Evidence map›Paper›PMID 40283085›Full record

ArticleLife (Basel, Switzerland)2025

Inherited Hemophilia-A Multidimensional Chronic Disease That Requires a Multidisciplinary Approach.

Cristina Claudia Tarniceriu, Loredana Liliana Hurjui, Daniela Maria Tanase, Anca Haisan, Razvan Tudor Tepordei, Gabriel Statescu, Simona Alice Partene Vicoleanu, Ancuta Lupu, Vasile Valeriu Lupu, Manuela Ursaru and 1 more

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Cristina Claudia TarniceriuDepartment of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Loredana Liliana HurjuiDepartment of Morpho-Functional Science II, Discipline of Physiology, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0003-3803-9405
Daniela Maria TanaseDepartment of Internal Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0002-7144-2506
Anca HaisanDepartment of Emergency Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0001-8073-8192
Razvan Tudor TepordeiDepartment of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0001-6325-7370
Gabriel StatescuDepartment of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Simona Alice Partene VicoleanuDepartment of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Ancuta LupuDepartment of Mother and Child, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0001-8147-3632
Vasile Valeriu LupuDepartment of Surgical Sciences I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0003-2640-8795
Manuela UrsaruDepartment of Surgical Sciences I, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Alin Horatiu NedelcuDepartment of Morpho-Functional Science I, Discipline of Anatomy, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.ORCID 0000-0002-0024-0237

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArticular damage is a marker of hereditary hemophilia, especially affecting the large joints of the upper and lower limbs. This retrospective study aimed to emphasize that hereditary coagulopathies, specifically hemophilia A and B, require a multidisciplinary approach due to their complex nature. The primary objectives of the paper are to determine the prevalence of hemophilic arthropathy among individuals with hemophilia in the northeastern region of Romania, identify the most frequently affected joints, and assess whether there is a correlation between the development of hemophilic arthropathy, the type of hemophilia, and the treatment received. The secondary objectives of the work are to identify a series of particularities regarding the occurrence of the comorbidities depending on the type of hemophilia and the treatment and severity of arthropathies. MATERIALS AND

methodsWe conducted a retrospective study that included 36 adults with hemophilia A and B. The status of the osteoarticular system was evaluated using the modified Hemophilia Joint Health Score (mHJHS). Twelve joints were evaluated using the following parameters: swelling, duration of swelling, muscle atrophy, joint pain, crepitus on motion, flexion loss, and extension loss. RESULTS AND DISCUSSIONS: The most severe damage was found in the joints of the knees, ankles, elbows, and wrists. In the knees, severe damage was noted significantly more frequently in the right knee (50% vs. 33.3%;

conclusionsIt is currently essential to determine methods for comprehensive hemophilia care that involves multidisciplinary medical services necessary for the diagnosis, treatment, and management of the condition and its complications and comorbidities.

Indexed as

arthropathiescomorbiditiesHCV infectionhemophiliajoint damage

Identifiers

PMID40283085
PMCPMC12028639

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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.