M. Pahor et al., LONG-TERM SURVIVAL AND USE OF ANTIHYPERTENSIVE MEDICATIONS IN OLDER PERSONS, Journal of the American Geriatrics Society, 43(11), 1995, pp. 1191-1197
OBJECTIVE: To determine whether older persons with hypertension who us
e specific calcium antagonists and ACE inhibitors have a different ris
k of mortality than those using beta-blockers. DESIGN: A prospective c
ohort study continuing from 1988 through 1992. SETTING: Three communit
ies of the Established Populations for Epidemiologic Studies of the El
derly. PARTICIPANTS: Hypertensive participants aged greater than or eq
ual to 71 years (n = 906) who had no evidence of congestive heart fail
ure and who were using either beta-blockers (n = 515), verapamil (n =
77), diltiazem (n = 92), nifedipine (n = 74), or ACE inhibitors (n = 1
48). Nifedipine was of the short acting variety. MEASUREMENTS: The mai
n outcome measure was all-cause mortality. Age, gender, smoking, HDL-c
holesterol, blood pressure, intake of digoxin and diuretics, physical
disability, self-perceived health, and comorbid conditions were examin
ed as confounders. RESULTS: During 3538 person-years of follow-up, 188
participants died (53 deaths per 1000 person-years). Compared with be
ta-blockers, after adjusting for age, gender, comorbid conditions and
other health-related factors, the relative risks (95% confidence inter
val) for mortality associated with use of verapamil, diltiazem, nifedi
pine, and ACE inhibitors were 0.8 (0.4-1.4), 1.3 (0.8-2.1), 1.7 (1.1-2
.7), and 0.9 (0.6-1.4), respectively. The results were unchanged after
excluding participants with other potential contraindications to beta
-blockers and after stratifying on coronary heart disease and use of d
iuretics. Higher doses of nifedipine were associated with higher morta
lity. CONCLUSION: Compared with beta-blockers, use of short acting nif
edipine was associated with decreased survival in older hypertensive p
ersons. However, selective factors influencing the use of specific dru
gs in higher risk patients could not be completely discounted, and fin
al conclusions will depend on clinical trials.