Evidence map›Paper›PMID 41606623›Full record

ArticleBMC women's health2026

Improvement in health‑related quality of life in patients with heavy menstrual bleeding after treatment and its association with hereditary bleeding disorders.

M A Cabrero Segurado, J M Bastida, C Gilabert, M Sánchez Barba, L Díaz-Ajenjo, A M Gonzalez-Galan, A Lama-Villanueva, P García-Jaen, M G de la Cruz Corral, M L Hernandez Hernandez and 10 more

Abstract read
In one paragraph

Article in BMC women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

M A Cabrero Segurado *Servicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain. macabrero@saludcastillayleon.es.
J M Bastida *Servicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
C GilabertServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
M Sánchez BarbaDepartamento de Estadística, Universidad de Salamanca (USAL), Salamanca, Spain.
L Díaz-AjenjoCentro de Investigación del Cáncer, Instituto de Investigación Biomédica de Salamanca (IBSAL), CSIC - Universidad de Salamanca (USAL), Universidad de Salamanca (USAL), Salamanca, Spain.
A M Gonzalez-GalanCentro de Investigación del Cáncer, Instituto de Investigación Biomédica de Salamanca (IBSAL), CSIC - Universidad de Salamanca (USAL), Universidad de Salamanca (USAL), Salamanca, Spain.
A Lama-VillanuevaCentro de Investigación del Cáncer, Instituto de Investigación Biomédica de Salamanca (IBSAL), CSIC - Universidad de Salamanca (USAL), Universidad de Salamanca (USAL), Salamanca, Spain.
P García-JaenServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
M G de la Cruz CorralServicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
M L Hernandez HernandezServicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
M Perez-GarciaUnidad de Enfermedades Raras del Adulto, Servicio de Medicina Interna, Instituto de Investigación Biomédica de Salamanca (IBSAL), Complejo Asistencial Universitario de Salamanca (CAUSA), Universidad de Salamanca (USAL), Salamanca, Spain.
N S Gutierrez-SampedroUnidad de Enfermedades Raras del Adulto, Servicio de Medicina Interna, Instituto de Investigación Biomédica de Salamanca (IBSAL), Complejo Asistencial Universitario de Salamanca (CAUSA), Universidad de Salamanca (USAL), Salamanca, Spain.
C Junco-DopicoUnidad de Enfermedades Raras del Adulto, Servicio de Medicina Interna, Instituto de Investigación Biomédica de Salamanca (IBSAL), Complejo Asistencial Universitario de Salamanca (CAUSA), Universidad de Salamanca (USAL), Salamanca, Spain.
S Alvaro-SanchezUnidad de Enfermedades Raras del Adulto, Servicio de Medicina Interna, Instituto de Investigación Biomédica de Salamanca (IBSAL), Complejo Asistencial Universitario de Salamanca (CAUSA), Universidad de Salamanca (USAL), Salamanca, Spain.
L Vazquez IglesiasServicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
R BenitoCentro de Investigación del Cáncer, Instituto de Investigación Biomédica de Salamanca (IBSAL), CSIC - Universidad de Salamanca (USAL), Universidad de Salamanca (USAL), Salamanca, Spain.
J M Hernandez-RivasServicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
M J Doyague SanchezServicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
T Costas Rodriguez *Servicio de Ginecología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain.
J R González-Porras *Servicio de Hematología, Complejo Asistencial Universitario de Salamanca (CAUSA), Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca (USAL), Salamanca, Spain. jrgp@usal.es.

Funding

Fundacion Castellano Leonesa de Hematologia y Hemoterapia FUCALHH 2020Gerencia Regional de Salud de Castilla y León GRS2147/A/2020Insituto de Salud Carlos III PI24/01987Instituto de Salud Carlos III PI24/01458
6 · The paper itself

Abstract

backgroundThe prevalence of hereditary bleeding disorders (HBDs) in heavy menstrual bleeding (HMB) and their impact on health-related quality of life (HRQoL) remain underexplored. We investigated the HRQoL of women with non-structural HMB and its association with HBDs.

methodA prospective longitudinal study of 100 women with HMB without structural gynecological pathology. HMB was defined as ≥ 8 days of bleeding or a PBAC score > 100 points. Four HRQoL questionnaires —SF-12®v2, EQ-5D-3 L, MBQ, and SAMANTA— were administered at baseline and 6 months. HBD diagnosis included hypermobility spectrum disorders, von Willebrand disease, platelet disorders, congenital coagulation factor deficiencies, and hyperfibrinolysis.

result88 women required treatment for HMB, anemia, or iron deficiency. Combined hormonal therapy (43%) and levonorgestrel intrauterine devices (14%) were the most frequently used treatments. Thirty-one women (31%) were diagnosed with HBD. After 6 months of treatment, SF-12®v2 results showed significant improvements in the mental and physical health components, particularly with respect to mobility, moderate activities, and pain perception. EQ-5D-3 L evaluations revealed significant improvements in anxiety and depression. MBQ and SAMANTA scores indicated significant reductions in menstrual bleeding and enhanced quality of life. However, at T6, HBD patients showed significantly lower improvements compared with non-HBD patients in physical health (SF-12 PCS, p = 0.035), EQ-5D index scores (p = 0.024), PBAC (p = 0.049), and MBQ (p = 0.028).

conclusionHBD is an important cause of HMB. Medical treatment improves mobility, moderate activities, pain perception, and anxiety/depression after 6 months, although HRQoL improvements are less pronounced in HBD patients.

Indexed as

Blood Coagulation Disorders, InheritedMenorrhagiaQuality of LifeAdultFemaleHumansLongitudinal StudiesMiddle AgedProspective StudiesSurveys and QuestionnairesYoung AdultHealth-related quality of lifeHeavy menstrual bleedingHereditary bleeding disordersMedical treatment outcomesMenstrual healthPatient-reported outcomes

Identifiers

PMID41606623
PMCPMC12924219

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LicenceCC BY-NC-ND
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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.