Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests

…, G Hülskamp, A Bush, SB Carr, R Castle, A Hoo… - Thorax, 2007 - thorax.bmj.com
Background: Lung clearance index (LCI), a measure of ventilation inhomogeneity derived
from the multiple-breath inert gas washout (MBW) technique, has been shown to detect …

Respiratory function among preterm infants whose mothers smoked during pregnancy

AF Hoo, M Henschen, C Dezateux… - American journal of …, 1998 - atsjournals.org
We examined whether the adverse effects of prenatal exposure to tobacco on lung
development are limited to the last weeks of gestation by comparing respiratory function in …

Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening

AF Hoo, LP Thia, A Bush, J Chudleigh, S Lum… - Thorax, 2012 - thorax.bmj.com
Background Long-term benefits of newborn screening (NBS) for cystic fibrosis (CF) have
been established with respect to nutritional status, but effects on pulmonary health remain …

Age and height dependence of lung clearance index and functional residual capacity

…, M Brown, P Aurora, P Subbarao, A Hoo… - European …, 2013 - Eur Respiratory Soc
The lung clearance index (LCI) is more sensitive than spirometry in detecting abnormal lung
function in children with cystic fibrosis. LCI is thought to be independent of age, but recent …

Sex-Specific Prediction Equations for V˙maxFRC in Infancy: A Multicenter Collaborative Study

AF Hoo, C Dezateux, JP Hanrahan, TJ Cole… - American journal of …, 2002 - atsjournals.org
Measurements of maximal flow at functional residual capacity (V˙ max FRC) from partial
forced expiratory maneuvers remain the most popular method for assessing small airway …

Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis

WJ Kozlowska, A Bush, A Wade, P Aurora… - American journal of …, 2008 - atsjournals.org
Rationale: After recent standardization of forced expiratory maneuvers for both infants and
preschool children, longitudinal measurements are now possible from birth. Objectives: The …

Evolution of lung function during the first year of life in newborn screened cystic fibrosis infants

LP Thia, AF Hoo, A Bush, P Aurora, A Wade… - Thorax, 2014 - thorax.bmj.com
Rationale Newborn screening (NBS) for cystic fibrosis (CF) allows early intervention. Design
of randomised controlled trials (RCT) is currently impeded by uncertainty regarding …

The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis

SC Ranganathan, J Stocks, C Dezateux… - American journal of …, 2004 - atsjournals.org
This study aimed to investigate the evolution of airway function in infants newly diagnosed
with cystic fibrosis (CF). FEV0. 5 was measured soon after diagnosis (median age of 28 …

Development of airway function in infancy after preterm delivery

AF Hoo, C Dezateux, M Henschen, K Costeloe… - The Journal of …, 2002 - Elsevier
Objective: To assess airway function at 1 year and compare this with similar measurements
made shortly after birth in preterm infants without clinical neonatal respiratory disease. Study …

Low birth weight for gestation and airway function in infancy: exploring the fetal origins hypothesis

C Dezateux, S Lum, AF Hoo, J Hawdon, K Costeloe… - Thorax, 2004 - thorax.bmj.com
Background: Poor fetal growth has been associated with impaired airway function in adult
life, but evidence linking birth weight and airway function in early childhood is sparse. We …