Evidence map›Paper›PMID 32801433›Full record

ArticleMedical archives (Sarajevo, Bosnia and Herzegovina)2020

Prevalence of FVIII Inhibitors Among Children with Hemophilia A: Experience at the Jordanian Royal Medical Services.

Raida Oudat, Muna Al-Maharmeh, Rasha Al-Ghrayeb, Tunia Ogeilat, Maher Kh Mustafa

Open access · greenAbstract read
In one paragraph

Article in Medical archives (Sarajevo, Bosnia and Herzegovina), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 53% 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, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
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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 2 institutions in 1 country.

Raida OudatDepartment of Hematopathology. Princess Iman Research and Laboratory Siences Centre, Royal Medical Services, Amman, Jordan.
Muna Al-MaharmehDepartment of Hematopathology. Princess Iman Research and Laboratory Siences Centre, Royal Medical Services, Amman, Jordan.
Rasha Al-GhrayebDepartment of Hematopathology. Princess Iman Research and Laboratory Siences Centre, Royal Medical Services, Amman, Jordan.
Tunia OgeilatDepartment of Hematopathology. Princess Iman Research and Laboratory Siences Centre, Royal Medical Services, Amman, Jordan.
Maher Kh MustafaDepartment of Pediatric Hematology and Medical Oncology, Queen Rania Hospital, Amman, Jordan.
King Hussein Medical Center · JOJordan Hospital · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionReplacement therapy is constantly required by Hemophilia A (HA) patients lacking coagulation factor VIII (FVIII). The most serious complication of this treatment is the development of neutralizing antibodies (inhibitors).

aimThe aim of this study is to determine the frequency of FVIII inhibitors among children treated for HA at the Jordanian Royal Medical Services.

methodsA total of 165 diagnosed HA patients receiving on-demand treatment, were tested for FVIII inhibitors between 2003 and 2018. The age range was 6 months to 16 years. Coagulation and inhibitor screening assays were performed, followed by Bethesda assay for inhibitor-positive samples to quantify FVIII inhibitor titers.

resultsOut of the 165 patients, 111 had severe hemophilia with FVIII level < 1%, 26 had moderate hemophilia with FVIII levels of 1-5% and 28 had mild hemophilia with FVIII levels of > 5%. Twenty patients had FVIII inhibitors, of whom 18 had high titers, 2 had low titers. The mean inhibitor level in low (titer) responders was 2.40 ± 0.85 BU, as opposed to 116.25 ±169.25 BU in high (titer) responders. In terms of disease severity, 18 of the 20 patients with FVIII inhibitors had severe HA, whereas two had moderate HA. No inhibitors were encountered in the mild HA group.

conclusionInhibitors only developed in moderate and severe cases of HA. The severity of the disease and age were the main contributing factors. The association between family history of inhibitors and the incidence of inhibitor formation warrants genetic evaluations to look for relevant mutations.

Indexed as

AdolescentAge FactorsAntibodies, NeutralizingBlood TransfusionChildChild, PreschoolFactor VIIIHemophilia AHumansImmunoglobulin GInfantJordanMaleSeverity of Illness IndexAntibodies, NeutralizingF8 protein, humanFactor VIIIImmunoglobulin GFVIII inhibitorsHemophilia A

Identifiers

PMID32801433
PMCPMC7406006
OpenAlexW3036678483

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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.