90-P02140
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