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      Outcomes of patients with hypertrophic cardiomyopathy and acute myocardial infarction: a propensity score-matched, 15-year nationwide population-based study in Asia

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          Abstract

          Objectives

          Hypertrophic cardiomyopathy (HCM) entails thickening of the myocardium and an increased risk of ischaemia. However, the prognosis of patients with HCM with acute myocardial infarction (AMI) is incompletely understood.

          Methods

          Medical information was retrieved from the Taiwan National Health Insurance Research Database in 1997–2011. The exclusion criteria were patients <18 years old, and history of AMI, coronary intervention, aortic valve disease, disease of the pericardium, heart surgery, device implantation, venous thromboembolism, cardiac transplant, congenital heart disease and end-stage renal disease on dialysis. Patients with HCM with AMI were compared with propensity score (PS)-matched patients with AMI without HCM. The primary endpoints were in-hospital and 1-year cardiovascular events.

          Results

          In total, 201 166 patients were admitted for AMI. There were 177 058 patients with new-onset AMI, 257 with HCM and 176 801 without HCM after exclusion criteria. Using 1:4 PS matching, the study population consisted of patients with AMI, 257 with HCM and 1028 without HCM. Patients with AMI with HCM received significantly less coronary intervention (OR=0.46; 95% CI 0.32 to 0.65; p<0.001), coronary intervention with stenting (OR=0.33; 95% CI 0.20 to 0.57; p<0.001) and coronary artery bypass graft surgery (OR=0.22; 95% CI 0.05 to 0.90; p=0.036), and fewer episodes of shock (OR=0.64; 95% CI 0.48 to 0.86; p=0.003) and in-hospital death (OR=0.46; 95% CI 0.30 to 0.70; p<0.001), compared with patients with AMI without HCM. Specifically, for patients with HCM with AMI, AMI occurred predominantly (82.5%) in the form of ischaemia without requiring coronary stenting. Patients with AMI with HCM had significantly better survival than patients without HCM (HR=0.66; 95% CI 0.51 to 0.85; p=0.001) during the 1-year follow-up.

          Conclusions

          This is the first PS-matched study to compare the prognosis of patients with AMI with and without HCM. Compared with patients with AMI without HCM, patients with HCM had significantly better in-hospital and within 1-year outcomes.

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          Most cited references8

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          Adjusted Kaplan-Meier estimator and log-rank test with inverse probability of treatment weighting for survival data.

          Estimation and group comparison of survival curves are two very common issues in survival analysis. In practice, the Kaplan-Meier estimates of survival functions may be biased due to unbalanced distribution of confounders. Here we develop an adjusted Kaplan-Meier estimator (AKME) to reduce confounding effects using inverse probability of treatment weighting (IPTW). Each observation is weighted by its inverse probability of being in a certain group. The AKME is shown to be a consistent estimate of the survival function, and the variance of the AKME is derived. A weighted log-rank test is proposed for comparing group differences of survival functions. Simulation studies are used to illustrate the performance of AKME and the weighted log-rank test. The method proposed here outperforms the Kaplan-Meier estimate, and it does better than or as well as other estimators based on stratification. The AKME and the weighted log-rank test are applied to two real examples: one is the study of times to reinfection of sexually transmitted diseases, and the other is the primary biliary cirrhosis (PBC) study. 2005 John Wiley & Sons, Ltd.
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            Clinical course of hypertrophic cardiomyopathy in a regional United States cohort.

