Ra. Kadir et al., Assessment of menstrual blood loss and gynaecological problems in patientswith inherited bleeding disorders, HAEMOPHILIA, 5(1), 1999, pp. 40-48
Menstrual blood loss and gynaecological problems in patients with inherited
bleeding disorders were assessed in this study. One hundred and sixteen wo
men, including 66 with von Willebrand's disease (vWD), 30 carriers of haemo
philia and 20 with factor XI (FXI) deficiency were interviewed and their gy
naecological history obtained. Their case records were also reviewed and me
nstrual loss was objectively assessed using a pictorial blood assessment ch
art (PBAC). Comparison with an age-matched control group (69 women) was per
formed. Menorrhagia (PBAC score > 100) was confirmed in 74%, 57% and 59% of
women with vWD, carriers of haemophilia and FXI deficiency, respectively,
in comparison with 29% in the control group (P = 0.001). PBAC scores were h
igher in vWD patients with a von Willebrand factor activity (vWF:Ac) of I 3
0 IU dL(-1) compared to those with higher levels, but the difference was no
t statistically significant. However, there was no relation between PBAC sc
ore and the severity of the disease in FXI deficient patients and carriers
of haemophilia. Duration of menstruation was significantly longer (P = 0.00
1) and episodes of flooding was significantly more common (P = 0.001) in pa
tients with inherited bleeding disorders compared to the control group. How
ever, there was no difference in the passage of clots during menstruation.
Forty-seven per cent of patients with inherited bleeding disorders had cons
ultations with their family practitioner or gynaecologist for menorrhagia,
36% had medical treatment and 27% had surgical procedures, including 10 hys
terectomies. Post-operative bleeding followed in four out of 28 cases of hy
steroscopy and/or dilatation and curettage. Bleeding complications followin
g hysterectomy were reported in five out of 10 patients. In conclusion, men
orrhagia is a common and major problem in patients with inherited bleeding
disorders, especially vWD. Increased awareness among gynaecologists and hae
matologists of the high prevalence of menorrhagia and the treatment options
available is necessary for optimal management of these patients. Appropria
te preoperative assessment and haemostatic control during any gynaecologica
l procedure, however minor, and in collaboration with the local haemophilia
centre is essential to minimize risks of haemorrhagic complications.