Abstract
Objectives
To determine whether international normalized ratio (INR), bilirubin, and creatinine predict bleeding risk following percutaneous liver biopsy.
Methods
A total of 870 consecutive patients (age 53 ± 14 years; 53% (459/870) male) undergoing non-targeted, ultrasound-guided, percutaneous liver biopsy at a single tertiary center from 01/2016 to 12/2019 were retrospectively reviewed. Results were analyzed using descriptive statistics and logistic regression models to evaluate the relationship between individual and combined laboratory values, and post-biopsy bleeding risk. Receiver operating characteristic (ROC) curves and area under ROC (AUC) curves were constructed to evaluate predictive ability.
Results
Post-biopsy bleeding occurred in 2.0% (17/870) of patients, with 0.8% (7/870) requiring intervention. The highest INR within 3 months preceding biopsy demonstrated the best predictive ability for post-biopsy bleeding and was superior to the most recent INR (AUC = 0.79 vs 0.61, p = 0.003). Total bilirubin is an independent predictor of bleeding (AUC = 0.73) and better than the most recent INR (0.61). Multivariate regression analysis of the highest INR and total bilirubin together yielded no improvement in predictive performance compared to INR alone (0.80 vs 0.79). The MELD score calculated using the highest INR (AUC = 0.79) and most recent INR (AUC = 0.74) were similar in their predictive performance. Creatinine is a poor predictor of bleeding (AUC = 0.61). Threshold analyses demonstrate an INR of > 1.8 to have the highest predictive accuracy for bleeding.
Conclusion
The highest INR in 3 months preceding ultrasound-guided percutaneous liver biopsy is associated with, and a better predictor for, post-procedural bleeding than the most recent INR and should be considered in patient risk stratification.
Clinical relevance statement
Despite correction of coagulopathic indices, the highest international normalized ratio within the 3 months preceding percutaneous liver biopsy is associated with, and a better predictor for, bleeding and should considered in clinical decision-making and determining biopsy approach.
Key Points
• Bleeding occurred in 2% of patients following ultrasound-guided liver biopsy, and was non-trivial in 41% of those patients who needed additional intervention and had an associated 23% 30-day mortality rate.
• The highest INR within 3 months preceding biopsy (AUC = 0.79) is a better predictor of bleeding than the most recent INR (AUC = 0.61).
• The MELD score is associated with post-procedural bleeding, but with variable predictive performance largely driven by its individual laboratory components.
Similar content being viewed by others
Abbreviations
- AUC:
-
Area under the curve
- INR:
-
International normalized ratio
- MELD:
-
Model for End-Stage Liver Disease
References
Rockey DC, Caldwell SH, Goodman ZD et al (2009) Liver biopsy. Hepatology 49:1017–1044. https://doi.org/10.1002/hep.22742
Weigand K, Weigand K (2009) Percutaneous liver biopsy: retrospective study over 15 years comparing 287 inpatients with 428 outpatients. J Gastroenterol Hepatol 24:792–799. https://doi.org/10.1111/j.1440-1746.2008.05718.x
Mueller M, Kratzer W, Oeztuerk S et al (2012) Percutaneous ultrasonographically guided liver punctures: an analysis of 1961 patients over a period of ten years. BMC Gastroenterol 12:173. https://doi.org/10.1186/1471-230X-12-173
Atwell TD, Spanbauer JC, McMenomy BP et al (2015) The timing and presentation of major hemorrhage after 18,947 image-guided percutaneous biopsies. AJR Am J Roentgenol 205:190–195. https://doi.org/10.2214/AJR.14.13002
