Occupational therapist-guided cognitive interventions in critically ill patients: a feasibility randomized controlled trial
Purpose Intensive care unit (ICU) delirium is a common complication of critical illness requiring a multimodal approach to management. We assessed the feasibility of a novel occupational therapist (OT)-guided cognitive intervention protocol, titrated according to sedation level, in critically ill pa...
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Veröffentlicht in: | Canadian journal of anesthesia 2023-01, Vol.70 (1), p.139-150 |
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creator | Deemer, Kirsten Myhre, Brittany Oviatt, Stephanie Parsons, Michelle Watson, Mallory Zjadewicz, Karolina Soo, Andrea Fiest, Kirsten Posadas-Calleja, Juan |
description | Purpose
Intensive care unit (ICU) delirium is a common complication of critical illness requiring a multimodal approach to management. We assessed the feasibility of a novel occupational therapist (OT)-guided cognitive intervention protocol, titrated according to sedation level, in critically ill patients.
Methods
Patients aged ≥ 18 yr admitted to a medical/surgical ICU were randomized to the standard delirium prevention protocol or to the OT-guided cognitive intervention protocol in addition to standard of care. The target enrolment number was
N
= 112. Due to the COVID-19 pandemic, the study enrolment period was truncated. The primary outcome was feasibility of the intervention as measured by the proportion of eligible cognitive interventions delivered by the OT. Secondary outcomes included feasibility of goal session length (20 min), participant clinical outcomes (delirium prevalence and duration, cognitive status, functional status, quality of life, and ICU length of stay), and a description of methodological challenges and solutions for future research.
Results
Seventy patients were enrolled and 69 patients were included in the final analysis. The majority of OT-guided sessions (110/137; 80%) were completed. The mean (standard deviation [SD]) number of sessions per patient was 4.1 (3.8). The goal session length was achieved (mean [SD], 19.8 [3.1] min), with few sessions (8/110; 7%) terminated early per patient request.
Conclusion
This novel OT-guided cognitive intervention protocol is feasible in medical/surgical ICU patients. A larger randomized controlled trial is required to determine the impact of such a protocol on delirium prevalence or duration.
Study registration
www.ClinicalTrials.gov
(NCT03604809); registered 18 June 2018. |
doi_str_mv | 10.1007/s12630-022-02351-9 |
format | Article |
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Intensive care unit (ICU) delirium is a common complication of critical illness requiring a multimodal approach to management. We assessed the feasibility of a novel occupational therapist (OT)-guided cognitive intervention protocol, titrated according to sedation level, in critically ill patients.
Methods
Patients aged ≥ 18 yr admitted to a medical/surgical ICU were randomized to the standard delirium prevention protocol or to the OT-guided cognitive intervention protocol in addition to standard of care. The target enrolment number was
N
= 112. Due to the COVID-19 pandemic, the study enrolment period was truncated. The primary outcome was feasibility of the intervention as measured by the proportion of eligible cognitive interventions delivered by the OT. Secondary outcomes included feasibility of goal session length (20 min), participant clinical outcomes (delirium prevalence and duration, cognitive status, functional status, quality of life, and ICU length of stay), and a description of methodological challenges and solutions for future research.
Results
Seventy patients were enrolled and 69 patients were included in the final analysis. The majority of OT-guided sessions (110/137; 80%) were completed. The mean (standard deviation [SD]) number of sessions per patient was 4.1 (3.8). The goal session length was achieved (mean [SD], 19.8 [3.1] min), with few sessions (8/110; 7%) terminated early per patient request.
Conclusion
This novel OT-guided cognitive intervention protocol is feasible in medical/surgical ICU patients. A larger randomized controlled trial is required to determine the impact of such a protocol on delirium prevalence or duration.
