Ref. |
Year |
Country |
Study type |
Number of Pts |
Length of follow-up |
Mean ± SD, platelet count prior to PSE in
K/μL
|
Mean ± SD, WBC count prior to PSE in K/μL
|
Indication for PSE |
Extent of spleen targeted |
Mean ± SD, platelet count at 2 wk in K/μL
|
Mean ± SD, platelet count at 1 mo in K/μL
|
Mean ± SD, platelet count at 1 yr in K/μL
|
Mean ± SD, WBC count at 2 wk in |
Mean ± SD, WBC count at 1 mo in K/μL
|
Mean ± SD, WBC count at 1 yr in K/μL
|
Kim et al[11] |
2012 |
South Korea |
Case series report |
11 |
6-28 mo |
Not provided |
Not provided |
All patients S/P OLT; 6/11 w/thrombocytopenia, 5/11 w/refractory ascites |
70%-80% |
Not provided |
Not provided |
Not provided |
Not provided |
Not provided |
Not provided |
Elmonem et al[12] |
2010 |
Egypt |
Case series report |
23 |
2 yr |
41.3 ± 13.0 |
2.3 ± 0.47 |
Hypersplenism in Cirrhosis w/leukopenia and thrombocytopenia, no HCC, and no SBP |
50%-70% |
124.3 ± 23.9 |
115.8 ± 18.4 |
94.1 ± 12.9 |
8.26 ± 1.54 |
6.53 ± 1.74 |
4.62 ± 1.13 |
Zhu et al[14] |
2009 |
China |
Nonrandomized prospective trial |
Total 62 Group A: 12 Group B: 34 Group C: 16 |
5 yr |
Group A: 40.2 ± 13.0 Group B: 37.4 ± 12.3 Group C: 43.6 ± 11.7 |
Group A: 2.42 ± 0.44 Group B: 2.54 ± 0.57 Group C: 2.64 ± 0.4 |
Hypersplenism in Cirrhosis, w/thrombocytopenia or neutropenia. No SBP, no Severe Jaundice |
50%-70% |
Group A: 1701 Group B: 1301 Group C: 801
|
Group A: 1301 Group B: 1101 Group C: 701
|
Group A: 1001 Group B: 901 Group C: 501
|
Group A: 7.51 Group B: 6.51 Group C: 4.01
|
Group A: 6.01 Group B: 5.51 Group C: 3.71
|
Group A: 4.51 Group B: 4.01 Group C: 3.01
|
Amin et al[9] |
2009 |
Egypt |
Randomized control trial |
Total 40 PSE: 20 SPL: 20 |
6 mo |
PSE: 39.7 ± 9.7 SPL: 47.2 ± 10.3 |
PSE: 3.3 ± 0.7 SPL: 2.8 ± 1.1 |
Cirrhosis w/o bone marrow disease, ischemic heart disease, renal failure, malignancy, or medical unstability |
50% |
PSE: 211.5 ± 36.2 SPL: 240.7 ± 52.0 |
Not provided |
Not provided |
PSE: 12.6 ± 2.6 SPL: 7.7 ± 1.9 |
Not provided |
Not provided |
Zhu et al[16] |
2008 |
China |
Randomized control trial |
Total 60 GF: 32 PVA: 28 |
3 yr |
GF: 47.06 ± 14.85 PVA: 44.36 ± 16.67 |
GF: 2.62 ± 0.67 PVA: 2.57 ± 0.63 |
Hypersplenism in cirrhosis w/thrombocytopenia or neutropenia. No SBP, no HCC, no hyperbilirubinemia |
50%-70% |
GF: 135.4 ± 28.1 PVA: 153.4 ± 37.1 |
GF: 113.2 ± 17.6 PVA: 125.4 ± 23.3 |
GF: 95.8 ± 13.9 PVA: 106.2 ± 17.2 |
GF: 6.6 ± 1.5 PVA: 7.5 ± 1.7 |
GF: 5.1 ± 0.9 PVA: 5.7 ± 1.2 |
GF: 4.2 ± 0.6 PVA: 4.7 ± 1.0 |
Hayashi et al[17] |
2007 |
Japan |
Nonrandomized prospective trial |
42 |
1 yr |
45 ± 11.7 |
2.9 ± 1.0 |
Thrombocytopenia caused by hypersplenism due to cirrhosis |
70%-80% |
Not provided |
116 ± 51 |
103 ± 34 |
Not provided |
Not provided |
Not provided |
Lee et al[15] |
2007 |
China |
Nonrandomized prospective trial |
10 |
1 yr |
56 ± 8.0 |
Not provided |
Thrombocytopenia in setting of cirrhosis |
20%-40% |
192 |
Not provided |
145 |
Not provided |
Not provided |
Not provided |
N'Kontchou et al[13] |
2005 |
France |
Retrospective review |
32 |
1-87 mo |
48 ± 14 |
4.2 ± 1.6 |
Cirrhosis w/severe cytopenia/leukopenia preventing treatment or severe purpur, or painful splenomegaly |
50% |
Not provided |
137.5 ± 77.4 |
Not provided |
Not provided |
6.5 ± 2.9 |
Not provided |