围手术期接受塞来昔布作为标准多模式镇痛方案之一的患者择期髋关节置换术后急性肾损伤的发生率、严重程度和可逆性

Manson Tak Hei Chan, Timmy Chi Wing Chan, Henry Chi Yeung Mak, Will Shing Him Chan, Stanley Sau Ching Wong, Vincent Kai Chung Wong, Lewis Ping Keung Chan, C. Cheung
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摘要

背景:急性肾损伤(AKI)可并发高达10%的原发性下肢全关节置换术。然而,这些先前的研究都没有评估AKI的持续时间和可逆性。此外,没有专门评估围手术期塞来昔布对AKI发生率和严重程度的影响,特别是对既往存在肾脏损害的患者。本研究回顾性回顾短期围手术期塞来昔布治疗AKI的发生率、严重程度和持续时间。我们还旨在评估围手术期塞来昔布对存在或不存在肾脏损害患者AKI发生率和严重程度的影响。方法:回顾性分析2018年1月至2021年12月在香港玛丽医院就诊的1077例患者。数据从计算机病历系统中检索。结果:1077例患者中有100例(9.3%)发生术后AKI。888例(82.5%)患者围手术期使用塞来昔布,189例(17.5%)患者未使用。围手术期服用塞来昔布的患者AKI总发生率为9.2%,而未服用塞来昔布的患者AKI总发生率为9.5%。差异无统计学意义。围手术期使用塞来昔布与术后AKI无相关性。在围手术期接受塞来昔布治疗的患者中,既往存在肾功能损害(肾功能检查正常)的患者和未存在肾功能损害的患者术后AKI的总发生率分别为9.3%和9.2%。这在统计学上没有显著性。两组AKI持续时间均为4天。在这两组中,大多数AKI病例都是1期。结论:短期围手术期塞来昔布可能没有额外的AKI风险,即使是先前存在肾脏损害的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidence, Severity and Reversibility of Acute Kidney Injury after Elective Hip and Knee Arthroplasty in Patients Receiving Celecoxib Perioperatively as One of the Standard Multimodal Analgesic Protocols
Background: Acute Kidney Injury (AKI) may complicate up to 10% of primary lower-extremity total joint arthroplasties. However, none of these previous studies evaluated the duration and reversibility of AKI. Moreover, none specifically evaluated the impact of perioperative celecoxib on the incidence and severity of AKI, especially for patients with preexisting renal impairment. This study was to retrospectively review the incidence, severity and duration of AKI with short term perioperative celecoxib. We also aimed to evaluate the impact of perioperative celecoxib on the incidence and severity of AKI in patients with and without preexisting renal impairment. Methods: We retrospectively reviewed 1077 patients at Queen Mary Hospital, Hong Kong, from January 2018 to December 2021. Data were retrieved from the computerized medical records system. Results: One hundred of 1077 patients (9.3%) had postoperative AKI. Eight hundred eighty-eight patients (82.5%) were prescribed perioperative celecoxib, while 189 patients (17.5%) were not. The overall incidence of AKI in those taking perioperative celecoxib was 9.2%, while it was 9.5% in those not taking perioperative celecoxib. There was no statistically significant difference. There was no association between perioperative celecoxib and postoperative AKI. Among those who received perioperative celecoxib, the overall incidence of postoperative AKI in those with and without preexisting renal impairment (normal renal function test) was 9.3% and 9.2%, respectively. This was not statistically significant. The duration of AKI was 4 days for both groups. In both groups, most AKI cases were stage 1. Conclusions: Short term perioperative celecoxib probably had no additional AKI risk even in patients with preexisting renal impairment.
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