Department of Pediatric Radiology, Chair of General and Invasive Radiology, Poznan University of Medical Sciences, Poznań, Poland.
Department of Pulmonology, Pediatric Allergy and Clinical Immunology, Poznan University of Medical Sciences, Poznań, Poland.
PLoS One. 2019 Jul 10;14(7):e0215786. doi: 10.1371/journal.pone.0215786. eCollection 2019.
Cystic fibrosis (CF) is one of the most common genetic disorders among the White population. The disease has a progressive course and leads to a reduction in the quality of life and of life expectancy. Standard diagnostic procedures used in the monitoring of CF patients include methods which expose patients to ionizing radiation. With increasing life expectancy in CF the cumulative dose of ionising radiation increases, prompting clinicians' search for safer imaging studies. Despite its safety and availability lung ultrasound (LUS) is not routinely used in the diagnostic evaluation of CF patients. The aim of the study was to evaluate the diagnostic value of LUS in children with CF compared to a chest X-ray, and to assess the diagnostic value of the recently developed LUS score-CF-USS (Cystic Fibrosis Ultrasound Score). LUS was performed in 48 CF children and adolescents aged from 5 to 18 years (24 girls and 24 boys). LUS consisted of the assessment of the pleura, lung sliding, A-line and B-line artefacts, "lung rockets", alveolar consolidations, air bronchogram and pleural effusion. Chest radiography was performed in all patients and analyzed according to the modified Chrispin-Norman score. LUS was analyzed according to CF-USS. The correlation between the CF-USS and the modified Chrispin-Norman scores was moderate (R = 0.52, p = 0.0002) and strong in control studies. In 75% of patients undergoing LUS, small areas of subpleural consolidations were observed, which were not visible on x-rays. At the same time, LUS was not sensitive enough to visualize bronchial pathology, which plays an important role in assessing the progression of the disease. Conclusions: LUS constitutes an invaluable tool for the diagnosis of subpleural consolidations. CF-USS results correlate with the conventional x-ray modified Chrispin-Norman score. LUS should be considered a supplementary radiographic examination in the monitoring of CF patients, and CF-USS may provide clinicians with valuable information concerning the progression of the disease.
囊性纤维化 (CF) 是白人中最常见的遗传疾病之一。该疾病具有进行性病程,导致生活质量和预期寿命降低。监测 CF 患者时使用的标准诊断程序包括使患者暴露于电离辐射的方法。随着 CF 患者预期寿命的延长,电离辐射的累积剂量增加,促使临床医生寻找更安全的成像研究。尽管超声检查具有安全性和可用性,但在 CF 患者的诊断评估中并未常规使用。本研究的目的是评估与胸部 X 射线相比,超声检查在 CF 儿童中的诊断价值,并评估最近开发的超声评分-CF-USS(囊性纤维化超声评分)的诊断价值。对 48 名年龄在 5 至 18 岁的 CF 儿童和青少年(24 名女孩和 24 名男孩)进行了超声检查。超声检查包括评估胸膜、肺滑动、A 线和 B 线伪影、“肺火箭”、肺泡实变、空气支气管征和胸腔积液。所有患者均进行了胸部 X 射线检查,并根据改良 Chrispin-Norman 评分进行了分析。超声检查根据 CF-USS 进行了分析。CF-USS 与改良 Chrispin-Norman 评分之间的相关性为中度(R=0.52,p=0.0002),在对照研究中为强。在进行超声检查的 75%的患者中,观察到小面积的胸膜下实变,但 X 射线不可见。同时,超声检查不够敏感,无法观察到支气管病变,而支气管病变在评估疾病进展方面起着重要作用。结论:超声检查是诊断胸膜下实变的一种非常有价值的工具。CF-USS 结果与传统 X 射线改良 Chrispin-Norman 评分相关。超声检查应被视为 CF 患者监测的补充影像学检查,CF-USS 可能为临床医生提供有关疾病进展的有价值信息。