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新生儿筛查项目人群中术前镰状细胞病筛查的效果:一项队列研究。

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

机构信息

Department of Anesthesia and Pain Medicine, The Hospital for Sick Children, University of Toronto, ON, Canada.

出版信息

Can J Anaesth. 2013 Jan;60(1):54-9. doi: 10.1007/s12630-012-9807-4. Epub 2012 Oct 27.

Abstract

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.

摘要

目的

已发布的临床实践指南建议所有来自镰状细胞病(SCD)高发种族的患者都应进行这种血红蛋白病的术前筛查。安大略省新生儿筛查组织于 2006 年启动了一项针对镰状血红蛋白病的普遍筛查计划,作为其区域性新生儿筛查计划的一部分。本研究的主要目的是确定在安大略省(一个拥有普遍新生儿镰状血红蛋白病筛查计划的地区),根据高危种族进行有选择性的 SCD 术前筛查的有效性。

方法

检索我院血液学实验室数据库,以确定在 2006 年 11 月(新生儿镰状血红蛋白病筛查计划启动时)至 2010 年 4 月期间进行术前镰状细胞筛查的所有儿童。对所有血红蛋白分析呈阳性的儿童的病历进行审查,以确定围手术期结果。

结果

我们的搜索策略确定了 710 名在新生儿筛查后出生并接受术前筛查的儿童。这 35 名儿童的镰状溶解度测试异常 - 1 名(0.14%)为新诊断(未通过新生儿筛查发现),1 名先前已诊断,33 名(4.65%)被诊断为镰状细胞特征。60 名儿童进行了超过一次术前筛查(范围 2-4)。35 名镰状溶解度异常结果的儿童中有 6 名进行了重复检测。

结论

仅根据高危种族进行术前筛查是识别安大略省 SCD 儿童的一种无效方法,该人群进行了普遍的新生儿镰状血红蛋白病筛查。为避免不必要的重复检测,我们提出了一种算法,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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