Abstract
Objectives
The objectives of this project were to collect and analyze clinical governance documents related to family-centred care and cardiac arrest care in Canadian EMS organizations; and to improve the family-centredness of out-of-hospital cardiac arrest care through experience-based co-design.
Methods
We conducted qualitative document analysis of Canadian EMS clinical governance documents related to family-centred and cardiac arrest care, combining elements of content and thematic analysis methods. We then used experience-based co-design to develop a family-centred out-of-hospital cardiac arrest care policy and procedure template.
Results
Thirty-five Canadian EMS organizations responded to our requests, representing service area coverage for 80% of the Canadian population. Twenty documents were obtained for review and six overarching themes were identified: addressing family in event of in-home death, importance of family, family member escort, provider discretion and family presence discouraged. Informed by our qualitative analysis we then co-designed a policy and procedure template was created that prioritizes patient care while promotes family-centredness.
Conclusions
There were few directives to support family-centred care by Canadian EMS organizations. A family-centred out-of-hospital cardiac arrest care policy and procedure template was developed using experience-based co-design to assist EMS organizations improve the family-centredness of out-of-hospital cardiac arrest care.
Résumé
Objectifs
Les objectifs de ce projet étaient de recueillir et d’analyser des documents de gouvernance clinique liés aux soins centrés sur la famille et aux soins de l’arrêt cardiaque dans les organisations canadiennes de SMU; et d’améliorer le caractère centré sur la famille des soins en cas d’arrêt cardiaque à l’extérieur de l’hôpital grâce à une co-conception fondée sur l’expérience.
Méthodes
Nous avons effectué une analyse qualitative des documents de gouvernance clinique des SMU canadiens liés aux soins axés sur la famille et aux arrêts cardiaques, en combinant des éléments de contenu et des méthodes d’analyse thématique. Nous avons ensuite utilisé la co-conception fondée sur l’expérience pour élaborer un modèle de politique et de procédure de soins en cas d’arrêt cardiaque centrés sur la famille en dehors de l’hôpital.
Résultats
Trente-cinq organisations Canadiennes de SMU ont répondu à nos demandes, ce qui représente une couverture de zone de service pour 80 % de la population canadienne. Vingt documents ont été obtenus aux fins d’examen et six thèmes principaux ont été cernés: s’adresser à la famille en cas de décès à domicile, l’importance de la famille, accompagnement d’un membre de la famille, la discrétion du fournisseur et la présence de la famille découragée. Éclairés par notre analyse qualitative, nous avons ensuite co-conçu un modèle de politique et de procédure qui priorise les soins aux patients tout en favorisant l’orientation familial.
Conclusions
Il y avait peu de directives pour soutenir les soins axés sur la famille par les organisations canadiennes de SMU. Un modèle de politique de soins d’arrêt cardiaque centré sur la famille a été élaboré à l’aide d’une co-conception basée sur l’expérience pour aider les organisations de SMU à améliorer l’orientation familiale des soins en cas d’arrêt cardiaque hors hôpital.
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What is known about the topic? |
Cardiac arrest of a loved one has lasting impacts on families. When successfully adopted, family-centredness is associated with higher perceived quality of care |
What did this study ask? |
What clinical governance documents exist among Canadian EMS organizations with regards to family-centred cardiac arrest care? |
What did this study find? |
There are very few clinical documents to support family-centred cardiac arrest care in Canadian EMS organizations |
Why does this study matter to clinicians? |
This study uses qualitative document analysis and experience-based co-design to create a policy and procedure template that describes practical strategies to improve the family-centredness of out-of-hospital cardiac arrest care |
“I was doing the compressions you know, the CPR like the person on the phone was telling me to do, but when the paramedics arrived they took me out of our bedroom, they wouldn’t let me be with him anymore, they kept me away from my own husband, in our bedroom, and I lost that time with him, I will never get it back.”—Family-centred cardiac arrest care project collaborator #17.
“The paramedics were amazing, they were so good, they explained to me what they were doing and why, they told me my Mum had like ventricular fibrillating and they shocked her. The supervisor, she even drove me to the hospital while the crew took Mum in the ambulance. I wish I could let the crew know how much I appreciated all they did for Mum and me”—Family-centred cardiac arrest care project collaborator #21.
