Shickle D, May A
Department of Haematology, University of Wales College of Medicine, Cardiff.
J Med Genet. 1989 Feb;26(2):109-12. doi: 10.1136/jmg.26.2.109.
A questionnaire was sent to 164 principal general practitioners working in Cardiff. A response rate of 81% was achieved. A total of 70% of respondents had had professional contact with a carrier for thalassaemia and a similar number for sickle cell disease, while 57% had recommended that a patient should be screened for haemoglobinopathy status. GPs tended to underestimate greatly the prevalence of haemoglobinopathies in South Glamorgan, and were uncertain of the ethnic minorities that were at particular risk. A carrier screening programme was considered justified by the majority of GPs in Cardiff and reasons for this opinion were examined. However, before a screening programme is started, information on whom to screen and their relative risk needs to be made more widely available.
一份问卷被发送给在加的夫工作的164名主要全科医生。回复率达到了81%。共有70%的受访者与地中海贫血携带者有过专业接触,镰状细胞病的接触比例与之相似,而57%的受访者曾建议对患者进行血红蛋白病状态筛查。全科医生往往大大低估了南格拉摩根郡血红蛋白病的患病率,并且不确定哪些少数民族群体面临特别风险。加的夫的大多数全科医生认为开展携带者筛查项目是合理的,并对持此观点的原因进行了研究。然而,在启动筛查项目之前,关于筛查对象及其相对风险的信息需要更广泛地传播。