The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?
•It is debated whether the Guillain-Barré syndrome (GBS) subtypes can be diagnosed by a single electrophysiological study.•GBS pathophysiology is dynamic and serial studies allow a more accurate diagnosis of subtypes.•At a first study, Uncini’s or Rajabally’s criteria can be employed for an indicati...
Gespeichert in:
Veröffentlicht in: | Clinical neurophysiology 2018-12, Vol.129 (12), p.2586-2593 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2593 |
---|---|
container_issue | 12 |
container_start_page | 2586 |
container_title | Clinical neurophysiology |
container_volume | 129 |
creator | Uncini, Antonino Kuwabara, Satoshi |
description | •It is debated whether the Guillain-Barré syndrome (GBS) subtypes can be diagnosed by a single electrophysiological study.•GBS pathophysiology is dynamic and serial studies allow a more accurate diagnosis of subtypes.•At a first study, Uncini’s or Rajabally’s criteria can be employed for an indicative subtype diagnosis.
It is controversial as to whether the electrophysiological Guillain-Barré syndrome (GBS) subtypes can be diagnosed on the basis of a single study and which criteria sets and cut-offs should be used. Serial electrophysiologic studies have shown that a significant number of patients changed electrodiagnostic subtype largely because of the recognition of reversible conduction failure as a possible evidence of axonal pathology. However, other reports concluded that electrodiagnosis can be made by a single study, the subtypes depending on the characteristic of the criteria set applied. Such divergent views, although explicable by the different methodology employed, can be confusing in the everyday practice. We argue that the pathophysiology of GBS is dynamic and that serial studies allow a more accurate diagnosis of subtypes. A second study, although not always practicable, is recommended in patients showing no clear demyelinating features, low amplitude distal compound muscle action potentials or conduction block without temporal dispersion. For practical purposes, we propose that at a first study Uncini’s or Rajabally’s criteria sets can be employed for an indicative subtype diagnosis. Finally, although the GBS subtype diagnosis has currently no impact on treatment, we believe that is important for understanding the underlying pathophysiology and prognostication. |
doi_str_mv | 10.1016/j.clinph.2018.09.025 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2132728409</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1388245718312598</els_id><sourcerecordid>2132728409</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-f0f65277809d9468e69b518b781a7e01f8477ddca19a3fae8feac43b00af9b813</originalsourceid><addsrcrecordid>eNp9kM9u1DAQxi1URP_AGyCUYy8JY8dZ2xyoStUuSEVcFnG0HHvMepWNt3ZStI_Ec_TF8GoLR04zGn3ffDM_Qt5SaCjQxftNY4cw7tYNAyobUA2w7gU5o1KwWqqOnZS-lbJmvBOn5DznDQAI4OwVOW2BU9UBOyNfV2uscEA7peiC-TnGHHIVfbWcwzCYMNafTEpPv6u8H12KW6zy3E_7HeYP1Y81JqxcrH6V6WRGd_WavPRmyPjmuV6Q73e3q5vP9f235Zeb6_vacian2oNfdEwICcopvpC4UH1HZS8kNQKBesmFcM4aqkzrDUqPxvK2BzBe9ZK2F-TyuHeX4sOMedLbkC2Wg0eMc9aMtkwwyUEVKT9KbYo5J_R6l8LWpL2moA8g9UYfQeoDSA1KF5DF9u45Ye636P6Z_pIrgo9HAZY_HwMmnW3A0aILqdDULob_J_wBMtWGzA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2132728409</pqid></control><display><type>article</type><title>The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Uncini, Antonino ; Kuwabara, Satoshi</creator><creatorcontrib>Uncini, Antonino ; Kuwabara, Satoshi</creatorcontrib><description>•It is debated whether the Guillain-Barré syndrome (GBS) subtypes can be diagnosed by a single electrophysiological study.•GBS pathophysiology is dynamic and serial studies allow a more accurate diagnosis of subtypes.•At a first study, Uncini’s or Rajabally’s criteria can be employed for an indicative subtype diagnosis.
