Clinical characteristics and survival of children with hypertrophic cardiomyopathy in China: A multicentre retrospective cohort study

被引:12
|
作者
Chan, Wenxiu [1 ]
Yang, Shiwei [2 ]
Wang, Jian [3 ]
Tong, Shilu [4 ]
Lin, Minyin [5 ]
Lu, Pengtao [2 ]
Yao, Ruen [3 ]
Wu, Lanping [1 ]
Chen, Lijun [1 ]
Guo, Ying [1 ]
Shen, Jie [1 ]
Liu, Tingliang [1 ]
Li, Fen [1 ]
Chen, Huiwen [6 ]
Zhang, Hao [6 ]
Wang, Shushui [5 ]
Fu, Lijun [1 ,7 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Dept Cardiol, Shanghai Childrens Med Ctr, 1678 Dongfang Rd, Shanghai 200127, Peoples R China
[2] Nanjing Med Univ, Childrens Hosp, Dept Cardiol, Nanjing 210008, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Res Div Birth Defects, Inst Paediat Translat Med,Shanghai Childrens Med, Shanghai 200127, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Dept Clin Epidemiol & Biostat, Shanghai Childrens Med Ctr, Shanghai 200127, Peoples R China
[5] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Paediat Cardiol, Guangdong Cardiovasc Inst, Guangzhou 510080, Peoples R China
[6] Shanghai Clin Res Ctr Rare Paediat Dis, 1678 Dongfang Rd, Shanghai 200127, Peoples R China
[7] Shanghai Jiao Tong Univ, Sch Med, Res Div Cardiovasc Dis, Inst Paediat Translat Med,Shanghai Childrens Med, Shanghai 200127, Peoples R China
关键词
Cohort study; Hypertrophic cardiomyopathy; Paediatrics; Survival; DISEASE TYPE-II; PEDIATRIC CARDIOMYOPATHY; AMERICAN-COLLEGE; DIAGNOSIS; OUTCOMES; EPIDEMIOLOGY; ATAXIA; ASSOCIATION; PREDICTORS; FREQUENCY;
D O I
10.1016/j.eclinm.2022.101466
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Few data on paediatric hypertrophic cardiomyopathy (HCM) are available in developing countries. A multicentre, retrospective, cohort study was conducted to profile the clinical characteristics and survival of children with HCM in China. Methods We collected longitudinal data on children with HCM aged 0-18 years at three participating institutions between January 1, 2010 and December 31, 2019. Patients were identified by searching for the diagnosis using ICD-10 codes from the electronic medical records database. HCM was diagnosed morphologically with echocardiography or cardiovascular magnetic resonance imaging. The exclusion criteria were secondary aetiologies of myocardial hypertrophy. The primary outcomes were all-cause death or heart transplantation. The Kaplan-Meier method was used to estimate the survival rate of different groups. Findings A total of 564 children were recruited, with a median age at diagnosis of 1.0 year (interquartile range, IQR: 0.4-8.0 years), followed for a median of 2.6 years (1977 patient-years, IQR:0.5, 5.9 years). The underlying aetiology was sarcomeric (382, 67.7%), inborn errors of metabolism (IEMs) (108, 19.2%), and RASopathies (74, 13.1%). A total of 149 patients (26.4%) died and no patients underwent heart transplantation during follow-up. The survival probability was 71.1% (95% confidence interval [CI], 66.3%- 75.3%) at 5 years. Patients with IEMs or those diagnosed during infancy had the poorest outcomes, with an estimated 5-year survival rate of 16.9% (95% CI, 7.7%-29.1%) and 56.0% (95% CI, 48.8%-62.5%), respectively. Heart failure was the leading cause of death in the cohort (90/149, 60.4%), while sudden cardiac death was the leading cause in patients with sarcomeric HCM (32/66, 48.5%). Interpretation There is a high proportion of patients with IEM and a low proportion of patients with neuromuscular disease in children with HCM in China. Overall, mortality remains high in China, especially in patients with IEMs and those diagnosed during infancy.
