Doris Barwich - Academia.edu (original) (raw)
Papers by Doris Barwich
Patient Education and Counseling, Oct 1, 2023
American Journal of Hospice and Palliative Medicine, Oct 21, 2022
Objective: Primary care providers play an important role in providing early palliative care, howe... more Objective: Primary care providers play an important role in providing early palliative care, however they often lack practical supports to operationalize this approach in practice. CAPACITI is a virtual training program aimed at providing practical tips, strategies, and action plans to help primary care providers offer an early palliative approach to care. The CAPACITI pilot program consisted of 10 facilitated, monthly training sessions, covering identification and assessment, communication, and engaging caregivers and specialists. We present the findings of an evaluation of the pilot program. Method: We conducted a single cohort study of primary care providers who participated in CAPACITI. Study outcomes were the change in the percentage of caseload reported as requiring palliative care and improved confidence in competencies measured on a 20-item, study-created survey. Pre and post survey data were analyzed using paired t-tests. Results: Twenty-two teams representing 127 care providers (including 36 physicians and 28 Nurse Practitioners) completed CAPACITI. Paired comparisons showed a moderate improvement in confidence across the competencies covered (.6 to 1.3 mean improvement across items using seven-point scales, all P < .05). Pre-CAPACITI, clinician prescribers ( N = 32) identified a mean of 1.2% of their caseload requiring a palliative approach to care, which increased to 1.6% post-program ( P = .02). Said differently, the total group of paired clinician prescribers identified 338 patients as requiring palliative care in their caseloads at baseline vs 482 patients following the intervention, for an overall increase of 144 patients in their collective caseloads. Conclusion: CAPACITI improved self-assessed palliative care identification and provider confidence in core competencies. The program demonstrated potential for building palliative care capacity in primary care teams.
Family Practice, Sep 19, 2019
BMJ supportive & palliative care, Jun 1, 2011
BMJ supportive & palliative care, Jun 1, 2012
PubMed, 2015
This is a knowledge translation project to promote the uptake of best practices in end-of-life (E... more This is a knowledge translation project to promote the uptake of best practices in end-of-life (EOL) care within the primary care setting in British Columbia (BC) through the use of tools embedded into electronic medical records (EMRs). The knowledge-to-action model is used to engage primary care providers in co-designing, adopting and evaluating the EOL care toolkit built for 3 EMRs. The toolkit has a set of EMR-specific data entry templates, query/report functions and access to additional downloadable resources. It is based on the EOL learning module designed and offered by the BC General Practice Services Committee's Practice Support Program to improve EOL care by primary care providers in the province. Our web-based distribution method allows providers to download and install the toolkit then take part to evaluate its use and impact. Initial feedback from phases 1-3 (of 4) has been favorable and has led to iterative improvements.
Oxford Scholarship Online, 2018
This chapter describes how advance care planning (ACP) is being implemented in Canada. It highlig... more This chapter describes how advance care planning (ACP) is being implemented in Canada. It highlights the use of an organizing National Framework for Advance Care Planning and a recent conceptual framework of end-of-life communication and decision making. A feature of the Canadian landscape are networks of collaboration and partnerships including research and non-governmental organizations, and examples of regional and national initiatives are presented in the boxes. A summary is provided of barriers, facilitators, the cultural milieu, and future opportunities for ACP in Canada. Implementation of ACP in Canada has followed a multi-faceted approach, with significant national leadership, key stakeholder participation and consumer engagement strategies, with important outcomes demonstrated.
Health Expectations, 2021
Questionnaire asking patients about engagement in advance care planning. (DOCX 37Â kb)
Palliative Medicine: A Case-Based Manual, 2021
The increasing professionalization and specialization of palliative care over the last 40 years h... more The increasing professionalization and specialization of palliative care over the last 40 years has had enormous impact and benefit for millions, especially with respect to symptom management. However, it may have also inadvertently created an expectation that all palliative care needs can and should be met through improving access to health services. Given the inherently social nature of dying, there is an urgent need to embrace palliative care as a public health issue and adopt models and approaches that allow communities, service delivery organizations, and policymakers to work together to improve well-being and quality of care, not just at end of life, but throughout the serious illness journey.
Healthcare quarterly, 2021
This paper reports findings from a modified World Café conducted at a palliative care professiona... more This paper reports findings from a modified World Café conducted at a palliative care professional conference in 2019, where input on tools to support advance care planning (ACP) was solicited from healthcare practitioners, managers and family members of patients. Barriers to ACP tool use included insufficient structures and resources in healthcare, death-avoidance culture and inadequate patient and family member engagement. Recommendations for tool use included clarification of roles and processes, training, mandates and monitoring, leadership support, greater reflection of diversity in tools and methods for public engagement. This paper illuminates factors to consider when implementing ACP tools in healthcare.
