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Infection in DiGeorge Following CHD Surgery

This study has been terminated.
Information provided by (Responsible Party):
Children's Healthcare of Atlanta Identifier:
First received: January 13, 2006
Last updated: March 14, 2012
Last verified: March 2008
We propose a retrospective review of patients with DiGeorge syndrome having undergone cardiac surgery to evaluate the incidence of blood stream and/or surgical site infection. The hypothesis is that we will find an increased number of infections for this sub-group. We will compare the incidence of infection to children of similar age and diagnosis to evaluate for variances in the incidence of infection.

DiGeorge Syndrome
Congenital Heart Defects

Study Type: Observational
Study Design: Time Perspective: Retrospective
Official Title: Incidence of Infection in the Patient With DiGeorge Syndrome Following Surgery for Congenital Heart Disease

Resource links provided by NLM:

Further study details as provided by Children's Healthcare of Atlanta:

Enrollment: 400
Study Start Date: January 1998
Study Completion Date: March 2008
Primary Completion Date: March 2008 (Final data collection date for primary outcome measure)
Detailed Description:
DiGeorge syndrome is a common genetic disorder that frequently results in congenital heart defects such as truncus arteriousus, coarctation of the aorta, interrupted aortic arch, tetralogy of Fallot, pulmonary atresia with VSD, and several others. The defect is usually due to a deletion in the long arm of chromosome 22. Approximately 25% of patients with DiGeorge have a congenital heart defect. These patients also have varying degrees of thymic hypoplasia with associated T cell dysfunction. They are at increased risk of infections and can be at risk for opportunistic infections when the degree of T cell dysfunction is severe. Children undergoing cardiac surgery are at risk for infections in the post-operative period, prolonging hospital stay and increasing morbidity and mortality. The patient with DiGeorge syndrome may have higher rates of infection due to associated immune system dysfunction, however, this has not been previously reported from a large group of DiGeorge syndrome patients. Children's Healthcare of Atlanta follows over 200 patients with DiGeorge syndrome, with the majority having previously undergone cardiac surgery. This group of patients may benefit from more extensive antibiotic prophylaxis following surgery if they indeed have significantly higher rates of infection, but the true incidence needs to be determined.

Ages Eligible for Study:   up to 15 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
DiGeorge Syndrome Cardiac Surgery

Inclusion Criteria:

  • Children's Healthcare of Atlanta patients, Egleston DiGeorge Syndrome Cardiac Surgery 200 medical charts between Jan 1, 1998 and April 31, 2005 with cardiac surgery and DiGeorge Syndrome 200 medical charts between Jan 1, 1998 and April 31,2005 with cardiac surgery and no DiGeorge Syndrome

Exclusion Criteria:

  • Those who do not meet inclusion criteria
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Please refer to this study by its identifier: NCT00278005

United States, Georgia
Children's Healthcare of Atlanta
Atlanta, Georgia, United States, 30322
Sponsors and Collaborators
Children's Healthcare of Atlanta
Principal Investigator: Kevin O Maher, MD Children's Healthcare of Atlanta, Sibley Heart Center Cardiology
  More Information

Responsible Party: Children's Healthcare of Atlanta Identifier: NCT00278005     History of Changes
Other Study ID Numbers: 05-134
Study First Received: January 13, 2006
Last Updated: March 14, 2012

Keywords provided by Children's Healthcare of Atlanta:
DiGeorge Syndrome
Congenital heart defects
Cardiac surgery

Additional relevant MeSH terms:
Heart Defects, Congenital
DiGeorge Syndrome
Pathologic Processes
Cardiovascular Abnormalities
Cardiovascular Diseases
Heart Diseases
Congenital Abnormalities
22q11 Deletion Syndrome
Craniofacial Abnormalities
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Lymphatic Abnormalities
Lymphatic Diseases
Abnormalities, Multiple
Chromosome Disorders
Genetic Diseases, Inborn
Parathyroid Diseases
Endocrine System Diseases processed this record on April 27, 2017