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首页> 外文期刊>Journal of assisted reproduction and genetics >Expanded carrier screening for recessively inherited disorders: economic burden and factors in decision-making when one individual in a couple is identified as a carrier
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Expanded carrier screening for recessively inherited disorders: economic burden and factors in decision-making when one individual in a couple is identified as a carrier

机译:扩展的载体筛查用于隐性遗传的疾病:当一对夫妇中的一个人被确定为承运人时,经济负担和决策中的因素

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Purpose When undergoing expanded carrier screening (ECS), couples are often screened sequentially to reduce need for a second individual's test. It is unknown how often partners of individuals found to be carriers complete the recommended testing with a sequential approach and what factors contribute to decision-making regarding partner testing. Additionally, the economic burden placed on individuals by ECS testing and its effect on partner testing has not been evaluated. Methods In part 1, all individuals at a university-affiliated reproductive endocrinology and infertility practice identified to be carriers of a recessively inherited mutation using the Counsyl/Foresight ECS were included. Conditions were categorized by severity according to a previously described classification system. In part 2, all individuals who underwent ECS with a single test provider between September 1, 2013 and February 1, 2020 were contacted via email to complete a confidential and anonymized online survey. Results In part 1, a total of 2061 patients were screened. 36.9% were carriers of one or more recessively inherited disorders. Twenty-seven percent of positively screened individuals did not have their partner screened. Carriers of a moderate condition had a trend towards a reduced odds for having their partner screened compared to a profound condition (OR 0.36, 95% CI 0.12-1.05, p = 0.06). Number of conditions was not predictive of subsequent partner screening (OR 0.95, 95% CI 0.72-1.25, p = 0.72). In part 2, the cost of ECS was not covered by insurance for 54.5% (103/189) and most paid over $300 out-of-pocket for testing (47.6%). The most common reason for not completing partner testing was that the results would not alter their course when seeking conception (33.3%). 73.5% of patients knew that the largest benefit of ECS comes from knowing a partner's results as well as their own. Conclusions Not all carriers of recessively inherited disorders choose to undergo partner screening. Patients found to be carrier of more debilitating genetic disorders may be more likely to screen their reproductive partners. For many, ECS testing is not covered by insurance, and this test may impose a significant economic burden. For some patients, the results of ECS would not change what they would do when seeking conception. Providers should evaluate whether a patient's ECS result would change their treatment course prior to testing.
机译:目的:在进行扩大携带者筛查(ECS)时,夫妇通常会按顺序进行筛查,以减少第二次个体检测的需要。目前尚不清楚被发现为携带者的个人的合作伙伴以顺序方法完成推荐测试的频率,以及哪些因素有助于合作伙伴测试的决策。此外,ECS测试给个人带来的经济负担及其对合作伙伴测试的影响尚未评估。方法在第1部分中,使用Counsyl/Foresight ECS,将大学附属生殖内分泌和不孕不育机构中确定为隐性遗传突变携带者的所有个体纳入研究。根据之前描述的分类系统,根据严重程度对病情进行分类。在第2部分中,通过电子邮件联系了2013年9月1日至2020年2月1日期间与单一测试提供商进行ECS测试的所有个人,以完成一项保密的匿名在线调查。结果第一部分共筛查2061例患者。36.9%为一种或多种隐性遗传疾病携带者。27%的筛查阳性个体没有对伴侣进行筛查。与重度携带者相比,中度携带者接受伴侣筛查的几率有降低的趋势(OR 0.36,95%可信区间0.12-1.05,p=0.06)。条件的数量不能预测随后的伴侣筛查(OR 0.95,95%可信区间0.72-1.25,p=0.72)。在第二部分中,54.5%(103/189)的ECS费用不在保险范围内,大多数ECS的测试费用超过300美元(47.6%)。未完成伴侣测试的最常见原因是,在寻求受孕时,测试结果不会改变他们的过程(33.3%)。73.5%的患者知道ECS的最大益处来自了解伴侣的结果以及他们自己的结果。结论并非所有隐性遗传疾病携带者都选择进行伴侣筛查。被发现携带更具衰弱性的遗传疾病的患者可能更有可能筛查他们的生殖伴侣。对许多人来说,ECS测试不在保险范围内,这种测试可能会带来巨大的经济负担。对于一些患者来说,ECS的结果不会改变他们在寻求受孕时的行为。提供者应在测试前评估患者的ECS结果是否会改变其治疗过程。

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