Evidence map›Paper›PMID 37965233›Full record

ArticleCureus2023

Characteristics of Patients Diagnosed With Guillain-Barré Syndrome at King Abdulaziz University Hospital, Jeddah, Saudi Arabia, From 2000 to 2018.

Shahad Almalki, Lama Alghamdi, Jumana Khayyat, Rawan T Harun, Mayar Alyousef, Rana Hakeem, Sarah Alsamiri, Zienab Alrefaie, Ahmed K Bamaga

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Article in Cureus, 2023. 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
0.2field-weighted citation impact, top 40% 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, 1 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

9 authors at 3 institutions in 2 countries.

Shahad AlmalkiDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Lama AlghamdiDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Jumana KhayyatDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Rawan T HarunDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Mayar AlyousefDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Rana HakeemDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Sarah AlsamiriDepartment of Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Zienab AlrefaieDepartment of Physiology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
Ahmed K BamagaDepartment of Pediatric Neurology, Faculty of Medicine, King Abdulaziz University, Jeddah, SAU.
King Abdulaziz Hospital · SACzech Academy of Sciences, Institute of Physiology · CZKing Abdulaziz University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGuillain-Barré syndrome (GBS) is the leading cause of non-polio acute flaccid paralysis worldwide, emphasizing the importance of epidemiological studies on this condition. Therefore, well-designed epidemiological studies in different populations can provide a better understanding of the characteristics of patients with GBS and the nature of the disease. To our knowledge, no previous study has attempted to describe the characteristics of patients with GBS in Kingdom of Saudi Arabia (KSA) based on disease subtypes and clinical features in both adult and pediatric patients. This study aimed to assess the frequencies of GBS subtypes and their relationships with patient characteristics and clinical data in a tertiary hospital in Jeddah, KSA.

methodsThis was a retrospective review of patients diagnosed with GBS between January 2000 and January 2018 at King Abdulaziz University Hospital (KAUH), a tertiary center in Jeddah, KSA.

resultsIn total, 47 patients with GBS (median age: seven years for pediatric and 36 years for adult patients) were included in the current study. There were six male and three female pediatric patients and 19 male and 19 female adult patients. Among patients with GBS who were classified into a specific electrophysiological subtype (n = 28), 13 (46.2%) had acute inflammatory demyelinating polyneuropathy (AIDP), 11 (39%) had an axonal subtype, and four (14%) had Miller Fisher syndrome (MFS). Patients required prolonged hospitalization of approximately 20 ± 22 days (2.83 ± 3.11 weeks). Patients with MFS were more likely to have higher cytoalbuminologic dissociation than those with other subtypes.

conclusionAIDP was the most frequent type of GBS, followed by the axonal type. Patients required prolonged hospitalization of approximately 20 ± 22 days (2.83 ± 3.11 weeks). Patients with MFS were more likely to have higher cytoalbuminologic dissociation than those with other subtypes. GBS type did not show a relationship with ICU admission or mechanical ventilation use. There was no association between specific therapies and different GBS subtypes and no significant difference in outcomes between different patterns of clinical presentation. Intravenous immunoglobulin (IVIg) and plasma exchange (PE) treatments both had the same efficacy in relation to outcomes for patients with GBS.

Indexed as

acute inflammatory demyelinating polyneuropathyepidemiology studyguillain–barré syndromemyelin sheathparalysisprognostic factor

Identifiers

PMID37965233
PMCPMC10641031
OpenAlexW4388619300

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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.