Mc. Houston et al., THE EFFECTS OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS ON BLOOD PRESSURESOF PATIENTS WITH HYPERTENSION CONTROLLED BY VERAPAMIL, Archives of internal medicine, 155(10), 1995, pp. 1049-1054
Background: Nonsteroidal anti-inflammatory drugs may attenuate the ant
ihypertensive effects of diuretics, beta-blockers, angiotensin-convert
ing enzyme inhibitors, central alpha-agonists, and other vasodilators.
Their effects on the antihypertensive efficacy of calcium channel blo
ckers are inadequately studied in small numbers of patients but appear
to be minimal. Methods: A three-phase, randomized, double-blind, plac
ebo-controlled multicenter study included 162 patients aged 18 to 75 y
ears with essential hypertension. After diastolic blood pressure was c
ontrolled to 90 mm Hg or less with once-daily verapamil hydrochloride,
patients received ibuprofen, naproxen, or placebo matching capsules f
or 3 weeks, and blood pressure, heart rate, weight, and adverse effect
s were evaluated. A general linear model with 95% confidence intervals
was used to compare each nonsteroidal anti-inflammatory drug treatmen
t group with the placebo group. Results: No significant differences in
sitting, standing, or supine blood pressure were noted with naproxen
or ibuprofen compared with placebo. The percentages of patients in eac
h treatment group with increases of 10 mm Hg or more in either systoli
c or diastolic blood pressure were similar. Statistically significant
increases in weight were seen with both nonsteroidal anti-inflammatory
drug therapies. Changes in pulse rate were not significant. The incid
ence of adverse effects was similar across all three treatment groups.
Conclusions: The addition of naproxen or ibuprofen to the treatment o
f hypertensive patients in whom blood pressure is controlled by once-d
aily verapamil does not cause an increase in blood pressure. Verapamil
may therefore offer considerable advantages in maintaining control of
blood pressure in patients who regularly receive nonsteroidal anti-in
flammatory drug therapy.