Evidence map›Paper›PMID 41145132›Full record

Observational studyArquivos de neuro-psiquiatria2025

Patient journey and treatment pattern in myasthenia gravis: real-world data from the Brazilian public health system.

Renata Andrade, Wilson Marques Junior, Luiza Vasconcelos, Paula Pungartnik, Thaís Zamboni Berra, Lucas Vieira Cortez, Daiane Beneduzzi

Abstract readObservational Study
In one paragraph

Observational study in Arquivos de neuro-psiquiatria, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Renata AndradeHospital Metropolitano Oeste Pelópidas Silveira, Real Hospital Português, Divisão de Doenças Raras, Recife PE, Brazil.ORCID 0000-0002-4228-2275
Wilson Marques JuniorFaculdade de Medicina de Ribeirão Preto, Hospital das Clínicas, Ribeirão Preto SP, Brazil.ORCID 0000-0002-4589-2749
Luiza VasconcelosAstrazeneca, São Paulo SP, Brazil.ORCID 0000-0003-1403-4167
Paula PungartnikIQVIA, Real World Evidence, São Paulo SP, Brazil.ORCID 0000-0002-9415-4283
Thaís Zamboni BerraIQVIA, Real World Evidence, São Paulo SP, Brazil.ORCID 0000-0002-4163-8719
Lucas Vieira CortezIQVIA, Real World Evidence, São Paulo SP, Brazil.ORCID 0000-0001-7762-1997
Daiane BeneduzziAstrazeneca, São Paulo SP, Brazil.ORCID 0009-0009-2212-9132

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is a rare neurological disease and the most common autoimmune disorder, characterized by muscle weakness. In Brazil, there is limited data on these patients within the Brazilian public healthcare system (SUS, from Sistema Único de Saúde, in Portuguese).To assess patients with MG in the Brazilian public healthcare system to understand their characteristics, patient journey, and treatment patterns.A retrospective observational study using real-world data from SUS to analyze patients with MG from January 2010 to December 2023. Data were extracted from the DATASUS, focusing on the Outpatient Procedure (SIA) and Hospital Admissions (SIH) information systems. Probabilistic record linkage compiled longitudinal patient data, assessing epidemiology, demographics, clinical characteristics, and treatment patterns, including medications, doses, and lines of treatment (LOT).A total of 13,476 patients with MG were identified. Admissions in healthcare units increased over the years, with 30.4% experiencing exacerbations and 9% crises. The mean age was 45.6 years, with a majority being female (65.4%) and white (53.4%). The case-fatality rate rose from 0.76% in 2011 to 1.90% in 2023. Treatment patterns showed frequent transitions between LOT, indicating constant instability and inadequate symptom control, with azathioprine and pyridostigmine being the most used medications. Some patients started treatment with intravenous immunoglobulin (IVIg), used in combination with other medications, and continued it continuously.The study highlights the increasing burden of MG on SUS, emphasizing the challenges of disease management and the need for continuous advancements in diagnostic and therapeutic strategies to improve patient outcomes.

Indexed as

Myasthenia GravisAdolescentAdultAgedBrazilChildFemaleHospitalizationHumansImmunoglobulins, IntravenousMaleMiddle AgedRetrospective StudiesYoung AdultImmunoglobulins, Intravenous

Identifiers

PMID41145132
PMCPMC12558700

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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.