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The Patient Perspective on Living with Acute Myeloid Leukemia
INTRODUCTION: Acute myeloid leukemia (AML) imposes significant burden on patients, their families, and the healthcare system. Published literature has reported many AML signs and symptoms, as well as their impact on patients. However, there are no publications on the experience of living with AML fr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315065/ https://www.ncbi.nlm.nih.gov/pubmed/28261652 http://dx.doi.org/10.1007/s40487-016-0029-8 |
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author | Tomaszewski, Erin L. Fickley, Catherine E. Maddux, LeAnne Krupnick, Robert Bahceci, Erkut Paty, Jean van Nooten, Floortje |
author_facet | Tomaszewski, Erin L. Fickley, Catherine E. Maddux, LeAnne Krupnick, Robert Bahceci, Erkut Paty, Jean van Nooten, Floortje |
author_sort | Tomaszewski, Erin L. |
collection | PubMed |
description | INTRODUCTION: Acute myeloid leukemia (AML) imposes significant burden on patients, their families, and the healthcare system. Published literature has reported many AML signs and symptoms, as well as their impact on patients. However, there are no publications on the experience of living with AML from the patient's perspective. In this study, we performed qualitative interviews with patients with AML to understand their experience. METHODS: Participants were recruited from the US and Japan. All patients were screened to assess eligibility, and were divided into four subgroups (i.e., newly-diagnosed, high-intensity chemotherapy; newly-diagnosed, low-intensity chemotherapy; relapse/refractory; and post-transplant). Patients were interviewed over the phone by a trained researcher and asked about their day-to-day experience with AML. Signs/symptoms and impacts were coded, analyzed using Atlas.ti software, and reported as frequencies, with the medians of patient-reported disturbance levels (0–10) computed for each symptom and impact. RESULTS: The most commonly reported sign/symptom in the US was fatigue (95.7%), followed by bruising and weakness (both 78.3%), and in Japan, nausea (94.4%), followed by fatigue and headache (both 88.9%). The most commonly reported impact in the US was a decreased ability to maintain social/familial roles (91.3%), followed by anxiety and a decreased ability to function (both 87.0%), and most commonly reported in Japan was anxiety, a decreased ability to function, and remission uncertainty (94.4%). CONCLUSION: Although the frequency of signs/symptoms and their level of disturbance varied between the US and Japan, there was remarkable consistency in the types of signs/symptoms and impacts reported across all patients. The consistency in the experience of the disease across patients suggests that measurement of AML experience can be achieved by using the same tool for most, if not all, of these patients. FUNDING: Astellas Pharma Inc., Northbrook, IL, USA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40487-016-0029-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5315065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-53150652017-03-02 The Patient Perspective on Living with Acute Myeloid Leukemia Tomaszewski, Erin L. Fickley, Catherine E. Maddux, LeAnne Krupnick, Robert Bahceci, Erkut Paty, Jean van Nooten, Floortje Oncol Ther Original Research INTRODUCTION: Acute myeloid leukemia (AML) imposes significant burden on patients, their families, and the healthcare system. Published literature has reported many AML signs and symptoms, as well as their impact on patients. However, there are no publications on the experience of living with AML from the patient's perspective. In this study, we performed qualitative interviews with patients with AML to understand their experience. METHODS: Participants were recruited from the US and Japan. All patients were screened to assess eligibility, and were divided into four subgroups (i.e., newly-diagnosed, high-intensity chemotherapy; newly-diagnosed, low-intensity chemotherapy; relapse/refractory; and post-transplant). Patients were interviewed over the phone by a trained researcher and asked about their day-to-day experience with AML. Signs/symptoms and impacts were coded, analyzed using Atlas.ti software, and reported as frequencies, with the medians of patient-reported disturbance levels (0–10) computed for each symptom and impact. RESULTS: The most commonly reported sign/symptom in the US was fatigue (95.7%), followed by bruising and weakness (both 78.3%), and in Japan, nausea (94.4%), followed by fatigue and headache (both 88.9%). The most commonly reported impact in the US was a decreased ability to maintain social/familial roles (91.3%), followed by anxiety and a decreased ability to function (both 87.0%), and most commonly reported in Japan was anxiety, a decreased ability to function, and remission uncertainty (94.4%). CONCLUSION: Although the frequency of signs/symptoms and their level of disturbance varied between the US and Japan, there was remarkable consistency in the types of signs/symptoms and impacts reported across all patients. The consistency in the experience of the disease across patients suggests that measurement of AML experience can be achieved by using the same tool for most, if not all, of these patients. FUNDING: Astellas Pharma Inc., Northbrook, IL, USA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40487-016-0029-8) contains supplementary material, which is available to authorized users. Springer Healthcare 2016-09-02 /pmc/articles/PMC5315065/ /pubmed/28261652 http://dx.doi.org/10.1007/s40487-016-0029-8 Text en © Springer Healthcare 2016 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial 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. |
spellingShingle | Original Research Tomaszewski, Erin L. Fickley, Catherine E. Maddux, LeAnne Krupnick, Robert Bahceci, Erkut Paty, Jean van Nooten, Floortje The Patient Perspective on Living with Acute Myeloid Leukemia |
title | The Patient Perspective on Living with Acute Myeloid Leukemia |
title_full | The Patient Perspective on Living with Acute Myeloid Leukemia |
title_fullStr | The Patient Perspective on Living with Acute Myeloid Leukemia |
title_full_unstemmed | The Patient Perspective on Living with Acute Myeloid Leukemia |
title_short | The Patient Perspective on Living with Acute Myeloid Leukemia |
title_sort | patient perspective on living with acute myeloid leukemia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315065/ https://www.ncbi.nlm.nih.gov/pubmed/28261652 http://dx.doi.org/10.1007/s40487-016-0029-8 |
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