Optimising local therapy during oral surgery in patients with von Willebrand disease: effective results from a retrospective analysis of 63 cases

被引:0
作者
Federici, AB
Sacco, R
Stabile, F
Carpenedo, M
Zingaro, E
Mannucci, PM
机构
[1] IRCCS Maggiore Hosp, Angelo Bianchi Bonomi Haemophilia & Thrombisis Ct, Milan, Italy
[2] IRCCS Maggiore Hosp, Dept Internal Med, Milan, Italy
[3] Univ Milan, Milan, Italy
[4] Ist Stomatol Italiano, Milan, Italy
关键词
desmopressin; factor VIII; Willebrand concentrates; oral surgery; tranexamic acid; von Willebrand disease;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bleeding after dental extractions is very frequent in patients with von Willebrand disease (vWD) and in the past often necessitated transfusions with factor VIII/von Willebrand factor concentrates (vWFc). To evaluate the benefits of a standard local therapy on bleeding complications during oral surgery, 63 consecutive patients with vWD were analysed retrospectively. All types of vWD were included: type 1 (n = 31), type 2 (n = 22) and type 3 (n = 10). All the patients had dental extractions or periodontal surgery at the same hospital by the same oral surgeons. All cases had been given tranexamic acid (TA) before and for 7 days after surgery. As additional local therapy fibrin glue (FG) was used during surgery in several patients. Additional systemic therapies were: desmopressin (DDAVP, 0.3 mu g kg(-1)) and fVIII/vWF concentrates (vWFc, 40 U kg(-1)) given as a single dose before surgery. The 29 subjects (46%) treated locally did not bleed. Among the remaining cases, 24 (38%) were given DDAVP as additional systemic therapy and 6 (9.5%) received vWFc. There was bleeding after surgery in only two cases who had been given local FG (type 2 B) or systemic vWFc (type 3), but bleeding was stopped with an additional local application of FG. Our data suggest that a standard local therapy with TA and FG with DDAVP can prevent bleeding complications during oral surgery in the majority of patients (84%) with vWD and reduce the need for concentrates, with all their possible complications and high costs.
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页码:71 / 77
页数:7
相关论文
共 25 条
[1]  
BOND L, 1988, NEW ENGL J MED, V318, P121
[2]  
Casonato A, 1999, THROMB HAEMOSTASIS, V81, P224
[3]   FACTOR-VIII-C INCREASES AFTER DESMOPRESSIN IN A SUBGROUP OF PATIENTS WITH AUTOSOMAL RECESSIVE SEVERE VON-WILLEBRAND DISEASE [J].
CASTAMAN, G ;
LATTUADA, A ;
MANNUCCI, PM ;
RODEGHIERO, F .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 89 (01) :147-151
[4]  
Chiarini L, 1997, Minerva Stomatol, V46, P115
[5]  
DJULBEGOVIC B, 1995, BLOOD, V85, P598
[6]   Diagnosis of von Willebrand disease [J].
Federici, AB .
HAEMOPHILIA, 1998, 4 (04) :654-660
[7]  
Federici AB, 1998, HAEMOPHILIA, V4, P7
[8]  
FEDERICI AB, 1998, HAEMOPHILIA, V4, P289
[9]   UNCONTROLLED BLEEDING DURING ENDODONTIC TREATMENT AS THE 1ST SYMPTOMS FOR DIAGNOSING VONWILLEBRANDS DISEASE - A CASE-REPORT [J].
KEILA, S ;
KAUFMAN, A ;
ITCKOWITCH, D .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1990, 69 (02) :243-246
[10]   Treatment of von Willebrand disease [J].
Mannucci, PM .
HAEMOPHILIA, 1998, 4 (04) :661-664