Pritzker School of Medicine, University of Chicago, IL 60637, USA.
Am J Perinatol. 2011 Mar;28(3):169-76. doi: 10.1055/s-0030-1265828. Epub 2010 Sep 9.
In Illinois, newborn screening (NBS) for sickle cell disease (SCD) began in 1989 and for cystic fibrosis (CF) in 2008. We measured pediatricians' knowledge and attitudes regarding CF and SCD, the significance of carrier status, and NBS methodologies. Of 730 eligible Illinois pediatricians randomly selected from the American Academy of Pediatrics Web-based directory, 391 (54%) fully or partially completed the survey. Approximately three-fifths were women, two-thirds were Caucasians, and one-quarter had specialty training. Ninety-seven percent (377/390) and 93% (364/391) of respondents have at one point cared for a patient with SCD and CF, respectively, and virtually all support NBS for SCD (389/391, 99.5%) and CF (382/389, 98%). Overall mean knowledge of SCD (81.2%) and CF (84.5%) was high but did not correlate with self-reported familiarity. Questions regarding the interpretation of NBS results were less well understood, with 37% of our respondents unaware that Illinois NBS identifies all infants with sickle cell trait, and 28% unaware that Illinois NBS does NOT identify all infants who are CF carriers. Pediatricians support NBS but need additional education about the meaning of a positive and negative screen with respect to carrier detection to effectively counsel or appropriately refer.
在伊利诺伊州,新生儿镰状细胞病(SCD)筛查于 1989 年开始,囊性纤维化(CF)筛查于 2008 年开始。我们测量了儿科医生对 CF 和 SCD 的知识和态度、携带者状态的意义以及 NBS 方法。从美国儿科学会基于网络的目录中随机选择了 730 名符合条件的伊利诺伊州儿科医生,其中 391 名(54%)完整或部分完成了调查。大约五分之三是女性,三分之二是白种人,四分之一有专业培训。97%(377/390)和 93%(364/391)的受访者分别在某个时候照顾过患有 SCD 和 CF 的患者,几乎所有受访者都支持 SCD(389/391,99.5%)和 CF(382/389,98%)的 NBS。SCD(81.2%)和 CF(84.5%)的总体平均知识水平较高,但与自我报告的熟悉程度无关。关于 NBS 结果解释的问题理解得不够好,我们的 37%的受访者不知道伊利诺伊州 NBS 可以识别所有患有镰状细胞特征的婴儿,28%的受访者不知道伊利诺伊州 NBS 无法识别所有 CF 携带者的婴儿。儿科医生支持 NBS,但需要更多关于阳性和阴性筛查与携带者检测相关的含义的教育,以便有效地提供咨询或适当转介。