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        west china medical publishers
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        find Author "LI Lingya" 2 results
        • Outcomes of multivessel vs culprit lesion-only percutaneous coronary intervention in acute myocardial infarction and cardiogenic shock: a meta-analysis

          ObjectiveCompare the therapeutic effects of multivessel percutaneous coronary intervention (MV-PCI) and culprit-only revascularization strategy (C-PCI) in percutaneous coronary intervention (PCI) for patients with acute myocardial infarction complicated by cardiogenic shock (AMICS) and multivessel disease (MVD). MethodsThe PubMed, Embase, Cochrane Library, MEDLINE, Web of Science, CENTRAL, CNKI and WanFang Data databases were searched to collect studies comparing C-PCI vs. MV-PCI in patients with AMI and CS from inception to March 2, 2025. Methodological quality of the included studies was assessed using the Newcastle-Ottawa scale (NOS) and the risk of bias (ROB) tool. Meta-analysis was performed using RevMan software (version 5.4.0). ResultsA total of 18 studies (1 randomized controlled trial, 1 post-hoc analysis of a randomized controlled trial, and 16 retrospective observational studies), enrolling 101 693 patients. The results of the observational studies showed that MV-PCI was associated with higher risk of short-term mortality (OR=1.13, 95%CI 1.01 to 1.25, P=0.03), renal replacement therapy (OR=1.41, 95%CI 1.32 to 1.50, P<0.00001), and cerebrovascular accident events (OR=1.21, 95%CI 1.10 to 1.33, P=0.0001). No significant difference was observed in long-term mortality (OR=0.93, 95%CI 0.74 to 1.16, P=0.51), recurrent myocardial infarction (OR=1.16, 95%CI 0.97 to 1.39, P=0.10), repeat revascularization events (OR=0.83, 95%CI 0.58 to 1.20, P=0.33) and bleeding event rates (OR=1.01, 95%CI 0.71 to 1.34, P=0.97) between groups. The results remained consistent after adding the only randomized trial.ConclusionsIn patients with AMICS and concomitant MVD, C-PCI provides comparable survival benefits to MV-PCI and is associated with a reduced risk of all-cause mortality, cerebrovascular events, and the need for renal replacement therapy.

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        • The prognostic value of the triglyceride-glucose index in acute coronary syndrome: a meta-analysis

          ObjectiveTo systematically review the prognostic value of the triglyceride-glucose (TyG) index in predicting cardiovascular outcomes in patients with acute coronary syndrome (ACS). MethodsThe PubMed, Embase, Cochrane Library, Web of Science, CBM, WanFang Data and CNKI databases were electronically searched to collect cohort studies investigating the association between the TyG index and ACS prognosis from inception to January 25, 2025. Two reviewers independently screened literature, extracted data and assessed the risk of bias of the included studies. Meta-analysis was then performed by using RevMan 5.4 and Stata 18.0 software. ResultsA total of 18 studies involving 30 769 patients were included. The meta-analysis revealed that the TyG index was associated with ACS prognosis. When the TyG index was treated as a categorical variable, higher TyG index was significantly associated with an increased risk of MACE compared to lower TyG index (HR=1.94, 95%CI 1.62 to 2.31, P<0.001). Subgroup analysis indicated that the association between the TyG index and MACE remained independent of gender, age, participant characteristics, hypertension, and diabetes. In patients with ACS but without chronic kidney disease, the TyG index demonstrated a strong correlation with MACE (P=0.006). However, in ACS patients with concurrent chronic kidney disease, the TyG index did not appear to be a suitable predictor of MACE (P=0.22). ConclusionThe TyG index demonstrates a strong correlation with MACE in ACS patients, where a higher TyG index is associated with an increased incidence of MACE, indicating poorer prognosis. The TyG index may serve as a simple surrogate marker for prognostic prediction in ACS patients, independent of sex, age, participant characteristics, hypertension, and diabetes. However, its application is currently limited in ACS patients with comorbid CKD.

          Release date:2025-09-15 01:49 Export PDF Favorites Scan
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