Evidence map›Paper›PMID 37284359›Full record

ArticleCureus2023

A Case Report of Idiopathic Acquired Hemophilia Type A.

Liz A Amu-Hernández, Cristina Marzo-Alonso, Albert Tugues-Peiró, Eva P Vicente-Pascual, Paula Monteagudo-Aguilar

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

5 authors at 1 institution in 1 country.

Liz A Amu-HernándezHematology and Hemostasis, Arnau de Vilanova University Hospital, Lleida, ESP.
Cristina Marzo-AlonsoThrombosis and Hemostasis Unit, Arnau de Vilanova University Hospital, Lleida, ESP.
Albert Tugues-PeiróThrombosis and Hemostasis Unit, Arnau de Vilanova University Hospital, Lleida, ESP.
Eva P Vicente-PascualThrombosis and Hemostasis Unit, Arnau de Vilanova University Hospital, Lleida, ESP.
Paula Monteagudo-AguilarInternal Medicine, Arnau de Vilanova University Hospital, Lleida, ESP.
Hospital Universitari Arnau de Vilanova · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquired hemophilia A (AHA) is a rare hemorrhagic coagulopathy caused by the presence of autoantibodies that inhibit the activity of factor VIII (FVIII). Its diagnosis requires a high index of suspicion. It should be suspected in the presence of extensive hematomas or intense mucosal bleeding in patients with no history of previous trauma or hemorrhagic symptoms. We present two clinical cases of AHA, with different presentations and therapeutic management based on immunosuppression and hemostatic control through bypass agents such as activated recombinant FVII (rFVIIa; Novoseven®) and activated prothrombin complex concentrate (aPCC; Feiba®). The first case was an idiopathic AHA that presented with extensive subcutaneous hematomas with inhibitor titer >40 Bethesda units/ml (BU/mL), prolonged activated partial thromboplastin time (aPTT), and FVIII of 0.8%. In contrast, the second case involved a patient with a history of autoimmune disease, who presented with epistaxis and inhibitor titer of 10.8 BU/ml and FVIII of 5.3%.

Indexed as

acquired hemophiliaautoantibodiesauto immunebleeding disorderscoagulationfactor viiifactor viii inhibitorfeibanovoseven

Identifiers

PMID37284359
PMCPMC10241219
OpenAlexW4379599687

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.