TY - JOUR
T1 - Palliation of allograft vasculopathy with transluminal angioplasty
T2 - A decade of experience
AU - Benza, Raymond L.
AU - Zoghbi, Gilbert J.
AU - Tallaj, Jose
AU - Brown, Robert
AU - Kirklin, James K.
AU - Hubbard, Meloneysa
AU - Rayburn, Barry
AU - Foley, Brian
AU - McGiffin, David C.
AU - Pinderski, Laura J.
AU - Misra, Vijay
AU - Bourge, Robert C.
PY - 2004/6/2
Y1 - 2004/6/2
N2 - Objectives The goal of this study was to examine the outcomes of percutaneous coronary interventions (PCI) and the predictors for restenosis after cardiac transplantation. Background The role of PCI as definitive therapy for allograft coronary disease (ACD) remains contentious. Methods Between January 1, 1990 and December 31, 2000, 62 patients (1.5 to 15.5 years after transplant) underwent 151 procedures resulting in PCIs of 219 lesions. Follow-up after PCI angiography was usually obtained at three and six months, then yearly. Repeat PCI was routinely done to lesions with >60% restenosis. Results The primary procedural success was 97%. Repeat PCI occurred in 74 of 219 lesions (34%); PCI-related mortality was 2.6% (4 of 151). The freedom from re-PCI (of same vessel site) was 75% at six months, 65% at one year, and 57% at four years. The freedom from restenosis was 95% at one month, 81% at three months, and 57% at six months. Multivariate predictors of freedom from restenosis were the use of stents, higher anti-proliferative immunosuppressant dose, and an era effect. In the setting of one-vessel disease at first PCI, the two-year freedom for ACD death or graft loss was 74%, compared with 75% for two-vessel and 27% for three-vessel disease (p = 0.009). Conclusions Despite the increasing effectiveness of PCI for localized ACD, the survival after development of advanced ACD remains poor. Stents appear to increase effectiveness of PCI for ACD, but other factors in the current era contribute to improved outcomes.
AB - Objectives The goal of this study was to examine the outcomes of percutaneous coronary interventions (PCI) and the predictors for restenosis after cardiac transplantation. Background The role of PCI as definitive therapy for allograft coronary disease (ACD) remains contentious. Methods Between January 1, 1990 and December 31, 2000, 62 patients (1.5 to 15.5 years after transplant) underwent 151 procedures resulting in PCIs of 219 lesions. Follow-up after PCI angiography was usually obtained at three and six months, then yearly. Repeat PCI was routinely done to lesions with >60% restenosis. Results The primary procedural success was 97%. Repeat PCI occurred in 74 of 219 lesions (34%); PCI-related mortality was 2.6% (4 of 151). The freedom from re-PCI (of same vessel site) was 75% at six months, 65% at one year, and 57% at four years. The freedom from restenosis was 95% at one month, 81% at three months, and 57% at six months. Multivariate predictors of freedom from restenosis were the use of stents, higher anti-proliferative immunosuppressant dose, and an era effect. In the setting of one-vessel disease at first PCI, the two-year freedom for ACD death or graft loss was 74%, compared with 75% for two-vessel and 27% for three-vessel disease (p = 0.009). Conclusions Despite the increasing effectiveness of PCI for localized ACD, the survival after development of advanced ACD remains poor. Stents appear to increase effectiveness of PCI for ACD, but other factors in the current era contribute to improved outcomes.
KW - ACD
KW - allograft coronary disease
KW - anti-proliferative
KW - AP
KW - CAD
KW - coronary artery disease
KW - minimal luminal diameter
KW - MLD
KW - MMF
KW - mycophenolate mofetil
KW - PCI
KW - percutaneous coronary intervention
KW - percutaneous transluminal coronary angioplasty
KW - PTCA
UR - http://www.scopus.com/inward/record.url?scp=2542447364&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2004.02.045
DO - 10.1016/j.jacc.2004.02.045
M3 - Article
C2 - 15172400
AN - SCOPUS:2542447364
SN - 0735-1097
VL - 43
SP - 1973
EP - 1981
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 11
ER -