Evidence map›Paper›PMID 39991399›Full record

ArticleCureus2025

Clinical Outcomes of Rituximab Infusion Among Refractory Myasthenia Gravis Patients in the Philippines: A 10-Year Retrospective Study.

Alyssa Pauline C Co, Ludwig F Damian

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Alyssa Pauline C CoNeurology, St. Lukes Medical Center, Quezon City, PHL.
Ludwig F DamianNeurology, St. Lukes Medical Center, Quezon City, PHL.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyasthenia gravis (MG) is an autoimmune disorder causing muscle weakness, with 10%-20% of cases becoming refractory to standard treatments. Rituximab, a CD20-targeting monoclonal antibody, has shown promise in refractory MG but lacks data from low- and middle-income countries (LMICs), such as the Philippines.

methodsA retrospective, cross-sectional study was conducted in treatment-refractory MG patients in St. Luke's Medical Center in the Philippines between January 2014 and December 2023. Clinical outcomes were assessed before and after treatment, including MGFA scores, pyridostigmine dosage, and CD19/CD20 levels. Subgroup analyses were performed based on thymectomy and MG antibody status.

resultsTwenty-one MG patients (10 acetylcholine receptor (AChR) positive, eight seronegative, and three muscle-specific kinase (MuSK) positive) were identified. These patients (mean age 46.4 years, 76% female) showed significant improvement post-rituximab, with 50% achieving complete or near-complete remission (MGFA Class I). Pyridostigmine dosage decreased significantly, and CD19/CD20 levels dropped markedly. MuSK-positive patients responded most rapidly, and thymectomy did not considerably impact outcomes. Rituximab was well-tolerated, with mild infusion-related reactions in two patients.

conclusionRituximab is a safe and effective option for refractory MG, especially in MuSK-positive patients, offering a cost-effective alternative in LMICs where treatments like eculizumab are inaccessible.

Indexed as

acetylcholine receptorautoantibodiesimmunosupressionlow- and middle-income country (lmic)musk antibodymyasthenia gravisneuromuscular junctionrefractory myasthenia gravisrituximabthymectomy

Identifiers

PMID39991399
PMCPMC11846680

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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.