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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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