在高压氧环境中集成医疗设备的方法

P. Cony , D. Mathieu , R. Houman , J.-P. Macchi , P. Dubois , F. Wisson
{"title":"在高压氧环境中集成医疗设备的方法","authors":"P. Cony ,&nbsp;D. Mathieu ,&nbsp;R. Houman ,&nbsp;J.-P. Macchi ,&nbsp;P. Dubois ,&nbsp;F. Wisson","doi":"10.1016/j.rbmret.2005.09.002","DOIUrl":null,"url":null,"abstract":"<div><p>The use of medical devices within hyperbaric chambers has always been slowed down by the specific difficulties of this environment. Indeed, installing a medical device within a pressure level much higher than atmospheric pressure and in an oxygen enriched atmosphere is an interesting challenge. In fact, few manufacturers dare engage in this way. Besides, for many years numerous working groups have emerged in hyperbaric medecine. Currently a european standard is being finalized and based on a risk analysis identifying, among other things, a certain number of potential hazards. They can potentially generate dangers during the use of a hyperbaric chamber. Installing a medical device in a hyperbaric chamber is not an easy thing to do. Indeed, the risks induced by a use in a hyperbaric chamber cannot be minimized. Furthermore the medical device must not cause additional risks within the chamber or, anyway, the risks must be evaluated, reduced and accepted. Consequently, prior to installing a medical device, this study proposes a methodology which enables to evaluate the risk management concerning the use of a medical device. Once the methodology completed, the manager of hyperbaric oxygen therapy unit is able to decide whether to install the device or not.</p></div>","PeriodicalId":100733,"journal":{"name":"ITBM-RBM","volume":"26 5","pages":"Pages 363-370"},"PeriodicalIF":0.0000,"publicationDate":"2005-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbmret.2005.09.002","citationCount":"3","resultStr":"{\"title\":\"Méthodologie d'intégration de dispositifs médicaux en milieu hyperbare\",\"authors\":\"P. Cony ,&nbsp;D. Mathieu ,&nbsp;R. Houman ,&nbsp;J.-P. Macchi ,&nbsp;P. Dubois ,&nbsp;F. Wisson\",\"doi\":\"10.1016/j.rbmret.2005.09.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The use of medical devices within hyperbaric chambers has always been slowed down by the specific difficulties of this environment. Indeed, installing a medical device within a pressure level much higher than atmospheric pressure and in an oxygen enriched atmosphere is an interesting challenge. In fact, few manufacturers dare engage in this way. Besides, for many years numerous working groups have emerged in hyperbaric medecine. Currently a european standard is being finalized and based on a risk analysis identifying, among other things, a certain number of potential hazards. They can potentially generate dangers during the use of a hyperbaric chamber. Installing a medical device in a hyperbaric chamber is not an easy thing to do. Indeed, the risks induced by a use in a hyperbaric chamber cannot be minimized. Furthermore the medical device must not cause additional risks within the chamber or, anyway, the risks must be evaluated, reduced and accepted. Consequently, prior to installing a medical device, this study proposes a methodology which enables to evaluate the risk management concerning the use of a medical device. Once the methodology completed, the manager of hyperbaric oxygen therapy unit is able to decide whether to install the device or not.</p></div>\",\"PeriodicalId\":100733,\"journal\":{\"name\":\"ITBM-RBM\",\"volume\":\"26 5\",\"pages\":\"Pages 363-370\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2005-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.rbmret.2005.09.002\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ITBM-RBM\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S129795620500121X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ITBM-RBM","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S129795620500121X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

摘要

由于这种环境的特殊困难,在高压氧舱中使用医疗设备的速度一直很慢。事实上,在比大气压高得多的压力水平和富氧大气中安装医疗设备是一项有趣的挑战。事实上,很少有厂家敢这么干。此外,多年来在高压医学领域出现了许多工作组。目前,一项基于风险分析的欧洲标准正在最终确定,其中包括确定一定数量的潜在危害。在高压氧舱的使用过程中,它们可能会产生潜在的危险。在高压氧舱中安装医疗设备不是一件容易的事。实际上,在高压氧舱中使用所引起的风险是不能最小化的。此外,医疗器械不得在室内造成额外的风险,或者无论如何,必须评估、减少和接受风险。因此,在安装医疗设备之前,本研究提出了一种方法,可以评估有关使用医疗设备的风险管理。一旦方法完成,高压氧治疗单位的经理能够决定是否安装设备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Méthodologie d'intégration de dispositifs médicaux en milieu hyperbare

The use of medical devices within hyperbaric chambers has always been slowed down by the specific difficulties of this environment. Indeed, installing a medical device within a pressure level much higher than atmospheric pressure and in an oxygen enriched atmosphere is an interesting challenge. In fact, few manufacturers dare engage in this way. Besides, for many years numerous working groups have emerged in hyperbaric medecine. Currently a european standard is being finalized and based on a risk analysis identifying, among other things, a certain number of potential hazards. They can potentially generate dangers during the use of a hyperbaric chamber. Installing a medical device in a hyperbaric chamber is not an easy thing to do. Indeed, the risks induced by a use in a hyperbaric chamber cannot be minimized. Furthermore the medical device must not cause additional risks within the chamber or, anyway, the risks must be evaluated, reduced and accepted. Consequently, prior to installing a medical device, this study proposes a methodology which enables to evaluate the risk management concerning the use of a medical device. Once the methodology completed, the manager of hyperbaric oxygen therapy unit is able to decide whether to install the device or not.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Oxygéenateurs : évolution et nouveautés Oxygenators : evolution and update Sortie de CEC difficile : tableaux cliniques et modalités thérapeutiques Phase contact dans la réponse hémostatique et vasculaire vers un système intégré Place de l'aprotinine en chirurgie cardiaque Déficit acquis en Antithrombine et hemofiltration
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1