The validity of systemic sclerosis diagnoses in two university hospitals in Finland

dc.contributor.authorPaltta Johanna
dc.contributor.authorKortelainen Saara
dc.contributor.authorKäyrä Matti
dc.contributor.authorPirilä Laura
dc.contributor.authorHuhtakangas Johanna
dc.contributor.authorPalomäki Antti
dc.contributor.organizationfi=sisätautioppi|en=Internal Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.40502528769
dc.converis.publication-id175177585
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175177585
dc.date.accessioned2022-10-28T14:42:10Z
dc.date.available2022-10-28T14:42:10Z
dc.description.abstract<p><strong>Objective: </strong>This study aimed to determine the validity of systemic sclerosis (SSc) diagnoses in Finnish university hospitals.</p><p><strong>Method: </strong>Electronic medical records for 385 patients with a registered diagnosis of SSc (ICD-10 code M34) in two Finnish university hospitals from 2008 to 2018 were reviewed to assess whether each patient's diagnosis was correct.</p><p><strong>Results: </strong>The positive predictive value (PPV) of a diagnosis of SSc was 0.66 when fulfilment of the 2013 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria for SSc was required; the PPV was 0.75 if patients meeting the 2001 LeRoy and Medsger classification criteria for early SSc were also included. When a diagnosis of SSc was made in a department of rheumatology, the PPV was 0.78, and 0.90 when including patients with early SSc. For the more specific diagnosis of limited cutaneous SSc (lcSSc), the PPV was 0.80, and 0.95 when including early SSc. For an lcSSc diagnosis made in rheumatology, the PPV was 0.81, and 0.97 with early SSc included.</p><p><strong>Conclusion: </strong>These results demonstrate that in these two Finnish university hospitals, the diagnostic validity of a diagnosis of SSc was good if it was diagnosed in the department of rheumatology. For a more specific diagnosis of lcSSc, the most prevalent form of SSc in Finland, the validity was good even when registered in any department.</p>
dc.identifier.eissn1502-7732
dc.identifier.jour-issn0300-9742
dc.identifier.olddbid189773
dc.identifier.oldhandle10024/172867
dc.identifier.urihttps://www.utupub.fi/handle/11111/44896
dc.identifier.urlhttps://www.tandfonline.com/doi/full/10.1080/03009742.2022.2056999
dc.identifier.urnURN:NBN:fi-fe2022081155120
dc.language.isoen
dc.okm.affiliatedauthorPaltta, Johanna
dc.okm.affiliatedauthorKortelainen, Saara
dc.okm.affiliatedauthorPirilä, Laura
dc.okm.affiliatedauthorPalomäki, Antti
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherTaylor and Francis [Commercial Publisher]
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1080/03009742.2022.2056999
dc.relation.ispartofjournalScandinavian Journal of Rheumatology
dc.source.identifierhttps://www.utupub.fi/handle/10024/172867
dc.titleThe validity of systemic sclerosis diagnoses in two university hospitals in Finland
dc.year.issued2023

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