Development of a Consensus Statement for the Definition, Diagnosis, and Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis Using the Delphi Technique

Introduction There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). This reflects, in part, the limited evidence-base underpinning the management of AE-IPF. In the absence of high-quality evidence, the aim of this rese...

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Veröffentlicht in:Advances in therapy 2015-10, Vol.32 (10), p.929-943
Hauptverfasser: Maher, Toby M., Whyte, Moira K. B., Hoyles, Rachel K., Parfrey, Helen, Ochiai, Yuuki, Mathieson, Nicky, Turnbull, Alice, Williamson, Nicola, Bennett, Bryan M.
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container_end_page 943
container_issue 10
container_start_page 929
container_title Advances in therapy
container_volume 32
creator Maher, Toby M.
Whyte, Moira K. B.
Hoyles, Rachel K.
Parfrey, Helen
Ochiai, Yuuki
Mathieson, Nicky
Turnbull, Alice
Williamson, Nicola
Bennett, Bryan M.
description Introduction There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). This reflects, in part, the limited evidence-base underpinning the management of AE-IPF. In the absence of high-quality evidence, the aim of this research was to develop a clinician-led consensus statement for the definition, diagnosis and treatment of AE-IPF. Methods A literature review was conducted to obtain published material on the definition and treatment of AE-IPF. The results of this review were circulated to an online panel of clinicians for review. Statements were then shared with ten expert respiratory clinicians who regularly treat patients with IPF. A Delphi technique was then used to develop a consensus statement for the definition, diagnosis and treatment of AE-IPF. During the first round of review, clinicians rated the clarity of each statement, the extent to which the statement should be included and provided comments. In two subsequent rounds of review, clinicians were provided with the group median inclusion rating for each statement, and any revised wording of statements to aid clarity. Clinicians were asked to repeat the clarity and inclusion ratings for the revised statements. Results The literature review, online panel discussion, and face-to-face meeting generated 65 statements covering the definition, diagnosis, and management of AE-IPF. Following three rounds of blind review, 90% of clinicians agreed 39 final statements. These final statements included a definition of AE-IPF, approach to diagnosis, and treatment options, specifically: supportive measures, use of anti-microbials, immunosuppressants, anti-coagulants, anti-fibrotic therapy, escalation, transplant management, and long-term management including discharge planning. Conclusion This clinician-led consensus statement establishes the ‘best practice’ for the management and treatment of AE-IPF based on current knowledge, evidence, and available treatments. Funding Boehringer Ingelheim Ltd., Bracknell, West Berkshire, UK.
doi_str_mv 10.1007/s12325-015-0249-6
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B. ; Hoyles, Rachel K. ; Parfrey, Helen ; Ochiai, Yuuki ; Mathieson, Nicky ; Turnbull, Alice ; Williamson, Nicola ; Bennett, Bryan M.</creator><creatorcontrib>Maher, Toby M. ; Whyte, Moira K. B. ; Hoyles, Rachel K. ; Parfrey, Helen ; Ochiai, Yuuki ; Mathieson, Nicky ; Turnbull, Alice ; Williamson, Nicola ; Bennett, Bryan M.</creatorcontrib><description>Introduction There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). This reflects, in part, the limited evidence-base underpinning the management of AE-IPF. In the absence of high-quality evidence, the aim of this research was to develop a clinician-led consensus statement for the definition, diagnosis and treatment of AE-IPF. Methods A literature review was conducted to obtain published material on the definition and treatment of AE-IPF. The results of this review were circulated to an online panel of clinicians for review. Statements were then shared with ten expert respiratory clinicians who regularly treat patients with IPF. A Delphi technique was then used to develop a consensus statement for the definition, diagnosis and treatment of AE-IPF. During the first round of review, clinicians rated the clarity of each statement, the extent to which the statement should be included and provided comments. In two subsequent rounds of review, clinicians were provided with the group median inclusion rating for each statement, and any revised wording of statements to aid clarity. Clinicians were asked to repeat the clarity and inclusion ratings for the revised statements. Results The literature review, online panel discussion, and face-to-face meeting generated 65 statements covering the definition, diagnosis, and management of AE-IPF. Following three rounds of blind review, 90% of clinicians agreed 39 final statements. These final statements included a definition of AE-IPF, approach to diagnosis, and treatment options, specifically: supportive measures, use of anti-microbials, immunosuppressants, anti-coagulants, anti-fibrotic therapy, escalation, transplant management, and long-term management including discharge planning. Conclusion This clinician-led consensus statement establishes the ‘best practice’ for the management and treatment of AE-IPF based on current knowledge, evidence, and available treatments. Funding Boehringer Ingelheim Ltd., Bracknell, West Berkshire, UK.