Iatrogenic Creutzfeldt-Jakob disease and its neurosurgical implications

被引:15
作者
Simpson, DA
Masters, CL
Ohlrich, G
Purdie, G
Stuart, G
Tannenberg, AEG
机构
[1] UNIV MELBOURNE,DEPT PATHOL,MELBOURNE,VIC,AUSTRALIA
[2] QUEEN ELIZABETH HOSP,DEPT NEUROL,WOODVILLE,SA 5011,AUSTRALIA
[3] ROYAL BRISBANE HOSP,DEPT NEUROL,BRISBANE,QLD 4029,AUSTRALIA
[4] ROYAL BRISBANE HOSP,DEPT NEUROSURG,BRISBANE,QLD 4029,AUSTRALIA
关键词
Creutzfeldt-Jakob disease; cadaveric dural homografts; prion;
D O I
10.1016/S0967-5868(96)90003-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Creutzfeldt-Jakob (CJD) disease has been reported after the insertion of dural homografts. Two Australian cases of CJD, both following posterior fossa craniotomies done in 1982, are reported; the incubation periods were 5 and 12 years. It seems highly probable that the association is causal. CJD infective agents (prions) are resistant to many previously accepted means of sterilisation and it is postulated that cadaver dural material was either derived from subjects with CJD, or was contaminated during preparation, In Australia the use of dural homografts in neurosurgery was abandoned in 1987; as the mean incubation period (determined from a world-wide review) has been about 65 months, it is now hoped that this: cause of CJD will not recur in the Australian population, although it is premature to state this with confidence, However, precautions against case-to-case transmission remain necessary, and guidelines for this purpose should be enforced in theatre practice and in organ donations. (C) Pearson Professional 1996.
引用
收藏
页码:118 / 123
页数:6
相关论文
共 36 条