Neal-Cooper F, Scott R B
Virginia Sickle Cell Anemia Awareness Program, Medical College of Virginia, Richmond 23298.
Public Health Rep. 1988 Mar-Apr;103(2):174-8.
Beginning in 1970, a cohort of 74 sickle trait-carrying couples was identified who risked producing children with sickle cell anemia or other serious hemoglobinopathies. They were counseled concerning the disease and their risk, and their initial reactions, their stated intentions concerning birth control and childbearing, and their subsequent childbearing histories were documented. Initial responses to the risk information varied widely, and stated intentions of birth control or childbearing did not accurately predict subsequent childbearing. Among 25 couples for whom there were complete childbearing data, there were 31 pregnancies with 13 affected children prior to counseling. After counseling, there were 25 pregnancies resulting in 10 affected children. The majority of the subsequent pregnancies occurred in the group who had not borne children or an affected child before counseling. In young couples, concern for producing a child with sickle cell anemia is often offset by a strong desire to have children regardless of risk.
从1970年开始,确定了一组74对携带镰状细胞性状的夫妇,他们有可能生育患有镰状细胞贫血或其他严重血红蛋白病的孩子。就该疾病及其风险对他们进行了咨询,并记录了他们的初始反应、关于节育和生育的既定意图以及他们随后的生育史。对风险信息的初始反应差异很大,而且既定的节育或生育意图并不能准确预测随后的生育情况。在有完整生育数据的25对夫妇中,咨询前有31次怀孕,其中13名儿童受影响。咨询后,有25次怀孕,导致10名儿童受影响。随后的大多数怀孕发生在咨询前未生育或未生育过受影响孩子的群体中。在年轻夫妇中,尽管担心生育患有镰状细胞贫血的孩子,但想要孩子的强烈愿望往往会抵消这种担忧。