Reproducibility of a Standardized Titration Procedure for the Initiation of Continuous Positive Airway Pressure Therapy in Patients with Obstructive Sleep Apnoea
Background: Manual titration of continuous positive airway pressure (CPAP) under polysomnographic control is the method most commonly employed to establish the minimal effective pressure (P eff ) for the treatment of the obstructive sleep apnoea syndrome (OSA). To date, however, the reproducibility...
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description | Background: Manual titration of continuous positive airway pressure (CPAP) under polysomnographic control is the method most commonly employed to establish the minimal effective pressure (P eff ) for the treatment of the obstructive sleep apnoea syndrome (OSA). To date, however, the reproducibility of P eff titrated in this way has not been investigated in any detail. Objectives: The present study aims to establish the reproducibility of P eff determined by manual titrations of CPAP under polysomnographic control in the sleep lab. Methods: In a group of 50 patients (5 women), with a mean (SD) apnoea-hypopnoea index of 39.3 (21.8), apnoea index of 28.1 (20.9) and oxygen desaturation index of 39.3 (22.6), with newly diagnosed OSA, manual titration of CPAP was performed on two consecutive nights using the following standard titration protocol: starting at 4 mbar, CPAP was increased by steps of 1 mbar at intervals of at least 5 min, until no signs of airway obstruction could be seen, and arousals were no longer elicited. When no airway obstruction was detected over a period of 30 min, the pressure was lowered once during the night in steps of 1 mbar at intervals of at least 10 min, until obstructive events reappeared, whereupon the pressure was again increased as described above, until, once more, no signs of airway obstruction and no arousals occurred. The second titration was carried out in a blind manner, that is the lab technician did not know the results of the first pressure titration. Results: The mean (SD) P eff for all titrations was 8.1 mbar (2.9). A high level of correlation was found between the P eff titrated on the first night and that titrated on the second night (Spearman correlation coefficient = 0.89). In a few individual cases, however, differences of up to 3 mbar were found between P eff on the first night and P eff on the second night. On average, the P eff measured on the second night was 0.5 mbar (SD = 1.3, range: –2.0 to 3.0 mbar) higher than that of the first night. Conclusions: With standardization of the manual titration of CPAP, P eff is readily reproducible. In individual cases, however, a difference of as much as 3.0 mbar between the two titrations is possible. |
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To date, however, the reproducibility of P eff titrated in this way has not been investigated in any detail. Objectives: The present study aims to establish the reproducibility of P eff determined by manual titrations of CPAP under polysomnographic control in the sleep lab. Methods: In a group of 50 patients (5 women), with a mean (SD) apnoea-hypopnoea index of 39.3 (21.8), apnoea index of 28.1 (20.9) and oxygen desaturation index of 39.3 (22.6), with newly diagnosed OSA, manual titration of CPAP was performed on two consecutive nights using the following standard titration protocol: starting at 4 mbar, CPAP was increased by steps of 1 mbar at intervals of at least 5 min, until no signs of airway obstruction could be seen, and arousals were no longer elicited. When no airway obstruction was detected over a period of 30 min, the pressure was lowered once during the night in steps of 1 mbar at intervals of at least 10 min, until obstructive events reappeared, whereupon the pressure was again increased as described above, until, once more, no signs of airway obstruction and no arousals occurred. The second titration was carried out in a blind manner, that is the lab technician did not know the results of the first pressure titration. Results: The mean (SD) P eff for all titrations was 8.1 mbar (2.9). A high level of correlation was found between the P eff titrated on the first night and that titrated on the second night (Spearman correlation coefficient = 0.89). In a few individual cases, however, differences of up to 3 mbar were found between P eff on the first night and P eff on the second night. On average, the P eff measured on the second night was 0.5 mbar (SD = 1.3, range: –2.0 to 3.0 mbar) higher than that of the first night. Conclusions: With standardization of the manual titration of CPAP, P eff is readily reproducible. In individual cases, however, a difference of as much as 3.0 mbar between the two titrations is possible.