2020
DOI: 10.3390/jcm9040920
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The Public Health Burden of Cardiomyopathies: Insights from a Nationwide Inpatient Study

Abstract: Cardiomyopathies are responsible for heart failure and sudden cardiac death, but epidemiological data are scarce and the public health burden may be underestimated. We studied aggregating data from all public or private hospitals in France. Patients were categorized from relevant ICD-10 codes into dilated, hypertrophic, restrictive, or other cardiomyopathies (DCM, HCM, RCM, or OCM, respectively). Between 2008 and 2015, a total of 326,461 distinct patients had cardiomyopathy-related hospitalizations. The hospit… Show more

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Cited by 11 publications
(8 citation statements)
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“…Longitudinal, interinstitutional collaborations that leverage structured data elements and interoperability within pediatric oncology will be increasingly important as new agents with potential cardiotoxicity change the landscape of survivorship care in the future. 59,60 33 Allen et al, 35 and Khera et al 34…”
Section: Discussionmentioning
confidence: 99%
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“…Longitudinal, interinstitutional collaborations that leverage structured data elements and interoperability within pediatric oncology will be increasingly important as new agents with potential cardiotoxicity change the landscape of survivorship care in the future. 59,60 33 Allen et al, 35 and Khera et al 34…”
Section: Discussionmentioning
confidence: 99%
“…The application of established ICD-9-CM and ICD-10-CM coding schema for heart failure [33][34][35] illustrates the opportunity to capture early CVD for children with cancer. The use of dexrazoxane for cardioprotection may account for the lack of significant difference in cardiac events between the low and high anthracycline groups; however, this may also reflect insufficient power because of the small sample size.…”
Section: Discussionmentioning
confidence: 99%
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“…Cardiomyopathies are usually divided into four main subtypes [1]: hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy and arrhythmogenic right ventricular cardiomyopathy, with other non-classified subtypes. Hypertrophic cardiomyopathy (HCM) is a heart disease defined by the presence of increased left ventricular (LV) wall thickness without abnormal loading conditions (hypertension, aortic stenosis) [1][2][3][4]. Its prevalence ranges from 0.02% to 0.23% [1].…”
Section: Introductionmentioning
confidence: 99%
“…New imaging techniques, such as myocardial deformation, have been developed for the assessment of LV function. In HCM, longitudinal strain analysis allows us to detect early LV contraction abnormalities despite obvious preserved LV ejection fractions [4,9], and some studies suggest a prognostic interest in cardiovascular risk stratification in these patients [10,11].…”
Section: Introductionmentioning
confidence: 99%