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首页> 外文期刊>Transfusion medicine reviews >Relative risk of reducing the lifetime blood donation deferral for men who have had sex with men versus currently tolerated transfusion risks.
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Relative risk of reducing the lifetime blood donation deferral for men who have had sex with men versus currently tolerated transfusion risks.

机译:与目前有耐受性的输血风险相比,与男性发生性关系的男性减少终生献血推迟的相对风险。

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The risks of known and emerging transfusion-transmitted infections (TTIs) from reducing the current lifetime blood donation deferral for men who have had sex with men (MSM) to 1 or 5 years were compared to the risk from continuing to transfuse in the United States 12.5% of platelet doses as pooled whole-blood-derived (rather than single-donor) platelets. Assumptions made in mathematical models and blood donor/transfusion studies of the risks of TTIs since 2000 were evaluated. The number of HIV, hepatitis B virus, or hepatitis C virus TTIs from reducing the MSM deferral to 1 year is, respectively, 0.88, 2.94, or 66.9, many more than 10 times smaller than the risk from pooled platelets. If erroneous release of HIV-positive units (a risk independent of a donor's source of infection) is not considered, the MSM risk is 1 HIV-infectious donation per 17 to 56 million MSM donations. Any purportedly increased risk of human herpesvirus-8 transmission from MSM donors is far smaller than the risk of transfusion-associated sepsis from pooled platelets. Single-donor platelets from MSM after 5 years' abstinence are as safe or 5 times safer than our current pooled platelets--if the next TTI to emerge were transmitted, respectively, sexually or by another route. Thus, acceptance of MSM as blood donors after 1 or 5 years' abstinence may result in a postulated increase in risk that is so much smaller than the currently tolerated transfusion risk and so small in absolute terms that the ethical question of fairness to the MSM group justifies the change in policy.
机译:在美国,将已知的和正在出现的输血传播感染(TTI)的风险与将与男性发生性关系(MSM)的男性目前的终生献血推迟降低到1或5年的风险进行了比较,并将其与继续输血的风险进行了比较。合并全血(而非单供体)血小板的血小板剂量占血小板剂量的12.5%。评价了自2000年以来在数学模型和献血者/输血研究中对TTI风险的假设。将MSM延至1年的HIV,B型肝炎病毒或C型肝炎病毒TTI的数量分别为0.88、2.94或66.9,比血小板聚集的风险小10倍以上。如果不考虑错误释放HIV阳性单位(独立于捐赠者感染源的风险),则MSM风险为每17至5600万MSM捐赠中有1 HIV感染性捐赠。据称从MSM供体传播人疱疹病毒8的任何增加的风险都远小于合并血小板引起的与输血相关的败血症的风险。如果禁食5年后出现的下一个TTI是通过性途径或其他途径传播的,则禁食5年后MSM的单供体血小板的安全性或安全性是我们目前合并的血小板的5倍。因此,在禁酒1或5年后接受MSM作为献血者可能会导致假定的风险增加,该风险远小于目前耐受的输血风险,并且绝对值很小,以至于对MSM组公平的道德问题证明政策的改变是合理的。

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