Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia

© 2016 Informa UK Limited, trading as Taylor & Francis Group. Objectives: To study the clinical manifestations, outcomes, and survival of warm-type autoimmune hemolytic anemia (AIHA) patients. Methods: This study was a retrospective single-center study from 2002 to 2013. Clinical data of AIHA...

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Main Authors: Ekarat Rattarittamrong, Prot Eiamprapai, Adisak Tantiworawit, Thanawat Rattanathammethee, Sasinee Hantrakool, Chatree Chai-Adisaksopha, Lalita Norasetthada
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Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/56115
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spelling th-cmuir.6653943832-561152018-09-05T03:09:06Z Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia Ekarat Rattarittamrong Prot Eiamprapai Adisak Tantiworawit Thanawat Rattanathammethee Sasinee Hantrakool Chatree Chai-Adisaksopha Lalita Norasetthada Medicine © 2016 Informa UK Limited, trading as Taylor & Francis Group. Objectives: To study the clinical manifestations, outcomes, and survival of warm-type autoimmune hemolytic anemia (AIHA) patients. Methods: This study was a retrospective single-center study from 2002 to 2013. Clinical data of AIHA patients were reviewed and analyzed. Results: One hundred and one patients were included, of whom 77% were female with a median age of 43 years. Primary AIHA was found in 61% of the patients. The secondary causes were systemic lupus erythematosus (SLE) (64%), solid malignancies (13%), lymphomas (10%), drugs (8%), and infections (5%). Most patients (96%) responded to steroids, which were not different between primary and secondary AIHA. Second-line treatments were required in 33 patients (33%). The indications were steroid dependence (58%), relapse (30%), and others (12%). The most common second-line treatment was cyclophosphamide (52%). The response rate for second-line treatments was 93%. Relapse occurred in 50 patients (50%) in which 58% occurred more than 3 years after diagnosis. The SLE patients relapsed and received second-line therapy more than the non-SLE group (P < 0.001). At the median 53-month follow-up, the overall survival (OS) was 84%. The independent risk factors for OS were age more than 50 years and malignancy. Sepsis was the most common cause of death. Discussion and conclusion: AIHA has a good prognosis and long-term survival especially in young patients without malignancy. Most patients have responded initially to steroids and have a high response rate to second-line therapy. Carefully adjusted and rapid taper of immunosuppressant is necessary to avoid sepsis complications. 2018-09-05T03:09:06Z 2018-09-05T03:09:06Z 2016-07-02 Journal 16078454 10245332 2-s2.0-84978493510 10.1080/10245332.2016.1138621 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84978493510&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/56115
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
spellingShingle Medicine
Ekarat Rattarittamrong
Prot Eiamprapai
Adisak Tantiworawit
Thanawat Rattanathammethee
Sasinee Hantrakool
Chatree Chai-Adisaksopha
Lalita Norasetthada
Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
description © 2016 Informa UK Limited, trading as Taylor & Francis Group. Objectives: To study the clinical manifestations, outcomes, and survival of warm-type autoimmune hemolytic anemia (AIHA) patients. Methods: This study was a retrospective single-center study from 2002 to 2013. Clinical data of AIHA patients were reviewed and analyzed. Results: One hundred and one patients were included, of whom 77% were female with a median age of 43 years. Primary AIHA was found in 61% of the patients. The secondary causes were systemic lupus erythematosus (SLE) (64%), solid malignancies (13%), lymphomas (10%), drugs (8%), and infections (5%). Most patients (96%) responded to steroids, which were not different between primary and secondary AIHA. Second-line treatments were required in 33 patients (33%). The indications were steroid dependence (58%), relapse (30%), and others (12%). The most common second-line treatment was cyclophosphamide (52%). The response rate for second-line treatments was 93%. Relapse occurred in 50 patients (50%) in which 58% occurred more than 3 years after diagnosis. The SLE patients relapsed and received second-line therapy more than the non-SLE group (P < 0.001). At the median 53-month follow-up, the overall survival (OS) was 84%. The independent risk factors for OS were age more than 50 years and malignancy. Sepsis was the most common cause of death. Discussion and conclusion: AIHA has a good prognosis and long-term survival especially in young patients without malignancy. Most patients have responded initially to steroids and have a high response rate to second-line therapy. Carefully adjusted and rapid taper of immunosuppressant is necessary to avoid sepsis complications.
format Journal
author Ekarat Rattarittamrong
Prot Eiamprapai
Adisak Tantiworawit
Thanawat Rattanathammethee
Sasinee Hantrakool
Chatree Chai-Adisaksopha
Lalita Norasetthada
author_facet Ekarat Rattarittamrong
Prot Eiamprapai
Adisak Tantiworawit
Thanawat Rattanathammethee
Sasinee Hantrakool
Chatree Chai-Adisaksopha
Lalita Norasetthada
author_sort Ekarat Rattarittamrong
title Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
title_short Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
title_full Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
title_fullStr Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
title_full_unstemmed Clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
title_sort clinical characteristics and long-term outcomes of warm-type autoimmune hemolytic anemia
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84978493510&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56115
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