Pulmonary complications of predominantly antibody immunodeficiencies in a tertiary lung center.

Q2 Medicine
Seyed Alireza Mahdaviani, Sepideh Darougar, Davood Mansouri, Sabereh Tashayoie-Nejad, Mahshid Movahedi, Karim Rahimi Aghdam, Hosseinali Ghaffaripour, Nooshin Baghaie, Maryam Hassanzad, Alireza Eslaminejad, Atefeh Fakharian, Guitti Pourdowlat, Jalal Heshmatnia, Mehrdad Bakhshayeshkaram, Mohammadreza Boloursaz, Payam Tabarsi, Seyed Karen Hashemitari, Ali Akbar Velayati
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引用次数: 3

Abstract

Background and aims: Respiratory infections are expressed very soon in the life in humoral immunodeficiencies and often lead to chronic irreversible complications such as bronchiectasis and chronic airflow limitation. This study was conducted to evaluate the pulmonary complications of predominantly antibody immunodeficiencies to show the benefits of timely diagnosis and appropriate therapy.

Patients and methods: The information of 48 patients involved with a type of predominantly antibody immunodeficiencies, including sex, type of primary immunodeficiency, age at the onset of symptoms, age at diagnosis, recurrent infections, respiratory symptoms, and pulmonary radiological and functional abnormalities were recorded and analyzed.

Results: In 48 patients evaluated, the mean age at diagnosis was 25.63 years. The mean diagnostic delay was estimated to be 13.62 years. The most recurring clinical manifestations, sinusitis (69.6%), otitis (43.5%), and recurrent pneumonia were the cause of frequent admissions in 68.8% of these patients. Bronchiectasis was frequently found (58.3%) in these patients mostly involving the middle and lower lobes (48.8% and 41.5%, respectively).

Conclusions: Respiratory complications, infectious or non-infectious, determine the prognosis of the disease in patients with predominantly antibody immunodeficiencies. Timely diagnosis and appropriate management may improve life expectancy and the quality of life in these patients.

Abstract Image

三期肺中心以抗体免疫缺陷为主的肺部并发症。
背景与目的:呼吸道感染在生命中以体液免疫缺陷的形式迅速表达,常导致慢性不可逆并发症,如支气管扩张和慢性气流受限。本研究旨在评估以抗体免疫缺陷为主的肺部并发症,以显示及时诊断和适当治疗的益处。患者和方法:记录并分析48例以抗体免疫缺陷为主的患者的信息,包括性别、原发性免疫缺陷类型、发病年龄、诊断年龄、复发感染、呼吸道症状、肺部放射学和功能异常。结果:48例患者的平均诊断年龄为25.63岁。平均诊断延迟估计为13.62年。其中以鼻窦炎(69.6%)、中耳炎(43.5%)和肺炎复发最为常见,占68.8%。支气管扩张多发(58.3%),主要累及中下叶(分别为48.8%和41.5%)。结论:呼吸道并发症,传染性或非传染性,决定了主要抗体免疫缺陷患者的预后。及时的诊断和适当的管理可以改善这些患者的预期寿命和生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Interventional Medicine and Applied Science
Interventional Medicine and Applied Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.60
自引率
0.00%
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0
审稿时长
15 weeks
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