The present study has several important strengths. The real-world study design and the large sample size of high-quality national registry data from primary care settings adequately reflect the general population and clinical practice in Sweden. Nevertheless, this study also has certain limitations. The retrospective study design introduces the potential for bias and confounding due to variables that may not have been accounted for in our analysis. Although all patients had physician-diagnosed COPD, the accuracy of COPD diagnoses and the severity of disease could not be verified, as spirometry data were not available in many patients. Due to lack of spirometry data, it was not possible to assess the impact of disease severity on the incidence of T2DM. This study was conducted only in Swedish patients; it is therefore uncertain whether these findings can be extrapolated to a more diverse group of patients and to other healthcare systems.
Hence, we conclude that patients with COPD who initiate treatment with ICS, especially with high dose, may have an elevated risk of developing T2DM.
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