Evidence map›Paper›PMID 32199584›Full record

SynthesisBritish journal of anaesthesia2020

Effect of tranexamic acid by baseline risk of death in acute bleeding patients: a meta-analysis of individual patient-level data from 28 333 patients.

Francois-Xavier Ageron, Angele Gayet-Ageron, Katharine Ker, Timothy J Coats, Haleema Shakur-Still, Ian Roberts, Antifibrinolytics Trials Collaboration

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in British journal of anaesthesia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Francois-Xavier AgeronClinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK; Emergency Department, Lausanne University Hospital, CHUV, Lausanne, Switzerland. Electronic address: fxageron@gmail.com.
Angele Gayet-AgeronDivision of Clinical Epidemiology, University Hospitals of Geneva, Geneva, Switzerland.
Katharine KerClinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK.
Timothy J CoatsEmergency Medicine, University of Leicester, Leicester, UK.
Haleema Shakur-StillClinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK.
Ian RobertsClinical Trials Unit, London School of Hygiene and Tropical Medicine, London, UK.
Antifibrinolytics Trials Collaboration
University of London · GBLondon School of Hygiene & Tropical Medicine · GBUniversity Hospital of Geneva · CHUniversity of Leicester · GB

Funding

Department of Health 06/303/20Department of Health 11/01/04Department of Health 14/190/01Medical Research Council MR/M009211/1
6 · The paper itself

Abstract

backgroundEarly administration of the antifibrinolytic drug tranexamic acid reduces death from bleeding in trauma and postpartum haemorrhage. We examined how the effectiveness and safety of antifibrinolytic drugs varies by the baseline risk of death as a result of bleeding.

methodsWe performed an individual patient-level data meta-analysis of randomised trials including more than 1000 patients that assessed antifibrinolytics in acute severe bleeding. We identified trials performed between January 1, 1946 and July 5, 2018 (PROSPERO, number 42016052155).

resultsTwo randomised trials were selected where 28 333 patients received tranexamic acid treatment within 3 h after the onset of acute bleeding. Baseline characteristics to estimate the risk of death as a result of bleeding were divided into four categories: Low (0-5%), intermediate (6-10%), high (11-20%), and very high (>20%). Most patients had a low baseline risk of death as a result of bleeding (23 008 [81%]). Deaths as a result of bleeding occurred in all baseline risk categories with 240 (1%), 202 (8%), 232 (14%), and 357 (30%) deaths in the low-, intermediate-, high-, and very high-risk categories, respectively. The effectiveness of tranexamic acid did not vary by baseline risk when given within 3 h after bleeding onset (P=0.51 for interaction term). There was no increased risk of vascular occlusive events with tranexamic acid and it did not vary by baseline risk categories (P=0.25).

conclusionsTranexamic acid appears to be safe and effective regardless of baseline risk of death. Because many deaths are in patients at low and intermediate risk, tranexamic acid use should not be restricted to the most severely injured or bleeding patients.

Indexed as

Acute DiseaseAdultAntifibrinolytic AgentsFemaleHemorrhageHumansMaleRandomized Controlled Trials as TopicRiskTranexamic AcidYoung AdultAntifibrinolytic AgentsTranexamic Acidantifibrinolyticsbleedingcoagulopathymortalitypostpartum haemorrhagetrauma

Identifiers

PMID32199584
PMCPMC7271662
OpenAlexW3010729818

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.