Review
Copyright ©2014 Baishideng Publishing Group Inc.
World J Radiol. May 28, 2014; 6(5): 160-168
Published online May 28, 2014. doi: 10.4329/wjr.v6.i5.160
Table 1 Study demographics and outcomes of partial splenic embolization
Ref.YearCountryStudy typeNumber of PtsLength of follow-upMean ± SD, platelet count prior to PSE inK/μLMean ± SD, WBC count prior to PSE in K/μLIndication for PSEExtent of spleen targetedMean ± SD, platelet count at 2 wk in K/μLMean ± SD, platelet count at 1 mo in K/μLMean ± SD, platelet count at 1 yr in K/μLMean ± SD, WBC count at 2 wk inMean ± SD, WBC count at 1 mo in K/μLMean ± SD, WBC count at 1 yr in K/μL
Kim et al[11]2012South KoreaCase series report116-28 moNot providedNot providedAll patients S/P OLT; 6/11 w/thrombocytopenia, 5/11 w/refractory ascites70%-80%Not providedNot providedNot providedNot providedNot providedNot provided
Elmonem et al[12]2010EgyptCase series report232 yr41.3 ± 13.02.3 ± 0.47Hypersplenism in Cirrhosis w/leukopenia and thrombocytopenia, no HCC, and no SBP50%-70%124.3 ± 23.9115.8 ± 18.494.1 ± 12.98.26 ± 1.546.53 ± 1.744.62 ± 1.13
Zhu et al[14]2009ChinaNonrandomized prospective trialTotal 62 Group A: 12 Group B: 34 Group C: 165 yrGroup A: 40.2 ± 13.0 Group B: 37.4 ± 12.3 Group C: 43.6 ± 11.7Group A: 2.42 ± 0.44 Group B: 2.54 ± 0.57 Group C: 2.64 ± 0.4Hypersplenism in Cirrhosis, w/thrombocytopenia or neutropenia. No SBP, no Severe Jaundice50%-70%Group A: 1701 Group B: 1301 Group C: 801Group A: 1301 Group B: 1101 Group C: 701Group A: 1001 Group B: 901 Group C: 501Group A: 7.51 Group B: 6.51 Group C: 4.01Group A: 6.01 Group B: 5.51 Group C: 3.71Group A: 4.51 Group B: 4.01 Group C: 3.01
Amin et al[9]2009EgyptRandomized control trialTotal 40 PSE: 20 SPL: 206 moPSE: 39.7 ± 9.7 SPL: 47.2 ± 10.3PSE: 3.3 ± 0.7 SPL: 2.8 ± 1.1Cirrhosis w/o bone marrow disease, ischemic heart disease, renal failure, malignancy, or medical unstability50%PSE: 211.5 ± 36.2 SPL: 240.7 ± 52.0Not providedNot providedPSE: 12.6 ± 2.6 SPL: 7.7 ± 1.9Not providedNot provided
Zhu et al[16]2008ChinaRandomized control trialTotal 60 GF: 32 PVA: 283 yrGF: 47.06 ± 14.85 PVA: 44.36 ± 16.67GF: 2.62 ± 0.67 PVA: 2.57 ± 0.63Hypersplenism in cirrhosis w/thrombocytopenia or neutropenia. No SBP, no HCC, no hyperbilirubinemia50%-70%GF: 135.4 ± 28.1 PVA: 153.4 ± 37.1GF: 113.2 ± 17.6 PVA: 125.4 ± 23.3GF: 95.8 ± 13.9 PVA: 106.2 ± 17.2GF: 6.6 ± 1.5 PVA: 7.5 ± 1.7GF: 5.1 ± 0.9 PVA: 5.7 ± 1.2GF: 4.2 ± 0.6 PVA: 4.7 ± 1.0
Hayashi et al[17]2007JapanNonrandomized prospective trial421 yr45 ± 11.72.9 ± 1.0Thrombocytopenia caused by hypersplenism due to cirrhosis70%-80%Not provided116 ± 51103 ± 34Not providedNot providedNot provided
