Sporadic Creutzfeldt-Jakob disease in a 18-year-old in the UK

The Lancet ◽  
1995 ◽  
Vol 346 (8983) ◽  
pp. 1155-1156 ◽  
Author(s):  
D. Bateman ◽  
D. Hilton ◽  
S. Love ◽  
M. Zeidler ◽  
J. Beck ◽  
...  
Keyword(s):  
2002 ◽  
Vol 6 (33) ◽  
Author(s):  
◽  
◽  

Variant Creutzfeldt-Jakob disease (vCJD) has been confirmed in a resident of Saskatchewan, Canada (1). The patient, a man under the age of 50, was first notified to the Canadian national CJD surveillance system at Health Canada in April 2002 when his clinical presentation, age, and history of residence in the United Kingdom (UK) led Canadian doctors to suspect vCJD. Post-mortem examination of brain tissues by experts in Canada and the UK has now confirmed the diagnosis of vCJD. Since 1998, when the national CJD surveillance system was launched, all suspect cases of CJD are reported to Health Canada through a national network of specialist physicians. Incidence data are also shared with European and other allied countries as part of the Collaborative Study Group of CJD (EUROCJD, http://www.eurocjd.ed.ac.uk/euroindex.htm). This patient is the first case of vCJD reported in Canada, which together with 6 cases reported in France and one each in the Republic of Ireland, Italy and USA, brings the total number of cases with onset outside the UK to 10 (personal communication National CJD Surveillance Unit, Edinburgh).


2003 ◽  
Vol 7 (18) ◽  
Author(s):  
N J Andrews

Five new cases of variant Creutzfeldt-Jakob disease (vCJD) were diagnosed in the United Kingdom (UK) in the first quarter of 2003, bringing the total number of confirmed or probable cases to 134 (1). Five deaths occurred in the first quarter, bringing the total number of deaths to 126. The total number of onsets and deaths by year are shown in the table.


2003 ◽  
Vol 7 (51) ◽  
Author(s):  

Following the information made available yesterday by the UK Secretary of State for Health about the possibility of transmission of variant Creutzfeld-Jakob Disease


2003 ◽  
Vol 12 (3) ◽  
pp. 235-246 ◽  
Author(s):  
Simon Cousens ◽  
Dawn Everington ◽  
Hester JT Ward ◽  
Jerome Huillard ◽  
Robert G Will ◽  
...  

Science ◽  
2001 ◽  
Vol 294 (5547) ◽  
pp. 1729-1731 ◽  
Author(s):  
J. N. H. d'Aignaux
Keyword(s):  

2012 ◽  
Vol 24 (7) ◽  
pp. 1183-1185 ◽  
Author(s):  
Kavita Das ◽  
Rebecca Davis ◽  
Brett DuToit ◽  
Brian Parsons

ABSTRACTSporadic Creutzfeldt-Jakob disease (sCJD) is a rare and devastating illness. It is the most frequently encountered form of the spongiform encephalopathies with 50 new cases a year in the UK. It presents with a myriad of symptoms reflecting central nervous system dysfunction and is characterized by a rapidly progressive dementia leading to death. The disease process can pose multiple challenges: diagnostic conundrums, complexities in management, and palliative care issues. Good coordinated care between services and information is paramount in adequate management and delivery of care for patients suffering from sCJD.Psychiatry services frequently become involved in the assessment and management of sCJD.


Vox Sanguinis ◽  
2006 ◽  
Vol 91 (3) ◽  
pp. 221-230 ◽  
Author(s):  
P. E. Hewitt ◽  
C. A. Llewelyn ◽  
J. Mackenzie ◽  
R. G. Will

2006 ◽  
Vol 3 (11) ◽  
pp. 757-766 ◽  
Author(s):  
Tini Garske ◽  
Hester J.T Ward ◽  
Paul Clarke ◽  
Robert G Will ◽  
Azra C Ghani

While the number of variant Creutzfeldt–Jakob disease (vCJD) cases continues to decline, concern has been raised that transmission could occur directly from one person to another through routes including the transfer of blood and shared use of surgical instruments. Here we firstly present data on the surgical procedures undertaken on vCJD patients prior to onset of clinical symptoms, which supports the hypothesis that cases via this route are possible. We then apply a mathematical framework to assess the potential for self-sustaining epidemics via surgical procedures. Data from hospital episode statistics on the rates of high- and medium-risk procedures in the UK were used to estimate model parameters, and sensitivity to other unknown parameters about surgically transmitted vCJD was assessed. Our results demonstrate that a key uncertainty determining the scale of an epidemic and whether it is self-sustaining is the number of times a single instrument is re-used, alongside the infectivity of contaminated instruments and the effectiveness of cleaning. A survey into the frequency of re-use of surgical instruments would help reduce these uncertainties.


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