It is controversial as to whether the electrophysiological Guillain-Barré syndrome (GBS) subtypes can be diagnosed on the basis of a single study and which criteria sets and cut-offs should be used. Serial electrophysiologic studies have shown that a significant number of patients changed electrodiagnostic subtype largely because of the recognition of reversible conduction failure as a possible evidence of axonal pathology. However, other reports concluded that electrodiagnosis can be made by a single study, the subtypes depending on the characteristic of the criteria set applied. Such divergent views, although explicable by the different methodology employed, can be confusing in the everyday practice. We argue that the pathophysiology of GBS is dynamic and that serial studies allow a more accurate diagnosis of subtypes. A second study, although not always practicable, is recommended in patients showing no clear demyelinating features, low amplitude distal compound muscle action potentials or conduction block without temporal dispersion. For practical purposes, we propose that at a first study Uncini’s or Rajabally’s criteria sets can be employed for an indicative subtype diagnosis. Finally, although the GBS subtype diagnosis has currently no impact on treatment, we believe that is important for understanding the underlying pathophysiology and prognostication.</description><identifier>ISSN: 1388-2457</identifier><identifier>EISSN: 1872-8952</identifier><identifier>DOI: 10.1016/j.clinph.2018.09.025</identifier><identifier>PMID: 30419502</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acute inflammatory demyelinating polyradiculoneuropathy ; Axonal Guillain-Barré syndrome ; Electrodiagnosis - methods ; Electrodiagnosis - standards ; Electrodiagnostic criteria ; Guillain-Barre Syndrome - classification ; Guillain-Barre Syndrome - diagnosis ; Guillain-Barre Syndrome - physiopathology ; Guillain-Barré syndrome ; Humans ; Neural Conduction ; Reversible conduction failure ; Serial electrophysiological studies</subject><ispartof>Clinical neurophysiology, 2018-12, Vol.129 (12), p.2586-2593</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-f0f65277809d9468e69b518b781a7e01f8477ddca19a3fae8feac43b00af9b813</citedby><cites>FETCH-LOGICAL-c428t-f0f65277809d9468e69b518b781a7e01f8477ddca19a3fae8feac43b00af9b813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.clinph.2018.09.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30419502$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uncini, Antonino</creatorcontrib><creatorcontrib>Kuwabara, Satoshi</creatorcontrib><title>The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?</title><title>Clinical neurophysiology</title><addtitle>Clin Neurophysiol</addtitle><description>•It is debated whether the Guillain-Barré syndrome (GBS) subtypes can be diagnosed by a single electrophysiological study.•GBS pathophysiology is dynamic and serial studies allow a more accurate diagnosis of subtypes.•At a first study, Uncini’s or Rajabally’s criteria can be employed for an indicative subtype diagnosis.
It is controversial as to whether the electrophysiological Guillain-Barré syndrome (GBS) subtypes can be diagnosed on the basis of a single study and which criteria sets and cut-offs should be used. Serial electrophysiologic studies have shown that a significant number of patients changed electrodiagnostic subtype largely because of the recognition of reversible conduction failure as a possible evidence of axonal pathology. However, other reports concluded that electrodiagnosis can be made by a single study, the subtypes depending on the characteristic of the criteria set applied. Such divergent views, although explicable by the different methodology employed, can be confusing in the everyday practice. We argue that the pathophysiology of GBS is dynamic and that serial studies allow a more accurate diagnosis of subtypes. A second study, although not always practicable, is recommended in patients showing no clear demyelinating features, low amplitude distal compound muscle action potentials or conduction block without temporal dispersion. For practical purposes, we propose that at a first study Uncini’s or Rajabally’s criteria sets can be employed for an indicative subtype diagnosis. Finally, although the GBS subtype diagnosis has currently no impact on treatment, we believe that is important for understanding the underlying pathophysiology and prognostication.</description><subject>Acute inflammatory demyelinating polyradiculoneuropathy</subject><subject>Axonal Guillain-Barré syndrome</subject><subject>Electrodiagnosis - methods</subject><subject>Electrodiagnosis - standards</subject><subject>Electrodiagnostic criteria</subject><subject>Guillain-Barre Syndrome - classification</subject><subject>Guillain-Barre Syndrome - diagnosis</subject><subject>Guillain-Barre Syndrome - physiopathology</subject><subject>Guillain-Barré syndrome</subject><subject>Humans</subject><subject>Neural Conduction</subject><subject>Reversible conduction failure</subject><subject>Serial electrophysiological studies</subject><issn>1388-2457</issn><issn>1872-8952</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9u1DAQxi1URP_AGyCUYy8JY8dZ2xyoStUuSEVcFnG0HHvMepWNt3ZStI_Ec_TF8GoLR04zGn3ffDM_Qt5SaCjQxftNY4cw7tYNAyobUA2w7gU5o1KwWqqOnZS-lbJmvBOn5DznDQAI4OwVOW2BU9UBOyNfV2uscEA7peiC-TnGHHIVfbWcwzCYMNafTEpPv6u8H12KW6zy3E_7HeYP1Y81JqxcrH6V6WRGd_WavPRmyPjmuV6Q73e3q5vP9f235Zeb6_vacian2oNfdEwICcopvpC4UH1HZS8kNQKBesmFcM4aqkzrDUqPxvK2BzBe9ZK2F-TyuHeX4sOMedLbkC2Wg0eMc9aMtkwwyUEVKT9KbYo5J_R6l8LWpL2moA8g9UYfQeoDSA1KF5DF9u45Ye636P6Z_pIrgo9HAZY_HwMmnW3A0aILqdDULob_J_wBMtWGzA</recordid><startdate>201812</startdate><enddate>201812</enddate><creator>Uncini, Antonino</creator><creator>Kuwabara, Satoshi</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201812</creationdate><title>The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?