</description><identifier>ISSN: 0025-7931</identifier><identifier>EISSN: 1423-0356</identifier><identifier>DOI: 10.1159/000050484</identifier><identifier>PMID: 11287828</identifier><identifier>CODEN: RESPBD</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adult ; Aged ; Biological and medical sciences ; Clinical Investigations ; Continuous positive airway pressure ; Female ; Humans ; Investigative techniques of respiratory function ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Pneumology ; Polysomnography ; Positive-Pressure Respiration ; Reproducibility of Results ; Respiratory system : syndromes and miscellaneous diseases ; Sleep Apnea, Obstructive - physiopathology ; Sleep Apnea, Obstructive - therapy</subject><ispartof>Respiration, 2001, Vol.68 (2), p.145-150</ispartof><rights>2001 S. Karger AG, Basel</rights><rights>2001 INIST-CNRS</rights><rights>Copyright 2001 S. Karger AG, Basel</rights><rights>Copyright (c) 2001 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c383t-27a90c7adff3c86b720dc942dff1203886ba73a27e5583e8247e20ba5d1a62543</citedby><cites>FETCH-LOGICAL-c383t-27a90c7adff3c86b720dc942dff1203886ba73a27e5583e8247e20ba5d1a62543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2423,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=928859$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11287828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wiest, G.H.</creatorcontrib><creatorcontrib>Fuchs, F.S.</creatorcontrib><creatorcontrib>Harsch, I.A.</creatorcontrib><creatorcontrib>Pour Schahin, S.</creatorcontrib><creatorcontrib>Lampert, S.</creatorcontrib><creatorcontrib>Brueckl, W.M.</creatorcontrib><creatorcontrib>Hahn, E.G.</creatorcontrib><creatorcontrib>Ficker, J.H.</creatorcontrib><title>Reproducibility of a Standardized Titration Procedure for the Initiation of Continuous Positive Airway Pressure Therapy in Patients with Obstructive Sleep Apnoea</title><title>Respiration</title><addtitle>Respiration</addtitle><description>Background: Manual titration of continuous positive airway pressure (CPAP) under polysomnographic control is the method most commonly employed to establish the minimal effective pressure (P eff ) for the treatment of the obstructive sleep apnoea syndrome (OSA). To date, however, the reproducibility of P eff titrated in this way has not been investigated in any detail. Objectives: The present study aims to establish the reproducibility of P eff determined by manual titrations of CPAP under polysomnographic control in the sleep lab. Methods: In a group of 50 patients (5 women), with a mean (SD) apnoea-hypopnoea index of 39.3 (21.8), apnoea index of 28.1 (20.9) and oxygen desaturation index of 39.3 (22.6), with newly diagnosed OSA, manual titration of CPAP was performed on two consecutive nights using the following standard titration protocol: starting at 4 mbar, CPAP was increased by steps of 1 mbar at intervals of at least 5 min, until no signs of airway obstruction could be seen, and arousals were no longer elicited. When no airway obstruction was detected over a period of 30 min, the pressure was lowered once during the night in steps of 1 mbar at intervals of at least 10 min, until obstructive events reappeared, whereupon the pressure was again increased as described above, until, once more, no signs of airway obstruction and no arousals occurred. The second titration was carried out in a blind manner, that is the lab technician did not know the results of the first pressure titration. Results: The mean (SD) P eff for all titrations was 8.1 mbar (2.9). A high level of correlation was found between the P eff titrated on the first night and that titrated on the second night (Spearman correlation coefficient = 0.89). In a few individual cases, however, differences of up to 3 mbar were found between P eff on the first night and P eff on the second night. On average, the P eff measured on the second night was 0.5 mbar (SD = 1.3, range: –2.0 to 3.0 mbar) higher than that of the first night. Conclusions: With standardization of the manual titration of CPAP, P eff is readily reproducible. In individual cases, however, a difference of as much as 3.0 mbar between the two titrations is possible.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Clinical Investigations</subject><subject>Continuous positive airway pressure</subject><subject>Female</subject><subject>Humans</subject><subject>Investigative techniques of respiratory function</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pneumology</subject><subject>Polysomnography</subject><subject>Positive-Pressure Respiration</subject><subject>Reproducibility of Results</subject><subject>Respiratory system : syndromes and miscellaneous diseases</subject><subject>Sleep Apnea, Obstructive - physiopathology</subject><subject>Sleep Apnea, Obstructive - therapy</subject><issn>0025-7931</issn><issn>1423-0356</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkV9rFDEUxYModq0--CxIUBB8WM2fySbzuCxVC4WW7vo8ZJI7bupsMk0ylu236Tc12122IOYlJPd37j3JQegtJV8oFfVXUpYglaqeoQmtGJ8SLmbP0YQQJqay5vQEvUrphhAqlGIv0QmlTEnF1AQ9XMMQgx2Na13v8haHDmu8zNpbHa27B4tXLkedXfD4KgYDdoyAuxBxXgM-9y67fbEIF8Fn58cwJnwVUqn8ATx38U5vixRS2ilXa4h62GJX2hUh-JzwnctrfNmmHEfzKFr2AAOeDz6Afo1edLpP8Oawn6Kf385Wix_Ti8vv54v5xdRwxfOUSV0TI7XtOm7UrJWMWFNXrJwpI1yVKy25ZhKEUBwUqyQw0mphqZ4xUfFT9Gnft_zH7QgpNxuXDPS99lBe1EhJmJSSF_DDP-BNGKMv3hrGFGdKCVKgz3vIxJBShK4ZotvouG0oaXahNcfQCvv-0HBsN2CfyENKBfh4AHQyuu-i9salI1fvRtZPvn7r-AvisXx9tnyc0wy2K9C7_0J7J38BxDe1Gg</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Wiest, G.H.</creator><creator>Fuchs, F.S.</creator><creator>Harsch, I.A.</creator><creator>Pour Schahin, S.</creator><creator>Lampert, S.</creator><creator>Brueckl, W.M.</creator><creator>Hahn, E.G.</creator><creator>Ficker, J.H.