Evidence map›Paper›PMID 41369909›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

High-Risk Bleeding in Acute Myeloid Leukemia: Clinical Presentation, Laboratory Markers, and Mortality Trends.

Mohammed Abdulgayoom, Yousef Al-Asa'd, Ahmed Ali, Abdulrahman F Al-Mashdali, Hawra Shawaylia, Dina Sameh Soliman, Deena Mudawi, Feryal Abbas, Omran Almokdad, Anil Ellahie and 2 more

Abstract read
In one paragraph

Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. 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

12 authors.

Mohammed AbdulgayoomDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.ORCID 0000-0003-0622-8455
Yousef Al-Asa'dDepartment of Internal Medicine, Hamad General Hospital, HMC, Doha, Qatar.
Ahmed AliDepartment of Internal Medicine, Hamad General Hospital, HMC, Doha, Qatar.
Abdulrahman F Al-MashdaliDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.ORCID 0000-0002-1393-5302
Hawra ShawayliaDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.
Dina Sameh SolimanDepartment of Laboratory Medicine and Pathology, National Center for Cancer Care and Research, Doha, Qatar.
Deena MudawiDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.
Feryal AbbasDepartment of Laboratory Medicine and Pathology, National Center for Cancer Care and Research, Doha, Qatar.
Omran AlmokdadDepartment of Clinical Imaging, Interventional Radiology Section, Hamad General Hospital, HMC, Doha, Qatar.
Anil EllahieDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.
Honar CherifDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.
Shehab MohamedDepartment of Hematology, National Center for Cancer Care and Research, HMC, Doha, Qatar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundSevere bleeding is a major complication in acute myeloid leukemia (AML), contributing to early mortality. While thrombocytopenia and coagulopathy are known risk factors, the clinical and laboratory features surrounding haemorrhagic events in real-world AML cohorts require further elucidation.ObjectivesTo assess the frequency, sites, clinical features, laboratory findings, and outcomes of Grade ≥3 bleeding in AML patients.MethodsThis retrospective study reviewed 214 AML patients treated between 2012 and 2021 at a tertiary centre in Qatar. Patients with WHO Grade ≥3 bleeding were analysed for clinical, laboratory, cytogenetic, and outcome data.ResultsThirty-five patients (16.3%) had Grade ≥3 bleeding, most commonly intracranial (86%), presenting with neurological symptoms (80%). Events occurred mainly during or soon after induction chemotherapy (40%). Median haemoglobin and platelet count at bleeding were 7.1 g/dL and 11 × 10

Indexed as

HemorrhageLeukemia, Myeloid, AcuteAdolescentAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedQatarRetrospective StudiesRisk FactorsYoung Adultacute myeloid leukemiaAMLbleedinghemorrhageintracranial hemorrhage

Identifiers

PMID41369909
PMCPMC12696292

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Registered trials

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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.