Approach to complications of prematurity (late): Clinical sciences

Last updated: May 05, 2025

Approach to complications of prematurity (late): Clinical sciences

STAGE DE PÉDIATRIE

STAGE DE PÉDIATRIE

Henoch-Schonlein purpura: Clinical sciences
Approach to inborn errors of metabolism (progressive or chronic): Clinical sciences
Meningitis (pediatrics): Clinical sciences
Approach to anemia in the newborn and infant (destruction and blood loss): Clinical sciences
Approach to anemia in the newborn and infant (underproduction): Clinical sciences
Approach to anemia (destruction and sequestration): Clinical sciences
Approach to anemia (underproduction): Clinical sciences
Sickle cell disease: Clinical sciences
Sepsis (pediatrics): Clinical sciences
Approach to constipation (pediatrics): Clinical sciences
Approach to a cough (pediatrics): Clinical sciences
Bronchiolitis: Clinical sciences
Pneumonia (pediatrics): Clinical sciences
Upper respiratory tract infections: Clinical sciences
Influenza: Clinical sciences
Croup and epiglottitis: Clinical sciences
Congestive heart failure: Clinical sciences
Asthma: Clinical sciences
Approach to diarrhea (pediatrics): Clinical sciences
Infectious gastroenteritis (acute) (pediatrics): Clinical sciences
Infectious gastroenteritis (subacute) (pediatrics): Clinical sciences
Approach to a fever (over 2 months): Clinical sciences
Osteomyelitis (pediatrics): Clinical sciences
Pharyngitis, peritonsillar abscess, and retropharyngeal abscess (pediatrics): Clinical sciences
Otitis media and externa (pediatrics): Clinical sciences
Septic arthritis and transient synovitis (pediatrics): Clinical sciences
Stevens-Johnson syndrome and toxic epidermal necrolysis: Clinical sciences
Urinary tract infection (pediatrics): Clinical sciences
Approach to viral exanthems (pediatrics): Clinical sciences
Approach to bacterial causes of fever and rash (pediatrics): Clinical sciences
Juvenile idiopathic arthritis: Clinical sciences
Kawasaki disease: Clinical sciences
Acute group A streptococcal infections and sequelae (pediatrics): Clinical sciences
Approach to congenital infections: Clinical sciences
Staphylococcal scalded skin syndrome and impetigo: Clinical sciences
Approach to head and neck masses (pediatrics): Clinical sciences
Periorbital and orbital cellulitis (pediatrics): Clinical sciences
Approach to a murmur (pediatrics): Clinical sciences
Approach to congenital heart diseases (cyanotic): Clinical sciences
Approach to hematuria (pediatrics): Clinical sciences
Nephritic syndromes (pediatrics): Clinical sciences
Approach to leukocoria (pediatrics): Clinical sciences
Hepatitis B: Clinical sciences
Approach to a limp (pediatrics): Clinical sciences
Approach to common musculoskeletal injuries (pediatrics): Clinical sciences
Developmental dysplasia of the hip: Clinical sciences
Legg-Calve-Perthes disease and slipped capital femoral epiphysis: Clinical sciences
Human immunodeficiency virus (HIV) infection: Clinical sciences
Approach to proteinuria (pediatrics): Clinical sciences
Approach to a red eye: Clinical sciences
Conjunctival disorders: Clinical sciences
Eyelid disorders: Clinical sciences
Approach to vomiting (newborn and infant): Clinical sciences
Approach to vomiting (pediatrics): Clinical sciences
Gastroesophageal reflux disease (pediatrics): Clinical sciences
Approach to increased intracranial pressure: Clinical sciences
Peptic ulcers, gastritis, and duodenitis (pediatrics): Clinical sciences
Large bowel obstruction: Clinical sciences
Small bowel obstruction: Clinical sciences
Approach to acid-base disorders: Clinical sciences
Approach to metabolic acidosis: Clinical sciences
Approach to metabolic alkalosis: Clinical sciences
Approach to respiratory acidosis: Clinical sciences
Approach to respiratory alkalosis: Clinical sciences
Approach to hypocalcemia (pediatrics): Clinical sciences
Approach to hypoglycemia (pediatrics): Clinical sciences
Approach to hypernatremia (pediatrics): Clinical sciences
Approach to hyponatremia (pediatrics): Clinical sciences
Adrenal insufficiency: Clinical sciences
Syndrome of inappropriate antidiuretic hormone secretion: Clinical sciences
Approach to a fever (0-60 days): Clinical sciences
Approach to hypotonia (newborn and infant): Clinical sciences
Approach to jaundice (newborn and infant): Clinical sciences
Approach to poor feeding (newborn and infant): Clinical sciences
Approach to complications of prematurity (early): Clinical sciences
Approach to complications of prematurity (late): Clinical sciences
Necrotizing enterocolitis: Clinical sciences
Neonatal respiratory distress syndrome: Clinical sciences
Approach to prenatal teratogen exposure: Clinical sciences
Respiratory failure (pediatrics): Clinical sciences
Foreign body aspiration and ingestion (pediatrics): Clinical sciences
Approach to upper airway obstruction (pediatrics): Clinical sciences
Anaphylaxis: Clinical sciences
Approach to epilepsy: Clinical sciences
Approach to a first unprovoked seizure (pediatrics): Clinical sciences
Febrile seizure (pediatrics): Clinical sciences
Diabetes mellitus (pediatrics): Clinical sciences
Dehydration (pediatrics): Clinical sciences
Brief, resolved, unexplained event (BRUE): Clinical sciences
Approach to bradycardia: Clinical sciences
Approach to tachycardia: Clinical sciences
Approach to melena and hematemesis (pediatrics): Clinical sciences
Burns: Clinical sciences
Approach to trauma (pediatrics): Clinical sciences
Approach to a child with Down syndrome (trisomy 21): Clinical sciences
Cystic fibrosis and primary ciliary dyskinesia: Clinical sciences
Approach to delay or regression in developmental milestones: Clinical sciences
Approach to growth faltering: Clinical sciences
Approach to neurodevelopmental disorders: Clinical sciences
Approach to short stature: Clinical sciences
Approach to feeding and eating disorders: Clinical sciences
Allergic rhinitis: Clinical sciences
Essential hypertension: Clinical sciences
Approach to a rash in the well newborn and infant: Clinical sciences
Immunizations (pediatrics): Clinical sciences
Well-child visit (newborn and infant): Clinical sciences
Well-child visit (toddler and child): Clinical sciences
Well-child visit (adolescent): Clinical sciences
Bacterial and viral skin infections: Pathology review
Nasal, oral and pharyngeal diseases: Pathology review
Pediatric musculoskeletal disorders: Pathology review
Viral exanthems of childhood: Pathology review
Seizures: Pathology review
Congenital TORCH infections: Pathology review
Central nervous system infections: Pathology review
Developmental and learning disorders: Pathology review
Breastfeeding
Anatomy clinical correlates: Eye

