Literature DB >> 25230989

Survival after arterial embolization therapy in patients with polycystic kidney and liver disease.

Junichi Hoshino1, Tatsuya Suwabe, Noriko Hayami, Keiichi Sumida, Koki Mise, Masahiro Kawada, Aya Imafuku, Rikako Hiramatsu, Masayuki Yamanouchi, Eiko Hasegawa, Naoki Sawa, Ryoji Takei, Kenmei Takaichi, Yoshifumi Ubara.   

Abstract

BACKGROUND: Transcatheter arterial embolization (TAE) has become a therapeutic option for symptomatic polycystic kidney disease (PKD) and polycystic liver disease (PLD). However, factors affecting survival with renal TAE remain unknown.
METHODS: All symptomatic patients with severe PKD and/or PLD who received renal and/or hepatic TAE at our center from October 1996 through March 2013 (n = 1,028) were followed until death. Their survival was compared with that of the general PKD population on dialysis in Japan. Factors affecting survival were analyzed using the Cox hazard model.
RESULTS: After renal TAE, 5- and 10-year survival was, respectively, 0.78 (95% confidence interval, 0.74-0.82) and 0.56 (0.49-0.63); with hepatic TAE, 0.69 (0.58-0.77) and 0.41 (0.22-0.60); and with dual TAE (renal and hepatic), 0.82 (0.72-0.88) and 0.45 (0.31-0.59). Survival after dialysis initiation was better among patients with renal TAE than among general PKD patients. Factors affecting survival after renal TAE were age [hazard ratio (HR) 3.02 (1.44-6.33) for every 10 years] and albumin [HR 0.70 (0.55-0.89) per 0.1 g/dl]. Kidney volume was not associated with patient death after TAE. The main causes of death among patients after renal TAE were similar to those of the general PKD population on dialysis whereas, after hepatic TAE, the main cause was cyst infection with liver failure (12.5% with PLD and 5.9% with PKD, p < 0.01).
CONCLUSION: Survival after renal TAE with severe PKD was better than for the general PKD population on dialysis, suggesting that renal TAE could overcome the disadvantage due to huge organ size.

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Year:  2014        PMID: 25230989     DOI: 10.1007/s40620-014-0138-0

Source DB:  PubMed          Journal:  J Nephrol        ISSN: 1121-8428            Impact factor:   3.902


  25 in total

1.  Intravascular embolization therapy in patients with enlarged polycystic liver.

Authors:  Junichi Hoshino; Yoshifumi Ubara; Tatsuya Suwabe; Keiichi Sumida; Noriko Hayami; Koki Mise; Rikako Hiramatsu; Eiko Hasegawa; Masayuki Yamanouchi; Naoki Sawa; Ryoji Takei; Kenmei Takaichi
Journal:  Am J Kidney Dis       Date:  2014-03-04       Impact factor: 8.860

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Authors:  F Temmerman; L Missiaen; B Bammens; W Laleman; D Cassiman; C Verslype; J van Pelt; F Nevens
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3.  Transcatheter renal arterial embolization therapy on a patient with polycystic kidney disease on hemodialysis.

Authors:  Y Ubara; H Katori; T Tagami; S Tanaka; M Yokota; Y Matsushita; F Takemoto; T Imai; S Inoue; K Kuzuhara; S Hara; A Yamada
Journal:  Am J Kidney Dis       Date:  1999-11       Impact factor: 8.860

4.  Liver cysts in patients with autosomal dominant polycystic kidney disease.

Authors:  J Milutinovic; P J Fialkow; T G Rudd; L Y Agodoa; L A Phillips; J I Bryant
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9.  Intravascular embolization therapy in a patient with an enlarged polycystic liver.

Authors:  Yoshifumi Ubara; Ryouji Takei; Jyunichi Hoshino; Tetsuo Tagami; Naoki Sawa; Masafumi Yokota; Hideyuki Katori; Fumi Takemoto; Shigeko Hara; Kenmei Takaichi
Journal:  Am J Kidney Dis       Date:  2004-04       Impact factor: 8.860

10.  Transcatheter arterial embolization therapy for a massive polycystic liver in autosomal dominant polycystic kidney disease patients.

Authors:  Hayne Cho Park; Chi Weon Kim; Han Ro; Ju-Young Moon; Kook-Hwan Oh; Yonsu Kim; Jung Sang Lee; Yong Hu Yin; Hwan Jun Jae; Jin Wook Chung; Curie Ahn; Young-Hwan Hwang
Journal:  J Korean Med Sci       Date:  2009-02-28       Impact factor: 2.153

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1.  Suitability of Patients with Autosomal Dominant Polycystic Kidney Disease for Renal Transcatheter Arterial Embolization.

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2.  Tolvaptan in Japanese patients with later-stage autosomal dominant polycystic kidney disease.

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3.  Transarterial Embolization for Treatment of Symptomatic Polycystic Liver Disease: More than 2-year Follow-up.

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