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Gynecological bleeding in women with congenital bleeding disorders: A comprehensive cohort from Iran.
Zafarani, Alireza; Ghodratnia, Elnaz; Amirzargar, Mohammad Reza; Poriafar, Yasaman; Tabibian, Shadi.
Afiliación
  • Zafarani A; Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran; Department of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran.
  • Ghodratnia E; Department of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran.
  • Amirzargar MR; Department of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran.
  • Poriafar Y; Department of Hematology and Blood Banking, Faculty of Allied Medicine, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran.
  • Tabibian S; Iranian Comprehensive Hemophilia Care Center, Tehran, Islamic Republic of Iran. Electronic address: Sh.tabibian@gmail.com.
Transfus Apher Sci ; 63(4): 103941, 2024 Apr 30.
Article en En | MEDLINE | ID: mdl-38735129
ABSTRACT

BACKGROUND:

Gynecological bleeding including menorrhagia and postpartum hemorrhage (PPH) face women's quality of life constantly with difficulties, especially those suffering from inherited bleeding disorders. In this study, we aim to evaluate gynecological bleeding particularly menorrhagia among Iranian women patients with inherited bleeding disorders admitted to the Iranian Comprehensive Hemophilia Care Center (ICHCC).

METHODS:

This study was conducted on 156 females aged ≥ 12 diagnosed with an inherited bleeding disorder in ICHCC. Demographic and laboratory data were documented for all patients. Bleeding questionnaires (the International Society on Thrombosis and Hemostasis bleeding assessment tool (ISTH-BAT), Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand disease (MCMDM-1), and Pictorial blood loss assessment chart (PBAC)) were filled out for all patients. For comparing metric and categorical parameters, Mann-Whitney was performed. Spearman's rho test was used for analyzing correlation.

RESULTS:

The mean age of patients was 33. Von Willebrand disease (VWD), Factor (F) VII deficiency and combined factor deficiency were the most diagnosed disorders. The median of ISTH-BAT, MCMDM-1, and PBAC was 7,7, and 517, respectively. Menorrhagia was the most common reason for diagnosis. Menorrhagia and PPH domain scores ≥ 2 were recorded in 82 and 34 patients, respectively, and PBAC scores > 100 were seen in 118 patients. Significant positive correlations were observed between bleeding scores and menorrhagia and PPH scores. No significant correlations were recorded for VWF Ag and VWF RCo with menorrhagia and PPH scores; however, significant correlations were seen for VWF Ag and VWF RCo with bleeding score questionnaires.

CONCLUSION:

Menorrhagia is the most common problem in females affected by different types of inherited bleeding disorders, particularly VWD. Increased awareness among gynecologists and hematologists about bleeding disorders in cases with unexplained menorrhagia is an essential step for optimal management.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Transfus Apher Sci Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Transfus Apher Sci Asunto de la revista: HEMATOLOGIA Año: 2024 Tipo del documento: Article