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Individualized Perioperative Blood Pressure Management in Patients Undergoing Major Abdominal Surgery: The IMPROVE-multi Randomized Clinical Trial.

JAMA2025-10-12PubMed
Total: 81.0Rigor: 9Innovation: 6Journal: 10Clinical: 8

Summary

In 1142 high-risk patients undergoing major abdominal surgery at 15 German centers, individualized MAP targets based on preoperative nighttime MAP did not reduce a 7-day composite of AKI, myocardial injury, nonfatal cardiac arrest, or death versus routine care (RR 1.10; 95% CI 0.93-1.30; P=.31). None of 22 secondary outcomes differed, including infections and a 90-day major adverse event composite.

Key Findings

  • Composite primary outcome occurred in 33.5% with individualized MAP vs 30.5% with routine care (RR 1.10; 95% CI 0.93-1.30; P=.31).
  • No significant differences across 22 secondary outcomes, including 7-day infections (15.9% vs 17.1%; P=.63) and 90-day KRT/MI/cardiac arrest/death composite (5.7% vs 3.5%; P=.12).
  • Intervention set intraoperative MAP targets using preoperative mean nighttime MAP from ambulatory monitoring; control targeted MAP ≥65 mm Hg.

Clinical Implications

Maintain standard MAP targets of ≥65 mm Hg during major abdominal surgery; do not escalate complexity by aligning targets to nighttime MAP, as this did not improve early organ injury or mortality.

Why It Matters

A large, multicenter RCT directly tests personalized MAP targeting using ambulatory data and finds no clinical benefit, challenging the adoption of individualized perioperative BP strategies.

Limitations

  • Single-blind design may allow performance bias at the provider level
  • Generalizability limited to German university hospitals and major abdominal surgery; short primary follow-up (7 days)

Future Directions

Test perfusion-guided strategies (e.g., autoregulation indices, organ-specific perfusion monitoring), evaluate microcirculatory endpoints, and assess different populations and longer-term outcomes.

Study Information

Study Type
RCT
Research Domain
Treatment
Evidence Level
I - Randomized, multicenter clinical trial with predefined outcomes
Study Design
OTHER