Suppr超能文献

使用临床和放射学评分对儿童非囊性纤维化支气管扩张症的评估

Evaluation of Noncystic Fibrosis Bronchiectasis Using Clinical and Radiological Scorings in Children.

作者信息

Başaran Abdurrahman Erdem, Başaran Ayşen, Maslak İbrahim Cemal, Arslan Gökhan, Bingöl Ayşen

机构信息

Division of Pediatric Pulmonology, Akdeniz University School of Medicine, Antalya, Turkey.

Department of Pediatrics, Akdeniz University School of Medicine, Antalya, Turkey.

出版信息

Turk Thorac J. 2018 Sep 13;19(4):159-164. doi: 10.5152/TurkThoracJ.2018.17081. Print 2018 Oct.

Abstract

OBJECTIVES

The aim of this study was to evaluate radiological, clinical, and demographic data of patients with noncystic fibrosis bronchiectasis and to compare high-resolution computed tomography (HRCT) scores based on the demographic and clinical characteristics.

MATERIALS AND METHODS

A total of 34 patients (18 male, 16 female) were assessed in terms of age at symptom onset, age at diagnosis, annual attack frequency, cough severity score, physical examination findings, and pulmonary function test results. Modified Bhalla scoring system (B total) and anatomical prevalence degree score (D total) were used for HRCT examination.

RESULTS

There was a strong negative correlation between forced expiratory volume at first second (FEV) and bronchial dilatation degree (SBRDIL). There was a moderate negative correlation of FEV, forced vital capacity (FVC), and maximum mid-expiratory flow rate (MEF; 25-75) with bronchiectasis degree (EXBRNC), bronchial wall thickness degree (SBWTHICK), and mucus accumulation in the major airways (PMPLA). The B total, D total, EXBRNC, and SBRDIL scores were significantly higher in patients with hemoptysis and sputum. In comparing B and D total scoring systems, B total provided better results in terms of rale, annual exacerbation frequency (AEF), cough severity score (CSS), and FEV values.

CONCLUSION

As it is proved using HRCT, pulmonary function impairment, sputum production, hemoptysis, and increase in AEF strongly correlating with objective HRCT scoring can be accepted as markers for pathological changes due to bronchiectasis.

摘要

目的

本研究旨在评估非囊性纤维化支气管扩张症患者的放射学、临床和人口统计学数据,并根据人口统计学和临床特征比较高分辨率计算机断层扫描(HRCT)评分。

材料与方法

共评估了34例患者(18例男性,16例女性),记录症状出现年龄、诊断年龄、年发作频率、咳嗽严重程度评分、体格检查结果和肺功能测试结果。HRCT检查采用改良的巴拉评分系统(B总分)和解剖学患病率评分(D总分)。

结果

第1秒用力呼气量(FEV)与支气管扩张程度(SBRDIL)之间存在强负相关。FEV、用力肺活量(FVC)和最大呼气中期流速(MEF;25 - 75)与支气管扩张程度(EXBRNC)、支气管壁厚度(SBWTHICK)和主气道黏液积聚(PMPLA)之间存在中度负相关。咯血和咳痰患者的B总分、D总分、EXBRNC和SBRDIL评分显著更高。在比较B总分和D总分评分系统时,B总分在啰音、年加重频率(AEF)、咳嗽严重程度评分(CSS)和FEV值方面提供了更好的结果。

结论

正如HRCT所证实的,肺功能损害、咳痰、咯血以及与客观HRCT评分密切相关的AEF增加可被视为支气管扩张所致病理变化的标志物。

相似文献

1
Evaluation of Noncystic Fibrosis Bronchiectasis Using Clinical and Radiological Scorings in Children.
Turk Thorac J. 2018 Sep 13;19(4):159-164. doi: 10.5152/TurkThoracJ.2018.17081. Print 2018 Oct.
7
Effect of radiological extent and severity of bronchiectasis on pulmonary function.
Multidiscip Respir Med. 2011 Oct 31;6(5):284-90. doi: 10.1186/2049-6958-6-5-284.
8
9
Annual FEV Loss in Patients with Noncystic Fibrosis Bronchiectasis and Affecting Factors.
South Med J. 2022 May;115(5):328-332. doi: 10.14423/SMJ.0000000000001394.

引用本文的文献

1
Usefulness of High-resolution Computed Tomography for Macrolide Therapy of Idiopathic Bronchiectasis.
Open Respir Med J. 2023 Aug 29;17:e187430642307250. doi: 10.2174/18743064-v17-230822-2022-27. eCollection 2023.
3
Relationships Between Bronchoscopy, Microbiology, and Radiology in Noncystic Fibrosis Bronchiectasis.
Pediatr Allergy Immunol Pulmonol. 2021 Jun;34(2):46-52. doi: 10.1089/ped.2020.1319. Epub 2021 May 14.
4
Measuring airway clearance outcomes in bronchiectasis: a review.
Eur Respir Rev. 2020 Apr 29;29(156). doi: 10.1183/16000617.0161-2019. Print 2020 Jun 30.

本文引用的文献

1
Hiatal hernias are correlated with increased severity of non-cystic fibrosis bronchiectasis.
Respirology. 2015 Jul;20(5):749-57. doi: 10.1111/resp.12522. Epub 2015 Apr 14.
2
Effect of radiological extent and severity of bronchiectasis on pulmonary function.
Multidiscip Respir Med. 2011 Oct 31;6(5):284-90. doi: 10.1186/2049-6958-6-5-284.
3
Do New Zealand children with non-cystic fibrosis bronchiectasis show disease progression?
Pediatr Pulmonol. 2011 Feb;46(2):131-8. doi: 10.1002/ppul.21331. Epub 2010 Aug 17.
4
Exacerbations in cystic fibrosis: 4--Non-cystic fibrosis bronchiectasis.
Thorax. 2008 Mar;63(3):269-76. doi: 10.1136/thx.2006.060913.
5
Non-cystic-fibrosis bronchiectasis: a perspective from South America.
Paediatr Respir Rev. 2006 Dec;7(4):275-80. doi: 10.1016/j.prrv.2006.04.008. Epub 2006 Oct 12.
6
Non cystic fibrosis bronchiectasis.
Paediatr Respir Rev. 2000 Mar;1(1):64-70. doi: 10.1053/prrv.2000.0011.
7
Non-CF bronchiectasis: does knowing the aetiology lead to changes in management?
Eur Respir J. 2005 Jul;26(1):8-14. doi: 10.1183/09031936.05.00127704.
8
Non-cystic-fibrosis bronchiectasis in children: a persisting problem in developing countries.
Respiration. 2005 May-Jun;72(3):233-8. doi: 10.1159/000085362.
9
Bronchiectasis: the consequence of late diagnosis in chronic respiratory symptoms.
J Trop Pediatr. 2005 Dec;51(6):362-5. doi: 10.1093/tropej/fmi036. Epub 2005 May 12.
10
New Zealand national incidence of bronchiectasis "too high" for a developed country.
Arch Dis Child. 2005 Jul;90(7):737-40. doi: 10.1136/adc.2004.066472. Epub 2005 May 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验