Literature DB >> 20232470

Effect of cumulative oxygen exposure on respiratory symptoms during infancy among VLBW infants without bronchopulmonary dysplasia.

Timothy P Stevens1, Andrew Dylag, Indira Panthagani, Gloria Pryhuber, Jill Halterman.   

Abstract

UNLABELLED: Very low birth weight (VLBW) infants, even those without bronchopulmonary dysplasia (BPD) are at risk for pulmonary morbidity during infancy. Although some studies have found an association between the level of neonatal oxygen exposure and later morbidity, others have not. A possible explanation for these inconsistent findings is that the cumulative dosage of neonatal supplemental oxygen to which infants are exposure is difficult to accurately quantify.
METHODS: A prospective cohort study of VLBW infants without BPD was performed to test the hypothesis that cumulative oxygen exposure in the neonatal period summarized using an area under the curve analysis (Oxygen(AUC)) is predictive of later pulmonary symptoms. Risk factors tested in the analysis included both neonatal and outpatient respiratory exposures. Outcome measures included respiratory symptoms and use of medications and health services to treat those symptoms.
RESULTS: The prevalence of pulmonary symptoms after NICU discharge was 48% (36 of 75 patients). Oxygen(AUC) as early as 72 hr of age predicts respiratory symptoms and respiratory-related health service and medication use during infancy in a dose dependent manner. Oxygen(AUC) is a stronger predictor of later respiratory symptoms than is the number of days of supplemental oxygen or positive pressure respiratory therapy or integrated mean airway pressure (MAP(AUC)).
CONCLUSIONS: Oxygen(AUC) as early as 72 hr of age is predictive of later respiratory symptoms and use of health services and medications to treat those symptoms. Supplemental oxygen therapy should be monitored carefully to minimize oxygen exposure and risk of later respiratory symptoms in VLBW infants.

Entities:  

Mesh:

Year:  2010        PMID: 20232470     DOI: 10.1002/ppul.21199

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  25 in total

1.  Lung development and the host response to influenza A virus are altered by different doses of neonatal oxygen in mice.

Authors:  Bradley W Buczynski; Min Yee; B Paige Lawrence; Michael A O'Reilly
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2012-03-09       Impact factor: 5.464

2.  Cumulative neonatal oxygen exposure predicts response of adult mice infected with influenza A virus.

Authors:  Echezona T Maduekwe; Bradley W Buczynski; Min Yee; Tiruamalai Rangasamy; Timothy P Stevens; B Paige Lawrence; Michael A O'Reilly
Journal:  Pediatr Pulmonol       Date:  2014-05-22

3.  Early Cumulative Supplemental Oxygen Predicts Bronchopulmonary Dysplasia in High Risk Extremely Low Gestational Age Newborns.

Authors:  Katherine C Wai; Michael A Kohn; Roberta A Ballard; William E Truog; Dennis M Black; Jeanette M Asselin; Philip L Ballard; Elizabeth E Rogers; Roberta L Keller
Journal:  J Pediatr       Date:  2016-07-26       Impact factor: 4.406

4.  Neonatal hyperoxia promotes asthma-like features through IL-33-dependent ILC2 responses.

Authors:  In Su Cheon; Young Min Son; Li Jiang; Nicholas P Goplen; Mark H Kaplan; Andrew H Limper; Hirohito Kita; Sophie Paczesny; Y S Prakash; Robert Tepper; Shawn K Ahlfeld; Jie Sun
Journal:  J Allergy Clin Immunol       Date:  2017-12-15       Impact factor: 10.793

5.  T cell developmental arrest in former premature infants increases risk of respiratory morbidity later in infancy.

Authors:  Kristin M Scheible; Jason Emo; Nathan Laniewski; Andrea M Baran; Derick R Peterson; Jeanne Holden-Wiltse; Sanjukta Bandyopadhyay; Andrew G Straw; Heidie Huyck; John M Ashton; Kelly Schooping Tripi; Karan Arul; Elizabeth Werner; Tanya Scalise; Deanna Maffett; Mary Caserta; Rita M Ryan; Anne Marie Reynolds; Clement L Ren; David J Topham; Thomas J Mariani; Gloria S Pryhuber
Journal:  JCI Insight       Date:  2018-02-22

6.  Cumulative exposure to gamma interferon-dependent chemokines CXCL9 and CXCL10 correlates with worse outcome after lung transplant.

Authors:  D C Neujahr; S D Perez; A Mohammed; O Ulukpo; E C Lawrence; F Fernandez; A Pickens; S D Force; M Song; C P Larsen; A D Kirk
Journal:  Am J Transplant       Date:  2011-12-07       Impact factor: 8.086

7.  Neonatal hyperoxia causes pulmonary vascular disease and shortens life span in aging mice.

Authors:  Min Yee; R James White; Hani A Awad; Wendy A Bates; Sharon A McGrath-Morrow; Michael A O'Reilly
Journal:  Am J Pathol       Date:  2011-05-06       Impact factor: 4.307

8.  Preterm cord blood CD4⁺ T cells exhibit increased IL-6 production in chorioamnionitis and decreased CD4⁺ T cells in bronchopulmonary dysplasia.

Authors:  Ravi Misra; Syed Shah; Deborah Fowell; Hongyue Wang; Kristin Scheible; Sara Misra; Heidie Huyck; Claire Wyman; Rita M Ryan; Anne Marie Reynolds; Tom Mariani; Philip J Katzman; Gloria S Pryhuber
Journal:  Hum Immunol       Date:  2015-03-20       Impact factor: 2.850

Review 9.  Rodent models of respiratory control and respiratory system development-Clinical significance.

Authors:  Andrew M Dylag; Thomas M Raffay
Journal:  Respir Physiol Neurobiol       Date:  2019-07-14       Impact factor: 1.931

Review 10.  The role of hyperoxia in the pathogenesis of experimental BPD.

Authors:  Bradley W Buczynski; Echezona T Maduekwe; Michael A O'Reilly
Journal:  Semin Perinatol       Date:  2013-04       Impact factor: 3.300

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