Comparison of comorbidities of stroke collected in administrative data, surveys, clinical trials and cohort studies

Author:

Kilkenny Monique F12ORCID,Dalli Lachlan L1ORCID,Sanders Ailie1,Olaiya Muideen T1ORCID,Kim Joosup12ORCID,Ung David3ORCID,Andrew Nadine E3ORCID

Affiliation:

1. Department of Medicine, School of Clinical Sciences at Monash Health, Monash University, Clayton, VIC, Australia

2. The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Heidelberg, VIC, Australia

3. Peninsula Clinical School, Central Clinical School, Monash University, Frankston, VIC, Australia

Abstract

Background Administrative data are used extensively for research purposes, but there remains limited information on the quality of these data for identifying comorbidities related to stroke. Objective To compare the prevalence of comorbidities of stroke identified using International Classification Diseases, Australian Modification (ICD-10-AM) or Anatomical Therapeutic Chemical codes, with those from (i) self-reported data and (ii) published studies. Method The cohort included patients with stroke or transient ischaemic attack admitted to hospitals (2012–2016; Victoria and Queensland) in the Australian Stroke Clinical Registry (N = 26,111). Data were linked with hospital and pharmaceutical datasets to ascertain comorbidities using published algorithms. The sensitivity, specificity, and positive predictive value of these comorbidities were compared with survey responses from 623 patients (reference standard). An indirect comparison was also performed with clinical data from published stroke studies. Results The sensitivity of hospital ICD-10-AM data was poor for most comorbidities, except for diabetes (93.0%). Specificity was excellent for all comorbidities (87–96%), except for hypertension (70.5%). Compared to published stroke studies (3 clinical trials and 1 incidence study), the prevalence of diabetes and atrial fibrillation in our cohort was similar using ICD-10-AM codes, but lower for dyslipidaemia and anxiety/depression. Whereas in the pharmaceutical dispensing data, the sensitivity was excellent for dyslipidaemia (94%) and modest for anxiety/depression (77%). In the pharmaceutical data, specificity was modest for hypertension (78%) and anxiety or depression (76%), but specificity was poor for dyslipidaemia (19%) and heart disease (46%). Conclusion Variation was observed in the reporting of comorbidities of stroke in administrative data, and consideration of multiple sources of data may be necessary for research. Further work is needed to improve coding and clinical documentation for reporting of comorbidities in administrative data.

Funder

Australian Government

National Health and Medical Research Council

National Heart Foundation of Australia

Publisher

SAGE Publications

Subject

Health Policy,Leadership and Management

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