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Comparison of EUS-Guided and Percutaneous Liver Biopsy Needles for Diagnostic Yield and Tissue Adequacy in Explanted Cirrhotic Livers: A Prospective Comparative Study
Poster Abstract

Aims

Endoscopic ultrasound–guided liver biopsy (EUS-LB) isincreasingly used as an alternative to percutaneous liver biopsy (PC-LB), butcomparative evidence on optimal needle selection remains limited. This studycompared diagnostic yield and tissue adequacy of EUS and percutaneous biopsy needles using explanted cirrhotic livers.

Methods

In this prospective, comparative ex-vivo study, 30 adult explanted cirrhotic livers underwent biopsies using four needles: PC-16G, PC-18G, EUS-19G FNB, and EUS-22G FNB from both lobes (total 240 biopsies). Tissueadequacy was defined as specimen length >15 mm and ≥11 complete portaltracts (CPT). Histopathology was assessed by a blinded pathologist. Repeated-measures ANOVA, Cochran’s Q, and McNemar tests were used.

Results

Mean total specimen length was highest with EUS-19G (26.8 ± 14.9mm), followed by PC-16G (18.8 ± 5.5 mm), PC-18G (17.9 ± 6.2 mm), and EUS-22G (12.9 ± 8.2 mm) (p<0.001). Mean CPT was comparable between EUS-19G(13.5 ± 3.8) and PC-16G (13.4 ± 2.8), but significantly lower with EUS-22G (8.9 ±3.2, p<0.001). Tissue adequacy was achieved in 98% with PC-16G, 93% with PC-18G, 92% with EUS-19G, and 50% with EUS-22G (p<0.001). Cirrhosis was most accurately identified with PC-16G and EUS-19G, while EUS-22G had higher non-diagnostic rates and lower fibrosis staging accuracy.

 

 

DIAGNOSTIC ACCURACY OF EUS AND PC NEEDLES

Sl no.

Needles

Stage 2

n (%)

Stage 3

n (%)

Stage 4

n (%)

1

PC 16 G

1 (3.3%)

1 (3.3%)

58 (96.6%)

2

PC 18 G

0

8 (13.3%)

52 (86.6%)

3

EUS 19 G

0

21 (35%)

39 (65%)

4

EUS 22 G

16 (26.6%)

43 (71.6%)

1 (3.3%)

 

 

Conclusions

EUS-19G provides tissue adequacy and portal tract yieldcomparable to standard percutaneous biopsy needles and yields significantlylonger core specimens. EUS-22G is inferior for diagnostic liver biopsy. EUS-19Grepresents a reliable alternative to PC-LB in appropriately selected patients.