2018
Long-term outcomes after treatment of bare-metal stent restenosis with paclitaxel-coated balloon catheters or everolimus-eluting stents: 3-year follow-up of the TIS clinical study
PLEVA, Leos, Pavel KUKLA, Jana ZAPLETALOVA a Ota HLINOMAZZákladní údaje
Originální název
Long-term outcomes after treatment of bare-metal stent restenosis with paclitaxel-coated balloon catheters or everolimus-eluting stents: 3-year follow-up of the TIS clinical study
Autoři
PLEVA, Leos (203 Česká republika, garant), Pavel KUKLA (203 Česká republika), Jana ZAPLETALOVA (203 Česká republika) a Ota HLINOMAZ (203 Česká republika, domácí)
Vydání
Catheterization and Cardiovascular Interventions, Hoboken, Wiley-Blackwell, 2018, 1522-1946
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.551
Kód RIV
RIV/00216224:14110/18:00105325
Organizační jednotka
Lékařská fakulta
UT WoS
000451188300007
Klíčová slova anglicky
everolimus-eluting stent; in-stent restenosis; paclitaxel-eluting balloon
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 10. 2. 2019 15:37, Soňa Böhmová
Anotace
V originále
Background The efficacy of paclitaxel-eluting balloon catheters (PEB) and drug-eluting stents for treatment of bare-metal stent restenosis (BMS-ISR) have been demonstrated in several studies with follow-up times of 9 to 12 months; however, the long-term outcomes of ISR treatment are less defined. Objectives Methods We aimed to compare the long-term efficacy of PEB and everolimus-eluting stents (EES) for the treatment of BMS-ISR. We analyzed 3-year clinical follow-up data from patients included in the TIS randomized clinical study. A total of 136 patients with BMS-ISR were allocated to receive treatment with either PEB or EES (68 patients with 74 ISR lesions per group). Results Conclusions The PEB and EES groups did not significantly differ in major adverse cardiac events-free survival (MACE; P = .211; including individual events: CV death: P = .622; myocardial infarction: P = .650 or target vessel revascularization: P = .286) at 3-year clinical follow-up. No event-free survival differences were found between the groups regarding overall mortality (P = .818), definite stent thrombosis (P = .165) or the second MACE (P = .270). At the 3-year follow-up, no significant differences in clinical outcomes were found between iopromide-coated PEB and EES for the treatment of BMS-ISR. (; ; NCT01735825).