22 results on '"Sarah Brennenstuhl"'
Search Results
2. Intensity of end-of-life care among children with life-threatening conditions: a national population-based observational study
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Kimberley Widger, Sarah Brennenstuhl, Katherine E. Nelson, Hsien Seow, Adam Rapoport, Harold Siden, Christina Vadeboncoeur, Sumit Gupta, and Peter Tanuseputro
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End-of-life care ,High intensity care ,Life-threatening conditions ,Pediatrics ,RJ1-570 - Abstract
Abstract Background Children with life-threatening conditions frequently experience high intensity care at the end of life, though most of this research only focused on children with cancer. Some research suggests inequities in care provided based on age, disease type, socioeconomic status, and distance that the child lives from a tertiary hospital. We examined: 1) the prevalence of indicators of high intensity end-of-life care (e.g., hospital stays, intensive care unit [ICU] stays, death in ICU, use of cardiopulmonary resuscitation [CPR], use of mechanical ventilation) and 2) the association between demographic and diagnostic factors and each indicator for children with any life-threatening condition in Canada. Methods We conducted a population-based retrospective cohort study using linked health administrative data to examine care provided in the last 14, 30, and 90 days of life to children who died between 3 months and 19 years of age from January 1, 2008 to December 31, 2014 from any underlying life-threatening medical condition. Logistic regression was used to model the association between demographic and diagnostic variables and each indicator of high intensity end-of-life care except number of hospital days where negative binomial regression was used. Results Across 2435 child decedents, the most common diagnoses included neurology (51.1%), oncology (38.0%), and congenital illness (35.9%), with 50.9% of children having diagnoses in three or more categories. In the last 30 days of life, 42.5% (n = 1035) of the children had an ICU stay and 36.1% (n = 880) died in ICU. Children with cancer had lower odds of an ICU stay (OR = 0.47; 95% CI = 0.36–0.62) and ICU death (OR = 0.37; 95%CI = 0.28–0.50) than children with any other diagnoses. Children with 3 or more diagnoses (vs. 1 diagnosis) had higher odds of > 1 hospital stay in the last 30 days of life (OR = 2.08; 95%CI = 1.29–3.35). Living > 400 km (vs
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- 2023
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3. Evaluating knowledge and attitudes scales for the care of older adults among nursing students in Ghana
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Diana Abudu-Birresborn, Sarah Brennenstuhl, Martine Puts, Lynn McCleary, Vida Yakong, Charlene H. Chu, and Lisa Cranley
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Knowledge ,Attitudes ,Older adults ,Nursing students ,Instrument evaluation ,Ghana ,Nursing ,RT1-120 - Abstract
Abstract Background Understanding nursing students’ knowledge about and attitudes toward older adults’ using context-specific survey instruments can help to identify and design effective learning and teaching materials to improve the care for persons 60 years and above. However, there are no validated instruments to examine nursing students’ knowledge and attitudes toward the care for older adults in the African context. The study aimed to evaluate the items on the Knowledge about Older Patients Quiz and Kogan's Attitudes towards Old People Scale suitable for the African context. Methods A cross-sectional study was conducted using second-and third-year nursing students from two public Nursing Training Institutions in Ghana. Using Sahin’s rule of sample size estimate of at least 150 participants for unidimensional dichotomous scales, 170 nursing students were recruited to participate after an information session in their classrooms. Data were collected from December 2019—March 2020 using the Knowledge about Older Patients Quiz and Kogan’s Attitudes Towards Old People Scale. Item response theory was employed to evaluate the Knowledge about Older Patients Quiz difficulty level and discrimination indices. Corrected item-to-total correlation analysis was conducted for Kogan's Attitudes towards Old People Scale. The internal consistency for both scales was examined. Results Of the 170 participants, 169 returned completed surveys. The mean age of participants was 21 years (SD = 3.7), and (54%) were female. Of the 30-items of the Knowledge about Older Patients Quiz, seven items were very difficult for most students to choose the correct response, and one was easy, as most of the students chose the correct response. Although 22 items demonstrated appropriate difficulty level, discrimination indices were used to select the final 15- items that discriminated moderately between upper and lower 25% performing students. The Kuder-Richardson-20 reliability was. 0.30, which was low. Considering Kogan's Attitudes towards Old People scale, 10-items were removed following negative and low corrected item-to-total correlation and a high Alpha coefficient if items were deleted. The final 22-items had a Cronbach alpha coefficient of 0.65, which was moderately satisfactory. Conclusion Evaluation of the scales demonstrated essential content validity and moderate internal consistency for the context of our study. Further research should focus on ongoing context-specific refinement of the survey instruments to measure nursing students’ knowledge about and attitudes toward caring for older adults in the African context.
