Why the study?
Intraoperative hypotension is common during surgery, but the optimal mean arterial pressure target in hypertensive patients remains unclear.
Does a higher intraoperative MAP target (≥80 mmHg) improve postoperative outcomes compared to a standard MAP target (≥65 mmHg) in high-risk hypertensive patients undergoing elective abdominal surgery?
Does a higher intraoperative MAP target (≥80 mmHg) improve postoperative outcomes compared to a standard MAP target (≥65 mmHg) in high-risk hypertensive patients undergoing elective abdominal surgery?
The HISTAP trial protocol outlines a randomized study to determine whether targeting a higher intraoperative mean arterial pressure (≥80 mmHg) reduces 30-day mortality and major organ dysfunction compared to standard targets (≥65 mmHg) in high-risk hypertensive patients undergoing major abdominal surgery.
Background The intraoperative period is often characterized by hemodynamic instability, and intraoperative hypotension is a common complication. The optimal mean arterial pressure (MAP) target in hypertensive patients is still not clear. We hereby describe the protocol and detailed statistical analysis plan for the high versus standard blood pressure target in hypertensive high-risk patients undergoing elective major abdominal surgery: the HISTAP randomized clinical trial. The HISTAP trial aims at addressing whether the use of a higher intraoperative MAP target in high-risk hypertensive surgical patients scheduled for elective abdominal surgery would improve postoperative outcomes, as compared to the standard and recommended perioperative MAP, by using a composite outcome including a 30-day mortality from surgical intervention and at least one major organ dysfunction or new onset of sepsis and septic shock occurring 7 days after surgery. Methods The HISTAP trial is an investigator-initiated, pragmatic, parallel-grouped, randomized, stratified, analyst-blinded trial with adequate allocation sequence generation, and allocation concealment. We will allocate 636 patients to a MAP target ≥ 80 mmHg (treatment group) or to a MAP target ≥65 mmHg (control group). The primary outcome is a composite outcome including a 30-day mortality from the operation and major organ complications. Secondary outcomes are mortality at 30 days, intensive care unit (ICU) length of stay, ICU readmission, Sequential Organ Failure Assessment (SOFA) scores recorded up to postoperative day 7, overall intraoperative fluid balance, vasopressors use, and the need for reoperation. An unadjusted χ 2 test will be used for the primary outcome analysis. A Cox proportional hazards model will be used to adjust the association between the primary outcome and baseline covariates. Conclusions The HISTAP trial results will provide important evidence to guide clinicians’ choice regarding the intraoperative MAP target in high-risk hypertensive patients scheduled for elective abdominal surgery.
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Messina et al. (2023) studied this question.
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