Low-dose cyclopenthiazide in the treatment of hypertension: a one-year community-based study

After an 8-week placebo period, 73 patients whose diastolic blood pressures were between 90 and 110 mmHg were randomly assigned to receive 125 micrograms (low dose) or 500 micrograms of cyclopenthiazide (standard dose) for a period of one year. Blood pressure was measured in the patient's home...

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Bibliographic Details
Published in:Quarterly journal of medicine 1991-02, Vol.78 (286), p.135
Main Authors: Johnston, G D, Wilson, R, McDermott, B J, McVeigh, G E, Duffin, D, Logan, J
Format: Article
Language:English
Subjects:
Adult
Aged
Apolipoproteins - blood
Blood Glucose - metabolism
Cholesterol - blood
Cyclopenthiazide - administration & dosage
Cyclopenthiazide - adverse effects
Cyclopenthiazide - therapeutic use
Drug Administration Schedule
Female
Glycated Hemoglobin A - metabolism
Humans
Hypertension - drug therapy
Hypertension - metabolism
Male
Middle Aged
Potassium - blood
Uric Acid - blood
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Summary:After an 8-week placebo period, 73 patients whose diastolic blood pressures were between 90 and 110 mmHg were randomly assigned to receive 125 micrograms (low dose) or 500 micrograms of cyclopenthiazide (standard dose) for a period of one year. Blood pressure was measured in the patient's home by the same observer at two-weekly intervals during an 8-week placebo run-in period, every 4 weeks for a further 12 weeks and at 24, 36 and 52 weeks thereafter. Serum potassium, urate, glucose, glycosylated haemoglobin, total and HDL cholesterol, and apolipoproteins were measured at the end of the placebo period and at 4, 8, 24 and 52 weeks of active treatment. Twelve of the 73 patients had an inadequate antihypertensive response--five on the higher dose and seven on the lower dose. One patient receiving 500 micrograms was withdrawn because of adverse effects. In the remaining 60 patients, systolic and diastolic blood pressures were significantly reduced when compared with pretreatment values in both treatment groups throughout the one year period. The decreases in blood pressure were not significantly different from each other (p greater than 0.65). Three patients on 500 micrograms required potassium supplements. Maximum decreases in the serum potassium of 0.52 mmol/l (500 micrograms dose) and 0.14 mmol/l (125 micrograms dose) were observed at 24 weeks of treatment in the remaining 57 patients. The differences between the two doses at this time were statistically significant (p less than 0.05), as were the increases in serum urate observed at 4, 8 and 24 weeks (p less than 0.05).
ISSN:0033-5622