The role of diastolic blood pressure when treating isolated systolic hypertension

Citation
Gw. Somes et al., The role of diastolic blood pressure when treating isolated systolic hypertension, ARCH IN MED, 159(17), 1999, pp. 2004-2009
Citations number
25
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
ARCHIVES OF INTERNAL MEDICINE
ISSN journal
00039926 → ACNP
Volume
159
Issue
17
Year of publication
1999
Pages
2004 - 2009
Database
ISI
SICI code
0003-9926(19990927)159:17<2004:TRODBP>2.0.ZU;2-R
Abstract
Objective: To assess the role of treated diastolic blood pressure (DBP) lev el in stroke, coronary heart disease (CHD), and cardiovascular disease (CVD ) in patients with isolated systolic hypertension (ISH). Design: An analysis of the 4736 participants in the Systolic Hypertension i n the Elderly Program (SHEP) was undertaken. The SHEP was a randomized mult icenter double-blind outpatient clinical trial of the impact of treating IS H in men and women aged 60 years and older. Main Outcome Measures: Cox proportional hazards regression analysis, with D BP and systolic blood pressure (SBP) as time-dependent covariables. Results: After adjustment for the baseline risk factors of race (black vs o ther), sex, use of antihypertensive medication before the study, a composit e variable (diabetes, previous heart attack, or stroke), age, and smoking h istory (ever vs never) and adjustment for the SEP as a time-dependent varia ble, we found, for the active treatment group only, that a decrease of 5 mm Hg in DBP increased the risk for stroke (relative risk, [RR], 1.14; 95% co nfidence interval [CI], 1.05-1.22),for CHD (RR, 1.08; 95% CI, 1.00-1.16), a nd for CVD (RR, 1.11; 95% CI, 1.05-1.16). Conclusions: Some patients with ISH may be treated to a level that uncovers subclinical disease, and some may be overtreated. Further studies need to determine whether excessively low DBP can be prevented by more careful titr ation of antihypertensive therapy while maintaining SEP control. It is reas suring that patients receiving treatment for ISH never perform worse than p atients receiving placebo in terms of CVD events.