Evidence map›Paper›PMID 41995531›Full record

ArticleMedicine2026

Appropriateness of terlipressin use and its association with clinical efficacy and safety: A real-world cohort study of 240 hospitalized patients.

Yifei Peng, Hongxia Duan, Meng Li, Ke Xiang, Jialin Li

Abstract read
In one paragraph

Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Yifei PengDepartment of Pharmacy, Leshan Hospital of Traditional Chinese Medicine, Affiliated to Chengdu University of Chinese Medicine, Leshan, China.ORCID 0009-0009-3187-1531
Hongxia Duan
Meng Li
Ke Xiang
Jialin Li

Funding

Leshan Science and Technology Program No. 25ZDYFSF0061
6 · The paper itself

Abstract

This study aimed to evaluate the appropriateness of terlipressin use and assess its effects on coagulation parameters in 240 hospitalized patients treated between January 2024 and January 2025 in a real-world, single-center retrospective cohort. Clinical appropriateness, encompassing diagnostic indication, initial dosing, and administration route, was rigorously evaluated against current clinical guidelines and the manufacturer's prescribing information. Key coagulation parameters - prothrombin time, thrombin time, activated partial thromboplastin time, and fibrinogen - were analyzed before and after treatment using paired-sample t tests, and patients were stratified into short-course (≤5 days) and long-course (≥6 days) therapy groups to examine the impact of treatment duration on outcomes using independent-sample t tests. The analysis revealed a high degree of appropriateness: 231 patients (96.3%) received terlipressin for guideline-consistent indications, 143 patients (59.6%) were administered the recommended initial bolus dose of 2 mg, and 185 cases (77.1%) employed the advised slow intravenous infusion route. Treatment with terlipressin significantly improved coagulation, with prothrombin time decreasing by a mean of 1.43 seconds and fibrinogen increasing by 0.11 g/L (both P < .01). However, extending the treatment course beyond 5 days offered no additional coagulation benefit, as no parameters showed significant improvement in the long-course compared with the short-course group (all P > .05). These results underscore that terlipressin use was largely appropriate for indication and route, but extending therapy beyond 5 days provided no additional coagulation benefit. This finding supports stricter adherence to guideline-recommended treatment duration to promote more rational and effective use of terlipressin in clinical practice.

Indexed as

Blood CoagulationTerlipressinVasoconstrictor AgentsAgedCohort StudiesFemaleFibrinogenHospitalizationHumansMaleMiddle AgedProthrombin TimeRetrospective StudiesTreatment OutcomeFibrinogenTerlipressinVasoconstrictor Agentsclinical rational drug usesomatostatinterlipressinupper gastrointestinal bleeding in cirrhosis

Identifiers

PMID41995531
PMCPMC13095263

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.