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From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation

OBJECTIVES: To gain insight into the experiences of patients with diffuse cutaneous systemic sclerosis during and after autologous hematopoietic stem cell transplantation. METHODS: Semi-structured interviews were conducted with patients who underwent hematopoietic stem cell transplantation in four u...

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Autores principales: Spierings, Julia, de Bresser, Carolijn JM, van Rhijn-Brouwer, Femke CC, Pieterse, Arwen, Vonk, Madelon C, Voskuyl, Alexandre E, de Vries-Bouwstra, Jeska K, van Laar, Jacob M, Kars, Marijke C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922627/
https://www.ncbi.nlm.nih.gov/pubmed/35382525
http://dx.doi.org/10.1177/2397198320920436
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author Spierings, Julia
de Bresser, Carolijn JM
van Rhijn-Brouwer, Femke CC
Pieterse, Arwen
Vonk, Madelon C
Voskuyl, Alexandre E
de Vries-Bouwstra, Jeska K
van Laar, Jacob M
Kars, Marijke C
author_facet Spierings, Julia
de Bresser, Carolijn JM
van Rhijn-Brouwer, Femke CC
Pieterse, Arwen
Vonk, Madelon C
Voskuyl, Alexandre E
de Vries-Bouwstra, Jeska K
van Laar, Jacob M
Kars, Marijke C
author_sort Spierings, Julia
collection PubMed
description OBJECTIVES: To gain insight into the experiences of patients with diffuse cutaneous systemic sclerosis during and after autologous hematopoietic stem cell transplantation. METHODS: Semi-structured interviews were conducted with patients who underwent hematopoietic stem cell transplantation in four university hospitals in the Netherlands. Interviews were transcribed verbatim and thematically analyzed. RESULTS: Nine male and seven female patients were interviewed, median age 47 years (range: 27–68). Patients mentioned their life was severely disrupted before hematopoietic stem cell transplantation and remained unsettled a long time after treatment. Uncertainty because of disease progression, loss of control over health and the sense of time and fear of treatment-related adverse events were common during hospitalization. After hematopoietic stem cell transplantation, patients experienced more physical limitations than they had expected, and recovery took longer and was mentally taxing. Going back to work and finding a new balance in personal relations and social life was complicated. Patients described various strategies to deal with challenges. Family and friends provided essential support, although many experienced a dwindling social circle. Most patients also appreciated peer support. All patients were satisfied with the low threshold for contact with physicians and nurses during hospitalization. However, aftercare focused on medical aspects rather than on psychological well-being and social issues. Moreover, patients would have preferred to be better prepared on what to expect after discharge, and lacked information about self-management, prognosis, optimal recovery, work, sexuality, and family planning. CONCLUSION: Hematopoietic stem cell transplantation has a major physical and psychological impact on patients with diffuse cutaneous systemic sclerosis. The course of recovery after this intensive therapy was unexpectedly long for some patients and offer of support was far less pro-active post-HSCT compared to pre-HSCT and during HSCT.
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spelling pubmed-89226272022-04-04 From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation Spierings, Julia de Bresser, Carolijn JM van Rhijn-Brouwer, Femke CC Pieterse, Arwen Vonk, Madelon C Voskuyl, Alexandre E de Vries-Bouwstra, Jeska K van Laar, Jacob M Kars, Marijke C J Scleroderma Relat Disord Original Articles OBJECTIVES: To gain insight into the experiences of patients with diffuse cutaneous systemic sclerosis during and after autologous hematopoietic stem cell transplantation. METHODS: Semi-structured interviews were conducted with patients who underwent hematopoietic stem cell transplantation in four university hospitals in the Netherlands. Interviews were transcribed verbatim and thematically analyzed. RESULTS: Nine male and seven female patients were interviewed, median age 47 years (range: 27–68). Patients mentioned their life was severely disrupted before hematopoietic stem cell transplantation and remained unsettled a long time after treatment. Uncertainty because of disease progression, loss of control over health and the sense of time and fear of treatment-related adverse events were common during hospitalization. After hematopoietic stem cell transplantation, patients experienced more physical limitations than they had expected, and recovery took longer and was mentally taxing. Going back to work and finding a new balance in personal relations and social life was complicated. Patients described various strategies to deal with challenges. Family and friends provided essential support, although many experienced a dwindling social circle. Most patients also appreciated peer support. All patients were satisfied with the low threshold for contact with physicians and nurses during hospitalization. However, aftercare focused on medical aspects rather than on psychological well-being and social issues. Moreover, patients would have preferred to be better prepared on what to expect after discharge, and lacked information about self-management, prognosis, optimal recovery, work, sexuality, and family planning. CONCLUSION: Hematopoietic stem cell transplantation has a major physical and psychological impact on patients with diffuse cutaneous systemic sclerosis. The course of recovery after this intensive therapy was unexpectedly long for some patients and offer of support was far less pro-active post-HSCT compared to pre-HSCT and during HSCT. SAGE Publications 2020-05-28 2020-10 /pmc/articles/PMC8922627/ /pubmed/35382525 http://dx.doi.org/10.1177/2397198320920436 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Spierings, Julia
de Bresser, Carolijn JM
van Rhijn-Brouwer, Femke CC
Pieterse, Arwen
Vonk, Madelon C
Voskuyl, Alexandre E
de Vries-Bouwstra, Jeska K
van Laar, Jacob M
Kars, Marijke C
From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title_full From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title_fullStr From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title_full_unstemmed From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title_short From “being at war” to “getting back on your feet”: A qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
title_sort from “being at war” to “getting back on your feet”: a qualitative study on experiences of patients with systemic sclerosis treated with hematopoietic stem cell transplantation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8922627/
https://www.ncbi.nlm.nih.gov/pubmed/35382525
http://dx.doi.org/10.1177/2397198320920436
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