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Published on: July 19, 2011
Renal failure in sick hypertensive premature infants receiving captopril therapy
1Edward Mallinckrodt Department of Pediatrics, Children's Hospital, Washington University School of Medicine, St. Louis, Missouri 63110.
Insights
Captopril effectively lowered high blood pressure in premature infants with chronic lung disease. However, close monitoring is crucial due to unpredictable drops in blood pressure and associated complications like oliguria and neurological signs.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Pharmacology
Background:
- Premature infants with chronic lung disease often develop systemic hypertension.
- Elevated peripheral renin values are common in this population.
- Renal abnormalities, including artery thrombosis and parenchymal disease, can contribute to hypertension.
Purpose of the Study:
- To evaluate the efficacy and complications of captopril therapy for systemic hypertension in sick premature infants.
- To assess the impact of captopril on blood pressure and identify associated adverse events.
Main Methods:
- A retrospective study of nine premature infants with chronic lung disease and hypertension.
- Captopril therapy was initiated at 0.3 mg/kg and dosages were subsequently halved.
- Blood pressure, renin values, renal scans, and clinical outcomes were monitored.
Main Results:
- Captopril significantly reduced systolic blood pressure (BP) in all infants after the initial dose.
- Reduced maintenance therapy led to unpredictable BP decreases (>40%) in 17 episodes.
- Four infants experienced severe hypotensive episodes with oliguria and neurological signs, unresponsive to standard treatment.
Conclusions:
- Captopril is effective in controlling hypertension in premature infants with chronic lung disease.
- Close monitoring of blood pressure is essential during captopril maintenance therapy due to the risk of severe, unpredictable hypotensive episodes.
- Further research is needed to understand and mitigate these complications.
Abstract:
A retrospective study of nine sick premature infants with chronic lung disease who received captopril for control of systemic hypertension (systolic blood pressure (BP) greater than 113 mm Hg) was carried out to determine efficacy of therapy and associated complications. All nine infants had markedly elevated peripheral renin values, 134.3 +/- 128.1 ng/mL/hr (mean +/- SD). Five infants had abnormal renal sonographic and perfusion scans with evidence of renal artery thrombosis, parenchymal disease, or both. Captopril therapy (0.3 mg/kg) was instituted at a postnatal age of 123 +/- 108 days. After the initial dose, the systolic BP decreased significantly in all infants, the decrease ranging from 21% to 58% of the pretreatment value. Dosage was subsequently halved in all infants. Seventeen episodes of unpredictable decreases in BP more than 40% from baseline occurred during the reduced maintenance therapy. Four infants had a total of seven episodes during which the BP decreased by 57 +/- 10% from baseline; this decrease persisted for 17 +/- 6 hours and was unresponsive to volume reexpansion and inotropic therapy. All seven episodes were accompanied by oliguria (urine output less than 1 mL/kg/hr) that persisted for 18 +/- 12 hours. These episodes were accompanied by neurologic signs (subtle seizures, lethargy, and/or apnea) within 18 +/- 6 hours after the onset of oliguria. The remaining five infants had a total of 13 episodes of decreased BP of 50 +/- 8% of baseline, which were of significantly shorter duration and responded to volume reexpanders, inotropic therapy, or both and were unaccompanied by oliguria. These data suggest the need for close observation of BP in infants receiving maintenance captopril therapy.
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