</description><identifier>ISSN: 0741-238X</identifier><identifier>EISSN: 1865-8652</identifier><identifier>DOI: 10.1007/s12325-015-0249-6</identifier><identifier>PMID: 26498943</identifier><language>eng</language><publisher>Cheshire: Springer Healthcare</publisher><subject>Cardiology ; Consensus ; Delphi Technique ; Endocrinology ; Humans ; Idiopathic Pulmonary Fibrosis - diagnosis ; Idiopathic Pulmonary Fibrosis - physiopathology ; Idiopathic Pulmonary Fibrosis - therapy ; Internal Medicine ; Medicine ; Medicine &amp; Public Health ; Oncology ; Original Research ; Patient Discharge ; Pharmacology/Toxicology ; Practice Guidelines as Topic ; Rheumatology</subject><ispartof>Advances in therapy, 2015-10, Vol.32 (10), p.929-943</ispartof><rights>The Author(s) 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c578t-4ab37011dbdc88d76db268e73308b8daf2593e73d99cd0502861f98d5ae075413</citedby><cites>FETCH-LOGICAL-c578t-4ab37011dbdc88d76db268e73308b8daf2593e73d99cd0502861f98d5ae075413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12325-015-0249-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12325-015-0249-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26498943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maher, Toby M.</creatorcontrib><creatorcontrib>Whyte, Moira K. B.</creatorcontrib><creatorcontrib>Hoyles, Rachel K.</creatorcontrib><creatorcontrib>Parfrey, Helen</creatorcontrib><creatorcontrib>Ochiai, Yuuki</creatorcontrib><creatorcontrib>Mathieson, Nicky</creatorcontrib><creatorcontrib>Turnbull, Alice</creatorcontrib><creatorcontrib>Williamson, Nicola</creatorcontrib><creatorcontrib>Bennett, Bryan M.</creatorcontrib><title>Development of a Consensus Statement for the Definition, Diagnosis, and Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis Using the Delphi Technique</title><title>Advances in therapy</title><addtitle>Adv Ther</addtitle><addtitle>Adv Ther</addtitle><description>Introduction There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). This reflects, in part, the limited evidence-base underpinning the management of AE-IPF. In the absence of high-quality evidence, the aim of this research was to develop a clinician-led consensus statement for the definition, diagnosis and treatment of AE-IPF. Methods A literature review was conducted to obtain published material on the definition and treatment of AE-IPF. The results of this review were circulated to an online panel of clinicians for review. Statements were then shared with ten expert respiratory clinicians who regularly treat patients with IPF. A Delphi technique was then used to develop a consensus statement for the definition, diagnosis and treatment of AE-IPF. During the first round of review, clinicians rated the clarity of each statement, the extent to which the statement should be included and provided comments. In two subsequent rounds of review, clinicians were provided with the group median inclusion rating for each statement, and any revised wording of statements to aid clarity. Clinicians were asked to repeat the clarity and inclusion ratings for the revised statements. Results The literature review, online panel discussion, and face-to-face meeting generated 65 statements covering the definition, diagnosis, and management of AE-IPF. Following three rounds of blind review, 90% of clinicians agreed 39 final statements. These final statements included a definition of AE-IPF, approach to diagnosis, and treatment options, specifically: supportive measures, use of anti-microbials, immunosuppressants, anti-coagulants, anti-fibrotic therapy, escalation, transplant management, and long-term management including discharge planning. Conclusion This clinician-led consensus statement establishes the ‘best practice’ for the management and treatment of AE-IPF based on current knowledge, evidence, and available treatments. Funding Boehringer Ingelheim Ltd., Bracknell, West Berkshire, UK.</description><subject>Cardiology</subject><subject>Consensus</subject><subject>Delphi Technique</subject><subject>Endocrinology</subject><subject>Humans</subject><subject>Idiopathic Pulmonary Fibrosis - diagnosis</subject><subject>Idiopathic Pulmonary Fibrosis - physiopathology</subject><subject>Idiopathic Pulmonary Fibrosis - therapy</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Oncology</subject><subject>Original Research</subject><subject>Patient Discharge</subject><subject>Pharmacology/Toxicology</subject><subject>Practice Guidelines as Topic</subject><subject>Rheumatology</subject><issn>0741-238X</issn><issn>1865-8652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9UcFu1DAQtRCILoUP4IJ85NAU20ls54JU7ba0UiWQ2ErcLMeebFwl9mInFfwPH4rDbiu4cBhZnnnz5s08hN5Sck4JER8SZSWrC0JzsKop-DO0opLXRQ72HK2IqGjBSvntBL1K6Z4QRkQtX6ITxqtGNlW5Qr828ABD2I_gJxw6rPE6-AQ-zQl_nfQEfwpdiHjqAW-gc95NLvgzvHF650Ny6Qxrb_E2gp4eWS7MPAG-_KENxFYv-LSkb6wLez31zuAv8zAGr-NPfOXauNDgu-T87jhm2PcOb8H03n2f4TV60ekhwZvje4ruri636-vi9vOnm_XFbWFqIaei0m0pCKW2tUZKK7htGZcgypLIVlrdsbop89c2jbGkJkxy2jXS1hryXSpanqKPB9793I5gTd4m6kHtoxuzUhW0U_9WvOvVLjyoipc1FVUmeH8kiCHrTpMaXTIwDNpDmJOigleCMM5EhtID1OTtU4TuaQwlanFXHdxV2V21uKt47nn3t76njkc7M4AdACmX_A6iug9z9Plm_2H9DQIUs-U</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Maher, Toby M.