临床实践研究数据链(CPRD) Aurum母婴链接的验证。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Catherine Vasilakis-Scaramozza, Rebecca Persson, George Kafatos, David Neasham, Katrina Wilcox Hagberg, Susan Jick
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引用次数: 0

摘要

目的:评估临床实践研究数据链(CPRD) Aurum母婴链(MBL)的有效性。方法:采用多种策略评估CPRD - Aurum MBL对的效度。我们的研究人群是基于100个CPRD Aurum实践样本中所有可用的MBL对。我们向MBL患者样本的全科医生发送了一份问卷,询问联系是否正确以及14天内的分娩日期是否正确。我们还比较了MBL分娩日期与CPRD Aurum匹配儿童的出生日期。最后,在医院事件统计(Hospital Episode Statistics, HES)符合条件的人群中,我们比较MBL分娩日期与分娩父母的HES分娩日期。结果:研究人群包括1224962对MBL, 1224962对活产,92118对分娩,122362对分娩。根据361份针对MBL人群的标准化问卷,85% (95% CI 74%-96%)的配对被确认为正确匹配。结论:我们对CPRD Aurum MBL的各种评估发现,绝大多数配对正确匹配,大多数分娩日期在14天内正确。某些研究可能需要进一步细化交货日期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Validation of Clinical Practice Research Datalink (CPRD) Aurum Mother-Baby Link.

Purpose: Assess the validity of the Clinical Practice Research Datalink (CPRD) Aurum Mother-Baby Link (MBL).

Methods: We assessed the validity of CPRD Aurum MBL pairs using several strategies. Our study population was based on all available MBL pairs in a 100-practice sample of CPRD Aurum. We sent a questionnaire to the general practitioner of a sample of MBL patients asking if linkage was correct and whether delivery date was correct within 14 days. We also compared MBL delivery date to the matched child's birth date in CPRD Aurum. Finally, in the Hospital Episode Statistics (HES) eligible population, we compared MBL delivery date to birthing parent's HES delivery date.

Results: The study population included 124 962 MBL pairs: 124 962 livebirths, 91 218 birthing parents, and 123 562 deliveries. Based on 361 questionnaire responses standardized to the MBL population, 85% (95% CI 74%-96%) of pairs were confirmed as correctly matched, <1% (0.04%-1.4%) were incorrectly matched, and 13% (10%-18%) could not be confirmed. For 71% (61%-82%) of the sample, delivery date was correct within 14 days. Among the entire population of 124 962 MBL pairs, 73% of MBL pairs had MBL delivery date within the baby's birth month recorded in CPRD Aurum. Among 79 834 patients with HES linkage, 94% of 107 080 MBL deliveries in CPRD Aurum were confirmed in HES.

Conclusions: Our various assessments of CPRD Aurum MBL found the great majority of pairs were correctly matched and most delivery dates were correct within 14 days. Further refinement of delivery dates may be necessary for some studies.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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