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METHODS article

Front. Pediatr., 21 November 2023
Sec. Pediatric Cardiology
This article is part of the Research Topic Fontan-Associated Liver Disease: Current status and future directions View all 3 articles

Routine follow-up transjugular liver biopsy in Fontan patients: technical considerations and safety of an initial case series and literature review

\r\nGuido Mandilaras
Guido Mandilaras1*Zora MeyerZora Meyer1Richard MühlbergRichard Mühlberg1Annabell BraunAnnabell Braun1Nikolaus A. HaasNikolaus A. Haas1Andre JakobAndre Jakob1Robert Dalla PozzaRobert Dalla Pozza1Moritz Wildgruber,&#x;Moritz Wildgruber2,†Marcus Fischer,&#x;\r\nMarcus Fischer1,†
  • 1Department of Pediatric Cardiology and Pediatric Intensive Care, University Hospital of Munich, Ludwig-Maximilian-University Munich, Munich, Germany
  • 2Department of Interventional Radiology, University Hospital of Munich, Ludwig-Maximilian-University Munich, Munich, Germany

Introduction: Patients with Fontan palliation are susceptible to congestive hepatopathy and Fontan-associated liver disease (FALD) because of hemodynamic changes. The staging of liver fibrosis involves various methods, including invasive biopsy. Transjugular liver biopsy (TJLB) offers a less invasive alternative, enhancing liver disease surveillance in routine cardiac catheterization. We detail the technical aspects, share initial outcomes, and discuss existing literature.

Methods/results: During routine follow-up cardiac catheterization indicated by hemodynamic or clinical alterations, four patients aged between 16 and 26 years with univentricular Fontan circulation and three patients with biventricular circulation underwent TJLB during routine surveillance catheterization. The examinations were performed under conscious sedation and local anesthesia without general anesthesia. Jugular access was obtained at the site of liver localization, and a 5 F multipurpose catheter was inserted into the liver veins. After hand angiography to delineate the local hepatic venous anatomy, an exchange wire was used to place the bioptome, and three consecutive biopsies were performed. There were no complications, especially perforation or bleeding. The technical success rate was 100%, with all obtained samples appropriate for histopathological diagnostics. The total additional procedure time was less than 20 min.

Conclusion: TJLB is an attractive alternative method for obtaining liver specimens in the scope of FALD care. We believe that it should be performed during routine hemodynamic evaluations in Fontan patients and can be performed safely with very low additional time expenditure. As the biopsy site is intravascular, the risk of external bleeding or hematoma is significantly reduced despite the high intrahepatic pressures and the usually impaired coagulation profile in these patients. Based on our initial experience and the lower complication rates compared with other techniques, TJLB should be considered a standard approach in these patients and used more often during the long-term follow-up of Fontan patients. It can be performed in the same setting whenever a hemodynamic assessment of patients with congenital heart defects is required.

1. Introduction

Patients with Fontan palliation are at risk of developing congestive hepatopathy and Fontan-associated liver disease (FALD), which is one of the severe long-term complications for this patient cohort. Hemodynamic changes, such as low cardiac output and chronic elevation of central venous pressure, contribute to the development of FALD. Chronic FALD may result in hepatic cirrhosis and hepatic cellular cancer, with possibly lethal consequences (1). The staging of liver fibrosis in FALD involves biochemical/hematological parameters, non-invasive fibrosis scores, sonographic liver elastography, and liver histology, in some cases.

Most centers caring for Fontan patients evaluate liver function using ultrasound-guided liver elastography, sometimes employing magnetic resonance elastography (MRE), and liver-specific laboratory parameters at regular intervals as part of their surveillance programs (2). When FALD progresses to severe hepatic congestion with progressive hepatic alterations, a liver biopsy is the gold standard diagnostic procedure. However, it is also highly invasive to estimate the severity of liver disease through a histopathological diagnosis (3).

