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Effect of spironolactone-hydrochlorothiazide on lung function in infants with chronic bronchopulmonary dysplasia
B Engelhardt1, W A Blalock, S DonLevy
1Department of Pediatrics, Vanderbilt University Medical School, Nashville, Tennessee 37232-2370.
Insights
Spironolactone-hydrochlorothiazide increased urine output in infants with bronchopulmonary dysplasia but did not improve lung function or oxygenation. Diuresis alone may not be sufficient for improving lung mechanics in these patients.
Area of Science:
- Pediatrics
- Neonatology
- Pulmonology
Background:
- Bronchopulmonary dysplasia (BPD) is a chronic lung disease in infants.
- Infants with BPD often require oxygen therapy and may have impaired lung function.
- Diuretic therapy is sometimes used in BPD management, but its efficacy on lung function is debated.
Purpose of the Study:
- To evaluate the effect of spironolactone-hydrochlorothiazide on urine output and lung function in infants with BPD.
- To determine if increased urine output correlates with improved respiratory parameters.
Main Methods:
- A randomized controlled trial involving 21 hospitalized infants with BPD.
- Infants received either spironolactone-hydrochlorothiazide (3 mg/kg/day) or no treatment for 6-8 days.
- Measurements included daily fluid/urine output, dynamic lung compliance, pulmonary resistance, and oxygen saturation.
Main Results:
- Spironolactone-hydrochlorothiazide significantly increased urine output.
- No significant improvements were observed in lung mechanics (compliance, resistance) or oxygenation.
- The diuretic effect was comparable to previous furosemide studies.
Conclusions:
- Spironolactone-hydrochlorothiazide effectively increases urine output in infants with BPD.
- The drug does not improve lung function or oxygenation in this population.
- Diuresis alone may not be the primary mechanism for lung function improvement with diuretic therapy in BPD.
Abstract:
To test the hypothesis that spironolactone-hydrochlorothiazide (Aldactazide) will improve urine output and lung function in infants with bronchopulmonary dysplasia, we studied 21 hospitalized, spontaneously breathing, oxygen-dependent infants with chronic bronchopulmonary dysplasia. Infants were randomly assigned to receive either a 1:1 mixture of spironolactone and hydrochlorothiazide orally (n = 12) (3 mg/kg/day of both compounds) or no treatment (n = 9) for 6 to 8 days each. Dynamic lung compliance, total pulmonary resistance, and hemoglobin oxygen saturation were measured on the first and last days of each study period. Fluid intake and urine output were measured each day. Although the treatment significantly increased urine output, neither lung mechanics nor oxygenation were improved by the drug. The magnitude of the diuresis achieved with spironolactone-hydrochlorothiazide treatment was comparable to the diuresis achieved in a previous study of furosemide treatment (J Pediatr 1986:109;1034-9). Statistical analysis indicated that a type II error was an unlikely explanation for our failure to detect a beneficial effect. In three patients, doubling the oral dose did not improve lung mechanics or oxygenation. We speculate that diuresis per se is not responsible for lung function improvement during treatment with other drugs with diuretic properties.
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