Study registration
www.ClinicalTrials.gov
(NCT03604809); registered 18 June 2018.</description><identifier>ISSN: 0832-610X</identifier><identifier>EISSN: 1496-8975</identifier><identifier>DOI: 10.1007/s12630-022-02351-9</identifier><identifier>PMID: 36385466</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Anesthesiology ; Cardiology ; Clinical trials ; Cognition ; Coronaviruses ; COVID-19 ; COVID-19 - therapy ; Critical Care Medicine ; Critical Illness - psychology ; Critical Illness - therapy ; Delirium ; Delirium - prevention & control ; Delirium - psychology ; Feasibility Studies ; Humans ; Intensive ; Intensive Care Units ; Intervention ; Medicine ; Medicine & Public Health ; Occupational Therapists ; Occupational therapy ; Pain Medicine ; Pandemics ; Patients ; Pediatrics ; Pneumology/Respiratory System ; Quality of Life ; Reports of Original Investigations</subject><ispartof>Canadian journal of anesthesia, 2023-01, Vol.70 (1), p.139-150</ispartof><rights>Canadian Anesthesiologists' Society 2022. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2022. Canadian Anesthesiologists' Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-bd54c285de14ce241074a2e6228589ed43def725005e31eaf949448564d3bcec3</citedby><cites>FETCH-LOGICAL-c441t-bd54c285de14ce241074a2e6228589ed43def725005e31eaf949448564d3bcec3</cites><orcidid>0000-0002-3674-3522</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12630-022-02351-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12630-022-02351-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36385466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deemer, Kirsten</creatorcontrib><creatorcontrib>Myhre, Brittany</creatorcontrib><creatorcontrib>Oviatt, Stephanie</creatorcontrib><creatorcontrib>Parsons, Michelle</creatorcontrib><creatorcontrib>Watson, Mallory</creatorcontrib><creatorcontrib>Zjadewicz, Karolina</creatorcontrib><creatorcontrib>Soo, Andrea</creatorcontrib><creatorcontrib>Fiest, Kirsten</creatorcontrib><creatorcontrib>Posadas-Calleja, Juan</creatorcontrib><title>Occupational therapist-guided cognitive interventions in critically ill patients: a feasibility randomized controlled trial</title><title>Canadian journal of anesthesia</title><addtitle>Can J Anesth/J Can Anesth</addtitle><addtitle>Can J Anaesth</addtitle><description>Purpose
Intensive care unit (ICU) delirium is a common complication of critical illness requiring a multimodal approach to management. We assessed the feasibility of a novel occupational therapist (OT)-guided cognitive intervention protocol, titrated according to sedation level, in critically ill patients.
Methods
Patients aged ≥ 18 yr admitted to a medical/surgical ICU were randomized to the standard delirium prevention protocol or to the OT-guided cognitive intervention protocol in addition to standard of care. The target enrolment number was
N
= 112. Due to the COVID-19 pandemic, the study enrolment period was truncated. The primary outcome was feasibility of the intervention as measured by the proportion of eligible cognitive interventions delivered by the OT. Secondary outcomes included feasibility of goal session length (20 min), participant clinical outcomes (delirium prevalence and duration, cognitive status, functional status, quality of life, and ICU length of stay), and a description of methodological challenges and solutions for future research.
Results
Seventy patients were enrolled and 69 patients were included in the final analysis. The majority of OT-guided sessions (110/137; 80%) were completed. The mean (standard deviation [SD]) number of sessions per patient was 4.1 (3.8). The goal session length was achieved (mean [SD], 19.8 [3.1] min), with few sessions (8/110; 7%) terminated early per patient request.
Conclusion
This novel OT-guided cognitive intervention protocol is feasible in medical/surgical ICU patients. A larger randomized controlled trial is required to determine the impact of such a protocol on delirium prevalence or duration.
Study registration
www.ClinicalTrials.gov
(NCT03604809); registered 18 June 2018.</description><subject>Anesthesiology</subject><subject>Cardiology</subject><subject>Clinical trials</subject><subject>Cognition</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - therapy</subject><subject>Critical Care Medicine</subject><subject>Critical Illness - psychology</subject><subject>Critical Illness - therapy</subject><subject>Delirium</subject><subject>Delirium - prevention & control</subject><subject>Delirium - psychology</subject><subject>Feasibility Studies</subject><subject>Humans</subject><subject>Intensive</subject><subject>Intensive Care Units</subject><subject>Intervention</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Occupational Therapists</subject><subject>Occupational therapy</subject><subject>Pain Medicine</subject><subject>Pandemics</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Pneumology/Respiratory System</subject><subject>Quality of Life</subject><subject>Reports of Original Investigations</subject><issn>0832-610X</issn><issn>1496-8975</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kU9LXDEUxYNU6qj9Al1IoJtuXs3_vNddEWsLghsFdyGT3DdmyLw3JnnCtF_ejDNV6MLFJffm_O4J5CD0mZJvlBB9nilTnDSEsVpc0qY7QDMqOtW0nZYf0Iy0nDWKkvsjdJzzkhDSKtl-REdc8VYKpWbo741z09qWMA424vIAya5DLs1iCh48duNiCCU8AQ5DgfQEw5bMdcIuVcHZGDc4xIi3HlXN37HFPdgc5iGGssHJDn5chT8vZkNJY4y1LSnYeIoOexszfNqfJ-ju5-Xtxa_m-ubq98WP68YJQUsz91I41koPVDhgghItLAPF6l3bgRfcQ6-ZJEQCp2D7TnRCtFIJz-cOHD9BX3e-6zQ-TpCLWYXsIEY7wDhlwzTXQslOyop--Q9djlOqX7OltKaaE04rxXaUS2POCXqzTmFl08ZQYrbRmF00pkZjXqIxXV0621tP8xX415V_WVSA74BcpWEB6e3td2yfAfzim-8</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Deemer, Kirsten</creator><creator>Myhre, Brittany</creator><creator>Oviatt, Stephanie</creator><creator>Parsons, Michelle</creator><creator>Watson, Mallory</creator><creator>Zjadewicz, Karolina</creator><creator>Soo, Andrea</creator><creator>Fiest, Kirsten</creator><creator>Posadas-Calleja, Juan</creator><general>Springer International Publishing</general><general>Springer Nature B.V</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>3V.