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Patients are part of a family network. When any person in a family becomes critically unwell and requires the assistance of an Intensive Care Unit (ICU), this has an impact on all members of that family.
COVID-19 changed visiting for all patients in hospitals across Scotland. It is not known what effect these restrictions will have on patients' recovery, nor do we understand the impact it may have on their relatives or staff caring for them. This study will look at the implications of the visiting restrictions as a consequence of the COVID-19 pandemic upon patients without COVID-19 who are in the cardiothoracic ICU. It will also explore the impact of these restrictions on them, their relatives and staff.
This study will be carried out within a single specialised intensive care unit in Scotland using mixed methods.
The first arm of this study will use retrospective data that is routinely collected in normal clinical practice. The investigators will compare patient outcomes prior to COVID-19 with outcomes following the implementation of COVID-19 visiting restrictions. The aim is to establish if the restrictions on visiting has an impact on the duration of delirium. Delirium is an acute mental confusion and is associated with longer hospital stays and worse outcomes in this patient group.
The second arm of this study involves semi-structured interviews with patients, relatives and staff that will allow deeper exploration of the issues around current visiting policy. The interviews will last approximately 1 hour and will address these issues. They will then be transcribed word for word and analysed using grounded theory, meaning the theories will develop from the data as it is analysed.
Full description
This study will look at the implications of visiting restrictions on patients without COVID-19 who are in the intensive care unit. It will also explore the impact of these restrictions on them, their relatives and staff.
The investigators hypothesise that the restriction of visiting has a negative impact on recovery of patients, families of patients and staff caring for patients without COVID-19 in the cardiothoracic ICU.
In order to answer this hypothesis, the wider implications of COVID-19 will be explored, not only with patients, but also relatives and staff involved in the care of these patients.
The research questions this study aims to answer are:
Is there a negative impact on the clinical outcomes due to the COVID-19 visitation restrictions? Is there an increase in the incidence and duration of delirium in patients who do not receive visitors? What experiences do patients recall during their ICU admission through the COVID-19 pandemic visitation restrictions? What experiences do relatives recall from their loved-ones during an ICU admission during the COVID-19 pandemic visitation restrictions? What impact, if any, do the changes to visiting have on staff?
In order to answer these research questions the investigators will carry out a single centre mixed method observational study. This study will consist of two arms.
The first arm of this study will utilise retrospective data that is routinely collected in normal clinical practice in this single centre. This will be used to compare to patient outcomes prior to COVID-19 with outcomes following the implementation of COVID-19 visiting restrictions.
The second arm of this study involves semi-structured interviews with patients, relatives and staff that allow deeper exploration of the issues around current visiting policy.
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Arm 1
Inclusion Criteria:
Length of stay within critical care > 4 days
Age > 18 years
Patients who have been admitted:
Exclusion Criteria:
Arm 2
Inclusion Criteria:
For Patients:
Length of stay within critical care > 4 days
Age > 18 years
Reason for admission
Provision of informed consent
For relatives:
Age > 18 years
Relative of a patient that has been in critical care > 4 days
Relative of a patient who has been admitted:
Relative of a patient admitted for > 4days
For Staff:
Exclusion:
For patients:
For relatives:
For Staff:
• Age < 18yrs
1,000 participants in 2 patient groups
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Central trial contact
Leah Hughes; Ben Shelley
Data sourced from clinicaltrials.gov
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