Department of Anaesthesia, Austin Health, Melbourne, VIC, Australia; Department of Critical Care, University of Melbourne, Melbourne, VIC, Australia.
Department of Critical Care, University of Melbourne, Melbourne, VIC, Australia.
Br J Anaesth. 2024 Dec;133(6):1439-1448. doi: 10.1016/j.bja.2023.11.053. Epub 2024 Jan 30.
Pharmaceuticals account for 19-32% of healthcare greenhouse gas (GHG) emissions. Paracetamol is a common perioperative analgesic agent. We estimated GHG emissions associated with i.v. and oral formulations of paracetamol used in the perioperative period.
Life-cycle assessment of GHG emissions (expressed as carbon dioxide equivalents COe) of i.v. and oral paracetamol preparations was performed. Perioperative paracetamol prescribing practices and costs for 26 hospitals in USA, UK, and Australia were retrospectively audited. For those surgical patients for whom oral formulations were indicated, COe and costs of actual prescribing practices for i.v. or oral doses were compared with optimal oral prescribing.
The carbon footprint for a 1 g dose was 38 g COe (oral tablet), 151 g COe (oral liquid), and 310-628 g COe (i.v. dependent on type of packaging and administration supplies). Of the eligible USA patients, 37% received paracetamol (67% was i.v.). Of the eligible UK patients, 85% received paracetamol (80% was i.v.). Of the eligible Australian patients, 66% received paracetamol (70% was i.v.). If the emissions mitigation opportunity from substituting oral tablets for i.v. paracetamol is extrapolated to USA, UK, and Australia elective surgical encounters in 2019, ∼5.7 kt COe could have been avoided and would save 98.3% of financial costs.
Intravenous paracetamol has 12-fold greater life-cycle carbon emissions than the oral tablet form. Glass vials have higher greenhouse gas emissions than plastic vials. Intravenous administration should be reserved for cases in which oral formulations are not feasible.
药品占医疗保健温室气体(GHG)排放量的 19-32%。对乙酰氨基酚是一种常见的围手术期镇痛剂。我们评估了围手术期使用的静脉注射和口服对乙酰氨基酚制剂相关的 GHG 排放。
对静脉注射和口服对乙酰氨基酚制剂的 GHG 排放(以二氧化碳当量 COe 表示)进行了生命周期评估。回顾性审核了美国、英国和澳大利亚 26 家医院的围手术期对乙酰氨基酚处方实践和费用。对于那些口服制剂适用的手术患者,比较了实际静脉或口服剂量的 COe 和成本与最佳口服处方。
1 克剂量的碳足迹为 38 克 COe(口服片剂)、151 克 COe(口服液体)和 310-628 克 COe(静脉注射,取决于包装和给药用品的类型)。在美国合格患者中,37%接受了对乙酰氨基酚(67%为静脉注射)。在英国合格患者中,85%接受了对乙酰氨基酚(80%为静脉注射)。在澳大利亚合格患者中,66%接受了对乙酰氨基酚(70%为静脉注射)。如果将用口服片剂替代静脉注射对乙酰氨基酚的减排机会外推到 2019 年美国、英国和澳大利亚的择期手术,大约可以避免 5.7 千吨 COe,并节省 98.3%的财务成本。
静脉注射对乙酰氨基酚的生命周期碳排放量比口服片剂形式高出 12 倍。玻璃小瓶比塑料小瓶的温室气体排放量更高。应保留静脉给药,用于口服制剂不可行的情况。