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Objective: To evaluate the real-world efficacy and safety of eculizumab in atypical hemolytic uremic syndrome (aHUS) within a Western Chinese cohort, with emphasis on treatment initiation timing and renal outcomes.
Methods: We conducted a retrospective analysis of 17 aHUS patients treated at Sichuan Provincial People's Hospital, focusing on the relationship between treatment timing and clinical prognosis. To evaluate timing effects, patients were categorized as Early Initiators (treatment within 7 days of symptom onset, n=9) versus Delayed Initiators (treatment beyond 7 days, n=8) The main outcome measures included hematological parameters, renal function, and adverse events.
Results: The cohort (n=17, 76.5% female, mean age 43.2 ± 20.0 years) demonstrated significant improvements post-eculizumab: creatinine decreased from 647.0 (439.0, 915.0) to 198.5 (86.5, 749.5) μmol/L, eGFR increased from 8.0 (5.0, 11.0) to 22.1 (6.4, 55.1) mL/min/1.73m², platelets rose from 75 ± 11 to 143 ± 33×10/L, and LDH declined from 787.5±908.0 to 232.8 ± 70.0 U/L (all P<0.001). Early treatment initiation (≤7 days, n=9) yielded superior outcomes versus delayed (>7 days, n=8): higher renal remission (88.9% vs 12.5%, P=0.003), hematological remission (100% vs 12.5%, P<0.001), and reduced dialysis dependence (0% vs 87.5%, P<0.001), with greater ΔeGFR (+(19.5 ± 3.1) vs +(2.3 ± 1.7 )mL/min/1.73m, P=0.016) and Δplatelets (+(67.8 ± 9.8) vs +(19.3 ± 7.2)×10/L, P=0.007). Renal survival favored early treatment (log-rank P<0.001), though residual renal impairment persisted. Two non-meningococcal bloodstream infections resolved with antibiotics.
Conclusion: Our findings provide the first Chinese evidence supporting early eculizumab initiation (≤7 days post-symptom onset) significantly improves hematological/renal outcomes and reduces dialysis dependence in Chinese aHUS patients. Despite residual renal impairment, prompt complement blockade mitigates ESRD risk, supporting time-sensitive intervention in resource-limited settings.
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http://dx.doi.org/10.3389/fendo.2025.1568082 | DOI Listing |
Clin Transplant
September 2025
Department of Pediatrics and Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Introduction: Atypical hemolytic uremic syndrome (aHUS) is a disease of complement dysregulation that may lead to kidney failure. Ravulizumab and eculizumab are complement C5 inhibitors approved for the treatment of aHUS. This study assessed the real-world effectiveness and safety of switching to ravulizumab from eculizumab in kidney transplant recipients with aHUS.
View Article and Find Full Text PDFNephrol Dial Transplant
August 2025
Middlesbrough Council.
Background And Hypothesis: Atypical haemolytic uraemic syndrome (aHUS) is a rare but severe condition caused by complement dysregulation. Eculizumab prophylaxis prevents recurrence and improves survival, yet the benefits of lifelong treatment for patients are uncertain and the long-term costs for health services are substantial. This economic evaluation applied the results from the Stopping Eculizumab Treatment Safely in aHUS (SETS aHUS) trial and assessed the cost-effectiveness of replacing lifelong eculizumab with a disease monitoring strategy over the long term.
View Article and Find Full Text PDFTransfus Med Hemother
August 2025
Alb-Fils Klinikum, Department of Hematology, Oncology, Infectiuous Disease and Palliative Care Medicine, Göppingen, Germany.
Background: Patients suffering from hemolytic anemia, thrombocytopenia, and organ damage may suffer from microangiopathic anemia, also called thrombotic microangiopathy (TMA). This condition is caused by many different pathogenic mechanisms and is always life-threatening due to vessel occlusion in vital organs. Rapid and careful workup is mandatory to identify the cause of TMA.
View Article and Find Full Text PDFBlood Adv
August 2025
Medical University of South Carolina, Charleston, South Carolina, United States.
Atypical hemolytic uremic syndrome (aHUS), a life-threatening complement-mediated disorder, is now treatable with terminal complement inhibitors like eculizumab. Although effective, these therapies are costly and increase susceptibility to infections, notably meningococcal disease, raising concerns about long-term use. The optimal duration of complement inhibition remains unclear, prompting efforts to explore the possibility of treatment discontinuation.
View Article and Find Full Text PDFCureus
July 2025
Pediatrics, Brooke Army Medical Center, San Antonio, USA.
A previously healthy seven-year-old boy presented with clinical and laboratory findings consistent with atypical hemolytic uremic syndrome (aHUS) given thrombocytopenia, microangiopathic hemolytic anemia (MAHA), and acute kidney injury in the setting of influenza A. Notably, he also met diagnostic criteria for disseminated intravascular coagulation (DIC) at the time of presentation with clinical findings including prolonged prothrombin time (PT), markedly elevated D-dimer, and low fibrinogen. While aHUS and DIC share overlapping clinical features, they are traditionally regarded as distinct entities, with aHUS driven by complement dysregulation and DIC by the widespread activation of the coagulation cascade resulting in microvascular thrombosis, consumptive coagulopathy, and secondary fibrinolysis.
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