Sputum Induction in Children and Adolescents with Problematic Severe Asthma: Success Rate, Safety and Tolerability

C. Ricci, L. Lasmar, P. Pitrez, R.F. Mascarenhas, P. Camargos
{"title":"Sputum Induction in Children and Adolescents with Problematic Severe Asthma: Success Rate, Safety and Tolerability","authors":"C. Ricci, L. Lasmar, P. Pitrez, R.F. Mascarenhas, P. Camargos","doi":"10.2174/1874838401508010007","DOIUrl":null,"url":null,"abstract":"Background: In problematic severe asthma (PSA), inflammatory phenotypes can by identified by assessing cel- lularity in induced sputum (IS) samples. However, there have been few studies employing sputum induction (SI) in pedi- atric patients. Objective: To assess the success rate, safety and tolerability of SI, as well as IS sample cellularity, in pediatric PSA pa- tients. Methods: We conducted a cross-sectional study involving 44 pediatric PSA patients. We collected IS samples using inha- lations of nebulized saline solution. On the basis of the post-bronchodilator forced expiratory volume in one second (FEV1, % of predicted), we administered nebulization with 4.5% hypertonic saline (for patients with an FEV1 � 60%) or 0.9% isotonic saline (for those with an FEV1 50%. Results: The observed success rate was 75% (95% CI: 60-86). Most of the patients provided satisfactory samples, al- though multiple SI sessions were required in some cases (27%). In comparison with the IS samples containing > 20% squamous cells, those containing � 20% showed significantly more neutrophils (P = 0.02) and eosinophils (P = 0.03). The most common adverse events were mild wheezing (in 14%) and salty taste (in 9%). In 8% of the sessions, there was a � 20% decrease in FEV1. Conclusion: In our sample of pediatric patients with PSA, sputum induction was safe and generally well tolerated, sug- gesting that it could be useful in the assessment of inflammatory processes in such patients.","PeriodicalId":22835,"journal":{"name":"The Open Allergy Journal","volume":"2011 1","pages":"7-13"},"PeriodicalIF":0.0000,"publicationDate":"2015-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Allergy Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874838401508010007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: In problematic severe asthma (PSA), inflammatory phenotypes can by identified by assessing cel- lularity in induced sputum (IS) samples. However, there have been few studies employing sputum induction (SI) in pedi- atric patients. Objective: To assess the success rate, safety and tolerability of SI, as well as IS sample cellularity, in pediatric PSA pa- tients. Methods: We conducted a cross-sectional study involving 44 pediatric PSA patients. We collected IS samples using inha- lations of nebulized saline solution. On the basis of the post-bronchodilator forced expiratory volume in one second (FEV1, % of predicted), we administered nebulization with 4.5% hypertonic saline (for patients with an FEV1 � 60%) or 0.9% isotonic saline (for those with an FEV1 50%. Results: The observed success rate was 75% (95% CI: 60-86). Most of the patients provided satisfactory samples, al- though multiple SI sessions were required in some cases (27%). In comparison with the IS samples containing > 20% squamous cells, those containing � 20% showed significantly more neutrophils (P = 0.02) and eosinophils (P = 0.03). The most common adverse events were mild wheezing (in 14%) and salty taste (in 9%). In 8% of the sessions, there was a � 20% decrease in FEV1. Conclusion: In our sample of pediatric patients with PSA, sputum induction was safe and generally well tolerated, sug- gesting that it could be useful in the assessment of inflammatory processes in such patients.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
诱导痰治疗儿童和青少年严重哮喘:成功率、安全性和耐受性
背景:在有问题的严重哮喘(PSA)中,炎症表型可以通过评估诱导痰(IS)样本中的细胞清晰度来识别。然而,在儿科患者中应用诱导痰的研究很少。目的:评估SI在儿童PSA患者中的成功率、安全性和耐受性,以及IS样本的细胞含量。方法:我们对44例儿童PSA患者进行了横断面研究。我们用吸入的雾化盐水溶液来收集IS样本。根据支气管扩张剂后一秒用力呼气量(FEV1,预测的%),我们给予4.5%高渗生理盐水(FEV1 - 60%)或0.9%等渗生理盐水(FEV1 50%)雾化。结果:观察成功率为75% (95% CI: 60-86)。大多数患者提供了满意的样本,尽管在某些情况下需要多次SI(27%)。与含有> 20%鳞状细胞的IS样品相比,含有- 20%鳞状细胞的IS样品中中性粒细胞(P = 0.02)和嗜酸性粒细胞(P = 0.03)显著增加。最常见的不良事件是轻度喘息(14%)和咸味(9%)。在8%的疗程中,FEV1下降了20%。结论:在我们的儿童PSA患者样本中,痰诱导是安全的,并且通常耐受性良好,这表明它可以用于评估此类患者的炎症过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Chronic Obstructive Pulmonary Disease (COPD) and Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome (ACOS) are Risk Factors for Cryptococcosis Association Between Endoscopic, Radiologic and Patient-reported Chronic Rhinosinusitis with Nasal Polyps Food Allergy Knowledge and Attitudes Among School Teachers in Jazan, Saudi Arabia Anaphylaxis to Glatiramer Acetate Dynamics of Plasma and Granule Membrane in Murine Bone Marrow- Derived Mast Cells after Re-stimulation
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1