Using a planetary health lens to quantify intravenous use of bioequivalent antimicrobials when oral administration is feasible.

IF 1.1 Q3 Medicine
JAMMI Pub Date : 2026-02-12 eCollection Date: 2026-03-01 DOI:10.3138/jammi-2025-0029
Meghan MacLaren, Rosanne Thalakada, Hui Zhu, Tim Ty Lau, Salomeh Shajari, Xiaotao Bi, Shaqil Peermohamed
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引用次数: 0

Abstract

Background: Health care accounts for 4.6% of Canada's greenhouse gas (GHG) emissions, 25% of which comes from medications. Antimicrobials with high bioavailability offer no additional benefit when given intravenously, except when oral (PO) administration is not feasible. Intravenous (IV) formulations have a higher carbon footprint than their PO counterparts. IV-to-PO switch strategies benefit patients and the health care system by reducing line-related adverse events, nursing time, length of hospital stay, and costs and can also reduce carbon emissions.Our primary objective was to quantify IV use of bioequivalent antimicrobials when PO administration is feasible. Secondary objectives were to determine GHG emissions and antimicrobial costs associated with unnecessary IV use of bioequivalent antimicrobials.

Methods: We performed a retrospective, cross-sectional study of hospitalized adults who received IV azithromycin, ciprofloxacin, clindamycin, cotrimoxazole, fluconazole, levofloxacin, linezolid, metronidazole, moxifloxacin, or voriconazole at Vancouver General Hospital on five dates. We determined the proportion of patients receiving these antimicrobials who met criteria for PO administration. We also applied a life cycle assessment (LCA) to assess the GHG emissions of the antimicrobial drug delivery systems using OpenLCA with the Ecoinvent database. Using these data, we calculated the GHG emissions and costs associated with unnecessary IV use.

Results: In total, 128 patients were identified. Seventy-eight (61%) met IV-to-PO switch criteria on the audit dates. Most eligible patients were admitted to general surgery, internal medicine, or critical care. The antimicrobial with the highest IV-to-PO switch eligibility was metronidazole (51%), most often prescribed for intra-abdominal infections. Over the five study dates, potential GHG savings were about 80,000 gCO2-eq. Potential annual cost savings were about $59,000.

Conclusion: Over 60% of patients receiving highly bioavailable IV antimicrobials were eligible for PO therapy, highlighting an opportunity to optimize prescribing. Promoting an IV-to-PO switch can improve patient outcomes and reduce environmental impact, supporting both patient-centred care and planetary health.

在口服给药可行的情况下,使用行星健康透镜量化静脉注射生物等效抗菌素。
背景:医疗保健占加拿大温室气体(GHG)排放量的4.6%,其中25%来自药物。具有高生物利用度的抗菌素在静脉注射时没有额外的益处,除非口服(PO)给药不可行。静脉(IV)制剂的碳足迹高于其PO对应物。IV-to-PO转换策略通过减少与线路相关的不良事件、护理时间、住院时间和成本,使患者和医疗保健系统受益,还可以减少碳排放。我们的主要目标是量化静脉使用生物等效抗菌剂时,PO管理是可行的。次要目标是确定与不必要的静脉使用生物等效抗菌素相关的温室气体排放和抗菌素成本。方法:我们对在温哥华总医院接受静脉注射阿奇霉素、环丙沙星、克林霉素、复方新诺明、氟康唑、左氧氟沙星、利奈唑胺、甲硝唑、莫西沙星或伏立康唑的住院成人进行回顾性、横断面研究。我们确定了接受这些抗菌剂的患者中符合PO给药标准的比例。我们还应用生命周期评估(LCA)来评估抗菌药物输送系统的温室气体排放,使用OpenLCA和Ecoinvent数据库。利用这些数据,我们计算了与不必要的静脉注射相关的温室气体排放量和成本。结果:共发现128例患者。78家(61%)在审核日期达到了IV-to-PO转换标准。大多数符合条件的患者接受普通外科、内科或重症监护。IV-to-PO切换资格最高的抗菌药物是甲硝唑(51%),最常用于腹腔感染。在五个研究期间,潜在的温室气体减排约为80,000 gco2当量。每年可能节省的成本约为5.9万美元。结论:接受高生物利用度静脉抗菌药物治疗的患者中,超过60%的患者符合PO治疗条件,这凸显了优化处方的机会。促进IV-to-PO转换可以改善患者的治疗效果,减少对环境的影响,支持以患者为中心的护理和全球健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JAMMI
JAMMI Medicine-Infectious Diseases
CiteScore
3.80
自引率
0.00%
发文量
48
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