Evidence map›Paper›PMID 39958127›Full record

ArticleCureus2025

Clinical Spectrum and Treatment Outcomes of Rare Bleeding Disorders in Female Patients: A Two-Center Experience in North Pakistan.

Muhammad Usman, Nighat Shahbaz, Mehreen Ali Khan, Hira Tariq, Rafia Mahmood, Saad Jamshed, Raheel Iftikhar, Mehwish Gilani, Maryum Khan, Tahira Zafar

Abstract read
In one paragraph

Article in Cureus, 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. Laboratory and Clinical Analysis of Rare Coagulation Factor Deficiencies-A Respective Study of a Single Center from Northwest China.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

10 authors.

Muhammad UsmanClinical Hematology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Nighat ShahbazClinical Hematology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Mehreen Ali KhanHematology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Hira TariqEpidemiology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Rafia MahmoodHematology, Armed Forces Institute of Pathology, Rawalpindi, PAK.
Saad JamshedHematology and Oncology, Rochester Regional Health, Rochester, USA.
Raheel IftikharHematology and Oncology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Mehwish GilaniChemical Pathology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Maryum KhanClinical Hematology, Armed Forces Bone Marrow Transplant Centre Rawalpindi, Rawalpindi, PAK.
Tahira ZafarHematology, Hemophilia Treatment Center, Rawalpindi, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Rare bleeding disorders (RBDs) result from genetic mutations in clotting factors. These RBDs vary in prevalence and are often underdiagnosed due to mild symptoms. Treatment is challenging due to limited clinical data and primarily involves substituting deficient factors and using adjuvant therapies. Women with RBDs face unique risks, including gynecologic bleeding, hemorrhagic ovarian cysts, and complications during pregnancy. These issues can significantly impact their quality of life and employment. This study was conducted to characterize the patterns of bleeding disorders, clinical manifestations, and treatment outcomes in female patients. Methods In this cross-sectional study, we included patients from the Hemophilia Treatment Center (HTC) and Armed Forces Bone Marrow Transplant Centre (AFBMTC) Rawalpindi between 2011 and 2023, using a convenience sampling technique. Data were extracted from patient files, including medical history, factor activity levels, symptoms, treatments, and medications. Eligible participants had congenital coagulation factor deficiencies, while those with platelet function or acquired coagulation disorders were excluded. Results In our study of 50 patients with RBD, the median age at bleeding presentation was two years; 72% of cases were born of consanguineous marriages, and 57% had a positive family history of bleeding disorders. Factor V deficiency was the most prevalent (28%), and major bleeding episodes occurred in 52% of cases. The predominant clinical presentations included menorrhagia (74%) and epistaxis (58%). Treatment primarily involved antifibrinolytics (98%) and FFP transfusions (96%), with significant associations identified among various risk factors related to bleeding. All patients were counseled regarding local measures for bleeding control. There was a moderate correlation found between factors V and VII with the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool (ISTH BAT) score. There is a weak correlation between factors X and XI with the ISTH BAT score. There was no correlation found in factor I, factor XI, factor XII, and combined factors V+VIII deficiency. Conclusion Women with RBDs face a spectrum of bleeding challenges, significantly impacting their quality of life and reproductive health. Early diagnosis and personalized treatment strategies are paramount in mitigating bleeding risks and enhancing patient outcomes.

Indexed as

clinical spectrumfactor deficiencynorth pakistanrare bleeding disorderswomen with rbds

Identifiers

PMID39958127
PMCPMC11830413

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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.