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- 2023
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4. The Development of Geriatric Assessment and Intervention Guidelines for an Online Geriatric Assessment Tool: A Canadian Modified Delphi Panel Study
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Martine Puts, Efthymios Papadopoulos, Sarah Brennenstuhl, Sara Durbano, Nazia Hossain, Brenda Santos, Kristin Cleverley, and Shabbir M. H. Alibhai
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geriatric assessment ,Delphi panel study ,geriatric oncology ,geriatric interventions ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Background: There are no guidelines available for what assessment tools to use in a patient’s self-completed online geriatric assessment (GA) with management recommendations. Therefore, we used a modified Delphi approach with Canadian expert clinicians to develop a consensus online GA plus recommendations tool. Methods: The panel consisted of experts in geriatrics, oncology, nursing, and pharmacy. Experts were asked to rate the importance and feasibility of assessments and interventions to be included in an online GA for patients. The items included in the first round were based on guidelines for in-person GA and literature review. The first two rounds were conducted using an online survey. A virtual 2 h meeting was held to discuss the items where no consensus was reached and then voted on in the final round. Results: 34 experts were invited, and 32 agreed to participate. In round 1, there were 85 items; in round 2, 50 items; and in round 3, 25 items. The final tool consists of fall history, assistive device use, weight loss, medication review, need help taking medication, social supports, depressive symptoms, self-reported vision and hearing, and current smoking status and alcohol use. Conclusion: This first multidisciplinary consensus on online GA will benefit research and clinical care for older adults with cancer.
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- 2022
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5. Cohort profile: Impact of Maternal and Paternal Mental Health – Assessing Concurrent Depression, Anxiety and Comorbidity in the Canadian Family (IMPACT study)
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Cindy-Lee Dennis, Simone Vigod, Rahman Shiri, Sarah Brennenstuhl, Kobra Falah-Hassani, Flavia Marini, Sophie Grigoriadis, Justine Dol, Hillary Brown, and Mark Wade
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Medicine - Abstract
Purpose This paper describes a prospective cohort, Impact of Maternal and Paternal Mental Health: Assessing Concurrent Depression, Anxiety and Comorbidity in The Canadian Family (IMPACT) study, which followed maternal–paternal dyads and their children across the first 2 years post partum.Participants A total of 3217 cohabitating maternal–paternal dyads were recruited into the study from 2014 to 2018. Each dyad member separately completed online questionnaires at baseline (
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- 2023
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6. Modification and adaptation of the general self-efficacy scale to determine nursing students’ belief in their capability to care for older adults
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Diana Abudu-Birresborn, Sarah Brennenstuhl, Martine Puts, Lynn McCleary, Vida Yakong Nyagre, Charlene H. Chu, and Lisa Cranley
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Gerontological nursing ,Geriatric education ,Guided mastery ,Self-efficacy ,Self-regulation ,Lower- and middle-income countries ,History of Africa ,DT1-3415 ,Nursing ,RT1-120 - Abstract
It is necessary to determine nursing students’ self-efficacy to care for person's 60 + years to identify opportunities and challenges to support, facilitate effective learning and performance, and enhance confidence in providing care for older adults. However, we did not find a validated survey instrument to determine self-efficacy to care for older adults. This paper aimed to describe the modification of the General Self-efficacy scale to the General Self-efficacy to Care for Older scale appropriate for the Africa context. A cross-sectional study was conducted with second- and third-year nursing students from two public Nursing and Midwifery Training Colleges in the northern and southern sectors of Ghana. The 13-item General Self-Efficacy Scale was expanded by adding 17 items specific to providing nursing care for older adults in acute care settings. Cognitive interviews were conducted to ensure the items added were understood by participants. The 30-items were tested using Exploratory Factor analysis. The mean age of participants was 21 years (SD = 3.73). More than half (54%) of the participants were female. An exploratory factor analysis yielded a two-factor model. Four items were removed due to low factors and cross-loadings on both factors. The remaining 26 items had fourteen items that loaded on Factor one and 12 items that loaded on Factor two. The Cronbach Alpha coefficient for the revised 26-item scale was 0.85 indicating good internal consistency. The modified scale is appropriate to examine nursing students’ self-efficacy to care for older adults in the African context.
