Where possible we have provided additional details of websites referenced, see the Support Directory.
Page 335: Records
British Paediatric Association (1990) Parent held and professional records used in child health surveillance, British Paediatric Association, London.
O’ Flaherty, S., Jandera, E., Llewellyn, J. Wall, M. (1987) Personal health records: an evaluation, Archives of Disease in Childhood, 67, 1152-5.
Emond, A. Howat, P., Evans, J. A. (1995) Reliability of parent-held child health records,Health Visitor, 68(8), 322-3.
Jeffs, D., Nossar, V., Bailey, F. Smith, W., Chey, T. (1994) Retention and use of personal health records: a population-based study, Journal of Paediatrics and Child Health, 30, 248-52.
Lakhani, A. D., Avery, A., Gordon, A., Tait, N. (1984) Evaluation of a home-based healh record booklet, Archives of Disease in Childhood, 59, 1076-81.
Dawson, C., Perkins, M., Draper, E., Johnson, A., Field, D. (1997) ARe outcome data regarding neonatal care available from routine sources?, Archives of Disease in Childhood,77, F206-10.
Page 339: Library of additional pages
A library of additional pages for the PCHR is held at the Royal College of Paedaitrics and Child Health. For details contact Maureen Robinson at firstname.lastname@example.org
Page 340: CHIC
‘Monitoring the health of the nation’s children – key indicators and the underlying essential core data set’. CHIC – RCPCH, May 2000. Website www.CHIConsortium.org.uk
Page 340: Australian data on minimum data set
Indicators for child health, development and wellbeing. A systematic review of the literature and recommendations for population monitoring. ISBN 0 9578286 3 2 April 2002.This is available for download at www.rchmelb.org/ccch/pub/index.cfm?doc_id=714 but is over 3MB in size
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