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1.
Eur J Neurol ; 29(4): 1222-1226, 2022 04.
Artículo en Inglés | MEDLINE | ID: mdl-34941016

RESUMEN

BACKGROUND AND PURPOSE: Creutzfeldt-Jakob disease (CJD) is lethal and transmissible. We assessed the impact of the COVID-19 pandemic on UK CJD surveillance. We hypothesized that (i) disruptions prolonged diagnostic latency; (ii) autopsy rates declined; and (iii) COVID-19 infection negatively affected diagnosis, care, and survival. METHODS: We retrospectively investigated the first year of the pandemic, using the preceding year as a comparator, quantifying numbers of individuals assessed by the UK National CJD Research & Surveillance Unit for suspected CJD, time to diagnosis, disease duration, and autopsy rates. We evaluated the impact of COVID-19 status on diagnosis, care, and survival in CJD. RESULTS: A total of 148 individuals were diagnosed with CJD in the pandemic (from a total of 166 individuals assessed) compared to 141 in the comparator (from 145 assessed). No differences were identified in disease duration or time to diagnosis. Autopsy rates were unchanged. Twenty individuals had COVID-19; 60% were symptomatic, and 10% had severe disease. Disruptions in diagnosis and care were frequently identified. Forty percent of COVID-19-positive individuals died; however, COVID-19 status did not significantly alter survival duration in CJD. CONCLUSIONS: The COVID-19 pandemic has not impacted UK CJD case ascertainment or survival, but diagnostic evaluation and clinical care of individuals have been affected.


Asunto(s)
COVID-19 , Síndrome de Creutzfeldt-Jakob , COVID-19/epidemiología , Síndrome de Creutzfeldt-Jakob/diagnóstico , Síndrome de Creutzfeldt-Jakob/epidemiología , Humanos , Pandemias , Atención al Paciente , Estudios Retrospectivos , SARS-CoV-2 , Reino Unido/epidemiología
2.
Ann Neurol ; 63(3): 347-54, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18074392

RESUMEN

OBJECTIVE: Although surgical transmission of Creutzfeldt-Jakob disease (CJD) has been demonstrated, these iatrogenic cases account for only a small proportion of all CJD cases. The majority are sporadic CJD (sCJD) cases of unknown cause. This study investigated whether some cases classified as sCJD might have an unrecognized iatrogenic basis through surgical or other medical procedures METHODS: This study compared medical risk factors from 431 sCJD cases referred 1998 to 2006 with 454 population control subjects. Possible geographic and temporal links between neurological and gynecological operations in 857 sCJD cases referred from 1990 to 2006 were investigated RESULTS: A reported history of ever having undergone surgery was associated with increased risk for sCJD (odds ratio, 2.0; 95% confidence interval, 1.3-2.1; p = 0.003). Increased risk was not associated with surgical categories chosen a priori but was confined to the residual category "other surgery," in which the increase in risk appeared most marked for three subcategories: skin stitches, nose/throat operations, and removal of growths/cysts/moles. No convincing evidence was found of links (same hospital, within 2 years) between cases undergoing neurosurgery or gynecological surgery INTERPRETATION: It is unlikely that a high proportion of UK sCJD cases are the result of transmission during surgery, but we cannot exclude the possibility that such transmission occurs occasionally. A study based on accurate surgical histories obtained from medical records is required to determine whether the increased risk associated with reported surgical history reflects a causal association or recall bias.


Asunto(s)
Síndrome de Creutzfeldt-Jakob/epidemiología , Síndrome de Creutzfeldt-Jakob/etiología , Adulto , Anciano , Anciano de 80 o más Años , Estudios de Casos y Controles , Síndrome de Creutzfeldt-Jakob/transmisión , Femenino , Procedimientos Quirúrgicos Ginecológicos/efectos adversos , Humanos , Masculino , Persona de Mediana Edad , Procedimientos Neuroquirúrgicos/efectos adversos , Factores de Riesgo
3.
Ann Neurol ; 59(1): 111-20, 2006 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-16287153

RESUMEN

OBJECTIVE: To investigate the potential risk factors for variant Creutzfeldt-Jakob disease (VCJD) in the United Kingdom. METHODS: Definite and probable vCJD cases (n = 136) were residing in Great Britain at disease onset, and were referred between May 1995 and November 2003. Control subjects (n = 922) were recruited between 2002 and 2003, from 100 randomly selected geographical clusters sampled to represent the geographical distribution of vCJD. RESULTS: Reported frequent consumption of beef and beef products thought likely to contain mechanically recovered or head meat, or both, including burgers and meat pies, was associated with increased risk for vCJD, as was reported frequent chicken consumption. Surgical operations were generally similarly reported for cases and control subjects, with the exception of a small group of minor operations, possibly attributable to underreporting in control subjects. Cases and control subjects had similar reported occupational histories and exposure to animals. INTERPRETATION: These findings are consistent with dietary exposure to contaminated beef products being the main route of infection of vCJD, but recall bias cannot be excluded. There was no convincing evidence of increased risk through medical, surgical, or occupational exposure or exposure to animals.


Asunto(s)
Síndrome de Creutzfeldt-Jakob/etiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Animales , Estudios de Casos y Controles , Bovinos , Niño , Síndrome de Creutzfeldt-Jakob/epidemiología , Dieta , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Factores de Riesgo , Encuestas y Cuestionarios , Reino Unido/epidemiología
4.
Nurs Times ; 101(20): 52-3, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15918466

RESUMEN

Creutzfeldt-Jakob disease is a rare, progressive brain disease that affects both men and women. It causes a relentless deterioration in the ability to function physically, mentally and emotionally. Many nurses will never have cared for patients with the disease and there are many misconceptions regarding its cause, progress and the implications for care. Blaire Smith-Bathgate examines these issues.


Asunto(s)
Síndrome de Creutzfeldt-Jakob/diagnóstico , Síndrome de Creutzfeldt-Jakob/enfermería , Adolescente , Adulto , Edad de Inicio , Anciano , Síndrome de Creutzfeldt-Jakob/clasificación , Síndrome de Creutzfeldt-Jakob/epidemiología , Electroencefalografía , Femenino , Salud Global , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Vigilancia de la Población , Reino Unido/epidemiología
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