Over 100,000 Canadians are bereaved by the sudden cardiac arrest of a family member every year [1]. Over the past 30 years there have been important advances in out-of-hospital cardiac arrest care with modest improvements in survival [2, 3] and little consideration of families. The long-term impacts of these events weigh heavily in the form of physiological and psychological stress [4, 5]. One year after a family member’s cardiac arrest, 40% of relatives experience after-effects such as disordered mood, post-traumatic stress, and anxiety [6, 7]. Mental health experts suggest the degree of symptomatology in family members may often be greater than the survivor of cardiac arrest [8].
Family-centred care is the collaboration of healthcare providers, patients, and families to optimize the quality of care [5]. It is well established in critical care [9] and paediatric emergency [10]. Family-centred care strategies in cardiac arrest care are believed by some to be a strategy to improve outcomes for patients and families [11, 12] yet barriers to their adoption in the prehospital setting have been identified [13].
A core component of a family-centred approach to cardiac arrest care is the facilitation of family presence [14]. However, offering presence during out-of-hospital cardiac arrest can be controversial as providers fear criticism or negative impacts on their performance [4, 13, 15]. The existence of family-centred cardiac arrest care policy, procedure or other clinical governance documents in Canadian EMS organizations is largely unknown. The overall aim of this project is to promote the adoption of family-centred cardiac arrest care into the prehospital setting.
The objectives of this project were to (i) collect and analyze clinical governance documents supporting family-centred care during out-of-hospital cardiac arrest in Canadian EMS organizations; and (ii) partner with survivors and family members to improve the family-centredness of out-of-hospital cardiac arrest care through the experience-based co-design of a policy and procedure template.
Methods
Study population and setting
We set out to obtain a representative sample of Canadian EMS organizations’ clinical governance documents (policies, procedures, protocols, guidelines etc.) We emailed Canadian EMS organizations asking for any documents related to family-centred care and cardiac arrest care. However, we accepted any documents that addressed family-centred care in general (presence, visitation, transport/escort) (see appendix for email template). We also conducted a Canadian grey literature search. We identified and emailed EMS organizations through the membership lists of the Canadian Resuscitation Outcomes Consortium (CanROC) and the Paramedic Chiefs of Canada. The province of Ontario required additional network sampling methods via the Ontario Association of Paramedic Chiefs website as they utilize over 50 individual services.
Collaborators with lived experience were engaged from the Family Centred Cardiac Arrest Care Project (https://osf.io/fxp5g/). This team has performed literature reviews and utilized experience-based co-design to developed various tools to improve cardiac arrest care [16, 17]. Twenty one persons with lived experience of cardiac arrest care from five Canadian provinces, (five survivors, eight family members of survivors and seven family members of non-survivors) participated in consultant, collaborator or co-investigator roles. They come from varied backgrounds, but include multiple practicing and retired healthcare professionals (physicians, nurses and allied health), a university professor, a theologian, a veterinarian, an unpaid caregiver, a pastor, a student, an artist and a yoga teacher.
Study design
We utilized qualitative document analysis methods for this study, a health policy research methodology [18]. The systematic four-step “R.E.A.D.” procedure was used to guide our research: (1) (R)eading of clinical governance documents, (2) (E)xtracting of relevant data, (3) (A)nalyzing data and (4) (D)istilling any findings, using meta-synthesis [18]. We reported this study in accordance with the Qualitative the Guidance for Reporting Involvement of Patients and the Public (GRIPP2) and the Standards for Reporting Qualitative Research (SRQR) (see appendix for both reporting documents) [19, 20].
Experience based co-design methods, (informed by our qualitative document analysis), were then used to develop a policy and procedure template. This type of co-design method is a form of participatory research utilizing lived experience of care providers and care recipients to improve care [21]. The method has also been described as a way for organizations to engage with care providers and care recipients to improve together [22]. Co-design workshops were undertaken during the COVID-19 pandemic using online synchronous and asynchronous tools such as Zoom [San Jose, California USA] and Jamboard, Draw, Docs and Sheets [The Alphabet company, Mountain View, California, USA]. Our co-design process had four phases: engage, gather, understand and improve [23]. See Fig. 1 for details.
Data collection
Each identified EMS organization was emailed up to three times between April 2020 and April 2021 (see appendix for email template) and invited to contribute clinical governance documents (policy, procedure, protocol or guidelines etc.) related to family-centred care and cardiac arrest care (see appendix for email invitation). If three attempts resulted in no reply, they were marked as “no response”. Our grey literature search had three phases: geographically restricted internet search engine (anonymous browser for de-personalized search without individual user bias), grey literature database (16 Canadian sources) and targeted website searching [24, 25]. See appendix (tables five, six and seven) for search strategy.
