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Published Online First: 4 May 2005. doi:10.1136/adc.2004.066472
Archives of Disease in Childhood 2005;90:737-740
Copyright © 2005 BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health.
Archives of Disease in Childhood 2005;90:737-740
© 2005 BMJ Publishing Group & Royal College of Paediatrics and Child Health

ORIGINAL ARTICLE

New Zealand national incidence of bronchiectasis "too high" for a developed country

J Twiss1,2, R Metcalfe2, E Edwards1,2, C Byrnes1,2

1 Starship Childrens’ Hospital, Auckland District Health Board, Auckland, New Zealand
2 University of Auckland, Auckland, New Zealand

Correspondence to:
Dr J Twiss
Starship Childrens’ Hospital, Private Bag 92024, Auckland, New Zealand; jacobt{at}adhb.govt.nz

Aims: To prospectively estimate the incidence of bronchiectasis among New Zealand (NZ) children, to consider aetiology and severity, and to evaluate regional and ethnic variation.

Methodology: NZ paediatricians were surveyed monthly for new cases of bronchiectasis during 2001 and 2002 via the NZ paediatric surveillance unit (with coverage of >94% of NZ paediatricians). Notified cases had their computed tomography scans reviewed and scored for severity. Confirmed cases were followed up by postal questionnaire one year after diagnosis. Demographic, aetiological, and severity data were collected.

Results: Ninety nine notifications were received. Sixty five cases were confirmed. An overall incidence of 3.7 per 100 000 under 15 year old children per year was estimated. Incidence was highest in Pacific children at 17.8 compared with 4.8 in Maori, 1.5 in NZ European, and 2.4 other per 100 000 per year. Incidence varied significantly by region. The median age at diagnosis was 5.2 years; the majority had symptoms for more than two years. Eighty three per cent had bilateral disease, with a median of three lobes affected, mean FEV1 of 77% predicted, and modified Bhalla HRCT score of 18.

Conclusions: The incidence of bronchiectasis is high in NZ children, nearly twice the rate for cystic fibrosis and seven times that of Finland, the only other country reporting a childhood national rate. Incidence varied substantially between ethnicities. Most cases developed disease in early childhood and had delayed diagnosis.

Abbreviations: CF, cystic fibrosis; FEV1, forced expiratory volume in one second; HRCT, high resolution computed tomography; NZPSU, New Zealand Paediatric Surveillance Unit

Keywords: bronchiectasis; incidence; New Zealand; indigenous


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