Evidence map›Paper›PMID 35067827›Full record

Observational studyNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2022

Very low peroneal nerve compound muscle action potential amplitude predicts poor outcome in patients with Guillain-Barré syndrome: a prospective cohort.

Juan Carlos López-Hernández, Javier Andrés Galnares-Olalde, Adib Jorge de Saráchaga, María Eugenia Briseño-Godínez, Esther Pérez-Valdez, Raúl Nathanael May-Mas, José Luis Arista-Ramírez, Lisette Bazán-Rodríguez, Elizabeth León-Manriquez, Jorge Burgos-Centeno and 1 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.7field-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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Guideline
  2. Prognostic value of modified Erasmus Guillaiun Barre' syndrome outcome score (mEGOS) in an Italian cohort of patients: Challenges, insights and limitations.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  3. 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

11 authors at 1 institution in 1 country.

Juan Carlos López-HernándezNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Javier Andrés Galnares-OlaldeNeurology Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Adib Jorge de SaráchagaNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
María Eugenia Briseño-GodínezNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Esther Pérez-ValdezNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Raúl Nathanael May-MasNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
José Luis Arista-RamírezNeurology Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Lisette Bazán-RodríguezNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Elizabeth León-ManriquezNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Jorge Burgos-CentenoNeurophysiology Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico.
Edwin Steven Vargas-CañasNeuromuscular Diseases Department, Instituto Nacional de Neurología Y Neurocirugía Manuel Velasco Suárez, Mexico City, Mexico. clinicaneuromuscular.innn@gmail.com.
Instituto Nacional de Neurología y Neurocirugía · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTwenty percent of patients with Guillain-Barré syndrome (GBS) have poor outcomes despite proper management. The aim of the study was to characterize electrophysiological factors related to poor outcome in patients with GBS.

methodsWe conducted an observational study from a prospective cohort of 91 patients with GBS in a tertiary healthcare center in Mexico, from 2017 to 2019. Demographics and nerve conduction studies were performed on admission, and a 3-month follow-up for GBS disability score was ensued, allocating patients in good (GBS disability score ≤ 2) and poor outcome (GBS disability score ≥ 3) groups. A logistic regression analysis for independent walk at 3 months was performed. Kaplan-Meier estimator curves for independent walk in very low (< 20% LLN) and low-normal ( ≥20% LLN) peroneal nerve CMAPs are presented.

resultsFrom the 91 GBS patients included, 37 (40.6%) did not regain independent walk at 3 months. Axonal variants were more common in the poor outcome group (31.4% vs 59.4%, p = 0.01) as well as AIDP variants with motor conduction block (6.6% vs 42.4%, p = 0.018). Univariable analysis was statistically significant for very low median, ulnar, tibial, and peroneal CMAP amplitudes in poor outcome patients; however, multivariable analysis was only significant for very low peroneal nerve CMAP amplitude (OR 3.6 [1.1-11.5, p = 0.024]). Conversely, a greater proportion of GBS patients with low-normal CMAPs recovered independent walk at 90 days (75% vs 30%, p < 0.001).

conclusionSevere axonal injury of the peroneal nerve, axonal, and AIDP with motor conduction block variants predicts worse functional outcome regarding independent walk at 3 months.

Indexed as

Guillain-Barre SyndromePeroneal NerveAction PotentialsHumansMusclesNeural ConductionProspective StudiesAxonalDemyelinatingGuillain-Barré syndromeNerve conduction studiesPeroneal nervePoor outcome

Identifiers

PMID35067827
OpenAlexW4207062579

What OpenQuestion holds

Textmetadata
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.