BMJ 1997;315:1504-1505 (6 December)

Papers

Underreporting of mortality from RhD haemolytic disease in Scotland and its implications: retrospective review

Charles R Whitfield, emeritus regius professor of midwifery,a Alaeddin Raafat, honorary lecturer in transfusion medicine,b Stanislaw J Urbaniak, honorary reader in transfusion medicine b

a Department of Obstetrics and Gynaecology, the Queen Mother's Maternity Hospital, University of Glasgow, Glasgow G3 8SH, b Academic Transfusion Medicine Unit, Department of Medicine and Therapeutics, University of Aberdeen, Regional Transfusion Centre, Foresterhill, Aberdeen AB9 2ZW

Correspondence to: Professor Whitfield


right arrow   Introduction

Clarke et al surveyed the decline in RhD haemolytic disease in England and Wales from 1977-92 by reviewing the statistics of the Office of Population Censuses and Surveys; during that time deaths attributable to RhD haemolytic disease had fallen from 18.4 to 1.3 per 100 000 live births.1 We surveyed RhD alloimmunisation in mothers resident in Scotland between 1987 and 91 and confirmed that fetal loss from RhD haemolytic disease was greater than that listed by the General Register Office in Scotland. Underreporting has serious implications for recognising, understanding, and preventing this potentially lethal disease.


right arrow   Subjects, methods, and results

Data on deaths attributable to RhD haemolytic disease during 1987-91 were obtained from: death certificates; details of pregnancies in Scottish residents who had antibody to RhD antigen and were managed at the Queen . . . [Full text of this article]


right arrow   Comment

right arrow   Acknowledgements

right arrow   References

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