Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients
Objective To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM). Methods We retrospectively reviewed the m...
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creator | Marie, I. Menard, J.‐F. Hatron, P. Y. Hachulla, E. Mouthon, L. Tiev, K. Ducrotte, P. Cherin, P. |
description | Objective
To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM).
Methods
We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations.
Results
Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients.
Conclusion
Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations. |
doi_str_mv | 10.1002/acr.20325 |
format | Article |
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To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM).
Methods
We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations.
Results
Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients.
Conclusion
Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</description><identifier>ISSN: 2151-464X</identifier><identifier>ISSN: 2151-4658</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.20325</identifier><identifier>PMID: 20722047</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Cancer ; Dermatomyositis ; Dermatomyositis - complications ; Dermatomyositis - drug therapy ; Drug Tolerance ; Dysphagia ; Enteral feeding ; Esophageal Diseases - drug therapy ; Esophageal Diseases - epidemiology ; Esophageal Diseases - etiology ; Esophagus ; Female ; Follow-Up Studies ; Gastroesophageal reflux ; Glucocorticoids - pharmacology ; Humans ; Immunoglobulins ; Immunoglobulins, Intravenous - administration & dosage ; Immunoglobulins, Intravenous - therapeutic use ; Immunologic Factors - administration & dosage ; Immunologic Factors - therapeutic use ; Intravenous administration ; Male ; medical records ; Middle Aged ; Mouth ; Muscle contraction ; Muscles ; Myopathy ; Pharynx ; Pneumonia ; Polymyositis ; Polymyositis - complications ; Polymyositis - drug therapy ; Prevalence ; Retrospective Studies ; Steroid hormones ; Thorax ; Treatment Outcome ; Young Adult</subject><ispartof>Arthritis care & research (2010), 2010-12, Vol.62 (12), p.1748-1755</ispartof><rights>Copyright © 2010 by the American College of Rheumatology</rights><rights>Copyright © 2010 by the American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</citedby><cites>FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Facr.20325$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.20325$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20722047$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marie, I.</creatorcontrib><creatorcontrib>Menard, J.‐F.</creatorcontrib><creatorcontrib>Hatron, P. Y.</creatorcontrib><creatorcontrib>Hachulla, E.</creatorcontrib><creatorcontrib>Mouthon, L.</creatorcontrib><creatorcontrib>Tiev, K.</creatorcontrib><creatorcontrib>Ducrotte, P.</creatorcontrib><creatorcontrib>Cherin, P.</creatorcontrib><title>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</title><title>Arthritis care & research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective
To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM).
Methods
We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations.
Results
Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients.
Conclusion
Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer</subject><subject>Dermatomyositis</subject><subject>Dermatomyositis - complications</subject><subject>Dermatomyositis - drug therapy</subject><subject>Drug Tolerance</subject><subject>Dysphagia</subject><subject>Enteral feeding</subject><subject>Esophageal Diseases - drug therapy</subject><subject>Esophageal Diseases - epidemiology</subject><subject>Esophageal Diseases - etiology</subject><subject>Esophagus</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroesophageal reflux</subject><subject>Glucocorticoids - pharmacology</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins, Intravenous - administration & dosage</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunologic Factors - administration & dosage</subject><subject>Immunologic Factors - therapeutic use</subject><subject>Intravenous administration</subject><subject>Male</subject><subject>medical records</subject><subject>Middle Aged</subject><subject>Mouth</subject><subject>Muscle contraction</subject><subject>Muscles</subject><subject>Myopathy</subject><subject>Pharynx</subject><subject>Pneumonia</subject><subject>Polymyositis</subject><subject>Polymyositis - complications</subject><subject>Polymyositis - drug therapy</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Steroid hormones</subject><subject>Thorax</subject><subject>Treatment Outcome</subject><subject>Young Adult</subject><issn>2151-464X</issn><issn>2151-4658</issn><issn>2151-4658</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1O3DAURq2qVUHAoi9QeUe7GPC_M92NRqVFQkKqqNRd5Dg3YOTEwXYGZccj8Iw8CYYBdvRufK91dBbfh9AXSo4oIezY2HjECGfyA9plVNKFULL6-LaLfzvoIKVrUoazquLLz2iHEc0YEXoX3Z8OOZoNDGFK2PX9NIRLH5rJuyHhLkScMsTg2oe7-whdNDaHOGNIYbwyl2A8dsMm-A30MGQcwZsMLc4Bj8HP_RySyy5hM7S4hdibHF7_fuAVThAdJBw6rDkeTXbFkfbRp874BAcv7x76e_LzYv17cXb-63S9OltYISu5UBWVHaiGa2uJpKzrGLGNaghdNlQrQQgVDVNESKspp225tRVtSxWxShPK99Dh1jvGcDNBynXvkgXvzQAli7r4pSxJqkJ--y9JyZILRbXmBf2-RW0MKZXA6jG63sS5QPVTW3Vpq35uq7BfX7RT00P7Rr52U4DjLXDrPMzvm-rV-s9W-Qgce6FO</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>Marie, I.</creator><creator>Menard, J.‐F.</creator><creator>Hatron, P. Y.</creator><creator>Hachulla, E.</creator><creator>Mouthon, L.</creator><creator>Tiev, K.</creator><creator>Ducrotte, P.</creator><creator>Cherin, P.</creator><general>John Wiley & Sons, Inc</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>201012</creationdate><title>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</title><author>Marie, I. ; Menard, J.