Data analysis
We conducted qualitative document analysis combining elements of content and thematic analysis [21]. Content analysis was used to identify, count and collate sections of document text. Thematic analysis was used to identify and examine patterns within and between the documents, developing key themes representative of the direction Canadian EMS care providers receive regarding family-centred and cardiac arrest care.
Documents were read repeatedly to develop in-depth knowledge of the data and searched to highlight key terms related to family-centred care (see table four appendix for key words used). Throughout the analysis phase, notes and codes were created and underwent further analysis until themes were identified and meta-synthesized. Meta-synthesis entailed grouping codes, comparing themes across documents, matching themes and generating higher-order analytical themes to go beyond the original documents and provide a superordinate interpretation [26]. Then, in partnership with survivors and family members with lived experience of out-of-hospital cardiac arrest, we performed co-design workshops, producing a universal policy and procedure template for family-centred cardiac arrest care. See Fig. 2 for a summary of our methods.
Ethics
This project was exempt from full ethics review (Alberta Research Ethics Community Consensus Initiative Ethics Screening Tool https://arecci.albertainnovates.ca/ethics-screening-tool/, “Low Risk”) as there were no human research participants—our partners with lived experience were engaged as consultants, collaborators and co-investigators. Documents were collected from EMS organizations under the condition of anonymity.
Results
Qualitative document analysis
Sixty EMS organizations were contacted. Their “responses” were categorized as (i) no response (n = 25, 41.6%), (ii) positive response with clinical governance documents provided (n = 14, 23.3%) and (iii) negative response without clinical governance documents provided (n = 21, 35%). 35 (58%) of the EMS organizations responded to our request for clinical governance documents. These 35 services provide care for over 80% of the Canadian population, or approximately 30 million Canadians and include all provincial service providers (excluding Quebec). The entirety of the non-responses were from regional services within Ontario. No additional clinical governance documents were obtained through grey literature search. See Fig. 2 for flow diagram. In total, 20 clinical governance documents from 14 different services were obtained (see Table 1 for results summary). Four documents were excluded upon receipt because they irrelevant to family-centred care or cardiac arrest care.
Five distinct and important themes were identified through our analysis: (1) Acknowledge the family when there is a death in the home; (2) Family members are important to the patient and patient care; (3) Family member escort options; (4) Provider discretion for family involvement; and (5) Family presence discouraged. Note, individual clinical governance documents could address more than one theme.
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1. Acknowledging family in event of in-home death
Four clinical governance documents guided the social-emotional approach EMS providers were to employ for a death in the home, but not cases of active resuscitation. These documents advised EMS providers to be sensitive towards the family in these scenarios. However, there were no actionable steps or guidance to assist providers in navigating these situations.
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2. Generalized importance of family
This theme included mentions of the term family-centred care, or addressed the patient and family dyad (for example, using terms like ‘patient and family’ rather than just patient). There were no specific actionable items, but an organizational culture that considered the patient and their family as a cohesive unit. Six documents provided guidance related to this theme and one was in the context of cardiac arrest care.
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3. Family member escort option
Eight of the 20 clinical governance documents identified and supported circumstances when EMS providers could facilitate taking a family member in the ambulance with the patient. The content of these policies and protocols addressed the need for a seatbelt, adherence to traffic laws and required family member to not be intoxicated or aggressive.
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4. Provider discretion
Six documents stated that the final decision to allow family presence was up to the EMS providers. In these examples, there was single statement explaining that the provider(s) had the discretion to determine the degree of closeness or involvement a family member could have while emphasizing that the EMS provider had the final say.
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5. Family presence discouraged
In three cases, family presence was discouraged. In one example, family presence was discouraged outright. In the other two documents, family members or support persons were encouraged to find their own transport and limited patient accompaniment was emphasized in high priority calls.
See Table 2 for a complete description and example quotes that exemplify themes.
Experience-based co-design for family-centred prehospital cardiac arrest care
An output of our co-design workshops was our conceptualization of family-centred prehospital cardiac arrest care that incorporates content and themes identified in the qualitative document analysis, as well as survivor and family knowledge and experience, and family-centredness concepts [27,28,29]. See appendix figure three for our conceptual framework.
We also drafted a policy and procedure template to help improve the family-centredness of out-of-hospital cardiac arrest care. The template addresses six domains: doing what is best for the patient, family-centredness, assigning a family liaison, caring for the non-transported patient, providing written information and document best practices. The domains were constructed based on our qualitative analysis, meta-synthesis as well as team members knowledge and experience. See Table 3 for our policy and procedure template.
