Bleeding Complications in Patients Receiving DDAVP at the Royal Brisbane (#55)
Background: Dental extractions challenge the body’s haemostatic
mechanism. Postoperative bleeding from extraction sockets can be
prolonged, or even life-threatening in patients with inherited bleeding
disorder. Pre- and post-operative clotting factor replacements or
systemic ddAVP have been advocated and employed at the Royal
Brisbane & Women’s Hospital (RBWH) to prevent bleeding complications
in these patients. This approach can be time-consuming, expensive,
limits patients to receive extractions as a hospital inpatient and is
associated with complications such as development of clotting factor
inhibitors.
Objectives: To assess the post-operative bleeding rate in patients
with inherited bleeding disorder that underwent dental extractions
at the RBWH between 2003-2012 with peri-operative clotting factor
replacement or systemic ddAVP cover.
Method: Patients with inherited bleeding disorder such as Haemophilia
A, Haemophilia B and von Willebrand’s disease were included. Chart
review was conducted and the following information was extracted: type
and severity of inherited bleeding disorder, number of teeth extracted, if
bone removal was required, if haemostatic agent was placed within the
socket, the type and amount of clotting factor and ddAVP used pre and
post-operatively, and if significant post-operative bleeding occurred.
Findings: 53 extraction events occurred in 45 patients between
2003-2012. All patients had peri-operative clotting factor or systemic
ddAVP cover. 10 out of 53 extraction events (18.9%) had post-operative
bleeding requiring further factor replacement or ddAVP. Post-operative
bleeding in 1 patient with mild Haemophilia A was complicated by the
development of inhibitors. Type and severity of bleeding disorder, bone
removal and use of local haemostatic agent did not have any significant
effect on post-operative bleeding.
Conclusion: Despite the use of peri-operative factor and ddAVP,
post-operative bleeding rate remains high for patients with inherited
bleeding disorder. More study is required to assess the effect of using
local haemostatic control to achieve haemostasis following extractions
in these patients.