Patricia Moreland
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Patricia Moreland has a total of 47 co-authors. Here are the top co-authors by number of shared publications:
- Marie Josée Mwiseneza
King Faisal Hospital Foundation, Kigali, Rwanda
3 shared publications - Absolomon Gashaija
Center for Impact, Innovation and Capacity Building in Health Information Systems and Nutrition (CIIC-HIN), Kigali, Rwanda
2 shared publications - Candide Girimpundu Mugeni
School of Nursing and Midwifery, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda
2 shared publications - Etienne Nsereko
School of Health Sciences, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda
2 shared publications - Japhet Ishimwe
Department of Community Health, School of Public Health, University of Rwanda, Kigali, Rwanda
2 shared publications - Richard Kalisa
Department of Community Health, School of Public Health, University of Rwanda, Kigali, Rwanda
2 shared publications
Latest Publications
- Open Access
- 13 June 2026
- Published by Springer Nature in BMC Pregnancy and Childbirth
- Vol. 26 (1)
Prevalence and determinants of low-birth-weight deliveries at four district hospitals in Kigali, Rwanda: a cross-sectional study
Low birth weight (LBW) is a significant public health concern, particularly in developing countries, because it is associated with increased neonatal and i
- 13 June 2026
- Published by Springer Nature in BMC Pregnancy and Childbirth
- Vol. 26 (1)
Open AccessPrevalence and determinants of low-birth-weight deliveries at four district hospitals in Kigali, Rwanda: a cross-sectional study
Low birth weight (LBW) is a significant public health concern, particularly in developing countries, because it is associated with increased neonatal and i
- 4 August 2021
- Published by Wolters Kluwer Health in Journal of Hospice & Palliative Nursing
- Vol. 23 (6) , 557-563
Palliative and End-of-Life Care Self-perceived Educational Needs of Physicians and Nurses in Rwanda
Palliative care access is an urgent and ethical imperative to effectively manage the increasing burden of serious health-related suffering worldwide. Understanding the palliative care educational needs of health care professionals is critical to support evidence-based clinical practice in Rwanda and other low- and middle-income countries. A cross-sectional study was conducted at 5 hospitals in Kigali, Rwanda, to assess the palliative/end-of-life educational needs of nurses and physicians. The End-of-Life Professional Caregiver Survey and a demographic form were used to collect data. Descriptive analyses and independent t tests were conducted. A total of 420 health care professionals participated in the study (response rate, 72%). Participants perceived their knowledge and skills in providing palliative/end-of-life care as low. Those who received palliative/end-of-life care training in the past 5 years, third- and fourth-year residents, and health care providers with 5 years of experience or more had significantly higher (P ≤ .05) mean scores on the End-of-Life Professional Caregiver Survey. Nurses scored higher than physicians in the patient- and family-centered communication (P = .049) and cultural and ethical values (P = .037) subscales. Pain management was identified as an educational need by 77% of participants. Our survey suggests the need for increased governmental investments in palliative/end-of-life care education among nurses and physicians in Rwanda.
- 4 August 2021
- Published by Wolters Kluwer Health in Journal of Hospice & Palliative Nursing
- Vol. 23 (6) , 557-563
Palliative and End-of-Life Care Self-perceived Educational Needs of Physicians and Nurses in Rwanda
Palliative care access is an urgent and ethical imperative to effectively manage the increasing burden of serious health-related suffering worldwide. Understanding the palliative care educational needs of health care professionals is critical to support evidence-based clinical practice in Rwanda and other low- and middle-income countries. A cross-sectional study was conducted at 5 hospitals in Kigali, Rwanda, to assess the palliative/end-of-life educational needs of nurses and physicians. The End-of-Life Professional Caregiver Survey and a demographic form were used to collect data. Descriptive analyses and independent t tests were conducted. A total of 420 health care professionals participated in the study (response rate, 72%). Participants perceived their knowledge and skills in providing palliative/end-of-life care as low. Those who received palliative/end-of-life care training in the past 5 years, third- and fourth-year residents, and health care providers with 5 years of experience or more had significantly higher (P ≤ .05) mean scores on the End-of-Life Professional Caregiver Survey. Nurses scored higher than physicians in the patient- and family-centered communication (P = .049) and cultural and ethical values (P = .037) subscales. Pain management was identified as an educational need by 77% of participants. Our survey suggests the need for increased governmental investments in palliative/end-of-life care education among nurses and physicians in Rwanda.
