Role of partial splenic artery embolization in corpuscular correction in cirrhotic patients before anti-viral therapy: a recent update study among Egyptian patients

Abstract

Background

To evaluate the role of partial splenic artery embolization in corpuscular correction in cirrhotic patients.

Results

Bleeding tendency was experienced in two thirds of patients (66.7%) and anemia in 63.3%. Splenic size ranged from 14.3 to 22 cm. PV diameter ranged from 11 to 18 mm. The mean platelet at the pre-operative laboratory was 34.9 ± 10.3 × 10³, corrected to 137.6 ± 37.1 × 10³ within 1 month follow-up, and then 140 × 10³ after 6 months. The mean of RBCs was 3.6 ± 0.3 × 10⁶, then 4 ± 0.5 × 10⁶ at 1 month follow-up period. WBCs showed correction at the early post-operative period, 3.3 ± 0.4 × 10³, compared to 5.4 ± 1.4 × 10³ at 1 month. Reduction in splenic size was achieved by 3–6 months. All patients (100%) had post-embolization syndrome. Gelfoam was used in 20 patients, PVA was used in 5 patients, and microspheres were used in 5 patients. Antiviral treatment regimen was started after an adequate rise in corpuscular counts in all patients.

Conclusion

Partial splenic artery embolization is an effective alternative method to surgery in treatment of hypersplenism particularly in cirrhotic patients prepared for antiviral treatment with correction of the associated thrombocytopenia.

Background

Hypersplenism refers to a clinical syndrome characterized by splenomegaly, anemia, leukopenia, thrombocytopenia, and compensatory bone marrow hyperplasia [1]. Hypersplenism represents increased pooling and destruction of the corpuscular elements of the blood, mainly platelets by the enlarged spleen [2], which is seen in many disorders, including cirrhosis with portal hypertension [3], hematologic abnormalities such as idiopathic thrombocytopenic purpura, thalassemia major, and hereditary spherocytosis, and diffuse splenic infiltration from primary malignancies such as leukemia and lymphoma [4]. The frequency of hypersplenism in patients with chronic liver disease varies between 30 and 70% [5]. Total splenectomy may be an effective treatment for hypersplenism, but it impairs the body’s ability to produce antibodies against encapsulated microorganisms and predisposes patients to sepsis; also, lifelong vaccination may be needed post-surgery [3].

Since 1973, splenic artery embolization for hypersplenism was usually performed. Initially, total aggressive embolization of the splenic parenchyma was performed, but severe complications, such as splenic abscess, overwhelming pneumonia, sepsis, hematoma and bleeding, pancreatic infarction, and even death, limited the usage of this technique. Since then, many authors start to practice incomplete or partial splenic arterial embolization, in which a portion of the splenic parenchyma is left viable to preserve the splenic tissue for immunologic function allowing defense against infections [3, 6].

Since then, transcatheter embolization of splenic parenchyma is often widely used for management of hypersplenism [2] and has been thought to be an effective safe alternative to splenectomy [7, 8] with subsequent improvement of anemia, leukopenia, and thrombocytopenia [9] especially in patients with comorbidity, like liver cirrhosis. This study aimed to evaluate the role of partial splenic artery embolization in correcting thrombocytopenia in cirrhotic patients with clinical manifestations of hypersplenism.

Methods

Patients

The study was approved by the local institutional ethics and review committee of our university. Informed consent was obtained from all participants. This study included 30 patients which presented with clinical manifestations of hypersplenism secondary to chronic liver disease; all patients underwent partial splenic embolization to correct thrombocytopenia. All patients were proved clinically and in the laboratory. All were referred from the hepatology departments and outpatient clinics of university hospitals. The study time frame was from January 2015 to December 2017.

All patients were subjected to the following.

