A real-world study evaluating ultrasound-guided percutaneous non-targeted liver biopsy needle failures and pathology sample-quality assessment in both end-cut and side-notch needles
Objectives: To determine biopsy device failures, causative factors, complications and sample quality of the 16G end-cut Biopince (TM) - and side-notch Bard (TM) - needles. Methods: All ultrasound-guided non-targeted liver biopsies between 01/01/2016 and 31/12/2018 were included. Operator, device, nu...
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Veröffentlicht in: | British journal of radiology 2021-09, Vol.94 (1125), p.20210475-20210475, Article 20210475 |
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Zusammenfassung: | Objectives: To determine biopsy device failures, causative factors, complications and sample quality of the 16G end-cut Biopince (TM) - and side-notch Bard (TM) - needles.
Methods: All ultrasound-guided non-targeted liver biopsies between 01/01/2016 and 31/12/2018 were included. Operator, device, number of failures, complications and repeat biopsies were recorded. Histopathology samples were reviewed for all cases of needle failure and a group with no failures, and graded "yes/no" for the presence of steatosis, inflammation and fibrosis. The pathology slides from these cases were reviewed to assess biopsy sample quality (length and portal tract number). The failure and no-failure groups were compared in terms of device type/histology, and sample quality was compared between the needle types.
Results: 1004 patients were included. 93.8% (n = 942) required one needle pass to obtain a sample and 6,2% (n = 62) required >1pass due to needle failure. Total of 76 needle failures, more with end-cut than side-notch needles (8.7% vs 2.9%) (p < 0.001). No needle failures resulted in complication. The presence of liver fibrosis was associated with fewer needle failures (p = 0.036). The major complication rate was 0.4% (4/1044). A biopsy with >10 portal tracts was obtained in 90.2% of specimens > 20mm long, compared with 66% of 16-20mm biopsies and 21% of 10 portal tracts was achieved in 10/26 (38.5%) of side-notch biopsies and 64/90 (71.1%) of end-cut biopsies (p = 0.004).
Conclusion: Ultrasound-guided liver biopsy is safe and sample quality is consistently good when a core >20mm long is obtained. The end-cut biopsy device generated reliably good quality biopsy samples; however, the needle failure rate was significantly higher than the side-cut needle.
Advances in knowledge: Ultrasound-guided liver biopsy specimen quality is consistently good when a core >20mm long is obtained which can be achieved with a single pass using the 16G Biopince TM end-cut needle, although the needle failure rate is significantly higher than the 16G Max-Core - Bard - side-notch needle. |
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ISSN: | 0007-1285 1748-880X |
DOI: | 10.1259/bjr.20210475 |