Key result
In a nationwide cohort of 570,157 ischemic heart disease patients, temporal disease trajectories revealed that the sequence of diagnoses varies across subpopulations, such as atrial fibrillation marking distinct IHD subgroups.
Why the study?
Patients with ischemic heart disease are increasingly multi-morbid, but few studies have analyzed the full spectrum of this multi-morbidity.
Cohort (n=570,157)
The sequence of diagnoses is crucial for characterizing multi-morbidity in IHD patients, revealing distinct subpopulations based on the timing of conditions like atrial fibrillation and osteoarthritis.
May inform IHD multimorbidity phenotyping by diagnosis sequence; leaves open whether trajectories predict outcomes or guide therapy.
BACKGROUND: Patients diagnosed with ischemic heart disease (IHD) are becoming increasingly multi-morbid, and studies designed to analyze the full spectrum are few. METHODS: Disease trajectories, defined as time-ordered series of diagnoses, were used to study the temporality of multi-morbidity. The main data source was The Danish National Patient Register (NPR) comprising 7,179,538 individuals in the period 1994-2018. Patients with a diagnosis code for IHD were included. Relative risks were used to quantify the strength of the association between diagnostic co-occurrences comprised of two diagnoses that were overrepresented in the same patients. Multiple linear regression models were then fitted to test for temporal associations among the diagnostic co-occurrences, termed length two disease trajectories. Length two disease trajectories were then used as basis for constructing disease trajectories of three diagnoses. RESULTS: In a cohort of 570,157 IHD disease patients, we identified 1447 length two disease trajectories and 4729 significant length three disease trajectories. These included 459 distinct diagnoses. Disease trajectories were dominated by chronic diseases and not by common, acute diseases such as pneumonia. The temporal association of atrial fibrillation (AF) and IHD differed in different IHD subpopulations. We found an association between osteoarthritis (OA) and heart failure (HF) among patients diagnosed with OA, IHD, and then HF only. CONCLUSIONS: The sequence of diagnoses is important in characterization of multi-morbidity in IHD patients as the disease trajectories. The study provides evidence that the timing of AF in IHD marks distinct IHD subpopulations; and secondly that the association between osteoarthritis and heart failure is dependent on IHD.
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Haue et al. (2022) conducted a cohort in Ischemic heart disease (n=570,157). Observation of disease trajectories was evaluated on Temporal associations among diagnostic co-occurrences (disease trajectories). In a nationwide cohort of 570,157 ischemic heart disease patients, temporal disease trajectories revealed that the sequence of diagnoses varies across subpopulations, such as atrial fibrillation marking distinct IHD subgroups.
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