Literature DB >> 10028306

Quality of life during menstruation in patients with inherited bleeding disorders.

R A Kadir1, C A Sabin, D Pollard, C A Lee, D L Economides.   

Abstract

Menorrhagia is a common and major problem for patients with inherited bleeding disorders, especially vWD. Quality of life during menstruation was assessed in 99 patients with inherited bleeding disorders including vWD (n = 57), carriers of haemophilia A (n = 17), carriers of haemophilia B (n = 7) and FXI deficiency (n = 18), and comparison was performed with an age-matched control group (n = 69). A questionnaire was used that included four main sections: (i) general health, (ii) health and daily activities, (iii) dysmenorrhea and (iv) quality of life during the menstrual period. Although patients with inherited bleeding disorders felt that their health (in general) was very good, they had significantly poorer quality of life on all the scales used than controls. Thirty-nine per cent reported having cut down on the amount of time spent on work and other activities as a result of their menstruation; 47% felt that they accomplished less than they would like during this period, 38% felt that they were limited in the kind of work and other activities that they could do, and 40% found that it took extra effort to perform their work. Fifty-one per cent experienced moderate, severe or very severe dysmenorrhoea. Quality of life was statistically poorer in patients with vWD, menstrual scores > 100 according to the pictorial blood assessment chart (PBAC), those who had periods > or = 8 days and those who experienced flooding or passage of clots. In conclusion, menstruation has a negative effect on the quality of life in patients with inherited bleeding disorders especially in those with objectively confirmed menorrhagia.

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Year:  1998        PMID: 10028306     DOI: 10.1046/j.1365-2516.1998.00208.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  7 in total

1.  Single-Center Experience of von Willebrand Disease (vWD) Among Patients with Menorrhagia: A Diagnosis which could be Missed.

Authors:  Rosline Hassan; Wan Aswani Wan Yusof; Nik Hazlina Nik Hussain; Wan Zaidah Abdullah
Journal:  Indian J Hematol Blood Transfus       Date:  2012-02-01       Impact factor: 0.900

2.  Haemophilia A carriers experience reduced health-related quality of life.

Authors:  L Gilbert; A Paroskie; D Gailani; M R Debaun; R F Sidonio
Journal:  Haemophilia       Date:  2015-04-30       Impact factor: 4.287

3.  Depression and post-traumatic stress disorder in individuals with hereditary hemorrhagic telangiectasia: A cross-sectional survey.

Authors:  Shruti Chaturvedi; Marianne Clancy; Nicole Schaefer; Olalekan Oluwole; Keith R McCrae
Journal:  Thromb Res       Date:  2017-03-09       Impact factor: 3.944

4.  Bleeding disorders, menorrhagia and iron deficiency: impacts on health-related quality of life.

Authors:  C Rae; W Furlong; J Horsman; E Pullenayegum; C Demers; J St-Louis; D Lillicrap; R Barr
Journal:  Haemophilia       Date:  2012-09-21       Impact factor: 4.287

5.  Prevalence, burden and treatment effects of vaginal bleeding in women with (suspected) congenital platelet disorders throughout life: a cross-sectional study.

Authors:  Marieke C Punt; Nienke D Ruigrok; Kitty W M Bloemenkamp; Nanda Uitslager; Rolf T Urbanus; Evelyn Groot; Idske C L Kremer Hovinga; Roger E G Schutgens; Karin P M van Galen
Journal:  Br J Haematol       Date:  2021-09-18       Impact factor: 8.615

Review 6.  The lived experience of women with a bleeding disorder: A systematic review.

Authors:  Anna Sanigorska; Steve Chaplin; Mike Holland; Kate Khair; Debra Pollard
Journal:  Res Pract Thromb Haemost       Date:  2022-02-03

Review 7.  How I manage severe von Willebrand disease.

Authors:  Frank W G Leebeek; Ferdows Atiq
Journal:  Br J Haematol       Date:  2019-09-09       Impact factor: 6.998

  7 in total

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