</creator><creator>Whyte, Moira K. 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B. ; Hoyles, Rachel K. ; Parfrey, Helen ; Ochiai, Yuuki ; Mathieson, Nicky ; Turnbull, Alice ; Williamson, Nicola ; Bennett, Bryan M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c578t-4ab37011dbdc88d76db268e73308b8daf2593e73d99cd0502861f98d5ae075413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Cardiology</topic><topic>Consensus</topic><topic>Delphi Technique</topic><topic>Endocrinology</topic><topic>Humans</topic><topic>Idiopathic Pulmonary Fibrosis - diagnosis</topic><topic>Idiopathic Pulmonary Fibrosis - physiopathology</topic><topic>Idiopathic Pulmonary Fibrosis - therapy</topic><topic>Internal Medicine</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Oncology</topic><topic>Original Research</topic><topic>Patient Discharge</topic><topic>Pharmacology/Toxicology</topic><topic>Practice Guidelines as Topic</topic><topic>Rheumatology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maher, Toby M.</creatorcontrib><creatorcontrib>Whyte, Moira K. B.</creatorcontrib><creatorcontrib>Hoyles, Rachel K.</creatorcontrib><creatorcontrib>Parfrey, Helen</creatorcontrib><creatorcontrib>Ochiai, Yuuki</creatorcontrib><creatorcontrib>Mathieson, Nicky</creatorcontrib><creatorcontrib>Turnbull, Alice</creatorcontrib><creatorcontrib>Williamson, Nicola</creatorcontrib><creatorcontrib>Bennett, Bryan M.</creatorcontrib><collection>Springer Nature OA Free Journals</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Advances in therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maher, Toby M.</au><au>Whyte, Moira K. B.</au><au>Hoyles, Rachel K.</au><au>Parfrey, Helen</au><au>Ochiai, Yuuki</au><au>Mathieson, Nicky</au><au>Turnbull, Alice</au><au>Williamson, Nicola</au><au>Bennett, Bryan M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a Consensus Statement for the Definition, Diagnosis, and Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis Using the Delphi Technique</atitle><jtitle>Advances in therapy</jtitle><stitle>Adv Ther</stitle><addtitle>Adv Ther</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>32</volume><issue>10</issue><spage>929</spage><epage>943</epage><pages>929-943</pages><issn>0741-238X</issn><eissn>1865-8652</eissn><abstract>Introduction There is a lack of agreed and established guidelines for the treatment of acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). This reflects, in part, the limited evidence-base underpinning the management of AE-IPF. In the absence of high-quality evidence, the aim of this research was to develop a clinician-led consensus statement for the definition, diagnosis and treatment of AE-IPF. Methods A literature review was conducted to obtain published material on the definition and treatment of AE-IPF. The results of this review were circulated to an online panel of clinicians for review. Statements were then shared with ten expert respiratory clinicians who regularly treat patients with IPF. A Delphi technique was then used to develop a consensus statement for the definition, diagnosis and treatment of AE-IPF. During the first round of review, clinicians rated the clarity of each statement, the extent to which the statement should be included and provided comments. In two subsequent rounds of review, clinicians were provided with the group median inclusion rating for each statement, and any revised wording of statements to aid clarity. Clinicians were asked to repeat the clarity and inclusion ratings for the revised statements. Results The literature review, online panel discussion, and face-to-face meeting generated 65 statements covering the definition, diagnosis, and management of AE-IPF. Following three rounds of blind review, 90% of clinicians agreed 39 final statements. These final statements included a definition of AE-IPF, approach to diagnosis, and treatment options, specifically: supportive measures, use of anti-microbials, immunosuppressants, anti-coagulants, anti-fibrotic therapy, escalation, transplant management, and long-term management including discharge planning. Conclusion This clinician-led consensus statement establishes the ‘best practice’ for the management and treatment of AE-IPF based on current knowledge, evidence, and available treatments. Funding Boehringer Ingelheim Ltd., Bracknell, West Berkshire, UK.</abstract><cop>Cheshire</cop><pub>Springer Healthcare</pub><pmid>26498943</pmid><doi>10.1007/s12325-015-0249-6</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
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subjects Cardiology
Consensus
Delphi Technique
Endocrinology
Humans
Idiopathic Pulmonary Fibrosis - diagnosis
Idiopathic Pulmonary Fibrosis - physiopathology
Idiopathic Pulmonary Fibrosis - therapy
Internal Medicine
Medicine
Medicine & Public Health
Oncology
Original Research
Patient Discharge
Pharmacology/Toxicology
Practice Guidelines as Topic
Rheumatology
title Development of a Consensus Statement for the Definition, Diagnosis, and Treatment of Acute Exacerbations of Idiopathic Pulmonary Fibrosis Using the Delphi Technique
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