High versus standard blood pressure target in hypertensive high-risk patients undergoing elective major abdominal surgery: a study protocol for the HISTAP randomized clinical trial.

Antonio Messina, Andrea Cortegiani, Stefano Romagnoli, Giovanni Sotgiu, Federico Piccioni, Katia Donadello, Massimo Girardis, Alberto Noto, Salvatore Maurizio Maggiore, Massimo Antonelli, Maurizio Cecconi
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Abstract

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 χ2 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.

接受选择性腹部大手术的高血压高危患者的高与标准血压目标:一项HISTAP随机临床试验的研究方案
背景:术中以血流动力学不稳定为特征,术中低血压是常见的并发症。高血压患者的最佳平均动脉压(MAP)目标尚不清楚。我们在此描述高血压高危患者择期腹部大手术的高与标准血压目标的方案和详细的统计分析计划:HISTAP随机临床试验。与标准和推荐的围手术期MAP相比,HISTAP试验旨在通过使用包括手术干预30天死亡率和术后7天发生至少一个主要器官功能障碍或新发败血症和感染性休克在内的综合结果,探讨在计划进行择期腹部手术的高危高血压手术患者中使用更高的术中MAP目标是否会改善术后结果。方法:HISTAP试验是一项研究者发起的、实用的、平行分组的、随机的、分层的、分析盲法的试验,具有充分的分配序列生成和分配隐藏。我们将636例患者分配到MAP目标≥80 mmHg(治疗组)或MAP目标≥65 mmHg(对照组)。主要转归是一个综合转归,包括手术30天死亡率和主要器官并发症。次要结局是30天死亡率、重症监护病房(ICU)住院时间、ICU再入院、术后第7天前记录的序贯器官衰竭评估(SOFA)评分、术中总体液体平衡、血管加压药物的使用以及再次手术的需要。主要结局分析采用未经校正的χ2检验。Cox比例风险模型将用于调整主要结局和基线协变量之间的关联。结论:HISTAP试验结果将为指导临床医生择期腹部手术高危高血压患者术中MAP靶点的选择提供重要依据。
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