Automated Cardioverter Defibrillator in Children

Sponsor
Children's Healthcare of Atlanta (Other)
Overall Status
Completed
CT.gov ID
NCT00268021
Collaborator
(none)
34
1

Study Details

Study Description

Brief Summary

Automated implantable cardioverter defibrillators ,AICD, and Biventricular,BiV, Pacemakers have been shown in randomized trials to offer an advantage in adults with decreased ventricular ejection fraction, heart failure, spontaneous non-sustained ventricular tachycardia VT, inducible non-suppressible VT and the combination of low ejection fraction and prior myocardial infarction,14. Pediatric patients with a variety of different heart abnormalities are at high risk for life threatening arrhythmias and poor ventricular function or heart failure,16. Therefore, extrapolating this adult data, AICDs and BiV pacemakers have been used with increasing frequency in the pediatric and congenital heart disease population. Improvements in device size and lead design allows AICD and BiV implantation in the very young, in small size patients and in patients with complex cardiac anomalies,1. The use of BiV pacemakers and the patterns of AICD discharge are similar in young patients and in adults, suggesting that the risk of life threatening arrhythmia and heart failure are also similar,16. However, this patient population behaves differently from the adult population in the incidence of pacemaker complications, circadian arrhythmias,7, and more importantly, a relatively high incidence of complications related to AICD insertion, 8. There is a need for more studies to establish the risk-benefit ratio of these devices in the pediatric setting.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This is a retrospective review of all the patients that had an AICD or BiV pacemakers inserted at Children's Healthcare of Atlanta at Egleston, Emory University, between January 1st, 1998 and July 30th, 2004. The goal of our study is to establish the prevalence of beneficial and adverse effects in the AICD and BiV patient population.

    Demographic, clinical and electrophysiologic characteristics during the hospitalization as well as at follow-up will be obtained from the medical records and are summarized in the following tables Note: We defined infection as elevated temperature above 38.1 C associated with elevated WBC and positive cultures.

    Appendix A

    We plan to collect the following demographic information. Age Weight Delivery method Gestational age Weight at birth Delivery complications Cardiac anomalies Other anomalies

    We plan to collect the following medical information/diagnoses. Indication Cardiac arrest Sustained ventricular tachycardia Inducible ventricular tachycardia Syncope Palpitations Severe hypertrophic cardiomyopathy Congenital heart disease Primary electrical disease Hypertrophic cardiomyopathy Idiopathic dilated cardiomyopathy

    We will collect the following AICD information. Lead Transvenous Subcutaneous array Epicardial patches Generator type

    We will collect the following outcomes information (AICD and BiV). Variable Appropriate discharge (AICD only) Inappropriate discharge (AICD only) Lead failure Overall survival Hospital Length of Stay Infection Blood transfusion/bleeding Hospital Re-admission Mortality/Morbidity information Cause of inappropriate AICD discharge/shock Long term complications

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    34 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    The Use of Automated Cardioverter Defibrillator in Children (AICD)
    Study Start Date :
    Jan 1, 1998

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A to 21 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      No
      Inclusion Criteria:
      • patients with AICD inserted at Children's Healthcare of Atlanta

      • patients with BiV pacemaker inserted at Children's Healthcare of Atlanta

      • insertions between 1.1.1998 and 7.30.2004

      Exclusion Criteria:
      • those patients who do not meet inclusion criteria

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Children's Healthcare of Atlanta Atlanta Georgia United States 30322

      Sponsors and Collaborators

      • Children's Healthcare of Atlanta

      Investigators

      • Principal Investigator: Kirk R Kanter, MD, Children's Healthcare of Atlanta

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      Children's Healthcare of Atlanta
      ClinicalTrials.gov Identifier:
      NCT00268021
      Other Study ID Numbers:
      • 04-082
      First Posted:
      Dec 22, 2005
      Last Update Posted:
      Dec 2, 2014
      Last Verified:
      Nov 1, 2014
      Keywords provided by Children's Healthcare of Atlanta

      Study Results

      No Results Posted as of Dec 2, 2014