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“Like not having an arm”: a qualitative study of the impact of visitor restrictions on cancer care during the COVID-19 pandemic
by
Verano, Mae
, Schapira, Lidia
, Tabor, Holly K.
, Lessios, Anna Sophia
, Holdsworth, Laura M.
, Aslakson, Rebecca
, Siden, Rachel
, Wong, Bonnie O.
in
Arm
/ Burnout
/ Cancer
/ Cancer patients
/ Care and treatment
/ Caregivers
/ Caregivers - psychology
/ Clinical outcomes
/ COVID-19
/ COVID-19 - prevention & control
/ Decision making
/ Epidemics
/ Health aspects
/ Hospitals
/ Humans
/ Medical care
/ Medical decision making
/ Medical treatment
/ Medicine
/ Medicine & Public Health
/ Negative experiences
/ Neoplasms - psychology
/ Neoplasms - therapy
/ Nursing
/ Nursing Research
/ Oncology
/ Oncology, Experimental
/ Pain Medicine
/ Palliative care
/ Palliative treatment
/ Pandemics
/ Pandemics - prevention & control
/ Patients
/ Physicians
/ Practitioner patient relationship
/ Psychosocial factors
/ Qualitative Research
/ Quality management
/ Quality of care
/ Rehabilitation Medicine
/ Restrictions
/ Therapeutic alliances
2024
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“Like not having an arm”: a qualitative study of the impact of visitor restrictions on cancer care during the COVID-19 pandemic
by
Verano, Mae
, Schapira, Lidia
, Tabor, Holly K.
, Lessios, Anna Sophia
, Holdsworth, Laura M.
, Aslakson, Rebecca
, Siden, Rachel
, Wong, Bonnie O.
in
Arm
/ Burnout
/ Cancer
/ Cancer patients
/ Care and treatment
/ Caregivers
/ Caregivers - psychology
/ Clinical outcomes
/ COVID-19
/ COVID-19 - prevention & control
/ Decision making
/ Epidemics
/ Health aspects
/ Hospitals
/ Humans
/ Medical care
/ Medical decision making
/ Medical treatment
/ Medicine
/ Medicine & Public Health
/ Negative experiences
/ Neoplasms - psychology
/ Neoplasms - therapy
/ Nursing
/ Nursing Research
/ Oncology
/ Oncology, Experimental
/ Pain Medicine
/ Palliative care
/ Palliative treatment
/ Pandemics
/ Pandemics - prevention & control
/ Patients
/ Physicians
/ Practitioner patient relationship
/ Psychosocial factors
/ Qualitative Research
/ Quality management
/ Quality of care
/ Rehabilitation Medicine
/ Restrictions
/ Therapeutic alliances
2024
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Do you wish to request the book?
“Like not having an arm”: a qualitative study of the impact of visitor restrictions on cancer care during the COVID-19 pandemic
by
Verano, Mae
, Schapira, Lidia
, Tabor, Holly K.
, Lessios, Anna Sophia
, Holdsworth, Laura M.
, Aslakson, Rebecca
, Siden, Rachel
, Wong, Bonnie O.
in
Arm
/ Burnout
/ Cancer
/ Cancer patients
/ Care and treatment
/ Caregivers
/ Caregivers - psychology
/ Clinical outcomes
/ COVID-19
/ COVID-19 - prevention & control
/ Decision making
/ Epidemics
/ Health aspects
/ Hospitals
/ Humans
/ Medical care
/ Medical decision making
/ Medical treatment
/ Medicine
/ Medicine & Public Health
/ Negative experiences
/ Neoplasms - psychology
/ Neoplasms - therapy
/ Nursing
/ Nursing Research
/ Oncology
/ Oncology, Experimental
/ Pain Medicine
/ Palliative care
/ Palliative treatment
/ Pandemics
/ Pandemics - prevention & control
/ Patients
/ Physicians
/ Practitioner patient relationship
/ Psychosocial factors
/ Qualitative Research
/ Quality management
/ Quality of care
/ Rehabilitation Medicine
/ Restrictions
/ Therapeutic alliances
2024
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“Like not having an arm”: a qualitative study of the impact of visitor restrictions on cancer care during the COVID-19 pandemic
Journal Article
“Like not having an arm”: a qualitative study of the impact of visitor restrictions on cancer care during the COVID-19 pandemic
2024
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Overview
Purpose
Visitor restriction policies to prevent the spread of COVID-19 among patients and clinicians were widespread during the pandemic, resulting in the exclusion of caregivers at key points of cancer care and treatment decision-making. The aim of this study was to explore how visitor restrictions impacted cancer treatment decision-making and care from patient and physician perspectives.
Methods
Sixty-seven interviews, including 48 cancer patients and 19 cancer and palliative care physicians from four academic cancer centers in the USA between August 2020 and July 2021.
Results
Visitor restrictions that prevented caregivers from participating in clinic appointments and perioperative hospital care created challenges in cancer care that spanned three domains: practical, social, and informational. We identified eight themes that characterized challenges within the three domains across all three groups, and that these challenges had negative emotional and psychological consequences for both groups. Physicians perceived that patients’ negative experiences due to lack of support through the physical presence of caregivers may have worsened patient outcomes.
Conclusions
Our data demonstrate the tripartite structure of the therapeutic relationship in cancer care with caregivers providing critical support in the decision-making and care process to both patients and physicians. Caregiver absences led to practical, psychosocial, and informational burdens on both groups, and likely increased the risk of burnout among physicians. Our findings suggest that the quality of cancer care can be enhanced by engaging caregivers and promoting their physical presence during clinical encounters.
Publisher
Springer Berlin Heidelberg,Springer,Springer Nature B.V
Subject
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