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- Publisher Website: 10.1136/bmjopen-2023-075518
- Scopus: eid_2-s2.0-85169758496
- PMID: 37669840
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Article: Comorbidities, symptoms and end-of-life medication use in hospitalised decedents before and during the COVID-19 pandemic: a retrospective regional cohort study in Ottawa, Canada
Title | Comorbidities, symptoms and end-of-life medication use in hospitalised decedents before and during the COVID-19 pandemic: a retrospective regional cohort study in Ottawa, Canada |
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Authors | Lawlor, PeterCohen, LeilaAdeli, Samantha RoseBesserer, EllaGratton, ValérieMurphy, RebekahWarmels, GraceBruni, AdriannaKabir, MonishaNoel, ChelseaHeidinger, BrandonAnderson, KobyArsenault-Mehta, KyleWooller, KristaLapenskie, JulieWebber, ColleenBedard, DanielEnright, PaulaDesjardins, IsabelleBhimji, KhadijaDyason, ClaireIyengar, AkshaiBush, Shirley H.Isenberg, SarinaTanuseputro, PeterVanderspank-Wright, BrandiDownar, JamesParsons, Henrique |
Keywords | adult intensive & critical care adult palliative care COVID-19 pain management |
Issue Date | 2023 |
Citation | BMJ Open, 2023, v. 13, n. 9, article no. e075518 How to Cite? |
Abstract | Objective To compare comorbidities, symptoms and end-of-life (EoL) palliative medication (antisecretories, opioids, antipsychotics and sedatives) use among decedents before and during the COVID-19 pandemic. Design In a retrospective cohort study, decedent records in three acute care hospitals were abstracted, generating a prepandemic (November 2019-February 2020) group (pre-COVID) and two intrapandemic (March-August 2020, wave 1) groups, one without (COVID-ve) and one with COVID-19 infection (COVID+ve). Control group decedents were matched 2:1 on age, sex and care service (medicine/intensive care unit (ICU)) with COVID+ve decedents. Setting Three regional acute care teaching hospitals in Ottawa, Canada Participants Decedents (N=425): COVID+ve (n=85), COVID-ve (n=170) and pre-COVID (n=170). Main outcome measures Data were abstracted regarding demographics, admission comorbidities and symptoms, and EoL medication use; opioid doses were standardised to parenteral morphine equivalent daily dose (MEDD), and the predictors of upper quartile MEDD in the last 24 hours of life were examined in multivariable logistic regression with adjusted ORs (aORs) and 95% CIs. Results The prevalence of dementia (41% vs 28% and 26%, p=0.03), breathlessness (63.5% vs 42% and 47%, p<0.01), cough (40% vs 27% and 19%, p<0.01) and fever (54% vs 9% and 13.5%) was higher in COVID+ve versus pre-COVID and COVID-ve groups, respectively. The median (IQR) of MEDD over the last 72 hours of life was 16.7 (9-36.5) vs 13.5 (5.7-21.8) and 10.5 (5.3-23.8) for COVID+ve versus pre-COVID and COVID-ve groups, respectively, (p=0.007). Male sex, COVID+ve grouping, ICU death and high-flow nasal cannula use predicted upper quartile MEDD dose, aORs (95% CIs): 1.84 (1.05 to 3.22), 2.62 (1.29 to 5.3), 5.14 (2.47 to 10.7) and 1.93 (1.05 to 3.52), respectively. COVID+ve group decedents used highest lorazepam and propofol doses. Conclusions COVID-19 decedents, particularly those in ICU, required higher EoL opioid and sedating medication doses than matched prepandemic or intrapandemic controls. These findings should inform and guide clinical practice. |
Persistent Identifier | http://hdl.handle.net/10722/347064 |
DC Field | Value | Language |
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dc.contributor.author | Lawlor, Peter | - |
dc.contributor.author | Cohen, Leila | - |
dc.contributor.author | Adeli, Samantha Rose | - |
dc.contributor.author | Besserer, Ella | - |
dc.contributor.author | Gratton, Valérie | - |
dc.contributor.author | Murphy, Rebekah | - |
dc.contributor.author | Warmels, Grace | - |
dc.contributor.author | Bruni, Adrianna | - |
dc.contributor.author | Kabir, Monisha | - |
dc.contributor.author | Noel, Chelsea | - |
