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Damus-Stansel-Kaye procedure: current indications and results
The Annals of Thoracic Surgery
|July 1, 1993
Summary
The Damus-Stansel-Kaye procedure shows promising long-term results for complex congenital heart disease, with 88% survival at 5 years and a low reoperation rate for this critical intervention.
Area of Science:
- Cardiovascular Surgery
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- The Damus-Stansel-Kaye procedure is a palliative surgical technique used for complex congenital heart disease.
- It addresses conditions such as restrictive bulboventricular foramen and subaortic stenosis.
Purpose of the Study:
- To evaluate the outcomes of the Damus-Stansel-Kaye procedure in patients with complex univentricular and biventricular congenital heart disease.
- To assess early mortality, long-term survival, and reoperation rates.
Main Methods:
- A retrospective review of 29 consecutive Damus-Stansel-Kaye procedures performed between October 1983 and August 1991.
- Analysis of patient demographics, indications for surgery, concurrent procedures (including Fontan procedure), age at operation, outflow tract gradients, and follow-up data.
Main Results:
- Three early deaths (10%) occurred, with two in patients who also had a concurrent Fontan procedure.
- Actuarial freedom from cardiac-related death was 88% at 5 years.
- Ten percent of patients required reoperation, primarily for aortic valve insufficiency or gradient across the anastomosis, with 90% freedom from reoperation related to the Damus-Stansel-Kaye procedure at 4 years.
Conclusions:
- The Damus-Stansel-Kaye procedure demonstrates acceptable early and long-term outcomes for selected patients with complex congenital heart disease.
- While reoperations may be necessary, the procedure offers a viable option for palliation, with good survival rates and manageable reoperation risks.