scholarly journals Sevelamer-associated ischemic colitis with perforation

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Rachel Hudacko ◽  
Peter Kaye

We present a case of an 83-year-old woman with end-stage renal disease and hyperphosphatemia treated with sevelamer carbonate, who underwent subtotal colectomy for diffuse bowel necrosis and two perforations in the transverse colon. Histologic examination revealed ischemic colitis with crystals consistent with sevelamer carbonate embedded in ulcer debris and within the colonic wall in areas of transmural necrosis. This is a novel cause of drug-induced ischemic colitis with subsequent perforation that has not yet been reported in the literature. Clinicians and pathologists should be aware of the potential complications of sevelamer use and the histologic features of sevelamer-induced colonic injury.

2012 ◽  
Vol 22 (3) ◽  
pp. 189 ◽  
Author(s):  
G Abraham ◽  
V Kher ◽  
S Saxena ◽  
M Jayakumar ◽  
D Chafekar ◽  
...  

1994 ◽  
Vol 331 (25) ◽  
pp. 1711-1712 ◽  
Author(s):  
Pierre M. Ronco ◽  
Antoine Flahault

2020 ◽  
Vol 115 (1) ◽  
pp. S68-S68
Author(s):  
Eric Then ◽  
Dustin Uhlenhopp ◽  
Michell Lopez ◽  
Srikanth Maddika ◽  
Tagore Sunkara ◽  
...  

2021 ◽  
Vol 14 (9) ◽  
pp. e245228
Author(s):  
Aishwarya Sharma ◽  
Devendranath Mannuru ◽  
Abhishek Matta ◽  
Amit Kaushal

A 62-year-old woman with a history of end-stage renal disease on haemodialysis, essential hypertension and type 2 diabetes mellitus was diagnosed with sepsis and placed on 600 mg oral linezolid every 12 hours and 1 g intravenous ceftriaxone every 24 hours. Blood cultures grew Streptococcus dysgalactiae, and she was switched to intravenous ceftriaxone 2 g daily. Platelet counts slowly trended down after starting ceftriaxone reaching 5 K/μL on day 12 of treatment. Ceftriaxone was discontinued and heparin-induced thrombocytopaenia was ruled out. She was switched to vancomycin and her platelet count improved. Given the temporal relationship between changing platelet counts and starting and discontinuing ceftriaxone, a diagnosis of drug-induced thrombocytopaenia was made.


2016 ◽  
Vol 9 (3) ◽  
pp. 481-485 ◽  
Author(s):  
Guillermo Rosa-Diez ◽  
Armando Luis Negri ◽  
Maria Soledad Crucelegui ◽  
Romina Philippi ◽  
Hernán Perez-Teysseyre ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
T. Lai ◽  
A. Frugoli ◽  
B. Barrows ◽  
M. Salehpour

Hyperphosphatemia is a common and well-described complication of end-stage renal disease. Despite strict dietary constraints and compliance, phosphate binders such as calcium acetate and/or sevelamer carbonate are also needed to treat secondary hyperparathyroidism. This case vignette describes an underrecognized adverse effect of a phosphate binder, sevelamer carbonate, inducing colitis in a 47-year-old male with insulin-dependent diabetes complicated by end-stage renal disease. He presented for recurrent abdominal pain with associated nausea and was found to have multiple circumferential lesions on computed tomography including distal ascending, transverse, and proximal descending colon. Colonoscopy demonstrated nearly obstructing lesions worrisome for colonic ischemia or inflammatory bowel disease. Pathological review of histology demonstrated ragged colonic mucosa with ulcerative debris and nonpolarizing crystalline material at the sites of ulceration, morphologically consistent with the phosphate binder, sevelamer carbonate. Sevelamer carbonate was discontinued, and the patient was transitioned to calcium carbonate with strict dietary restrictions. His symptoms improved with the cessation of sevelamer, and he was subsequently discharged home. He eventually underwent renal transplant without redevelopment of symptoms. Recognition of this underreported complication of sevelamer carbonate, phosphate binder, is of utmost importance in directing appropriate therapy with cessation of this medication in the setting of gastrointestinal complaints or more specifically enteritis and colitis. Clinicians providing care to end-stage renal patients taking either sevelamer and/or sodium polystyrene sulfonate should have increased awareness of the possible gastrointestinal side effects.


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