引用
收藏
页数:12
相关论文
共 50 条
  • [21] Atrial fibrillation and the risk of sudden cardiac arrest in patients with hypertrophic cardiomyopathy - A nationwide cohort study
    Liao, Min-Tsun
    Wu, Cho-Kai
    Juang, Jyh-Ming Jimmy
    Lin, Ting-Tse
    Wu, Chih-Cheng
    Lin, Lian-Yu
    ECLINICALMEDICINE, 2021, 34
  • [22] Clinical manifestation and outcomes of children with hypertrophic cardiomyopathy in Kosovo
    Bejiqi, Ramush A.
    Retkoceri, Ragip
    Zeka, Nairn
    Vuciterna, Armend
    Mustafa, Aferdita
    Maloku, Arlinda
    Bejiqi, Rinor
    TURKISH JOURNAL OF PEDIATRICS, 2020, 62 (02) : 215 - 223
  • [23] The clinical profile, genetic basis and survival of childhood cardiomyopathy: a single-center retrospective study
    Yuan, Wenjing
    Jia, Zhongli
    Li, Jiajin
    Liu, Lingjuan
    Tian, Jie
    Huang, Xupei
    Quan, Junjun
    EUROPEAN JOURNAL OF PEDIATRICS, 2024, 183 (03) : 1389 - 1401
  • [24] Prevalence, characteristics, and natural history of apical phenotype in a large cohort of patients with hypertrophic cardiomyopathy
    Rouskas, Pavlos
    Zegkos, Thomas
    Ntelios, Dimitris
    Gossios, Thomas
    Parcharidou, Despoina
    Papanastasiou, Christos A.
    Karamitsos, Theodoros
    Vassilikos, Vassilis
    Kouskouras, Kostantinos
    Efthimiadis, Georgios K.
    HELLENIC JOURNAL OF CARDIOLOGY, 2023, 73 : 8 - 15
  • [25] Clinical melanoma characteristics and survival-a single-center retrospective study between 2000 and 2010
    Feichtenschlager, Valentin
    Weihsengruber, Felix
    Richter, Leo
    vujic, Igor
    Rappersberger, Klemens
    Posch, Christian
    WIENER MEDIZINISCHE WOCHENSCHRIFT, 2019, 169 (13-14) : 323 - 330
  • [26] The China Hypertrophic Cardiomyopathy Project (CHCMP): The Rationale and Design of a Multicenter, Prospective, Registry Cohort Study
    Du, Zhi
    Wang, Kai
    Cui, Yawei
    Xie, Xudong
    Zhu, Ruoyu
    Dong, Fanghong
    Guo, Xiaogang
    JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2024, 17 (03) : 732 - 738
  • [27] Clinical Outcome of Hypertrophic Cardiomyopathy in Probands with the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort Study
    Vodnjov, Nina
    Maver, Ales
    Teran, Natasa
    Peterlin, Borut
    Toplisek, Janez
    Writzl, Karin
    JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2025, 18 (01) : 110 - 120
  • [28] Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathy
    Lopes, Luis Rocha
    Brito, Dulce
    Belo, Adriana
    Cardim, Nuno
    INTERNATIONAL JOURNAL OF CARDIOLOGY, 2019, 278 : 173 - 179
  • [29] Nutritional status associated with clinical outcomes in children with solid tumors: A retrospective cohort study from China
    Li, Yongzhen
    Lu, Zhongying
    Ma, Ao
    Yao, Wei
    Dong, Rui
    Li, Kai
    Wu, Min
    Dong, Kuiran
    Qian, Tian
    CANCER MEDICINE, 2024, 13 (01):
  • [30] Hypertrophic cardiomyopathy with latent obstruction: Clinical characteristics and surgical results
    Ji, Qiang
    Wang, YuLin
    Liu, FangYu
    Yang, Ye
    Xia, LiMin
    Ding, WenJun
    Lai, Hao
    Wang, ChunSheng
    JOURNAL OF CARDIOLOGY, 2022, 79 (01) : 42 - 49