先天性和非先天性畸形儿童的平喘处方:一项欧洲数据关联研究。

IF 1.6 Q3 HEALTH CARE SCIENCES & SERVICES International Journal of Population Data Science Pub Date : 2022-08-25 DOI:10.23889/ijpds.v7i3.1889
Natalie Divin, E. Garne, J. Morris, M. Loane
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引用次数: 0

摘要

目的哮喘是儿童最常见的慢性疾病,但对先天性异常儿童哮喘和喘息的发病率知之甚少。本研究探讨了6个欧洲地区/国家先天性异常儿童与非异常儿童接受抗哮喘处方的患病率和风险。这是一项基于EUROlinkCAT人群的连锁队列研究,涉及2000-2014年间出生的0-9岁儿童。来自六个EUROCAT登记处的先天性异常数据与国家/生命统计中的出生数据和电子处方数据库相关联。各地区的处方/药房配药记录被标准化为通用数据模型。以R03开头的解剖治疗化学分类代码用于识别抗哮喘处方。进行随机效应荟萃分析,以确定一年内相对于参照组接受bbb1抗哮喘处方的相对风险(RR),以及不同登记中心和年龄组患病率的异质性。结果5.1%的先天性异常患儿和4.9%的对照患儿因未关联而被排除在研究之外。与对照儿童(n=1,722,912)相比,先天性异常儿童(n=60,662)使用bbb1类抗哮喘药物的比例更高,服用抗哮喘药物的风险也明显更高(RR=1.41, 95% CI 1.35-1.48)。风险的增加在所有年龄组中都是一致的。有先天性异常的儿童更可能使用β -2激动剂(RR=1.71, 95% CI 1.60-1.83)和吸入皮质类固醇(RR=1.74, 95% CI 1.61-1.87)。与对照儿童相比,患有食管闭锁、膈疝、遗传综合征和染色体异常的儿童服用抗哮喘药物的风险超过两倍。确定了抗哮喘处方患病率和风险的地区差异。结论1岁儿童抗哮喘处方具有跨年龄组和跨欧洲地区的特点。本研究表明,可以通过数据链接获得有关已开/配发的抗哮喘处方的患病率信息,以监测患病率随时间的变化。
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Anti-asthmatic prescriptions in children with and without congenital anomalies: a European data linkage study.
ObjectivesAsthma is the most common chronic disease in childhood, yet little is known about rates of asthma and wheezing in children with congenital anomalies. This study explored the prevalence and risk of receiving anti-asthmatic prescriptions in children with congenital anomalies compared to children without anomalies in six European regions/countries. ApproachThis was a EUROlinkCAT population-based linkage cohort study involving children from 0-9 years of age born between 2000-2014. Congenital anomaly data from six EUROCAT registries were linked to births data in national/vital statistics and to electronic prescription databases. Prescription/pharmacy dispensing records across regions were standardised to a Common Data Model. Anatomical Therapeutic Chemical classification codes beginning with R03 were used to identify anti-asthmatic prescriptions. Random-effects meta-analyses were performed to identify both the relative risk (RR) of receiving >1 anti-asthmatic prescription in a year relative to the reference group, and the heterogeneity of prevalence rates across registries and age group. ResultsA total of 5.1% of children with congenital anomalies and 4.9% of reference children were dropped from the study as they were not linked. Children with congenital anomalies (n=60,662) had a higher prevalence of >1 anti-asthmatic prescription and a significantly higher risk of being prescribed anti-asthmatics (RR=1.41, 95% CI 1.35-1.48) compared to reference children (n=1,722,912). The increased risk was consistent across all age groups. Children with congenital anomalies were more likely to be prescribed beta-2 agonists (RR=1.71, 95% CI 1.60-1.83) and inhaled corticosteroids (RR=1.74, 95% CI 1.61-1.87). Children with oesophageal atresia, diaphragmatic hernia, genetic syndromes and chromosomal anomalies had over twice the risk of being prescribed anti-asthmatics compared to reference children. Regional differences in prevalence and risk of anti-asthmatic prescriptions were identified. ConclusionChildren aged <10 years with congenital anomalies consistently had higher prevalence and risk of receiving >1 anti-asthmatic prescription across age group and across European regions. This study demonstrates that information on the prevalence of anti-asthmatic prescriptions issued/dispensed can be obtained through data linkage to monitor changes in prevalence over time.
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0.00%
发文量
386
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20 weeks
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