Literature DB >> 12574883

[Hygenic measures for Creutzfeldt-Jakob disease].

H-J Knopf1.   

Abstract

The Creutzfeldt-Jakob disease (CJD) belongs to the so-called prion diseases or transmissible spongiform encephalopathies. The iatrogenic transmission of the pathogen by direct contact with infectious tissue, tissue extracts and surgical instruments has been demonstrated. CJD is not an infectious disease in the usual sense. Transmission is not possible by normal social contact nor by nursing measures just as CJD can not be transferred by normal skin contact or contact with blood, serum or other patient' secretions. Therefore, CJD patients do not have to be isolated, because strict conformity to the generally recognized rules of hygiene is completely sufficient. The high resistance of prions to environmental influences requires the combination of different disinfection and sterilization measures before inactivation of the pathogen occurs and it is possible to exclude transmission by medical products.

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Mesh:

Year:  2002        PMID: 12574883     DOI: 10.1007/s00120-002-0269-0

Source DB:  PubMed          Journal:  Urologe A        ISSN: 0340-2592            Impact factor:   0.639


  6 in total

Review 1.  Prion diseases and the BSE crisis.

Authors:  S B Prusiner
Journal:  Science       Date:  1997-10-10       Impact factor: 47.728

2.  [The Creutzfeld-Jakob disease. A sphinx of current neurobiology].

Authors:  S Poser; I Zerr; W J Schulz-Schaeffer; H A Kretzschmar; K Felgenhauer
Journal:  Dtsch Med Wochenschr       Date:  1997-09-12       Impact factor: 0.628

3.  Creutzfeldt-Jakob disease associated with cadaveric dura mater grafts -- Japan, January 1979-May 1996.

Authors: 
Journal:  MMWR Morb Mortal Wkly Rep       Date:  1997-11-14       Impact factor: 17.586

4.  Detection of scrapie agent in the peripheral nervous system of a diseased sheep.

Authors:  M H Groschup; F Weiland; O C Straub; E Pfaff
Journal:  Neurobiol Dis       Date:  1996       Impact factor: 5.996

Review 5.  Iatrogenic Creutzfeldt-Jakob disease at the millennium.

Authors:  P Brown; M Preece; J P Brandel; T Sato; L McShane; I Zerr; A Fletcher; R G Will; M Pocchiari; N R Cashman; J H d'Aignaux; L Cervenáková; J Fradkin; L B Schonberger; S J Collins
Journal:  Neurology       Date:  2000-10-24       Impact factor: 9.910

6.  Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering.

Authors:  C L Masters; J O Harris; D C Gajdusek; C J Gibbs; C Bernoulli; D M Asher
Journal:  Ann Neurol       Date:  1979-02       Impact factor: 10.422

  6 in total

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