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Volumn 330, Issue 7496, 2005, Pages 877-879
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A feasibility study of signed consent for the collection of patient identifiable information for a national paediatric clinical audit database
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
CHILDHOOD MORTALITY;
DATA BASE;
DISEASE SEVERITY;
ETHNOLOGY;
FEASIBILITY STUDY;
INFORMED CONSENT;
INTENSIVE CARE UNIT;
LAW;
LENGTH OF STAY;
MEDICAL AUDIT;
MEDICAL RECORD;
MEDICAL SOCIETY;
NATIONAL HEALTH SERVICE;
PARENT;
PRIORITY JOURNAL;
REFUSAL TO PARTICIPATE;
REGRESSION ANALYSIS;
UNITED KINGDOM;
ADOLESCENT;
ADULT;
BIOMEDICAL AND BEHAVIORAL RESEARCH;
CLINICAL TRIAL;
EMPIRICAL APPROACH;
FACTUAL DATABASE;
FEMALE;
HUMAN;
INFANT;
INFORMATION PROCESSING;
INTENSIVE CARE;
MALE;
MANAGEMENT;
METHODOLOGY;
MULTICENTER STUDY;
NEWBORN;
PRESCHOOL CHILD;
STATISTICS;
BIOMEDICAL AND BEHAVIORAL RESEARCH;
EMPIRICAL APPROACH;
ADOLESCENT;
ADULT;
CHILD, PRESCHOOL;
CONSENT FORMS;
DATA COLLECTION;
DATABASES, FACTUAL;
ENGLAND;
FEASIBILITY STUDIES;
FEMALE;
HUMANS;
INFANT;
INFANT, NEWBORN;
INTENSIVE CARE UNITS, PEDIATRIC;
MALE;
PATIENT IDENTIFICATION SYSTEMS;
THIRD-PARTY CONSENT;
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EID: 17244382963
PISSN: 09598146
EISSN: None
Source Type: Journal
DOI: 10.1136/bmj.38404.650208.AE Document Type: Article |
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Times cited : (23)
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References (4)
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