Boyum JH, Atwell TD, Schmit GD et al (2016) Incidence and risk factors for adverse events related to image-guided liver biopsy. Mayo Clin Proc 91:329–335. https://doi.org/10.1016/j.mayocp.2015.11.015
Midia M, Devang O, Department of Radiology, McMaster University School of Medicine, Hamilton, ON, Canada et al (2019) Predictors of bleeding complications following percutaneous image-guided liver biopsy: a sco** review. Diagn Interv Radiol 25:71–80. https://doi.org/10.5152/dir.2018.17525
Patel IJ, Rahim S, Davidson JC et al (2019) Society of interventional radiology consensus guidelines for the periprocedural management of thrombotic and bleeding risk in patients undergoing percutaneous image-guided interventions—part ii: recommendations. J Vasc Interv Radiol 30:1168-1184.e1. https://doi.org/10.1016/j.jvir.2019.04.017
Pandey S, Vyas GN (2012) Adverse effects of plasma transfusion: adverse effects of plasma transfusion. Transfusion 52:65S-79S. https://doi.org/10.1111/j.1537-2995.2012.03663.x
Singal AK, Kamath PS (2013) Model for end-stage liver disease. J Clin Exp Hepatol 3:50–60. https://doi.org/10.1016/j.jceh.2012.11.002
Malinchoc M, Kamath PS, Gordon FD et al (2000) A model to predict poor survival in patients undergoing transjugular intrahepatic portosystemic shunts. Hepatology 31:864–871. https://doi.org/10.1053/he.2000.5852
Montgomery A, Ferral H, Vasan R, Postoak DW (2005) MELD score as a predictor of early death in patients undergoing elective transjugular intrahepatic portosystemic shunt (TIPS) procedures. Cardiovasc Intervent Radiol 28:307–312. https://doi.org/10.1007/s00270-004-0145-y
DeLong ER, DeLong DM, Clarke-Pearson DL (1988) Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics 44:837–845. https://doi.org/10.2307/2531595
Chang Y, Kim JI, Lee B et al (2020) Clinical application of ultrasonography-guided percutaneous liver biopsy and its safety over 18 years. Clin Mol Hepatol 26:318–327. https://doi.org/10.3350/cmh.2019.0019n
Skelly MM, James PD, Ryder SD (2001) Findings on liver biopsy to investigate abnormal liver function tests in the absence of diagnostic serology. J Hepatol 35:195–199. https://doi.org/10.1016/s0168-8278(01)00094-0
Spycher C, Zimmermann A, Reichen J (2001) The diagnostic value of liver biopsy. BMC Gastroenterol 1:12. https://doi.org/10.1186/1471-230X-1-12
Myers RP, Fong A, Shaheen AAM (2008) Utilization rates, complications and costs of percutaneous liver biopsy: a population-based study including 4275 biopsies. Liver Int 28:705–712. https://doi.org/10.1111/j.1478-3231.2008.01691.x
Stanworth SJ, Brunskill SJ, Hyde CJ et al (2004) Is fresh frozen plasma clinically effective? A systematic review of randomized controlled trials. Br J Haematol 126:139–152. https://doi.org/10.1111/j.1365-2141.2004.04973.x
Holland L, Sarode R (2006) Should plasma be transfused prophylactically before invasive procedures? Curr Opin Hematol 13:447–451. https://doi.org/10.1097/01.moh.0000245688.47333.b6
Yang L, Stanworth S, Hopewell S et al (2012) Is fresh-frozen plasma clinically effective? An update of a systematic review of randomized controlled trials. Transfusion 52:1673–1686. https://doi.org/10.1111/j.1537-2995.2011.03515.x. (quiz 1673)
Rassi AB, d’Amico EA, Tripodi A et al (2020) Fresh frozen plasma transfusion in patients with cirrhosis and coagulopathy: effect on conventional coagulation tests and thrombomodulin-modified thrombin generation. J Hepatol 72:85–94. https://doi.org/10.1016/j.jhep.2019.09.008
Goretti S, Ochi M, Jagannathan P, Chebaa BR et al (2021) ID: 3526988 pre-procedure fresh frozen plasma does not reduce bleeding risk in patients with cirrhosis and coagulopathy undergoing invasive procedures. Gastrointestinal Endoscopy 93:AB60–AB61. https://doi.org/10.1016/j.gie.2021.03.177
