Assessment of Intravenous versus Oral Antimicrobials in a Large Regional Health Authority.

IF 0.6 Q4 PHARMACOLOGY & PHARMACY CANADIAN JOURNAL OF HOSPITAL PHARMACY Pub Date : 2022-04-04 DOI:10.4212/cjhp.v75i2.3173
Manpreet Dulku, Tina Sekhon, A. Tejani
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Abstract

Background Many antimicrobials given by the intravenous (IV) route have oral (PO) formulations with high oral bioavailability. The advantages of using the PO rather than the IV formulation include lower risk of adverse reactions, shorter length of hospital stay, and lower health care costs. Objectives The primary objective was to determine the proportions of patients who received the IV and PO formulations of antimicrobials with high oral bioavailability. The secondary objectives were to determine the proportion of patients who were eligible to receive PO antimicrobials from the start of treatment, the proportion who qualified for IV-to-PO step-down, and areas of improvement to increase use of PO antimicrobials. Methods A retrospective chart review was conducted in hospitals in the Fraser Health Authority, British Columbia, between October 18, 2019, and March 5, 2020. Two hundred charts were randomly selected for patients who had received either azithromycin, ciprofloxacin, clindamycin, fluconazole, levofloxacin, linezolid, moxifloxacin, metronidazole, sulfamethoxazole-trimethoprim, or voriconazole. Results Of the 200 patients, 124 (62.0%) received the PO formulations, while 76 (38.0%) received the IV formulations. Of the 76 patients receiving IV antimicrobials, 39 (51.3%; 95% confidence interval 44.7%-57.9%) were eligible to receive PO antimicrobials from the start of treatment or could have been stepped down from IV to PO administration. Conclusions More than half of patients who received IV therapy were eligible to receive the PO formulation of antimicrobials known to have high oral bioavailability; relative to earlier studies, this proportion has not improved over time. This finding highlights the need for continued vigilance in encouraging the use of PO rather than IV formulations for hospitalized patients.
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某大型地区卫生当局对静脉注射与口服抗菌素的评估
背景许多通过静脉(IV)途径给药的抗菌药物都有口服(PO)制剂,具有较高的口服生物利用度。使用PO而不是IV制剂的优点包括不良反应风险较低、住院时间较短和医疗费用较低。目的主要目的是确定接受口服高生物利用度抗菌药物IV和PO制剂的患者比例。次要目标是确定从治疗开始就有资格接受PO抗菌药物的患者比例、有资格接受静脉注射至PO降压的患者比例,以及增加PO抗菌药物使用的改进领域。方法于2019年10月18日至2020年3月5日在不列颠哥伦比亚省弗雷泽卫生局的医院进行回顾性图表审查。随机选择200张图表,用于接受阿奇霉素、环丙沙星、克林霉素、氟康唑、左氧氟沙星、利奈唑胺、莫西沙星、甲硝唑、磺胺甲恶唑甲氧苄啶或伏立康唑治疗的患者。结果在200例患者中,124例(62.0%)接受PO制剂,76例(38.0%)接受IV制剂。在76名接受静脉注射抗菌药物的患者中,39名(51.3%;95%置信区间44.7%-57.9%)从治疗开始就有资格接受PO抗菌药物治疗,或者可以从静脉注射减少到PO给药。结论超过一半接受静脉注射治疗的患者有资格接受口服生物利用度高的抗菌药物PO制剂;与早期的研究相比,这一比例并没有随着时间的推移而提高。这一发现突出表明,在鼓励住院患者使用PO而非IV制剂时,需要继续保持警惕。
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来源期刊
CANADIAN JOURNAL OF HOSPITAL PHARMACY
CANADIAN JOURNAL OF HOSPITAL PHARMACY PHARMACOLOGY & PHARMACY-
CiteScore
1.10
自引率
0.00%
发文量
64
期刊介绍: The CJHP is an academic journal that focuses on how pharmacists in hospitals and other collaborative health care settings optimize safe and effective drug use for patients in Canada and throughout the world. The aim of the CJHP is to be a respected international publication serving as a major venue for dissemination of information related to patient-centred pharmacy practice in hospitals and other collaborative health care settings in Canada and throughout the world.
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