Due to contraindications for performing a percutaneous liver biopsy (PLB), such as coagulopathy or ascites because of liver failure, transjugular liver biopsy (TJLB) has been gaining ground as an alternative method among adult patients for liver disease surveillance (4). In Fontan patients, this method may play an important role in the long-term assessment of liver pathology. Fontan patients often require a hemodynamic assessment because of clinical or hemodynamic alterations in the long-term follow-up (i.e., protein-losing enteropathy, reduced exercise performance, and increasing cyanosis). Whenever catheter investigations are planned, TJLB can be added to the procedure with minimal effort and performed safely by cardiac interventionalists without requiring major additional time. Therefore, we introduced TJLB in our routine cardiac catheter program. This article reports the technical aspects of this procedure, our initial results, and the potential benefits for this patient cohort. In addition, a review of the literature is provided.

2. Patients and methods

Since 2020, patients with biventricular circulation or especially those with univentricular heart diseases who present with clinical signs of right heart failure, elevated central venous pressure, high estimated pulmonary vascular resistance in the Fontan circulation, and signs of hepatopathy undergo TJLB during routine hemodynamic surveillance catheterization in our department (Division of Pediatric Cardiology and Pediatric Intensive Care of the University Hospital of Munich).

We present the clinical course and technical aspects of our initial four patients, aged between 16 and 26 years, with failing Fontan circulation and FALD and three patients with biventricular congenital heart defects, aged between 12 and 55 years, who underwent cardiac catheterizations and TJLB during the same procedure (see Table 1). As a standard of care in our institution, the examinations were performed under conscious sedation and local anesthesia, without general anesthesia.

TABLE 1
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Table 1. Patients’ characteristics and history.

Initially, a hemodynamic assessment was performed in room air (FiO2 21%) before angiography and included measurements of aortic and ventricular pressure, superior and inferior vena cava pressure, Fontan tunnel pressures, pulmonary artery pressure, and pulmonary capillary wedge pressure. Angiography was performed in each case to identify possible Fontan pathway stenosis, venovenous collaterals, stenosis of the pulmonary arteries, or arterial–pulmonary collaterals.

In general, additional procedures, such as interventional closure of collaterals, dilatation and/or stenting of stenotic Fontan pathways, or endomyocardial biopsy, are performed whenever indicated after the initial hemodynamic assessment.

2.1. Technical aspects

Subsequently, jugular access was obtained in all patients at the site of liver localization using a 5 F Cook sheath, which was then exchanged for an 8 F sheath. A 5 F multipurpose catheter was inserted into the liver veins under fluoroscopic guidance. After performing hand angiography to delineate the local hepatic venous anatomy, an extra stiff x-change wire (Amplatz Super Stiff; Boston Scientific, Boston, MA, USA) was used to place the 10 F long sheath using a curved metal stiffener (Cook Flexor® Check-Flo®). The bioptome (Cook Medical Coaxial Biopsy Needle Set Quick-Core® 18 G) was inserted over the stiff wire through the long sheath and positioned with its tip about 1.5 cm distal to the vein origin, presenting enough thickness of the hepatic parenchyma to reduce the risk of capsular perforation. The 18 G biopsy needle was then maneuvered into the hepatic vein. Under fluoroscopy, the curved metal stiffener was turned anteriorly and inserted preferably into the right hepatic vein. The biopsy needle was then pushed through the vein wall into the hepatic parenchyma with a short thrust. The biopsy needle has a 2 cm throw and a 1.7 cm specimen notch. Three biopsies were obtained from either hepatic segment 5 or segment 8 (see Figures 1, 2). After completing the biopsies, the bioptome and sheath were retracted, and manual pressure was applied to the puncture site. A sonographic examination of the liver was performed within 10 min in the Cath lab to exclude hepatic perforation or subcapsular hematoma. There were no complications, especially perforation or bleeding. The technical success rate was 100%, with all obtained samples appropriate for histopathological diagnostics. The total additional procedure time was less than 20 min.

