Early, intensive BP drop benefits stroke patients



LONDON – Receipt of early, intensive blood pressure–lowering treatment improved functional outcomes in patients with acute intracerebral hemorrhage in a large, randomized trial.

There was a significant, favorable shift in the distribution of modified Rankin Scale (mRS) scores with a more intensive approach to blood pressuring lowering than guideline-recommended treatment, resulting in lower levels of disability (odds ratio, 0.87; P = .04).

Sara Freeman/IMNG Medical Media

Dr. Craig Anderson

However, the results of the eagerly anticipated INTERACT2 trial showed only a modest and nonsignificant reduction in the primary endpoint of death and disability (OR, 0.87; P less than .06).

The trial’s findings are still clinically relevant, the study’s investigators believe, and the approach now warrants implementation in routine clinical practice in most patients with acute intracerebral hemorrhage (ICH), particularly as there were no undue safety concerns when compared with the guideline-recommended approach.

"Blood pressure lowering in acute ICH is safe, so go early, go intensive, and go sustained in most of our patients because it improves the chances of a better recovery in survivors," said Dr. Craig Anderson, of the George Institute for Global Health in Sydney, Australia. "Ultimately, that’s what patients and families want us to do."

Dr. Anderson, who is the study’s chief investigator and is also professor of stroke medicine and clinical neuroscience at the University of Sydney, presented the study’s findings on May 29 at the annual European Stroke Conference; the results were also published simultaneously in the New England Journal of Medicine (doi: 10.1056/NEJMoa1214609).

Design of INTERACT2

INTERACT2 (Second Intensive Blood Pressure Reduction in Acute Cerebral Haemorrhage Trial) was an international, multicenter, prospective, open-label, blinded-endpoint, randomized trial of 2,839 patients. Patients were recruited within 6 hours of onset of spontaneous ICH and had elevated systolic blood pressure (150-220 mm Hg). The mean age was 63.5 years, and most patients were men (63%), Chinese (68%), and hypertensive (72%).

Patients were centrally allocated to randomly receive either intensive (n = 1,399) or guideline-recommended (n = 1,430) blood pressure–lowering treatment. Intensive treatment aimed to lower the systolic blood pressure rapidly, within 1 hour, to a target of less than 140 mm Hg. By contrast, guideline-recommended treatment aimed to reduce systolic blood pressure below a target of 180 mm Hg with no time limit.

The antihypertensive agents used were not stipulated in the study protocol, and hence a variety of agents were used by the 141 hospitals that participated in the trial. Intravenous agents were used in 90% of patients in the intensive-treatment arm versus 43% in the conventionally treated arm. Intensively managed patients were more likely to receive an IV bolus dose and an infusion (30% vs. 18%) or multiple agents (27% vs. 8%). The most commonly used agent was urapidil, an alpha-blocker available in some parts of Europe, but not in the United States.

Key findings

The primary measure of a poor outcome, defined as an mRS score of 3-6 at 90 days, was observed in 719 (52%) of intensively treated patients versus 785 (55.6%) of guideline-treated patients. An mRS score of 6 indicates death, and 3-5 denotes major disability.

An ordinal analysis of the mRS showed lower scores with the intensive than with the guideline-recommended blood pressure–lowering approach, with more patients able to remain independent despite having some level of disability (mRS score 0-2 in 48% of intensively treated vs. 44% of guideline-treated patients).

Sara Freeman/IMNG Medical Media

Dr. Christian Stapf

Health-related quality of life was assessed using the European Quality of Life-5 Dimensions questionnaire, and intensively treated patients reported fewer problems in mobility (64% vs. 67%; P = .13), self-care (47% vs. 52%; P = .02), usual activities (61% vs. 66%; P = .006), pain or discomfort (40% vs. 45%; P = .01), and anxiety or depression (34% vs. 38%, P = .05) than did those in the standard-treatment arm.

"I’ve never seen this in a clinical trial before," Dr. Anderson observed. "It’s very hard to find a signal in clinical trials, and I guess I was surprised by the degree of significance in benefit on usual activities, which is a very high measure of functional recovery when the patient is home."

Nonfatal serious adverse events occurred in a similar proportion of intensively treated and guideline-treated patients (23.3% and 23.6%, respectively). "The important thing is that we tried to look for any hazard, and we found no excess harms any way we looked at it," Dr. Anderson reported.

Implications for current practice

"If the results of this study with respect to the primary outcome were not as robust as some may have hoped, practitioners should be reassured by the safety data," Dr. Jennifer Frontera of the Cleveland Clinic Foundation commented in an editorial accompanying the NEJM paper.


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