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根据术后疼痛强度提供理想静脉患者自控镇痛的截止值:一项回顾性观察研究。

Cutoff Values for Providing the Ideal Intravenous Patient-Controlled Analgesia According to the Intensity of Postoperative Pain-A Retrospective Observational Study.

机构信息

Department of Anesthesiology and Pain Medicine, School of Medicine, Chosun University, 309 Pilmun-daero, Dong-Gu, Gwangju 61452, Korea.

Department of Anesthesiology and Pain Medicine, Chosun University Hospital, 365 Pilmun-daero, Dong-Gu, Gwangju 61453, Korea.

出版信息

Medicina (Kaunas). 2021 Oct 6;57(10):1065. doi: 10.3390/medicina57101065.

Abstract

The cutoff values were analyzed for providing the ideal intravenous patient-controlled analgesia (PCA) that could reduce rescue analgesics or antiemetics requirements, based on the grades of postoperative pain intensity (PPI). PCA regimens of 4106 patients were retrospectively analyzed, and they were allocated into three groups with low, moderate, and high PPI grades (groups L, M, and H, respectively) based on numeric rating scores obtained 6 h postoperatively. Opioid and non-opioid analgesic doses were converted into fentanyl-equivalent doses (DOSE-FEN-OP and DOSE-FEN-NONOP, respectively). The primary endpoint was the cutoff values of these parameters. With respect to the PCA settings to reduce rescue analgesic and antiemetic requirements, group L required a background infusion rate (BIR) of 1.75-3 mL/h, bolus volume of 0.5-1.25 mL, and lockout interval of ≤12.5 min. Group M required a BIR of 1.75 mL/h, bolus volume of 0.5-1.75 mL, and lockout interval of ≤5 min. Group H required a BIR of 1.75 mL/h, bolus volume of 0.5 mL, and lockout interval of ≤5 min. In assessments of the analgesic doses to reduce rescue analgesic requirement, the DOSE-FEN-OP was at least 950 μg of fentanyl regardless of group, while the DOSE-FEN-NONOP was ≥250 μg, ≥550 μg, and ≥700 μg for the L, M, and H groups, respectively. In assessments of the analgesic doses to reduce rescue antiemetic requirement, DOSE-FEN-OP was ≤950 μg for groups L and M and ≤850 μg for Group H, while DOSE-FEN-NONOP was ≤50 μg, ≤450 μg, and ≤700 μg for groups L, M, and H, respectively. The ideal PCA for reduction in rescue analgesics or antiemetics can be achieved by adjustment of PCA settings and drug dosages carefully with these cutoff values depending on the expected grades of PPI. Especially, the ideal PCA can be provided by adjusting the lockout interval and bolus volume rather than BIR and by applying smaller bolus doses and shorter lockout intervals with an increasing PPI grade.

摘要

基于术后疼痛强度(PPI)等级,分析了截断值,以提供可减少解救性镇痛或止吐药需求的理想静脉患者自控镇痛(PCA)。回顾性分析了 4106 例患者的 PCA 方案,并根据术后 6 小时获得的数字评分将其分为低、中、高 PPI 等级组(分别为 L、M 和 H 组)。将阿片类药物和非阿片类药物的剂量转换为芬太尼等效剂量(DOSE-FEN-OP 和 DOSE-FEN-NONOP)。主要终点是这些参数的截断值。为了降低 PCA 对解救性镇痛和止吐药的需求,L 组需要背景输注率(BIR)为 1.75-3 mL/h、推注量为 0.5-1.25 mL 和锁定间隔≤12.5 min。M 组需要 BIR 为 1.75 mL/h、推注量为 0.5-1.75 mL 和锁定间隔≤5 min。H 组需要 BIR 为 1.75 mL/h、推注量为 0.5 mL 和锁定间隔≤5 min。在评估减少解救性镇痛需求的镇痛剂量时,DOSE-FEN-OP 至少为 950μg 芬太尼,而 DOSE-FEN-NONOP 分别为 L、M 和 H 组的≥250μg、≥550μg 和≥700μg。在评估减少解救性止吐药需求的镇痛剂量时,L 和 M 组的 DOSE-FEN-OP≤950μg,H 组的 DOSE-FEN-OP≤850μg,而 DOSE-FEN-NONOP 分别为 L、M 和 H 组的≤50μg、≤450μg 和≤700μg。根据预期的 PPI 等级,通过仔细调整这些截断值的 PCA 设置和药物剂量,可以实现减少解救性镇痛或止吐药的理想 PCA。特别是,可以通过调整锁定间隔和推注量,而不是 BIR,并随着 PPI 等级的增加应用较小的推注剂量和较短的锁定间隔来提供理想的 PCA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a65c/8541173/3201bcdaa905/medicina-57-01065-g001.jpg

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