</title><author>Uncini, Antonino ; Kuwabara, Satoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-f0f65277809d9468e69b518b781a7e01f8477ddca19a3fae8feac43b00af9b813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acute inflammatory demyelinating polyradiculoneuropathy</topic><topic>Axonal Guillain-Barré syndrome</topic><topic>Electrodiagnosis - methods</topic><topic>Electrodiagnosis - standards</topic><topic>Electrodiagnostic criteria</topic><topic>Guillain-Barre Syndrome - classification</topic><topic>Guillain-Barre Syndrome - diagnosis</topic><topic>Guillain-Barre Syndrome - physiopathology</topic><topic>Guillain-Barré syndrome</topic><topic>Humans</topic><topic>Neural Conduction</topic><topic>Reversible conduction failure</topic><topic>Serial electrophysiological studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uncini, Antonino</creatorcontrib><creatorcontrib>Kuwabara, Satoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical neurophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uncini, Antonino</au><au>Kuwabara, Satoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand?</atitle><jtitle>Clinical neurophysiology</jtitle><addtitle>Clin Neurophysiol</addtitle><date>2018-12</date><risdate>2018</risdate><volume>129</volume><issue>12</issue><spage>2586</spage><epage>2593</epage><pages>2586-2593</pages><issn>1388-2457</issn><eissn>1872-8952</eissn><abstract>•It is debated whether the Guillain-Barré syndrome (GBS) subtypes can be diagnosed by a single electrophysiological study.•GBS pathophysiology is dynamic and serial studies allow a more accurate diagnosis of subtypes.•At a first study, Uncini’s or Rajabally’s criteria can be employed for an indicative subtype diagnosis.
It is controversial as to whether the electrophysiological Guillain-Barré syndrome (GBS) subtypes can be diagnosed on the basis of a single study and which criteria sets and cut-offs should be used. Serial electrophysiologic studies have shown that a significant number of patients changed electrodiagnostic subtype largely because of the recognition of reversible conduction failure as a possible evidence of axonal pathology. However, other reports concluded that electrodiagnosis can be made by a single study, the subtypes depending on the characteristic of the criteria set applied. Such divergent views, although explicable by the different methodology employed, can be confusing in the everyday practice. We argue that the pathophysiology of GBS is dynamic and that serial studies allow a more accurate diagnosis of subtypes. A second study, although not always practicable, is recommended in patients showing no clear demyelinating features, low amplitude distal compound muscle action potentials or conduction block without temporal dispersion. For practical purposes, we propose that at a first study Uncini’s or Rajabally’s criteria sets can be employed for an indicative subtype diagnosis. Finally, although the GBS subtype diagnosis has currently no impact on treatment, we believe that is important for understanding the underlying pathophysiology and prognostication.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30419502</pmid><doi>10.1016/j.clinph.2018.09.025</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1388-2457 |
ispartof | Clinical neurophysiology, 2018-12, Vol.129 (12), p.2586-2593 |
issn | 1388-2457 1872-8952 |
language | eng |
recordid | cdi_proquest_miscellaneous_2132728409 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Acute inflammatory demyelinating polyradiculoneuropathy Axonal Guillain-Barré syndrome Electrodiagnosis - methods Electrodiagnosis - standards Electrodiagnostic criteria Guillain-Barre Syndrome - classification Guillain-Barre Syndrome - diagnosis Guillain-Barre Syndrome - physiopathology Guillain-Barré syndrome Humans Neural Conduction Reversible conduction failure Serial electrophysiological studies |
title | The electrodiagnosis of Guillain-Barré syndrome subtypes: Where do we stand? |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T09%3A29%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20electrodiagnosis%20of%20Guillain-Barr%C3%A9%20syndrome%20subtypes:%20Where%20do%20we%20stand?&rft.jtitle=Clinical%20neurophysiology&rft.au=Uncini,%20Antonino&rft.date=2018-12&rft.volume=129&rft.issue=12&rft.spage=2586&rft.epage=2593&rft.pages=2586-2593&rft.issn=1388-2457&rft.eissn=1872-8952&rft_id=info:doi/10.1016/j.clinph.2018.09.025&rft_dat=%3Cproquest_cross%3E2132728409%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2132728409&rft_id=info:pmid/30419502&rft_els_id=S1388245718312598&rfr_iscdi=true |