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ID 62282
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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 ORCID Kaken ID publons researchmap
Wada, Koichiro Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science ORCID researchmap
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 ORCID Kaken ID
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 ORCID Kaken ID publons researchmap
Kitagawa, Masashi Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science Kaken ID
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 Kaken ID publons
Sugiyama, Hitoshi Department of Nephrology, Rheumatology, Endocrinology, and Metabolism, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science ORCID Kaken ID publons researchmap
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 Kaken ID publons researchmap
Watanabe, Toyohiko Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science ORCID Kaken ID publons researchmap
Nasu, Yasutomo Department of Urology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Science Kaken ID publons researchmap
Abstract
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.
Note
© 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] .
Published Date
2021-4-28
Publication Title
Transplantation Proceedings
Volume
volume53
Issue
issue5
Publisher
Elsevier BV
Start Page
1494
End Page
1500
ISSN
0041-1345
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
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isVersionOf https://doi.org/10.1016/j.transproceed.2021.03.043