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Volume 19, Issue 4, Pages 243-246 (April 2010)


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Mid-term Results of the Hancock II Valve and Carpentier-Edward Perimount Valve in the Pulmonary Portion in Congenital Heart Disease

Jae Gun Kwak, MDa, Jeong Ryul Lee, MDbCorresponding Author Informationemail address, Woong-Han Kim, MDb, Yong Jin Kim, MDb

Received 10 March 2009; received in revised form 28 August 2009; accepted 31 October 2009.

Background

As the number of cases with artificial pulmonary valve implantation increases for congenital heart disease, the number of young adults with artificial pulmonary valves has also increased.

Methods

From 2000 to 2007, 146 artificial valves, such as the Carpentier-Edward Perimount, Hancock II, Biocor, homograft and hand-made valves were implanted for pulmonary valve in 132 patients with various forms of congenital heart disease. Among them, the outcomes of the Carpentier-Edward Perimount (n=63) and the Hancock II (n=40) valves were reviewed retrospectively. The mean age at initial implantation was 12.8±6.6 years. The overall duration of follow up was 36.0±24.2 months.

Results

There was an early death due to right ventricular failure with intractable ventricular arrhythmia and 3 late deaths due to progressive right ventricular failure, dilated cardiomyopathy and infective endocarditis. The overall survival and re-operation free rate was 96.3% and 89.8% respectively. Eight out of 63 Carpentier-Edward patients (12.6%) underwent re-replacement at 49.2±25.2 months. The re-operation free rates were 97.7%, 87.7% and 50% at 1, 3 and 5 years respectively. There was no re-operation required for the 40 Hancock II patients over 18.0±10.8 months. There was no statistical significance in the re-operation free rates between these 2 valves (p-value=0.51).

Conclusions

The overall survival rate associated with pulmonary valve bioprosthetic valve implantation was acceptable. However, the re-operation freedom rate was not satisfactory at mid-term for the Carpentier-Edward.

a Department of Thoracic and Cardiovascular Surgery, Sejong General Hospital, Bucheon, Republic of Korea

b Department of Thoracic and Cardiovascular Surgery, Seoul National University Children's Hospital, 28 Yeongun Dong, Jongno Gu, Seoul, Republic of Korea

Corresponding Author InformationCorresponding author. Tel.: +82 11 9989 1081.

PII: S1443-9506(09)01102-0

doi:10.1016/j.hlc.2009.10.009


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