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dc.contributor.authorObel, A. O
dc.contributor.authorKoech, D. K
dc.date.accessioned2013-06-11T08:35:53Z
dc.date.available2013-06-11T08:35:53Z
dc.date.issued1991
dc.identifier.citationJ Cardiovasc Pharmacol. 1991 Mar;17(3):504-7.en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/1711614
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31280
dc.description.abstractEighty-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.isoenen
dc.titlePotassium supplementation versus bendrofluazide in mildly to moderately hypertensive Kenyansen
dc.typeArticleen


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