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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s10157-011-0503-4</subfield>
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   <subfield code="a">Safety and efficacy of administering the maximal dose of candesartan in renal transplant recipients</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Masayoshi Okumi, Noritaka Kawada, Naotsugu Ichimaru, Harumi Kitamura, Toyofumi Abe, Ryoichi Imamura, Yasuyuki Kojima, Yukito Kokado, Yoshitaka Isaka, Hiromi Rakugi, Norio Nonomura, Toshiki Moriyama, Shiro Takahara]</subfield>
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   <subfield code="a">Background: The regular dose of an angiotensin II type-1 receptor blocker (ARB) in renal transplant patients for hypertension is shown to be safe and effective; however, information on the appropriate dosing of ARBs in renal transplant patients is limited. We evaluate the efficacy and safety of the maximal dose of candesartan administered to renal transplant patients. Methods: Sixty-nine recipients were enrolled in this study. Patients were divided into three groups based on the basal dose of candesartan: patients not taking candesartan (Group A); patients taking a low to medium dose of candesartan (2-4mg/day; Group B); and patients taking a high dose of candesartan (8mg/day; Group C). During the course of the study, the dose of candesartan was gradually increased to a final dose of 12mg/day. Physiological and biochemical parameters were measured before and after the 12-month study period. Results: Ninety-one percent of patients succeeded in continuing their administration of candesartan for 1year and 75% tolerated the administration of the maximal dose of candesartan. Significant differences in proteinuria, albuminuria, serum creatinine, and estimated glomerular filtration rate (eGFR) level among the groups were detected. In Group A, candesartan reduced systolic blood pressure, decreased the levels of proteinuria, albuminuria, eGFR, and hemoglobin and increased plasma potassium, creatinine level, and plasma renin activity. Conclusion: The gradual increase of an ARB to its maximal dose in renal transplant patients is safe when carefully monitored. We were able to demonstrate the impact of maximal renin−angiotensin system (RAS) blockade on both proteinuria and albuminuria, which indicates the need for future, long-term randomized prospective trials to further establish the impact of maximal RAS blockade on renal and cardiovascular protection in transplant patients.</subfield>
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   <subfield code="a">Japanese Society of Nephrology, 2011</subfield>
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   <subfield code="a">Anemia</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Hyperkalemia</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Albuminuria</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Okumi</subfield>
   <subfield code="D">Masayoshi</subfield>
   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
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   <subfield code="a">Kawada</subfield>
   <subfield code="D">Noritaka</subfield>
   <subfield code="u">Division of Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
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   <subfield code="a">Ichimaru</subfield>
   <subfield code="D">Naotsugu</subfield>
   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
   <subfield code="4">aut</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
   <subfield code="a">Kitamura</subfield>
   <subfield code="D">Harumi</subfield>
   <subfield code="u">Division of Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
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   <subfield code="a">Abe</subfield>
   <subfield code="D">Toyofumi</subfield>
   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Imamura</subfield>
   <subfield code="D">Ryoichi</subfield>
   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="a">Kojima</subfield>
   <subfield code="D">Yasuyuki</subfield>
   <subfield code="u">Soryukai Inoue Hospital, Suita, Osaka, Japan</subfield>
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   <subfield code="u">Division of Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
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   <subfield code="D">Hiromi</subfield>
   <subfield code="u">Division of Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
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   <subfield code="a">Nonomura</subfield>
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   <subfield code="u">Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, 565-0871, Suita, Osaka, Japan</subfield>
   <subfield code="4">aut</subfield>
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   <subfield code="u">Health Care Center, Osaka University, Suita, Osaka, Japan</subfield>
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   <subfield code="a">Takahara</subfield>
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   <subfield code="u">Department of Advanced Technology for Transplantation, Osaka University Graduate School of Medicine, Suita, Osaka, Japan</subfield>
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   <subfield code="t">Clinical and Experimental Nephrology</subfield>
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   <subfield code="g">15/6(2011-12-01), 907-915</subfield>
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   <subfield code="q">15:6&lt;907</subfield>
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