Clinical history taking

Clinical history taking includes the following:

• Relevant history, like bilharziasis with previous anti-bilharzial therapy, blood transfusion, and other risk factors that can contribute in the determination of the etiology of liver disease

• History of blood disease (anemia or leukemia) or bleeding tendency

• Presence of portal hypertension, hematemesis, or melena

• History of chronic liver disease or liver cell failure or precoma

Laboratory investigations

Laboratory investigations include the following:

• Complete blood picture with stress on platelet count

• Antiplatelet antibodies

• Liver profile including liver enzymes (ALT and AST), total and direct bilirubin, and serum albumin

• Prothrombin time, concentration, and INR

• Viral markers (HBsAg and HCVAbs)

• Renal function tests (serum creatinine and blood urea)

• Bone marrow aspiration to exclude bone marrow causes of thrombocytopenia

Abdominal ultrasonography with color Doppler study

Color Doppler US examination was done by GE logic P5 and P8, and all patients kept fasting overnight prior to the ultrasonography examination.

Spleen: Size, echogenicity, presence of focal lesions, splenic vein diameter and patency as well as duplex study, with stress upon the splenic maximal length, SV diameter, and blood flow velocity within.

Liver: Size, surface, echogenicity, presence of focal lesions and portal vein ultrasonographic, and duplex examination.

Portal trunk was scanned longitudinally. The portal vein diameter was measured directly about 1.5–2.5 cm before the bifurcation to the right and left branches. The portal flow velocity (PFV) in centimeters per second (cm/s) was averaged by Doppler traces of 2–3 cardiac cycles, as well as direction of portal blood flow; the cross-sectional area of PV was also measured with the calculation of congestion index as well as the presence of ascites and collaterals.

Child-Pugh classifications of the patients in the study

In this study, most of the patients (25 patients) were Child-P A classification with good general condition and good liver function, with no ascites or encephalopathy.

Only few cases (5 cases) were early Child B classification (B7) and were embolized to save the patient’s life; however, no major complications were noted within.

Inclusion criteria

• Cases of hypersplenism secondary to chronic liver disease

• Platelet count less than (50,000\μL)

• Child-P classification A or early B

• Good general performance status

• Absence of ascites

Exclusion criteria

• Child-Pugh C classification

• Moderate and marked ascites

• Portal or splenic vein thrombosis or reversed flow of portal vein on color Doppler US

• Allergy to contrast media

• Aortoiliac or bilateral femoral artery occlusion

• Hypocellular bone marrow

Pre-embolization and patient preparation

The benefits and potential risks of splenic embolization were explained to each patient, and informed consent was obtained.

The participants were asked to fast for 12 h. All patients received broad spectrum antibiotics prophylaxis 6 h before embolization (which consisted of 3rd generation cephalosporins, combined ampicillin-sulbactam and metronidazole). Good sterilization of the patient was routinely done.

Embolization protocol

The patient lies supine in the angiography suite, both groins were prepped by betadine, and percutaneous femoral puncture was performed using cutaneous and perivascular local anesthesia infiltration to induce arterial vasculoplegia and to reduce pain during and post-procedure.

Seldinger’s technique was then used for the 6F femoral sheath insertion. Unilateral femoral artery approach was usually used for partial splenic artery embolization technique (used almost in all patients, only one patient underwent transradial approach).

To catheterize the celiac trunk, a 0.035 hydrophilic guide wire (Radiofocus Inc.) and 5 Fr Cobra catheter (Angiodynamic/Cordis Inc.) were used. Splenic artery was then selectively catheterized; by advancing the catheter over the guidewire, preliminary splenic arteriography was obtained to determine the exact splenic size, configuration of the splenic artery, and location of the pancreatic branches. The catheter was then advanced forward as distal as possible, so that its tip lies distal to the pancreatic branches. Very particular attention was paid to the dorsal pancreatic artery to avoid any potential reflux of the embolic agents.

Approaches for partial splenic artery embolization

The first approach was non-selective approach that was used in the majority of cases (25 patients); it was performed when the splenic artery was tortuous and difficult to selectively catheterize distal splenic branches. In these cases, the catheter tip was positioned more proximally in the main splenic artery as distal as we can, beyond the last major pancreatic branch.

