Abstract
Objective: To validate the Danish National Patient Register’s (NPR) diagnoses of pediatric acquired demyelinating syndromes (ADS) including multiple sclerosis (MS). Study design and setting: We identified ADS diagnostic groups using International Classification of Diseases (ICD) codes and reviewed medical records to validate the NPR diagnoses during 2008–2015. Results: Among 409 children in the study, 184 children had a validated and final ADS diagnosis after reviewing medical records as follows: optic neuritis (ON; n=46), transverse myelitis (TM; n=16), acute disseminated encephalomyelitis (ADEM; n=50), clinically isolated syndrome (CIS) including dissemination in space (CIS [DIS]) but not dissemination in time (n=6), neuromyelitis optica spectrum disorder (NMOsd; n=5), and MS (n=61). During the mean follow-up of 4.6 years, 33% of children initially diagnosed with monophasic ADS progressed to MS. Positive predictive value (PPV) was 0.71 (95% confidence interval [CI] =0.62–0.80) for ON, 0.64 (95% CI =0.43–0.82) for TM, 0.93 (95% CI =0.84–0.98) for MS, 0.27 (95% CI =0.19–0.35) for CIS, 0.43 (95% CI =0.10–0.82) for NMOsd, and 0.15 (95% CI =0.10–0.20) for ADEM. Assuming complete coverage for non-MS ADS, the sensitivity was 0.99 (95% CI =0.93–1.00) for ON, 0.83 (95% CI =0.36–1.00) for CIS (DIS), and 0.80 (95% CI =0.56–0.94) for TM, but only 0.58 (95% CI =0.43–0.72) for ADEM and 0.60 (95% CI =0.15–0.95) for NMOsd. Conclusion: PPV was high for MS and considered acceptable for ON and TM; therefore, these ICD revision 10 (ICD-10) codes from the NPR are useful for epidemiological studies. Conversely, PPV was low for CIS and ADEM; NMOsd was inconclusive.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Clinical Epidemiology |
| Vol/bind | 10 |
| Sider (fra-til) | 391-399 |
| ISSN | 1179-1349 |
| DOI | |
| Status | Udgivet - 2018 |
Finansiering
We thank the chief physicians at Danish pediatric and neurological departments for their collaboration in accessing medical records. The study was supported by the Danish MS society (grant numbers A29625 and A31526), Novartis, Teva, and Genzyme. MSB has served on a scientific advisory board for Teva and has received speaker honoraria for lecturing from Novartis and support for congress participation from Teva, Novartis, and Roche. MM has served on a scientific advisory board for Biogen Idec, Novartis, and Merck Serono, has received honoraria for lecturing from Biogen Idec, Merck Serono, Novartis, and Genzyme, and has received support for congress participation from Biogen Idec, Novartis, Genzyme, and Teva. APB has received speaker honoraria from Novartis and has served on an advisory board for Biogen Idec. LCT has received honoraria for lecturing from Rigshospitalet (Copenhagen, Denmark), Statistics Denmark, and SanofiA-vensis. This study was financially supported by the Danish MS Society, TEVA, Novartis and Genzyme. The authors report no other conflicts of interest in this work.
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