Utility of transient elastography in evaluation and follow-up of Budd-Chiari syndrome patients after endovascular intervention

Abstract

Background

Liver stiffness measurement (LSM) using transient elastography (TE) is a common noninvasive method for assessing hepatic fibrosis. The purpose of this study was to show the utility of LSM in the evaluation and short-term follow-up of Budd-Chiarri syndrome (BCS) patients as well as to investigate the relationships between LSM, hepatic venous pressure, and liver fibrosis. We conducted a prospective cohort study in which 25 patients with a confirmed diagnosis of primary BCS underwent endovascular intervention for BCS treatment. All patients had pressure gradient changes across the stenosed hepatic veins/inferior vena cava (HV/IVC) measured before and after the procedure, a transvenous liver biopsy during the procedure, and LSM (using Transient Elastography 3 days before and 3 months after the intervention as a short-term follow-up). Comparisons and correlations were made between liver stiffness, hepatic venous pressure, and fibrosis.

Results

The HV/IVC pressure gradient measured immediately before and after the intervention had a direct proportionate correlation with the LS measured 3 days before and 3 months after the intervention (r = 0.41 & 0.44, p: 0.04 & 0.03, respectively). LSM drops significantly 3 months after intervention (from 51.62 ± 22 kPa to 28.80 ± 19.25 kPa (p: 0.001)). There is a significant improvement in LSM post-intervention among patients with moderate to severe fibrosis (METAVIR scores of ≥ F2 before intervention (p: 0.001).

Conclusions

LSM in BCS patients reflects congestion rather than fibrosis stage. TE can be used for the short-term monitoring of patients with BCS following the endovascular intervention as a noninvasive tool.

Background

In BCS, hepatic venous outflow obstruction causes venous stasis, post-sinusoidal portal hypertension, and a decrease in portal perfusion, culminating in ischemic damage to hepatocytes and hepatic cell inflammation. These biological factors all contribute to increased liver stiffness, which can be measured using one-dimensional transient elastography (TE) [1].

Liver stiffness (LS) is a noninvasive method for estimating liver fibrosis. Although previously thought to be inappropriate for BCS due to liver congestion, LS is now thought to be capable of monitoring treatment outcomes in BCS after balloon angioplasty, albeit without correlating with liver fibrosis [2].

LSM correlates with the hepatic venous pressure gradient (HVPG) [3, 4], the gold standard of portal hypertension (PH) evaluation [5], and thus could be used to indirectly assess PH in patients with advanced chronic liver disease (ACLD) [6].

According to the most recent Baveno Consensus on PH, LSM values greater than 20–25 kPa can noninvasively rule in clinically significant PH (CSPH) in ACLD patients [3].

LSM, on the other hand, does not only reflect liver fibrosis but also many other conditions [7,8,9,10], including liver congestion [9]. As a result, LSM could play a role in the evaluation of BCS because the hepatic venous flow obstruction found in these patients typically leads to liver congestion and a post-sinusoidal form of PH.

The goal of treatment (via endovascular intervention) in patients with BCS is to relieve hepatic congestion, thereby improving hepatocyte function and allowing portal hypertension to resolve, and TE can measure this indirectly [11, 12].

The current study aimed to demonstrate the utility of TE in the diagnosis, staging, and follow-up of liver fibrosis in patients with BCS before and after the endovascular intervention. In addition, TE was used to determine if there is a correlation between the preintervention fibrosis stage (using Meta-analysis of Histological Data in Viral Hepatitis (METAVIR)) and posttreatment LSM.

Only a few studies, mostly case series, have looked at the role of TE in the diagnosis of liver fibrosis in BCS patients, as well as the possibility of using TE as a noninvasive tool to monitor these patients after endovascular intervention.

Methods

Patients

This prospective cohort study enrolled 25 Egyptian patients who had primary BCS confirmed by Doppler ultrasound (described in the following section) performed by a single radiologist from our group. Before participating, all patients provided written informed consent, and the local Research Ethical Committee approved the study protocol, in accordance with the ethical guidelines of the 1975 Declaration of Helsinki.