            Hypertrophic cardiomyopathy (HCM) has been regarded as a disease that causes substantial disability, with annual mortality rates of up to 6%, based largely on reports from tertiary referral centers. To assess the clinical course of HCM in a patient cohort more closely resembling the true disease state. Retrospective cohort study. A regional cohort from Minnesota and adjoining regions, free of referral center bias, studied at Minneapolis Heart Institute. Two hundred seventy-seven consecutively studied HCM patients, none referred for specialized HCM care, managed clinically in a standard fashion. Mortality and clinical course of HCM. During a mean (SD) follow-up of 8.1 (6.6) years, 45 patients died and 29 of these deaths were directly related to HCM; however, 8 of the 29 HCM deaths were not premature (occurring >75 years of age). Annual HCM mortality rate was 1.3% (0.7% for sudden cardiac death). Patients identified in adulthood (n = 234) showed no statistically significant difference in mortality when compared with expected mortality, as calculated for the general US or Minnesota populations (P=.17). Patients identified as children (n=43) showed decreased survival compared with the general population (P<.001). At most recent clinical evaluation, 192 patients (69%) had no or mild symptoms and 69 (25%) experienced incapacitating symptoms or HCM-related death; 53 (19%) of the patients had achieved estimated life expectancy of 75 years or older. More advanced symptoms at diagnosis-occurrence of atrial fibrillation (often associated with stroke), the presence of basal outflow obstruction of at least 30 mm Hg, and marked left ventricular wall thickness of more than 25 mm-were clinically important independent predictors of HCM mortality. In a regionally selected patient population most closely resembling the true disease state, HCM did not significantly increase the risk of premature death or adversely affect overall life expectancy. Prevailing misconceptions of HCM as a generally unfavorable condition may largely be related to the skewed patient referral patterns characteristic of tertiary care centers. Hypertrophic cardiomyopathy is nevertheless a highly complex disease capable of serious clinical consequences and premature death in some patients.
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              Decreased coronary flow reserve in hypertrophic cardiomyopathy is related to remodeling of the coronary microcirculation.

              Ischemia occurs frequently in hypertrophic cardiomyopathy (HCM) without evidence of epicardial stenosis. This study evaluates the hypothesis that the occurrence of ischemia in HCM is related to remodeling of the coronary microcirculation. End-diastolic septal wall thickness was significantly increased in patients with HCM (25.8+/-2.9 mm) in comparison with cardiac transplant recipients (control subjects: 11.4+/-3.0 mm; P<0.05). Although the diameter of the left anterior descending coronary artery was similar in both groups (3.0+/-0.8 versus 3.0+/-0.5 mm, P=NS), the coronary resistance reserve (CRR=CRRbasal/CRRhyperemic), corrected for extravascular compression (end-diastolic left ventricular pressure), was reduced to 1.5+/-0.6 in HCM (P<.05; control, 2.6+/-0.8). Arteriolar lumen (AL) divided by wall area was lower in HCM (21+/-5% versus 30+/-4%; P<.05), and capillary density tended to decrease (from 1824+/-424 to 1445+/-513 per mm2, P=.11) in HCM. CRR was linearly related to normalized AL according to the formula CRR=O.1 AL-0.45 (r=.57; P<.05). Further analysis revealed that CRR, AL, and capillary density were all linearly related to the degree of hypertrophy. Decrements in CRR were related to changes of the coronary microcirculation. Both the decrease in CRR and these changes in the coronary microcirculation were related to the degree of hypertrophy. All these factors might contribute to the well-known occurrence of ischemia in this patient group.
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                Author and article information

                Journal
                BMJ Open
                BMJ Open
                bmjopen
                bmjopen
                BMJ Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2044-6055
                2018
                23 August 2018
                : 8
                : 8
                : e019741
                Affiliations
                [1 ] departmentDivision of Cardiology , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                [2 ] departmentDepartment of Cardiology , Chang Gung Memorial Hospital Keelung Branch , Keelung, Taiwan
                [3 ] departmentDivision of Cardiovascular Medicine, Miriam and Rhode Island Hospital , Warren Alpert School of Medicine, Brown University , Providence, Rhode Island, USA
                [4 ] departmentDepartment of Cardiothoracic and Vascular Surgery , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                [5 ] departmentDepartment of Nephrology , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                [6 ] departmentDepartment of Neurology , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                [7 ] departmentDepartment of Neurosurgery , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                [8 ] departmentDepartment of Physical Medicine and Rehabilitation , Chang Gung Memorial Hospital, Linkou Medical Center , Taoyuan City, Taiwan
                Author notes
                [Correspondence to ] Dr Victor Chien-Chia Wu; victorcwu@ 123456hotmail.com
                Article
                bmjopen-2017-019741
                10.1136/bmjopen-2017-019741
                6112399
                30139891
                386ef97d-5282-4a04-814f-c7604de62e13
                © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 22 September 2017
                : 20 June 2018
                : 31 July 2018
                Categories
                Cardiovascular Medicine
                Research
                1506
                1683
                Custom metadata
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                Medicine
                hypertrophic cardiomyopathy,acute myocardial infarction,outcome
                Medicine
                hypertrophic cardiomyopathy, acute myocardial infarction, outcome

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