</creator><general>Karger</general><general>S. Karger AG</general><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>7RQ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>U9A</scope><scope>7X8</scope></search><sort><creationdate>2001</creationdate><title>Reproducibility of a Standardized Titration Procedure for the Initiation of Continuous Positive Airway Pressure Therapy in Patients with Obstructive Sleep Apnoea</title><author>Wiest, G.H. ; Fuchs, F.S. ; Harsch, I.A. ; Pour Schahin, S. ; Lampert, S. ; Brueckl, W.M. ; Hahn, E.G. ; Ficker, J.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-27a90c7adff3c86b720dc942dff1203886ba73a27e5583e8247e20ba5d1a62543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Clinical Investigations</topic><topic>Continuous positive airway pressure</topic><topic>Female</topic><topic>Humans</topic><topic>Investigative techniques of respiratory function</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pneumology</topic><topic>Polysomnography</topic><topic>Positive-Pressure Respiration</topic><topic>Reproducibility of Results</topic><topic>Respiratory system : syndromes and miscellaneous diseases</topic><topic>Sleep Apnea, Obstructive - physiopathology</topic><topic>Sleep Apnea, Obstructive - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wiest, G.H.</creatorcontrib><creatorcontrib>Fuchs, F.S.</creatorcontrib><creatorcontrib>Harsch, I.A.</creatorcontrib><creatorcontrib>Pour Schahin, S.</creatorcontrib><creatorcontrib>Lampert, S.</creatorcontrib><creatorcontrib>Brueckl, W.M.</creatorcontrib><creatorcontrib>Hahn, E.G.</creatorcontrib><creatorcontrib>Ficker, J.H.</creatorcontrib><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>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</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 Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Respiration</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wiest, G.H.</au><au>Fuchs, F.S.</au><au>Harsch, I.A.</au><au>Pour Schahin, S.</au><au>Lampert, S.</au><au>Brueckl, W.M.</au><au>Hahn, E.G.</au><au>Ficker, J.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reproducibility of a Standardized Titration Procedure for the Initiation of Continuous Positive Airway Pressure Therapy in Patients with Obstructive Sleep Apnoea</atitle><jtitle>Respiration</jtitle><addtitle>Respiration</addtitle><date>2001</date><risdate>2001</risdate><volume>68</volume><issue>2</issue><spage>145</spage><epage>150</epage><pages>145-150</pages><issn>0025-7931</issn><eissn>1423-0356</eissn><coden>RESPBD</coden><abstract>Background: Manual titration of continuous positive airway pressure (CPAP) under polysomnographic control is the method most commonly employed to establish the minimal effective pressure (P eff ) for the treatment of the obstructive sleep apnoea syndrome (OSA). To date, however, the reproducibility of P eff titrated in this way has not been investigated in any detail. Objectives: The present study aims to establish the reproducibility of P eff determined by manual titrations of CPAP under polysomnographic control in the sleep lab. Methods: In a group of 50 patients (5 women), with a mean (SD) apnoea-hypopnoea index of 39.3 (21.8), apnoea index of 28.1 (20.9) and oxygen desaturation index of 39.3 (22.6), with newly diagnosed OSA, manual titration of CPAP was performed on two consecutive nights using the following standard titration protocol: starting at 4 mbar, CPAP was increased by steps of 1 mbar at intervals of at least 5 min, until no signs of airway obstruction could be seen, and arousals were no longer elicited. When no airway obstruction was detected over a period of 30 min, the pressure was lowered once during the night in steps of 1 mbar at intervals of at least 10 min, until obstructive events reappeared, whereupon the pressure was again increased as described above, until, once more, no signs of airway obstruction and no arousals occurred. The second titration was carried out in a blind manner, that is the lab technician did not know the results of the first pressure titration. Results: The mean (SD) P eff for all titrations was 8.1 mbar (2.9). A high level of correlation was found between the P eff titrated on the first night and that titrated on the second night (Spearman correlation coefficient = 0.89). In a few individual cases, however, differences of up to 3 mbar were found between P eff on the first night and P eff on the second night. On average, the P eff measured on the second night was 0.5 mbar (SD = 1.3, range: –2.0 to 3.0 mbar) higher than that of the first night. Conclusions: With standardization of the manual titration of CPAP, P eff is readily reproducible. In individual cases, however, a difference of as much as 3.0 mbar between the two titrations is possible.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>11287828</pmid><doi>10.1159/000050484</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Biological and medical sciences Clinical Investigations Continuous positive airway pressure Female Humans Investigative techniques of respiratory function Investigative techniques, diagnostic techniques (general aspects) Male Medical sciences Middle Aged Pneumology Polysomnography Positive-Pressure Respiration Reproducibility of Results Respiratory system : syndromes and miscellaneous diseases Sleep Apnea, Obstructive - physiopathology Sleep Apnea, Obstructive - therapy |
title | Reproducibility of a Standardized Titration Procedure for the Initiation of Continuous Positive Airway Pressure Therapy in Patients with Obstructive Sleep Apnoea |
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