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Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center
BACKGROUND: Palliative sedation (PS) is an intervention to treat refractory symptoms and to relieve suffering at the end of life. Its prevalence and practice patterns vary widely worldwide. The aim of our study was to evaluate the frequency, clinical indications and outcomes of PS in advanced cancer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755023/ https://www.ncbi.nlm.nih.gov/pubmed/29301574 http://dx.doi.org/10.1186/s12904-017-0264-2 |
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author | Prado, Bernard Lobato Gomes, Diogo Bugano Diniz Usón Júnior, Pedro Luiz Serrano Taranto, Patricia França, Monique Sedlmaier Eiger, Daniel Mariano, Rodrigo Coutinho Hui, David Del Giglio, Auro |
author_facet | Prado, Bernard Lobato Gomes, Diogo Bugano Diniz Usón Júnior, Pedro Luiz Serrano Taranto, Patricia França, Monique Sedlmaier Eiger, Daniel Mariano, Rodrigo Coutinho Hui, David Del Giglio, Auro |
author_sort | Prado, Bernard Lobato |
collection | PubMed |
description | BACKGROUND: Palliative sedation (PS) is an intervention to treat refractory symptoms and to relieve suffering at the end of life. Its prevalence and practice patterns vary widely worldwide. The aim of our study was to evaluate the frequency, clinical indications and outcomes of PS in advanced cancer patients admitted to our tertiary comprehensive cancer center. METHODS: We retrospectively studied the use of PS in advanced cancer patients who died between March 1st, 2012 and December 31st, 2014. PS was defined as the use of continuous infusion of midazolam or neuroleptics for refractory symptoms in the end of life. This study was approved by the Research Ethics Committee of our institution (project number 2481–15). RESULTS: During the study period, 552 cancer patients died at the institution and 374 met the inclusion criteria for this study. Main reason for exclusion was death in the Intensive Care Unit. Among all included patients, 54.2% (n = 203) received PS. Patients who received PS as compared to those not sedated were younger (67.8 vs. 76.4 years-old, p < 0.001) and more likely to have a diagnosis of lung cancer (23% vs. 14%, p = 0.028). The most common indications for sedation were dyspnea (55%) and delirium (19.7%) and the most common drugs used were midazolam (52.7%) or midazolam and a neuroleptic (39.4%). Median initial midazolam infusion rate was 0.75 mg/h (interquartile range – IQR - 0.6-1.5) and final rate was 1.5 mg/h (IQR 0.9–3.0). Patient survival (length of hospital stay from admission to death) of those who had PS was more than the double of those who did not (33.6 days vs 16 days, p < 0.001). The palliative care team was involved in the care of 12% (n = 25) of sedated patients. CONCLUSIONS: PS is a relatively common practice in the end-of-life of cancer patients at our hospital and it is not associated with shortening of hospital stay. Involvement of a dedicated palliative care team is strongly recommended if this procedure is being considered. Further research is needed to identify factors that may affect the frequency and outcomes associated with PS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12904-017-0264-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5755023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57550232018-01-08 Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center Prado, Bernard Lobato Gomes, Diogo Bugano Diniz Usón Júnior, Pedro Luiz Serrano Taranto, Patricia França, Monique Sedlmaier Eiger, Daniel Mariano, Rodrigo Coutinho Hui, David Del Giglio, Auro BMC Palliat Care Research Article BACKGROUND: Palliative sedation (PS) is an intervention to treat refractory symptoms and to relieve suffering at the end of life. Its prevalence and practice patterns vary widely worldwide. The aim of our study was to evaluate the frequency, clinical indications and outcomes of PS in advanced cancer patients admitted to our tertiary comprehensive cancer center. METHODS: We retrospectively studied the use of PS in advanced cancer patients who died between March 1st, 2012 and December 31st, 2014. PS was defined as the use of continuous infusion of midazolam or neuroleptics for refractory symptoms in the end of life. This study was approved by the Research Ethics Committee of our institution (project number 2481–15). RESULTS: During the study period, 552 cancer patients died at the institution and 374 met the inclusion criteria for this study. Main reason for exclusion was death in the Intensive Care Unit. Among all included patients, 54.2% (n = 203) received PS. Patients who received PS as compared to those not sedated were younger (67.8 vs. 76.4 years-old, p < 0.001) and more likely to have a diagnosis of lung cancer (23% vs. 14%, p = 0.028). The most common indications for sedation were dyspnea (55%) and delirium (19.7%) and the most common drugs used were midazolam (52.7%) or midazolam and a neuroleptic (39.4%). Median initial midazolam infusion rate was 0.75 mg/h (interquartile range – IQR - 0.6-1.5) and final rate was 1.5 mg/h (IQR 0.9–3.0). Patient survival (length of hospital stay from admission to death) of those who had PS was more than the double of those who did not (33.6 days vs 16 days, p < 0.001). The palliative care team was involved in the care of 12% (n = 25) of sedated patients. CONCLUSIONS: PS is a relatively common practice in the end-of-life of cancer patients at our hospital and it is not associated with shortening of hospital stay. Involvement of a dedicated palliative care team is strongly recommended if this procedure is being considered. Further research is needed to identify factors that may affect the frequency and outcomes associated with PS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12904-017-0264-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-04 /pmc/articles/PMC5755023/ /pubmed/29301574 http://dx.doi.org/10.1186/s12904-017-0264-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Prado, Bernard Lobato Gomes, Diogo Bugano Diniz Usón Júnior, Pedro Luiz Serrano Taranto, Patricia França, Monique Sedlmaier Eiger, Daniel Mariano, Rodrigo Coutinho Hui, David Del Giglio, Auro Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title | Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title_full | Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title_fullStr | Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title_full_unstemmed | Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title_short | Continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
title_sort | continuous palliative sedation for patients with advanced cancer at a tertiary care cancer center |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755023/ https://www.ncbi.nlm.nih.gov/pubmed/29301574 http://dx.doi.org/10.1186/s12904-017-0264-2 |
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