AI Article Synopsis

  • - The study examines variations in lung cancer survival across countries involved in the International Cancer Benchmarking Partnership (ICBP) and explores how comorbid diseases might affect these differences but highlights a lack of quantifiable data on this impact.
  • - Researchers analyzed lung cancer registry and hospital data from nine jurisdictions, using three different comorbidity scores (Charlson, Elixhauser, and inpatient bed day) related to patients' health prior to their diagnosis, involving over 233,000 individuals.
  • - Findings suggest that while it was possible to create valid comorbidity scores for each jurisdiction, the differences in coding and admission practices limit the comparability of this data internationally, indicating a need for a standardized comorbidity index before assessing its

Article Abstract

Introduction: The International Cancer Benchmarking Partnership (ICBP) identified significant international differences in lung cancer survival. Differing levels of comorbid disease across ICBP countries has been suggested as a potential explanation of this variation but, to date, no studies have quantified its impact. This study investigated whether comparable, robust comorbidity scores can be derived from the different routine population-based cancer data sets available in the ICBP jurisdictions and, if so, use them to quantify international variation in comorbidity and determine its influence on outcome.

Methods: Linked population-based lung cancer registry and hospital discharge data sets were acquired from nine ICBP jurisdictions in Australia, Canada, Norway and the UK providing a study population of 233 981 individuals. For each person in this cohort Charlson, Elixhauser and inpatient bed day Comorbidity Scores were derived relating to the 4-36 months prior to their lung cancer diagnosis. The scores were then compared to assess their validity and feasibility of use in international survival comparisons.

Results: It was feasible to generate the three comorbidity scores for each jurisdiction, which were found to have good content, face and concurrent validity. Predictive validity was limited and there was evidence that the reliability was questionable.

Conclusion: The results presented here indicate that interjurisdictional comparability of recorded comorbidity was limited due to probable differences in coding and hospital admission practices in each area. Before the contribution of comorbidity on international differences in cancer survival can be investigated an internationally harmonised comorbidity index is required.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870453PMC
http://dx.doi.org/10.1136/thoraxjnl-2017-210362DOI Listing

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