{"id":2419,"date":"2011-07-26T13:05:50","date_gmt":"2011-07-26T13:05:50","guid":{"rendered":"https:\/\/medicalcriteria.com\/web\/neugbs\/"},"modified":"2025-05-13T20:28:50","modified_gmt":"2025-05-13T20:28:50","slug":"neugbs","status":"publish","type":"post","link":"https:\/\/medicalcriteria.com\/web\/neugbs\/","title":{"rendered":"Diagnostic Criteria for Guillain-Barre Syndrome (GBS)"},"content":{"rendered":"<div class=\"99c380e4b4a7b96c35d7ddf7dcb434e8\" data-index=\"1\" style=\"float: none; margin:0px 0 0px 0; text-align:center;\">\n<script async src=\"https:\/\/pagead2.googlesyndication.com\/pagead\/js\/adsbygoogle.js\"><\/script>\r\n<!-- MC 2019- Horizontal -->\r\n<ins class=\"adsbygoogle\"\r\n     style=\"display:block\"\r\n     data-ad-client=\"ca-pub-0127150553352455\"\r\n     data-ad-slot=\"3806776041\"\r\n     data-ad-format=\"auto\"\r\n     data-full-width-responsive=\"true\"><\/ins>\r\n<script>\r\n     (adsbygoogle = window.adsbygoogle || []).push({});\r\n<\/script>\n<\/div>\n<p>The Guillain-Barre syndrome (GBS) or Landry-Guillain-Barre-Strohl syndrome, also known as post-infectious polyneuropathy or acute idiopathic polyneuritis, is an acute acquired, frequently severe, monophasic autoimmune illness of the peripheral nervous system (PNS). GBS manifests itself with the clinical picture characterised by gait disturbance, pain, weakness, rapidly ascending symmetric flaccid muscle paralysis, areflexia with distal predominance (involving lower motor neuron), sensory disturbance, variable autonomic involvement, and increased cerebrospinal fluid protein without pleocytosis.<br \/>\n<!--more--><br \/>\n<strong>Diagnostic criteria<\/strong><br \/>\nAssessment of current diagnostic criteria for Guillain-Barre syndrome<br \/>\nRequired features<\/p>\n<ul>\n<li>Progressive weakness in both arms and legs<\/li>\n<li>Areflexia (or hyporeflexia).<\/li>\n<\/ul>\n<p>Features supportive of diagnosis<\/p>\n<ul>\n<li>Progression of symptoms over days to 4 weeks<\/li>\n<li>Relative symmetry<\/li>\n<li>Mild sensory signs or symptoms<\/li>\n<li>Cranial nerve involvement, especially bilateral facial weakness<\/li>\n<li>Recovery beginning 2 to 4 weeks after progression ceases<\/li>\n<li>Autonomic dysfunction<\/li>\n<li>Absence of fever at onset<\/li>\n<li>Typical CSF (albumino-cytologic dissociation)<\/li>\n<li>EMG\/nerve conduction studies (characteristic signs of a demyelinating process in the peripheral nerves)<\/li>\n<\/ul>\n<p>Features casting doubt on the diagnosis<\/p>\n<ul>\n<li>Asymmetrical weakness<\/li>\n<li>Persistent bladder and bowel dysfunction<\/li>\n<li>Bladder or bowel dysfunction at onset<\/li>\n<li>&gt;50 mononuclear leukocytes\/mm<sup>3<\/sup> or presence of polymorphonuclear leukocytes in CSF<\/li>\n<li>Distinct sensory level.<\/li>\n<\/ul>\n<p>Features that rule out the diagnosis<\/p>\n<ul>\n<li>Hexacarbon abuse<\/li>\n<li>Abnormal porphyrin metabolism<\/li>\n<li>Recent diphtheria infection<\/li>\n<li>Lead intoxication<\/li>\n<li>Other similar conditions: poliomyelitis, botulism, hysterical paralysis, toxic neuropathy.<\/li>\n<\/ul>\n<p><strong>Guillain-Barr\u00e9 Syndrome Disability Scale (Hughes)<\/strong><\/p>\n<table style=\"border-collapse: collapse; width: 100%;\" border=\"1\">\n<tbody>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">0<\/td>\n<td style=\"width: 95.116%;\">Healthy<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">1<\/td>\n<td style=\"width: 95.116%;\">Minor symptoms or signs of neuropathy but capable of manual work\/capable of running<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">2<\/td>\n<td style=\"width: 95.116%;\">Able to walk without support of a stick (5m across an open space) but incapable of manual work\/running<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">3<\/td>\n<td style=\"width: 95.116%;\">Able to walk with a stick, appliance or support (5m across an open space)<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">4<\/td>\n<td style=\"width: 95.116%;\">Confined to bed or chair bound<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">5<\/td>\n<td style=\"width: 95.116%;\">Requiring assisted ventilation (for any part of the day or night)<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 4.7619%; text-align: center;\">6<\/td>\n<td style=\"width: 95.116%;\">Death<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>&nbsp;<\/p>\n<p><strong>References: <\/strong><\/p>\n<ol>\n<li>Asbury AK, Cornblath DR. Assessment of current diagnostic criteria for Guillain-Barr\u00e9 syndrome. Ann Neurol. 1990;27 Suppl:S21-4.\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/2194422\/\" target=\"_blank\" rel=\"noopener noreferrer\">[Medline]<\/a><\/li>\n<li>Hughes RA, Swan AV, van Doorn PA. Intravenous immunoglobulin for Guillain-Barr\u00e9 syndrome. Cochrane Database Syst Rev. 2010;(6):CD002063.\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/20556755\/\" target=\"_blank\" rel=\"noopener noreferrer\">[Medline]<\/a><\/li>\n<\/ol>\n<p>&nbsp;<\/p>\n<p>Created Jul 28, 2011.<\/p>\n\n<div style=\"font-size: 0px; height: 0px; line-height: 0px; margin: 0; padding: 0; clear: both;\"><\/div>","protected":false},"excerpt":{"rendered":"<p>Sorry, this entry is only available in Espa\u00f1ol.<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_lmt_disableupdate":"","_lmt_disable":"","_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"categories":[2],"tags":[1190,16,15,14,13,1189,1188,5,4],"class_list":["post-2419","post","type-post","status-publish","format-standard","hentry","category-neurology","tag-barre","tag-criteria","tag-criterios","tag-diagnostic","tag-diagnostico","tag-gbs","tag-guillain","tag-sindrome","tag-syndrome"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - 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