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OpenTrials
Completed

NCT Number: NCT00446160

Adult Congenital Heart Disease Surgery

It is now estimated that the number of adults with congenital heart disease in the U.S is over 800,000. Unfortunately, these patients, in some way, have become a lost population. They have congenital abnormalities familiar to a children's hospital, yet have surpassed the age cutoff for admission.

Recently, we have developed a specialized program to care for this unique patient population. Dedicated programs such as ours hope to optimize patient care, consolidate specialized resources, provide sufficient patient numbers for training and maintain expertise and facilitate research in this unique population.

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Key information

Age range

19 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Emory University

Atlanta, Georgia, 30322, United States

About this study

In the United States, approximately 30,000 children are born with congenital heart disease every year. As technology, operative technique, and critical care medicine have improved significantly over the years, more of these children are surviving into adulthood.

Care of the congenital cardiac surgical patient requires a concerted effort on the part of the surgeons, perfusionists, anesthesiologists, intensivists, nurses, respiratory therapists, rehabilitation services and social workers. It is hoped that the same excellent care received in a children's congenital heart surgery program can be continued as these patients graduate into an adult program.

This is a retrospective chart review examining patients over the age of 18 years who have undergone operations for congenital heart disease. The primary interest of the study is to look at the breakdown of our adult congenital program in regards to location, personnel, and case type. All charts reviewed will be of patients who had their surgery at Children's Healthcare of Atlanta or Emory University between January 1, 2000 and December 31, 2006. We will review approximately 225 charts for this study.

The first aim of the study would be to examine the demographics of the adult congenital heart surgery program itself. The following information will be collected:

  • Location of the surgery - children's hospital vs adult hospital
  • Surgeon - adult cardiac surgeon vs congenital cardiac surgeon

The second aim of the study would be to analyze the types of surgeries being performed. The following information will be collected:

  • Pathologic diagnosis
  • Number of re-operative sternotomies
  • Number of open-heart surgeries

The third aim of the study would be to analyze our outcomes. The following information will be collected:

  • Number of surgical mortalities

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • surgery at Children's Healthcare of Atlanta or Emory University between 1.1.2000 and 12.31.2007
  • surgery on patients after 18 years to approximately 65 years of age

Exclusion criteria

  • Those who do not meet inclusion criteria

Treatment and study plan

Primary outcomes

  1. The primary interest of the study is to look at the breakdown of our adult congenital program in regards to location, personnel, and case type.

    Time frame: Retrospective chart review

Sponsors and collaborators

Lead sponsor

Emory University

Other

Registry information

Official study title

Proposal for Retrospective Review of an Adult Congenital Heart Surgery Program

Important dates

Study start
2000
Primary completion
2016
Study completion
2016
First posted
Mar 12, 2007
Registry last updated
Feb 21, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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