The impact of pre-procedure heart rate on adverse clinical outcomes in patients undergoing percutaneous coronary intervention

The prognostic impact of pre-procedure heart rate (PHR) following percutaneous coronary intervention (PCI) has not yet been fully investigated. This post-hoc analysis sought to assess the impact of PHR on medium-term outcomes among patients having PCI, who were enrolled in the "all-comers"...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Wang Rutao
Takahashi Kuniaki
Chichareon Ply
Gao Chao
Kogame Norihiro
Modolo Rodrigo
Tomaniak Mariusz
Kawashima Hideyuki
Ono Masafumi
Hara Hironori
Schächinger Volker
Tonev Gincho
Ungi Imre
Botelho Roberto
Eeckhout Eric
Dokumentumtípus: Cikk
Megjelent: 2020
Sorozat:ATHEROSCLEROSIS 303
Tárgyszavak:
doi:10.1016/j.atherosclerosis.2020.04.010

mtmt:31361460
Online Access:http://publicatio.bibl.u-szeged.hu/22344
Leíró adatok
Tartalmi kivonat:The prognostic impact of pre-procedure heart rate (PHR) following percutaneous coronary intervention (PCI) has not yet been fully investigated. This post-hoc analysis sought to assess the impact of PHR on medium-term outcomes among patients having PCI, who were enrolled in the "all-comers" GLOBAL LEADERS trial.The primary endpoint (composite of all-cause death or new Q-wave myocardial infarction [MI]) and key secondary safety endpoint (bleeding according to Bleeding Academic Research Consortium [BARC] type 3 or 5) were assessed at 2 years. PHR was available in 15,855 patients, and when evaluated as a continuous variable (5 bpm increase) and following adjustment using multivariate Cox regression, it significantly correlated with the primary endpoint (hazard ratio [HR] 1.06, 95% confidence interval [CI] 1.03-1.09, p < 0.001). Using dichotomous cut-off criteria, a PHR>67 bpm was associated with increased all-cause mortality (HR 1.38, 95%CI 1.13-1.69, p = 0.002) and more frequent new Q-wave MI (HR 1.41, 95%CI 1.02-1.93, p = 0.037). No significant association was found between PHR and BARC 3 or 5 bleeding (HR 1.04, 95% CI 0.99-1.09, p = 0.099). There was no interaction with the primary (p-inter = 0.236) or secondary endpoint (p-inter = 0.154) when high and low PHR was analyzed according to different antiplatelet strategies.Elevated PHR was an independent predictor of all-cause mortality at 2 years following PCI in the "all-comer" GLOBAL LEADERS trial. The prognostic value of increased PHR on outcomes was not affected by the different antiplatelet strategies in this trial.
Terjedelem/Fizikai jellemzők:1-7
ISSN:0021-9150