Abstract

BackgroundBenchmarking outcomes across settings commonly requires risk-adjustment for co-morbidities that must be derived from extant sources that were designed for other purposes. A question arises as to the extent to which differing available sources for health data will be concordant when inferring the type and severity of co-morbidities, how close are these to the “truth”. We studied the level of concordance for same-patient comorbidity data extracted from administrative data (coded from International Classification of Diseases, Australian modification,10th edition [ICD-10 AM]), from the medical chart audit, and data self-reported by men with prostate cancer who had undergone a radical prostatectomy.MethodsWe included six hospitals (5 public and 1 private) contributing to the Prostate Cancer Outcomes Registry-Victoria (PCOR-Vic) in the study. Eligible patients from the PCOR-Vic underwent a radical prostatectomy between January 2017 and April 2018.Health Information Manager’s in each hospital, provided each patient’s associated administrative ICD-10 AM comorbidity codes. Medical charts were reviewed to extract comorbidity data. The self-reported comorbidity questionnaire (SCQ) was distributed through PCOR-Vic to eligible men.ResultsThe percentage agreement between the administrative data, medical charts and self-reports ranged from 92 to 99% in the 122 patients from the 217 eligible participants who responded to the questionnaire. The presence of comorbidities showed a poor level of agreement between data sources.ConclusionRelying on a single data source to generate comorbidity indices for risk-modelling purposes may fail to capture the reality of a patient’s disease profile. There does not appear to be a ‘gold-standard’ data source for the collection of data on comorbidities.

Highlights

  • Benchmarking outcomes across settings commonly requires risk-adjustment for co-morbidities that must be derived from extant sources that were designed for other purposes

  • Clinical notes might be incomplete, the patient may not be informed of all comorbidities and the coding system may not document all comorbidities. The aim of this project was to examine the completeness and agreement of comorbidity data and cancer status obtained from three data sources: International Classification of Diseases (ICD) coded administrative data, medical charts and self-reports in men contributing to Prostate Cancer Outcomes Registry (PCOR)-Vic who have had a radical prostatectomy following a diagnosis of prostate cancer

  • Men contributing to PCOR-Vic who had undergone a radical prostatectomy between January 2017 and April 2018 at one of six convenient hospitals were eligible to participate in this study

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Summary

Introduction

Benchmarking outcomes across settings commonly requires risk-adjustment for co-morbidities that must be derived from extant sources that were designed for other purposes. The Prostate Cancer Outcome Registry-Victoria (PCORVic) was developed in 2009 as a clinical quality registry, to measure and report on quality of care, using benchmarking of performance at a clinician and hospital level. PCOR-Vic collects data on aspects relating to the diagnosis, treatment, quality of life and clinical outcomes of men diagnosed with CaP [5]. Indicators were categorised according to whether they assessed structures, processes or outcomes of care [7]. Both clinical (e.g. positive surgical margins and 90-day prostate cancer specific mortality (PCSM) following treatment) and patient-reported outcomes (urinary, bowel and sexual quality of life) are reported

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