CYSTIC-FIBROSIS - SCORING SYSTEM WITH THIN-SECTION CT
CYSTIC-FIBROSIS - SCORING SYSTEM WITH THIN-SECTION CT
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DOI：
10.1148/radiology.179.3.2027992
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发表时间：
1991-06-01
期刊：
影响因子：
19.7
通讯作者：
NAIDICH, DP
中科院分区：
文献类型：
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作者：
BHALLA, M;TURCIOS, N;NAIDICH, DP
通过胸部X线检查评估囊性纤维化（CF）患者肺部疾病的进展。采用Chrispin或Birmingham方法对各种影像学改变的严重程度和范围进行评分，该方法涉及使用不精确和主观的术语，如线状阴影，大的肺部阴影和结节性囊性病变。虽然计算机断层扫描（CT）已被证明是有帮助的肺部疾病的CF的评价，没有评分系统或其他客观标准已开发的评估范围广泛的肺部变化，在这些患者。设计了一个CT评分系统，该系统包含CF患者肺部的所有变化。这样的评分系统可以促进现有的和新开发的治疗方案的客观评价，并可能是一个有价值的工具，在术前评估的患者被认为是肺叶切除术或肺大疱切除术，并在肺移植患者的选择。
The progression of lung disease in patients with cystic fibrosis (CF) was evaluated with chest radiography. The severity and extent of the various radiographic changes were scored with the Chrispin or the Birmingham method, which involves the use of imprecise and subjective terms, such as line shadows, large pulmonary shadows, and nodular cystic lesions. Although computed tomography (CT) has been shown to be helpful in the evaluation of lung disease in CF, no scoring system or other objective criteria have been developed for the evaluation of the wide range of pulmonary changes in these patients. A CT scoring system was devised that incorporates all of the changes seen in the lungs of patients with CF. Such a scoring system may facilitate objective evaluation of existing and newly developed therapeutic regimens and may be a valuable tool in the preoperative evaluation of patients being considered for lobectomy or bullectomy and in the selection of patients for lung transplantation.