At birth, the respiratory and circulatory systems undergo rapid adaptation. Lung fluid is absorbed, pulmonary vascular resistance falls, systemic resistance rises, and two critical foetal shunts close:
Functional closure occurs within hours of birth as left atrial pressure exceeds right atrial pressure (reversal of foetal gradient). Anatomical closure may take weeks to months. Persistence = patent foramen ovale (PFO), relevant in cyanotic disease.
Functionally closes within 24–72 hours in term neonates due to rising PaO2 and falling prostaglandin E2 (PGE2). In preterm infants, the duct often remains patent (PDA). Indomethacin or ibuprofen promote closure; surgical ligation reserved for refractory cases.
| Parameter | Term (≥37 wks) | Late Preterm (34–36 wks) | Preterm (<32 wks) |
|---|---|---|---|
| Heart Rate (bpm) | 120–160 | 120–160 | 120–170 |
| Respiratory Rate (/min) | 40–60 | 40–60 | 40–65 |
| SpO2 target (post-ductal) | 94–98% | 93–97% | 91–95% |
| Systolic BP (mmHg) | 60–80 | 50–70 | 45–65 |
| Temperature (°C axillary) | 36.5–37.5 | 36.5–37.5 | 36.5–37.5 |
| Blood glucose (mmol/L) | 2.6–7.0 | 2.6–7.0 | 2.6–7.0 |
Assessed at 1 minute (response to resuscitation) and 5 minutes (short-term outcome indicator). Total maximum = 10. Score <7 at 5 minutes warrants continued reassessment.
| Criterion | 0 | 1 | 2 |
|---|---|---|---|
| Appearance (colour) | Blue/pale all over | Pink body, blue extremities | Pink all over |
| Pulse (heart rate) | Absent | <100 bpm | ≥100 bpm |
| Grimace (reflex irritability) | No response | Grimace/weak cry | Cough/sneeze/vigorous cry |
| Activity (muscle tone) | Limp/flaccid | Some flexion of limbs | Active motion |
| Respiration | Absent | Weak/irregular | Regular, strong cry |
Total Ballard score mapped to gestational age chart. New Ballard Score (NBS) valid from 20–44 weeks. Best performed within 12–96 hours of birth.
| Parameter | Target | Action if Outside Range |
|---|---|---|
| SpO2 (term, first 10 min) | 60% at 1 min → 91–95% by 10 min | Titrate FiO2 |
| Blood glucose | 2.6–7.0 mmol/L | Dextrose infusion; check feeds |
| Temperature | 36.5–37.5°C | Warm/cool as needed; cooling if HIE criteria met |
| Blood pressure | MAP ≥ gestational age (in mmHg) | Dopamine/dobutamine; volume if shocked |
| pH | 7.25–7.45 | Ventilation adjustment; sodium bicarbonate rarely |
| Drug | Source | Dose |
|---|---|---|
| Poractant alfa (Curosurf) | Porcine | 100–200 mg/kg intratracheally |
| Beractant (Survanta) | Bovine | 100 mg/kg intratracheally |
| Calfactant (Infasurf) | Bovine | 105 mg/kg intratracheally |
Hyperoxia causes abnormal retinal neovascularisation in preterm infants. Strict oxygen targeting is a key nursing responsibility in NICU.
| Gestation | SpO2 Target | Rationale |
|---|---|---|
| <32 weeks (NICU phase) | 91–95% | Reduces ROP risk; avoids free radical damage |
| 32–36 weeks | 93–97% | Lower ROP risk; broader target acceptable |
| Term/corrected ≥37 weeks | 94–98% | Normal physiological target |
| During procedures (suction/repositioning) | Allow transient dips; respond if <85% >30 seconds | Minimise unnecessary FiO2 increases |
ROP screening: ophthalmology review at 31–32 weeks corrected age (or 4 weeks chronological age, whichever is later) for all infants <32 weeks or <1500g.
