低剂量甲氨蝶呤和甲氧苄啶-磺胺甲恶唑联合处方与老年人30天死亡风险:一项队列研究

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Hasti Sadeghi, Fatemeh Ahmadi, Eric McArthur, Jessica M Sontrop, Sheikh S Abdullah, Brad L Urquhart, Richard B Kim, Flory T Muanda
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引用次数: 0

摘要

目的:本研究的目的是表征老年人联合使用低剂量甲氨蝶呤和TMP-SMX与低剂量甲氨蝶呤和头孢菌素的死亡风险。方法:我们在加拿大安大略省(2002年4月1日至2022年8月1日)进行了一项回顾性、基于人群的新用户队列研究,使用相关的行政保健数据。服用低剂量甲氨蝶呤的老年人新联合处方TMP-SMX (n = 1602)与新联合处方头孢菌素的老年人1:1匹配。主要终点是抗生素配药日期后30天内的死亡。次要结局包括全因住院、因骨髓抑制住院和因主要诊断为持续感染住院。倾向评分匹配用于平衡各组基线健康指标。风险比(RR)采用修正泊松回归计算。结果:在3204名服用低剂量甲氨蝶呤的成年人的倾向评分匹配队列中,成人联合使用TMP-SMX和头孢菌素的30天死亡风险相似(14/1602[0.87%]比15/1602 [0.94%];Rr 0.93 [95% ci 0.45-1.93])。接受TMP-SMX治疗的成人全因住院(RR 1.49 [95% CI 1.13-1.97])和感染(RR 2.78 [95% CI 1.30-5.95])的风险高于接受头孢菌素治疗的成人。结论:在服用低剂量甲氨蝶呤的老年人中,联合使用TMP-SMX与头孢菌素与更高的30天死亡风险无关,但与更高的30天全因住院和持续感染住院风险相关。如果得到证实,这些风险应与联合使用TMP-SMX和低剂量甲氨蝶呤的益处相平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-prescription of low-dose methotrexate and trimethoprim-sulfamethoxazole and the 30-day risk of death among older adults: A cohort study.

Aims: The aim of this study was to characterize the risk of death in older adults co-prescribed low-dose methotrexate and TMP-SMX vs. low-dose methotrexate and a cephalosporin.

Methods: We conducted a retrospective, population-based, new-user cohort study in Ontario, Canada (April 1, 2002-August 1, 2022) using linked administrative healthcare data. Older adults taking low-dose methotrexate who were newly co-prescribed TMP-SMX (n = 1602) were matched 1:1 with those who were newly co-prescribed a cephalosporin. The primary outcome was death within 30 days of the antibiotic dispensing date. Secondary outcomes included all-cause hospitalization, a hospital visit with myelosuppression and a hospitalization with persistent infection defined as the main diagnosis. Propensity score matching was used to balance comparison groups on indicators of baseline health. Risk ratios (RR) were obtained using modified Poisson regression.

Results: In a propensity-score matched cohort of 3204 adults taking low-dose methotrexate, the 30-day risk of death was similar in adults co-prescribed TMP-SMX vs. a cephalosporin (14/1602 [0.87%] vs. 15/1602 [0.94%]; RR 0.93 [95% CI 0.45-1.93]). The risk of all-cause hospitalization (RR 1.49 [95% CI 1.13-1.97]) and infection (RR 2.78 [95% CI 1.30-5.95]) was higher in adults treated with TMP-SMX than those treated with cephalosporins.

Conclusions: In older adults taking low-dose methotrexate, co-prescription of TMP-SMX vs. a cephalosporin was not associated with a higher 30-day risk of death but was associated with a higher 30-day risk of all-cause hospitalization and hospital admission with persistent infection. If verified, these risks should be balanced against the benefits of co-prescribing TMP-SMX and low-dose methotrexate.

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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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