全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Diagnostic Value of Exhaled Carbon Monoxide as an Early Marker of Exacerbation in Children with Chronic Lung Diseases

DOI: 10.5402/2012/859873

Full-Text   Cite this paper   Add to My Lib

Abstract:

Chronic airways infection and inflammation are leading causes of morbidity and mortality in chronic lung diseases (CLD). Pulmonary exacerbations are major causes of morbidity in CLD. Exhaled carbon monoxide (eCO) is a product of endogenous metabolic processes whose presence in exhaled breath is considered an index of inflammatory processes. Objective. To evaluate carbon monoxide (eCO) as inflammatory marker for early detection of acute exacerbation in CLD. Methods. Case control study included 40 children with CLD (twenty in exacerbation, group I and twenty in quiescent period, group II) recruited from the Chest Clinic, Children’s Hospital, Ain Shams University. Twenty apparently healthy children were included as controls (group III). Results. Patients’ mean age was 9.98 ± 3.29 years: 24 (60%) males and 16 (40%) females. The mean eCO level among patients during exacerbation was 5.35 ± 1.35 (ppm) compared to 2.65 ± 0.49 (ppm) in quiescent stage and 1.30 ± 0.47 (ppm) in controls. eCO cutoff value discriminating cases and control was 1.5 (ppm) (sensitivity; 100% and specificity 70%) and cutoff value discriminating group I from group II was 3 (ppm) (sensitivity: 100% and specificity: 100%). Conclusion. Exhaled CO can be considered a noninvasive early marker of acute exacerbation of CLD. 1. Introduction Chronic lung diseases (CLDs) including cystic fibrosis, asthma, chronic obstructive pulmonary disease (COPD), and other types of bronchiectasis represent a major challenge for health care [1]. Chronic infection and inflammation of the airways are the leading causes of morbidity and mortality in CLD [2]. Pulmonary exacerbations are a major cause of morbidity and decreased quality of life for patients with chronic lung diseases [3]. Exhaled breath analysis has enormous potential as an easy, non invasive means of monitoring inflammation and oxidative stress in the airway [4]. CO represents a product of endogenous metabolic processes whose presence on exhaled breath is considered as indices of inflammatory processes [5]. Exhaled Co not only can be used as an oxidative stress marker, but also can reflect the severity of chronic lung diseases (CLD). Also exhaled CO could serve as an indicator of acute exacerbations in children with CLD [6]. 1.1. Aim of the Work The present study aimed to detect the diagnostic value of carbon monoxide (CO) as inflammatory marker for early detection of acute exacerbation of chronic lung diseases. 2. Patients and Method 2.1. Study Case control study was carried at the Chest Clinic, Children’s hospital, Ain Sham University in the period

