Effect of Prophylactic Dose of Trimethoprim-Sulfamethoxazole on Serum Creatinine in Japanese Patients With Connective Tissue Diseases

R. Kawato, R. Rokutanda, M. Okada, M. Matsushita, K. Yamaji, N. Tamura
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Abstract

Objectives: At normal doses of trimethoprim-sulfamethoxazole (TMP/SMX), trimethoprim inhibits tubular creatinine secretion, leading to a rapid but reversible increase in serum creatinine (SCr). Although patients with connective tissue diseases are often in the state of immunosuppression and TMP/SMX is an important prophylactic drug, clinicians often have to stop or reduce the dosage due to concerns regarding its effect on renal function. This study aimed to evaluate the effect of a prophylactic dose of TMP/SMX on SCr in Japanese patients with connective tissue diseases, the extent of SCr level elevation and the independent risk factors for creatinine elevation. Methods: A retrospective cohort study was undertaken. Participants included patients with connective tissue diseases who were treated with a prophylactic dose of TMP/SMX between 2004 and 2018. Using single and multiple regression analyses, the risk factors that affected SCr elevation were evaluated. Results: A total of 262 patients, females, n = 181; age, median (range) = 59 (19-89) years, were included. The median baseline SCr level before treatment was 0.62 (0.16-2.1) mg/dL. The median SCr elevation value was 0.07 (−0.54 to 0.84) mg/dL in 4 weeks after TMP/SMX initiation. Five (2%) participants had ⩾0.3 mg/dL SCr elevation. Multiple regression analyses, including age, baseline SCr, diuretic use, nonsteroidal anti-inflammatory drug use and diabetes mellitus, indicated that baseline SCr and advanced age were independent risk factors of SCr elevation. Conclusions: These results demonstrated that baseline SCr and advanced age were associated with SCr elevation by a prophylactic dose of TMP/SMX. However, a prophylactic dose of TMP/SMX rarely elevated the SCr level significantly. Therefore, other causes can be considered if patients show an SCr elevation ⩾0.3 mg/dL.
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甲氧苄啶-磺胺甲恶唑预防剂量对日本结缔组织病患者血清肌酐的影响
目的:在正常剂量的甲氧苄啶-磺胺甲恶唑(TMP/SMX)下,甲氧苄啶抑制小管肌酐分泌,导致血清肌酐(SCr)快速但可逆的升高。虽然结缔组织疾病患者常处于免疫抑制状态,TMP/SMX是重要的预防性药物,但临床医生经常因担心其对肾功能的影响而不得不停止或减少剂量。本研究旨在评估TMP/SMX预防剂量对日本结缔组织疾病患者SCr的影响、SCr水平升高的程度以及肌酐升高的独立危险因素。方法:采用回顾性队列研究。参与者包括结缔组织疾病患者,他们在2004年至2018年期间接受了预防性剂量的TMP/SMX治疗。采用单因素和多因素回归分析,评估影响SCr升高的危险因素。结果:共262例患者,女性,n = 181;年龄中位数(范围)= 59(19-89)岁。治疗前的中位基线SCr水平为0.62 (0.16-2.1)mg/dL。在TMP/SMX开始治疗4周后,SCr中位升高值为0.07(- 0.54至0.84)mg/dL。5名(2%)参与者的SCr升高小于0.3 mg/dL。包括年龄、基线SCr、利尿剂使用情况、非甾体抗炎药使用情况和糖尿病等因素的多元回归分析显示,基线SCr和高龄是SCr升高的独立危险因素。结论:这些结果表明,通过预防剂量的TMP/SMX,基线SCr和高龄与SCr升高相关。然而,预防性剂量的TMP/SMX很少显著提高SCr水平。因此,如果患者的SCr升高大于或等于0.3 mg/dL,可以考虑其他原因。
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CiteScore
4.40
自引率
0.00%
发文量
14
审稿时长
8 weeks
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