Dillon JF, Simpson KJ, Hayes PC (1994) Liver biopsy bleeding time: an unpredictable event. J Gastroenterol Hepatol 9:269–271. https://doi.org/10.1111/j.1440-1746.1994.tb01722.x
McVay PA, Toy PT (1990) Lack of increased bleeding after liver biopsy in patients with mild hemostatic abnormalities. Am J Clin Pathol 94:747–753. https://doi.org/10.1093/ajcp/94.6.747
Intagliata NM, Rahimi RS, Higuera-de-la-Tijera F et al (2023) Procedural-related bleeding in hospitalized patients with liver disease (PROC-BLeeD): an international, prospective, multicenter observational study. Gastroenterology 165:717–732. https://doi.org/10.1053/j.gastro.2023.05.046
Lisman T, Porte RJ (2010) Rebalanced hemostasis in patients with liver disease: evidence and clinical consequences. Blood 116:878–885. https://doi.org/10.1182/blood-2010-02-261891
Mohanty A, Kapuria D, Canakis A et al (2021) Fresh frozen plasma transfusion in acute variceal haemorrhage: results from a multicentre cohort study. Liver Int 41:1901–1908. https://doi.org/10.1111/liv.14936
Caldwell S, Northup PG (2010) Bleeding complication with liver biopsy: is it predictable? Clin Gastroenterol Hepatol 8:826–829. https://doi.org/10.1016/j.cgh.2010.06.010
Willis J, Carroll C, Planz V, Galgano SJ (2022) Thromboelastography: a review for radiologists and implications on periprocedural bleeding risk. Abdom Radiol (NY) 47:2697–2703. https://doi.org/10.1007/s00261-022-03539-9
Wikkelsø A, Wetterslev J, Møller AM, Afshari A (2016) Thromboelastography (TEG) or thromboelastometry (ROTEM) to monitor haemostatic treatment versus usual care in adults or children with bleeding. Cochrane Database Syst Rev. https://doi.org/10.1002/14651858.CD007871.pub3
Perelman AD, Limaye M, Blakemore J, Hoskins IA (2022) Thromboelastography versus standard coagulation assays in patients with postpartum hemorrhage. Am J Perinatol. https://doi.org/10.1055/a-1974-5055
Hartmann J, Dias JD, Pivalizza EG, Garcia-Tsao G (2023) Thromboelastography-guided therapy enhances patient blood management in cirrhotic patients: a meta-analysis based on randomized controlled trials. Semin Thromb Hemost 49:162–172. https://doi.org/10.1055/s-0042-1753530
Funding
The authors state that this work has not received any funding.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Guarantor
The scientific guarantor of this publication is Dr. Olga R. Brook, MD.
Conflict of interest
Dr. Michael P. Curry has research grants with Mallinckrodt, Sonic Incytes, and is a paid consultant for Mallinckrodt, Sonic Incutes, Albireo, Alexion.
Dr. Bettina Siewert receives royalties from Wolter Kluwer and is a reviewer for Up-To-Date.
The remaining authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.
Statistics and biometry
One of the authors (Dr. Alexander Brook, PhD) has significant statistical expertise.
Informed consent
Written informed consent was waived by the Institutional Review Board due to its retrospective nature.
Ethical approval
Institutional Review Board approval was obtained.
Study subjects or cohorts overlap
Study subjects or cohorts have not been previously reported elsewhere.
Methodology
• retrospective
• case–control study
• performed at one institution
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Vo, N.H., Sari, M.A., Grimaldi, E. et al. Highest 3-month international normalized ratio (INR): a predictor of bleeding following ultrasound-guided liver biopsy. Eur Radiol (2024). https://doi.org/10.1007/s00330-024-10692-w
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00330-024-10692-w