Is One Pass Enough for the Diagnosis of the Pancreatic Masses During EUS-FNB? A Prospective Study
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 79
- 试验地点
- 1
- 主要终点
- The diagnostic accuracy of one pass EUS-FNB.
研究概览
简要总结
Endoscopic ultrasonography (EUS) with tissue acquisition (TA) is nowadays a well-established technique for the sampling of solid lesions pancreatic and non-pancreatic lesions. Major complications after EUS-TA of solid masses are rare. Several studies have been published in the last recent years aimed to identify factors related to a non-diagnostic or false-negative EUS-FNA, and to improve its diagnostic yield using different needle gauge and different tissue acquisition technique as fanning technique, slow-pull stylet extraction or suction technique.
To overcome this problem, new EUS-TA needles entered in clinical practice to obtain histological specimens increasing the accuracy of the EUS-TA. Preliminary result with these new needles, called EUS-fine needle biopsy (FNB) are promising with an accuracy rate more than 90%.
Recently, Leungh et al. conducted an observational study to evaluate the role of macroscopic on-site evaluation (MOSE) on the diagnostic accuracy of 22G Franseen-tip needle. The study demonstrated that MOSE using the 22G Franseen tip needle could limit needle passes by accurately estimating histologic core fragments. However, the study limitations such as the small sample size and the lack of control group, hampered the value of the conclusions.
So, nowadays, no definitive data regarding how many needle passes need to be performed with FNB needles, neither regarding the use of MOSE to evaluate the specimens obtained with FNB needle. The MOSE technique of the acquired tissue was proposed for the first time by Iwashita et al, using a 19G needle and is nowadays a well-established technique with high accuracy in the final diagnosis.
The aim of our study is to evaluate if during EUS-FNB of pancreatic masses only one needle pass with MOSE evaluation can be satisfactory to obtain a correct diagnosis.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age greater than 18, both genders.
- •Both in-patient and out-patients.
- •Presence of a solid lesion. In the presence of a cystic component, the solid part of the lesion should be more 75% of the total.
- •FNB performed by a 22G needle Acquire® (Boston Scientific).
- •Tissue acquisition with fanning technique.
- •Able to obtained informed consent.
排除标准
- •Patients underwent EUS-FNA with or without ROSE
- •Patients underwent EUS-FNB plus ROSE.
- •Previous biopsy of the lesion with diagnosis of malignancy
- •Presence of an uncorrectable coagulopathy as defined by abnormal prothrombin time (PT) or partial thromboplastin time (PTT) that does not normalize after administration of fresh frozen plasma.
- •Pregnancy or breast-feeding.
- •Patients unable to understand and/or read the consent form.
结局指标
主要结局
The diagnostic accuracy of one pass EUS-FNB.
时间窗: 24 months
EUS-FNB only one needle pass inside the target lesions with MOSE evaluation can be satisfactory to obtain a correct diagnosis.
次要结局
未报告次要终点
