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Longer-Term All-Cause and Cardiovascular Mortality With Intensive Blood Pressure Control: A Secondary Analysis of a Randomized Clinical Trial.
Jaeger, Byron C; Bress, Adam P; Bundy, Joshua D; Cheung, Alfred K; Cushman, William C; Drawz, Paul E; Johnson, Karen C; Lewis, Cora E; Oparil, Suzanne; Rocco, Michael V; Rapp, Stephen R; Supiano, Mark A; Whelton, Paul K; Williamson, Jeff D; Wright, Jackson T; Reboussin, David M; Pajewski, Nicholas M.
Affiliation
  • Jaeger BC; Department of Biostatistics and Data Science, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Bress AP; Informatics, Decision-Enhancement, and Analytic Sciences (IDEAS) Center, Veterans Affairs, Salt Lake City Health Care System, Salt Lake City, Utah.
  • Bundy JD; Department of Population Health Sciences, University of Utah School of Medicine, Salt Lake City.
  • Cheung AK; Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Cushman WC; Renal Section, Veterans Affairs Salt Lake City Healthcare System, Salt Lake City, Utah.
  • Drawz PE; Division of Nephrology and Hypertension, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City.
  • Johnson KC; Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis.
  • Lewis CE; Division of Renal Diseases and Hypertension, University of Minnesota, Minneapolis.
  • Oparil S; Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis.
  • Rocco MV; Department of Epidemiology, University of Alabama at Birmingham.
  • Rapp SR; Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham.
  • Supiano MA; Section on Nephrology, Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Whelton PK; Department of Psychiatry and Behavioral Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Williamson JD; Department of Social Science and Health Policy, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
  • Wright JT; Division of Geriatrics, University of Utah School of Medicine, Salt Lake City.
  • Reboussin DM; Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana.
  • Pajewski NM; Section on Gerontology and Geriatric Medicine, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina.
JAMA Cardiol ; 7(11): 1138-1146, 2022 11 01.
Article in En | MEDLINE | ID: mdl-36223105
ABSTRACT
Importance The Systolic Blood Pressure Intervention Trial (SPRINT) showed that intensive blood pressure control reduced cardiovascular morbidity and mortality. However, the legacy effect of intensive treatment is unknown.

Objective:

To evaluate the long-term effects of randomization to intensive treatment with the incidence of cardiovascular and all-cause mortality approximately 4.5 years after the trial ended. Design, Setting, and

Participants:

In this secondary analysis of a multicenter randomized clinical trial, randomization began on November 8, 2010, the trial intervention ended on August 20, 2015, and trial close-out visits occurred through July 2016. Patients 50 years and older with hypertension and increased cardiovascular risk but without diabetes or history of stroke were included from 102 clinic sites in the US and Puerto Rico. Analyses were conducted between October 2021 and February 2022.

Interventions:

Randomization to systolic blood pressure (SBP) goal of less than 120 mm Hg (intensive treatment group; n = 4678) vs less than 140 mm Hg (standard treatment group; n = 4683). Main Outcomes and

Measures:

Extended observational follow-up for mortality via the US National Death Index from 2016 through 2020. In a subset of 2944 trial participants, outpatient SBP from electronic health records during and after the trial were examined.

Results:

Among 9361 randomized participants, the mean (SD) age was 67.9 (9.4) years, and 3332 (35.6%) were women. Over a median (IQR) intervention period of 3.3 (2.9-3.9) years, intensive treatment was beneficial for both cardiovascular mortality (hazard ratio [HR], 0.66; 95% CI, 0.49-0.89) and all-cause mortality (HR, 0.83; 95% CI, 0.68-1.01). However, at the median (IQR) total follow-up of 8.8 (8.3-9.3) years, there was no longer evidence of benefit for cardiovascular mortality (HR, 1.02; 95% CI, 0.84-1.24) or all-cause mortality (HR, 1.08; 95% CI, 0.94-1.23). In a subgroup of participants, the estimated mean outpatient SBP among participants randomized to intensive treatment increased from 132.8 mm Hg (95% CI, 132.0-133.7) at 5 years to 140.4 mm Hg (95% CI, 137.8-143.0) at 10 years following randomization. Conclusions and Relevance The beneficial effect of intensive treatment on cardiovascular and all-cause mortality did not persist after the trial. Given increasing outpatient SBP levels in participants randomized to intensive treatment following the trial, these results highlight the importance of consistent long-term management of hypertension. Trial Registration ClinicalTrials.gov Identifier NCT01206062.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hypertension / Antihypertensive Agents Type of study: Clinical_trials / Incidence_studies / Prognostic_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Cardiol Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hypertension / Antihypertensive Agents Type of study: Clinical_trials / Incidence_studies / Prognostic_studies Limits: Aged / Female / Humans / Male Language: En Journal: JAMA Cardiol Year: 2022 Document type: Article