Devastating bowel inflammation/necrosis primarily in preterm infants; one of the leading causes of mortality and morbidity in the NICU.
| Stage | Classification | Systemic Signs | Abdominal Signs | Radiological Signs |
|---|---|---|---|---|
| Stage I | Suspected NEC | Temperature instability, apnoea, bradycardia | Mild distension, feeding intolerance, pre-feed aspirates | Normal or mild ileus |
| Stage II | Confirmed NEC | As above + metabolic acidosis, thrombocytopenia | Gross distension, absent bowel sounds, bloody stools | Pneumatosis intestinalis (gas in bowel wall), portal venous gas |
| Stage III | Advanced NEC | Shock, DIC, hypotension, severe apnoea | Peritonitis, erythema of abdominal wall, severe tenderness | Pneumoperitoneum (free air = perforation) |
Bleeding originating in the germinal matrix (highly vascularised, fragile tissue present until ~34 weeks), extending into the ventricles. Primarily affects preterm infants <32 weeks.
| Grade | Description | Prognosis |
|---|---|---|
| Grade I | Germinal matrix haemorrhage only; no ventricular extension | Excellent; usually no long-term deficit |
| Grade II | Blood in ventricles; <50% ventricular volume; no dilation | Good; minor risk of neurodevelopmental problems |
| Grade III | Blood fills >50% of ventricle; ventricular dilation | Significant risk of neurodevelopmental impairment |
| Grade IV | Periventricular haemorrhagic infarction (PVHI); parenchymal extension | High mortality/severe disability risk |
All criteria must be met:
Persistence of the foetal communication between pulmonary artery and descending aorta. Clinically significant PDA causes left-to-right shunting, pulmonary overcirculation, and systemic steal.
| Phase | Volume | Rationale |
|---|---|---|
| Trophic / Minimal Enteral Feeds (MEF) | 10–20 mL/kg/day | Primes gut; stimulates gut hormones; does not provide full nutrition — TPN concurrent |
| Incremental advancement | Increase by 15–20 mL/kg/day | Allows gut adaptation; monitor tolerance at each increment |
| Full enteral feeds | 150–180 mL/kg/day (preterm) | Full nutritional requirements met; aim within 7–14 days in stable preterm |
| Fortification | Human milk fortifier (HMF) added | Adds protein/calcium/phosphorus to breast milk for growing preterm (<34 weeks, <1800g) |
| Component | Day 1 | Target |
|---|---|---|
| Amino acids (protein) | 1.5 g/kg/day | 3.5–4 g/kg/day |
| Lipid emulsion | 0.5–1 g/kg/day | 3 g/kg/day |
| Glucose | 6–8 mg/kg/min GIR | Maintain BG 2.6–10 mmol/L |
| Total fluid | 60–80 mL/kg/day | 150–180 mL/kg/day (EBM included) |
Neonatal Individualised Developmental Care and Assessment Program (NIDCAP) — minimises sensory overload and supports neurodevelopment in the NICU environment.
The issue of donor breast milk in GCC NICUs intersects with Islamic law on rada'a (milk kinship/fosterage). Islamic jurisprudence holds that if a woman breastfeeds an infant 5 or more times (per most madhabs), a milk-kinship relationship is established, creating marriage prohibitions similar to blood relations. This has historically led to reluctance among Muslim families to use donor breast milk from unknown donors.
However, the contemporary scholarly consensus — including rulings from the International Islamic Fiqh Academy (IIFA), Saudi Arabia's Council of Senior Scholars, and UAE fatwa bodies — is that:
Nursing practice recommendation: provide families with written information in Arabic about the milk bank process, the fatwa position, and the medical evidence. Offer an interpreter and, where requested, facilitate a meeting with a hospital Islamic scholar. Respect parental decision-making and document the discussion in the medical record.
GCC countries have among the highest rates of assisted reproductive technology (ART) globally. IVF multiple pregnancies (twins, triplets) significantly increase preterm birth rates, NICU admissions, and complex neonatal presentations.
High consanguinity rates in GCC (20–60% in some populations) increase autosomal recessive conditions: metabolic disorders (PKU, organic acidaemias), haemoglobinopathies, congenital anomalies — these may present in the NICU.
Prevalence up to 25% in some Gulf populations (X-linked recessive; affects males more severely). Presents as severe early-onset jaundice, haemolytic anaemia. Standard neonatal screening in most GCC countries. Avoid triggers throughout life.
| Country | Number of Conditions | Notable Inclusions |
|---|---|---|
| Saudi Arabia (MOH) | ~12 conditions | G6PD, CH, PKU, CAH, galactosaemia, biotinidase, haemoglobinopathies, amino acid disorders |
| UAE (DHA/DOH) | ~9 conditions | G6PD, CH, PKU, CAH, galactosaemia; expanding programme |
| Qatar (NCDC) | ~20+ conditions | Expanded NBS panel including fatty acid oxidation disorders |
| Kuwait, Bahrain, Oman | Variable; 5–15+ | Core conditions; programmes expanding |
Based on NICE NG98 thresholds. For clinical decision-support only — always apply clinical judgement and consult senior clinician.