Exclusion criteria

Patients with other etiologies of liver disease unrelated to BCS (e.g., viral, autoimmune, or metabolic), those who had BCS due to secondary causes (e.g., tumoral hepatic venous (HV) or inferior vena caval (IVC) invasion or compression), patients who had a contraindication for transjugular intrahepatic portosystemic shunt (TIPS) (such as severe congestive heart failure, uncontrolled sepsis, and advanced liver disease), and patients who had one or more confounder which could affect the proper assessment of liver stiffness (LS) (e.g., BMI > 30, acute hepatitis, and extrahepatic cholestasis) were excluded.

Tools of the study

Complete histories and clinical examinations were recorded for all included patients, and laboratory investigations included a complete blood count (CBC), a liver profile, and a coagulation profile. As part of our protocol, we performed a thorough thrombophilia workup for all patients with a confirmed diagnosis of primary BCS to determine the underlying etiology (s).

Abdominal Doppler ultrasonography was performed to assess: liver and splenic size, ascites status, caudate lobe enlargement, mottled parenchyma, presence of hepatic focal lesions, the status of the major HVs whether patent or occluded (long or short segment occlusion), and the number of occluded veins; the status of IVC, pattern of vascular occlusion (i.e., hepatic vein occlusion (HVO) and/or IVC occlusion (IVCO)), portal vein (PV) and intra & extrahepatic collaterals. In cases of nonconclusive Doppler ultrasound findings or the presence of hepatic focal lesions, data from multi-slice computed tomography (CT) with venography and portography and/or magnetic resonance venography (MRV) and dynamic MRI were recorded to clarify their nature. Following that, all patients underwent upper endoscopy to determine the status of gastroesophageal varices and portal hypertensive gastropathy and to treat them accordingly before beginning the anticoagulation therapy.

Endovascular intervention and pressure gradient measurement

The intervention was chosen based on the location and extent of the venous occlusion. TIPS was performed on 18 patients, with 7 undergoing angioplasty in the form of IVC balloon dilatation without stenting (5 patients) and hepatic vein stenting (2 patients). Pressure gradients were measured both before and after the procedure. Pressure gradients were measured using 4F or 5F multipurpose catheters across the stenosed HV segment between the patent distal HV segment and the IVC or right atrium in patients undergoing HV angioplasty and/or stent implantation. Gradients were measured in patients with IVC occlusion or stenosis across the patent segment of the IVC and right atrium. Portosystemic gradients were measured after TIPS creation.

LS measurement technique

All included patients had their liver stiffness assessed using a Fibroscan Echosens 502 (M probe and XL probe) by a single well-trained operator. For all patients, the LSM was taken twice, 3 days before the endovascular intervention and 3 months later as a short-term follow-up. Patients who had significant large ascites before the examination underwent paracentesis. Patients were placed on their backs in the dorsal decubitus position, with their right arm in full abduction. The right hepatic lobe was used for LS measurements. In a right intercostal space, a 3.5-MHz US transducer mounted on the axis of a vibrator was placed. As for elastic shear waves, a 50-Hz vibration with an amplitude of 2 mm and a pulse tracking frequency of 3.5 MHz was propagated into the liver. The mean LS value was calculated in kilopascals for each patient who had at least ten successful measurements. The range of LSM values is 0–75.4 kPa. The approximate range of LSM values from F0 to F4 corresponds to different stages of fibrosis:

• F0: 0–4.9 kPa

• F1: 5–7.4 kPa

• F2: 7.5–9.9 kPa

• F3: 10–14.9 kPa

• F4: 15–75 kPa

Liver biopsy

All patients had a percutaneous transjugular liver biopsy once during the interventional procedure. The METAVIR scoring system was used to assess the fibrosis stage [13]. The patients were divided into two groups: those with a fibrosis score < F2 and those with a fibrosis score ≥ F2. The differences in changes in LS measurements after interventional procedures between these groups were analyzed.

Statistical techniques

A biomedical statistician carried this study’s statistical review out. Data was gathered, revised, coded, and entered using the Statistical Package for Social Science (SPSS) version 23.