The second approach used was selective approach (done in five patients); in this approach, few distal branches of the splenic artery are selectively catheterized using micro-catheter to reach this position (2.4–3 Fr Renegade ® Hi Flo™ Microcatheter (Boston Scientific, Natick, MA) with a 0.027-in. inner diameter, and embolization is performed to achieve complete stasis in these in the targeted branches.

Embolic particles were mixed with the contrast material and injected slowly until stasis, with the parenchymal blush produced.

Either temporary (Gelfoam) or permanent occluding materials (Microspheres and PVA) were used as embolizing material in the study; Gelfoam particles were the most used embolizing materials in our study, used in 20 patients, while the permanent occluding materials were used only in 10 patients (PVA or Embosphere, Boston Scientific); 355- to 500-μm particles were usually used with size of up to 500 to 700 μm for splenic artery. These particles were mixed with 80 g gentamicin and contrast material, and the mixture was injected slowly. The endpoint of embolization was usually determined when angiography showed that an estimated 50–70% of the splenic parenchyma was successfully embolized, evaluated during the parenchymal phase of serial arteriograms, and then the procedure was terminated.

Post-embolization regimen

All patients were admitted before the procedure and remained in the hospital until the post-embolization syndrome or any significant complications disappear. Analgesic management was followed routinely and combined with an anti-inflammatory agent. Supportive care includes appropriate hydro-electrolytic infusions, broad spectrum antibiotics (3rd generation cephalosporins, amoxicillin-clavulanate (3 g/day) and ofloxacin (400 mg/day) for at least 7 days after the procedure, and analgesics (paracetamol and even morphine if needed). The clinical assessment was performed by the patient’s physician at discharge and consultations at 1 month, 3 months, and 6 months after the procedure.

Follow-up

The post-procedure result and follow-up was analyzed from the medical and radiologic files.

The laboratory tests included CBC stressing on platelet count and liver and renal functions before discharge, and then CBC was repeated at 1, 3, and 6 months after embolization.

Morphologic verification by CT examination took place 1 month after embolization to assess the volume of the infarcted areas and detect any post-embolization complications. In the follow-up visits, CBC and abdominal ultrasonography were done routinely.

Statistical test

The data were coded, entered, and processed on an IBM-PC compatible computer using SPSS (version 19).

Results

This study included 30 patients which presented with clinical manifestations of hypersplenism secondary to chronic liver disease; all patients were proved clinically and in the laboratory as they were on the regimen for anti-viral therapy. Eight patients were females, and the rest were males (Table 1, Fig. 1).

Table 1 Demographic data of the study group

Fig. 1

Sex variation in the study group

Thrombocytopenia and bleeding tendency were the most distressing symptom that was experienced in two thirds of patients (66.7%) and anemia and its associated manifestations in 19 out of 30 patients (63.3%). Dull aching left hypochondrial pain elicited in 15 out of 30 patients (50%).

The splenic size of the patients included ranged from 14.3 to 22 cm (mean 17.8 ± 2.1 cm). Portal vein diameter ranged from 11 to 18 mm (mean 14.7 mm ± 1.9 mm) with P value (< 0.001). Three patients had minimal ascites. Five patients had a recent history of upper GIT endoscopy and local control of esophageal varices (Table 2).

Table 2 Pre-embolization relevant US findings

Platelets were the first blood element to be corrected at the early post-embolization period; it was the most reliable indicator for technical success. Comparison of the mean platelet count at the pre-operative laboratory was 34.9 ± 10.3 × 10³, then corrected to 137.6 ± 37.1 × 10³ within 1 month follow-up duration, and then there were some fluctuations at 3- and 6-month follow-up periods; most results were ranking in the figures of around 140 × 10³ with P value (< 0.001) (Table 3).

Table 3 Laboratory response based on platelet count

In RBCs, the mean was 3.6 ± 0.3 × 10⁶ compared with 4 ± 0.5 × 10⁶ at 1 month follow-up period, with slight steady elevation during 3- and 6-month durations. WBCs also showed correction at the early post-operative period, 3.3 ± 0.4 × 10³, compared to 5.4 ± 1.4 × 10³ at 1 month, with no significant rise at the late 3rd and 6th month follow-up periods which persists at 5.3 ± 0.8 × 10³ with P value (<0.001) (Tables 4 and 5).

