Adults with Congenital Heart Disease (CHD) are a new and growing population of patients who pose a challenge to both medicine and nursing. Medical and surgical advances have increased the number of adults with CHD. These advances may create Quality of Life (QOL) issues which were not previously considered. The purpose of this study was to collect data describing the QOL of adults with CHD in order for health professionals to develop appropriate information, counseling, and anticipatory guidance. This study was a case-control study design utilizing a QOL assessment tool, the Sickness impact Profile (SIP), along with a demographic questionnaire
