Section of Interventional Pulmonology, Division of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, 1800 Orleans Street, Suite 7125M, Baltimore, MD 21287, USA.
Ann Am Thorac Soc. 2013 Apr;10(2):121-6. doi: 10.1513/AnnalsATS.201209-074OC.
Most bronchoscopic procedures are performed using moderate sedation achieved by combining a short-acting benzodiazepine with an opioid agent. Propofol (2.6-diisopropylphenol), a short-acting hypnotic agent, has been increasingly used to provide deep sedation in the endoscopy community with an acceptable safety profile.
To compare the impact of moderate versus deep sedation on the adequacy and diagnostic yield of endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA).
A retrospective review of prospectively collected data was performed at two academic institutions with interventional pulmonary fellowships using two methods of sedation during EBUS (deep vs. moderate sedation). Rapid on-site cytologic evaluation was used on all procedures in both groups. EBUS-TBNA nodal sampling was considered adequate if the aspirate yielded a specific diagnosis or lymphocytes. EBUS-TBNA was considered diagnostic if a lymph node aspirate yielded a specific diagnosis or if subsequent surgical sampling or prolonged radiographic surveillance revealed no nodal pathology.
No difference was observed in the indication for EBUS-TBNA between the two groups. More lymph nodes were sampled per patient in the deep sedation group (314 nodes from 163 patients; 2.2 nodes per patient) than in the moderate sedation group (181 lymph nodes from 146 patients; 1.4 nodes per patient; P < 0.01). The EBUS-TBNA diagnostic yield was higher for the deep sedation group (80% of patients) than for the moderate sedation group (66% of patients; P < 0.01).
Diagnostic yield and number of lymph nodes sampled using deep sedation is superior to moderate sedation in patients undergoing EBUS-TBNA. Prospective studies accounting for other factors including patient selection and cost are needed.
大多数支气管镜检查是通过将短效苯二氮䓬类药物与阿片类药物联合使用来实现中度镇静来完成的。丙泊酚(2.6-二异丙基苯酚),一种短效催眠药物,已被越来越多地用于提供深度镇静,在接受内镜检查的人群中具有可接受的安全性。
比较中度镇静与深度镇静对支气管内超声引导经支气管针吸活检(EBUS-TBNA)的充分性和诊断效果的影响。
在两家拥有介入性肺科奖学金的学术机构中,通过两种方法对支气管镜检查进行镇静(深度镇静与中度镇静),对前瞻性收集的数据进行回顾性分析。在这两组中,所有操作均使用快速现场细胞学评估。如果抽吸物获得特定诊断或淋巴细胞,则认为 EBUS-TBNA 淋巴结取样是充分的。如果淋巴结抽吸物获得特定诊断,或者随后的手术取样或延长的放射学监测未显示出任何淋巴结病变,则认为 EBUS-TBNA 是诊断性的。
两组之间 EBUS-TBNA 的适应证无差异。深度镇静组(163 例患者 314 个淋巴结;每个患者 2.2 个淋巴结)每个患者采集的淋巴结数量多于中度镇静组(146 例患者 181 个淋巴结;每个患者 1.4 个淋巴结;P<0.01)。深度镇静组的 EBUS-TBNA 诊断率(80%的患者)高于中度镇静组(66%的患者;P<0.01)。
在接受 EBUS-TBNA 的患者中,使用深度镇静进行诊断率和采样淋巴结数量优于中度镇静。需要进行前瞻性研究,考虑包括患者选择和成本在内的其他因素。