Clinical Utility of Short-Term Blood Pressure Measures to Inform Long-Term Blood Pressure Management

Author:

Wang Nelson123ORCID,Harris Katie1ORCID,Woodward Mark1ORCID,Harrap Stephen4,Mancia Giuseppe5ORCID,Poulter Neil6ORCID,Chalmers John1ORCID,Rodgers Anthony1,

Affiliation:

1. The George Institute for Global Health UNSW, Sydney, Australia (N.W., K.H., M.W., J.C., A.R.).

2. Royal Prince Alfred Hospital, Sydney, Australia (N.W.).

3. Sydney Medical School, University of Sydney, Australia (N.W.).

4. Royal Melbourne Hospital, University of Melbourne, Victoria, Australia (S.H.).

5. University of Milano-Bicocca, Italy (G.M.).

6. School of Public Health, Imperial College London, United Kingdom (N.P.).

Abstract

Background: Decisions about hypertension management are substantially influenced by blood pressure (BP) levels measured before and soon after starting BP lowering drugs. We aimed to assess the utility of short-term BP changes in individuals in terms of long-term treatment response. Methods: Post hoc analyses of 2 randomized trials with 4-to-6 weeks active run-in for all participants, followed by randomization to active BP lowering treatment (combination perindopril±indapamide) or placebo. We categorized individuals by degree of systolic BP (SBP) change during active run-in treatment and assessed associations with subsequent postrandomization placebo-corrected BP reduction, cardiovascular events, and tolerability. We included individuals with baseline BP ≥140/90 mm Hg from the PROGRESS trial (Perindopril Protection Against Recurrent Stroke Study; 4275 individuals with cerebrovascular disease) and ADVANCE trial (The Action in Diabetes and Vascular Disease: Preterax and Diamicron-MR Controlled Evaluation; 6610 individuals with diabetes). Results: During the active run-in period, the proportion of participants with initial SBP changes in 4 categories (SBP increase, 0–9.9 mm Hg decrease, 10–19.9 mm Hg decrease, and ≥20 mm Hg decrease) were 17%, 27%, 28%, and 28% in PROGRESS and 21%, 22%, 24%, and 33% in ADVANCE. Randomization to active therapy achieved similar placebo-corrected long-term BP reductions across the 4 initial SBP change groups in both trials ( P -values for heterogeneity >0.1). There was no significant difference in achieving BP <140/90 mm Hg at follow-up, major cardiovascular events, nor treatment tolerability according to the SBP change during active run-in period (all P -values >0.1). Conclusions: An individual’s apparent BP change immediately after commencing therapy has limited clinical utility. Therefore, more emphasis should be given to use of evidence-based regimens and measures over the long-term to ensure sustained BP control. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT00145925.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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