BMJ Supportive & Palliative Care, 2012
ACP is an established standard of care in many settings. However, no validated tool exists to eva... more ACP is an established standard of care in many settings. However, no validated tool exists to evaluate patients' and their families' perspectives on ACP. The purpose of this study was to develop and validate a novel questionnaire to evaluate the quantity and quality of ACP from the perspective of a patient and their family member. To develop the questionnaire, items were generated from focus groups with health care professionals and face to face interviews with hospitalised patients. This questionnaire was then piloted and evaluated by a sample of hospitalised patients who had advanced illnesses and their family members. The questionnaire was divided into 2 parts, the first part covering ACP activities before hospital admission (6 questions) and the second part relating to' goals of care' discussions that occurred during hospitalisation (8 questions). 27 patients and 24 family members participated in the pilot. All respondents rated the language, clarity, fit, accept...
Canadian family physician Medecin de famille canadien, 2018
OBJECTIVE To identify barriers to and enablers of advance care planning (ACP) perceived by physic... more OBJECTIVE To identify barriers to and enablers of advance care planning (ACP) perceived by physicians and other health professionals in primary care. DESIGN Cross-sectional, self-administered survey. SETTING Ontario, Alberta, and British Columbia. PARTICIPANTS Family physicians (n = 117) and other health professionals (n = 64) in primary care. MAIN OUTCOME MEASURES Perceived barriers relating to the clinician, characteristics of patients, and system factors, rated on a 7-point scale from 0 (not at all) to 6 (an extreme amount), and enablers reported using an open-ended question. RESULTS Between November 2014 and June 2015, questionnaires were returned by 72.2% (117 of 162) of family physicians and 68.8% (64 of 93) of the other health professionals. Physicians rated insufficient time, inability to electronically transfer the advance care plan across care settings, decreased interaction with patients near the end of life owing to transfer of care, and patients' difficulty understa...
OBJECTIVE To assess primary care patients' engagement in advance care planning (ACP) and pred... more OBJECTIVE To assess primary care patients' engagement in advance care planning (ACP) and predictors of engagement. DESIGN Cross-sectional survey using a revised version of a validated questionnaire. SETTING Alberta, Ontario, and British Columbia. PARTICIPANTS Convenience sample of 20 family practices that provided a consecutive sample of 810 patients aged 50 years and older. MAIN OUTCOME MEASURES Engagement in ACP activities, and sociodemographic and health-related predictors of having engaged in ACP activities. RESULTS Patients had a mean age of 66 years (55.6% women). Two-thirds of patients (68.5%; 555) had thought about the kinds of medical treatments they would want or not want if they were sick and in hospital, 52.8% (n = 428) had talked with someone about what they would want, 32.0% (n = 259) had written down their wishes, 50.4% (n = 408) had named someone to be their substitute decision maker, and 23.0% (n = 186) had engaged in all 4 key ACP activities. Of those patients ...
Patient Education and Counseling, Oct 1, 2023
American Journal of Hospice and Palliative Medicine, Oct 21, 2022
Objective: Primary care providers play an important role in providing early palliative care, howe... more Objective: Primary care providers play an important role in providing early palliative care, however they often lack practical supports to operationalize this approach in practice. CAPACITI is a virtual training program aimed at providing practical tips, strategies, and action plans to help primary care providers offer an early palliative approach to care. The CAPACITI pilot program consisted of 10 facilitated, monthly training sessions, covering identification and assessment, communication, and engaging caregivers and specialists. We present the findings of an evaluation of the pilot program. Method: We conducted a single cohort study of primary care providers who participated in CAPACITI. Study outcomes were the change in the percentage of caseload reported as requiring palliative care and improved confidence in competencies measured on a 20-item, study-created survey. Pre and post survey data were analyzed using paired t-tests. Results: Twenty-two teams representing 127 care providers (including 36 physicians and 28 Nurse Practitioners) completed CAPACITI. Paired comparisons showed a moderate improvement in confidence across the competencies covered (.6 to 1.3 mean improvement across items using seven-point scales, all P < .05). Pre-CAPACITI, clinician prescribers ( N = 32) identified a mean of 1.2% of their caseload requiring a palliative approach to care, which increased to 1.6% post-program ( P = .02). Said differently, the total group of paired clinician prescribers identified 338 patients as requiring palliative care in their caseloads at baseline vs 482 patients following the intervention, for an overall increase of 144 patients in their collective caseloads. Conclusion: CAPACITI improved self-assessed palliative care identification and provider confidence in core competencies. The program demonstrated potential for building palliative care capacity in primary care teams.
Family Practice, Sep 19, 2019
BMJ supportive & palliative care, Jun 1, 2011
BMJ supportive & palliative care, Jun 1, 2012
PubMed, 2015
This is a knowledge translation project to promote the uptake of best practices in end-of-life (E... more This is a knowledge translation project to promote the uptake of best practices in end-of-life (EOL) care within the primary care setting in British Columbia (BC) through the use of tools embedded into electronic medical records (EMRs). The knowledge-to-action model is used to engage primary care providers in co-designing, adopting and evaluating the EOL care toolkit built for 3 EMRs. The toolkit has a set of EMR-specific data entry templates, query/report functions and access to additional downloadable resources. It is based on the EOL learning module designed and offered by the BC General Practice Services Committee's Practice Support Program to improve EOL care by primary care providers in the province. Our web-based distribution method allows providers to download and install the toolkit then take part to evaluate its use and impact. Initial feedback from phases 1-3 (of 4) has been favorable and has led to iterative improvements.
