Total embolization of the main splenic artery as a supplemental treatment modality for hypersplenism

AIM: To study the safety and feasibility of total embolization of the main splenic artery as a supplemental treatment modality for hypersplenism with thrombocy topenia or leukocytopenia accompanying liver cirrhosis. METHODS: Fifteen consecutive patients with hyper- splenism due to cirrhosis were enr...

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Published in:World journal of gastroenterology : WJG Vol. 17; no. 24; pp. 2953 - 2957
Main Authors: He, Xin-Hong, Li, Wen-Tao, Peng, Wei-Jun, Li, Guo-Dong, Wang, Sheng-Ping, Xu, Li-Chao
Format: Journal Article
Language:English
Published: United States Baishideng Publishing Group Co., Limited 28-06-2011
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Summary:AIM: To study the safety and feasibility of total embolization of the main splenic artery as a supplemental treatment modality for hypersplenism with thrombocy topenia or leukocytopenia accompanying liver cirrhosis. METHODS: Fifteen consecutive patients with hyper- splenism due to cirrhosis were enrolled in this study from January 2006 to June 2010. All patients underwent total embolization of the main splenic artery. Clinical symp- toms, white blood cell (WBC) and platelet (PLT) counts, splenic volume, and complications of the patients were recorded. The patients were followed up for 1 and 6 mo, and 1, 2, 3 years, respectively, after operation. RESULTS: Total embolization of the main splenic artery was technically successful in all patients. Minor complications occurred in 13 patients after the procedure, but no major complications were found. The WBC and PLT counts were significantly higher and the residual splenic volume was significantly lower 1 and 6 mo, and 1, 2, 3 years after the procedure than before the procedure (P 〈 0.01). Moreover, the residual splenic volume increased very slowly with the time after embolization. All patients were alive during the follow-up period. CONCLUSION: Total embolization of the main splenic artery is a safe and feasible procedure and may serve as a supplemental treatment modality for hypersplenism with thrombocytopenia or leukocytopenia accompanying liver cirrhosis.
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AIM: To study the safety and feasibility of total embolization of the main splenic artery as a supplemental treatment modality for hypersplenism with thrombocy topenia or leukocytopenia accompanying liver cirrhosis. METHODS: Fifteen consecutive patients with hyper- splenism due to cirrhosis were enrolled in this study from January 2006 to June 2010. All patients underwent total embolization of the main splenic artery. Clinical symp- toms, white blood cell (WBC) and platelet (PLT) counts, splenic volume, and complications of the patients were recorded. The patients were followed up for 1 and 6 mo, and 1, 2, 3 years, respectively, after operation. RESULTS: Total embolization of the main splenic artery was technically successful in all patients. Minor complications occurred in 13 patients after the procedure, but no major complications were found. The WBC and PLT counts were significantly higher and the residual splenic volume was significantly lower 1 and 6 mo, and 1, 2, 3 years after the procedure than before the procedure (P 〈 0.01). Moreover, the residual splenic volume increased very slowly with the time after embolization. All patients were alive during the follow-up period. CONCLUSION: Total embolization of the main splenic artery is a safe and feasible procedure and may serve as a supplemental treatment modality for hypersplenism with thrombocytopenia or leukocytopenia accompanying liver cirrhosis.
Liver cirrhosis; Hypersplenism; Coil embolization, Splenic artery
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Author contributions: He XH, Li WT and Peng WJ designed the research; He XH, Li WT, Li GD, Wang SP and Xu LC performed the research; Li WT, Peng WJ and Li GD provided the new reagents/analytic tools; Wang SP and Xu LC analyzed the data; He XH and Wang SP wrote the paper.
Telephone: +86-21-64175590 Fax: +86-21-64049870
Correspondence to: Wen-Tao Li, Professor, Department of Radiology, Fudan University Shanghai Cancer Center, Shanghai 200032, China. wentao.li.sh@gmail.com
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v17.i24.2953