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Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study
BACKGROUND: Patterns of medication administration prior to in-hospital cardiac arrest (I-HCA) and the potential impact of these on patient outcomes is not well-established. Accordingly, types of medications administered in the 72 h prior to I-HCA were examined in relation to initial rhythms of I-HC...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104360/ https://www.ncbi.nlm.nih.gov/pubmed/33969325 http://dx.doi.org/10.1016/j.resplu.2020.100026 |
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author | Attin, Mina Abiola, Simeon Magu, Rijul Rosero, Spencer Apostolakos, Michael Groth, Christine M. Block, Robert Lin, C.D. (Joey) Intrator, Orna Hurley, Deborah Arcoleo, Kimberly |
author_facet | Attin, Mina Abiola, Simeon Magu, Rijul Rosero, Spencer Apostolakos, Michael Groth, Christine M. Block, Robert Lin, C.D. (Joey) Intrator, Orna Hurley, Deborah Arcoleo, Kimberly |
author_sort | Attin, Mina |
collection | PubMed |
description | BACKGROUND: Patterns of medication administration prior to in-hospital cardiac arrest (I-HCA) and the potential impact of these on patient outcomes is not well-established. Accordingly, types of medications administered in the 72 h prior to I-HCA were examined in relation to initial rhythms of I-HCA and survival. METHODS: A retrospective, pilot study was conducted among 96 patients who experienced I-HCA. Clinical characteristics and treatments including medications were extracted from electronic health records. Relative risk (RR) of medications or class of medications associated with the initial rhythms of I-HCA and return of spontaneous circulation (ROSC) were calculated. RESULTS: Two distinct sub-groups were identified that did not survive to hospital discharge (n = 31): 1) those who received either vasopressin/ desmopressin (n = 16) and 2) those who received combinations of psychotherapeutic agents with anxiolytics, sedatives, and hypnotics (n = 15) prior to I-HCA. The risk of pulseless electrical activity and asystolic arrest was high in patients who received sympathomimetic agents alone or in combination with β-Adrenergic blocking agents, (RR = 1.40, 1.41, respectively). Vasopressin and a combination of vasopressin and fentanyl were associated with risk of unsuccessful ROSC (RR = 2.50, 2.38, respectively). CONCLUSIONS: The types of medications administered during inpatient care may serve as a surrogate marker for identifying patients at risk of specific initial rhythms of I-HCA and survival. |
format | Online Article Text |
id | pubmed-8104360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81043602021-05-07 Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study Attin, Mina Abiola, Simeon Magu, Rijul Rosero, Spencer Apostolakos, Michael Groth, Christine M. Block, Robert Lin, C.D. (Joey) Intrator, Orna Hurley, Deborah Arcoleo, Kimberly Resusc Plus Clinical Paper BACKGROUND: Patterns of medication administration prior to in-hospital cardiac arrest (I-HCA) and the potential impact of these on patient outcomes is not well-established. Accordingly, types of medications administered in the 72 h prior to I-HCA were examined in relation to initial rhythms of I-HCA and survival. METHODS: A retrospective, pilot study was conducted among 96 patients who experienced I-HCA. Clinical characteristics and treatments including medications were extracted from electronic health records. Relative risk (RR) of medications or class of medications associated with the initial rhythms of I-HCA and return of spontaneous circulation (ROSC) were calculated. RESULTS: Two distinct sub-groups were identified that did not survive to hospital discharge (n = 31): 1) those who received either vasopressin/ desmopressin (n = 16) and 2) those who received combinations of psychotherapeutic agents with anxiolytics, sedatives, and hypnotics (n = 15) prior to I-HCA. The risk of pulseless electrical activity and asystolic arrest was high in patients who received sympathomimetic agents alone or in combination with β-Adrenergic blocking agents, (RR = 1.40, 1.41, respectively). Vasopressin and a combination of vasopressin and fentanyl were associated with risk of unsuccessful ROSC (RR = 2.50, 2.38, respectively). CONCLUSIONS: The types of medications administered during inpatient care may serve as a surrogate marker for identifying patients at risk of specific initial rhythms of I-HCA and survival. Elsevier 2020-10-09 /pmc/articles/PMC8104360/ /pubmed/33969325 http://dx.doi.org/10.1016/j.resplu.2020.100026 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Paper Attin, Mina Abiola, Simeon Magu, Rijul Rosero, Spencer Apostolakos, Michael Groth, Christine M. Block, Robert Lin, C.D. (Joey) Intrator, Orna Hurley, Deborah Arcoleo, Kimberly Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title | Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title_full | Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title_fullStr | Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title_full_unstemmed | Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title_short | Polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: A pilot study |
title_sort | polypharmacy prior to in-hospital cardiac arrest among patients with cardiopulmonary diseases: a pilot study |
topic | Clinical Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104360/ https://www.ncbi.nlm.nih.gov/pubmed/33969325 http://dx.doi.org/10.1016/j.resplu.2020.100026 |
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