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1.
Ned Tijdschr Geneeskd ; 1682024 03 05.
Article in Dutch | MEDLINE | ID: mdl-38470255

ABSTRACT

This article presents a small interview study with non-intensive care physicians concerning their experiences with tissue donation conversations with families of deceased potential donors.


Subject(s)
Physicians , Tissue and Organ Procurement , Humans , Tissue Donors , Communication
2.
PLoS One ; 18(8): e0286978, 2023.
Article in English | MEDLINE | ID: mdl-37616248

ABSTRACT

BACKGROUND: The COVID-19 pandemic has prompted many countries to formulate guidelines on how to deal with a worst-case scenario in which the number of patients needing intensive care unit (ICU) care exceeds the number of available beds. This study aims to explore the experiences of triage teams when triaging fictitious patients with the Dutch triage guidelines. It provides an overview of the factors that influence decision-making when performing ICU triage with triage guidelines. METHODS: Eight triage teams from four hospitals were given files of fictitious patients needing intensive care and instructed to triage these patients. Sessions were observed and audio-recorded. Four focus group interviews with triage team members were held to reflect on the sessions and the Dutch guidelines. The results were analyzed by inductive content analysis. RESULTS: The Dutch triage guidelines were the main basis for making triage decisions. However, some teams also allowed their own considerations (outside of the guidelines) to play a role when making triage decisions, for example to help avoid using non-medical criteria such as prioritization based on age group. Group processes also played a role in decision-making: triage choices can be influenced by the triagists' opinion on the guidelines and the carefulness with which they are applied. Intensivists, being most experienced in prognostication of critical illness, often had the most decisive role during triage sessions. CONCLUSIONS: Using the Dutch triage guidelines is feasible, but there were some inconsistencies in prioritization between teams that may be undesirable. ICU triage guideline writers should consider which aspects of their criteria might, when applied in practice, lead to inconsistencies or ethically questionable prioritization of patients. Practical training of triage team members in applying the guidelines, including explanation of the rationale underlying the triage criteria, might improve the willingness and ability of triage teams to follow the guidelines closely.


Subject(s)
Intensive Care Units , Practice Guidelines as Topic , Humans , COVID-19/epidemiology , Critical Care , Pandemics , Triage
3.
Ned Tijdschr Geneeskd ; 1652021 09 08.
Article in Dutch | MEDLINE | ID: mdl-34523829

ABSTRACT

In Spring 2020, the Netherlands appeared to be poorly prepared for 'code black': a situation in which Intensive Care Unit (ICU) bed shortage would be a reality. Guidelines were developed with medical and non-medical considerations for ICU triage. In recent months, we organized eight simulated triage sessions in four hospitals, as part of a research project. We asked triage teams to prioritize cases of patients in need of ICU care, aided by the guidelines. Data are still being analyzed; here we share some preliminary observations and lessons learned. In our sessions, it was striking how much triage depends on the input of the intensivist, especially when it comes to crucial expertise regarding prognosis and length of stay. Differences in prioritization predominantly depended on different estimations of prognosis and length of stay. The guidelines provide direction, but prioritizing ICU patients can be mentally burdensome for triagists. This requires support and aftercare for triage teams.


Subject(s)
Pandemics , Triage , Aftercare , Critical Care , Humans , Intensive Care Units
4.
Patient Educ Couns ; 104(5): 1206-1212, 2021 05.
Article in English | MEDLINE | ID: mdl-33041158

ABSTRACT

OBJECTIVE: To explore how shared decision-making (SDM) is learned in clinical practice according to professionals and patients. METHODS: Focus group and individual interviews with interns (n = 9), residents (n = 12), senior physicians (n = 13), and (former) patients and relatives (n = 13) in fertility care and intensive care. RESULTS: Patients and professionals identified barriers and drivers for SDM related to patient, caregiver, and context. Participants agreed: the nuances of SDM are learned in practice, not during undergraduate medical education. Through observing and copying from other professionals, interns and residents describe building their personal "repertoire" of SDM skills, knowledge, and attitude. Professionals indicated it was helpful to see many different examples - both good and bad - of physicians in action. CONCLUSION: Learning SDM is a complicated task for both students and professionals in healthcare. Relevant factors are the involvement of patients, the role of informal learning processes and role models, and the importance of reflective practice. PRACTICE IMPLICATIONS: Learning SDM in practice requires 1) measures to lessen pressures on a meso and macro level that hinder SDM in practice, 2) inventive and precise training and education and paying explicit attention to informal learning processes in clinical practice and learning through role models.


Subject(s)
Patient Participation , Physicians , Attitude of Health Personnel , Decision Making , Decision Making, Shared , Focus Groups , Humans
5.
Ned Tijdschr Geneeskd ; 1632019 05 03.
Article in Dutch | MEDLINE | ID: mdl-31120229

ABSTRACT

Dementia expressed in metaphors In healthcare, both patients and doctors use a lot of metaphors in their communication. Generally, not a lot of attention is paid to this, however, the use of metaphors is important to the patients' experience of both quality of life and quality of care. In our society, many negative metaphors are used about people with dementia, and these reflect the general way dementia is perceived by society. We investigated the sort of metaphors that people with dementia themselves use when talking about their lives with dementia. We found that people with dementia use a variety of metaphors to describe their disease. When doctors become more sensitive to the use of metaphors by themselves and their patients, this could lead to better insight into the specific experience patients go through and to healthcare that is better adjusted to these experiences.


Subject(s)
Communication , Dementia/psychology , Metaphor , Physician-Patient Relations , Quality of Life , Humans
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