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A Successful Approach to Kidney Transplantation in Patients with Secondary Hyperoxaluria.

J. Roodnat,1 A. Mik-van Egmond,2 W. Visser,2 S. Berger,3 W. van der Meijden,4 F. Knauf,5 M. Agteren van,1 M. Betjes,1 E. Hoorn.1

1Internal Medicine, Erasmus MC, Rotterdam, Netherlands
2Dietetics, Erasmus MC, Rotterdam, Netherlands
3Internal Medicine, University Hospital, Groningen, Netherlands
4Internal Medicine, Radboud University, Nijmegen, Netherlands
5Nephrology and Hypertension, Friedrich-Alexander-Universität, Erlangen-Nürnberg, Germany.

Meeting: 2016 American Transplant Congress

Abstract number: B232

Keywords: Graft failure, Kidney transplantation, Metabolic disease, Recurrence

Session Information

Session Name: Poster Session B: Kidney: Cardiovascular and Metabolic

Session Type: Poster Session

Date: Sunday, June 12, 2016

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Halls C&D

Chronic oxalate nephropathy is observed secondary to enteric hyperoxaluria that is associated with malabsorption e.g. in short bowel syndrome. Kidney transplantation can be challenging given the risk of recurrence resulting in graft dysfunction. We studied whether a strategy to decrease serum oxalic acid prior to transplantation may allow successful kidney transplantation.

A protocol was developed to reduce serum oxalic acid levels pre and post kidney transplantation based on reduced intake and increased removal of oxalic acid via intensified hemodialysis (HD). Months before transplantation a low oxalic acid diet (40 mg/day), cholestyramine, potassium citrate, and calcium carbonate were started. One week before transplantation (living donor transplantation) or immediately after surgery (deceased donor transplantation), an oxalic-acid free drip-feed and daily 6h HD session were started. When a urine output>2L was reached HD was stopped and 40mg oxalic acid diet was re-started. Patients were instructed to maintain diuresis > 2L/day.

We report three patients with short bowel syndrome following surgery for Crohn's disease who presented as potential kidney transplant recipients. All three patients had elevated serum oxalic acid levels and biopsy-proven calcium oxalate depositions in their native or transplanted kidney. The protocol reduced serum oxalic acid levels from 102, 112, and 48 to 23, 13, and 11 [mu]mol/l. Patients 1 and 2 received a living donor kidney and had immediate functioning grafts. Patient 3 received a deceased donor kidney and achieved urine output >2L/day after 3 weeks. The post-transplantation periods were complicated by sepsis in Patient 1 and symptomatic native kidney stones in Patient 2 requiring temporary re-institution of the protocol. The patients are currently 12, 11, and 7 months after transplantation with stable estimated glomerular filtration rates of 40, 46, and 50 ml/min/1.73 m2, respectively.

We conclude that successful kidney transplantation in patients with secondary hyperoxaluria is feasible by implementing a strategy aimed at reducing serum oxalic acid levels in the peri-transplantation period.

CITATION INFORMATION: Roodnat J, Mik-van Egmond A, Visser W, Berger S, van der Meijden W, Knauf F, Agteren van M, Betjes M, Hoorn E. A Successful Approach to Kidney Transplantation in Patients with Secondary Hyperoxaluria. Am J Transplant. 2016;16 (suppl 3).

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To cite this abstract in AMA style:

Roodnat J, Egmond AMik-van, Visser W, Berger S, Meijden Wvander, Knauf F, van MAgteren, Betjes M, Hoorn E. A Successful Approach to Kidney Transplantation in Patients with Secondary Hyperoxaluria. [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/a-successful-approach-to-kidney-transplantation-in-patients-with-secondary-hyperoxaluria/. Accessed May 8, 2025.

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