What are the recommended systolic blood pressure targets for a patient with acute intracerebral hemorrhage on day 1 (first 24 hours) and from day 2 onward?

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Last updated: February 17, 2026View editorial policy

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Blood Pressure Targets in Acute Intracerebral Hemorrhage

For patients with acute intracerebral hemorrhage presenting with systolic blood pressure 150–220 mmHg, target a systolic BP of 140 mmHg (acceptable range 130–150 mmHg) within 1 hour of treatment initiation and maintain this target continuously for at least 7 days—this applies equally to day 1 and day 2 onward. 1, 2

Day 1 (First 24 Hours): Aggressive Early Control

Primary Target and Timing

  • Initiate antihypertensive therapy within 2 hours of symptom onset to maximize reduction in hematoma expansion 1, 2
  • Achieve systolic BP of 140 mmHg (range 130–150 mmHg) within 1 hour of starting treatment 1, 2
  • This aggressive early approach is supported by the 2022 American Heart Association/American Stroke Association guidelines (Class I, Level A recommendation) 1, 2

Critical Safety Boundaries on Day 1

  • Never lower systolic BP below 130 mmHg—this carries a Class III: Harm recommendation and is associated with worse neurological outcomes and increased mortality 1, 2
  • Avoid dropping systolic BP by more than 70 mmHg within the first hour, particularly in patients presenting with systolic BP ≥220 mmHg, as this increases risk of acute kidney injury and neurological deterioration 1, 3
  • Maintain cerebral perfusion pressure ≥60 mmHg at all times, especially if intracranial pressure is elevated 1, 2

Preferred Pharmacologic Agent

  • Intravenous nicardipine is the first-line agent: start at 5 mg/hour and titrate by 2.5 mg/hour every 5 minutes up to a maximum of 15 mg/hour 1
  • Nicardipine allows precise titration and sustained BP control, which is critical for minimizing blood pressure variability 1
  • Labetalol is an acceptable alternative when nicardipine is unavailable or contraindicated 1

Monitoring Intensity on Day 1

  • Measure BP every 15 minutes until target is reached, then every 30–60 minutes for the first 24 hours 1
  • Use continuous arterial line monitoring for patients on continuous IV antihypertensives 2
  • Minimize BP variability—large fluctuations in systolic BP independently worsen functional outcomes, even when mean BP is within target 1, 4

Day 2 Onward (Through Day 7): Sustained Control

Unchanged Target Range

  • Continue targeting systolic BP 130–150 mmHg for at least 7 days after ICH onset 1, 2
  • The target does NOT change after day 1—the same 140 mmHg goal (range 130–150 mmHg) applies throughout the acute hospitalization 1, 2

Rationale for Sustained Control

  • The therapeutic window extends beyond the first 24 hours; smooth, sustained BP control through day 7 limits variability-related harm and prevents delayed hematoma expansion 1, 2
  • High BP variability during the first 24–48 hours is independently associated with death and severe disability at 90 days 1, 4

Transition Strategy

  • Continue continuous IV infusion (nicardipine or labetalol) as long as needed to maintain smooth control without peaks 1
  • Transition to oral antihypertensives only when BP is stable and variability is minimized 2
  • Avoid intermittent boluses, which increase BP variability 5

Special Populations and Caveats

Patients with Initial Systolic BP ≥220 mmHg

  • Exercise extreme caution: intensive BP lowering in this subgroup is associated with higher rates of neurological deterioration (15.5% vs 6.8%) and acute kidney injury without benefit in reducing death or severe disability 3
  • In these patients, do not drop systolic BP by more than 70 mmHg in the first hour 1, 3

Large or Surgically Decompressed ICH

  • The safety and efficacy of intensive BP lowering are uncertain in patients with large hematomas or those requiring surgical decompression 1, 2
  • In these cases, accept slightly higher systemic BP targets (e.g., 150–160 mmHg) if intracranial pressure is markedly elevated, provided cerebral perfusion pressure remains ≥60 mmHg 1, 5

Patients with Glasgow Coma Scale <5

  • Evidence for intensive BP lowering is limited in patients with severe ICH (GCS <5), as they were largely excluded from INTERACT2 and ATACH-2 trials 2

Common Pitfalls to Avoid

  • Delaying treatment beyond 2 hours from symptom onset markedly narrows the therapeutic window 1, 2
  • Allowing BP to drift above 160 mmHg increases risk of hematoma expansion 1
  • Lowering BP below 130 mmHg is harmful and associated with worse outcomes 1, 2, 4
  • Permitting large BP variability (peaks and fluctuations) worsens functional outcomes independent of mean BP achieved 1, 4
  • Using glyceryl trinitrate (GTN) should be avoided, as the RIGHT-2 trial showed it was associated with greater hematoma growth and poorer outcomes 1

Contrast with Older Guidelines

The 2010 AHA/ASA guidelines suggested a more conservative approach, with a systolic BP target of <180 mmHg for patients presenting with systolic BP 150–220 mmHg 6. However, the 2022 guidelines represent a paradigm shift based on INTERACT2 and ATACH-2 trial data, establishing 140 mmHg (range 130–150 mmHg) as the optimal target with Class I, Level A evidence 1, 2. The older, more permissive target of <180 mmHg is no longer recommended for patients in the 150–220 mmHg range 6, 1.

References

Guideline

Blood Pressure Management in Hemorrhagic Stroke

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Acute Blood Pressure Management in Intracerebral Hemorrhage

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Management of Blood Pressure in Chronic Subdural Hematoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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