Intensive Blood Pressure Reduction is Associated with Reduced Hematoma Growth in Fast Bleeding Intracerebral Hemorrhage A Secondary Analysis of the ATACH-2 Randomized Clinical Trial. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: Spontaneous intracerebral hemorrhage (ICH) patients at highest risk of hematoma growth are those with the most potential to benefit from anti-expansion treatment. Large clinical trials have not definitively shown a clear benefit of blood pressure (BP) reduction. We aim to determine whether intensive blood pressure reduction could benefit patients with fast bleeding ICH. METHODS: An exploratory analysis of data from the Antihypertensive Treatment of Acute Cerebral Hemorrhage 2 (ATACH-2) randomized controlled trial was performed. In order to capture not just early bleeding (even if a small amount), but the rate of bleeding (mL/hour), we restricted the study to "Fast bleeding ICH," defined as an ICH volume/onset-to-CT time >5mL/hr. Hematoma growth, as defined as an increase of hematoma volume > 33% between baseline and 24 hours. RESULTS: A total of 940 patients were included (mean age 62.1 years, 61.5% male), of whom 214 (22.8%) experienced hematoma expansion. Of these, 567(60.3%) met the definition of "fast bleeding" with baseline ICH volume/time to presentation of at least 5mL/hr. Intensive blood pressure reduction was associated with a significantly lower rate of hematoma growth in fast bleeding patients (20.6% vs 31.0%, p=0.005). In a subgroup of 266 (46.9%) fast-bleeding patients who received treatment within 2 hours after symptom onset, intensive BP lowering was associated with improved functional independence (OR, 1.98; 95% CI,1.06-3.69; p=0.031). INTERPRETATION: Our results suggest that early use of intensive BP reduction may reduce hematoma growth and improve outcome in fast bleeding patients. This article is protected by copyright. All rights reserved.

publication date

  • September 14, 2023

Identity

Digital Object Identifier (DOI)

  • 10.1002/ana.26795

PubMed ID

  • 37706569