Literature DB >> 26262578

Adults with congenital heart disease transition.

Koichiro Niwa1.   

Abstract

PURPOSE OF REVIEW: At present, 85-90% of those born with congenital heart disease (CHD) grow up to become adults. With few exceptions, reparative surgery is not curative and requires long-term surveillance. Caregivers could be changed from pediatric cardiologists to adult CHD specialists (or cardiologists) during this process. This study will focus on the current practice of transition in CHD. RECENT
FINDINGS: Residua and sequelae may progress in severity with age and induce late complications, such as arrhythmias, cardiac failure, thromboembolism, sudden cardiac death, reoperation, cardiac intervention, and arrhythmia ablation. There are other obstacles that further complicate adult CHD, including pregnancy and delivery, noncardiac surgery, psychosocial problems, health insurance coverage, and extracardiac complications, making close follow-up and proper management mandatory. Because of this, several specialized centers have been established to respond to this need, and several studies focusing on transition have been published recently.
SUMMARY: Provision of comprehensive care by multidisciplinary teams including adult CHD specialists, adult and pediatric cardiologists and cardiovascular surgeons, specialized nurses, and other specific disciplines are the fundamental features in care facilities for adult CHD. Training and education should be focused on adult CHD fellows who represent the next generation that will assume responsibility for this patient population. Proper transition from pediatric cardiologists and cardiovascular surgeons to adult CHD care team, including adult CHD specialists and/or cardiologists trained in this field, is mandatory.

Entities:  

Mesh:

Year:  2015        PMID: 26262578     DOI: 10.1097/MOP.0000000000000270

Source DB:  PubMed          Journal:  Curr Opin Pediatr        ISSN: 1040-8703            Impact factor:   2.856


  7 in total

Review 1.  Pediatric heart transplantation: long-term outcomes.

Authors:  Anne I Dipchand; Jessica A Laks
Journal:  Indian J Thorac Cardiovasc Surg       Date:  2019-05-29

Review 2.  Postoperative residua and sequelae in adults with repaired tetralogy of Fallot.

Authors:  Munetaka Masuda
Journal:  Gen Thorac Cardiovasc Surg       Date:  2016-04-26

Review 3.  Metabolic syndrome and coronary artery disease in adults with congenital heart disease.

Authors:  Koichiro Niwa
Journal:  Cardiovasc Diagn Ther       Date:  2021-04

4.  HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.

Authors:  Juan Wang; Xiao-Qing Hu; Yu-Han Guo; Jian-Yun Gu; Jia-Hong Xu; Yan-Jie Li; Ning Li; Xiao-Xiao Yang; Yi-Qing Yang
Journal:  Pediatr Cardiol       Date:  2016-12-10       Impact factor: 1.655

5.  Fortune favours the brave: composite first-person narrative of adolescents with congenital heart disease.

Authors:  Giovanni Biglino; Sofie Layton; Lindsay-Kay Leaver; Jo Wray
Journal:  BMJ Paediatr Open       Date:  2017-11-17

6.  Piloting the Use of Patient-Specific Cardiac Models as a Novel Tool to Facilitate Communication During Cinical Consultations.

Authors:  Giovanni Biglino; Despina Koniordou; Marisa Gasparini; Claudio Capelli; Lindsay-Kay Leaver; Sachin Khambadkone; Silvia Schievano; Andrew M Taylor; Jo Wray
Journal:  Pediatr Cardiol       Date:  2017-02-18       Impact factor: 1.838

7.  Changes of hospitalization trend in the pediatric cardiology division of a single center by increasing adult with congenital heart disease.

Authors:  Sang-Yun Lee; Gi-Beom Kim; Hye-Won Kwon; Mi-Kyoung Song; Eun Jung Bae; Sungkyu Cho; Jae Gun Kwak; Hong-Gook Lim; Woong-Han Kim; Jeong-Ryul Lee
Journal:  BMC Cardiovasc Disord       Date:  2020-05-15       Impact factor: 2.298

  7 in total

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