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Blood Pressure-Attained Analysis of ATACH 2 Trial
Adnan I Qureshi1, Yuko Y Palesch2, Lydia D Foster2
1From the Department of Neurology, Zeenat Qureshi Stroke Research Center, University of Minnesota, Minneapolis (A.I.Q., M.H.Q.) qureshai@gmail.com.
Insights
Intensive blood pressure reduction in intracerebral hemorrhage patients did not lower death or disability rates. However, it led to increased neurological deterioration and cardiac events, indicating risks associated with aggressive SBP management.
Area of Science:
- Neurology
- Cardiology
- Critical Care Medicine
Background:
- Intracerebral hemorrhage (ICH) is a critical condition often associated with high blood pressure.
- Effective management of systolic blood pressure (SBP) in ICH patients is crucial for improving outcomes.
- Previous studies have investigated various SBP targets, but the optimal strategy remains debated.
Purpose of the Study:
- To compare the rates of death or disability at 3 months in ICH patients based on post-treatment systolic blood pressure (SBP) attained.
- To evaluate the impact of achieving and maintaining a lower SBP target on clinical outcomes and adverse events.
Main Methods:
- A randomized trial involving 1000 ICH patients with SBP ≥180 mm Hg, randomized within 4.5 hours of symptom onset.
- Patients were grouped based on achieving SBP <140 mm Hg within 2 hours: reduced and maintained, or reduced but not maintained.
- Outcomes including death, disability (modified Rankin Scale 4-6), neurological deterioration, and cardiac events were assessed.
Main Results:
- Achieving and maintaining SBP <140 mm Hg within 2 hours did not significantly alter the rate of death or disability at 3 months compared to no reduction.
- Significantly higher rates of neurological deterioration within 24 hours were observed in both the reduced and maintained (10.4%) and reduced but not maintained (11.5%) groups.
- Cardiac-related adverse events within 7 days were more frequent in the group with reduction and maintenance of SBP <140 mm Hg (11.2%) compared to the reference group (6.4%).
Conclusions:
- Intensive SBP reduction to <140 mm Hg in ICH patients, whether maintained or not, did not improve 3-month death or disability rates.
- Aggressive SBP management was associated with increased risks of neurological deterioration and cardiac-related adverse events.
- These findings suggest caution when applying intensive SBP reduction strategies in the acute phase of intracerebral hemorrhage.
Background And Purpose:
We compared the rates of death or disability, defined by modified Rankin Scale score of 4 to 6, at 3 months in patients with intracerebral hemorrhage according to post-treatment systolic blood pressure (SBP)-attained status.
Methods:
We divided 1000 subjects with SBP ≥180 mm Hg who were randomized within 4.5 hours of symptom onset as follows: SBP <140 mm Hg achieved or not achieved within 2 hours; subjects in whom SBP <140 mm Hg was achieved within 2 hours were further divided: SBP <140 mm Hg for 21 to 22 hours (reduced and maintained) or SBP was ≥140 mm Hg for at least 2 hours during the period between 2 and 24 hours (reduced but not maintained).
Results:
Compared with subjects without reduction of SBP <140 mm Hg within 2 hours, subjects with reduction and maintenance of SBP <140 mm Hg within 2 hours had a similar rate of death or disability (relative risk of 0.98; 95% confidence interval, 0.74-1.29). The rates of neurological deterioration within 24 hours were significantly higher in reduced and maintained group (10.4%; relative risk, 1.98; 95% confidence interval, 1.08-3.62) and in reduced but not maintained group (11.5%; relative risk, 2.08; 95% confidence interval, 1.15-3.75) compared with reference group. The rates of cardiac-related adverse events within 7 days were higher among subjects with reduction and maintenance of SBP <140 mmHg compared to subjects without reduction (11.2% versus 6.4%).
Conclusions:
No decline in death or disability but higher rates of neurological deterioration and cardiac-related adverse events were observed among intracerebral hemorrhage subjects with reduction with and without maintenance of intensive SBP goals.
Clinical Trial Registration:
URL: https://www.clinicaltrials.gov. Unique identifier: NCT01176565.
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