Decision-Making Tree

Transcript

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Preterm birth before 37 weeks of gestation can result in various complications that increase an infant’s morbidity and mortality. These complications are most common among patients who are born before 32 weeks of gestation or those with very low birth weight under 1500 grams. Late complications of prematurity can develop after the first month of life, and because they don’t typically cause acute or obvious signs and symptoms, many are identified through screening.

Now, if a pediatric patient presents with a chief concern suggesting a late complication of prematurity, first obtain a focused history and physical examination. Then, review your findings to determine if your patient requires further evaluation.

Let’s start by assessing your patient’s oxygen requirement. If your patient required supplemental oxygen for 28 days or more, consider bronchopulmonary dysplasia, or BPD. History will reveal an infant born before 32 weeks of gestation. They may have had a patent ductus arteriosus, required mechanical ventilation, or had prolonged exposure to hyperoxia. The exam might reveal chest retractions and audible pulmonary rales. And when attempting to wean your patient’s supplemental oxygen, they will usually become hypoxemic and tachypneic within 60 minutes.

Even though BPD is a clinical diagnosis, you can consider ordering a chest X-ray to support the diagnosis, determine disease severity, and identify complications. Typically, the chest X-ray will reveal diffuse hazy opacifications and hyperinflation, with or without cystic lucencies. This combination of clinical and imaging findings confirms your diagnosis of bronchopulmonary dysplasia.

Okay, here’s your first clinical pearl! In severe cases of BPD, disrupted pulmonary vascular development leads to increased pulmonary vascular resistance and ultimately pulmonary hypertension. Over time, the right ventricle hypertrophies in order to maintain cardiac output. These patients can experience pulmonary hypertensive crises, during which an acute increase in pulmonary arterial pressure overwhelms the right ventricle and causes right-sided heart failure.

Okay, you’ll also assess your patient for signs and symptoms of anemia. Premature infants are physiologically predisposed to anemia, due to limited iron stores, impaired erythropoietin production, and a short fetal red blood cell lifespan. Newborns with anemia may have poor weight gain, apneic episodes, or a history of frequent lab draws. Keep in mind that some patients are asymptomatic, and the anemia might be discovered as an incidental lab finding. On physical exam, your patient might be hypoxemic, tachypneic, or tachycardic; and you’ll often detect pallor, especially on the conjunctivae and the palms of the hands and soles of the feet.

With these signs and symptoms, consider anemia of prematurity. To confirm the diagnosis, obtain hemoglobin levels, a hematocrit, and a reticulocyte count. If the hemoglobin and hematocrit are below reference range for age, and the reticulocyte count is low, diagnose anemia of prematurity.

Next, assess the need to screen for periventricular leukomalacia, or PVL. Since PVL is caused by an ischemic injury to the premature brain, these patients may have had a previous episode of hypoxemia or hypotension, or they may have been diagnosed with intraventricular hemorrhage, sepsis, or necrotizing enterocolitis. The physical exam may reveal an uncoordinated suck-swallow, increased muscle tone, or spastic diplegia. With these findings, consider PVL and order a cranial ultrasound. If it shows characteristic white matter injury, with or without cysts, diagnose PVL.

Now here’s a clinical pearl! PVL is often asymptomatic during the first weeks or months of life, so to identify it, you’ll need to perform routine screening with cranial ultrasound. For all infants with risk factors, such as a gestational age of 30 weeks of gestation or less, order the first ultrasound within the first 7 days of life, then again at 4 to 6 weeks of life, and at least once more before your patient is discharged from the hospital.

Sources

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