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Ocular myasthenia gravis: Predictive value of single-fiber electromyography
Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological...
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Published in: | Muscle & nerve 1999-09, Vol.22 (9), p.1222-1227 |
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description | Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. Fifty‐eight percent of patients with an abnormal SFEMG developed GMG, whereas 82% of those with a normal study remained with OMG. Thus, a normal SFEMG was associated with MG remaining restricted to the extraocular muscles. (P = 0.036, Fisher's exact test), but an abnormal SFEMG was not predictive of subsequent development of GMG. © 1999 John Wiley & Sons, Inc. Muscle Nerve 22: 1222–1227, 1999 |
doi_str_mv | 10.1002/(SICI)1097-4598(199909)22:9<1222::AID-MUS8>3.0.CO;2-R |
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More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. Fifty‐eight percent of patients with an abnormal SFEMG developed GMG, whereas 82% of those with a normal study remained with OMG. Thus, a normal SFEMG was associated with MG remaining restricted to the extraocular muscles. (P = 0.036, Fisher's exact test), but an abnormal SFEMG was not predictive of subsequent development of GMG. © 1999 John Wiley & Sons, Inc. Muscle Nerve 22: 1222–1227, 1999</description><identifier>ISSN: 0148-639X</identifier><identifier>EISSN: 1097-4598</identifier><identifier>DOI: 10.1002/(SICI)1097-4598(199909)22:9<1222::AID-MUS8>3.0.CO;2-R</identifier><identifier>PMID: 10454717</identifier><identifier>CODEN: MUNEDE</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Disease Progression ; Diseases of striated muscles. Neuromuscular diseases ; Electromyography ; Female ; Fingers ; generalized ; Humans ; Male ; Medical sciences ; Middle Aged ; Muscle Fibers, Skeletal - physiology ; myasthenia gravis ; Myasthenia Gravis - physiopathology ; Neurology ; ocular ; Ocular Motility Disorders - physiopathology ; Oculomotor Muscles - physiopathology ; Predictive Value of Tests ; prognosis ; Prospective Studies ; single-fiber electromyography</subject><ispartof>Muscle & nerve, 1999-09, Vol.22 (9), p.1222-1227</ispartof><rights>Copyright © 1999 John Wiley & Sons, Inc.</rights><rights>1999 INIST-CNRS</rights><rights>Copyright 1999 John Wiley & Sons, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4308-a036cf1fec3778beff9d319a695c8b212e60a8bd126231d5d0e3a50e42a1ee103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1950937$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10454717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weinberg, David H.</creatorcontrib><creatorcontrib>Rizzo III, Joseph F.</creatorcontrib><creatorcontrib>Hayes, Michael T.</creatorcontrib><creatorcontrib>Kneeland, Michael D.</creatorcontrib><creatorcontrib>Kelly Jr, John J.</creatorcontrib><title>Ocular myasthenia gravis: Predictive value of single-fiber electromyography</title><title>Muscle & nerve</title><addtitle>Muscle Nerve</addtitle><description>Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. Fifty‐eight percent of patients with an abnormal SFEMG developed GMG, whereas 82% of those with a normal study remained with OMG. Thus, a normal SFEMG was associated with MG remaining restricted to the extraocular muscles. (P = 0.036, Fisher's exact test), but an abnormal SFEMG was not predictive of subsequent development of GMG. © 1999 John Wiley & Sons, Inc. Muscle Nerve 22: 1222–1227, 1999</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease Progression</subject><subject>Diseases of striated muscles. Neuromuscular diseases</subject><subject>Electromyography</subject><subject>Female</subject><subject>Fingers</subject><subject>generalized</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscle Fibers, Skeletal - physiology</subject><subject>myasthenia gravis</subject><subject>Myasthenia Gravis - physiopathology</subject><subject>Neurology</subject><subject>ocular</subject><subject>Ocular Motility Disorders - physiopathology</subject><subject>Oculomotor Muscles - physiopathology</subject><subject>Predictive Value of Tests</subject><subject>prognosis</subject><subject>Prospective Studies</subject><subject>single-fiber electromyography</subject><issn>0148-639X</issn><issn>1097-4598</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkNtu00AQQFcIRNPCLyA_INQ-OOzFt02hUuVCGjUQlFLgbbRej9sFOw67dsB_j02iFAkknkYjzRwdHUJeMzpmlPKXx9ezdHbCqIz9IJTJMZNSUnnC-US-Yrwfk_PZhf_u5jo5E2M6Then3F8-IKP9x0MyoixI_EjILwfk0LmvlFKWRPFjcsBoEAYxi0fkaqHbUlmv6pRr7nBllHdr1ca4iffBYm50YzbobVTZolcXnjOr2xL9wmRoPSxRN7auurp_Wd91T8ijQpUOn-7mEbl5--ZjeunPF9NZej73dSBo4isqIl2wArWI4yTDopC5YFJFMtRJxhnHiKokyxmPuGB5mFMUKqQYcMUQGRVH5MWWu7b19xZdA5VxGstSrbBuHURSJoEMmNgLaFs7Z7GAtTWVsh0wCkNlgKEyDM1gaAbbysA5SBgqA_SVYagMAiikC-Cw7LnPdgJtVmH-B3WbtT94vjtQTquysGqljbu_kyGVIr73-2FK7P6S-5_bP9R-7z3X33KNa_DnnqvsN4hiEYfw-f0Ulhdifjm9msMn8QuZB7Sm</recordid><startdate>199909</startdate><enddate>199909</enddate><creator>Weinberg, David H.