TY - JOUR
T1 - A systematic review and meta-Analysis of clinical outcomes of patients undergoing chronic total occlusion percutaneous coronary intervention
AU - Simsek, Bahadir
AU - Kostantinis, Spyridon
AU - Karacsonyi, Judit
AU - Alaswad, Khaldoon
AU - Megaly, Michael
AU - Karmpaliotis, Dimitrios
AU - Masoumi, Amirali
AU - Jaber, Wissam A.
AU - Nicholson, William
AU - Rinfret, Stephane
AU - Mashayekhi, Kambis
AU - Werner, Gerald S.
AU - McEntegart, Margaret
AU - Lee, Seung Whan
AU - Khatri, Jaikirshan J.
AU - Harding, Scott A.
AU - Avran, Alexandre
AU - Jaffer, Farouc A.
AU - Doshi, Darshan
AU - Kao, Hsien Li
AU - Sianos, Georgios
AU - Yamane, Masahisa
AU - Milkas, Anastasios
AU - Azzalini, Lorenzo
AU - Garbo, Roberto
AU - Tammam, Khalid
AU - Rafeh, Nidal Abi
AU - Nikolakopoulos, Ilias
AU - Vemmou, Evangelia
AU - Rangan, Bavana V.
AU - Nicholas Burke, M.
AU - Garcia, Santiago
AU - Croce, Kevin J.
AU - Wu, Eugene B.
AU - Tsuchikane, Etsuo
AU - Di Mario, Carlo
AU - Galassi, Alfredo R.
AU - Gagnor, Andrea
AU - Knaapen, Paul
AU - Jang, Yangsoo
AU - Kim, Byeong Keuk
AU - Poommipanit, Paul B.
AU - Brilakis, Emmanouil S.
N1 - Publisher Copyright:
© 2022 HMP Global.
PY - 2022/11
Y1 - 2022/11
N2 - Objectives. Chronic total occlusion (CTO) percutaneous coronary intervention (PCI) can improve patient symptoms, but it remains controversial whether it impacts subsequent clinical outcomes. Methods. In this systematic review and meta-Analysis, we queried PubMed, ScienceDirect, Cochrane Library, Web of Science, and Embase databases (last search: September 15, 2021). We investigated the impact of CTO-PCI on clinical events including all-cause mortality, cardiovascular death, myocardial infarction (MI), major adverse cardiovascular event (MACE), stroke, subsequent coronary artery bypass surgery, target-vessel revascularization, and heart failure hospitalizations. Pooled analysis was performed using a random-effects model. Results. A total of 58 publications with 54,540 patients were included in this analysis, of which 33 were observational studies of successful vs failed CTO-PCI, 19 were observational studies of CTO-PCI vs no CTO-PCI, and 6 were randomized controlled trials (RCTs). In observational studies, but not RCTs, CTO-PCI was associated with better clinical outcomes. Odds ratios (ORs) and 95% confidence intervals (CIs) for all-cause mortality, MACE, and MI were 0.52 (95% CI, 0.42-0.64), 0.46 (95% CI, 0.37-0.58), 0.66 (95% CI, 0.50-0.86), respectively for successful vs failed CTO-PCI studies; 0.38 (95% CI, 0.31-0.45), 0.57 (95% CI, 0.42-0.78), 0.65 (95% CI, 0.42-0.99), respectively, for observational studies of CTO-PCI vs no CTO-PCI; 0.72 (95% CI, 0.39-1.32), 0.69 (95% CI, 0.38-1.25), and 1.04 (95% CI, 0.46-2.37), respectively for RCTs. Conclusions. CTO-PCI is associated with better subsequent clinical outcomes in observational studies but not in RCTs. Appropriately powered RCTs are needed to conclusively determine the impact of CTO-PCI on clinical outcomes.
AB - Objectives. Chronic total occlusion (CTO) percutaneous coronary intervention (PCI) can improve patient symptoms, but it remains controversial whether it impacts subsequent clinical outcomes. Methods. In this systematic review and meta-Analysis, we queried PubMed, ScienceDirect, Cochrane Library, Web of Science, and Embase databases (last search: September 15, 2021). We investigated the impact of CTO-PCI on clinical events including all-cause mortality, cardiovascular death, myocardial infarction (MI), major adverse cardiovascular event (MACE), stroke, subsequent coronary artery bypass surgery, target-vessel revascularization, and heart failure hospitalizations. Pooled analysis was performed using a random-effects model. Results. A total of 58 publications with 54,540 patients were included in this analysis, of which 33 were observational studies of successful vs failed CTO-PCI, 19 were observational studies of CTO-PCI vs no CTO-PCI, and 6 were randomized controlled trials (RCTs). In observational studies, but not RCTs, CTO-PCI was associated with better clinical outcomes. Odds ratios (ORs) and 95% confidence intervals (CIs) for all-cause mortality, MACE, and MI were 0.52 (95% CI, 0.42-0.64), 0.46 (95% CI, 0.37-0.58), 0.66 (95% CI, 0.50-0.86), respectively for successful vs failed CTO-PCI studies; 0.38 (95% CI, 0.31-0.45), 0.57 (95% CI, 0.42-0.78), 0.65 (95% CI, 0.42-0.99), respectively, for observational studies of CTO-PCI vs no CTO-PCI; 0.72 (95% CI, 0.39-1.32), 0.69 (95% CI, 0.38-1.25), and 1.04 (95% CI, 0.46-2.37), respectively for RCTs. Conclusions. CTO-PCI is associated with better subsequent clinical outcomes in observational studies but not in RCTs. Appropriately powered RCTs are needed to conclusively determine the impact of CTO-PCI on clinical outcomes.
KW - Chronic total occlusion
KW - Clinical outcomes
KW - Meta-Analysis
KW - Percutaneous coronary intervention
KW - Systematic review
UR - http://www.scopus.com/inward/record.url?scp=85146063963&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:85146063963
SN - 1042-3931
VL - 34
SP - E763-E775
JO - Journal of Invasive Cardiology
JF - Journal of Invasive Cardiology
IS - 11
ER -