dc.contributor.author | Obel, A. O | |
dc.contributor.author | Koech, D. K | |
dc.date.accessioned | 2013-06-11T08:35:53Z | |
dc.date.available | 2013-06-11T08:35:53Z | |
dc.date.issued | 1991 | |
dc.identifier.citation | J Cardiovasc Pharmacol. 1991 Mar;17(3):504-7. | en |
dc.identifier.uri | http://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/1711614 | |
dc.identifier.uri | http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31280 | |
dc.description.abstract | Eighty-four consecutive black patients who had confirmed but untreated hypertension participated in a double-blind randomized clinical trial involving potassium supplement (64 mmol/day) versus bendrofluazide (10 mg/day). Diastolic blood pressure (DBP) of the 42 patients receiving potassium supplementation (group A) decreased from a mean (+/- SD) of 108 +/- 3 to 88 +/- 4 mm Hg (p less than 0.001; paired t test) after 28 weeks of medication. DBP of the 42 patients receiving bendrofluazide (group B) decreased from a mean of 108 +/- 2 to 84 +/- 4 mm Hg (p less than 0.001; paired t test). There was no statistically significant difference between the magnitude of decrease in DBP in group A and B patients (unpaired t test). No clinical, biochemical, or ECG abnormalities occurred in group A patients. Eight group B patients showed hyperuricemia; 4 patients in the same group had hyperglycemia and 3 other patients had hypokalemia. The results support the notion that potassium supplementation may be an effective therapeutic approach to mildly hypertensive blacks. | en |
dc.language.iso | en | en |
dc.title | Potassium supplementation versus bendrofluazide in mildly to moderately hypertensive Kenyans | en |
dc.type | Article | en |