dc.contributor.author | Heidinger, Brandon | - |
dc.contributor.author | Anderson, Koby | - |
dc.contributor.author | Arsenault-Mehta, Kyle | - |
dc.contributor.author | Wooller, Krista | - |
dc.contributor.author | Lapenskie, Julie | - |
dc.contributor.author | Webber, Colleen | - |
dc.contributor.author | Bedard, Daniel | - |
dc.contributor.author | Enright, Paula | - |
dc.contributor.author | Desjardins, Isabelle | - |
dc.contributor.author | Bhimji, Khadija | - |
dc.contributor.author | Dyason, Claire | - |
dc.contributor.author | Iyengar, Akshai | - |
dc.contributor.author | Bush, Shirley H. | - |
dc.contributor.author | Isenberg, Sarina | - |
dc.contributor.author | Tanuseputro, Peter | - |
dc.contributor.author | Vanderspank-Wright, Brandi | - |
dc.contributor.author | Downar, James | - |
dc.contributor.author | Parsons, Henrique | - |
dc.date.accessioned | 2024-09-17T04:15:07Z | - |
dc.date.available | 2024-09-17T04:15:07Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | BMJ Open, 2023, v. 13, n. 9, article no. e075518 | - |
dc.identifier.uri | http://hdl.handle.net/10722/347064 | - |
dc.description.abstract | Objective To compare comorbidities, symptoms and end-of-life (EoL) palliative medication (antisecretories, opioids, antipsychotics and sedatives) use among decedents before and during the COVID-19 pandemic. Design In a retrospective cohort study, decedent records in three acute care hospitals were abstracted, generating a prepandemic (November 2019-February 2020) group (pre-COVID) and two intrapandemic (March-August 2020, wave 1) groups, one without (COVID-ve) and one with COVID-19 infection (COVID+ve). Control group decedents were matched 2:1 on age, sex and care service (medicine/intensive care unit (ICU)) with COVID+ve decedents. Setting Three regional acute care teaching hospitals in Ottawa, Canada Participants Decedents (N=425): COVID+ve (n=85), COVID-ve (n=170) and pre-COVID (n=170). Main outcome measures Data were abstracted regarding demographics, admission comorbidities and symptoms, and EoL medication use; opioid doses were standardised to parenteral morphine equivalent daily dose (MEDD), and the predictors of upper quartile MEDD in the last 24 hours of life were examined in multivariable logistic regression with adjusted ORs (aORs) and 95% CIs. Results The prevalence of dementia (41% vs 28% and 26%, p=0.03), breathlessness (63.5% vs 42% and 47%, p<0.01), cough (40% vs 27% and 19%, p<0.01) and fever (54% vs 9% and 13.5%) was higher in COVID+ve versus pre-COVID and COVID-ve groups, respectively. The median (IQR) of MEDD over the last 72 hours of life was 16.7 (9-36.5) vs 13.5 (5.7-21.8) and 10.5 (5.3-23.8) for COVID+ve versus pre-COVID and COVID-ve groups, respectively, (p=0.007). Male sex, COVID+ve grouping, ICU death and high-flow nasal cannula use predicted upper quartile MEDD dose, aORs (95% CIs): 1.84 (1.05 to 3.22), 2.62 (1.29 to 5.3), 5.14 (2.47 to 10.7) and 1.93 (1.05 to 3.52), respectively. COVID+ve group decedents used highest lorazepam and propofol doses. Conclusions COVID-19 decedents, particularly those in ICU, required higher EoL opioid and sedating medication doses than matched prepandemic or intrapandemic controls. These findings should inform and guide clinical practice. | - |
dc.language | eng | - |
dc.relation.ispartof | BMJ Open | - |
dc.subject | adult intensive & critical care | - |
dc.subject | adult palliative care | - |
dc.subject | COVID-19 | - |
dc.subject | pain management | - |
dc.title | Comorbidities, symptoms and end-of-life medication use in hospitalised decedents before and during the COVID-19 pandemic: a retrospective regional cohort study in Ottawa, Canada | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1136/bmjopen-2023-075518 | - |
dc.identifier.pmid | 37669840 | - |
dc.identifier.scopus | eid_2-s2.0-85169758496 | - |
dc.identifier.volume | 13 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | article no. e075518 | - |
dc.identifier.epage | article no. e075518 | - |
dc.identifier.eissn | 2044-6055 | - |