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Screening bleeding disorders in adolescents and young women with menorrhagia.
Caki Kiliç, Suar; Sarper, Nazan; Zengin, Emine; Aylan Gelen, Sema.
Afiliación
  • Caki Kiliç S; Kocaeli University Medical Faculty, Department of Pediatric Hematology, Kocaeli, Turkey.
  • Sarper N; Kocaeli University Medical Faculty, Department of Pediatric Hematology, Kocaeli, Turkey.
  • Zengin E; Kocaeli University Medical Faculty, Department of Pediatric Hematology, Kocaeli, Turkey.
  • Aylan Gelen S; Kocaeli University Medical Faculty, Department of Pediatric Hematology, Kocaeli, Turkey.
Turk J Haematol ; 30(2): 168-76, 2013 Jun.
Article en En | MEDLINE | ID: mdl-24385781
ABSTRACT

OBJECTIVE:

Chronic menorrhagia causes anemia and impairment of life quality. In this study the aim was the screening of bleeding disorders in adolescents and young women with menorrhagia. MATERIALS AND

METHODS:

The study was performed prospectively by pediatric hematologists. A form including demographic characteristics of the patients, bleedings other than menorrhagia, familial bleeding history, characteristics of the menorrhagia, and impairment of life quality due to menorrhagia was filled out by the researcher during a face-to-face interview with the patient. A pictorial blood assessment chart was also used for evaluation of blood loss. All patients underwent pelvic ultrasound sonography testing and women also received pelvic examination by gynecologists. Whole blood count, peripheral blood smear, blood group, serum transaminases, urea, creatinine, ferritin, PFA-100, PT, aPTT, INR, TT, fibrinogen, VWFAg, VWFRCo, FVIII, and platelet aggregation assays were performed. Platelet aggregations were studied by lumiaggregometer.

RESULTS:

Out of 75 patients enrolled, 60 patients completed the study. The mean age was 20.68±10.34 (range 10-48) years and 65% (n=39) of the patients were younger than 18 years. In 18 (46%) of the adolescents, menorrhagia subsided spontaneously. In 20% (n=12) of the patients, a bleeding disorder was detected (1 case of type 3 von Willebrand disease, 2 patients with low VWFAg, 1 case of probable von Willebrand disease, 3 cases of Bernard-Soulier syndrome, 2 cases of Glanzmann thrombasthenia, 2 cases of immune thrombocytopenic purpura, 1 case of congenital factor VII deficiency).

CONCLUSION:

In patients with menorrhagia, at least complete blood count, peripheral smear, aPTT, PT, VWFAg, VWFRCo, FVIII, and fibrinogen assays must be performed. When there is history of nose and gum bleeding, platelet function assay by lumiaggregometer must also be performed. In nearly 50% of adolescents, menorrhagia is dysfunctional and transient. Detailed coagulation assays can be postponed in adolescents if bleeding history other than menorrhagia and/or family history of bleeding and/or parental consanguinity is absent. All subjects with menorrhagia must consult with gynecologists and hematologists. CONFLICT OF INTEREST None declared.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: Turk J Haematol Año: 2013 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Qualitative_research / Screening_studies Idioma: En Revista: Turk J Haematol Año: 2013 Tipo del documento: Article País de afiliación: Turquía