Clinical Features and Treatment Outcomes of Childhood Autoimmune Hemolytic Anemia: A Retrospective Analysis of 68 Cases. Issue 2 (March 2016)
- Record Type:
- Journal Article
- Title:
- Clinical Features and Treatment Outcomes of Childhood Autoimmune Hemolytic Anemia: A Retrospective Analysis of 68 Cases. Issue 2 (March 2016)
- Main Title:
- Clinical Features and Treatment Outcomes of Childhood Autoimmune Hemolytic Anemia
- Authors:
- Fan, Junjie
He, Hailong
Zhao, Wenli
Wang, Yi
Lu, Jun
Li, Jie
Li, Jianqin
Xiao, Peifang
Lu, Ye
Chai, Yihuan
Hu, Shaoyan - Abstract:
- Abstract : Autoimmune hemolytic anemia (AIHA) is a rare disease in children, and its clinical severity varies. To better understand disease manifestation and treatment outcome, we analyzed 68 children diagnosed as AIHA for clinical characteristics, laboratory findings, and treatment outcomes. Data show that primary AIHA accounted for 39.7% of all patients, whereas secondary AIHA accounted for 60.3%. Among them, Evans syndrome (ES) accounted for 20 cases (29.4%). Average hemoglobin was lower in the 1-year or below age group than in the above 1-year age group, combined-antibody group than single-antibody group, and IgM-contained group than non–IgM-contained group ( P <0.05 for all). The duration of therapy in the ES group was longer than that in the AIHA-only group ( P <0.05). During the follow-up period, 29 cases (29/45, 64.4%) remained in continuous remission. In total, 35.6% of patients relapsed after first complete remission and 56.3% of them still showed good response to glucocorticoid after relapse. There was no difference in the duration of therapy or relapse rate between the intravenous immunoglobulin (IVIG)-treatment group and the non–IVIG-treatment group. In conclusion, the severity of anemia correlates with age and serologic types of direct antiglobulin test. Glucocorticoid is efficacious for AIHA regardless of whether it is a first attack or relapse in this cohort of young patients. ES needs longer treatment duration. IVIG does not improve the outcome of AIHA.Abstract : Autoimmune hemolytic anemia (AIHA) is a rare disease in children, and its clinical severity varies. To better understand disease manifestation and treatment outcome, we analyzed 68 children diagnosed as AIHA for clinical characteristics, laboratory findings, and treatment outcomes. Data show that primary AIHA accounted for 39.7% of all patients, whereas secondary AIHA accounted for 60.3%. Among them, Evans syndrome (ES) accounted for 20 cases (29.4%). Average hemoglobin was lower in the 1-year or below age group than in the above 1-year age group, combined-antibody group than single-antibody group, and IgM-contained group than non–IgM-contained group ( P <0.05 for all). The duration of therapy in the ES group was longer than that in the AIHA-only group ( P <0.05). During the follow-up period, 29 cases (29/45, 64.4%) remained in continuous remission. In total, 35.6% of patients relapsed after first complete remission and 56.3% of them still showed good response to glucocorticoid after relapse. There was no difference in the duration of therapy or relapse rate between the intravenous immunoglobulin (IVIG)-treatment group and the non–IVIG-treatment group. In conclusion, the severity of anemia correlates with age and serologic types of direct antiglobulin test. Glucocorticoid is efficacious for AIHA regardless of whether it is a first attack or relapse in this cohort of young patients. ES needs longer treatment duration. IVIG does not improve the outcome of AIHA. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Journal of pediatric hematology/oncology. Volume 38:Issue 2(2016)
- Journal:
- Journal of pediatric hematology/oncology
- Issue:
- Volume 38:Issue 2(2016)
- Issue Display:
- Volume 38, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 38
- Issue:
- 2
- Issue Sort Value:
- 2016-0038-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-03
- Subjects:
- autoimmune hemolytic anemia (AIHA) -- Evans syndrome (ES) -- children -- glucocorticoid
Pediatric hematology -- Periodicals
Tumors in children -- Periodicals
618.9215 - Journal URLs:
- http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://gateway.tx.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=00043426-000000000-00000 ↗
http://www.jpho-online.com/ ↗
http://journals.lww.com/jpho-online/pages/default.aspx ↗
http://journals.lww.com ↗ - DOI:
- 10.1097/MPH.0000000000000476 ↗
- Languages:
- English
- ISSNs:
- 1077-4114
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5030.183000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5277.xml