Evidence map›Paper›PMID 40914739›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2025

Efficacy and safety of efgartigimod versus intravenous immunoglobulin in early intervention of acetylcholine receptor antibody-positive impending myasthenic crisis: A retrospective cohort study.

Rongjing Guo, Chao Sun, Xiaoxi Huang, Sijia Hao, Qingqing Wang, Zhe Ruan, Ting Gao, Yonglan Tang, Xiangqi Cao, Yu Liu and 2 more

Abstract readComparative Study
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Observational
  9. Review
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

12 authors.

Rongjing GuoDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Chao SunDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Xiaoxi HuangDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Sijia HaoDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Qingqing WangDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Zhe RuanDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Ting GaoDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Yonglan TangDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Xiangqi CaoDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Yu LiuDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Zhuyi LiDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Ting ChangDepartment of Neurology, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China. Electronic address: changting1981@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early intervention in impending myasthenic crisis (IMC) is critical to avert life-threatening progression. This study compared the clinical effectiveness and safety of the novel FcRn antagonist efgartigimod versus intravenous immunoglobulin (IVIg) in IMC management. In this retrospective cohort study, we analyzed 51 acetylcholine receptor antibody-positive (AChR-Ab+) IMC patients who received either efgartigimod (n ​= ​30) or IVIg (n ​= ​21) from June 2023 to November 2024. Efficacy was assessed based on changes in Myasthenia Gravis Activities of Daily Living (MG-ADL) and Quantitative Myasthenia Gravis (QMG) scores over four weeks. From weeks 2-4, the efgartigimod group showed significantly greater improvements in MG-ADL and QMG scores (both P ​< ​0.05), with a similar trend after baseline adjustment. By week 4, the results of the clinically meaningful improvement (CMI) analysis indicated that a higher proportion of patients in the efgartigimod group achieved MG-ADL improvement ≥7 points (90.0 ​% vs. 57.1 ​%) and greater QMG scores improvement. The proportion of patients reaching minimal symptom expression (MSE) was 80.0 ​% in the efgartigimod group compared to 14.3 ​% in the IVIg group, with mean improvement rates of 91.5 ​% vs. 60.7 ​%, respectively. One case of myasthenic crisis-related death occurred in the IVIg group, while no severe adverse events were reported in the remaining patients. Efgartigimod has been shown to effectively alleviate IMC symptoms, prevent progression to myasthenic crisis (MC), and significantly reduce in complications without substantially increasing the economic costs. These findings suggest its potential as a first-line therapeutic option for AChR-Ab-positive IMC patients.

Indexed as

AutoantibodiesImmunoglobulins, IntravenousMyasthenia GravisReceptors, CholinergicActivities of Daily LivingAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAutoantibodiesImmunoglobulins, IntravenousReceptors, CholinergicEfficacyEfgartigimodImpending myasthenic crisisIntravenous immunoglobulinMyasthenia gravis

Identifiers

PMID40914739
PMCPMC12664453

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Registered trials

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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.