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儿科研究带来的风险略高于最低风险且无直接受益前景:对45 CFR 46.406提出挑战。

Pediatric research posing a minor increase over minimal risk and no prospect of direct benefit: challenging 45 CFR 46.406.

作者信息

Iltis Ana

机构信息

Saint Louis University, Center for Health Care Ethics, St. Louis, Missouri 63103-2006, USA.

出版信息

Account Res. 2007 Jan-Mar;14(1):19-34. doi: 10.1080/08989620601104782.

Abstract

Subpart D of the Common Rule establishes 4 categories of research that may be conducted on children. One category, 45 CFR 46.406, permits research posing a minor increase over minimal risk and no prospect of direct benefit but expected to yield vital knowledge about the subjects' disorder or condition. To include other children in research posing a minor increase over minimal risk and no prospect of direct benefit requires federal review and approval of the Secretary of Health and Human Services under 45 CFR 46.407. It is widely held that children generally should not be exposed to more than minimal risk in research without the prospect of direct benefit. To justify deviating from this norm, as 406 allows, two claims must be true: (1) When there is vital knowledge to be gained from studying children, it is permissible to expose some children to a minor increase over minimal risk with no prospect of direct benefit; (2) It is permissible for locally reviewed and approved research to expose only children with the disorder or condition under investigation to greater risk with no prospect of direct benefit. The justification for (1) appears to be grounded in the magnitude of benefit to society combined with the need to study children. This article demonstrates that, even if the necessity and magnitude of benefit to society justify exposing children to increased risk, the decision to categorically restrict participation in such research to children with the disorder or condition under investigation (unless the study is federally reviewed and approved) is not justified. Subpart D should be revised.

摘要

《通用准则》D 子部分规定了可以在儿童身上开展的 4 类研究。其中一类,即 45 CFR 46.406,允许开展风险仅比最低风险略有增加且无直接受益前景,但有望产生有关受试者疾病或状况的重要知识的研究。要将其他儿童纳入风险仅比最低风险略有增加且无直接受益前景的研究,需要根据 45 CFR 46.407 获得美国卫生与公众服务部部长的联邦审查和批准。人们普遍认为,在没有直接受益前景的情况下,儿童一般不应在研究中面临超过最低限度的风险。为了像 406 所允许的那样偏离这一规范,必须满足两项主张:(1)当通过研究儿童能够获得重要知识时,允许让一些儿童面临比最低风险略有增加且无直接受益前景的情况;(2)经当地审查和批准的研究仅允许让患有正在研究的疾病或状况的儿童面临更大风险且无直接受益前景。对(1)的理由似乎基于对社会的益处大小以及研究儿童的必要性。本文表明,即使对社会的益处的必要性和大小证明让儿童面临更高风险是合理的,但将此类研究的参与明确限制于患有正在研究的疾病或状况的儿童(除非该研究经过联邦审查和批准)这一决定也是不合理的。D 子部分应予修订。

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