Literature DB >> 16705008

Preschool healthcare utilisation related to home oxygen status.

A Greenough1, J Alexander, S Burgess, J Bytham, P A J Chetcuti, J Hagan, W Lenney, S Melville, N J Shaw, J Boorman, S Coles, F Pang, J Turner.   

Abstract

OBJECTIVE: To determine, in prematurely born children who had bronchopulmonary dysplasia (BPD), if respiratory morbidity, healthcare utilisation, and cost of care during the preschool years were influenced by use of supplementary oxygen at home after discharge from the neonatal intensive care unit.
DESIGN: Observational study.
SETTING: Four tertiary neonatal intensive care units. PATIENTS: 190 children, median gestational age 27 weeks (range 22-31), 70 of whom received supplementary oxygen when discharged home.
INTERVENTIONS: Review of hospital and general practitioner records together with a parent completed respiratory questionnaire. MAIN OUTCOME MEASURES: Healthcare utilisation, cost of care, cough, wheeze, and use of an inhaler.
RESULTS: Seventy children had supplementary oxygen at home (home oxygen group), but only one had a continuous requirement for home oxygen beyond 2 years of age. There were no significant differences in the gestational age or birth weight of the home oxygen group compared with the rest of the cohort. However, between 2 and 4 years of age inclusive, the home oxygen group had more outpatient attendances (p = 0.0021) and specialist attendances (p = 0.0023), and, for respiratory problems, required more prescriptions (p<0.0001). Their total cost of care was higher (p<0.0001). In addition, more of the home oxygen group wheezed more than once a week (p = 0.0486) and were more likely to use an inhaler (p<0.0001).
CONCLUSIONS: Children with BPD who have supplementary oxygen at home after discharge have increased respiratory morbidity and healthcare utilisation in the preschool years.

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Year:  2006        PMID: 16705008      PMCID: PMC2672834          DOI: 10.1136/adc.2005.088823

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN: 1359-2998            Impact factor:   5.747


  12 in total

1.  Home oxygen status and rehospitalisation and primary care requirements of infants with chronic lung disease.

Authors:  A Greenough; J Alexander; S Burgess; P A J Chetcuti; S Cox; W Lenney; F Turnbull; N J Shaw; A Woods; J Boorman; S Coles; J Turner
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2.  Health care utilisation of infants with chronic lung disease, related to hospitalisation for RSV infection.

Authors:  A Greenough; S Cox; J Alexander; W Lenney; F Turnbull; S Burgess; P A Chetcuti; N J Shaw; A Woods; J Boorman; S Coles; J Turner
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Authors:  Anne Greenough; John Alexander; Sal Burgess; Phillip A J Chetcuti; Sarah Cox; Warren Lenney; Francis Turnbull; Nigel J Shaw; Alison Woods; Jill Boorman; Stephen Coles; Jackie Turner
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10.  Health care utilisation of prematurely born, preschool children related to hospitalisation for RSV infection.

Authors:  A Greenough; J Alexander; S Burgess; J Bytham; P A J Chetcuti; J Hagan; W Lenney; S Melville; N J Shaw; J Boorman; S Coles; J Turner; F Pang
Journal:  Arch Dis Child       Date:  2004-07       Impact factor: 3.791

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4.  Respiratory morbidity, healthcare utilisation and cost of care at school age related to home oxygen status.

Authors:  Anne Greenough; John Alexander; Jill Boorman; Philip A J Chetcuti; Ian Cliff; Warren Lenney; Colin Morgan; Nigel J Shaw; Karl P Sylvester; Jackie Turner
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5.  Health Care and Societal Costs of Bronchopulmonary Dysplasia.

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7.  The impact of bronchopulmonary dysplasia on caregiver health related quality of life during the first 2 years of life.

Authors:  Sharon A McGrath-Morrow; Timothy Ryan; Kristin Riekert; Maureen A Lefton-Greif; Michelle Eakin; Joseph M Collaco
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Review 8.  Bronchopulmonary dysplasia early changes leading to long-term consequences.

Authors:  Anne Hilgendorff; Michael A O'Reilly
Journal:  Front Med (Lausanne)       Date:  2015-02-12

9.  Comparison of Follow-up Courses after Discharge from Neonatal Intensive Care Unit between Very Low Birth Weight Infants with and without Home Oxygen.

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10.  Lung CD103+dendritic cells and Clec9a signaling are required for neonatal hyperoxia-induced inflammatory responses to rhinovirus infection.

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