Neuromuscular disease and respiratory failure
Neurologists should be able to anticipate and recognise the onset of respiratory failure in patients with neuromuscular disorders. Symptoms will differ depending on the speed of onset of the respiratory muscle weakness. Careful monitoring of respiratory function is particularly important in acute di...
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Veröffentlicht in: | Practical neurology 2008-08, Vol.8 (4), p.229-237 |
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description | Neurologists should be able to anticipate and recognise the onset of respiratory failure in patients with neuromuscular disorders. Symptoms will differ depending on the speed of onset of the respiratory muscle weakness. Careful monitoring of respiratory function is particularly important in acute disorders such as Guillain-Barré syndrome. Patients with an unrecognised neuromuscular disorder may occasionally present with respiratory failure. Important investigations include vital capacity, mouth pressures, arterial blood gases, chest x ray and sometimes overnight respiratory monitoring. Patients with Guillain-Barré and other acute conditions may require short-term ventilatory support in the intensive care unit. Patients with some chronic disorders, such as motor neuron disease and Duchenne dystrophy, can be successfully treated with non-invasive ventilation, usually in collaboration with a respiratory physician. New-onset weakness of limb and respiratory muscles in the intensive care unit is usually due to critical illness myopathy or critical illness polyneuropathy, and treatment is supportive. |
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Symptoms will differ depending on the speed of onset of the respiratory muscle weakness. Careful monitoring of respiratory function is particularly important in acute disorders such as Guillain-Barré syndrome. Patients with an unrecognised neuromuscular disorder may occasionally present with respiratory failure. Important investigations include vital capacity, mouth pressures, arterial blood gases, chest x ray and sometimes overnight respiratory monitoring. Patients with Guillain-Barré and other acute conditions may require short-term ventilatory support in the intensive care unit. Patients with some chronic disorders, such as motor neuron disease and Duchenne dystrophy, can be successfully treated with non-invasive ventilation, usually in collaboration with a respiratory physician. 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Symptoms will differ depending on the speed of onset of the respiratory muscle weakness. Careful monitoring of respiratory function is particularly important in acute disorders such as Guillain-Barré syndrome. Patients with an unrecognised neuromuscular disorder may occasionally present with respiratory failure. Important investigations include vital capacity, mouth pressures, arterial blood gases, chest x ray and sometimes overnight respiratory monitoring. Patients with Guillain-Barré and other acute conditions may require short-term ventilatory support in the intensive care unit. Patients with some chronic disorders, such as motor neuron disease and Duchenne dystrophy, can be successfully treated with non-invasive ventilation, usually in collaboration with a respiratory physician. New-onset weakness of limb and respiratory muscles in the intensive care unit is usually due to critical illness myopathy or critical illness polyneuropathy, and treatment is supportive.</description><subject>Abdomen</subject><subject>Biological and medical sciences</subject><subject>Chronic Disease</subject><subject>Congenital diseases</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Diagnosis, Differential</subject><subject>Diaphragm (Anatomy)</subject><subject>Dyspnea</subject><subject>Guillain-Barre syndrome</subject><subject>Humans</subject><subject>Lungs</subject><subject>Medical sciences</subject><subject>Motor neurone disease</subject><subject>Muscular Diseases - complications</subject><subject>Muscular Diseases - pathology</subject><subject>Muscular Diseases - physiopathology</subject><subject>Muscular dystrophy</subject><subject>Neurological disorders</subject><subject>Neurology</subject><subject>Neuromuscular Diseases - complications</subject><subject>Neuromuscular Diseases - pathology</subject><subject>Neuromuscular Diseases - physiopathology</subject><subject>Patients</subject><subject>Respiration</subject><subject>Respiration, Artificial - standards</subject><subject>Respiratory failure</subject><subject>Respiratory Insufficiency - etiology</subject><subject>Respiratory Insufficiency - pathology</subject><subject>Respiratory Insufficiency - physiopathology</subject><subject>Respiratory Muscles - innervation</subject><subject>Respiratory Muscles - pathology</subject><subject>Respiratory Muscles - physiopathology</subject><subject>Respiratory Paralysis - etiology</subject><subject>Respiratory Paralysis - pathology</subject><subject>Respiratory Paralysis - physiopathology</subject><subject>Respiratory Physiological