在加拿大建立国家乳房植入物登记处的理由。

IF 2.2 4区 医学 Q2 SURGERY
Canadian Journal of Surgery Pub Date : 2024-03-07 Print Date: 2024-01-01 DOI:10.1503/cjs.007123
Jan Willem Cohen Tervaert
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引用次数: 0

摘要

摘要下议院卫生常务委员会于 2022 年提议启动国家乳房植入物登记制度。下文将概述为什么要这样做以及需要哪些要求。乳房植入物产品并不总是符合国际规范和标准,由于行业欺诈,已经发生了多起丑闻。要追踪哪些患者的乳房植入物存在缺陷,一个良好的登记册是绝对必要的。此外,一些疾病,如淋巴瘤、自身免疫性疾病和所谓的乳房植入疾病,据信与乳房植入物有关。目前还缺乏对这些疾病在乳房植入物患者中发生频率的准确估计。通过登记,不仅可以记录手术数据,还可以记录患者报告的结果测量值,从而更好地了解患者的治疗效果和设备性能。该登记处不应是自愿("选择加入")登记处,而应是强制("选择退出")登记处,只有患者(而非外科医生)可以选择是否参与。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The case for a national breast implant registry in Canada.

SummaryThe House of Commons Standing Committee on Health proposed in 2022 to start a national registry for breast implants. Why, and what requirements are needed, will be outlined. Breast implant products are not always in compliance with international norms and standards, and several scandals have occurred because of industry fraud. To trace which patients have defective breast implants, a good registry is an absolute must. Furthermore, some diseases, such as lymphomas, autoimmune diseases, and so-called breast implant illness, are believed to be associated with breast implants. An accurate estimation of how often these diseases occur in patients with breast implants is lacking. A registry in which not only surgical data but also patient-reported outcome measurements are recorded will result in a better understanding of patient outcomes and device performance. The registry should not be a voluntary ("opt-in") registry but a mandatory ("opt-out") registry, in which only the patient (and not the surgeon) has the choice whether to participate.

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来源期刊
CiteScore
3.00
自引率
8.00%
发文量
120
审稿时长
6-12 weeks
期刊介绍: The mission of CJS is to contribute to the meaningful continuing medical education of Canadian surgical specialists, and to provide surgeons with an effective vehicle for the dissemination of observations in the areas of clinical and basic science research.
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