Table 4 Laboratory response based on RBC count

Table 5 Laboratory response based on WBC count

Preoperative splenic size was ranged from 14.3 to 22 cm with the mean = 17.8 ± 2.1 cm with P value < 0.001; also, splenic artery and its branches as well as collateral circulation (lienorenal and gastric) were mapped and studied to pre-plane for the procedure itself to avoid the possibility of non-target embolization. Variable degrees of splenic parenchymal infarctions were achieved in the early post-embolization period, monitored by abdominal CT scans; by the time of 1 month, we started to notice mild reduction in splenic size, which ranged 14–20 cm (16.7 ± 1.8). Progressive reduction in size also was achieved by 3 and 6 months follow-up which were 13–19 cm (15.6 ± 1.8) and 12.5–17 cm (14.6 ± 1.4) respectively (Table 6) (Figs.2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, and 13).

Table 6 Splenic size changes pre- and post-embolization

Fig. 2

Male patient, 55 years old, with HCV, complaining left hypochondrial pain and bleeding tendency. Pre-embolization. Contrast abdominal CT examination at the artery. a–d Axial cuts at the arterial phase showing cirrhotic liver with splenomegaly. The splenic artery seen originates from the celiac trunk. CT at the portovenous phase. a–d Axial images. e Coronal reformats

Fig. 3

PSE. DSA pre- and post-embolization. a, b Selective DSA of splenic artery before embolization showing enlarged spleen with diffuse homogeneous contrast enhancement of splenic parenchyma. c, d Digital subtraction splenic angiography post-embolization showing areas of splenic infarctions about (70%) with sparing of areas near the splenic hilum

Fig. 4

Post-PSE. Follow-up abdominal CT examination (3 months) post-splenic embolization. a, b Axial images showing multiple hypodense non-enhanced areas of infarctions seen involving most of the splenic parenchyma with some areas spared. c–f Coronal and sagittal reformatted images showed the extent of infarction

Fig. 5

Male patient, 57 years old, with thrombocytopenia corrected only by fresh frozen plasma transfusion. a, b Selective DSA of splenic artery before embolization showing splenic artery and its segmental divisions. c, d Delayed images showed the parenchymal phase. DSA post-embolization. a, b Multiple areas of splenic infarctions about (70%) of the splenic parenchyma

Fig. 6

Follow-up abdominal CT late arterial phase. a, b Axial images. c, d Multiplanar coronal reformatted images. Multiple large well-defined non-enhanced geographically distributed hypodense areas involving most of the splenic parenchyma (about 70%) with other smaller normally perfused areas enhanced with contrast material, denoting residual variable splenic tissue after embolization

Fig. 7

Female patient, 45 years old, complaining of bleeding tendency and anemic manifestations. Pre embolization CT. Abdominal multislice CT examination post-contrast study. a, b Axial images. c, d Coronal images. e Sagittal images at the portovenous phase showing mild hepatosplenomegaly

Fig. 8

PSE. Selective digital subtraction splenic angiography. a, b DSA of the splenic artery showing the tortuous splenic artery. The tip of the catheter reaching as distal as possible nears the splenic hilum. DSA. a, b Splenic angiography post-embolization showing multiple areas of splenic infarctions (mainly peripherally located) representing about 50% of the splenic parenchyma

Fig. 9

Post-embolization follow-up CT examination. a–d Multiple axial cuts at the portovenous phase revealed multiple hypodense areas of near fluid density seen involving most of splenic parenchyma with mainly peripheral distribution, denoting post-embolization multiple infarctions

Fig. 10

Female patient, 48 years old, with chronic HCV, referred for correction of thrombocytopenia. Pre-embolization post-contrast CT examination. a–d Axial images at the arterial phase showing diffuse hepatic disease with mild splenomegaly. e, f Multiplanar reformatted coronal and sagittal images at the portovenous phase confirming presence of mild splenomegaly

