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Meta-Analysis
. 2018 Nov;97(48):e13437.
doi: 10.1097/MD.0000000000013437.

Terlipressin for the treatment of acute variceal bleeding: A systematic review and meta-analysis of randomized controlled trials

Xinmiao Zhou  1   2   3 , Dhiraj Tripathi  4 , Tingxue Song  1   3 , Lichun Shao  3 , Bing Han  1   2 , Jia Zhu  1   5 , Dan Han  1 , Fufang Liu  1   2 , Xingshun Qi  1
Affiliations
Meta-Analysis

Terlipressin for the treatment of acute variceal bleeding: A systematic review and meta-analysis of randomized controlled trials

Xinmiao Zhou et al. Medicine (Baltimore). 2018 Nov.

Abstract

Background and aim: Acute variceal bleeding (AVB) is life-threatening. We aimed to systematically review the current evidence regarding the efficacy and safety of terlipressin for AVB in liver cirrhosis.

Methods: We searched the PubMed, EMBASE, and Cochrane Library databases. The reference list was also hand-searched. Using a random-effect model, we combined the data obtained according to the different time points when the events developed. Odds ratio (OR) and weighted mean difference (WMD) were calculated. Quality of evidence was evaluated by the GRADE methodology.

Results: Thirty randomized controlled trials with 3344 patients were included. Compared with no vasoactive drug, terlipressin significantly improved the control of bleeding within 48 hours (OR = 2.94, P = .0008) and decreased the in-hospital mortality (OR = 0.31, P = .008). Compared with somatostatin, terlipressin had a significantly higher risk of complications (OR = 2.44, P = .04). Compared with octreotide, terlipressin had a significantly inferior control of bleeding within 24 hours (OR = 0.37, P = .007). Compared with vasopressin, terlipressin had a significantly lower risk of complications (OR = 0.15, P = .02). Compared with terlipressin combined with endoscopic variceal ligation, terlipressin alone had significantly higher 5-day treatment failure (OR = 14.46, P = .01) and transfusion requirements within 49 to 120 hours (WMD = 1.20, P = .002). No outcome was significantly different between terlipressin and sclerotherapy. Compared with balloon tamponade, terlipressin significantly decreased the 30-day rebleeding (OR = 0.05, P = .001) and transfusion requirements (WMD = -2.70, P = .02). Quality of evidence was very low to moderate.

Conclusion: Our findings were in accordance with the current recommendations regarding terlipressin for the treatment of AVB in cirrhosis. However, due to low quality of evidence, further studies are recommended.

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Conflict of interest statement

The authors have no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Flow chart of study selection.
Figure 2
Figure 2
Forest plot showing the difference in the control of bleeding in patients treated with terlipressin compared with no vasoactive drugs.
Figure 3
Figure 3
Forest plot showing the difference in the mortality in patients treated with terlipressin compared with no vasoactive drugs.
Figure 4
Figure 4
Forest plot showing the difference in the rebleeding in patients treated with terlipressin compared with balloon tamponade.
Figure 5
Figure 5
An overview of our findings.
See this image and copyright information in PMC

References

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