References

[1]  I. Horváth and R. Gajdócsy, “Exhaled carbon monoxide in airway diseases: from research findings to clinical relevance,” Journal of Breath Research, vol. 4, no. 4, Article ID 047102, 2010.
[2]  J. Zhao, P. D. Schloss, L. M. Kalikin et al., “Decade-long bacterial community dynamics in cystic fibrosis airways,” Proceedings of the National Academy of Sciences, vol. 109, no. 15, pp. 5809–5814, 2012.
[3]  C. H. Goss and J. L. Burns, “Exacerbations in cystic fibrosis·1: epidemiology and pathogenesis,” Thorax, vol. 62, no. 4, pp. 360–367, 2007.
[4]  W. B. M. Gerritsen, J. Asin, P. Zanen, J. M. M. van den Bosch, and F. J. L. M. Haas, “Markers of inflammation and oxidative stress in exacerbated chronic obstructive pulmonary disease patients,” Respiratory Medicine, vol. 99, no. 1, pp. 84–90, 2005.
[5]  L. A. Hoffman, J. Choi, G. W. Rodway, and J. M. Sethi, “Markers of lung disease in exhaled breath: nitric oxide,” Biological Research for Nursing, vol. 7, no. 4, pp. 241–255, 2006.
[6]  E. Babusikova, M. Jesenak, P. Durdik, D. Dobrota, and P. Banovcin, “Exhaled carbon monoxide as a new marker of respiratory diseases in children,” Journal of Physiology and Pharmacology, vol. 59, no. 6, pp. 9–17, 2008.
[7]  H. Grasemann, I. Ioannidis, R. P. Tomkiewicz, H. De Groot, B. K. Rubin, and F. Ratjen, “Nitric oxide metabolites in cystic fibrosis lung disease,” Archives of Disease in Childhood, vol. 78, no. 1, pp. 49–53, 1998.
[8]  J. Kanga, R. Kuhn, L. Craigmyle, D. Haverstock, and D. Church, “Cystic fibrosis clinical score: a new scoring system to evaluate acute pulmonary exacerbation,” Clinical Therapeutics, vol. 21, no. 8, pp. 1343–1356, 1999.
[9]  D. M. G. Halpin and D. P. Tashkin, “Defining disease modification in chronic obstructive pulmonary disease,” Journal of Chronic Obstructive Pulmonary Disease, vol. 6, no. 3, pp. 211–225, 2009.
[10]  T. A. Laguna, B. D. Wagner, B. Starcher et al., “Urinary desmosine: a biomarker of structural lung injury during CF pulmonary exacerbation,” Pediatric Pulmonology, vol. 47, no. 9, pp. 856–863, 2012.
[11]  I. D. Freire, F. A. De Abreu E Silva, and M. ?. De Araújo, “Comparison among pulmonary function test results, the Shwachman-Kulczycki score and the Brasfield score in patients with cystic fibrosis,” Jornal Brasileiro de Pneumologia, vol. 34, no. 5, pp. 280–287, 2008.
[12]  C. D. A. D. Alves, R. A. Aguiar, A. C. S. Alves, and M. A. Santana, “Diabetes mellitus in patients with cystic fibrosis,” Jornal Brasileiro de Pneumologia, vol. 33, no. 2, pp. 213–221, 2007.
[13]  H. R. Rabin, S. M. Butler, M. E. B. Wohl et al., “Pulmonary exacerbations in cystic fibrosis,” Pediatric Pulmonology, vol. 37, no. 5, pp. 400–406, 2004.
[14]  N. Kapur, I. B. Masters, P. S. Morris, J. Galligan, and R. Ware, “Defining pulmonary exacerbation in children with non-cystic fibrosis bronchiectasis,” Pediatric Pulmonology, vol. 47, pp. 68–75, 2012.
[15]  I. Eichler, M. Nilsson, R. Rath, I. Enander, P. Venge, and D. Y. Koller, “Human neutrophil lipocalin, a highly specific marker for acute exacerbation in cystic fibrosis,” European Respiratory Journal, vol. 14, no. 5, pp. 1145–1149, 1999.
[16]  A. C. Tanrikulu, A. Abakay, O. Evliyaoglu, and Y. Palanci, “Coenzyme Q10, Copper, Zinc, and Lipid Peroxidation levels in serum of patients with chronic obstructive pulmonary disease,” Biological Trace Element Research, pp. 659–667, 2010.
[17]  M. Y. El-Seify, T. A. Kamel, M. I. El-Mogy, and S. H. Ossman, “Serum human neutrophil lipocalin in pediatric chronic lung diseases: a novel marker of ongoing neutrophilic inflammation,” Egyptian Journal of Bronchology, vol. 5, no. 1, 2011.
[18]  D. B. Sanders, R. C. L. Bittner, M. Rosenfeld, G. J. Redding, and C. H. Goss, “Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis,” Pediatric Pulmonology, vol. 46, no. 4, pp. 393–400, 2011.
[19]  J. D. Antuni, S. A. Kharitonov, D. Hughes, M. E. Hodson, and P. J. Barnes, “Increase in exhaled carbon monoxide during exacerbations of cystic fibrosis,” Thorax, vol. 55, no. 2, pp. 138–142, 2000.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133