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Proc Natl Acad Sci U S A. 2012 Apr 10;109(15):5809-14. doi: 10.1073/pnas.1120577109. Epub 2012 Mar 26.
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Urinary desmosine: a biomarker of structural lung injury during CF pulmonary exacerbation.尿脱氧异皮质酮:CF 肺部恶化期间结构肺损伤的生物标志物。
Pediatr Pulmonol. 2012 Sep;47(9):856-63. doi: 10.1002/ppul.22525. Epub 2012 Mar 19.
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Defining pulmonary exacerbation in children with non-cystic fibrosis bronchiectasis.定义非囊性纤维化支气管扩张症儿童的肺部恶化。
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Exhaled carbon monoxide in airway diseases: from research findings to clinical relevance.气道疾病中的呼出气一氧化碳:从研究结果到临床相关性。
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Coenzyme Q10, copper, zinc, and lipid peroxidation levels in serum of patients with chronic obstructive pulmonary disease.慢性阻塞性肺疾病患者血清中辅酶 Q10、铜、锌和脂质过氧化水平。
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Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis.在成人和儿童囊性纤维化患者中,肺部恶化与随后的 FEV1 下降有关。
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Exhaled carbon monoxide as a new marker of respiratory diseases in children.呼出一氧化碳作为儿童呼吸道疾病的新标志物。
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Comparison among pulmonary function test results, the Shwachman-Kulczycki score and the Brasfield score in patients with cystic fibrosis.囊性纤维化患者肺功能测试结果、施瓦赫曼-库尔奇茨基评分和布拉斯菲尔德评分的比较。
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呼出气一氧化碳作为慢性肺部疾病患儿病情加重早期标志物的诊断价值

Diagnostic value of exhaled carbon monoxide as an early marker of exacerbation in children with chronic lung diseases.

作者信息

Abd El Khalek Karima A, El Seify Magda Y, Youssef Omneya I, Badr Mona M

机构信息

Department of Pediatrics, Faculty of Medicine, Ain Shams University, Cairo 11321, Egypt.

出版信息

ISRN Pediatr. 2012;2012:859873. doi: 10.5402/2012/859873. Epub 2012 Sep 11.

DOI:10.5402/2012/859873
PMID:22997589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3446676/
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.

摘要

慢性气道感染和炎症是慢性肺部疾病(CLD)发病和死亡的主要原因。肺部急性加重是CLD发病的主要原因。呼出一氧化碳(eCO)是内源性代谢过程的产物,其在呼出气体中的存在被认为是炎症过程的指标。目的:评估一氧化碳(eCO)作为CLD急性加重早期检测的炎症标志物。方法:病例对照研究纳入了从艾因夏姆斯大学儿童医院胸科诊所招募的40名CLD儿童(20名处于急性加重期,为I组;20名处于静止期,为II组)。另外纳入20名明显健康的儿童作为对照组(III组)。结果:患者的平均年龄为9.98±3.29岁:男性24名(60%),女性16名(40%)。急性加重期患者的平均eCO水平为5.35±1.35(ppm),而静止期为2.65±0.49(ppm),对照组为1.30±0.47(ppm)。区分病例和对照组的eCO临界值为1.5(ppm)(敏感性为100%,特异性为70%),区分I组和II组的临界值为3(ppm)(敏感性为100%,特异性为100%)。结论:呼出CO可被视为CLD急性加重的非侵入性早期标志物。