Phenomena</subject><subject>Ventilation</subject><issn>1474-7758</issn><issn>1474-7766</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0E1r3DAQBmARUpJ0k2uPYSG0kIOdGcuSrGNr2jSQpgm0oTchW2Pwxl-VbGj-fR1stpBLTyOYRy_Dy9g7hBiRy6uhixOALEaRSMQDdoKpSiOlpDzcv0V2zN6GsANApbk-YseYyTTVoE9YdEeT79splFNj_dbVgWygre3c1lMYam_H3j9vK1s3k6dT9qayTaCzdW7Yzy-ff-Rfo9vv1zf5x9uo4DwbI14UqCERWGop0FZOEWoHPOFQyFJgCiSctlVWEIESSkiHylmAquBWO-Ib9mHJHXz_e6IwmrYOJTWN7aifgpGap5DNeRt28Qru-sl3820GVYZSKJXpWcWLKn0fgqfKDL5urX82COalRjN05qVGs9Q4fzhfY6eiJfePr73N4P0KbChtU3nblXXYuwQEl5Co2UWLq8NIf_Z765-MVFwJc_eYG_x0_w1_PUiTz_5y8UW7-9-RfwHH5pSd</recordid><startdate>200808</startdate><enddate>200808</enddate><creator>Hutchinson, D</creator><creator>Whyte, K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ</general><general>BMJ Publishing Group LTD</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200808</creationdate><title>Neuromuscular disease and respiratory failure</title><author>Hutchinson, D ; Whyte, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b338t-3bb190251c9651afd7e19d03230b6c5140e5d9af8bee075756d17da00fb3a9de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Abdomen</topic><topic>Biological and medical sciences</topic><topic>Chronic Disease</topic><topic>Congenital diseases</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Diagnosis, Differential</topic><topic>Diaphragm (Anatomy)</topic><topic>Dyspnea</topic><topic>Guillain-Barre syndrome</topic><topic>Humans</topic><topic>Lungs</topic><topic>Medical sciences</topic><topic>Motor neurone disease</topic><topic>Muscular Diseases - complications</topic><topic>Muscular Diseases - pathology</topic><topic>Muscular Diseases - physiopathology</topic><topic>Muscular dystrophy</topic><topic>Neurological disorders</topic><topic>Neurology</topic><topic>Neuromuscular Diseases - complications</topic><topic>Neuromuscular Diseases - pathology</topic><topic>Neuromuscular Diseases - physiopathology</topic><topic>Patients</topic><topic>Respiration</topic><topic>Respiration, Artificial - standards</topic><topic>Respiratory failure</topic><topic>Respiratory Insufficiency - etiology</topic><topic>Respiratory Insufficiency - pathology</topic><topic>Respiratory Insufficiency - physiopathology</topic><topic>Respiratory Muscles - innervation</topic><topic>Respiratory Muscles - pathology</topic><topic>Respiratory Muscles - physiopathology</topic><topic>Respiratory Paralysis - etiology</topic><topic>Respiratory Paralysis - pathology</topic><topic>Respiratory Paralysis - physiopathology</topic><topic>Respiratory Physiological Phenomena</topic><topic>Ventilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hutchinson, D</creatorcontrib><creatorcontrib>Whyte, K</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>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Practical neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hutchinson, D</au><au>Whyte, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuromuscular disease and respiratory failure</atitle><jtitle>Practical neurology</jtitle><addtitle>Pract Neurol</addtitle><date>2008-08</date><risdate>2008</risdate><volume>8</volume><issue>4</issue><spage>229</spage><epage>237</epage><pages>229-237</pages><issn>1474-7758</issn><eissn>1474-7766</eissn><abstract>Neurologists should be able to anticipate and recognise the onset of respiratory failure in patients with neuromuscular disorders. Symptoms will differ depending on the speed of onset of the respiratory muscle weakness. Careful monitoring of respiratory function is particularly important in acute disorders such as Guillain-Barré syndrome. Patients with an unrecognised neuromuscular disorder may occasionally present with respiratory failure. Important investigations include vital capacity, mouth pressures, arterial blood gases, chest x ray and sometimes overnight respiratory monitoring. Patients with Guillain-Barré and other acute conditions may require short-term ventilatory support in the intensive care unit. Patients with some chronic disorders, such as motor neuron disease and Duchenne dystrophy, can be successfully treated with non-invasive ventilation, usually in collaboration with a respiratory physician. New-onset weakness of limb and respiratory muscles in the intensive care unit is usually due to critical illness myopathy or critical illness polyneuropathy, and treatment is supportive.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd</pub><pmid>18644909</pmid><doi>10.1136/pn.2008.152611</doi><tpages>9</tpages></addata></record> |
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subjects | Abdomen Biological and medical sciences Chronic Disease Congenital diseases Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Diagnosis, Differential Diaphragm (Anatomy) Dyspnea Guillain-Barre syndrome Humans Lungs Medical sciences Motor neurone disease Muscular Diseases - complications Muscular Diseases - pathology Muscular Diseases - physiopathology Muscular dystrophy Neurological disorders Neurology Neuromuscular Diseases - complications Neuromuscular Diseases - pathology Neuromuscular Diseases - physiopathology Patients Respiration Respiration, Artificial - standards Respiratory failure Respiratory Insufficiency - etiology Respiratory Insufficiency - pathology Respiratory Insufficiency - physiopathology Respiratory Muscles - innervation Respiratory Muscles - pathology Respiratory Muscles - physiopathology Respiratory Paralysis - etiology Respiratory Paralysis - pathology Respiratory Paralysis - physiopathology Respiratory Physiological Phenomena Ventilation |
title | Neuromuscular disease and respiratory failure |
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