Discussion
Interpretation
We collected and analyzed clinical governance documents related to family-centred care and cardiac arrest care in Canadian EMS organizations. Few documents were obtained that directed a family-centred approach. Organizational practices varied in their family-centredness from acknowledging the patient and family as a dyad to actively discouraging family involvement. No single organization’s documents included all components of family-centred cardiac arrest care identified in a recent review (i. primary focus on resuscitation; ii. consideration of family context, iii. collaboration between resuscitation team and family; iv. provisions for the family’s post-resuscitation needs; and iv. dedicated policies, procedures and education) [28], signalling a potential opportunity for improvement.
Previous studies
Past research on prehospital family-centred care has identified numerous barriers to its provision including the belief it interferes with patient care, the unfamiliar environment, limited personnel, multi-tasking medical care and concern for patient care interference [13]. Adoption of family-centred care principles into training and clinical governance structures may help both front line EMS providers and physicians providing medical consultation overcome these barriers and improve care for their patients and families [27]. This is particularly relevant given that many EMS organizations are moving towards managing and terminating resuscitations on scene for reasons such as lack of benefit from transport, minimizing interruptions in CPR and minimizing exposure to additional health care providers [30, 31]. In these instances, undertaking simple low resource actions such as providing frequent updates, offering presence and answering questions may help families cope with the cardiac arrest experience.
Strengths and limitations
This study analyzed clinical governance documents from Canadian EMS organizations that provide pre-hospital care to a large proportion of the population. Rather than just identifying a gap, this study contributes a potential solution by providing an experience-based co-designed policy and procedure template for future clinical governance document development.
Our results were obtained through a document review process which does not perfectly represent clinical care. Our request was for clinical governance documents related to family-centred care and cardiac arrest care; however, family-centredness may be built into other documents not obtained through our search. We also acknowledge that Canadian EMS organizations, specifically Canada’s highly trained and professional prehospital providers, are already providing family-centred care, regardless of the presence or absence of clinical governance documents. Furthermore, the EMS organizations that provided documents were primarily from provincial services and metropolitan centers, therefore EMS organizations from northern, Indigenous and French-speaking communities are under-represented in our findings. The impact of providing family-centred prehospital cardiac arrest care on scene times or important patient outcomes, is unknown.
Clinical and research implications
Cardiac arrest of a family member is one of the most psychologically impactful and devastating life events [32,33,34]. Providing prehospital family-centred cardiac arrest care requires the ability to address intense emotional responses, address existential questions and competence in transitioning from patient care to family care [35]. To develop greater competence in family-centred care, and improve the experience of family members, organizational buy-in, training and clinical governance processes are required [22]. When successfully adopted, family-centredness is associated with higher quality of care and satisfaction for providers and families [36,37,38].
Conclusion
We analyzed clinical governance documents related to family-centred care and cardiac arrest care from EMS organizations that care for approximately 80% of the population of Canada and found there were few directives to support family-centred care, especially as it relates to out-of-hospital cardiac arrest. Our qualitative document review employed patient and public involvement and identified various themes: addressing the family when there is a death in the home, the importance of family, family escort options and provider discretion. Informed by our document review, an experience-based co-design project was employed to create a family-centred out-of-hospital cardiac arrest care policy and procedure template to assist EMS organizations incorporate family-centredness in future clinical governance.
References
Heart and Stroke Foundation of Canada. Cardiac arrest in the pool [Internet]. 2020 [cited 2021 Feb 16]. http://www.heartandstroke.ca/articles/cardiac-arrest-in-the-pool
Sasson C, Rogers MAM, Dahl J, Kellermann AL. Predictors of survival from out-of-hospital cardiac arrest: a systematic review and meta-analysis. Circ Cardiovasc Qual Outcomes. 2010;3(1):63–81.
Buick JE, Drennan IR, Scales DC, Brooks SC, Byers A, Cheskes S, et al. Improving temporal trends in survival and neurological outcomes after out-of-hospital cardiac arrest. Circ Cardiovasc Qual Outcomes. 2018. https://doi.org/10.1161/CIRCOUTCOMES.117.003561.
Jabre P, Tazarourte K, Azoulay E, Borron SW, Belpomme V, Jacob L, et al. Offering the opportunity for family to be present during cardiopulmonary resuscitation: 1-year assessment. Intensive Care Med. 2014;40(7):981–7.
