Evidence map›Paper›PMID 38630312›Full record

ArticleJournal of neurology2024

Occurrence of area postrema syndrome during follow-up: phenotype and influence over NMOSD activity in LATAM in real-world settings.

Claudia Pestchanker, Brenda Bertado Cortez, Marco A Lana Peixoto, José Ignacio Gortari, Sheila Castro Suarez, Cesar Caparo Zamalloa, Graciana Galiana, Francisco Peñalver, Vanesa Daccach Marques, Katharina Messias and 21 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2024. 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
0.8field-weighted citation impact, top 29% of its field
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, 2 citations in OpenAlex.

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

31 authors at 18 institutions in 6 countries.

Claudia PestchankerNeurology Department, Dr. Ramón Carrillo Central Hospital, San Luis, Argentina.
Brenda Bertado CortezClínica de Enfermedades Desmielinizantes (CED) del Centro Médico Nacional Siglo XXI, del Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Marco A Lana PeixotoCIEM MS Research Center, Federal University of Minas Gerais Medical School, Belo Horizonte, Brazil.
José Ignacio GortariPrivate Neurology Office, Pereira, Colombia.
Sheila Castro SuarezCentro Básico de Investigación en Demencia y Enfermedades Desmielinizantes del Sistema Nervioso, National Institute of Neurological Science, Lima, Peru.
Cesar Caparo ZamalloaCentro Básico de Investigación en Demencia y Enfermedades Desmielinizantes del Sistema Nervioso, National Institute of Neurological Science, Lima, Peru.
Graciana GalianaNeurology Department, Lagomaggiore Hospital, Mendoza, Argentina.
Francisco PeñalverNeurology Department, Lagomaggiore Hospital, Mendoza, Argentina.
Vanesa Daccach MarquesHospital das Clínicas da Faculda de de Medicina de Ribeirão Preto, Universidade de São Paulo, São Paulo, Brazil.
Katharina MessiasHospital das Clínicas da Faculda de de Medicina de Ribeirão Preto, Universidade de São Paulo, São Paulo, Brazil.
Lorna GalleguillosNeurology Department, Clínica Alemana de Santiago, Santiago, Chile.
Fernando GarcíaNeurology Department, Santo Tomás Hospital, Universidad Interamericana de Panamá, Panama City, Panama.
Juan I RojasCentro Esclerosis Múltiple Buenos Aires (CEMBA), Buenos Aires, Argentina.
Liliana PatruccoCentro Esclerosis Múltiple Buenos Aires (CEMBA), Buenos Aires, Argentina.
Edgardo CristianoCentro Esclerosis Múltiple Buenos Aires (CEMBA), Buenos Aires, Argentina.
Verónica TkachukNeuroimmunology Unit, Neurology Department, Hospital de Clínicas, Buenos Aires, Argentina.
Susana LiwackiNeurology Unit, Hospital Córdoba, Córdoba, Argentina.
Jorge CorrealeServicio de Neuroinmunología y Enfermedades Desmielinizantes, Departamento de Neurología, Fleni, Buenos Aires, Argentina.
Mariano MarrodanServicio de Neuroinmunología y Enfermedades Desmielinizantes, Departamento de Neurología, Fleni, Buenos Aires, Argentina.
María C YsraelitServicio de Neuroinmunología y Enfermedades Desmielinizantes, Departamento de Neurología, Fleni, Buenos Aires, Argentina.
Carlos VrechNeurology Department, Sanatorio Allende, Córdoba, Argentina.
Norma DeriCENyR, Ciudad de Buenos Aires, Buenos Aires, Argentina.
Felisa LeguizamonHospital de Agudos, Dr. Teodoro Álvarez, Buenos Aires, Argentina.
Darío TavoliniINECO Neurociencias Oroño, Santa Fe, Argentina.
Carolina MainellaHospital Español de Rosario, Santa Fe, Argentina.
Gisela ZangaUnidad Asistencial César Milstein, Buenos Aires, Argentina.
Marina Alonso SerenaÁrea de Investigación en Medicina Interna, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Ethel CiampiHospital Dr. Sótero del Río y Universidad Católica de Chile, Santiago, Chile.
Herval Ribeiro Soares NetoHospital Do Servidor Estadual de São Paulo, São Paulo, Brazil.
Pablo LopezNeuroimmunology Unit, Department of Neurosciences, Hospital Aleman, Buenos Aires, Argentina.
Edgar Carnero ContenttiNeuroimmunology Unit, Department of Neurosciences, Hospital Aleman, Buenos Aires, Argentina. ecarnerocontentti@hospitalaleman.com.ORCID http://orcid.org/0000-0001-7435-5726
Hospital Alemán · ARHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRInstituto Nacional de Enfermedades Neoplásicas · PEUniversity of Mendoza · ARClínica Alemana · CLFundacion Allende · ARHospital César Milstein · ARHospital Clínico de la Universidad Católica · CLHospital de Clínicas "José de San Martín" · ARHospital do Servidor Público Estadual · BRHospital General de Agudos Dr. TEODORO ALVAREZ · ARHospital Italiano de Buenos Aires · ARHospital Provincial de Rosario · ARInstituto de Neurología Cognitiva · ARMexican Social Security Institute · MXServicio Diabetología Hospital Córdoba · ARUniversidade Federal de Minas Gerais · BRUniversidad Interamericana de Panamá · PA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe aimed to assess the frequency, duration, and severity of area postrema syndrome (APS) during follow-up in neuromyelitis optica spectrum disorder (NMOSD) patients, as well as its association with inflammatory activity and prognostic factors of APS severity in a real-world setting.

methodsWe conducted a retrospective study on a cohort of Latin American (LATAM) NMOSD patients who had experienced APS during their follow-up. Patients from Mexico, Peru, Brazil, Colombia, Panama, Chile and Argentina patients who met 2015 NMOSD criteria were included. We evaluated data on symptom type (nausea, vomiting and/or hiccups), frequency, duration, severity (measured by APS severity scale), association with other NMOSD core relapses, and acute treatments (symptomatic and immunotherapy or plasmapheresis). Logistic regression was conducted to evaluate factors associated with APS severity (vs. mild-moderate).

resultsOut of 631 NMOSD patients, 116 (18.3%) developed APS during their follow-up. The most common APS phenotype was severe. Inflammatory activity (i.e., relapses) significantly decreased after the onset of APS. Half of the patients experienced isolated APS with a median duration of 10 days, and the most frequently used acute treatment was IV steroids. All three symptoms were present in 44.6% of the patients. APS symptoms resolved following immunotherapy. Logistic regression did not identify independent factors associated with the severity of APS.

conclusionsOur findings indicate that 18.3% of NMOSD patients developed APS during the follow-up period, with most patients fulfilling criteria for severe APS. The inflammatory activity decreased after the onset of APS compared to the previous year.

Indexed as

Neuromyelitis OpticaPhenotypeAdultArea PostremaFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesSeverity of Illness IndexArea postrema syndromeNMOSDPhenotypeSeverity

Identifiers

PMID38630312
OpenAlexW4394872893

What OpenQuestion holds

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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.