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Predictors of refractoriness to therapy and healthcare resource utilization in 378 patients with primary autoimmune hemolytic anemia from eight Italian reference centers

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TLDR
A mechanistic investigation of thrombotic microangiopathy associated with IV abuse of Opana ER and the experience of the Oklahoma registry and the blood Center of Wisconsin shows promising results.
Abstract
REFERENCES 1. Al-Nouri ZL, Reese JA, Terrell DR, Vesely SK, George JN. Drug-induced thrombotic microangiopathy: a systematic review of published reports. Blood. 2015;125:616-618. 2. Reese JA, Bougie DW, Curtis BR, et al. Drug-induced thrombotic microangiopathy: experience of the Oklahoma registry and the blood Center of Wisconsin. Am J Hematol. 2015;90:406-410. 3. Miller PJ, Farland AM, Knovich MA, Batt KM, Owen J. Successful treatment of intravenously abused oral Opana ER-induced thrombotic microangiopathy without plasma exchange. Am J Hematol. 2014;89: 695-697. 4. Hunt R, Yalamanoglu A, Tumlin J, et al. A mechanistic investigation of thrombotic microangiopathy associated with IV abuse of Opana ER. Blood. 2017;129:896-905. 5. Yui JC, Dispenzieri A, Leung N. Ixazomib-induced thrombotic microangiopathy. Am J Hematol. 2017;92:E53-E55. 6. George JN, Morton JM, Liles NW, Nester CM. After the party's over. N Engl J Med. 2017;371:74-80.

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The Changing Landscape of Autoimmune Hemolytic Anemia

TL;DR: On the whole, the double-edged sword of new pathogenetic insights and therapies has changed the landscape of AIHA, both providing enthusiastic knowledge and complicating the clinical management of this disease.
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New Insights in Autoimmune Hemolytic Anemia: From Pathogenesis to Therapy Stage 1.

TL;DR: A comprehensive review of the main clinical characteristics, diagnosis, and pathogenic mechanisms of AIHA are provided, along with classic and new therapeutic approaches.
Journal ArticleDOI

How I treat warm autoimmune hemolytic anemia.

TL;DR: Warm autoimmune hemolytic anemia (wAIHA) is caused by increased erythrocyte destruction by immunoglobulin G (IgG) autoantibodies, with or without complement activation as discussed by the authors.
References
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Journal ArticleDOI

Drug-induced thrombotic microangiopathy: a systematic review of published reports

TL;DR: Criteria to assess the strength of evidence for a causal association of a drug with TMA is established and data can provide support for clinicians evaluating patients with suspected TMA.
Journal ArticleDOI

How I treat autoimmune hemolytic anemia

TL;DR: The parameters present in diagnostic testing that allow for prognostic insight and present algorithms for both diagnosis and treatment of the AIHA patient in diverse situations are reviewed in the hope that this review may offer guidance in regard to personalized therapy recommendations.
Journal ArticleDOI

Splenectomy for Immune Thrombocytopenia: Down but not out

TL;DR: Avoid splenectomy within the first 12 months after ITP diagnosis for most patients to allow for spontaneous or therapy-induced remissions, particularly in older patients who have increased surgical morbidity and lower rates of response, and in young children.
Journal ArticleDOI

How I manage patients with cold agglutinin disease.

TL;DR: Therapies targeting the classical complement pathway are promising, and the complement C1s inhibitor, BIVV009, has shown favourable results in preliminary studies.
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