肾移植患者使用非甾体抗炎药:一项回顾性研究。

Pub Date : 2023-01-01 DOI:10.3233/JRS-220065
Kannan Sridharan, Shamik Shah
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引用次数: 0

摘要

背景:肾移植患者通常服用非甾体抗炎药(NSAIDs)以达到镇痛目的:考虑到数据匮乏,我们开展了本研究,以评估各种非甾体抗炎药的使用情况和移植患者急性肾损伤(AKI)的发生率:2020年1月至12月期间,我们在巴林王国萨尔曼尼亚医疗中心肾内科对至少服用过一剂非甾体抗炎药的肾移植患者进行了一项回顾性研究。研究人员获得了患者的人口统计学资料、血清肌酐值以及与药物相关的详细信息。肾病改善全球结果(KDIGO)标准用于定义 AKI:结果:共纳入 87 名患者。43名患者服用了双氯芬酸,60名患者服用了布洛芬,6名患者服用了吲哚美辛,10名患者服用了甲灭酸,11名患者服用了萘普生。由于非甾体抗炎药处方有多个疗程,因此共发现 70 个双氯芬酸处方、80 个布洛芬处方、6 个吲哚美辛处方、11 个甲灭酸处方和 16 个萘普生处方。非甾体抗炎药之间的血清肌酐绝对值变化(p = 0.08)和百分比变化(p = 0.1)均无明显差异。28个(15.2%)非甾体抗炎药疗程符合KDIGO的AKI标准。年龄(OR:1.1,95% CI:1.007,1.2;p = 0.02)、同时服用依维莫司(OR:483,95% CI:4.3,54407;p = 0.01)和霉酚酸酯+环孢素+硫唑嘌呤(OR:63.4E+006,95% CI:203.2157 至 19.8E+012;p = 0.005)与非甾体抗炎药诱发 AKI 的显著风险有关:结论:在肾移植患者中,我们观察到非甾体抗炎药可能诱发的 AKI 约占 15.2%。结论:在我们的肾移植患者中,我们观察到非甾体抗炎药可能诱发的 AKI 约为 15.2%,各种非甾体抗炎药之间的 AKI 发生率无明显差异,且无一人发生移植失败或死亡。
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Use of non-steroidal anti-inflammatory drugs in renal transplant patients: A retrospective study.

Background: Renal transplants are often prescribed non-steroidal anti-inflammatory drugs (NSAIDs) for analgesic purposes.

Objective: Considering the dearth of data, we carried out the present study to evaluate the use of various NSAIDs and the incidence of acute kidney injury (AKI) in transplant patients.

Methods: A retrospective study amongst renal transplant patients prescribed at least one dose of NSAID was carried between January and December 2020 at the Department of Nephrology, Salmaniya Medical Complex, Kingdom of Bahrain. The patients' demographic details, serum creatinine values, and drug-related details were obtained. The Kidney Disease Improving Global Outcomes (KDIGO) criteria were used for defining AKI.

Results: Eighty-seven patients were included. Forty-three patients were prescribed diclofenac, 60 received ibuprofen, six received indomethacin, 10 were administered mefenamic acid, and 11 received naproxen. Due to multiple courses of NSAID prescription, a total of 70 prescriptions were identified for diclofenac, 80 for ibuprofen, six for indomethacin, 11 for mefenamic acid, and 16 for naproxen. No significant differences were observed in the absolute (p = 0.08) and percent changes in serum creatinine (p = 0.1) between the NSAIDs. Twenty-eight (15.2%) courses of NSAID therapy met the KDIGO criteria for AKI. Age (OR: 1.1, 95% CI: 1.007, 1.2; p = 0.02), concomitant everolimus (OR: 483, 95% CI: 4.3, 54407; p = 0.01), and mycophenolate + cyclosporine + azathioprine (OR: 63.4E+006, 95% CI: 203.2157 to 19.8E+012; p = 0.005) administration were observed with significant risk of NSAID-induced AKI.

Conclusion: We observed possible NSAID-induced AKI to an extent of around 15.2% in our renal transplant patients. No significant differences were observed in the incidence of AKI between various NSAIDs and none of them had either graft failure or death.

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