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During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Pigment nephropathy is characterized by a rapid decline in renal function as a consequence of rhabdomyolysis or hemolysis.
This was a retrospective observational study done at our tertiary care centre to analyze the etiology, clinical manifestations, laboratory profile and outcomes in patients with biopsy-proven pigment-induced nephropathy between January 2017 and January 2024. History, clinical examination findings, laboratory investigations and outcomes were documented.
Our study population included 103 patients, out of which 60% were males. The mean follow-up was 12 ± 2.5 months. Mean age was 41.8 ± 14 years. 88% (90) had oliguria and mean serum creatinine at presentation was 6.7 ± 2.5 mg/dL. Rhabdomyolysis was noted in 68% (70) and hemolysis in 32% (33). Etiology of rhabdomyolysis include snake envenomation (11), seizures (7), trauma (24), sepsis (8), pancreatitis (6), drug induced (5), thyroid myopathy (2) and multiple substance abuse (7). Etiology of hemolysis include rifampicin induced (3), leptospirosis (5), mismatched blood transfusion reaction (3), snake bite (17), sepsis (3) and sickle cell disease (2).The mean duration of hospital stay was 10 ± 2.36 days. 73 patients (71 %) required hemodialysis (HD) during hospital stay and mean number of HD sessions was 10 ± 5. Mortality was 18% (18). On statistical analysis, there was no significant difference between AKI due to rhabdomyolysis and hemolysis except for high creatine phosphokinase in patients with rhabdomyolysis and Lactate dehydrogenase level in patients with hemolysis. At follow-up, 9% (9) progressed to chronic kidney disease (CKD).
Pigment nephropathy due to rhabdomyolysis and hemolysis is an important cause of dialysis requiring AKI . The prognosis was relatively good and depends on the etiology and complications