Suppr超能文献

低剂量处方:将药物对社会和环境的“副作用”降至最低。

Lower-dose prescribing: minimizing "side effects" of pharmaceuticals on society and the environment.

机构信息

Environmental Sciences Division, National Exposure Research Laboratory, U.S. Environmental Protection Agency, 944 East Harmon Avenue, Las Vegas, NV 89119, USA.

出版信息

Sci Total Environ. 2013 Jan 15;443:324-37. doi: 10.1016/j.scitotenv.2012.10.092. Epub 2012 Nov 29.

Abstract

The prescribed use of pharmaceuticals can result in unintended, unwelcomed, and potentially adverse consequences for the environment and for those not initially targeted for treatment. Medication usage frequently results in the collateral introduction to the environment (via excretion and bathing) of active pharmaceutical ingredients (APIs), bioactive metabolites, and reversible conjugates. Imprudent prescribing and non-compliant patient behavior drive the accumulation of unused medications, which pose major public health risks from diversion as well as risks for the environment from unsound disposal, such as flushing to sewers. The prescriber has the unique wherewithal to reduce each of these risks by modifying various aspects of the practice of prescribing. By incorporating consideration of the potential for adverse environmental impacts into the practice of prescribing, patient care also could possibly be improved and public health better protected. Although excretion of an API is governed by its characteristic pharmacokinetics, this variable can be somewhat controlled by the prescriber in selecting APIs possessing environment-friendly excretion profiles and in selecting the lowest effective dose. This paper presents the first critical examination of the multi-faceted role of drug dose in reducing the ambient levels of APIs in the environment and in reducing the incidence of drug wastage, which ultimately necessitates disposal of leftovers. Historically, drug dose has been actively excluded from consideration in risk mitigation strategies for reducing ambient API levels in the environment. Personalized adjustment of drug dose also holds the potential for enhancing therapeutic outcomes while simultaneously reducing the incidence of adverse drug events and in lowering patient healthcare costs. Optimizing drug dose is a major factor in improving the sustainability of health care. The prescriber needs to be cognizant that the "patient" encompasses the environment and other "bystanders," and that prescribed treatments can have unanticipated, collateral impacts that reach far beyond the healthcare setting.

摘要

药物的规定使用可能会对环境和最初未被治疗的人群产生意外、不受欢迎且潜在的不利后果。药物使用经常导致活性药物成分 (API)、生物活性代谢物和可逆轭合物通过排泄和洗浴等途径意外引入环境。轻率的处方和不遵守医嘱的患者行为导致未使用的药物积累,这不仅会因为药物滥用而产生重大公共卫生风险,还会因为处理不当(如冲入下水道)而对环境造成风险。通过修改处方实践的各个方面,处方者具有减少这些风险的独特能力。将环境不良影响的可能性纳入处方实践,可以改善患者护理并更好地保护公共健康。虽然 API 的排泄受其特征药代动力学控制,但通过选择具有环保排泄特征的 API 并选择最低有效剂量,处方者可以在一定程度上控制这种变异性。本文首次对药物剂量在降低环境中 API 浓度和减少药物浪费发生率(最终需要处理剩余药物)方面的多方面作用进行了批判性检查。历史上,在降低环境中 API 水平的风险缓解策略中,药物剂量一直被积极排除在外。药物剂量的个性化调整也有可能提高治疗效果,同时减少不良药物事件的发生和降低患者的医疗保健成本。优化药物剂量是改善医疗保健可持续性的主要因素。处方者需要认识到“患者”包括环境和其他“旁观者”,并且规定的治疗可能会产生意想不到的、附带的影响,远远超出医疗保健环境。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验