How quickly should we titrate antihypertensive medication? Systematic review modelling blood pressure response from trial data.

CONTEXT: There are no evidence syntheses available to guide clinicians on when to titrate antihypertensive medication after initiation. OBJECTIVE: To model the blood pressure (BP) response after initiating antihypertensive medication. Data sources electronic databases including Medline, Embase, Coch...

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Những tác giả chính: Lasserson, D, Buclin, T, Glasziou, P
Định dạng: Journal article
Ngôn ngữ:English
Được phát hành: 2011
Miêu tả
Tóm tắt:CONTEXT: There are no evidence syntheses available to guide clinicians on when to titrate antihypertensive medication after initiation. OBJECTIVE: To model the blood pressure (BP) response after initiating antihypertensive medication. Data sources electronic databases including Medline, Embase, Cochrane Register and reference lists up to December 2009. STUDY SELECTION: Trials that initiated antihypertensive medication as single therapy in hypertensive patients who were either drug naive or had a placebo washout from previous drugs. DATA EXTRACTION: Office BP measurements at a minimum of two weekly intervals for a minimum of 4 weeks. An asymptotic approach model of BP response was assumed and non-linear mixed effects modelling used to calculate model parameters. RESULTS AND CONCLUSIONS: Eighteen trials that recruited 4168 patients met inclusion criteria. The time to reach 50% of the maximum estimated BP lowering effect was 1 week (systolic 0.91 weeks, 95% CI 0.74 to 1.10; diastolic 0.95, 0.75 to 1.15). Models incorporating drug class as a source of variability did not improve fit of the data. Incorporating the presence of a titration schedule improved model fit for both systolic and diastolic pressure. Titration increased both the predicted maximum effect and the time taken to reach 50% of the maximum (systolic 1.2 vs. 0.7 weeks; diastolic 1.4 vs. 0.7 weeks). CONCLUSIONS: Estimates of the maximum efficacy of antihypertensive agents can be made early after starting therapy. This knowledge will guide clinicians in deciding when a newly started antihypertensive agent is likely to be effective or not at controlling BP.