Comparison of 12-to 24-Hour Versus 72-Hour Intravenous Terlipressin in Patients With Acute Esophageal Variceal Bleeding: A Systematic Review and Meta-analysis

被引:0
作者
Al Hayek, Mohammad [1 ]
Sawaf, Bisher [2 ]
Abbarh, Shahem [3 ]
Dhoop, Sudheer [2 ]
Khashan, Abdallah [4 ]
Hassan, Ahmed [5 ]
Alzubi, Alhasan Saleh [6 ]
Abdelwahed, Abdelrahman F. [7 ]
Alzein, Abdussalam I. A. [8 ]
Nounou, Mohamedhen Vall [9 ]
Alastal, Yaseen [10 ]
Elhadi, Muhammed [11 ]
机构
[1] Damascus Univ, Fac Med, Damascus, Syria
[2] Univ Toledo, Internal Med, 4430 Holland,Sylvania, Toledo, OH 43623 USA
[3] Georgetown Univ, Internal Med, MedStar Hlth, Baltimore, MD USA
[4] Henrico Doctors Hosp, Richmond, VA USA
[5] South Valley Univ, Fac Med, Qena, Egypt
[6] Marshall Univ, Joan C Edwards Sch Med, Internal Med, Huntington, WV USA
[7] East Carolina Univ, Internal Med, Greenville, NC USA
[8] Sebha Univ, Fac Med, Sebha, Libya
[9] Univ Nouakchott Al Aasriya, Fac Med, Nouakchott, Mauritania
[10] Univ Toledo, Dept Gastroenterol, Toledo, OH USA
[11] Korea Univ, Coll Med, 145 Anam Ro, Seoul, South Korea
关键词
esophageal variceal; terlipressin; meta-analysis; bleeding; vasopressors; MANAGEMENT; CIRRHOSIS; LIGATION; MULTICENTER; HEMORRHAGE; DIAGNOSIS; GUIDANCE; RISK;
D O I
10.1177/87551225241311444
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To compare the efficacy and safety of 12-24 hours versus 72 hours of intravenous terlipressin therapy in patients with acute esophageal variceal bleeding (AVB). Data sources: A systematic search was conducted using PubMed, Scopus, Cochrane Library, Google Scholar, Web of Science, VHL, and ClinicalTrials.gov for studies published up to February 24, 2024. The search terms included "terlipressin," "variceal bleeding," "short-course," and "72-hour treatment." Study selection and data extraction: Randomized controlled trials (RCTs) comparing 12 to 24 hours with 72 hours of terlipressin therapy in patients with AVB were included. Studies not meeting these criteria or focusing on unrelated outcomes were excluded. Two authors conducted data extraction and bias assessment independently, with discrepancies resolved by a third reviewer. Baseline characteristics and outcomes (rebleeding and mortality within 5 days) were recorded. Results: Four RCTs with 469 patients were included in the analysis. There were no significant differences observed in 5-day rebleeding rates (OR = 0.943; 95% CI [0.384, 2.317]; P = 0.898) or mortality rates (OR = 0.386; 95% CI [0.066, 2.260]; P = 0.291) between terlipressin treatment durations of 12 to 24 hours and 72 hours within the first 5 days posttreatment. In addition, no heterogeneity was found in both variables (P > 0.1). Conclusion: This meta-analysis indicates that there is no significant difference in rebleeding rates or mortality between 12 to 24 hours and 72 hours of terlipressin therapy for AVB within 5 days posttreatment. Shorter treatment durations may offer advantages in terms of resource utilization and adverse event risk but require further validation through studies involving larger patient populations.
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