Davidson JE, Aslakson RA, Long AC, Puntillo KA, Kross EK, Hart J, et al. Guidelines for family-centered care in the neonatal, pediatric, and adult ICU. Crit Care Med. 2017;45(1):103–28.
Middelkamp W, Moulaert VR, Verbunt JA, van Heugten CM, Bakx WG, Wade DT. Life after survival: long-term daily life functioning and quality of life of patients with hypoxic brain injury as a result of a cardiac arrest. Clin Rehabil. 2007;21(5):425–31.
Wachelder EM, Moulaert VRMP, van Heugten C, Verbunt JA, Bekkers SCAM, Wade DT. Life after survival: long-term daily functioning and quality of life after an out-of-hospital cardiac arrest. Resuscitation. 2009;80(5):517–22.
Košir M, Simonič B, Gostečnik C, Noč M, Tadel Kocjančič Š, Jazbec A, et al. Relational family therapy in the treatment of sudden cardiac arrest survivors and their relatives. Pers Chall J Theol Educ Canon Law Soc Stud Inspired Pope John Paul II. 2021;11(1):249.
Goldfarb MJ, Bibas L, Bartlett V, Jones H, Khan N. outcomes of patient- and family-centered care interventions in the ICU: a systematic review and meta-analysis. Crit Care Med. 2017;45(10):1751–61.
American Academy of Pediatrics, Committee on Pediatric Emergency Medicine, American College of Emergency Physicians, Pediatric Emergency Medicine Committee. Patient- and family-centered care and the role of the emergency physician providing care to a child in the emergency department. Pediatrics. 2006;118(5):2242–4.
Case R, Mazzagatti E, Stub D, Andrews E, Bray J, Smith K. Consequences of cardiac arrest: the psychosocial functioning of survivors and family members. Resuscitation. 2018;130: e91.
Sawyer KN, Camp-Rogers TR, Kotini-Shah P, del Rios M, Gossip MR, Moitra VK, et al. Sudden cardiac arrest survivorship: a scientific statement from the American Heart Association. Circulation. 2020. https://doi.org/10.1161/CIR.0000000000000747.
Ayub EM, Sampayo EM, Shah MI, Doughty CB. Prehospital providers’ perceptions on providing patient and family centered care. Prehosp Emerg Care. 2017;21(2):233–41.
Doyle CJ, Post H, Burney RE, Maino J, Keefe M, Rhee KJ. Family participation during resuscitation: an option. Ann Emerg Med. 1987;16(6):673–5.
Compton S, Madgy A, Goldstein M, Sandhu J, Dunne R, Swor R. Emergency medical service providers’ experience with family presence during cardiopulmonary resuscitation. Resuscitation. 2006;70(2):223–8.
Douma MJ, Ali S, Bone A, Dainty KN, Dennett L, Smith KE, et al. The needs of families during cardiac arrest care: a survivor- and family-led scoping review protocol. J Emerg Nurs. 2021;47(5):778–88.
Douma MJ, Graham TAD, Bone A, Ali S, Dennett L, Brindley PG, et al. What are the care needs of families experiencing cardiac arrest care? A survivor and family-performed systematic review and qualitative meta-synthesis protocol. Int J Qual Methods. 2021;20:160940692110486.
Dalglish SL, Khalid H, McMahon SA. Document analysis in health policy research: the READ approach. Health Policy Plan. 2020;35:1424–31.
Staniszewska S, Brett J, Simera I, Seers K, Mockford C, Goodlad S, et al. GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research. BMJ. 2017. https://doi.org/10.1136/bmj.j3453.
O’Brien BC, Harris IB, Beckman TJ, Reed DA, Cook DA. Standards for reporting qualitative research: a synthesis of recommendations. Acad Med. 2014;89(9):1245–51.
Dewar B, Mackay R, Smith S, Pullin S, Tocher R. Use of emotional touchpoints as a method of tapping into the experience of receiving compassionate care in a hospital setting. J Res Nurs. 2010;15(1):29–41.
Bate P, Robert G. Toward more user-centric OD: lessons from the field of experience-based design and a case study. J Appl Behav Sci. 2007;43(1):41–66.
Dimopoulos-Bick TL, O’Connor C, Montgomery J, Szanto T, Fisher M, Sutherland V, et al. “Anyone can co-design?”: a case study synthesis of six experience-based co-design (EBCD) projects for healthcare systems improvement in New South Wales, Australia. Patient Exp J. 2019;6(2):93–104.
