SESSION TITLE: Medical Student/Resident Critical Care Posters SESSION TYPE: Med Student/Res Case Rep Postr PRESENTED ON: October 18-21, 2020 INTRODUCTION: Thrombotic microangiopathy (TMA) is characterized by many etiologies, however it is not often described as a complication of Endoscopic Retrograde Cholangiopancreatography (ERCP). Failure to identify the relationship between TMA and ERCP may result in delay of diagnosis and poor patient outcomes. We present a case of a young healthy female who developed TMA after ERCP. CASE PRESENTATION: A 26-year-old woman presented to the hospital with complaints of abdominal pain, nausea and vomiting. An abdominal CT scan showed cholelithiasis and choledocholithiasis and the patient was scheduled for ERCP. She tolerated the procedure well with no immediate complications. However, a day after procedure, labs showed elevated serum lipase and amylase levels with renewed abdominal pain. Two days after ERCP she developed fever, severe thrombocytopenia, anemia and acute kidney injury (AKI) evidenced by elevated serum creatinine. A preliminary diagnosis of thrombotic thrombocytopenic purpura (TMA) was considered. Plasma exchange therapy with platelet transfusion and high dose steroids was initiated. She also received multiple packed red cell transfusion for severe anemia. ADAMTS13 antibody testing returned low at 53% with negative anti-ADAMTS13 IgG. After 7 daily sessions of plasma exchange platelets improved, AKI and anemia resolved, and the patient was discharged from the hospital. DISCUSSION: Literature review shows only about 4 cases of ERCP induced TMA. A well-known complication of ERCP is pancreatitis and a rare unfortunate sequela of this is TMA. There is a known correlation between TMA and pancreatitis, though the mechanism by which this occurs is still not well understood. Endothelial damage, cytokine release and platelet activation are thought to be the pathophysiological links between these two conditions (1). Cytokines cause release of ultra-large von-Willebrand factor (VWf) molecules that attach to activated platelets promoting aggregation, clumping and thrombus formation. There is concomitant reduction in serum ADAMTS13, which would normally cleave the ultra-large VWf, due to pancreatic enzyme degradation. CONCLUSIONS: This case illustrates how complicated the diagnosis of TMA can be, but also points out how clinical judgment is imperative to prompt early treatment and increase favorable outcomes. TMA caused by ERCP is rare, but recognizing this link is important for immediate initiation of life saving treatment. Reference #1: 1. Malik, F., Ali, N., Ahsan, I., Ghani, A. R., & Fidler, C. (2016). Eculizumab refractory thrombotic thrombocytopenic purpura secondary to post-endoscopic retrograde cholangiopancreatography pancreatitis in a patient. Journal of community hospital internal medicine perspectives, 6(6), 32310. DISCLOSURES: No relevant relationships by Kitson Deane, source=Web Response No relevant relationships by Abidemi Idowu, source=Web Response