Autoimmune Rheumatic Diseases and Outcomes Following Percutaneous Coronary Intervention: A Systematic Review and Meta-Analysis

被引:0
|
作者
Ang, Song Peng [1 ]
Chia, Jia Ee [2 ]
Misra, Kanchan [3 ]
Krittanawong, Chayakrit [4 ,5 ]
Iglesias, Jose [1 ,6 ]
Gewirtz, Daniel [1 ]
Mukherjee, Debabrata [2 ,7 ]
机构
[1] Rutgers Hlth Community Med Ctr, Dept Internal Med, 99 Highway 37 West, Toms River, NJ 08755 USA
[2] Texas Tech Univ, Dept Internal Med, Hlth Sci Ctr, El Paso, TX USA
[3] Rutgers Robert Wood Johnson Med Sch, Dept Radiol, New Brunswick, NJ USA
[4] NYU Langone Hlth, Cardiol Div, New York, NY USA
[5] NYU, Sch Med, New York, NY USA
[6] Hackensack Meridian Sch Med, Dept Internal Med, Nutley, NJ USA
[7] Texas Tech Univ, Dept Cardiovasc Med, Hlth Sci Ctr, El Paso, TX USA
关键词
autoimmune rheumatic diseases; percutaneous coronary intervention; lupus; rheumatoid arthritis; mortality; cardio-rheumatology; LONG-TERM OUTCOMES; CARDIOVASCULAR-DISEASE; LUPUS-ERYTHEMATOSUS; ARTERY-DISEASE; RISK-FACTORS; ARTHRITIS; ATHEROSCLEROSIS; INFLAMMATION; MECHANISMS; SYMPTOMS;
D O I
10.1177/00033197241255167
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Autoimmune Rheumatic Diseases (AIRDs) are associated with increased cardiovascular mortality. However, the post-percutaneous coronary intervention (PCI) outcomes in this population present a research gap, given the limited and discordant findings in existing studies. We conducted a systematic review and meta-analysis to assess the relationship between AIRDs and clinical outcomes after PCI; 9 studies with 7,027,270 patients (126,914 with AIRD, 6,900,356 without AIRD) were included. The AIRD cohort was characterized by an older age, a predominantly female demographic, and a greater prevalence of hypertension and diabetes mellitus. Over a mean follow-up period of 4.6 +/- 3.5 years, AIRD patients demonstrated significantly higher odds of all-cause mortality (odds ratio (OR) 1.45, 95% CI: 1.25-1.78, P < .001) and major adverse cardiovascular events (MACE) (OR 1.63, 95% CI: 1.01-2.62, P = .04) compared with non-AIRD patients. Sensitivity analysis using adjusted estimates, confirmed the higher all-cause mortality (hazard ratio 1.32, 95% CI: 1.05-1.64, P = .01). Patients with rheumatoid arthritis had a significantly elevated odds of all-cause mortality (OR 1.50, 95% CI: 1.27-1.77) and MACE (OR 1.18, 95% CI: 1.14-1.21). Our study demonstrated an association between AIRDs and suboptimal long-term outcomes post-PCI. Prospective studies are warranted to explore the risk factors of unfavorable prognoses in patients with AIRDs.
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