Hypotension prediction index for prevention of intraoperative hypotension in patients undergoing general anesthesia: a randomized controlled trial.

IF 2 3区 医学 Q2 ANESTHESIOLOGY Perioperative Medicine Pub Date : 2024-06-15 DOI:10.1186/s13741-024-00414-7
Chih-Jun Lai, Ya-Jung Cheng, Yin-Yi Han, Po-Ni Hsiao, Pei-Lin Lin, Ching-Tang Chiu, Jang-Ming Lee, Yu-Wen Tien, Kuo-Liong Chien
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Abstract

Background: Intraoperative hypotension is a common side effect of general anesthesia. Here we examined whether the Hypotension Prediction Index (HPI), a novel warning system, reduces the severity and duration of intraoperative hypotension during general anesthesia.

Methods: This randomized controlled trial was conducted in a tertiary referral hospital. We enrolled patients undergoing general anesthesia with invasive arterial monitoring. Patients were randomized 1:1 either to receive hemodynamic management with HPI guidance (intervention) or standard of care (control) treatment. Intraoperative hypotension treatment was initiated at HPI > 85 (intervention) or mean arterial pressure (MAP) < 65 mmHg (control). The primary outcome was hypotension severity, defined as a time-weighted average (TWA) MAP < 65 mmHg. Secondary outcomes were TWA MAP < 60 and < 55 mmHg.

Results: Of the 60 patients who completed the study, 30 were in the intervention group and 30 in the control group. The patients' median age was 62 years, and 48 of them were male. The median duration of surgery was 490 min. The median MAP before surgery presented no significant difference between the two groups. The intervention group showed significantly lower median TWA MAP < 65 mmHg than the control group (0.02 [0.003, 0.08] vs. 0.37 [0.20, 0.58], P < 0.001). Findings were similar for TWA MAP < 60 mmHg and < 55 mmHg. The median MAP during surgery was significantly higher in the intervention group than that in the control group (87.54 mmHg vs. 77.92 mmHg, P < 0.001).

Conclusions: HPI guidance appears to be effective in preventing intraoperative hypotension during general anesthesia. Further investigation is needed to assess the impact of HPI on patient outcomes.

Trial registration: ClinicalTrials.gov (NCT04966364); 202105065RINA; Date of registration: July 19, 2021; The recruitment date of the first patient: July 22, 2021.

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预防全身麻醉患者术中低血压的低血压预测指数:随机对照试验。
背景:术中低血压是全身麻醉的常见副作用。在此,我们研究了低血压预测指数(HPI)这一新型预警系统能否降低全身麻醉期间术中低血压的严重程度并缩短其持续时间:这项随机对照试验在一家三级转诊医院进行。我们招募了接受有创动脉监测的全身麻醉患者。患者按 1:1 随机分配,接受 HPI 指导下的血液动力学管理(干预)或标准护理(对照)治疗。术中低血压治疗在 HPI > 85(干预)或平均动脉压 (MAP) 结果时启动:在完成研究的 60 名患者中,干预组和对照组各占 30 人。患者的中位年龄为 62 岁,其中 48 人为男性。手术时间中位数为 490 分钟。两组患者术前的中位血压无明显差异。结论:HPI 引导似乎能有效预防全身麻醉期间的术中低血压。需要进一步调查以评估 HPI 对患者预后的影响:试验注册:ClinicalTrials.gov (NCT04966364);202105065RINA;注册日期:2021年7月19日:注册日期:2021年7月19日;首例患者招募日期:2021年7月22日:首例患者招募日期:2021 年 7 月 22 日。
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审稿时长
10 weeks
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