Schaefer Philipp J, Schaefer Fritz K W, Heller Martin, Jahnke Thomas
Department of Diagnostic Radiology, University Hospital Schleswig-Holstein Campus Kiel, Arnold-Heller-Strasse 9, 24105 Kiel, Germany.
J Vasc Interv Radiol. 2007 Oct;18(10):1241-8. doi: 10.1016/j.jvir.2007.06.036.
To characterize a new protocol of computed tomographic (CT) fluoroscopy-guided biopsy of the lung and upper abdomen to minimize the intervention time, complication rate, and exposure to ionizing radiation for both the patient and the radiologist.
Fifty patients (23 women, 27 men; mean age, 64.3 years; age range, 36-83 years) with lung (n = 41) or upper abdomen (n = 9) nodules 15 mm or smaller underwent CT fluoroscopy-guided biopsy from November 2005 to October 2006. The mean nodule diameter was 12.6 mm (range, 8-15 mm), the mean depth to skin was 57.3 mm (range, 20-114 mm), and the mean depth of nodules from pleura and/or peritoneum was 18.9 mm (range, 1-77 mm). Histopathologic evaluation of samples was performed on the day of the procedure. A CT fluoroscopy-guided biopsy protocol was established as follows: (a) native CT with breath-holding at an intermediate respiration level, (b) selection of section position with target nodule and insertion of an 18-gauge coaxial biopsy needle extrapleurally and/or extraperitoneally virtually targeting at nodule, (c) start of CT fluoroscopy (130 kVp, 30 mAs, 5-mm-thick sections) at inspiration level with the patient expiring, (d) stop of CT fluoroscopy when the target nodule reaches the section position, short breath-hold, needle advancement to the target nodule, (e) control of needle position with CT fluoroscopy, and (f) biopsy.
The mean total table time was 23.8 minutes (range, 15-41 minutes), the mean duration of CT fluoroscopy was 8.2 seconds (range, 4-23 seconds), and the mean duration of breath-holding--including needle insertion to target nodule and control CT fluoroscopy--was 10.3 seconds (range, 5-15 seconds). There were three minor pneumothoraces that required no further intervention, seven minor pulmonary hemorrhages, three moderate pulmonary hemorrhages with hemoptysis, and one moderate liver hematoma. There were no major complications. The diagnostic accuracy of biopsy samples was 96%.
The presented modification of CT fluoroscopy-guided biopsy of mobile pulmonary and upper abdominal lesions is a rapid and safe procedure, requiring only short exposure to ionizing radiation.
描述一种新的计算机断层扫描(CT)透视引导下肺和上腹部活检方案,以尽量减少患者和放射科医生的干预时间、并发症发生率及电离辐射暴露。
2005年11月至2006年10月,50例患者(23例女性,27例男性;平均年龄64.3岁;年龄范围36 - 83岁),其肺(n = 41)或上腹部(n = 9)存在直径15 mm或更小的结节,接受了CT透视引导下活检。结节平均直径为12.6 mm(范围8 - 15 mm),平均皮肤深度为57.3 mm(范围20 - 114 mm),结节距胸膜和/或腹膜的平均深度为18.9 mm(范围1 - 77 mm)。在操作当天对样本进行组织病理学评估。CT透视引导下活检方案如下确立:(a)在中等呼吸水平屏气时进行平扫CT;(b)选择包含目标结节的截面位置,并在胸膜外和/或腹膜外虚拟靶向结节插入18号同轴活检针;(c)在患者呼气时吸气水平开始CT透视(130 kVp,30 mAs,5 mm厚截面);(d)当目标结节到达截面位置时停止CT透视,短暂屏气,将针推进至目标结节;(e)用CT透视控制针的位置;(f)进行活检。
平均总检查时间为23.8分钟(范围15 - 41分钟),CT透视平均持续时间为8.2秒(范围4 - 23秒),屏气平均持续时间(包括将针插入目标结节和控制CT透视)为10.3秒(范围5 - 15秒)。出现3例无需进一步干预的少量气胸、7例少量肺出血、3例伴有咯血的中度肺出血和1例中度肝血肿。无严重并发症。活检样本的诊断准确率为96%。
所提出的对可移动肺部和上腹部病变的CT透视引导活检的改进是一种快速且安全的操作,仅需短时间暴露于电离辐射。