Background and AimsEndoscopic ultrasound-guided liver biopsy (EUS-LB) technique-related factors as a determinant of specimen yield have not been studied. We used a modified technique to study adequacy, safety and technical determinants in patients with or without cirrhosis. MethodsEUS-LB was performed with a 19G Franseen tip needle by wet heparinized suction. One or two passes with a variable number of actuations were taken, the end-point being the aspiration of blood. Primary outcomes were tissue core adequacy and definitive histologic diagnosis. Secondary outcomes were a correlation between the number and depth of actuations with total specimen length (TSL), longest specimen length (LSL) and adverse events (AE). Early and late adverse events (AE) were also accessed. ResultsAdequate samples were seen in 48/50 and histologic diagnosis could be achieved in 49/50 patients. Mean TSL, LSL and depth of actuation were 7.98±3.74cm, 1.89±0.80cm and 4.29±0.98cm, respectively. The median complete portal tracts(CPT) were 23 (range, 7-50) and number of actuations was 7 (range, 4-12) The correlation between TSL with number and depth of actuation was r=0.71 vs 0.53 & r=0.55 vs 0.51 and for LSL were r=0.28 vs 0.11 & r=0.74 vs 0.55 in non-cirrhotic and cirrhotic patients respectively. No major and 7(14%) minor adverse events were observed. ConclusionsThis modified EUS-LB technique results in adequate tissue acquisition and is safe in non-cirrhotic and cirrhotic patients. Technical factors like the number and depth of actuations determine specimen yield.
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