| Literature DB >> 27497856 |
Ronald S Go1, Jeffrey L Winters2, Nelson Leung3, David L Murray2, Maria A Willrich2, Roshini S Abraham2, Hatem Amer3, William J Hogan4, Ariela L Marshall4, Sanjeev Sethi2, Cheryl L Tran5, Dong Chen2, Rajiv K Pruthi4, Aneel A Ashrani4, Fernando C Fervenza3, Carl H Cramer5, Vilmarie Rodriguez6, Alexandra P Wolanskyj4, Stephan D Thomé7, C Christopher Hook8.
Abstract
Thrombotic microangiopathies (TMAs) comprise a heterogeneous set of conditions linked by a common histopathologic finding of endothelial damage resulting in microvascular thromboses and potentially serious complications. The typical clinical presentation is microangiopathic hemolytic anemia accompanied by thrombocytopenia with varying degrees of organ ischemia. The differential diagnoses are generally broad, while the workup is frequently complex and can be confusing. This statement represents the joint recommendations from a multidisciplinary team of Mayo Clinic physicians specializing in the management of TMA. It comprises a series of evidence- and consensus-based clinical pathways developed to allow a uniform approach to the spectrum of care including when to suspect TMA, what differential diagnoses to consider, which diagnostic tests to order, and how to provide initial empiric therapy, as well as some guidance on subsequent management.Entities:
Mesh:
Year: 2016 PMID: 27497856 DOI: 10.1016/j.mayocp.2016.05.015
Source DB: PubMed Journal: Mayo Clin Proc ISSN: 0025-6196 Impact factor: 7.616