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Risk Factors of Death or Chronic Renal Replacement Therapy Requirements in Patients with Thrombotic Microangiopathies Without ADAMTS-13 Deficiency.

Miguel G. Uriol-Rivera,Bernardo Lopez Andrade,Antonio Mas Bonet,Aina Obrador Mulet, Carmen Ballester Ruiz,Leonor Perianez Parraga,Javier Lumbreras, Jose Ignacio Ayestaran Rota, Mireia Ferreruela Servalos, Joana Ferrer Balaguer, Lucio Pallares Ferreres, Maria Jose Picado Valles, Rosa Maria Ruiz de Gopegui Valero, Susana Tarongi Sanchez, Ana Garcia Martin, Juan Rodriguez Garcia, Cristina Gomez Cobo, Daniel Ramis-Cabrer

EUROPEAN JOURNAL OF HAEMATOLOGY(2024)

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摘要
Thrombotic microangiopathy (TMA), characterized by microangiopathic hemolytic anemia, thrombocytopenia, and multisystem organ dysfunction, is a life-threatening disease. Patients with TMA who do not exhibit a severe ADAMTS-13 deficiency (defined as a disintegrin-like and metalloprotease with thrombospondin type 1 motif no. 13 activity ≥10%: TMA-13n) continue to experience elevated mortality rates. This study explores the prognostic indicators for augmented mortality risk or necessitating chronic renal replacement therapy (composite outcome: CO) in TMA-13n patients. We included 42 TMA-13n patients from January 2008 to May 2018. Median age of 41 years and 60% were female. At presentation, 62% required dialysis, and 57% warranted intensive care unit admission. CO was observed in 45% of patients, including a 9-patient mortality subset. Multivariate logistic regression revealed three independent prognostic factors for CO: early administration of eculizumab (median time from hospitalization to eculizumab initiation: 5 days, range 0-19 days; odds ratio [OR], 0.14; 95% confidence interval [CI], 0.02-0.94), presence of neuroradiological lesions (OR, 6.67; 95% CI, 1.12-39.80), and a PLASMIC score ≤4 (OR, 7.39; 95% CI, 1.18-46.11). In conclusion, TMA-13n patients exhibit a heightened risk of CO in the presence of low PLASMIC scores and neuroradiological lesions, while early eculizumab therapy was the only protective factor.
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brain damage,PLASMIC score,renal failure and mortality,thrombotic microangiopathy
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