‐F. ; Hatron, P. Y. ; Hachulla, E. ; Mouthon, L. ; Tiev, K. ; Ducrotte, P. ; Cherin, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4585-6815fe6b37cc0512ff20cb6b019b17640014b26045c7131d0017c4dd160c67013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer</topic><topic>Dermatomyositis</topic><topic>Dermatomyositis - complications</topic><topic>Dermatomyositis - drug therapy</topic><topic>Drug Tolerance</topic><topic>Dysphagia</topic><topic>Enteral feeding</topic><topic>Esophageal Diseases - drug therapy</topic><topic>Esophageal Diseases - epidemiology</topic><topic>Esophageal Diseases - etiology</topic><topic>Esophagus</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroesophageal reflux</topic><topic>Glucocorticoids - pharmacology</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Immunoglobulins, Intravenous - administration & dosage</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunologic Factors - administration & dosage</topic><topic>Immunologic Factors - therapeutic use</topic><topic>Intravenous administration</topic><topic>Male</topic><topic>medical records</topic><topic>Middle Aged</topic><topic>Mouth</topic><topic>Muscle contraction</topic><topic>Muscles</topic><topic>Myopathy</topic><topic>Pharynx</topic><topic>Pneumonia</topic><topic>Polymyositis</topic><topic>Polymyositis - complications</topic><topic>Polymyositis - drug therapy</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Steroid hormones</topic><topic>Thorax</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marie, I.</creatorcontrib><creatorcontrib>Menard, J.‐F.</creatorcontrib><creatorcontrib>Hatron, P. Y.</creatorcontrib><creatorcontrib>Hachulla, E.</creatorcontrib><creatorcontrib>Mouthon, L.</creatorcontrib><creatorcontrib>Tiev, K.</creatorcontrib><creatorcontrib>Ducrotte, P.</creatorcontrib><creatorcontrib>Cherin, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis care & research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marie, I.</au><au>Menard, J.‐F.</au><au>Hatron, P. Y.</au><au>Hachulla, E.</au><au>Mouthon, L.</au><au>Tiev, K.</au><au>Ducrotte, P.</au><au>Cherin, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients</atitle><jtitle>Arthritis care & research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2010-12</date><risdate>2010</risdate><volume>62</volume><issue>12</issue><spage>1748</spage><epage>1755</epage><pages>1748-1755</pages><issn>2151-464X</issn><issn>2151-4658</issn><eissn>2151-4658</eissn><abstract>Objective
To assess the long‐term outcome of esophageal complications in the group of patients receiving intravenous immunoglobulins (IVIG) for the treatment of severe steroid‐refractory esophageal involvement related to polymyositis/dermatomyositis (PM/DM).
Methods
We retrospectively reviewed the medical records of 73 patients (39 with PM, 34 with DM) with steroid‐resistant esophageal involvement. Esophageal involvement was evaluated by clinical and manometric investigations.
Results
Seventy‐three patients with steroid‐refractory esophageal involvement related to PM/DM received IVIG therapy (2 gm/kg monthly). The median interval between PM/DM diagnosis and the onset of esophageal complications was 6 months. The most common clinical manifestations revealing esophageal dysfunction were dysphagia (69.9%), coughing while eating (61.6%), and gastroesophageal reflux into the pharynx and/or mouth (34.2%). Twenty‐five patients exhibited life‐threatening esophageal complications requiring exclusive enteral feeding; 33 patients (45.2%) with esophageal impairment developed aspiration pneumonia. Sixty patients (82.2%) exhibited resolution of esophageal clinical manifestations, leading to a return to normal oral feeding and ablation of feeding enteral tubes. Four other patients (5.5%) improved, although they still experienced mild dysphagia intermittently. Because of impaired cricopharyngeal muscle relaxation, another patient successfully underwent cricopharyngeal myotomy. Eight patients died from aspiration pneumonia (n = 6) and cancer (n = 2). Muscle weakness, thoracic myopathy, and aspiration pneumonia were independent predictive factors of IVIG‐treated esophageal complications in PM/DM patients.
Conclusion
Our findings indicate that IVIG should be considered in life‐threatening esophageal impairment complicating steroid‐resistant PM/DM. We also suggest that combined therapy of IVIG and high‐dose steroids may be the first‐line therapy in PM/DM patients with life‐threatening esophageal manifestations.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>20722047</pmid><doi>10.1002/acr.20325</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Cancer Dermatomyositis Dermatomyositis - complications Dermatomyositis - drug therapy Drug Tolerance Dysphagia Enteral feeding Esophageal Diseases - drug therapy Esophageal Diseases - epidemiology Esophageal Diseases - etiology Esophagus Female Follow-Up Studies Gastroesophageal reflux Glucocorticoids - pharmacology Humans Immunoglobulins Immunoglobulins, Intravenous - administration & dosage Immunoglobulins, Intravenous - therapeutic use Immunologic Factors - administration & dosage Immunologic Factors - therapeutic use Intravenous administration Male medical records Middle Aged Mouth Muscle contraction Muscles Myopathy Pharynx Pneumonia Polymyositis Polymyositis - complications Polymyositis - drug therapy Prevalence Retrospective Studies Steroid hormones Thorax Treatment Outcome Young Adult |
title | Intravenous immunoglobulins for steroid‐refractory esophageal involvement related to polymyositis and dermatomyositis: A series of 73 patients |
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