Ramipril in the treatment of hypertension and proteinuria in children with chronic kidney diseases
Language English Country United States Media print
Document type Comparative Study, Evaluation Study, Journal Article
PubMed
15110900
DOI
10.1016/j.amjhyper.2004.01.008
PII: S0895706104000342
Knihovny.cz E-resources
- MeSH
- Antihypertensive Agents therapeutic use MeSH
- Chronic Disease MeSH
- Circadian Rhythm drug effects MeSH
- Diastole drug effects MeSH
- Child MeSH
- Adult MeSH
- Hypertension drug therapy physiopathology MeSH
- Angiotensin-Converting Enzyme Inhibitors therapeutic use MeSH
- Infant MeSH
- Blood Pressure drug effects MeSH
- Humans MeSH
- Adolescent MeSH
- Kidney Diseases drug therapy physiopathology MeSH
- Child, Preschool MeSH
- Prospective Studies MeSH
- Proteinuria drug therapy physiopathology MeSH
- Ramipril therapeutic use MeSH
- Child Welfare MeSH
- Statistics as Topic MeSH
- Severity of Illness Index MeSH
- Systole drug effects MeSH
- Treatment Outcome MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Infant MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Comparative Study MeSH
- Names of Substances
- Antihypertensive Agents MeSH
- Angiotensin-Converting Enzyme Inhibitors MeSH
- Ramipril MeSH
BACKGROUND: Angiotensin-converting enzyme inhibitors are the drugs of choice in renal hypertension. The efficacy and safety of ramipril in adults has been proved; however, data on effectiveness of ramipril in children are few. The aim of the present study was to investigate the effect of ramipril on blood pressure (BP) and proteinuria in children with chronic kidney diseases. METHODS: A total of 31 children (median age 11.3 years, range 1.9-19.8 years) with various chronic nephropathies and hypertension or proteinuria were prospectively treated with ramipril for 6 months. Blood pressure was evaluated using ambulatory BP monitoring and hypertension was defined as mean BP equal to or greater than the 95th percentile for healthy children. Proteinuria was defined as protein excretion > or =100 mg/m(2)/24 h. The starting dose of ramipril was 1.5 mg/m(2)/24 h once daily. In 27 children it was given as monotherapy. RESULTS: The median decrease in ambulatory BP was 11 mm Hg for daytime systolic, 10 mm Hg for daytime and nighttime diastolic, and 8 mm Hg for nighttime systolic BP. Hypertension normalized in 55% of the children. Proteinuria decreased in 84% of the children with pathologic proteinuria; the median decrease was 51%. A positive correlation was found between initial proteinuria and change of proteinuria (r = 0.95, P <.001). Glomerular filtration rate and serum potassium level did not change significantly. One child developed a cough that was believed to be related to ramipril. CONCLUSIONS: Ramipril is an effective and safe drug in children with chronic kidney diseases associated with hypertension, proteinuria, or both.
References provided by Crossref.org
Narrative update of clinical trials with antihypertensive drugs in children and adolescents