Ophthalmic surgery and Creutzfeldt-Jakob disease

Although the evidence does not suggest that contaminated ophthalmic instruments represent a risk of onward transmission of sporadic CJD, this conclusion should be treated with caution The occurrence of variant Creutzfeldt-Jakob disease (vCJD) and the probable causal link with bovine spongiform encephalopathy (BSE) in cattle have increased interest in the search for possible environmental sources of sporadic CJD (sCJD). Presumed iatrogenic CJD is rare. Up to the year 2000 there had been 267 cases reported worldwide: three cases secondary to human corneal grafting (one confirmed, one probable, and one possible case), 114 related to human dura mater grafts, 139 related to human growth hormone treatment, four related to human pituitary gonadotrophin therapy, and seven linked to neurosurgical procedures or stereotactic EEG electrodes.1 Because of the marked resistance of the infectious agent of CJD to conventional sterilisation techniques, there is concern about the possibility of transmission of infection via surgical instruments in contact with infected tissue, especially in neurosurgery or ophthalmic surgery. The presence of infection in the eye in sCJD was first demonstrated following the intracerbral inoculation of pooled sCJD eye tissue in non-human primates.2 Recently the infectious form of prion protein (PrPSc) has been identified in the neural retina, optic nerve, and in retinal pigmented epithelium in variant and sporadic CJD using immunohistochemistry or western blot,3,4 with comparable levels to those found in brain. PrPSc was not detected in other ocular tissues. Although this suggests that there may be a greater risk of contaminating surgical instruments in procedures involving the posterior segment of the eye, infectivity has been demonstrated in animal and human cornea,5 and circumstantial evidence has implicated corneal transplantation as a mechanism of transmission of iatrogenic CJD.6 Experimental infection has been achieved following conjunctival installation of scrapie infectivity in …

[1]  London,et al.  The lighter side , 2003 .

[2]  A. Tullo Creutzfeldt-Jakob disease and eye surgery--new disease, old disease. , 2003, Journal of cataract and refractive surgery.

[3]  P. Klöhn,et al.  Transmission of prions , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[4]  C. V. van Duijn,et al.  Sporadic Creutzfeldt–Jakob disease and surgery: A case–control study using community controls , 2002, Neurology.

[5]  C. V. van Duijn,et al.  Creutzfeldt-Jakob disease 38 years after diagnostic use of human growth hormone , 2002, Journal of neurology, neurosurgery, and psychiatry.

[6]  J. Collinge,et al.  Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay , 2001, The Lancet.

[7]  C. Lueck,et al.  Creutzfeldt-Jakob disease and the eye. I. Background and patient management , 2000, Eye.

[8]  C. Masters,et al.  Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study , 1999, The Lancet.

[9]  E. Granieri,et al.  Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95 , 1998, The Lancet.

[10]  A. Druschky,et al.  Transmission of Creutzfeldt-Jakob disease via a corneal transplant , 1997, Journal of neurology, neurosurgery, and psychiatry.

[11]  S. Cousens,et al.  Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96 , 1997, BMJ.

[12]  P. Brown,et al.  Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease , 1994, Annals of neurology.

[13]  H. Fraser,et al.  Conjunctival instillation of scrapie in mice can produce disease. , 1993, Veterinary microbiology.

[14]  R. Will,et al.  Evidence for case-to-case transmission of Creutzfeldt-Jakob disease , 1982, Journal of neurology, neurosurgery, and psychiatry.

[15]  L. Manuelidis,et al.  Experimental creutzfeldt-jakob disease transmitted via the eye with infected cornea. , 1977, The New England journal of medicine.

[16]  J. Ironside,et al.  Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease. , 2003, Investigative ophthalmology & visual science.

[17]  P. Brown,et al.  Risk of prion disease transmission from ocular donor tissue transplantation. , 1999, Cornea.