All patients will receive standard medical care and no experimental interventions will be performed. Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) is a well-established procedure commonly used for the investigation of lesions within or adjacent to the gastrointestinal (GI) lumen (i.e. pancreas, liver, mediastinal masses, left adrenal gland, lymph nodes, and subepithelial lesions). EUS-guided tissue sampling has been commonly performed with different size and types of aspiration and core biopsy needles.
Endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) is a well-established procedure commonly used for the investigation of lesions within or adjacent to the gastrointestinal (GI) lumen (i.e. pancreas, liver, mediastinal masses, left adrenal gland, lymph nodes, and subepithelial lesions). EUS-guided tissue sampling has been commonly performed with different size and types of aspiration and core biopsy needles. More recently, a novel through-the-needle microforceps has been introduced. The MorayTM microforceps fits through a 19-gauge FNA needle and allows targeted tissue sampling under EUS visualization. Aim - To prospectively evaluate the safety and diagnostic yield of the through-the-needle microforceps for pancreatic and non-pancreatic solid, cystic and mixed solid/cystic lesions.
Study Type
OBSERVATIONAL
Enrollment
54
EUS- guided tissue sampling of solid and/or cystic pancreatic and non-pancreatic lesions as part of their medical care.
University of Florida
Gainesville, Florida, United States
Overall diagnostic yield of EUS-TS
Time frame: 2 months
Diagnostic Yield of EUS-guided tissue sampling solid lesions
Time frame: 2 months
Diagnostic Yield of EUS-guided tissue sampling cystic lesions
Time frame: 2 months
Diagnostic yield of EUS-TS using through-the-needle micro forceps
Time frame: 2 months
Diagnostic yield of EUS-TS using fine-needle aspiration
Time frame: 2 months
Diagnostic yield of EUS-TS using core biopsy needle
Time frame: 2 months
Rate of adverse events associated with EUS-TS
Adverse events defined based on previously established criteria by the American Society of Gastrointestinal Endoscopy (ASGE)
Time frame: 48 hours
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