Rhekiss--德国炎症性风湿病儿童祝寿和怀孕登记册。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Anja Strangfeld, Yvette Meissner, Anja Weiß, Tatjana Rudi, Angela Zink, Tanja Ellmann, Tim Filla, Peer Aries, Xenofon Baraliakos, Christina Bungartz, Cornelia Glaser, Jörg Henes, Hanns-Martin Lorenz, Matthias Schneider, Susanna Späthling-Mestekemper, Christof Specker, Jutta G Richter, Rebecca Fischer-Betz
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引用次数: 0

摘要

药物流行病学需要可靠的数据来判断药物治疗对妊娠、妊娠结局和母乳喂养婴儿的影响。由于孕妇和哺乳期妇女通常被排除在随机临床试验之外,因此需要进行观察研究。其中一个数据来源是专门针对某些疾病或疾病群体而开发的妊娠登记册。德国的 Rhekiss 登记册调查了患有慢性炎症性风湿病(IRD)的妇女的妊娠情况。Rhekiss 是一项全国性的多中心纵向研究,18 岁或以上患有基础 IRD 的妇女可在计划怀孕时或怀孕前半期由风湿病医生登记。数据在定期随访时收集。风湿病医生和患者在受孕前(如果是在计划怀孕时登记)、怀孕期间和怀孕后通过网络系统提供信息。患者还可使用智能手机应用程序。所有疾病的孕产妇和临床信息、一般实验室指标、抗风湿药物和其他药物的治疗情况、不良事件、与妊娠过程和结果有关的项目以及婴儿的健康状况都将得到统一评估。IRD的个体信息包括分类标准、特定诊断的实验室参数、临床参数和测量疾病活动性或损害的有效工具。此外,还采集了患者报告的结果测量。该登记册共登记了 2013 名患者,提供了 1801 例妊娠的数据。总之,Rhekiss 是一个全面而复杂的登记册,可以回答有关慢性 IRD 妇女怀孕的各种研究问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhekiss-The German Register for Child Wish and Pregnancies in Inflammatory Rheumatic Diseases.

In pharmacoepidemiology, robust data are needed to judge the impact of drug treatment on pregnancy, pregnancy outcomes and breast-fed infants. As pregnant and breastfeeding women are usually excluded from randomised clinical trials, observational studies are required. One of those data sources are pregnancy registers specifically developed to focus on certain diseases or disease groups. The German Rhekiss register investigates pregnancies in women with chronic inflammatory rheumatic diseases (IRD). Rhekiss is a nationwide, multicentre, longitudinal study, in which women aged 18 years or older with an underlying IRD can be enrolled by a rheumatologist either when planning a pregnancy or in the first half of pregnancy. Data are collected prospectively at regular follow-up visits. Rheumatologists and patients provide information in a web-based system before conception (if enrolment was at the time of pregnancy planning), during and after pregnancy. A smartphone app is available for patients. Maternal and clinical information, general laboratory markers, treatment with antirheumatic and other drugs, adverse events, items related to course and outcome of pregnancy and the health of the child are uniformly assessed for all diseases. Individual information on the IRD includes classification criteria, diagnosis-specific laboratory parameters, clinical parameters and validated instruments to measure disease activity or damage. Furthermore, patient-reported outcome measures are captured. A total of 2013 individual patients have been enrolled in the register, and data on 1801 completed pregnancies are available. In summary, Rhekiss is a comprehensive and complex register that can answer various research questions about pregnancy in women with chronic IRDs.

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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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