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Kidney Week

Abstract: FR-PO611

Gastrointestinal Bleed in ESRD: An Unexpected Cause

Session Information

  • Trainee Case Reports - IV
    October 26, 2018 | Location: Exhibit Hall, San Diego Convention Center
    Abstract Time: 10:00 AM - 12:00 PM

Category: Trainee Case Reports

  • 701 Dialysis: Hemodialysis and Frequent Dialysis

Authors

  • Kodali, Ravi, Yale University School of Medicine, New Haven, Connecticut, United States
  • Chang, Eric, Yale University School of Medicine, New Haven, Connecticut, United States
  • Brewster, Ursula C., Yale University School of Medicine, New Haven, Connecticut, United States

Group or Team Name

  • Yale University
Introduction

ESRD patients have a fivefold higher risk of gastrointestinal (GI) bleed compared to those without CKD. Common causes include angiodysplasia, peptic ulcer disease, diverticular disease, ischemic colitis. A lesser known causes of GI bleed in this population is sevelamer induced GI ulcer.

Case Description

A 59-year-old African American man with type 2 diabetes mellitus, HTN, ESRD on hemodialysis, presented with severe headache and right sided weakness. He had intraventricular hemorrhage from severe hypertension. Routine labs showed hyperphosphatemia, so he was continued on sevelamer. On hospitalization day 20, he had multiple episodes of dark tarry stools with hemoglobin drop. Upper GI endoscopy revealed a large ulcer in the duodenum; he was started on pantoprazole. GI bleed recurred over the next weeks. A colonoscopy revealed a 3-5 cm segment of ulcerated and friable mucosa in the ascending colon. Biopsy of the colonic ulcer revealed presence of “fish scale” crystals previously associated with sevelamer, with inflammatory changes (Fig 1). A diagnosis of sevelamer induced colonic ulcer was made and sevelamer was stopped.

Discussion

Here we report 6 cases from our institution of GI ulcerations with deposition of sevelamer (Table 1). This is an underappreciated association and should be suspected in the right clinical scenario. Given the continued increase in use of sevelamer as a phosphate binder, it is important for the nephrologists to be cognizant of this entity.

Table 1
 Age (years)Dialysis vintage (years)Time on sevelamer (years)Presenting symptomsLocation of lesion
Patient 15955 years intermittent useMelena, hgb dropAscending colon
Patient 25875Abdominal Pain, diarrheaTransverse colon
Patient 3503 (PD)3Sigmoid perforationSigmoid colon
Patient 45622Rectosigmoid colitisColon NOS (random biopsy)
Patient 57532Rectal ulcers, hematocheziaRectosigmoid colon
Patient 66933Heme positive stools, anemiaColon

Sevelamer crystals in biopsy from colon