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      Age‐ and Lesion‐Related Comorbidity Burden Among US Adults With Congenital Heart Disease: A Population‐Based Study

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          Abstract

          Background

          As patients with congenital heart disease ( CHD) are living longer, understanding the comorbidities they develop as they age is increasingly important. However, there are no published population‐based estimates of the comorbidity burden among the US adult patients with CHD.

          Methods and Results

          Using the IBM MarketScan commercial claims database from 2010 to 2016, we identified adults aged ≥18 years with CHD and 2 full years of continuous enrollment. These were frequency matched with adults without CHD within categories jointly defined by age, sex, and dates of enrollment in the database. A total of 40 127 patients with CHD met the inclusion criteria (mean [ SD] age, 36.8 [14.6] years; and 48.2% were women). Adults with CHD were nearly twice as likely to have any comorbidity than those without CHD ( P<0.001). After adjusting for covariates, patients with CHD had a higher prevalence risk ratio for “previously recognized to be common in CHD” (risk ratio, 9.41; 95% CI, 7.99–11.1), “other cardiovascular” (risk ratio, 1.73; 95% CI, 1.66–1.80), and “noncardiovascular” (risk ratio, 1.47; 95% CI, 1.41–1.52) comorbidities. After adjusting for covariates and considering interaction with age, patients with severe CHD had higher risks of previously recognized to be common in CHD and lower risks of other cardiovascular comorbidities than age‐stratified patients with nonsevere CHD. For noncardiovascular comorbidities, the risk was higher among patients with severe than nonsevere CHD before, but not after, the age of 40 years.

          Conclusions

          Our data underscore the unique clinical needs of adults with CHD compared with their peers. Clinicians caring for CHD may want to use a multidisciplinary approach, including building close collaborations with internists and specialists, to help provide appropriate care for the highly prevalent noncardiovascular comorbidities.

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          Most cited references28

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          Comorbidity measures for use with administrative data.

          This study attempts to develop a comprehensive set of comorbidity measures for use with large administrative inpatient datasets. The study involved clinical and empirical review of comorbidity measures, development of a framework that attempts to segregate comorbidities from other aspects of the patient's condition, development of a comorbidity algorithm, and testing on heterogeneous and homogeneous patient groups. Data were drawn from all adult, nonmaternal inpatients from 438 acute care hospitals in California in 1992 (n = 1,779,167). Outcome measures were those commonly available in administrative data: length of stay, hospital charges, and in-hospital death. A comprehensive set of 30 comorbidity measures was developed. The comorbidities were associated with substantial increases in length of stay, hospital charges, and mortality both for heterogeneous and homogeneous disease groups. Several comorbidities are described that are important predictors of outcomes, yet commonly are not measured. These include mental disorders, drug and alcohol abuse, obesity, coagulopathy, weight loss, and fluid and electrolyte disorders. The comorbidities had independent effects on outcomes and probably should not be simplified as an index because they affect outcomes differently among different patient groups. The present method addresses some of the limitations of previous measures. It is based on a comprehensive approach to identifying comorbidities and separates them from the primary reason for hospitalization, resulting in an expanded set of comorbidities that easily is applied without further refinement to administrative data for a wide range of diseases.
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            Congenital heart disease in the general population: changing prevalence and age distribution.

            Empirical data on the changing epidemiology of congenital heart disease (CHD) are scant. We determined the prevalence, age distribution, and proportion of adults and children with severe and other forms of CHD in the general population from 1985 to 2000. Where healthcare access is universal, we used administrative databases that systematically recorded all diagnoses and claims. Diagnostic codes conformed to the International Classification of Disease, ninth revision. Severe CHD was defined as tetralogy of Fallot, truncus arteriosus, transposition complexes, endocardial cushion defects, and univentricular heart. Prevalence of severe and other CHD lesions was determined in 1985, 1990, 1995, and 2000 using population numbers in Quebec. Children were subjects <18 years of age. The prevalence was 4.09 per 1000 adults in the year 2000 for all CHD and 0.38 per 1000 (9%) for those with severe lesions. Female subjects accounted for 57% of the adult CHD population. The median age of all patients with severe CHD was 11 years (interquartile range, 4 to 22 years) in 1985 and 17 years (interquartile range, 10 to 28 years) in 2000 (P<0.0001). The prevalence of severe CHD increased from 1985 to 2000, but the increase in adults was significantly higher than that observed in children. In the year 2000, 49% of those alive with severe CHD were adults. The prevalence in adults and median age of patients with severe CHD increased in the general population from 1985 to 2000. In 2000, there were nearly equal numbers of adults and children with severe CHD.
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              Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010.

              Our objective was to obtain contemporary lifetime estimates of congenital heart disease (CHD) prevalence using population-based data sources up to year 2010.
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                Author and article information

                Contributors
                anu.agarwal2@ucsf.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                02 October 2019
                15 October 2019
                : 8
                : 20 ( doiID: 10.1002/jah3.v8.20 )
                : e013450
                Affiliations
                [ 1 ] Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA
                [ 2 ] Department of Medicine Philip R. Lee Institute for Health Policy Studies School of Medicine, and Center for Healthcare Value University of California, San Francisco San Francisco CA
                [ 3 ] Adult Congenital Heart Disease Program Knight Cardiovascular Institute Oregon Health and Science University Portland OR
                [ 4 ] Division of Cardiology Children's National Health System Washington DC
                Author notes
                [*] [* ] Correspondence to: Anushree Agarwal, MD, Adult Congenital Cardiology Section, Cardiology Division, University of California, San Francisco, 500 Parnassus Ave, M‐1177B, Box 0124, San Francisco, CA 94143‐0124. E‐mail: anu.agarwal2@ 123456ucsf.edu
                Article
                JAH34508
                10.1161/JAHA.119.013450
                6818026
                31575318
                332d853b-6318-46a5-beba-3dba940494a7
                © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 30 May 2019
                : 11 September 2019
                Page count
                Figures: 2, Tables: 5, Pages: 11, Words: 7855
                Funding
                Funded by: American Heart Association Foundation
                Award ID: 17MCPRP33240000
                Categories
                Original Research
                Original Research
                Congenital Heart Disease
                Custom metadata
                2.0
                jah34508
                15 October 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.7.0 mode:remove_FC converted:15.10.2019

                Cardiovascular Medicine
                cohort study,comorbidities heart failure,congenital cardiac defect,health services,cardiovascular disease,epidemiology,risk factors

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