Fig. 11

Embolization procedure DSA of the celiac trunk and splenic artery before embolization. a, b The origin of splenic artery. Images showing both guide wide and cobra catheter advancement proximally within splenic artery. Selective splenic artery angiographic images showed segmental branches of the splenic artery with no pancreatic or gastric branches denoting very good position for embolization. Post-embolization angiography. a, b Splenic angiography after the beginning of the embolization showing insufficient embolized areas

Fig. 12

Angiography after injection of more embolizing material for achieving 50% embolization

Fig. 13

Multislice CT study of the abdomen at the post-contrast phase. a, b Axial images. c, d Coronal reformatted images showing multiple peripherally located hypodense areas of splenic infarctions

Partial splenic artery embolization like any endovascular procedures is not absolutely safe procedure; it has its own complications; all complications in our study were in the acceptable range with no deaths recorded. All patients (100%) had post-embolization syndrome in the form general weakness, fatigue, pain, vomiting, and fever. Twenty percent of patients developed ascites late within the first month of follow-up and persists up to 3 months. Infection was encountered only in two patients. Portal and splenic vein thrombosis was encountered in four patients at the early post-operative period. Mild encephalopathy was seen only in three patients; all were attributed to the Child-Pugh class of the patient at time of the procedure (all were Child-P class B). One uncommon complication happened among the patients; the patient developed ascites, fever, and mild encephalopathy and was diagnosed as spontaneous bacterial peritonitis and treated by antibiotics. No abscess formation could be seen among the treated patients even at the late follow-up periods. No splenic rupture could be seen in all patients (Table 7).

Table 7 PV diameter pre- and post-embolization

Gelfoam pledges are most widely used based on the splenic sinusoids which can accommodate a large amount of PVA or Embosphere which are very expensive. In the study, Gelfoam was used in 20 patients (66.7% of cases), while PVA was used in 5 cases (16.66%), and microspheres were also used 5 patients (16.66% of cases). We noticed no significant post-embolization differences in imaging among the patients with different types of embolizing materials (Table 8).

Table 8 Post-procedure complications in the study group

Antiviral treatment regimen was started after an adequate rise in corpuscular counts in all patients (Table 9).

Table 9 Type of embolizing materials used in different patients

Discussion

Egypt has been reported as having the highest prevalence rate of HCV worldwide, with HCV antibodies. In turn, the reported incidence of hypersplenism in chronic liver diseases was reported as high as 68% [10].

With the development of interventional radiology, partial splenic embolization has been widely applied in clinical treatment of hypersplenism especially in patient prepared to antiviral therapy. PSE has fewer risks compared with surgery, shorter hospital stays, and better clinical effects. The open or laparoscopic splenectomy was the cornerstone to treat hypersplenism. However, there are certain limitations and contraindications, like those patients with advanced liver disease associated with considerable morbidity and mortality [11].

In this study, all patients were treated by partial splenic artery embolization with preservation of a part of the splenic tissue with no specific predilection to a certain embolizing material to do this mission, either temporary occluding materials like Gelfoam pledgets or permanent embolizing particles like microspheres and PVA; all induced tissue ischemia and infarction with subsequent corpuscular correction. The widely available and cheap Gelfoam particles was the dominant embolizing material (66.7%); all of the patients were treated effectively, 16.6% by microspheres and also 16.66% by PVA. This agrees with Hickman et al. [6] who successfully used gelatin sponge pledgets and polyvinyl alcohol particles as embolizing materials.

Absorbable gelatin sponge (Gelfoam) is the most commonly described embolic material for partial splenic embolization, but it has been criticized, predominantly because of its temporary nature, but the short time needed for tissue destruction with subsequent irreversible damage of splenic tissue made Gelfoam particles to be enough for this mission [12].

