Evidence map›Paper›PMID 30520671›Full record

ArticlePlatelets2019

Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding.

Gillian C Lowe, Roksana Fickowska, Rashid Al Ghaithi, Annabel Maclachlan, Paul Harrison, Will Lester, Steve P Watson, Bethan Myers, Justin Clark, Neil V Morgan

Open access · hybridAbstract read
In one paragraph

Article in Platelets, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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

10 authors at 4 institutions in 1 country.

Gillian C Lowea Comprehensive Care Haemophilia Centre , University Hospital Birmingham NHS Foundation Trust , Birmingham , UK.
Roksana Fickowskab Institute of Cardiovascular Sciences, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.
Rashid Al Ghaithic Institute of Inflammation and Ageing, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.
Annabel Maclachlanb Institute of Cardiovascular Sciences, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.
Paul Harrisonc Institute of Inflammation and Ageing, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.ORCID http://orcid.org/0000-0003-4610-8909
Will Lestera Comprehensive Care Haemophilia Centre , University Hospital Birmingham NHS Foundation Trust , Birmingham , UK.
Steve P Watsonb Institute of Cardiovascular Sciences, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.ORCID http://orcid.org/0000-0002-7846-7423
Bethan Myersd Department of Haematology , Lincoln County Hospital , Lincoln , UK.
Justin Clarkf Department of Gynaecology , Birmingham Women's and Children's NHS Foundation Trust , Birmingham , UK.
Neil V Morganb Institute of Cardiovascular Sciences, College of Medical and Dental Sciences , University of Birmingham , Birmingham , UK.ORCID http://orcid.org/0000-0001-6433-5692
University of Birmingham · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBBirmingham Women’s and Children’s NHS Foundation Trust · GBLincoln County Hospital · GB

Funding

British Heart Foundation CH/03/003/15571British Heart Foundation FS/13/70/30521British Heart Foundation FS/15/18/31317British Heart Foundation PG/13/36/30275British Heart Foundation RG/09/007
6 · The paper itself

Abstract

Heavy menstrual bleeding (HMB) is often undiagnosed in women and can cause discomfort and distress. A haemostatic cause for excessive bleeding is often not routinely investigated and can lead to hysterectomy at an early age. A prospective cohort study was carried out to determine whether certain patients with unexplained HMB have an underlying platelet function defect (PFD). The Genotyping and Phenotyping of Platelets (GAPP) study recruited 175 women with HMB and 44 unrelated volunteers from 25 Haemophilia Centres across the UK, and a tertiary gynaecology service. Bleeding history was assessed using the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool (ISTH-BAT). Platelet count, platelet size, haemoglobin and mean corpuscular volume were measured in whole blood using the Sysmex XN-1000 Haematology Analyzer. Platelet function testing using lumiaggregometry and flow cytometry was performed in patients included in this study. A PFD was identified in 47% (82/175) of patients with HMB. Cutaneous bleeding was the most frequent additional bleeding symptom (89% in PFD and 83% with no PFD). Whole blood platelet count was significantly lower (P < 0.0001) between the PFD group and no PFD group. The prevalence of anaemia did not differ between patients and healthy volunteers. Clinical evaluation alone is insufficient to determine presence of an underlying PFD in patients with HMB. Platelet function tests may be considered and clinical guidelines may include them in their algorithms. An appropriate diagnosis and subsequent tailored management of HMB may prevent unnecessary surgery and help manage future haemostatic challenges.

Indexed as

AdultBlood Cell CountBlood CoagulationBlood PlateletsFemaleHumansMean Platelet VolumeMenorrhagiaMiddle AgedPhenotypePlatelet AggregationPlatelet CountPlatelet Function TestsAggregometrybleedingheavy menstrual bleedingplatelet function defectsplatelet function testsplatelets

Identifiers

PMID30520671
PMCPMC6406209
OpenAlexW2903596421

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.