The qualitative data were presented as numbers and percentages, whereas the quantitative data were presented in the form of mean, standard deviations (SD), and ranges. Multiple comparisons between groups were carried out. LSD (post hoc range test) was used to make multiple comparisons between pairs of groups, with the findings displayed as mean and SD. To compare clinical data before and after the intervention, the MacNemar test was performed. The statistical significance of the variations in LSM values before and after the endovascular operation was determined using a paired samples t test. Pearson’s correlation coefficient was used to analyze the correlations between changes in pressure gradients across stenosed HVs/IVC and LS measures after interventional operations. The relationship between LSM before and after the intervention and METAVIR score was determined using a marginal homogeneity test. SPSS version 17 was used to analyze all of the data. A p value of less than 0.05 was deemed significant.

Results

In this study, 25 Egyptian patients with primary BCS were included. There were 13 males and 12 females. The average age was 36.24 ± 9.34 years (range: 19–55 years). In 80% of patients with BCS, the chronic presentation was the most common, with painful hepatomegaly and increasing abdominal enlargement leading to ascites being the most common symptoms. TIPS was performed on 18 patients, whereas 7 underwent angioplasty ± stenting in the form of IVC balloon dilatation (5 patients) and hepatic vein stenting (2 patients). One of the patients became pregnant shortly after the intervention and was lost to follow-up; LSM was not used on her.

There was a total clearance of ascites in 18 patients after the endovascular intervention, and only grade 1 ascites in 6 patients. In addition, liver functions improved significantly. Table 1 compares the clinical, laboratory, and radiological characteristics of patients before and 3 months after the intervention. Table 1 shows that following the intervention, the HV/IVC pressure gradient decreased markedly in all patients (p = 0.001).

The LSM measured at 3-month follow-up following the intervention showed significant improvement (p < 0.001) (Table 1 & Fig. 1).

Fig. 1

Liver stiffness measurement pre- and post-intervention

Correlation between HV/IVC pressure gradient & LSM

Before the intervention, the mean SD changes in HV/IVC pressure gradient in all patients were 23.8 ± 55 mmHg, and the mean SD changes in LSM in these patients were 51.62 ± 22 kPa, while the mean changes in HV/IVC pressure gradient were 8.00 ± 2 mmHg and in LSM were 28.80 ± 19.25 kPa at 3 months (Table 1).

The correlation coefficients between changes in pressure gradients and changes in LSM before and after the intervention were 0.41 and 0.44, indicating a moderate positive association between these two nonparametric measures (Fig. 2a & b).

Fig. 2

a Correlation between LSM and HV/IVC pressure gradient before intervention. b Correlation between LSM and HV/IVC pressure gradient at 3-month follow-up post-intervention

Correlation between LSM and METAVIR staging

When we used METAVIR staging to try to find a link between changes in LSM and histological fibrosis staging, we discovered a significant difference between the METAVIR score of the liver biopsy and the LSM, whether performed 3 days before the intervention or 3 months after the intervention (p = 0.001). However, the difference between the results of LSM post-intervention & liver biopsy staging became less compared with the difference before intervention (Table 2).

Table 1 Characteristics of patients before and after endovascular intervention

We found no significant improvement in LSM post-intervention in the group of patients with METAVIR scores of < F2 (n = 6), while there was a substantial improvement in LSM post-intervention in the group of patients whose METAVIR scores were ≥ F2 (n = 18) (Table 3).

Table 2 Relation between pre- & post-intervention LSM and liver biopsy (METAVIR score)

Table 3 Comparison between pre- & post-intervention LSM and different stages of METAVIR score (n = 24)

Discussion

The goal of this study was to demonstrate how useful TE was for diagnosing, staging, and monitoring liver fibrosis in patients with BCS before and after endovascular intervention, also to identify if there is a relation between LSM and the pre-intervention fibrosis stage (METAVIR).

All patients who underwent HV angioplasty/stenting or TIPS in the current study had a significant reduction in their HV/IVC pressure gradient following the intervention, resulting in an immediate reduction in hepatic congestion (p value = 0.001). This is supported by two recent studies involving 19 and 32 BCS patients, respectively. In these investigations, the pressure gradient drops significantly after the intervention [12, 14].