No significant impact on the extent of infarction or the end point results was attributed to the type of the particles used; this agrees with Hayashi et al. [13] who used in their study Gelfoam as the embolizing material, with the therapeutic endpoint being a splenic infarction rate of 70–80%. Different results were observed in the study by Zhu et al. [14]; he reported that PSE using Gelfoam particles or using PVA particles revealed good short- and long-term efficacy in relieving leukocytopenia and thrombocytopenia caused by hypersplenism, but the improvement in WBC and PLT counts was obviously better in the PVA group than in Gelfoam. Petermann et al. [15] concluded that effective splenic artery embolization for hypersplenism due to portal hypertension requires embolization of more than 50% of the parenchyma.

Pre-embolization mean platelet count was 34.9 ± 10.3 × 10³ that was corrected up to 137.6 ± 37.1 × 10³ within 1 month follow-up duration, which then showed some fluctuations at 3- and 6-month follow-up periods. There was some unexplained relapse of few cases that necessitated more treatment sessions. The results of our study revealed that PSE was a highly effective treatment in improving thrombocytopenia in patients with hypersplenism who started antiviral region after correction. Platelets were the first to be corrected at the early post-embolization period and as indicator for technical success. This runs close to the results reported by Zhu et al. [14] who found that the pre-embolization platelet count was 44.36 ± 16.67 × 10³, which then after 1 month became 125.36 ± 23.25 × 10³ and 6 months post-procedural became 111 ± 18.76 × 10³.

The ideal extent of splenic parenchymal infarction for the improvement in hematologic values remains unknown [16]. In our study, 50–70% embolization area is effective in the improvement of thrombocytopenia and leukocytopenia. Sangro et al. [17] noted that less than 50% splenic infarction was associated with a poor hematologic response but that 60–70% infarction was associated with more durable and substantial improvement in hematologic values.

Based on the amount of induced tissue infarction, a lot of studies attributed the variation of platelet count post-embolization matches the percentage of infarction which was 50–70% of splenic tissue in our study compared with that reported by Lee et al. [18] who observed a marked variation of platelet value between his study groups (low group; 30% embolization) and high embolization group (70% embolization). In another study by Ganesh et al. [19], the authors demonstrated that 65–70% embolization area is effective in platelet value improvement in liver cirrhosis patients with thrombocytopenia.

The post-embolization improvement in WBC count agreed with Palsson et al. [20], who estimated long-term leucocytes values after PSE; the mean WBC count was 8 × 10³/μL. RBCs also showed significant change after PSE with slight steady elevation during 3 and 6 month’s duration (4.4 ± 0.5 × 10⁶/μL). This disagrees with what was found in a study done by Zhu et al. [14] who noticed no significant elevation of the RBC count which was 3.24 ± 0.57 × 10⁶/μL before the procedure which became 3.33 ± 0.59 × 10⁶/μL after 6 months.

The pre-embolization mean splenic size in our study was 17.8 ± 2.1 cm, which reached 16.7 ± 1.8 cm after 1 month. Three months post-procedural, it was 15.6 ± 1.8 cm; however, by the end of 6 months, it was 14.6 ± 1.4 cm. He Xin-Hong et al. [21] found that splenic volume decreased significantly post-embolization 1 month after the procedures, and then gradually increased during the 4-year follow-up.

Significant decrease in portal vein diameter and portal venous pressure was achieved in this study. This agrees with the results of Nishida et al. [22] that found a drop in portal venous pressure after transient splenic artery occlusion.

Most of the complications encountered in our study were in the accepted range and secondary to tissue destruction and ischemia; post-embolization syndrome was the most common complication and occurred in almost all patients (100%). This agreed with Zhu et al. [14] who found that post-embolization syndrome was the most frequent side effect.

The limitations of this study include a small sample size, single-center data collection, and non-randomized design. The long duration of enrollment and prolonged follow-up of patients are the major strengths of our study.

Conclusion

Partial splenic artery embolization is an effective alternative method to surgery in treatment of hypersplenism particularly in cirrhotic patients prepared for antiviral treatment with correction of the associated thrombocytopenia.