Respiratory Research Review Issue 130:

1 December, 2016

This issue of Respiratory Research Review covers the topics of bronchiectasis and CF (cystic fibrosis).

Improving outcomes for children with bronchiectasis and preventing it altogether:

Byrnes, C.

6 November, 2015

Presentation to Respiratory Conference New Zealand November 2015.

The impact of respiratory disease in New Zealand: 2014 update:

Telfar Barnard, L., Baker, M., Pierse, N., & Zhang, J.

4 April, 2015

This report covers six respiratory disease indicators: asthma, bronchiectasis, childhood bronchiolitis and pneumonia, chronic obstructive pulmonary disease (COPD), and total respiratory disease.

NZ Respiratory Research Review Issue 94:

22 November, 2013

This issue focuses on-CF bronchiectasis.

​Prognostic value of bronchiectasis in patients with moderate-to-severe chronic obstructive pulmonary disease:

Martinez-Garcia, M., Carrillo, D., Soler-Cataluna, J., Donat-Sanz, Y., Serra, P., Lerma, M., et al.

7 February, 2013

Objectives: To assess the prognostic value of bronchiectasis in patients with moderate-to-severe COPD.

Respiratory health outcomes 1 year after admission with severe lower respiratory tract infection:

Trenholme, A. et al.

19 September, 2012

The aim of this study was to determine and to describe the presence of respiratory morbidity in young children 1 year after being hospitalized with a severe LRI.

Bronchiectasis secondary to primary immunodeficiency in children: Longitudinal changes in structure and function:

Haidopoulou, K., Calder, A., Jones, A., Jaffe, A., & Sonnappa, S.

9 June, 2009

​Primary immunodeficiency is a common cause of bronchiectasis in children. The term bronchiectasis suggests an irreversible process; however, disease progression following treatment is controversial. The aim of this study was to evaluate the progression of bronchiectasis in children with primary immunodeficiency after institution of treatment. The authors concluded that bronchiectasis secondary to primary immunodeficiency in childhood is not always a progressive condition, suggesting a potential to slow or prevent disease progression with appropriate treatment.

The need to redefine non-cystic fibrosis bronchiectasis in childhood:

​ Eastham, K., Fall, A., Mitchell, L., & Spencer, D.

26 November, 2003

This study undertook a clinical and radiological review of 93 children with non-CF bronchiectasis. The authors concluded that while bronchiectasis is currently defined as a condition which is both permanent and progressive, this term is not necessarily appropriate for all paediatric patients.

Reversible bronchial dilatation in children: Comparison of serial high-resolution computer tomography scans of the lungs:

Gaillard, E., Carty, H., & Smyth, R.

9 September, 2003

Bronchiectasis is generally considered irreversible in the adult population, largely based on studies employing bronchography in cases with a significant clinical history. It is assumed that the same is true for children. The objective of this study was to evaluate changes in appearance of bronchial dilatation, unrelated to cystic fibrosis in children, as assessed by sequential high-resolution computer tomography (HRCT) of the lungs. The authors concluded that a radiological diagnosis of bronchiectasis should be considered with caution in children as diagnostic criteria derived from studies in adults have not been validated in children and the condition is generally considered irreversible.