Tanriverdi L. H., Barrett A., Kalyanasundaram A., Zafar M. A., Ziganshin B. A., Elefteriades J. A.
VASCULAR PHARMACOLOGY, cilt.159, sa.107494, ss.1-8, 2025 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
159
Sayı:
107494
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Basım Tarihi:
2025
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Doi Numarası:
10.1016/j.vph.2025.107494
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Dergi Adı:
VASCULAR PHARMACOLOGY
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Derginin Tarandığı İndeksler:
Scopus, Science Citation Index Expanded (SCI-EXPANDED), Academic Search Premier, BIOSIS, CAB Abstracts, Chemical Abstracts Core, MEDLINE, Veterinary Science Database
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Sayfa Sayıları:
ss.1-8
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İnönü Üniversitesi Adresli:
Evet
Özet
Objective
Studies investigating the efficacy of β-blocker agents for patients with
thoracic aortic aneurysm (TAA) have produced heterogeneous and conflicting results. We assess the effects of β-blockers on clinical outcomes in patients with TAA.
Methods
A systematic literature search was performed through Ovid MEDLINE, EMBASE, Web of Science, Pubmed and Cochrane CENTRAL, all from inception to April 30, 2024.
Randomized controlled trials (RCTs) exploring the effect of β-blocker agents in patients with TAA were considered for inclusion, with no population restriction. Inverse variance–weighted random-effects model was used. The overall risk of bias assessment was conducted by Cochrane Risk of Bias 2 tool. The primary outcome was aortic events during follow-up.
Results
We included a total of 161 patients with TAA (mean age, 27.6 years; 80 [49.7 %] male, mean follow-up 6.7 years) in 4 RCTs. The pooled risk ratio in the β-blocker arm for aortic events was 0.74 [95 % CI (0.20; 2.71), I
2: 0 %,
p = 0.64, low certainty of evidence (CoE)] when compared to placebo or no treatment in patients with TAA. The pooled risk ratios for aortic dissection or death (all-cause mortality) or in the β-blocker arm were 0.45 (95 % CI (0.10; 1.98), I2: 0 %,
p = 0.29, low CoE) and 0.58 (95 % CI (0.15; 2.24), I
2: 0 %,
p = 0.43, low CoE), respectively. The risks of aortic dissection, rupture, or death were comparable, regardless of agent, disease, and age.Conclusion
We found no evidence of benefit from β-blocker treatment for patients with TAA. More robust RCTs are needed to establish evidence-based recommendations.