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Effectiveness of preoperative screening for sickle cell disease in a population with a newborn screening program: A cohort study

机译:一项队列研究:术前筛查镰状细胞病在新生儿筛查人群中的有效性

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Purpose: Published clinical practice guidelines recommend that all patients from ethnic groups with a high prevalence of sickle cell disease (SCD) undergo preoperative screening for this hemoglobinopathy. Newborn Screening Ontario initiated a universal sickle hemoglobinopathy screening program in 2006 as part of its regional newborn screening program. The primary objective of this study was to determine the effectiveness of selective preoperative screening for SCD based on at-risk ethnicity in Ontario, a region that has a universal newborn sickle hemoglobinopathy screening program. Methods: The hematology laboratory database at our hospital was searched to identify all children who underwent preoperative sickle cell screening in the 42-month period starting in November 2006 (when the newborn sickle hemoglobinopathy screening program was introduced) and ending in April 2010. Medical records of all children testing positive on hemoglobin analysis were reviewed to determine perioperative outcomes. Results: Our search strategy identified 710 children who were born after the introduction of newborn screening and who underwent preoperative screening. Thirty-five of these children had abnormal sickle solubility tests - one (0.14%) was a new diagnosis (not identified by newborn screening), one had been diagnosed previously, and 33 (4.65%) were identified as having sickle cell trait. Sixty children had more than one preoperative screening test performed (range, 2-4). Six of the 35 children with abnormal sickle solubility results underwent repeated testing. Conclusions: Preoperative screening based on at-risk ethnicity alone is an ineffective method of identifying additional children with SCD in Ontario, a population with universal newborn sickle hemoglobinopathy screening. In an effort to avoid unnecessary repeat testing, we propose an algorithm to help physicians decide whether to initiate preoperative sickle cell screening for children.
机译:目的:已发布的临床实践指南建议所有镰状细胞病(SCD)患病率较高的族裔患者均应接受术前筛查以检查这种血红蛋白病。新生儿筛查作为其区域新生儿筛查计划的一部分,安大略省于2006年启动了通用镰刀血红蛋白病筛查计划。这项研究的主要目的是根据安大略省的高危族裔来确定选择性SCD术前筛查的有效性,该地区具有普遍的新生儿镰刀血红蛋白病筛查计划。方法:从我院血液学实验室数据库中检索所有从2006年11月(引入新生儿镰刀血红蛋白病筛查计划)至2010年4月结束的42个月内接受过术前镰状细胞筛查的儿童。对所有在血红蛋白分析测试中呈阳性的儿童进行回顾,以确定围手术期的结局。结果:我们的搜索策略确定了710名在进行新生儿筛查后出生并接受术前筛查的儿童。这些儿童中有35名镰状细胞溶解度测试异常-一种是新诊断(未通过新生儿筛查确定)(0.14%),先前已被诊断出一种,而33名(4.65%)被诊断为具有镰状细胞性状。 60名儿童接受了一项以上的术前筛查测试(范围2-4)。在35名镰刀溶解度结果异常的儿童中,有6名接受了重复测试。结论:仅根据高危人群进行术前筛查是一种无法有效识别安大略省SCD儿童的有效方法,安大略省是一名普遍新生儿镰刀血红蛋白病筛查人群。为了避免不必要的重复测试,我们提出了一种算法,可以帮助医生决定是否对儿童进行术前镰状细胞筛查。

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