FIGURE 1
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Figure 1. Fluoroscopy (A) mapping of the venous liver anatomy via an angiography (B) biopsy needle inserted over the stiff wire through the long sheath and positioned with its tip about 1.5 cm distal to the vein origin, liver segment V.

FIGURE 2
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Figure 2. Obtained liver specimen.

3. Histopathological examination

In all cases, the fibrosis was graded using standard scoring systems, including the congestive hepatic fibrosis score (CHS) (stages 0–4) and the modified Ishak congestive hepatic fibrosis (ICHF) score.

4. Discussion

FALD, one of the most common late-onset complications of Fontan palliation, carries an unfavorable prognosis (5). Medical centers that care for Fontan patients evaluate liver function using scoring systems and routine laboratory parameters, and they determine liver stiffness through a hepatic ultrasound or MRE. While laboratory parameters tend to indicate liver failure in later stages, elastography (ultrasound/MRI) correlates with liver fibrosis but relies on the expertise of the examiner and can be influenced by factors such as abdominal air or ascites. A liver biopsy remains the gold standard for assessing FALD and the extent of hepatopathy (68).

TJLB is typically performed as a preferred alternative when PLB is contraindicated because of factors such as thrombocytopenia, coagulopathy, or ascites. Various studies comparing PLB and TJLB have demonstrated no significant difference in terms of technical success and complication rates. These facts influenced us to introduce TJLB in our routine surveillance program for patients with suspected liver fibrosis and heart disease. Although specimen sizes obtained through TJLB are generally smaller, the histopathological findings are as accurate as those obtained through PLB (911).

Potential complications after a liver biopsy include capsular perforation of the liver, perforation of other abdominal organs such as the kidneys, and hemobilia (3, 12). PLB has been associated with cases of pneumothorax and abdominal wall aneurysm (13), while TJLB may involve technical complications related to the implantation of the sheath in the jugular vein (10).

Hemorrhage is the most commonly reported complication after liver biopsy, and it may be more pronounced in patients with impaired coagulation profiles and elevated central venous pressure, such as in Fontan patients. The incidence of hemorrhage varies between 4% and 18.5%, depending on the biopsy technique (traditional biopsy, ultrasound-guided PLB, or TJLB), the anatomy of the patient, and the experience of the operator (9, 13).

Studies conducted on groups of Fontan patients have shown a lower incidence rate of hemorrhage after TJLB (3.2%) compared with PLB (7.4%) (3, 12). The reduced hemorrhage risk associated with TJLB could be attributed to the possibility of precise anatomical mapping of the patient's circulation through angiography before the procedure. In addition, any potential bleeding in TJLB results in venous auto-transfusion, which is less concerning than an abdominal hemorrhage, especially in patients with reduced coagulation and elevated central venous pressure. Therefore, TJLB appears to be the preferred method in these patients to minimize the risk of hemorrhage. In all our initial patients presented here, we could not identify any of these complications confirming this well-known safety aspect.

The retrospective study by Borquez et al. (3) focused on 125 Fontan patients, with a median age of 17 years (ranging from 2 to 50.5 years), who underwent TJLB. The study reported a complication rate of 3.2% (four out of 125 cases), including two capsular perforations, one renal hematoma, and one case of hemobilia.

In the study conducted by Srinivasan et al. (12), which investigated 68 cases of ultrasound-guided PLB performed on 67 Fontan patients, with a median age of 20.2 years (ranging from 7.2 to 39 years), the only complication reported was hemorrhage in five out of 68 interventions, resulting in a hemorrhage incidence rate of 7.4%.

