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The intermittent intrapulmonary deflation technique for airway clearance in patients with cystic fibrosis: A randomized trial
Cystic fibrosis (CF) is a muco-obstructive lung disease characterized by thick sputum with abnormal rheological properties. The intermittent intrapulmonary deflation (IID) is a new instrumental airway clearance technique (ACT) that aims to decrease the sputum viscoelastic properties. This study asse...
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Published in: | Respiratory medicine and research 2024-11, Vol.86, p.101094, Article 101094 |
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creator | de Macedo, Juliana Ribeiro Fonseca Franco Aubriot, Anne-Sophie Reychler, Gregory Penelle, Morgane Gohy, Sophie Poncin, William |
description | Cystic fibrosis (CF) is a muco-obstructive lung disease characterized by thick sputum with abnormal rheological properties. The intermittent intrapulmonary deflation (IID) is a new instrumental airway clearance technique (ACT) that aims to decrease the sputum viscoelastic properties. This study assessed the benefits of adding the IID technique to a conventional ACT in patients with CF hospitalized for intravenous antibiotic therapy.
Participants with CF accustomed to autogenic drainage (AD) as their standard ACT received, in a randomized order, a 30-min session of either AD alone or AD combined with IID (AD+IID). Sputum was collected during each ACT regimens and for a 24-hour period following both sessions. Sputum wet weight, dry weight, solids content and rheological properties were analyzed. Cough events occurring during and over 2 h post ACT were compared between both regimens.
Seventeen patients with CF (aged 29 ± 11 years; FEV1%: 57.1 ± 20.1) were analysed. The sputum wet weight collected during AD alone was significantly higher than during AD+IID (8.11 ± 6.93 vs 5.40 ± 4.11 respectively, p = 0.01). The sputum rheological properties did not significantly differ between group. There were more cough episodes during AD alone compared to AD+IID (median [IQR]: 8 [5–15.5] vs 5 [3.5–11.0] respectively, p = 0.02).
In participants with CF accustomed to AD, adding the IID technique in combination to AD does not confer a clear benefit on airway clearance in the short term. Clinical Trials register: NCT04157972 |
doi_str_mv | 10.1016/j.resmer.2024.101094 |
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Participants with CF accustomed to autogenic drainage (AD) as their standard ACT received, in a randomized order, a 30-min session of either AD alone or AD combined with IID (AD+IID). Sputum was collected during each ACT regimens and for a 24-hour period following both sessions. Sputum wet weight, dry weight, solids content and rheological properties were analyzed. Cough events occurring during and over 2 h post ACT were compared between both regimens.
Seventeen patients with CF (aged 29 ± 11 years; FEV1%: 57.1 ± 20.1) were analysed. The sputum wet weight collected during AD alone was significantly higher than during AD+IID (8.11 ± 6.93 vs 5.40 ± 4.11 respectively, p = 0.01). The sputum rheological properties did not significantly differ between group. There were more cough episodes during AD alone compared to AD+IID (median [IQR]: 8 [5–15.5] vs 5 [3.5–11.0] respectively, p = 0.02).
In participants with CF accustomed to AD, adding the IID technique in combination to AD does not confer a clear benefit on airway clearance in the short term. Clinical Trials register: NCT04157972</description><identifier>ISSN: 2590-0412</identifier><identifier>EISSN: 2590-0412</identifier><identifier>DOI: 10.1016/j.resmer.2024.101094</identifier><identifier>PMID: 38843595</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Adult ; Airway clearance technique ; Anti-Bacterial Agents - administration & dosage ; Cough - etiology ; Cystic fibrosis ; Cystic Fibrosis - complications ; Cystic Fibrosis - physiopathology ; Cystic Fibrosis - therapy ; Female ; Humans ; Intermittent intrapulmonary deflation ; Male ; Mucus and sputum ; Respiratory Therapy - methods ; Rheology ; Simeox ; Sputum ; Young Adult</subject><ispartof>Respiratory medicine and research, 2024-11, Vol.86, p.101094, Article 101094</ispartof><rights>2024 SPLF and Elsevier Masson SAS</rights><rights>Copyright © 2024 SPLF and Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1565-b20f6b725f26bbad0a2c1ff9cd09f3bf4aa28ef7d1d1887afd18ce6a9e2468503</cites><orcidid>0000-0002-4776-7503</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38843595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Macedo, Juliana Ribeiro Fonseca Franco</creatorcontrib><creatorcontrib>Aubriot, Anne-Sophie</creatorcontrib><creatorcontrib>Reychler, Gregory</creatorcontrib><creatorcontrib>Penelle, Morgane</creatorcontrib><creatorcontrib>Gohy, Sophie</creatorcontrib><creatorcontrib>Poncin, William</creatorcontrib><title>The intermittent intrapulmonary deflation technique for airway clearance in patients with cystic fibrosis: A randomized trial</title><title>Respiratory medicine and research</title><addtitle>Respir Med Res</addtitle><description>Cystic fibrosis (CF) is a muco-obstructive lung disease characterized by thick sputum with abnormal rheological properties. The intermittent intrapulmonary deflation (IID) is a new instrumental airway clearance technique (ACT) that aims to decrease the sputum viscoelastic properties. This study assessed the benefits of adding the IID technique to a conventional ACT in patients with CF hospitalized for intravenous antibiotic therapy.
