Evidence map›Paper›PMID 30937199›Full record

ArticleCase reports in hematology2019

A Case of Acquired Haemophilia A in a Patient with Chronic Myelomonocytic Leukaemia.

Takeshi Araki, Shinya Ohata, Kohei Okamoto, Kazuhide Morimoto, Mana Hiraishi, Shinichiro Yamada, Ishikazu Mizuno, Takeshi Sugimoto

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Case reports in hematology, 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
0.5field-weighted citation impact, top 34% 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, 3 citations in OpenAlex.

  1. Article
  2. 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

8 authors at 3 institutions in 1 country.

Takeshi ArakiDepartment of Hematology and Oncology, Kita-Harima Medical Center, Hyogo, Japan.
Shinya OhataDepartment of Hematology and Oncology, Kita-Harima Medical Center, Hyogo, Japan.
Kohei OkamotoDepartment of Nephrology, Kobe University Hospital, Hyogo, Japan.
Kazuhide MorimotoDivision of Laboratory Medicine, Kita-Harima Medical Center, Hyogo, Japan.
Mana HiraishiDepartment of Cardiology, Kita-Harima Medical Centre, Hyogo, Japan.
Shinichiro YamadaDepartment of Cardiology, Kita-Harima Medical Centre, Hyogo, Japan.
Ishikazu MizunoDepartment of Hematology, Hyogo Cancer Center, Akashi, Japan.
Takeshi SugimotoDepartment of Hematology and Oncology, Kita-Harima Medical Center, Hyogo, Japan.ORCID 0000-0002-8121-5323
Tokyo-Kita Medical Center · JPHyogo Prefectural Cancer Center · JPKobe University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 67-year-old male, with a known diagnosis of myelodysplastic syndromes with multilineage dysplasia (MDS-MLD) was admitted to our hospital with a primary complaint of subcutaneous bleeding in his left thigh. Laboratory data showed anaemia and prolongation of activated partial thromboplastin time (85.8 s, normal range 24-39 s) without thrombocytopenia. Coagulation factor VIII (FVIII) activity was less than 1% (normal range 60-150%), and a FVIII inhibitor was identified and quantified at 166 BU/mL to indicate a diagnosis of acquired haemophilia A (AHA). A recent, but sustained circulating monocytosis (>1 × 10

Identifiers

PMID30937199
PMCPMC6415290
OpenAlexW2916952651

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.