Algorithmic approach to finding people with multiple sclerosis using routine healthcare data in Wales.

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurology, Neurosurgery, and Psychiatry Pub Date : 2024-10-16 DOI:10.1136/jnnp-2024-333532
Richard Nicholas, Emma Clare Tallantyre, James Witts, Ruth Ann Marrie, Elaine M Craig, Sarah Knowles, Owen Rhys Pearson, Katherine Harding, Karim Kreft, J Hawken, Gillian Ingram, Bethan Morgan, Rodden M Middleton, Neil Robertson, Ukms Register Research Group
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Abstract

Background: Identification of multiple sclerosis (MS) cases in routine healthcare data repositories remains challenging. MS can have a protracted diagnostic process and is rarely identified as a primary reason for admission to the hospital. Difficulties in identification are compounded in systems that do not include insurance or payer information concerning drug treatments or non-notifiable disease.

Aim: To develop an algorithm to reliably identify MS cases within a national health data bank.

Method: Retrospective analysis of the Secure Anonymised Information Linkage (SAIL) databank was used to identify MS cases using a novel algorithm. Sensitivity and specificity were tested using two existing independent MS datasets, one clinically validated and population-based and a second from a self-registered MS national registry.

Results: From 4 757 428 records, the algorithm identified 6194 living cases of MS within Wales on 31 December 2020 (prevalence 221.65 (95% CI 216.17 to 227.24) per 100 000). Case-finding sensitivity and specificity were 96.8% and 99.9% for the clinically validated population-based cohort and sensitivity was 96.7% for the self-declared registry population.

Discussion: The algorithm successfully identified MS cases within the SAIL databank with high sensitivity and specificity, verified by two independent populations and has important utility in large-scale epidemiological studies of MS.

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利用威尔士常规医疗数据寻找多发性硬化症患者的算法方法。
背景:在常规医疗保健数据储存库中识别多发性硬化症(MS)病例仍具有挑战性。多发性硬化症的诊断过程可能很漫长,而且很少被确定为入院的主要原因。在不包括保险或支付方有关药物治疗或不可通报疾病的信息的系统中,识别的困难就更大了:方法:对安全匿名信息链接(SAIL)数据库进行回顾性分析,使用新算法识别多发性硬化症病例。利用现有的两个独立多发性硬化症数据集测试了灵敏度和特异性,其中一个数据集经过临床验证并以人群为基础,另一个数据集来自多发性硬化症国家登记处:截至 2020 年 12 月 31 日,该算法从 4 757 428 条记录中识别出威尔士境内 6194 例在世多发性硬化症病例(患病率为每十万人 221.65 例(95% CI 216.17 至 227.24))。经临床验证的人群队列的病例查找灵敏度和特异度分别为96.8%和99.9%,自我申报登记人群的灵敏度为96.7%:该算法在SAIL数据库中成功识别了多发性硬化症病例,具有很高的灵敏度和特异性,并得到了两个独立人群的验证,在大规模多发性硬化症流行病学研究中具有重要作用。
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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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