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评估流感疫苗效力的挑战及死亡率益处争议

Challenges in evaluating influenza vaccine effectiveness and the mortality benefits controversy.

作者信息

Nichol Kristin L

机构信息

Research Service (151), VA Medical Center, 1 Veterans Drive, Minneapolis, MN 55417, USA.

出版信息

Vaccine. 2009 Oct 23;27(45):6305-11. doi: 10.1016/j.vaccine.2009.07.006.

Abstract

Randomized, controlled trials are the gold standard study design. However, ethical constraints and practical considerations may necessitate other types of studies for evaluating influenza vaccine effectiveness in the elderly--a high priority group for annual vaccination in many countries. Observational studies therefore comprise the bulk of the vaccine effectiveness evidence in older persons, but these types of studies can be susceptible to selection bias and residual confounding. All observational studies should utilize strategies to minimize the impact of bias and confounding. Recent studies questioning the plausibility of reported mortality benefits among vaccinated elderly persons may themselves be based on assumptions that are susceptible to important limitations and multiple biases. Future studies that incorporate prospectively collected information on functional status, life expectancy, and other types of data may provide additional insights into these concerns. At present, even after taking into account the potential for residual bias and confounding, most studies confirm the benefits of vaccination among the elderly for reducing hospitalization and death.

摘要

随机对照试验是研究设计的金标准。然而,伦理限制和实际考量可能使得在评估流感疫苗对老年人(许多国家年度疫苗接种的重点人群)的有效性时需要采用其他类型的研究。因此,观察性研究构成了老年人疫苗有效性证据的主体,但这类研究可能容易受到选择偏倚和残余混杂因素的影响。所有观察性研究都应采用策略来尽量减少偏倚和混杂因素的影响。最近一些对已接种疫苗的老年人报告的死亡获益的合理性提出质疑的研究,其本身可能基于一些容易受到重大局限性和多种偏倚影响的假设。纳入前瞻性收集的功能状态、预期寿命和其他类型数据的未来研究,可能会为这些问题提供更多见解。目前,即使考虑到残余偏倚和混杂因素的可能性,大多数研究仍证实接种疫苗对老年人减少住院和死亡有益。

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