On the other hand, Govender et al. (13) evaluated the use of sonography-guided PLB in infants and children, including 470 patients who underwent 597 PLB procedures for various liver pathologies. The mean age of the patients was 10.5 years (ranging from 1 month to 21 years). In this study, 10 major complications were reported, representing a complication rate of 1.7%. These major complications included one case each of pneumothorax (0.2%) and abdominal wall pseudoaneurysm (0.2%), along with eight patients experiencing hemorrhage (1.3%). In addition, minor complications were noted in 49 patients (8.2%), with 35 cases (5.8%) of symptomatic subcapsular hematoma and 9 cases (1.5%) of small hemoperitoneum.

These studies provide valuable insights into the complication rates associated with TJLB and PLB in Fontan patients. TJLB appears to have a lower incidence of hemorrhage compared with PLB, making it a preferable approach in this patient population to reduce the risk of bleeding complications.

The study conducted by Meng et al. (9) involved comparing TJLB and PLB in 60 and 277 patients with various liver pathologies, respectively. In the TJLB group, the reported complications included one subcapsular hematoma, two cases of hematoma at the puncture site of the neck, and one case of paroxysmal supraventricular tachycardia. In contrast, the PLB group had 20 minor complications and four major complications. This study concludes that TJLB is a safe alternative to PLB.

Similarly, Sehmbhi et al. (10) performed a retrospective review of all liver biopsies conducted at a UK transplant center over 12 months. This study included 330 TJLB and 240 PLB procedures. The combined complication rate was 5.6%, with eight major complications (1.4%) and 24 minor complications (4.2%), and there was no significant difference between the two groups. However, the technical failure rate of TJLB was 4%, mainly because of difficulties in puncturing the internal jugular vein, failure to cannulate the hepatic vein, or an unstable sheath position.

In the comparison study by Hardman et al. (11), TJLB and image-guided PLB were performed in 36 and 202 cases, respectively. TJLB resulted in one major complication (2.8%) and two minor complications (5.5%), while PLB led to four major complications (1.9%) and 10 minor complications (4.9%). The authors concluded that both techniques showed similar efficacy and complication rates.

These studies collectively indicate that TJLB is a feasible and safe alternative to PLB in assessing liver pathology, especially in Fontan patients, and may offer advantages in terms of reduced risk of hemorrhage and overall complications. However, it is important to consider the specific clinical context and individual patient factors when deciding on the appropriate biopsy approach.

The modified ICHF score is considered a valuable tool for assessing liver biopsies in Fontan patients. Unlike other traditional histopathological scoring systems, the ICHF score is particularly suitable for evaluating the liver tissue in these patients.

In addition to the histopathological evaluation, investigations have shown that MRE is useful for the longitudinal follow-up of liver stiffness in Fontan patients. MRE allows non-invasive assessment of liver fibrosis by measuring liver stiffness, and it has been found to correlate significantly with the ICHF scoring and invasive hemodynamic parameters such as the mean pressure in the Fontan circulation and the cardiac index.

Therefore, when the MRE score is greater than 5 kPa, combining an invasive hemodynamic examination with a TJLB is recommended. This integrated approach can provide comprehensive information about the liver condition in Fontan patients and help manage their liver disease.

By using MRE and ICHF scoring in combination with TJLB, healthcare providers can better monitor the liver health of Fontan patients and make informed decisions regarding their treatment and long-term follow-up care (14).

Whenever there is a need for hemodynamic assessment in Fontan patients because of clinical or hemodynamic alterations during long-term follow-up (e.g., protein-losing enteropathy, reduced exercise performance, and increasing cyanosis), catheter investigations are commonly used to evaluate cardiac output and pulmonary pressures and calculate pulmonary vascular resistance. These investigations often require sedation or general anesthesia to ensure patient comfort and cooperation during the procedure.

Based on the literature reviewed and our initial results, we would support the management approach where TJLB can be easily incorporated into the catheter investigation procedure with minimal additional effort in these patients. The procedure itself is comparable to many other interventional measures; therefore, skilled cardiac interventionalists can safely perform the TJLB without significantly prolonging the overall procedure time. This approach streamlines patient management by reducing the number of separate investigations needed and, in turn, enhances patient comfort and convenience.