The pre-procedure LSM mean (51.62 ± 22 kPa, encompassing 23 patients in the F4 stage and 2 patients in the F3 range) in our data was higher than the cut-off value of 10.4 kPa (above which is widely believed to characterize F4 fibrosis (liver cirrhosis)) [15, 16]. Our data also demonstrated a considerable improvement in hepatic fibrosis after reducing liver congestion, going from 51.62 ± 22 kPa pre-intervention down to 28.8 ± 19.25 kPa 3 months afterward. This information could drive clinicians to request more imaging studies to confirm BCS diagnosis. Dajti et al. stated that such high LSM values are uncommon in other liver illnesses, such as advanced chronic liver disease (ACLD) or other disorders that cause hepatic congestion [17].

Pre- and post-intervention, LSM was found to be positively correlated with HV/IVC pressure gradient (r = 0.41, p = 0.04) and (r = 0.44, p = 0.03), respectively. As a result, TE follow-up monitoring can be used to assess the therapeutic benefits in BCS patients.

Wang et al. showed a direct association between HVPG and LSM before intervention (the coefficient of correlation between LSM and hepatic venous pressure before angioplasty was r = 0.701, (p 0.001)) [12], which is consistent with our findings.

Mukund et al., in contrast to our findings, observed no relation between changes in LSM and pressure gradient [14].

There was a significant difference between the histological stage of fibrosis and the LSM performed 3 days before intervention (p 0.001) and 3 months after intervention (p = 0.001) in the current study.

Our findings are consistent with those of Wang et al. [12], who found that LSM was related to hepatic venous pressure rather than the degree of fibrosis in BCS patients. They found that LSM did not correlate with the degree of fibrosis in histological specimens before angioplasty (r = 0.170, P = 0.22). LSM still did not correlate with the degree of fibrosis 2 days after the intervention (r = 0.223, p = 0.220), and there was no significant difference in LSM between different fibrosis stages before angioplasty [12]. These findings contradict prior findings that LSM is positively correlated with the severity of fibrosis [1, 14].

This is maybe because LSM is more affected by hepatic venous pressure (i.e., liver congestion due to post-sinusoidal portal hypertension in BCS patients leads to higher LSM).

Unlike Mukund et al., who found no significant difference in LS values post-intervention between both groups with METAVIR fibrosis scores of ≤ 2 (n = 7) and > 2 (n = 5), p = 0.5714, our findings showed no significant improvement in LSM post-intervention among the group of patients whose fibrosis stage was < F2 (n = 6, p = 0.07). However, among patients with moderate-to-severe fibrosis, there is a significant improvement in LSM post-intervention (scores ≥ F2, n = 18, p 0.001). The substantially varying outcomes of liver elasticity can explain this in relation to the METAVIR fibrosis score [18]. These findings supported the idea that hepatic congestion, rather than fibrosis score, is the primary determinant of liver elasticity in BCS patients [19].

Mancuso et al. recently claimed that LS alterations from baseline could predict BCS outcomes when treated with only medicinal therapy. They measured LS every 4–5 months with FibroScan Echosens, and after an average 10-month follow-up, three patients, two with improved LS and one with stable LS, had stable liver disease, whereas one with worsening LS developed refractory ascites, with an increase in both creatinine and bilirubin, and was referred for evaluation of both liver and kidney transplantation [20]. In two cases with BCS, a recent case report investigated the efficacy of the hepatic vein (HV) waveform by Doppler ultrasonography and quantified liver stiffness (LS) using transient elastography (TE) before and after percutaneous transhepatic angioplasty (PTA). Serial monitoring of the HV waveform and the LS value, according to the authors, allows for the safe management of patients with BCS who may require PTA [21].

Conclusions

Our findings imply we could utilize LSM as a sensitive noninvasive method to monitor hemodynamic changes in BCS patients after therapy, and that we might use it for short-term follow-up of BCS patients following endovascular intervention.

The limitations of the current study

The relatively small number of the studied patients and the limited duration of follow-up are the limitations of the current study. Frequent liver biopsies after the endovascular intervention with fibrosis staging using the METAVIR staging and comparing their results to the results of repeated LSM at the same time for validation of the role of LSM in long-term follow-up of BCS patients are recommended.

Recommendations

We highly encouraged a multicenter study or larger cohort with longer follow-up duration and serial LSM after endovascular interventions to confirm the role of LSM in short- and long-term follow-up of BCS patients, its potential prognostic value, and stratifying severity of the disease.