Oxford Scholarship Online, 2018
This chapter describes how advance care planning (ACP) is being implemented in Canada. It highlig... more This chapter describes how advance care planning (ACP) is being implemented in Canada. It highlights the use of an organizing National Framework for Advance Care Planning and a recent conceptual framework of end-of-life communication and decision making. A feature of the Canadian landscape are networks of collaboration and partnerships including research and non-governmental organizations, and examples of regional and national initiatives are presented in the boxes. A summary is provided of barriers, facilitators, the cultural milieu, and future opportunities for ACP in Canada. Implementation of ACP in Canada has followed a multi-faceted approach, with significant national leadership, key stakeholder participation and consumer engagement strategies, with important outcomes demonstrated.
Health Expectations, 2021
Questionnaire asking patients about engagement in advance care planning. (DOCX 37Â kb)
Palliative Medicine: A Case-Based Manual, 2021
The increasing professionalization and specialization of palliative care over the last 40 years h... more The increasing professionalization and specialization of palliative care over the last 40 years has had enormous impact and benefit for millions, especially with respect to symptom management. However, it may have also inadvertently created an expectation that all palliative care needs can and should be met through improving access to health services. Given the inherently social nature of dying, there is an urgent need to embrace palliative care as a public health issue and adopt models and approaches that allow communities, service delivery organizations, and policymakers to work together to improve well-being and quality of care, not just at end of life, but throughout the serious illness journey.
Healthcare quarterly, 2021
This paper reports findings from a modified World Café conducted at a palliative care professiona... more This paper reports findings from a modified World Café conducted at a palliative care professional conference in 2019, where input on tools to support advance care planning (ACP) was solicited from healthcare practitioners, managers and family members of patients. Barriers to ACP tool use included insufficient structures and resources in healthcare, death-avoidance culture and inadequate patient and family member engagement. Recommendations for tool use included clarification of roles and processes, training, mandates and monitoring, leadership support, greater reflection of diversity in tools and methods for public engagement. This paper illuminates factors to consider when implementing ACP tools in healthcare.
BMJ Supportive & Palliative Care, 2012
ACP is an established standard of care in many settings. However, no validated tool exists to eva... more ACP is an established standard of care in many settings. However, no validated tool exists to evaluate patients' and their families' perspectives on ACP. The purpose of this study was to develop and validate a novel questionnaire to evaluate the quantity and quality of ACP from the perspective of a patient and their family member. To develop the questionnaire, items were generated from focus groups with health care professionals and face to face interviews with hospitalised patients. This questionnaire was then piloted and evaluated by a sample of hospitalised patients who had advanced illnesses and their family members. The questionnaire was divided into 2 parts, the first part covering ACP activities before hospital admission (6 questions) and the second part relating to' goals of care' discussions that occurred during hospitalisation (8 questions). 27 patients and 24 family members participated in the pilot. All respondents rated the language, clarity, fit, accept...
Canadian family physician Medecin de famille canadien, 2018
OBJECTIVE To identify barriers to and enablers of advance care planning (ACP) perceived by physic... more OBJECTIVE To identify barriers to and enablers of advance care planning (ACP) perceived by physicians and other health professionals in primary care. DESIGN Cross-sectional, self-administered survey. SETTING Ontario, Alberta, and British Columbia. PARTICIPANTS Family physicians (n = 117) and other health professionals (n = 64) in primary care. MAIN OUTCOME MEASURES Perceived barriers relating to the clinician, characteristics of patients, and system factors, rated on a 7-point scale from 0 (not at all) to 6 (an extreme amount), and enablers reported using an open-ended question. RESULTS Between November 2014 and June 2015, questionnaires were returned by 72.2% (117 of 162) of family physicians and 68.8% (64 of 93) of the other health professionals. Physicians rated insufficient time, inability to electronically transfer the advance care plan across care settings, decreased interaction with patients near the end of life owing to transfer of care, and patients' difficulty understa...
OBJECTIVE To assess primary care patients' engagement in advance care planning (ACP) and pred... more OBJECTIVE To assess primary care patients' engagement in advance care planning (ACP) and predictors of engagement. DESIGN Cross-sectional survey using a revised version of a validated questionnaire. SETTING Alberta, Ontario, and British Columbia. PARTICIPANTS Convenience sample of 20 family practices that provided a consecutive sample of 810 patients aged 50 years and older. MAIN OUTCOME MEASURES Engagement in ACP activities, and sociodemographic and health-related predictors of having engaged in ACP activities. RESULTS Patients had a mean age of 66 years (55.6% women). Two-thirds of patients (68.5%; 555) had thought about the kinds of medical treatments they would want or not want if they were sick and in hospital, 52.8% (n = 428) had talked with someone about what they would want, 32.0% (n = 259) had written down their wishes, 50.4% (n = 408) had named someone to be their substitute decision maker, and 23.0% (n = 186) had engaged in all 4 key ACP activities. Of those patients ...