Participants with CF accustomed to autogenic drainage (AD) as their standard ACT received, in a randomized order, a 30-min session of either AD alone or AD combined with IID (AD+IID). Sputum was collected during each ACT regimens and for a 24-hour period following both sessions. Sputum wet weight, dry weight, solids content and rheological properties were analyzed. Cough events occurring during and over 2 h post ACT were compared between both regimens.
Seventeen patients with CF (aged 29 ± 11 years; FEV1%: 57.1 ± 20.1) were analysed. The sputum wet weight collected during AD alone was significantly higher than during AD+IID (8.11 ± 6.93 vs 5.40 ± 4.11 respectively, p = 0.01). The sputum rheological properties did not significantly differ between group. There were more cough episodes during AD alone compared to AD+IID (median [IQR]: 8 [5–15.5] vs 5 [3.5–11.0] respectively, p = 0.02).
In participants with CF accustomed to AD, adding the IID technique in combination to AD does not confer a clear benefit on airway clearance in the short term. Clinical Trials register: NCT04157972</description><subject>Adult</subject><subject>Airway clearance technique</subject><subject>Anti-Bacterial Agents - administration & dosage</subject><subject>Cough - etiology</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - complications</subject><subject>Cystic Fibrosis - physiopathology</subject><subject>Cystic Fibrosis - therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Intermittent intrapulmonary deflation</subject><subject>Male</subject><subject>Mucus and sputum</subject><subject>Respiratory Therapy - methods</subject><subject>Rheology</subject><subject>Simeox</subject><subject>Sputum</subject><subject>Young Adult</subject><issn>2590-0412</issn><issn>2590-0412</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoVrT_QCRHL61JNtnuehCk-AUFL_UcssmEpuxHTVJLBf-7WbaKJ0-ThOedyTwIXVIypYTmN-uph9CAnzLCeP9ESn6EzpgoyYRwyo7_nEdoHMKaEMLojJKCn6JRVhQ8E6U4Q1_LFWDXRvCNixHa2F-82mzrpmuV32MDtlbRdS2OoFete98Ctp3Hyvmd2mNdg_Kq1X0TvElgahHwzsUV1vsQncbWVb4LLtzie5xI0zXuEwyO3qn6Ap1YVQcYH-o5ent8WM6fJ4vXp5f5_WKiqcjFpGLE5tWMCcvyqlKGKKaptaU2pLRZZblSrAA7M9TQopgpm4qGXJXAeF4Ikp2j66HvxndpgRBl44KGulYtdNsgM5KLsuA0FwnlA6rTr4MHKzfeNcmEpET27uVaDu5l714O7lPs6jBhWzVgfkM_phNwNwCQ9vxwKR50kqXBOA86StO5_yd8A1gJmok</recordid><startdate>202411</startdate><enddate>202411</enddate><creator>de Macedo, Juliana Ribeiro Fonseca Franco</creator><creator>Aubriot, Anne-Sophie</creator><creator>Reychler, Gregory</creator><creator>Penelle, Morgane</creator><creator>Gohy, Sophie</creator><creator>Poncin, William</creator><general>Elsevier Masson SAS</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>7X8</scope><orcidid>https://orcid.org/0000-0002-4776-7503</orcidid></search><sort><creationdate>202411</creationdate><title>The intermittent intrapulmonary deflation technique for airway clearance in patients with cystic fibrosis: A randomized trial</title><author>de Macedo, Juliana Ribeiro Fonseca Franco ; Aubriot, Anne-Sophie ; Reychler, Gregory ; Penelle, Morgane ; Gohy, Sophie ; Poncin, William</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1565-b20f6b725f26bbad0a2c1ff9cd09f3bf4aa28ef7d1d1887afd18ce6a9e2468503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Airway clearance technique</topic><topic>Anti-Bacterial Agents - administration & dosage</topic><topic>Cough - etiology</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - complications</topic><topic>Cystic Fibrosis - physiopathology</topic><topic>Cystic Fibrosis - therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Intermittent intrapulmonary