ORAL MANIFESTATIONS AND DENTAL MANAGEMENT OF PATIENTS WITH HEREDITARY ANGIOEDEMA

被引:36
作者
ATKINSON, JC
FRANK, MM
机构
[1] NIAID,CLIN INVEST LAB,BETHESDA,MD 20892
[2] NIDR,PATIENT CARE BRANCH,BETHESDA,MD 20892
关键词
ANGIOEDEMA; HEREDITARY; COMPLEMENT; DENTAL TREATMENT;
D O I
10.1111/j.1600-0714.1991.tb00908.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Hereditary angioedema (HAE) is a genetic disorder in which affected individuals develop extensive, spontaneous angioedema of the extremities, gastrointestinal tract, and oropharynx. Dental treatment of unmedicated patients with HAE can trigger life-threatining pharyngeal edema. Previously, it was demonstrated that the administration of fresh frozen plasma (FFP) before surgery prevented angioedma attacks in 6 patients undergoing dental extractions. The present study examines the long term effectiveness of FFP in preventing angioedema from developing in 53 patients with HAE undergoing all types of dental treatment over a ten-year period. Only 3 of 45 patients (6.7%) covered with FFP had a minor angioedema attack after dental therapy in 10 yr. No attacks of moderate or severe swelling were seen. Attacks occurred independently of the disease activity of the patient and the trauma of the dental procedure. The use of fresh frozen plasma is effective in preventing attacks of angioedema in HAE patients undergoing all types of dental procedures.
引用
收藏
页码:139 / 142
页数:4
相关论文
共 17 条
[1]   MOLECULAR-BASIS FOR THE DEFICIENCY OF COMPLEMENT-1 INHIBITOR IN TYPE-I HEREDITARY ANGIONEUROTIC-EDEMA [J].
CICARDI, M ;
IGARASHI, T ;
ROSEN, FS ;
DAVIS, AE .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (03) :698-702
[2]   C1 INHIBITOR AND HEREDITARY ANGIONEUROTIC-EDEMA [J].
DAVIS, AE .
ANNUAL REVIEW OF IMMUNOLOGY, 1988, 6 :595-628
[3]  
DONALDSON VH, 1966, PEDIATRICS, V37, P1017
[4]  
DONALDSON VH, 1989, AM J MED, V87, pN49
[5]  
DONALDSON VH, 1962, J ALLERGY, V33, P316
[6]   HEREDITARY ANGIOEDEMA - CLINICAL SYNDROME AND ITS MANAGEMENT [J].
FRANK, MM ;
GELFAND, JA ;
ATKINSON, JP .
ANNALS OF INTERNAL MEDICINE, 1976, 84 (05) :580-593
[7]  
Frank MM, 1988, IMMUNOLOGICAL DIS, P203
[8]   ACQUIRED C1-INHIBITOR DEFICIENCY ASSOCIATED WITH ANTIIDIOTYPIC ANTIBODY TO MONOCLONAL IMMUNOGLOBULINS [J].
GEHA, RS ;
QUINTI, I ;
AUSTEN, KF ;
CICARDI, M ;
SHEFFER, A ;
ROSEN, FS .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (09) :534-540
[9]   ACQUIRED C1 ESTERASE INHIBITOR DEFICIENCY AND ANGIOEDEMA - REVIEW [J].
GELFAND, JA ;
BOSS, GR ;
CONLEY, CL ;
REINHART, R ;
FRANK, MM .
MEDICINE, 1979, 58 (04) :321-328
[10]   TREATMENT OF HEREDITARY ANGIOEDEMA WITH DANAZOL - REVERSAL OF CLINICAL AND BIOCHEMICAL ABNORMALITIES [J].
GELFAND, JA ;
SHERINS, RJ ;
ALLING, DW ;
FRANK, MM .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (26) :1444-1448