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Watari, Shogo
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Araki, Motoo
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Wada, Koichiro
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Yoshinaga, Kasumi
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Maruyama, Yuki
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Mitsui, Yosuke
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Sadahira, Takuya
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Kubota, Risa
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Nishimura, Shingo
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Kobayashi, Yasuyuki
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Takeuchi, Hidemi
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Tanabe, Katsuyuki
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Kitagawa, Masashi
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Morinaga, Hiroshi
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Kitamura, Shinji
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Sugiyama, Hitoshi
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Wada, Jun
Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
Watanabe, Masami
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Watanabe, Toyohiko
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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Nasu, Yasutomo
Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science
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抄録 | Background
We investigated the association between ABO-incompatible (ABO-I) kidney transplantation and early graft function. Methods We retrospectively analyzed 95 patients who underwent living donor kidney transplantation between May 2009 and July 2019. It included 61 ABO-compatible (ABO-C) and 34 ABO-I transplantations. We extracted data on immunologic profile, sex, age, cold ischemic time, type of immunosuppression, and graft function. Two definitions were used for slow graft function (SGF) as follows: postoperative day (POD) 3 serum creatinine level >3 mg/dL and estimated glomerular filtration rate (eGFR) <20 mL/min/1.73 m2. Logistic regression analysis was performed to analyze the effect of ABO-I on the incidence of SGF. Results The characteristics between the ABO-C and ABO-I were not different. ABO-I received rituximab and plasma exchange. Patients also received tacrolimus and mycophenolate mofetil for 2 weeks and prednisolone for 1 week before transplantation as preconditioning. Of the 95 study patients, 19 (20%) and 21 (22%) were identified with SGF according to POD 3 serum creatinine level or eGFR, respectively. Multivariable analysis revealed that ABO-I significantly reduced the incidence of SGF (odds ratio, 0.15; 95% confidence interval, 0.03-0.7; P = .02), and cold ischemic time >150 min increased the incidence of SGF (odds ratio, 6.5; 95% confidence interval, 1.7-25; P = .006). Similar results were identified in POD 3 eGFR. Inferior graft function in patients with SGF was identified up to 6 months after transplantation. Conclusion ABO-I reduces the incidence of SGF, which is associated with an inferior graft function up to 6 months. |
備考 | © 2021 Published by Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/.
This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.transproceed.2021.03.043] .
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発行日 | 2021-4-28
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出版物タイトル |
Transplantation Proceedings
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巻 | 53巻
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号 | 5号
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出版者 | Elsevier BV
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開始ページ | 1494
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終了ページ | 1500
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ISSN | 0041-1345
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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論文のバージョン | author
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PubMed ID | |
DOI | |
Web of Science KeyUT | |
関連URL | isVersionOf https://doi.org/10.1016/j.transproceed.2021.03.043
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