Evidence map›Paper›PMID 40392014›Full record

SynthesisAmerican journal of hematology2025

Mixed Autoimmune Hemolytic Anemia: A Systematic Review of Epidemiology, Clinical Characteristics, Therapies, and Outcomes.

Jeremy W Jacobs, Sheharyar Raza, Landon M Clark, Laura D Stephens, Elizabeth S Allen, Jennifer S Woo, Rachel Lane Walden, Cristina A Figueroa Villalba, Christopher A Tormey, Caroline G Stanek and 3 more

Abstract readSystematic Review
In one paragraph

Synthesis in American journal of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Jeremy W JacobsDepartment of Pathology, Microbiology & Immunology, Vanderbilt University, Nashville, Tennessee, USA.ORCID 0000-0002-5719-9685
Sheharyar RazaLaboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Landon M ClarkVanderbilt University School of Medicine, Nashville, Tennessee, USA.
Laura D StephensDepartment of Pathology, University of California San Diego, La Jolla, California, USA.
Elizabeth S AllenDepartment of Pathology, University of California San Diego, La Jolla, California, USA.
Jennifer S WooDepartment of Pathology, City of Hope Comprehensive Cancer Center, Irvine, California, USA.
Rachel Lane WaldenAnnette and Irwin Eskind Family Biomedical Library and Learning Center, Vanderbilt University, Nashville, Tennessee, USA.ORCID 0000-0002-5998-2083
Cristina A Figueroa VillalbaDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
Christopher A TormeyDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0003-1785-2245
Caroline G StanekDepartment of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0009-0006-4274-2354
Brian D AdkinsDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-9480-2762
Evan M BlochDivision of Transfusion Medicine, Department of Pathology, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-8181-9517
Garrett S BoothDepartment of Pathology, Microbiology & Immunology, Vanderbilt University, Nashville, Tennessee, USA.ORCID 0000-0002-8422-9480

Funding

The Malaria Transfusion Risk (MATRix) StudyK23HL151826 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI BLOCH, EVAN MARTIN · 2020 to 2024
$882k
NHLBI NIH HHS 1K23HL15182NHLBI NIH HHS K23 HL151826
6 · The paper itself

Abstract

Mixed autoimmune hemolytic anemia (AIHA) is a rare and clinically complex hematologic disorder defined by the simultaneous presence of both warm and cold autoantibodies, resulting in severe and often treatment-resistant hemolysis. Due to variability in diagnostic criteria and limited data, a comprehensive understanding of its epidemiology, clinical characteristics, and management remains incomplete. To address these gaps, we performed a systematic literature review employing stringent diagnostic criteria to evaluate epidemiologic patterns, clinical features, and therapeutic outcomes. Our analysis included 81 patients identified across 35 studies, revealing a median age of 45 years and a notable female predominance (2.25:1). Autoimmune diseases constituted the most frequent underlying etiology, followed by hematologic malignancies and infections. Patients exhibited significant anemia, with median nadir hemoglobin levels reaching 5.6 g/dL. Corticosteroids represented the most common therapeutic intervention; however, only 43% of patients achieved remission, while 37% experienced chronic hemolysis, and mortality reached 11%. Many patients required multiple lines of therapy, including rituximab and cytotoxic agents, highlighting the disease's refractory nature and management complexity. The substantial variability in diagnostic and therapeutic approaches emphasizes an urgent need for standardized diagnostic criteria, earlier integration of combination therapies, and exploration of innovative treatment modalities. Future prospective, multicenter studies are essential to refine disease recognition, optimize therapeutic strategies, and ultimately improve patient outcomes in mixed AIHA.

Indexed as

Anemia, Hemolytic, AutoimmuneAdrenal Cortex HormonesAdultAutoantibodiesFemaleHumansMaleMiddle AgedRituximabTreatment OutcomeAdrenal Cortex HormonesAutoantibodiesRituximabhemolysishemolytic anemiamixed AIHAmixed autoimmune hemolysismixed autoimmune hemolytic anemiamixed‐type autoimmune hemolytic anemia

Identifiers

PMID40392014
PMCPMC12232602

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.