Godin KM, Kirkpatrick SI, Hanning RM, Stapleton J, Leatherdale ST. Examining guidelines for school-based breakfast programs in Canada: a systematic review of the grey literature. Can J Diet Pract Res. 2017;78(2):92–100.
Douma MJ, MacKenzie E, Loch T, Tan MC, Anderson D, Picard C, et al. Prone cardiopulmonary resuscitation: a scoping and expanded grey literature review for the COVID-19 pandemic. Resuscitation. 2020;155:103–11.
Sandelowski M, Docherty S, Emden C. Qualitative metasynthesis: issues and techniques. Res Nurs Health. 1997;20(4):365–71.
Kokorelias KM, Gignac MAM, Naglie G, Cameron JI. Towards a universal model of family centered care: a scoping review. BMC Health Serv Res. 2019. https://doi.org/10.1186/s12913-019-4394-5.
Douma MJ, Graham TAD, Ali S, Dainty KN, Bone A, Smith KE, et al. What are the care needs of families experiencing cardiac arrest? A survivor and family led scoping review. Resuscitation. 2021;168:119–41.
Institute for Patient and Family Centered Care. BETTER TOGETHER: strategies for changing policies [Internet]. [cited 2021 Feb 16]. https://www.ipfcc.org/bestpractices/Strategies-for-Changing-Policies.pdf
Bailey ED, Wydro GC, Cone DC. Termination of resuscitation in the prehospital setting for adult patients suffering nontraumatic cardiac arrest. Prehosp Emerg Care. 2000;4(2):190–5.
Grunau B, Kime N, Leroux B, Rea T, Van Belle G, Menegazzi JJ, et al. Association of intra-arrest transport vs continued on-scene resuscitation with survival to hospital discharge among patients with out-of-hospital cardiac arrest. JAMA. 2020;324(11):1058.
Shear MK, Ghesquiere A, Glickman K. Bereavement and complicated grief. Curr Psychiatry Rep. 2013. https://doi.org/10.1007/s11920-013-0406-z.
Keyes KM, Pratt C, Galea S, McLaughlin KA, Koenen KC, Shear MK. The burden of loss: unexpected death of a loved one and psychiatric disorders across the life course in a national study. Am J Psychiatry. 2014;171(8):864–71.
Shinada K, Kohno T, Fukuda K, Higashitani M, Kawamatsu N, Kitai T, et al. Prevalence and determinants of complicated grief in bereaved caregivers of patients admitted for cardiovascular diseases. Eur Heart J. 2019;40(Supplement 1):1285.
Bremer A, Dahlberg K, Sandman L. Balancing between closeness and distance: emergency medical services personnel’s experiences of caring for families at out-of-hospital cardiac arrest and sudden death. Prehospital Disaster Med. 2012;27(1):42–52.
Brown K, Mace SE, Dietrich AM, Knazik S, Schamban NE. Patient and family-centred care for pediatric patients in the emergency department. CJEM. 2008;10(01):38–43.
Brady MT, Crim L, Caldwell L, Koranyi K. Family-centered care: a paradigm for care of the HIV-affected family. Pediatr AIDS HIV Infect. 1996;7(3):168–75.
Callahan HE. Families dealing with advanced heart failure: a challenge and an opportunity. Crit Care Nurs Q. 2003;26(3):230–43.
Acknowledgements
We acknowledge the generous contributions of the members of the Family Centred Cardiac Arrest Care Project in the completion of the policy and procedure template included in this study. Family Centred Cardiac Arrest Care Project: Samina Ali, Sheila Early, Kim Ruether, Kristin Flanary, Katherine E. Smith, Katie N. Dainty, Timothy A. D. Graham, Samir Z. A. Graham, Lynn Blomheart, Jesse Blommaert, Calah Myhre, Ella MacKenzie, Louise Jarratt, Katherine E. Smith
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Open Access funding provided by the IReL Consortium. This work is unfunded.
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Members of Family Centred Cardiac Arrest Care Project are listed in acknowledgements section.
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Loch, T., Drennan, I.R., Buick, J.E. et al. Caring for the invisible and forgotten: a qualitative document analysis and experience-based co-design project to improve the care of families experiencing out-of-hospital cardiac arrest. Can J Emerg Med 25, 233–243 (2023). https://doi.org/10.1007/s43678-023-00464-8
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DOI: https://doi.org/10.1007/s43678-023-00464-8