</creator><creator>Rizzo III, Joseph F.</creator><creator>Hayes, Michael T.</creator><creator>Kneeland, Michael D.</creator><creator>Kelly Jr, John J.</creator><general>John Wiley & Sons, Inc</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><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>199909</creationdate><title>Ocular myasthenia gravis: Predictive value of single-fiber electromyography</title><author>Weinberg, David H. ; Rizzo III, Joseph F. ; Hayes, Michael T. ; Kneeland, Michael D. ; Kelly Jr, John J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4308-a036cf1fec3778beff9d319a695c8b212e60a8bd126231d5d0e3a50e42a1ee103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Disease Progression</topic><topic>Diseases of striated muscles. Neuromuscular diseases</topic><topic>Electromyography</topic><topic>Female</topic><topic>Fingers</topic><topic>generalized</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle Fibers, Skeletal - physiology</topic><topic>myasthenia gravis</topic><topic>Myasthenia Gravis - physiopathology</topic><topic>Neurology</topic><topic>ocular</topic><topic>Ocular Motility Disorders - physiopathology</topic><topic>Oculomotor Muscles - physiopathology</topic><topic>Predictive Value of Tests</topic><topic>prognosis</topic><topic>Prospective Studies</topic><topic>single-fiber electromyography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weinberg, David H.</creatorcontrib><creatorcontrib>Rizzo III, Joseph F.</creatorcontrib><creatorcontrib>Hayes, Michael T.</creatorcontrib><creatorcontrib>Kneeland, Michael D.</creatorcontrib><creatorcontrib>Kelly Jr, John J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Muscle & nerve</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weinberg, David H.</au><au>Rizzo III, Joseph F.</au><au>Hayes, Michael T.</au><au>Kneeland, Michael D.</au><au>Kelly Jr, John J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ocular myasthenia gravis: Predictive value of single-fiber electromyography</atitle><jtitle>Muscle & nerve</jtitle><addtitle>Muscle Nerve</addtitle><date>1999-09</date><risdate>1999</risdate><volume>22</volume><issue>9</issue><spage>1222</spage><epage>1227</epage><pages>1222-1227</pages><issn>0148-639X</issn><eissn>1097-4598</eissn><coden>MUNEDE</coden><abstract>Extraocular muscle weakness is the most common presenting sign of myasthenia gravis (MG). More than half of patients presenting with symptoms isolated to these muscles (OMG) develop generalized myasthenia gravis (GMG) over the course of their illness. No clinical, laboratory, or electrophysiological features are recognized that identify these high‐risk patients. We have therefore assessed the ability of single‐fiber electromyography (SFEMG) to predict the development of GMG in patients presenting with OMG. Thirty‐nine consecutive patients presenting with OMG underwent SFEMG of the extensor digitorum communis muscle as well as a battery of other laboratory and imaging studies at the time of diagnosis. All patients were followed prospectively for a minimum of 24 months or until they developed GMG. Two patients were excluded, leaving 37 for assessment. Twenty remained with pure OMG for the entire follow‐up period (mean, 55 months). Twenty‐six of the 37 had abnormal SFEMG studies at presentation. Eleven of these remained with OMG and 15 developed GMG. Fifty‐eight percent of patients with an abnormal SFEMG developed GMG, whereas 82% of those with a normal study remained with OMG. Thus, a normal SFEMG was associated with MG remaining restricted to the extraocular muscles. (P = 0.036, Fisher's exact test), but an abnormal SFEMG was not predictive of subsequent development of GMG. © 1999 John Wiley & Sons, Inc. Muscle Nerve 22: 1222–1227, 1999</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10454717</pmid><doi>10.1002/(SICI)1097-4598(199909)22:9<1222::AID-MUS8>3.0.CO;2-R</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Biological and medical sciences Disease Progression Diseases of striated muscles. Neuromuscular diseases Electromyography Female Fingers generalized Humans Male Medical sciences Middle Aged Muscle Fibers, Skeletal - physiology myasthenia gravis Myasthenia Gravis - physiopathology Neurology ocular Ocular Motility Disorders - physiopathology Oculomotor Muscles - physiopathology Predictive Value of Tests prognosis Prospective Studies single-fiber electromyography |
title | Ocular myasthenia gravis: Predictive value of single-fiber electromyography |
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