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2002-2020 年:进展、挑战和行动呼吁——应对有害病原体,而非滥用药物。

BAD BUGS, NO DRUGS 2002-2020: PROGRESS, CHALLENGES, AND CALL TO ACTION.

机构信息

BOSTON, MASSACHUSETTS.

出版信息

Trans Am Clin Climatol Assoc. 2020;131:65-71.

Abstract

Antimicrobial resistance (AMR) requires a multifaceted response via a One Health approach. Antibiotics make procedures including joint replacement, transplantation, cancer chemotherapy, and premature newborn care possible. The U.S. Centers for Disease Control and Prevention (CDC) estimates that 2 million Americans are infected and >35,900 die from AMR, costing over $20 billion/year. Projections are that this will increase to 350 million cumulative AMR deaths by 2050. In its 2004 report entitled "Bad Bugs, No Drugs: As Antibiotic R&D Stagnates, A Public Health Crisis Brews," the Infectious Diseases Society of America (IDSA) raised alarm and proposed solutions. In the face of decreasing Food and Drug Administration (FDA) approvals and several program failures, scientific collaboration and regulatory innovation led to updated guidance for common, life-threatening infections. The IDSA and others worked to advance policies for discovery and development of drugs for the most resistant infections. Successes include legislation and public-private partnerships that provide push incentives. Need exists for pull incentives; several models are currently being explored.

摘要

抗菌药物耐药性(AMR)需要通过“同一健康”方法采取多方面的应对措施。抗生素使关节置换、移植、癌症化疗和早产儿护理等程序成为可能。美国疾病控制与预防中心(CDC)估计,有 200 万美国人受到感染,超过 35900 人死于 AMR,每年花费超过 2000 亿美元。预计到 2050 年,这一数字将增加到 3.5 亿例 AMR 累计死亡。在其 2004 年题为“坏细菌,无药可用:随着抗生素研发停滞不前,公共卫生危机迫在眉睫”的报告中,美国传染病学会(IDSA)发出了警报并提出了解决方案。面对食品和药物管理局(FDA)批准的减少和几个项目的失败,科学合作和监管创新为常见的、危及生命的感染提供了更新的指导。IDSA 和其他组织努力推进针对最耐药感染的药物发现和开发的政策。取得的成功包括提供推动激励措施的立法和公私合作伙伴关系。需要拉动激励措施;目前正在探索几种模式。

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