Evidence map›Paper›PMID 30772866›Full record

ArticleBMJ open2019

Novel use of tranexamic acid to reduce the need for Nasal Packing in Epistaxis (NoPac) randomised controlled trial: research protocol.

Adam Reuben, Andrew Appelboam, Andy Barton, Patricia Jane Vickery, Richard Body, Malcolm Hilton, Jason Coppell, Paul Ewings

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 3 institutions in 1 country.

Adam ReubenAcademic Department of Emergency Medicine, Royal Devon and Exeter Hospital NHS Foundation Trust, Exeter, UK.
Andrew AppelboamAcademic Department of Emergency Medicine, Royal Devon and Exeter Hospital NHS Foundation Trust, Exeter, UK.
Andy BartonResearch Design Service South West, Bristol, UK.
Patricia Jane VickeryPeninsula Clinical Trials Unit, Plymouth University, Plymouth, UK.
Richard BodyDepartment of Emergency Medicine, Manchester Royal Infirmary, Manchester, UK.
Malcolm HiltonDepartment of Otolaryngology, Royal Devon and Exeter Hospital, NHS Foundation Trust, Exeter, UK.
Jason CoppellDepartment of Haematology, Royal Devon and Exeter Hospital, NHS Foundation Trust, Exeter, UK.
Paul EwingsResearch Design Service South West, Bristol, UK.
Royal Devon and Exeter Hospital · GBManchester Royal Infirmary · GBUniversity of Plymouth · GB

Funding

Department of Health PB-PG-0215-36142Department of Health PDF-2012-05-193
6 · The paper itself

Abstract

introductionPatients presenting to emergency departments (EDs) with epistaxis uncontrolled by subsequent simple first aid measures or application of topical vasoconstrictors will typically undergo anterior nasal packing. Packing is effective, but can be extremely painful and unpleasant and patients usually need hospital admission. Tranexamic acid (TXA) is a cheap, safe, readily available antifibrinolytic agent known to be beneficial in a variety of clinical settings where uncontrolled bleeding may be a problem. Anecdotal evidence suggests that topical TXA may be of value in persistent epistaxis; however, further evaluation is required. METHODS AND ANALYSIS: This is a multicentre, double-blind, parallel group, randomised, controlled trial comparing the use of topical intranasal TXA with indistinguishable placebo in adults presenting to UK EDs with persistent atraumatic epistaxis. Follow-up is at 1 week by structured telephone review. The primary outcome measure is the subsequent need for anterior nasal packing in the ED. Key secondary outcomes include the need for hospital admission, blood transfusion and/or further treatment for epistaxis during the index ED attendance. Recruiting 450 patients will provide 90% power to demonstrate an absolute reduction in packing rate from 95% to 85%. An improvement of this magnitude would be of significant benefit to patients and healthcare providers and justify a change to standard practice. Given the low cost of TXA and its short administration time, a full economic evaluation is not being undertaken. ETHICS AND DISSEMINATION: The study has been approved by the South West-Bristol Research Ethics Committee (reference 17/SW/0010). We aim to publish the findings in a high impact, international peer-reviewed journal. Results will also be shared with the Hereditary Haemorrhagic Telangiectasia foundation and telangiectasia UK for dissemination through appropriate related forums. TRIAL REGISTRATION NUMBER: ISRCTN34153772 and EudraCT No: 2016-001530-10.

Indexed as

Emergency Service, HospitalAdministration, IntranasalAdministration, TopicalAntifibrinolytic AgentsDouble-Blind MethodEndotamponadeEpistaxisHumansMulticenter Studies as TopicRandomized Controlled Trials as TopicTranexamic AcidTreatment OutcomeAntifibrinolytic AgentsTranexamic Acidemergencyepistaxisintranasalpackingtopicaltranexamic acid

Identifiers

PMID30772866
PMCPMC6398761
OpenAlexW2911929055

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.