- 1 September 2020
- Published by Elsevier in International Journal of Nursing Studies
- Vol. 109, 103668
Rapid Investment in Nursing to Strengthen the Global COVID-19 Response
- 1 September 2020
- Published by Elsevier in International Journal of Nursing Studies
- Vol. 109, 103668
Rapid Investment in Nursing to Strengthen the Global COVID-19 Response
- 1 July 2018
- Published by Wolters Kluwer Health in Journal of Cardiovascular Nursing
- Vol. 33 (4) , 356-362
Illness Uncertainty and Posttraumatic Stress in Young Adults With Congenital Heart Disease
Background: Young adults with congenital heart disease (CHD) are at risk for chronic illness uncertainty in 4 domains: ambiguity about the state of their illness; lack of information about the disease, its treatment, and comorbidities; complexity of the healthcare system and relationship with healthcare providers; and unpredictability of the illness course and outcome. Chronic uncertainty has been associated with posttraumatic stress symptoms (PTSS) and posttraumatic stress disorder (PTSD). Objective: The aims of this study were to explore how young adults with CHD experience uncertainty and to describe the relationship between PTSS and the appraisal and management process. Methods: An exploratory, mixed methods design was used. Data were collected in person and via Skype from 25 participants (19–35 years old), who were diagnosed with CHD during childhood and able to read and write English. In-depth interviews and the University of California at Los Angeles Posttraumatic Stress Disorder Reaction Index were used to collect data. Qualitative data were analyzed using the constant comparative method. Results: The 4 domains of uncertainty were evident in the narratives. The PTSD mean (SD) score was 31.3 (7.7). Six participants met criteria for PTSD. Narrative analysis revealed a relationship between severity of PTSS and the appraisal and management of uncertainty. Participants with PTSD used management strategies that included avoidance, reexperiencing, and hyperarousal. Conclusions: Young adults with CHD may be at risk for the development of long-term psychological stress and PTSD in the setting of chronic uncertainty. Regular monitoring to identify PTSS/PTSD may be a means to promote treatment adherence and participation in healthcare.
- 1 July 2018
- Published by Wolters Kluwer Health in Journal of Cardiovascular Nursing
- Vol. 33 (4) , 356-362
Illness Uncertainty and Posttraumatic Stress in Young Adults With Congenital Heart Disease
Background: Young adults with congenital heart disease (CHD) are at risk for chronic illness uncertainty in 4 domains: ambiguity about the state of their illness; lack of information about the disease, its treatment, and comorbidities; complexity of the healthcare system and relationship with healthcare providers; and unpredictability of the illness course and outcome. Chronic uncertainty has been associated with posttraumatic stress symptoms (PTSS) and posttraumatic stress disorder (PTSD). Objective: The aims of this study were to explore how young adults with CHD experience uncertainty and to describe the relationship between PTSS and the appraisal and management process. Methods: An exploratory, mixed methods design was used. Data were collected in person and via Skype from 25 participants (19–35 years old), who were diagnosed with CHD during childhood and able to read and write English. In-depth interviews and the University of California at Los Angeles Posttraumatic Stress Disorder Reaction Index were used to collect data. Qualitative data were analyzed using the constant comparative method. Results: The 4 domains of uncertainty were evident in the narratives. The PTSD mean (SD) score was 31.3 (7.7). Six participants met criteria for PTSD. Narrative analysis revealed a relationship between severity of PTSS and the appraisal and management of uncertainty. Participants with PTSD used management strategies that included avoidance, reexperiencing, and hyperarousal. Conclusions: Young adults with CHD may be at risk for the development of long-term psychological stress and PTSD in the setting of chronic uncertainty. Regular monitoring to identify PTSS/PTSD may be a means to promote treatment adherence and participation in healthcare.