Health Informatics Journal, Volume 10

Volume 10, Number 1, March 2004

Louise R. Guillaume, Peter A. Bath:
The Impact of Health Scares on Parents' Information Needs and Preferred Information Sources: A Case Study of the MMR Vaccine Scare. 5-22
Leonidas Orfanidis, Panagiotis D. Bamidis, Barry Eaglestone:
Data Quality Issues in Electronic Health Records: An Adaptation Framework for the Greek Health System. 23-36
Lars Höglund, Elena Maceviciute, T. D. Wilson:
Trust in Healthcare: An Information Perspective. 37-48
Mark Hepworth, Janet Harrison:
A Survey of the Information Needs of People with Multiple Sclerosis. 49-69
Lars Andersson, Greta Petersen, Per Johnson, Fredrik Ståhl:
Finding Genes Contributing to the Arthritis Phenotype by Comparing Rat and Human Genome Data. 71-75
Y. W. Chow, T. Treasure, S. Gallivan:
Can the Internet Be Used to Collect Clinical Data for Research? 77-82
Lennart Magnusson, Elizabeth Hanson:
Working with Older People and Their Carers to Research and Develop Responsive ICT Support Services. 83-88

Julia Hippisley-Cox, Vicky Hammersley, Mike Pringle, Carol Coupland, N. Crown, L. Wright:
Methodology for Assessing the Usefulness of General Practice Data for Research in One Research Network. 91-109
Michael Goddard, David Mowat, Christopher Corbett, Cordell Neudorf, Parminder Raina, Vic Sahai:
The Impacts of Knowledge Management and Information Technology Advances on Public Health Decision-Making in 2010. 111-120
Peter A. Bath, David Clark, Michael Wright:
The International Observatory on End of Life Care (IOELC): An Information Resource for Palliative Care. 121-126
Riitta Söderlund:
The Role of Information and Communication Technology in Home Services: Telecare Does not Satisfy the Needs of the Elderly. 127-137
Stefan Ek:
Information Literacy as a Health Promoting Determinant. 139-153
Trefor Roscoe, Pat Lane:
An Assessment Tool for Medical Informatics Skills. 155-159

Rob Procter: Editorial. 163-164
Danielle L. Penn, Joan R. Burns, Andrew Georgiou, P. Gawaine Powell Davies, Mark F. Harris:
Evolution of a register recall system to enable the delivery of better quality of care in general practice. 165-176
Joan R. Burns, Mary-Ann Bonney, P. Gawaine Powell Davies, Mark F. Harris:
Utilization of the CARDIAB®^TM database system to promote quality of care in Australian general practice. 177-184
Laurence Alpay, Pieter J. Toussaint, Nicole P. M. Ezendam, Ton A. J. M. Rövekamp, Wilco C. Graafmans, Rudi G. J. Westendorp:
Easing Internet access of health information for elderly users. 185-194
Christopher W. Stokes, Cenwein Cannavina, Giuseppe Cannavina:
The state of readiness of student health professionals for web-based learning environments. 195-204
Omnia Allam, Alex Gray, Steve McIntosh, David Morrey:
A systems approach to a deeper understanding of a cancer care domain. 205-220
Rabiah Ahmad, Peter A. Bath:
The use of Cox regression and genetic algorithm (CoRGA) for identifying risk factors for mortality in older people. 221-236
Taina Mäntyranta, Outi Elonheimo, Timo Klaukka, Seppo Koskinen, Jukka Mattila, Mika Vuori, Olli Nylander, Pekka Nikka, Hannu Rintanen, Mikko Nenonen:
A system of key indicators for needs assessment at local level: The Finnish network of information producers. 237-247

Rob Procter: Special Issue Integrated care records: problems and solutions. 251-252
Matthew Jones:
Learning the lessons of history? Electronic records in the United Kingdom acute hospitals, 1988-2002. 253-263
Marilyn N. Kirshbaum:
Are we ready for the Electronic Patient Record? Attitudes and perceptions of staff from two NHS trust hospitals. 265-276
Bob Sugden, Rob Wilson:
Integrated care and electronic transmission of prescriptions: experience of the evaluation of ETP pilots. 277-290
Geraldine Fitzpatrick:
Integrated care and the working record. 291-302
Dave Martin, John Mariani, Mark Rouncefield:
Implementing an HIS project: everyday features and practicalities of NHS project work. 303-313
K. Neil Jenkings:
Problems encountered in integrated care records research. 314-324