By combining hemodynamic assessment with TJLB, healthcare providers can obtain comprehensive information about cardiac and liver health in univentricular Fontan patients or patients with other biventricular circulation during a single session. This integrated approach offers several benefits, including simplifying the overall evaluation process, reducing the need for multiple interventions, and ultimately increasing patient comfort and satisfaction.

5. Limitations

Its relatively modest sample size inherently constrains this case series. Nonetheless, given the novelty of the introduced method within our management portfolio, we were able to establish its feasibility and safety.

6. Conclusion

TJLB is a valuable procedure that can be performed during routine hemodynamic evaluations in patients, with minimal additional time required. By conducting TJLB during routine cardiac catheterization and under conscious sedation, both hemodynamic data and liver biopsies can be obtained simultaneously, reducing the procedure time and overall count of interventions.

This alternative method of obtaining liver specimens for FALD care has shown potentially lower complication rates, such as bleeding and hematoma, compared with other techniques, despite the challenges posed by elevated central venous pressure and reduced coagulation profiles in Fontan patients. In addition, during the catheterization, common vascular anomalies in Fontan anatomy (e.g., heterotaxy) can be easily assessed through angiography, further minimizing the risk of complications.

Furthermore, in the event of a possible hemorrhage during the TJLB, venous auto-transfusion occurs without clinical consequences, adding to the safety of the procedure.

Considering the lower complication rates reported, our own initial results, and the ease of assessing vascular anomalies, we recommend incorporating cardiac catheterization with simultaneous TJLB as a standard approach in the routine surveillance program for all patients with Fontan palliation, especially when clinical scores and/or liver elastography trends indicate a deterioration of liver function or worsening of FALD. This integrated approach ensures a comprehensive evaluation of both cardiac and liver health, promoting effective management and timely interventions when necessary.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

Ethics statement

Written informed consent was obtained from the minors’ legal guardians for the publication of any potentially identifiable images or data included in this article.

Author contributions

GM, MW, RD, AJ, and NH contributed to patient management, conception, and design of this study and the acquisition, analysis, and interpretation of the data for the work. AJ and GM organized the database. GM, MW, and MF wrote the first draft of the manuscript. ZM, AB, and RM wrote sections of the manuscript. MF and NH critically revised the manuscript. All authors contributed to the article and approved the submitted version.

Acknowledgments

The authors thank the colleagues of the Pathological Institute, University Hospital of Munich—LMU, Munich, for the excellent collaboration in diagnosing the mentioned patients.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Gordon-Walker TT, Bove K, Veldtman G. Fontan-associated liver disease: a review. J Cardiol. (2019) 74:223–32. doi: 10.1016/j.jjcc.2019.02.016

PubMed Abstract | CrossRef Full Text | Google Scholar

2. de Lange C, Möller T, Hebelka H. Fontan-associated liver disease: diagnosis, surveillance, and management. Front Pediatr. (2023) 11:1100514. doi: 10.3389/fped.2023.1100514

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Borquez AA, Silva-Sepulveda J, Lee JW, Vavinskaya V, Vodkin I, El-Sabrout H, et al. Transjugular liver biopsy for Fontan associated liver disease surveillance: technique, outcomes and hemodynamic correlation. Int J Cardiol. (2021) 328:83–8. doi: 10.1016/j.ijcard.2020.11.037

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Maji P, Malik R, Madhusudhan KS, Sharma S. Utility and safety of transjugular liver biopsy in children. Indian J Pediatr. (2021) 88:709–11. doi: 10.1007/s12098-020-03650-z

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Rathgeber SL, Guttman OR, Lee AF, Voss C, Hemphill NM, Schreiber RA, et al. Fontan-associated liver disease: spectrum of disease in children and adolescents. J Am Heart Assoc. (2020) 9:e012529. doi: 10.1161/JAHA.119.012529

