Zachariah Justin P, McNeal Catherine J, Copeland Laurel A, Fang-Hollingsworth Ying, Stock Eileen M, Sun FangFang, Song Joon Jin, Gregory Sean T, Tom Jeffrey O, Wright Eric A, VanWormer Jeffrey J, Cassidy-Bushrow Andrea E
Lillie Frank Abercrombie Section of Pediatric Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Department of Pediatrics, Baylor Scott & White Health, Temple, TX, USA; Department of Internal Medicine, Baylor Scott & White Health, Temple, TX, USA.
J Clin Lipidol. 2015 Sep-Oct;9(5 Suppl):S77-87. doi: 10.1016/j.jacl.2015.06.014. Epub 2015 Jul 9.
Pediatric lipid management recommendations have evolved from selective screening to universal screening to identify and target therapy for genetic dyslipidemias. Data on the success of the selective screening guidelines for lipid testing, dyslipidemia detection, and lipid management are conflicting.
To determine temporal trends in lipid testing, dyslipidemia categories and pharmacotherapy in a cohort of 653,642 individual youth aged 2 to 20 years from 2002 to 2012.
Summary data on lipid test results, lipid-lowering medicine (LLM) dispensings, and International Classification of Diseases, Ninth Revision diagnoses were compiled from the virtual data warehouses of 5 sites in the Cardiovascular Research Network. Temporal trends were determined using linear regression.
Among the average 255,160 ± 25,506 children enrolled each year, lipid testing declined from 16% in 2002 to 11% in 2012 (P < .001 for trend). Among the entire population, the proportion newly detected each year with low-density lipoprotein cholesterol >190 mg/dL, a value commonly used to define familial hypercholesterolemia, increased over time from 0.03% to 0.06% (P = .03 for trend). There was no significant change over time in the proportion of the yearly population initiated on LLM or statins specifically (0.045 ± 0.009%, P = .59 [LLM] and 0.028 ± 0.006%, P = .25 [statin]).
Although lipid testing declined during 2002 to 2012, the detection of familial hypercholesterolemia-level low-density lipoprotein cholesterol increased. Despite this increased detection, pharmacotherapy did not increase over time. These findings highlight the need to enhance lipid screening and management strategies in high-risk youth.
儿科血脂管理建议已从选择性筛查发展到普遍筛查,以识别和针对遗传性血脂异常进行治疗。关于血脂检测、血脂异常检测和血脂管理的选择性筛查指南的成功数据存在冲突。
确定2002年至2012年期间653642名2至20岁青少年队列中血脂检测、血脂异常类别和药物治疗的时间趋势。
从心血管研究网络5个站点的虚拟数据仓库中汇编血脂检测结果、降脂药物(LLM)配药和国际疾病分类第九版诊断的汇总数据。使用线性回归确定时间趋势。
在每年平均纳入的255160±25506名儿童中,血脂检测从2002年的16%下降到2012年的11%(趋势P<0.001)。在整个人口中,每年新检测出低密度脂蛋白胆固醇>190mg/dL(常用于定义家族性高胆固醇血症的值)的比例随时间从0.03%增加到0.06%(趋势P=0.03)。每年开始使用LLM或他汀类药物的人群比例随时间没有显著变化(0.045±0.009%,P=0.59[LLM]和0.028±0.006%,P=0.25[他汀类药物])。
尽管2002年至2012年期间血脂检测有所下降,但家族性高胆固醇血症水平的低密度脂蛋白胆固醇检测增加。尽管检测增加,但药物治疗并未随时间增加。这些发现凸显了加强高危青少年血脂筛查和管理策略的必要性。