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Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study

BACKGROUND: Cognitive impairment is commonly reported in patients receiving chemotherapy, but the acuity of onset is not known. This study utilized the psychomotor vigilance test (PVT) and trail-making test B (TMT-B) to assess cognitive impairment immediately post-chemotherapy. METHODS: Patients age...

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Autores principales: Khan, Omar F., Cusano, Ellen, Raissouni, Soundouss, Pabia, Mica, Haeseker, Johanna, Bosma, Nicholas, Ko, Jenny J., Li, Haocheng, Kumar, Aalok, Vickers, Michael M., Tang, Patricia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375158/
https://www.ncbi.nlm.nih.gov/pubmed/30764801
http://dx.doi.org/10.1186/s12885-019-5349-2
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author Khan, Omar F.
Cusano, Ellen
Raissouni, Soundouss
Pabia, Mica
Haeseker, Johanna
Bosma, Nicholas
Ko, Jenny J.
Li, Haocheng
Kumar, Aalok
Vickers, Michael M.
Tang, Patricia A.
author_facet Khan, Omar F.
Cusano, Ellen
Raissouni, Soundouss
Pabia, Mica
Haeseker, Johanna
Bosma, Nicholas
Ko, Jenny J.
Li, Haocheng
Kumar, Aalok
Vickers, Michael M.
Tang, Patricia A.
author_sort Khan, Omar F.
collection PubMed
description BACKGROUND: Cognitive impairment is commonly reported in patients receiving chemotherapy, but the acuity of onset is not known. This study utilized the psychomotor vigilance test (PVT) and trail-making test B (TMT-B) to assess cognitive impairment immediately post-chemotherapy. METHODS: Patients aged 18–80 years receiving first-line intravenous chemotherapy for any stage of breast or colorectal cancer were eligible. Patient symptoms, peripheral neuropathy and Stanford Sleepiness Scale were assessed. A five-minute PVT and TMT-B were completed on a tablet computer pre-chemotherapy and immediately post-chemotherapy. Using a mixed linear regression model, changes in reciprocal transformed PVT reaction time (mean 1/RT) were assessed. A priori, an increase in median PVT reaction times by > 20 ms (approximating PVT changes with blood alcohol concentrations of 0.04–0.05 g%) was considered clinically relevant. RESULTS: One hundred forty-two cancer patients (73 breast, 69 colorectal, median age 55.5 years) were tested. Post-chemotherapy, mean 1/RT values were significantly slowed compared to pre-chemotherapy baseline (p = 0.01). This corresponded to a median PVT reaction time slowed by an average of 12.4 ms. Changes in PVT reaction times were not correlated with age, sex, cancer type, treatment setting, or use of supportive medications. Median post-chemotherapy PVT reaction time slowed by an average of 22.5 ms in breast cancer patients and by 1.6 ms in colorectal cancer patients. Post-chemotherapy median PVT times slowed by > 20 ms in 57 patients (40.1%). Exploratory analyses found no statistically significant association between the primary outcome and self-reported anxiety, fatigue or depression. TMT-B completion speed improved significantly post-chemotherapy (p = 0.03), likely due to test-retest phenomenon. CONCLUSIONS: PVT reaction time slowed significantly immediately post-chemotherapy compared to a pre-chemotherapy baseline, and levels of impairment similar to effects of alcohol consumption in other studies was seen in 40% of patients. Further studies assessing functional impact of cognitive impairment on patients immediately after chemotherapy are warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5349-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-63751582019-02-26 Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study Khan, Omar F. Cusano, Ellen Raissouni, Soundouss Pabia, Mica Haeseker, Johanna Bosma, Nicholas Ko, Jenny J. Li, Haocheng Kumar, Aalok Vickers, Michael M. Tang, Patricia A. BMC Cancer Research Article BACKGROUND: Cognitive impairment is commonly reported in patients receiving chemotherapy, but the acuity of onset is not known. This study utilized the psychomotor vigilance test (PVT) and trail-making test B (TMT-B) to assess cognitive impairment immediately post-chemotherapy. METHODS: Patients aged 18–80 years receiving first-line intravenous chemotherapy for any stage of breast or colorectal cancer were eligible. Patient symptoms, peripheral neuropathy and Stanford Sleepiness Scale were assessed. A five-minute PVT and TMT-B were completed on a tablet computer pre-chemotherapy and immediately post-chemotherapy. Using a mixed linear regression model, changes in reciprocal transformed PVT reaction time (mean 1/RT) were assessed. A priori, an increase in median PVT reaction times by > 20 ms (approximating PVT changes with blood alcohol concentrations of 0.04–0.05 g%) was considered clinically relevant. RESULTS: One hundred forty-two cancer patients (73 breast, 69 colorectal, median age 55.5 years) were tested. Post-chemotherapy, mean 1/RT values were significantly slowed compared to pre-chemotherapy baseline (p = 0.01). This corresponded to a median PVT reaction time slowed by an average of 12.4 ms. Changes in PVT reaction times were not correlated with age, sex, cancer type, treatment setting, or use of supportive medications. Median post-chemotherapy PVT reaction time slowed by an average of 22.5 ms in breast cancer patients and by 1.6 ms in colorectal cancer patients. Post-chemotherapy median PVT times slowed by > 20 ms in 57 patients (40.1%). Exploratory analyses found no statistically significant association between the primary outcome and self-reported anxiety, fatigue or depression. TMT-B completion speed improved significantly post-chemotherapy (p = 0.03), likely due to test-retest phenomenon. CONCLUSIONS: PVT reaction time slowed significantly immediately post-chemotherapy compared to a pre-chemotherapy baseline, and levels of impairment similar to effects of alcohol consumption in other studies was seen in 40% of patients. Further studies assessing functional impact of cognitive impairment on patients immediately after chemotherapy are warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5349-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-14 /pmc/articles/PMC6375158/ /pubmed/30764801 http://dx.doi.org/10.1186/s12885-019-5349-2 Text en © The Author(s). 2019 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
Khan, Omar F.
Cusano, Ellen
Raissouni, Soundouss
Pabia, Mica
Haeseker, Johanna
Bosma, Nicholas
Ko, Jenny J.
Li, Haocheng
Kumar, Aalok
Vickers, Michael M.
Tang, Patricia A.
Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title_full Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title_fullStr Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title_full_unstemmed Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title_short Immediate-term cognitive impairment following intravenous (IV) chemotherapy: a prospective pre-post design study
title_sort immediate-term cognitive impairment following intravenous (iv) chemotherapy: a prospective pre-post design study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6375158/
https://www.ncbi.nlm.nih.gov/pubmed/30764801
http://dx.doi.org/10.1186/s12885-019-5349-2
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