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Serai SD, Wallihan DB, Venkatesh SK, Ehman RL, Campbell KM, Sticka J, et al. Magnetic resonance elastography of the liver in patients status-post Fontan procedure: feasibility and preliminary results: MRE in post-Fontan patients. Congenit Heart Dis. (2014) 9:7–14. doi: 10.1111/chd.12144

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Daniels CJ, Bradley EA, Landzberg MJ, Aboulhosn J, Beekman RH, Book W, et al. Fontan-associated liver disease. J Am Coll Cardiol. (2017) 70:3173–94. doi: 10.1016/j.jacc.2017.10.045

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Chen B, Schreiber RA, Human DG, Potts JE, Guttman OR. Assessment of liver stiffness in pediatric Fontan patients using transient elastography. Can J Gastroenterol Hepatol. (2016) 2016:7125193. doi: 10.1155/2016/7125193

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Meng H-C, Lin H-C, Huang C-C, Liao D-M, Lee F-Y, Lee S-D, et al. Transjugular liver biopsy: comparison with percutaneous liver biopsy. J Gastroenterol Hepatol. (1994) 9:457–61. doi: 10.1111/j.1440-1746.1994.tb01274.x

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Sehmbhi M, Doufexi D, Schoutens L, Mak C, Patch D, O’Beirne J, et al. PWE-134 transjugular liver biopsy versus percutaneous liver biopsy—indications, adequacy, quality of specimens and complications. Gut. (2015) 64:A272. doi: 10.1136/gutjnl-2015-309861.583

CrossRef Full Text | Google Scholar

11. Hardman RL, Perrich KD, Silas AM. Single-institution results of image-guided nonplugged percutaneous versus transjugular liver biopsy. Cardiovasc Intervent Radiol. (2011) 34:369–75. doi: 10.1007/s00270-010-9924-9

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Srinivasan A, Guzman AK, Rand EB, Rychik J, Goldberg DJ, Russo PA, et al. Percutaneous liver biopsy in Fontan patients. Pediatr Radiol. (2019) 49:342–50. doi: 10.1007/s00247-018-4311-9

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Govender P, Jonas MM, Alomari AI, Padua HM, Dillon BJ, Landrigan-Ossar MF, et al. Sonography-guided percutaneous liver biopsies in children. Am J Roentgenol. (2013) 201:645–50. doi: 10.2214/AJR.12.9802

CrossRef Full Text | Google Scholar

14. Silva-Sepulveda JA, Fonseca Y, Vodkin I, Vaughn G, Newbury R, Vavinskaya V, et al. Evaluation of Fontan liver disease: correlation of transjugular liver biopsy with magnetic resonance and hemodynamics. Congenit Heart Dis. (2019) 14:600–8. doi: 10.1111/chd.12770

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Fontan-associated liver disease, FALD, transjugular liver biopsy, congenital heart disease, pediatric cardiology

Citation: Mandilaras G, Meyer Z, Mühlberg R, Braun A, Haas NA, Jakob A, Dalla Pozza R, Wildgruber M and Fischer M (2023) Routine follow-up transjugular liver biopsy in Fontan patients: technical considerations and safety of an initial case series and literature review. Front. Pediatr. 11:1204545. doi: 10.3389/fped.2023.1204545

Received: 12 April 2023; Accepted: 13 October 2023;
Published: 21 November 2023.

Edited by:

Ornella Milanesi, University of Padua, Italy

Reviewed by:

Jenny Zablah, University of Colorado Hospital, United States
Natalie Soszyn, Children’s Hospital Colorado, United States

© 2023 Mandilaras, Meyer, Mühlberg, Braun, Haas, Jakob, Dalla Pozza, Wildgruber and Fischer. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Guido Mandilaras guido.mandilaras@med.uni-muenchen.de

These authors have contributed equally to this work and share last authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.