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本文引用的文献

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The missing voice of patients in drug-safety reporting.药物安全报告中患者缺失的声音。
N Engl J Med. 2010 Mar 11;362(10):865-9. doi: 10.1056/NEJMp0911494.
2
Adverse events in randomized trials: neglected, restricted, distorted, and silenced.随机试验中的不良事件:被忽视、受限、歪曲和沉默。
Arch Intern Med. 2009 Oct 26;169(19):1737-9. doi: 10.1001/archinternmed.2009.313.
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Data-based risk calculators becoming more sophisticated--and more popular.
JAMA. 2009 Aug 19;302(7):730-1. doi: 10.1001/jama.2009.1142.
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Statin-associated adverse cognitive effects: survey results from 171 patients.他汀类药物相关的不良认知效应:171例患者的调查结果
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Views of older persons with multiple morbidities on competing outcomes and clinical decision-making.患有多种疾病的老年人对相互竞争的结果和临床决策的看法。
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The impact of the format of graphical presentation on health-related knowledge and treatment choices.图形呈现形式对健康相关知识及治疗选择的影响。
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Physician response to patient reports of adverse drug effects: implications for patient-targeted adverse effect surveillance.医生对患者药物不良反应报告的反应:对以患者为目标的不良反应监测的影响。
Drug Saf. 2007;30(8):669-75. doi: 10.2165/00002018-200730080-00003.
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Physician-patient communication about prescription medication nonadherence: a 50-state study of America's seniors.医生与患者关于处方药不依从性的沟通:对美国老年人的一项涵盖50个州的研究。
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Primary prevention of cardiovascular diseases with statin therapy: a meta-analysis of randomized controlled trials.他汀类药物治疗对心血管疾病的一级预防:随机对照试验的荟萃分析
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益处和危害对老年人进行原发性心血管预防用药意愿的影响。

Effects of benefits and harms on older persons' willingness to take medication for primary cardiovascular prevention.

作者信息

Fried Terri R, Tinetti Mary E, Towle Virginia, O'Leary John R, Iannone Lynne

机构信息

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

Arch Intern Med. 2011 May 23;171(10):923-8. doi: 10.1001/archinternmed.2011.32. Epub 2011 Feb 28.

DOI:10.1001/archinternmed.2011.32
PMID:21357797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3101287/
Abstract

BACKGROUND

Quality-assurance initiatives encourage adherence to evidenced-based guidelines based on a consideration of treatment benefit. We examined older persons' willingness to take medication for primary cardiovascular disease prevention according to benefits and harms.

METHODS

In-person interviews were performed with 356 community-living older persons. Participants were asked about their willingness to take medication for primary prevention of myocardial infarction (MI) with varying benefits in terms of absolute 5-year risk reduction and varying harms in terms of type and severity of adverse effects.

RESULTS

Most (88%) would take medication, providing an absolute benefit of 6 fewer persons with MI out of 100, approximating the average risk reduction of currently available medications. Of participants who would not take it, 17% changed their preference if the absolute benefit was increased to 10 fewer persons with MI, and, of participants who would take it, 82% remained willing if the absolute benefit was decreased to 3 fewer persons with MI. In contrast, large proportions (48%-69%) were unwilling or uncertain about taking medication with average benefit causing mild fatigue, nausea, or fuzzy thinking, and only 3% would take medication with adverse effects severe enough to affect functioning.

CONCLUSIONS

Older persons' willingness to take medication for primary cardiovascular disease prevention is relatively insensitive to its benefit but highly sensitive to its adverse effects. These results suggest that clinical guidelines and decisions about prescribing these medications to older persons need to place emphasis on both benefits and harms.

摘要

背景

质量保证倡议鼓励根据对治疗益处的考量遵循循证指南。我们根据益处和危害研究了老年人服用预防原发性心血管疾病药物的意愿。

方法

对356名社区居住的老年人进行了面对面访谈。询问参与者对于服用预防心肌梗死(MI)药物的意愿,这些药物在5年绝对风险降低方面有不同益处,在不良反应的类型和严重程度方面有不同危害。

结果

大多数人(88%)愿意服药,若每100人中有6人因服药而减少患MI的情况,这接近目前可用药物的平均风险降低水平。在不愿服药的参与者中,如果绝对益处增加到每100人中有10人减少患MI,17%的人改变了他们的偏好;而在愿意服药的参与者中,如果绝对益处减少到每100人中有3人减少患MI,82%的人仍然愿意服药。相比之下,很大一部分人(48%-69%)不愿意或不确定是否服用会导致轻度疲劳、恶心或思维模糊等平均益处的药物,只有3%的人会服用不良反应严重到足以影响功能的药物。

结论

老年人服用预防原发性心血管疾病药物的意愿对其益处相对不敏感,但对其不良反应高度敏感。这些结果表明,关于向老年人开具这些药物的临床指南和决策需要同时强调益处和危害。