Polypharmacy and Therapeutic Inertia in Extreme Longevity: A Potential Clinical Ageism Scenario Secondary to Important Gaps in Clinical Evidence.

IF 2.8 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
María Viviana Pantoja, Ivan David Lozada-Martinez
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引用次数: 0

Abstract

Population aging is a global health priority due to the dramatic increase in the proportion of older persons worldwide. It is also expected that both global life expectancy and disability-free life expectancy will increase, leading to a significant rise in the proportion of individuals with extreme longevity, such as non-agenarians and centenarians. The inaccuracy of clinical evidence on therapeutic interventions for this demographic could lead to biased decision-making, influenced by age-related beliefs or misperceptions about their therapeutic needs. This represents a potential clinical ageism scenario stemming from gaps in clinical evidence. Such biases can result in 2 significant issues that adversely affect the health status and prognosis of older persons: polypharmacy and therapeutic inertia. To date, documents on polypharmacy in non-agenarians and centenarians account for less than 0.35% of the overall available evidence on polypharmacy. Furthermore, evidence regarding therapeutic inertia is non-existent. The purpose of this letter is to discuss polypharmacy and therapeutic inertia as potential clinical ageism scenarios resulting from the clinical evidence gaps in extreme longevity.

极端长寿人群的多重用药和治疗惰性:临床证据中的重要空白所导致的潜在临床老龄化问题。
由于全球老年人的比例急剧增加,人口老龄化已成为全球健康的优先事项。预计全球预期寿命和无残疾预期寿命都将延长,这将导致非长寿老人和百岁老人等极长寿人群的比例大幅上升。针对这一人群的治疗干预临床证据不准确,可能会导致决策出现偏差,受到与年龄有关的信念或对其治疗需求的误解的影响。这是一种潜在的临床老龄歧视,源于临床证据的不足。这种偏见会导致两个对老年人健康状况和预后产生不利影响的重大问题:多药治疗和治疗惰性。迄今为止,关于非长者和百岁老人多药治疗的文献还不到现有多药治疗证据总数的 0.35%。此外,有关治疗惰性的证据并不存在。本信旨在讨论多药治疗和治疗惰性问题,这两种情况可能是由于极度长寿的临床证据缺口而导致的临床年龄歧视。
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
Journal of Preventive Medicine and Public Health
Journal of Preventive Medicine and Public Health Medicine-Public Health, Environmental and Occupational Health
CiteScore
6.40
自引率
0.00%
发文量
60
审稿时长
8 weeks
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