出院时处方万古霉素胶囊与液体对难辨梭菌感染再入院的影响。

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Rachel Reise, Silken A Usmani, Earl J Morris, Asinamai M Ndai, Marvin A Dewar, Scott Martin Vouri
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引用次数: 0

摘要

免责声明:为了加快文章的发表,AJHP在接受稿件后将尽快在网上发布。被接受的稿件已经过同行评审和编辑,但在技术格式化和作者校对之前会在网上发布。这些手稿不是记录的最终版本,稍后将被最终文章(按照AJHP风格格式化并由作者校对)所取代。目的:艰难梭菌感染(CDI)是一种医院获得性感染,常用口服万古霉素治疗。一项旨在通过用复方液体万古霉素代替胶囊来降低成本的制度性政策可能会产生意想不到的后果,即在出院时处方液体制剂,由于药房缺乏可用性或缺乏保险覆盖,可能会延迟患者获得药物的时间。本研究旨在评估万古霉素胶囊或液体处方患者出院后的再入院率。方法:这是一项在一家学术医院进行的回顾性队列研究,使用6年时间内的电子健康记录数据。主要结果是出院30天内的全因和cdi特异性再入院率,次要结果包括60天和90天内的再入院率。基线特征比较采用卡方检验或Mann-Whitney U检验。采用Cox比例风险模型计算再入院风险比(HR),采用泊松回归模型分析再入院率。所有再入院病例均经病历审查确认。结果:共440例患者,其中女性61.3%;中位年龄为58岁);其中68% (n = 298)处方万古霉素液体,32% (n = 142)处方万古霉素胶囊。两组的基线特征相似,除了存在炎症性肠病(19.0% vs 6.4%, P < 0.0001)和中位住院时间(6天vs 8天,P = 0.010)。服用万古霉素液体的患者在30天内再入院的可能性并不比服用胶囊的患者高,全因再入院的调整HR为1.58 (95% CI, 0.92-2.73), cdi特异性再入院的调整HR为2.21 (95% CI, 0.72-6.76)。然而,处方液体的患者更有可能在60天内再次入院,全因再入院的调整HR为1.87 (95% CI, 1.19-2.94), cdi特异性再入院的调整HR为2.84 (95% CI, 1.14-7.06)。结论:降低用药成本的医院药学实践可能会影响出院时万古霉素的处方,进而可能对口服万古霉素治疗的CDI患者的再入院率产生负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of prescribing vancomycin capsules vs liquid at discharge on readmissions for C. difficile infection.

Purpose: Clostridioides difficile infection (CDI) is a hospital-acquired infection commonly treated with oral vancomycin. An institutional policy aimed at reducing costs by substituting compounded liquid vancomycin for capsules may have the unintended consequence of having the liquid formulation prescribed at discharge, potentially delaying patients' access due to a lack of availability in pharmacies or lack of insurance coverage. This study aimed to evaluate hospital readmission rates of patients prescribed either vancomycin capsules or liquid upon discharge.

Methods: This was a retrospective cohort study conducted at an academic hospital using electronic health records data over a 6-year timeframe. The primary outcomes were all-cause and CDI-specific readmission rates within 30 days of discharge, and secondary outcomes included readmission rates within 60 and 90 days. Baseline characteristics were compared using chi-square or Mann-Whitney U tests. The hazard ratio (HR) for readmission was calculated using a Cox proportional hazards model, and readmission rates were analyzed using a Poisson regression model. All readmissions were confirmed by chart review.

Results: A total of 440 patients (61.3% female; median age, 58 years) were included; of these, 68% (n = 298) were prescribed vancomycin liquid and 32% (n = 142) a capsule form. Baseline characteristics were similar in the 2 groups, with the exception of the presence of inflammatory bowel disease (19.0% vs 6.4%, P < 0.0001) and median length of stay (6 days vs 8 days, P = 0.010). Patients prescribed vancomycin liquid were not more likely to be readmitted within 30 days relative to those prescribed capsule, with an adjusted HR for all-cause readmission of 1.58 (95% CI, 0.92-2.73) and an adjusted HR for CDI-specific readmission of 2.21 (95% CI, 0.72-6.76). However, patients prescribed liquid were more likely to be readmitted within 60 days, with an adjusted HR for all-cause readmission of 1.87 (95% CI, 1.19-2.94) and an adjusted HR for CDI-specific readmission of 2.84 (95% CI, 1.14-7.06).

Conclusion: A hospital pharmacy practice implemented to reduce medication costs may impact vancomycin prescribing at discharge and, in turn, may negatively impact readmission rates for patients with CDI treated with oral vancomycin.

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来源期刊
CiteScore
2.90
自引率
18.50%
发文量
341
审稿时长
3-8 weeks
期刊介绍: The American Journal of Health-System Pharmacy (AJHP) is the official publication of the American Society of Health-System Pharmacists (ASHP). It publishes peer-reviewed scientific papers on contemporary drug therapy and pharmacy practice innovations in hospitals and health systems. With a circulation of more than 43,000, AJHP is the most widely recognized and respected clinical pharmacy journal in the world.
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