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The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients
BACKGROUND: Older patients are often users of prolonged Central Nervous System Depressants (CNSD) (Z-hypnotics, benzodiazepines and opioids), which may be associated with reduced cognition. The long-term effects of CNSD use and reduced cognitive function in older patients are unclear. The aim of thi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893618/ https://www.ncbi.nlm.nih.gov/pubmed/35239678 http://dx.doi.org/10.1371/journal.pone.0263024 |
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author | Siddiqui, Tahreem Ghazal Bjelkarøy, Maria Torheim Cheng, Socheat Kristoffersen, Espen Saxhaug Grambaite, Ramune Lundqvist, Christofer |
author_facet | Siddiqui, Tahreem Ghazal Bjelkarøy, Maria Torheim Cheng, Socheat Kristoffersen, Espen Saxhaug Grambaite, Ramune Lundqvist, Christofer |
author_sort | Siddiqui, Tahreem Ghazal |
collection | PubMed |
description | BACKGROUND: Older patients are often users of prolonged Central Nervous System Depressants (CNSD) (Z-hypnotics, benzodiazepines and opioids), which may be associated with reduced cognition. The long-term effects of CNSD use and reduced cognitive function in older patients are unclear. The aim of this study was to examine whether cognitive function and CNSD use at baseline hospitalisation were associated with all-cause mortality two years after discharge. METHODS: We conducted a prospective observational study, including baseline data (2017–2018) from previously hospitalised older patients (65–90 years), assessing all-cause mortality two years after discharge. We used logistic regression to assess the primary outcome, all-cause mortality two years after baseline hospitalisation. The primary predictors were cognitive function measured by The Mini Mental State Examination (MMSE) and prolonged CNSD use (continuous use ≥ 4 weeks). Adjustment variables: age, gender, education, the Hospital Anxiety and Depression Scale (HADS) and the Cumulative Illness Rating Scale for Geriatrics (CIRS-G), using receiver operating characteristics (ROC) to compare the predictive power of the models. In a sub-analysis we used, the Neurobehavioural Cognitive State Examination (Cognistat) and the Clock Drawing Test. RESULTS: Two years after discharge, out of 246 baseline patients, 43 were deceased at follow-up, among these 27 (63%) were CNSD users, and 16 (36%) were non-users at baseline, (p = 0.002). In the multivariable models cognitive function (MMSE score) was a predictor of mortality (OR 0.81 (95% CI 0.69; 0.96), p = 0.014). CNSD use was associated with mortality (OR 2.71 (95% CI 1.06; 6.95), p = 0.038), with ROC AUC: 0.74–0.77 for these models. Results using Cognistat supported the findings. The Clock Drawing Test was not significant predictor of mortality. CONCLUSION: Two years after discharge from the hospital, older patients with reduced cognitive function and CNSD use during hospital stay had higher mortality. This underlines that inappropriate (prolonged and concurrent) use of CNSDs should be avoided by older patients, particularly in patients with reduced cognitive function. TRIAL REGISTRATION: NCT03162081, 22 May 2017. |
format | Online Article Text |
id | pubmed-8893618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88936182022-03-04 The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients Siddiqui, Tahreem Ghazal Bjelkarøy, Maria Torheim Cheng, Socheat Kristoffersen, Espen Saxhaug Grambaite, Ramune Lundqvist, Christofer PLoS One Research Article BACKGROUND: Older patients are often users of prolonged Central Nervous System Depressants (CNSD) (Z-hypnotics, benzodiazepines and opioids), which may be associated with reduced cognition. The long-term effects of CNSD use and reduced cognitive function in older patients are unclear. The aim of this study was to examine whether cognitive function and CNSD use at baseline hospitalisation were associated with all-cause mortality two years after discharge. METHODS: We conducted a prospective observational study, including baseline data (2017–2018) from previously hospitalised older patients (65–90 years), assessing all-cause mortality two years after discharge. We used logistic regression to assess the primary outcome, all-cause mortality two years after baseline hospitalisation. The primary predictors were cognitive function measured by The Mini Mental State Examination (MMSE) and prolonged CNSD use (continuous use ≥ 4 weeks). Adjustment variables: age, gender, education, the Hospital Anxiety and Depression Scale (HADS) and the Cumulative Illness Rating Scale for Geriatrics (CIRS-G), using receiver operating characteristics (ROC) to compare the predictive power of the models. In a sub-analysis we used, the Neurobehavioural Cognitive State Examination (Cognistat) and the Clock Drawing Test. RESULTS: Two years after discharge, out of 246 baseline patients, 43 were deceased at follow-up, among these 27 (63%) were CNSD users, and 16 (36%) were non-users at baseline, (p = 0.002). In the multivariable models cognitive function (MMSE score) was a predictor of mortality (OR 0.81 (95% CI 0.69; 0.96), p = 0.014). CNSD use was associated with mortality (OR 2.71 (95% CI 1.06; 6.95), p = 0.038), with ROC AUC: 0.74–0.77 for these models. Results using Cognistat supported the findings. The Clock Drawing Test was not significant predictor of mortality. CONCLUSION: Two years after discharge from the hospital, older patients with reduced cognitive function and CNSD use during hospital stay had higher mortality. This underlines that inappropriate (prolonged and concurrent) use of CNSDs should be avoided by older patients, particularly in patients with reduced cognitive function. TRIAL REGISTRATION: NCT03162081, 22 May 2017. Public Library of Science 2022-03-03 /pmc/articles/PMC8893618/ /pubmed/35239678 http://dx.doi.org/10.1371/journal.pone.0263024 Text en © 2022 Siddiqui et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Siddiqui, Tahreem Ghazal Bjelkarøy, Maria Torheim Cheng, Socheat Kristoffersen, Espen Saxhaug Grambaite, Ramune Lundqvist, Christofer The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title | The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title_full | The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title_fullStr | The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title_full_unstemmed | The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title_short | The effect of cognitive function and central nervous system depressant use on mortality—A prospective observational study of previously hospitalised older patients |
title_sort | effect of cognitive function and central nervous system depressant use on mortality—a prospective observational study of previously hospitalised older patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893618/ https://www.ncbi.nlm.nih.gov/pubmed/35239678 http://dx.doi.org/10.1371/journal.pone.0263024 |
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