</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>8FQ</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3674-3522</orcidid></search><sort><creationdate>20230101</creationdate><title>Occupational therapist-guided cognitive interventions in critically ill patients: a feasibility randomized controlled trial</title><author>Deemer, Kirsten ; Myhre, Brittany ; Oviatt, Stephanie ; Parsons, Michelle ; Watson, Mallory ; Zjadewicz, Karolina ; Soo, Andrea ; Fiest, Kirsten ; Posadas-Calleja, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-bd54c285de14ce241074a2e6228589ed43def725005e31eaf949448564d3bcec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anesthesiology</topic><topic>Cardiology</topic><topic>Clinical trials</topic><topic>Cognition</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - therapy</topic><topic>Critical Care Medicine</topic><topic>Critical Illness - psychology</topic><topic>Critical Illness - therapy</topic><topic>Delirium</topic><topic>Delirium - prevention & control</topic><topic>Delirium - psychology</topic><topic>Feasibility Studies</topic><topic>Humans</topic><topic>Intensive</topic><topic>Intensive Care Units</topic><topic>Intervention</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Occupational Therapists</topic><topic>Occupational therapy</topic><topic>Pain Medicine</topic><topic>Pandemics</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Pneumology/Respiratory System</topic><topic>Quality of Life</topic><topic>Reports of Original Investigations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deemer, Kirsten</creatorcontrib><creatorcontrib>Myhre, Brittany</creatorcontrib><creatorcontrib>Oviatt, Stephanie</creatorcontrib><creatorcontrib>Parsons, Michelle</creatorcontrib><creatorcontrib>Watson, Mallory</creatorcontrib><creatorcontrib>Zjadewicz, Karolina</creatorcontrib><creatorcontrib>Soo, Andrea</creatorcontrib><creatorcontrib>Fiest, Kirsten</creatorcontrib><creatorcontrib>Posadas-Calleja, Juan</creatorcontrib><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>ProQuest Nursing and Allied Health Journals</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>Canadian Business & Current Affairs Database</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</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>Canadian journal of anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deemer, Kirsten</au><au>Myhre, Brittany</au><au>Oviatt, Stephanie</au><au>Parsons, Michelle</au><au>Watson, Mallory</au><au>Zjadewicz, Karolina</au><au>Soo, Andrea</au><au>Fiest, Kirsten</au><au>Posadas-Calleja, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Occupational therapist-guided cognitive interventions in critically ill patients: a feasibility randomized controlled trial</atitle><jtitle>Canadian journal of anesthesia</jtitle><stitle>Can J Anesth/J Can Anesth</stitle><addtitle>Can J Anaesth</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>70</volume><issue>1</issue><spage>139</spage><epage>150</epage><pages>139-150</pages><issn>0832-610X</issn><eissn>1496-8975</eissn><abstract>Purpose
Intensive care unit (ICU) delirium is a common complication of critical illness requiring a multimodal approach to management. We assessed the feasibility of a novel occupational therapist (OT)-guided cognitive intervention protocol, titrated according to sedation level, in critically ill patients.
Methods
Patients aged ≥ 18 yr admitted to a medical/surgical ICU were randomized to the standard delirium prevention protocol or to the OT-guided cognitive intervention protocol in addition to standard of care. The target enrolment number was
N
= 112. Due to the COVID-19 pandemic, the study enrolment period was truncated. The primary outcome was feasibility of the intervention as measured by the proportion of eligible cognitive interventions delivered by the OT. Secondary outcomes included feasibility of goal session length (20 min), participant clinical outcomes (delirium prevalence and duration, cognitive status, functional status, quality of life, and ICU length of stay), and a description of methodological challenges and solutions for future research.
Results
Seventy patients were enrolled and 69 patients were included in the final analysis. The majority of OT-guided sessions (110/137; 80%) were completed. The mean (standard deviation [SD]) number of sessions per patient was 4.1 (3.8). The goal session length was achieved (mean [SD], 19.8 [3.1] min), with few sessions (8/110; 7%) terminated early per patient request.
Conclusion
This novel OT-guided cognitive intervention protocol is feasible in medical/surgical ICU patients. A larger randomized controlled trial is required to determine the impact of such a protocol on delirium prevalence or duration.
Study registration
www.ClinicalTrials.gov
(NCT03604809); registered 18 June 2018.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>36385466</pmid><doi>10.1007/s12630-022-02351-9</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-3674-3522</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink |
subjects | Anesthesiology Cardiology Clinical trials Cognition Coronaviruses COVID-19 COVID-19 - therapy Critical Care Medicine Critical Illness - psychology Critical Illness - therapy Delirium Delirium - prevention & control Delirium - psychology Feasibility Studies Humans Intensive Intensive Care Units Intervention Medicine Medicine & Public Health Occupational Therapists Occupational therapy Pain Medicine Pandemics Patients Pediatrics Pneumology/Respiratory System Quality of Life Reports of Original Investigations |
title | Occupational therapist-guided cognitive interventions in critically ill patients: a feasibility randomized controlled trial |
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