Lee et al[15]2007ChinaNonrandomized prospective trial101 yr56 ± 8.0Not providedThrombocytopenia in setting of cirrhosis20%-40%192Not provided145Not providedNot providedNot provided
N'Kontchou et al[13]2005FranceRetrospective review321-87 mo48 ± 144.2 ± 1.6Cirrhosis w/severe cytopenia/leukopenia preventing treatment or severe purpur, or painful splenomegaly50%Not provided137.5 ± 77.4Not providedNot provided6.5 ± 2.9Not provided
Table 2 Complications in partial splenic artery embolization
Ref.YearCountryStudy typeComplication: Frequency of post embolization syndromeComplication: Mean length of post embolization syndrome-DaysMajor complications: Total numberPersistant thrombocytopeniaSplenomegalyPleural effusion/ascitesVariceal bleedingPortal vein thrombosisBacterial peritonitisSplenic abscessPSE-related deathRepeat embolization required
Kim et al[11]2012South KoreaCase series report100.00%Not provided0.00%0.00%0.00%0.00%0.00%0.00%0.00%0.00%0.00%0.00%
Elmonem et al[12]2010EgyptCase series report91.30%Not provided34.80%4.30%4.30%8.70%0.00%4.30%4.30%4.30%4.30%4.30%
Zhu et al[14]2009ChinaNonrandomized prospective trialTotal 85.5% Group A: 100% Group B: 91.2% Group C: 62.5%Group A: 13 Group B: 7 Group C: 3Total 14.5% Group A: 50% Group B: 8.8% Group C: 0%Total 0% Group A: 0% Group B: 0% Group C: 0%Total 0% Group A: 0% Group B: 0% Group C: 0%Total 4.8% Group A: 16.6% Group B: 2.9% Group C: 0%Total 1.6% Group A: 8.3% Group B: 0% Group C: 0%Total 1.6% Group A: 8.3% Group B: 0% Group C: 0%Total 1.6% Group A: 8.3% Group B: 2.9% Group C: 0%Total 1.6% Group A: 8.3% Group B: 0% Group C: 0%Total 1.6% Group A: 8.3% Group B: 0% Group C: 0%Total 0% Group A: 0% Group B: 0% Group C: 0%
Amin et al[9]2009EgyptRandomized control trialNot providedPSE: 2.1 (0.4) SPL: 4.3 (1.1)PSE: 25% SPL: 25%PSE: 0% SPL: 0%PSE: 0% SPL: 0%PSE: 10% SPL: 10%PSE: 0% SPL: 0%PSE: 5% SPL: 15%PSE: 0% SPL: 0%PSE: 5% SPL: 0%PSE: 5% SPL: 0%PSE: 0% SPL: 0%
Zhu et al[16]2008ChinaRandomized control trialGF: 90.6% PVA: 100%GF: 6.4 (3.6) PVA: 7.6 (2.8)GF: 25.0% PVA: 21.4%GF: 0% PVA: 0%GF: 0% PVA: 0%GF: 9.4% PVA: 10.7%GF: 3.1% PVA: 3.6%GF: 3.1% PVA: 7.1%GF: 6.3% PVA: 0%GF: 3.1% PVA: 0%GF: 3.1% PVA: 0%GF: 0% PVA: 0%
Hayashi et al[17]2007JapanNonrandomized prospective trial100.00%Not provided11.90%0.00%0.00%9.50%0.00%0.00%0.00%0.00%0.00%0.00%
Lee et al[15]2007ChinaNonrandomized prospective trial100.00%Not provided10.00%0.00%0.00%10.00%0.00%0.00%0.00%0.00%0.00%0.00%
N'Kontchou et al[13]2005FranceRetrospective review78.10%1428.10%3.10%0.00%6.30%0.00%6.30%0.00%6.30%6.3%13.10%