Source:http://linkedlifedata.com/resource/pubmed/id/11115053
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2000-12-22
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pubmed:abstractText |
The aim of this paper is to describe the development of a national hepatitis C register and the completeness of the data it contains. This is a descriptive report of the structure and function of the register, including case definitions, registration and follow-up procedures, and methods used to maximize data quality and to obtain comparative data sources. The register contains data on HCV-infected individuals who acquired their infections on a known date and by a known route; to date all are transfusion recipients identified during the UK lookback exercise, who tested positive or indeterminate for anti-HCV after receiving 'infected' blood issued before the introduction of routine testing of the blood supply for anti-HCV. By 31 December 1999, 871 (87%) of 996 eligible transfusion recipients had been registered, and 984 (99%) flagged in the NHS Central Registers. Registered patients had been infected for an average of 11.1 years (SEM 0.1); around half were being cared for by clinicians with a specialist interest in liver disease. Except for the information on tobacco use, current alcohol use, and hepatitis B status, data were more than 80% complete, and for most variables, more than 90% complete. The consistency of data abstraction was found to be 98% (SEM 0.5). In conclusion, the Register contains high quality anonymised data on one of the largest cohorts of individuals with HCV infections acquired on a known date and by a known route. It could serve as a model for other chronic disease registers; developers may find the structure, design, and methodological issues addressed useful.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1352-0504
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
420-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11115053-Adolescent,
pubmed-meshheading:11115053-Adult,
pubmed-meshheading:11115053-Aged,
pubmed-meshheading:11115053-Aged, 80 and over,
pubmed-meshheading:11115053-Blood Transfusion,
pubmed-meshheading:11115053-Child,
pubmed-meshheading:11115053-Child, Preschool,
pubmed-meshheading:11115053-Data Collection,
pubmed-meshheading:11115053-Female,
pubmed-meshheading:11115053-Great Britain,
pubmed-meshheading:11115053-Hepacivirus,
pubmed-meshheading:11115053-Hepatitis C,
pubmed-meshheading:11115053-Humans,
pubmed-meshheading:11115053-Infant,
pubmed-meshheading:11115053-Male,
pubmed-meshheading:11115053-Registries
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pubmed:year |
2000
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pubmed:articleTitle |
The HCV National Register: towards informing the natural history of hepatitis C infection in the UK.
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pubmed:affiliation |
Immunization Division, Communicable Disease Surveillance Centre, London, UK. hharris@phls.nhs.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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