deflation</topic><topic>Male</topic><topic>Mucus and sputum</topic><topic>Respiratory Therapy - methods</topic><topic>Rheology</topic><topic>Simeox</topic><topic>Sputum</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Macedo, Juliana Ribeiro Fonseca Franco</creatorcontrib><creatorcontrib>Aubriot, Anne-Sophie</creatorcontrib><creatorcontrib>Reychler, Gregory</creatorcontrib><creatorcontrib>Penelle, Morgane</creatorcontrib><creatorcontrib>Gohy, Sophie</creatorcontrib><creatorcontrib>Poncin, William</creatorcontrib><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>Respiratory medicine and research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Macedo, Juliana Ribeiro Fonseca Franco</au><au>Aubriot, Anne-Sophie</au><au>Reychler, Gregory</au><au>Penelle, Morgane</au><au>Gohy, Sophie</au><au>Poncin, William</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The intermittent intrapulmonary deflation technique for airway clearance in patients with cystic fibrosis: A randomized trial</atitle><jtitle>Respiratory medicine and research</jtitle><addtitle>Respir Med Res</addtitle><date>2024-11</date><risdate>2024</risdate><volume>86</volume><spage>101094</spage><pages>101094-</pages><artnum>101094</artnum><issn>2590-0412</issn><eissn>2590-0412</eissn><abstract>Cystic fibrosis (CF) is a muco-obstructive lung disease characterized by thick sputum with abnormal rheological properties. The intermittent intrapulmonary deflation (IID) is a new instrumental airway clearance technique (ACT) that aims to decrease the sputum viscoelastic properties. This study assessed the benefits of adding the IID technique to a conventional ACT in patients with CF hospitalized for intravenous antibiotic therapy.
Participants with CF accustomed to autogenic drainage (AD) as their standard ACT received, in a randomized order, a 30-min session of either AD alone or AD combined with IID (AD+IID). Sputum was collected during each ACT regimens and for a 24-hour period following both sessions. Sputum wet weight, dry weight, solids content and rheological properties were analyzed. Cough events occurring during and over 2 h post ACT were compared between both regimens.
Seventeen patients with CF (aged 29 ± 11 years; FEV1%: 57.1 ± 20.1) were analysed. The sputum wet weight collected during AD alone was significantly higher than during AD+IID (8.11 ± 6.93 vs 5.40 ± 4.11 respectively, p = 0.01). The sputum rheological properties did not significantly differ between group. There were more cough episodes during AD alone compared to AD+IID (median [IQR]: 8 [5–15.5] vs 5 [3.5–11.0] respectively, p = 0.02).
In participants with CF accustomed to AD, adding the IID technique in combination to AD does not confer a clear benefit on airway clearance in the short term. Clinical Trials register: NCT04157972</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>38843595</pmid><doi>10.1016/j.resmer.2024.101094</doi><orcidid>https://orcid.org/0000-0002-4776-7503</orcidid></addata></record> |
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subjects | Adult Airway clearance technique Anti-Bacterial Agents - administration & dosage Cough - etiology Cystic fibrosis Cystic Fibrosis - complications Cystic Fibrosis - physiopathology Cystic Fibrosis - therapy Female Humans Intermittent intrapulmonary deflation Male Mucus and sputum Respiratory Therapy - methods Rheology Simeox Sputum Young Adult |
title | The intermittent intrapulmonary deflation technique for airway clearance in patients with cystic fibrosis: A randomized trial |
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