Key result
Prazosin improved blood pressure control, though 45 of 93 patients discontinued therapy due to side effects (20.4%), failure to respond (11.8%), myocardial infarction (8.6%), or other reasons.
Why the study?
Does prazosin improve blood pressure control in patients with difficult-to-control hypertension?
Observational (n=93)
Open-label
No
Does prazosin improve blood pressure control in patients with difficult-to-control hypertension?
Prazosin is an effective third-line agent for refractory hypertension, but requires a very low initial dose to avoid first-dose hypotension.
Prazosin was associated with BP improvement in refractory hypertension despite high discontinuation; leaves open its third-line role pending randomized data.
Prazosin has been used as an antihypertensive drug in the treatment of 93 patients in Dunedin since 1971-1972, mainly those whose previous control was unsatisfactory. It has led to very significant improvement of control in many cases; 48 patients now receiving the drug have taken it for an average of 30 months. Forty-five patients have stopped taking the drug for various reasons, such as failure to respond (11-8%), side effects (20-4%), myocardial infarction (8-6%) or unrelated reasons (7-5%). This reflects to some extent the use ofa new drug in patients who are difficult to control, and its use initially without concomitant diuretic and beta-blocker therapy. We believe that the place of praxosin is primarily as a third drug for patients whose hypertension does not respond satisfactorirly to a diuretic and a beta-blocker. The first dose must be kept small, preferably 0-25 mg, and even with this dose a small proportion of patients receiving diuretic and beta-blocker therapy seem to become hypotensive; patients should be warned about this. The plasma half-life in normal volunteers was 3-8 hours but in some patients it seems to be considerably longer.
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Simpson et al. (1977) conducted an observational in Hypertension (n=93). Prazosin was evaluated on Discontinuation of therapy. Prazosin improved blood pressure control, though 45 of 93 patients discontinued therapy due to side effects (20.4%), failure to respond (11.8%), myocardial infarction (8.6%), or other reasons.
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