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- 2023
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7. Medical, behavioural and social preconception and interconception risk factors among pregnancy planning and recently pregnant Canadian women
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Hilary K Brown, Cindy-Lee Dennis, Sarah Brennenstuhl, Rhonda C Bell, Sarah Carsley, Flavia Marini, Stephanie Atkinson, Dragana Misita, Catherine Birken, Alessandra Prioreschi, and Nilusha Jiwani-Ebrahim
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Medicine (General) ,R5-920 - Abstract
Objectives The objective of this study is to describe the clustering of medical, behavioural and social preconception and interconception health risk factors and determine demographic factors associated with these risk clusters among Canadian women.Design Cross-sectional data were collected via an online questionnaire assessing a range of preconception risk factors. Prevalence of each risk factor and the total number of risk factors present was calculated. Multivariable logistic regression models determined which demographic factors were associated with having greater than the mean number of risk factors. Exploratory factor analysis determined how risk factors clustered, and Spearman’s r determined how demographic characteristics related to risk factors within each cluster.Setting Canada.Participants Participants were recruited via advertisements on public health websites, social media, parenting webpages and referrals from ongoing studies or existing research datasets. Women were eligible to participate if they could read and understand English, were able to access a telephone or the internet, and were either planning a first pregnancy (preconception) or had ≥1 child in the past 5 years and were thus in the interconception period.Results Most women (n=1080) were 34 or older, and were in the interconception period (98%). Most reported risks in only one of the 12 possible risk factor categories (55%), but women reported on average 4 risks each. Common risks were a history of caesarean section (33.1%), miscarriage (27.2%) and high birth weight (13.5%). Just over 40% had fair or poor eating habits, and nearly half were not getting enough physical activity. Three-quarters had a body mass index indicating overweight or obesity. Those without a postsecondary degree (OR 2.35; 95% CI 1.74 to 3.17) and single women (OR 2.22, 95% CI 1.25 to 3.96) had over twice the odds of having more risk factors. Those with two children or more had 60% lower odds of having more risk factors (OR 0.68, 95% CI 0.52 to 0.86). Low education and being born outside Canada were correlated with the greatest number of risk clusters.Conclusions Many of the common risk factors were behavioural and thus preventable. Understanding which groups of women are prone to certain risk behaviours provides opportunities for researchers and policy-makers to target interventions more efficiently and effectively.
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- 2022
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8. COVID-19 Pandemic Impact and Response in Canadian Pediatric Chronic Pain Care: A National Survey of Medical Directors and Pain Professionals
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Tieghan Killackey, Melanie Noel, Kathryn A. Birnie, Manon Choinière, M. Gabrielle Pagé, Lise Dassieu, Anaïs Lacasse, Chitra Lalloo, Sarah Brennenstuhl, Patricia Poulin, Pablo Ingelmo, Samina Ali, Marco Battaglia, Fiona Campbell, Andrew Smith, Lauren Harris, Vina Mohabir, Myles Benayon, Isabel Jordan, Justina Marianayagam, and Jennifer Stinson
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covid-19 ,pediatric pain ,pain clinics ,distance treatments ,e-health ,telehealth ,Medicine (General) ,R5-920 ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Background: The COVID-19 pandemic presents one of the greatest threats to pediatric pain care seen in generations. Due to public health restrictions, many pediatric pain clinics halted in-person appointments, delaying and disrupting access to care. There is no existing research on the impacts of COVID-19 on pediatric chronic pain care in Canada or the challenges experienced by health care professionals and pain clinics. Aims: The aim of this study was to evaluate the impact of COVID-19 on Canadian pediatric chronic pain care by documenting how health care professionals provided care during the first six months of the pandemic. Methods: Two Canadian online cross-sectional surveys were conducted: one among Canadian pediatric pain clinic directors (Study 1) and another among multidisciplinary pediatric pain health care professionals (Study 2). Results: Responses from 13/13 Canadian pediatric pain clinics/rehabilitation programs indicated that all clinics provided virtual care during the pandemic. No significant changes were reported on the frequency of appointment requests. Most clinics reported no perceived change in patient pain levels (n = 9/13, 69%) or occurrence of pain flares (n = 10/13, 77%). Results from 151 individual health care professionals indicated that the majority (90%) of non–emergency department respondents were providing virtual care. The main challenges of virtual care included technological barriers, financial concerns, infrastructure and logistics, privacy, and clinical challenges. Conclusions: This study documented the impact of the COVID-19 pandemic on pediatric chronic pain care in Canada and highlighted the rapid shift to using virtual solutions. Simultaneously, respondents outlined current challenges and potential solutions to consider in the development of virtual care guidelines and policy in Canada.
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- 2021
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9. Preconception risk factors and health care needs of pregnancy-planning women and men with a lifetime history or current mental illness: A nationwide survey.
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Cindy-Lee Dennis, Hilary K Brown, Sarah Brennenstuhl, Simone Vigod, Ainsley Miller, Rita Amiel Castro, Flavia Casasanta Marini, and Catherine Birken
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Medicine ,Science - Abstract
ObjectivesWhile depression and anxiety are common in women and men of reproductive age, preconception interventions to optimize the health of individuals with mental illness before pregnancy is limited and focuses primarily on psychotropic medication management. Comparing individuals with depression, anxiety, and comorbidity to those with neither condition, we identified areas of preconception care optimization related to psychosocial risk factors, general physical health, medication use, and uptake of high-risk health behaviours. We also investigated differences in preconception health care use, attitudes, and knowledge.MethodWe conducted a nationwide survey of 621 women (n = 529) and men (n = 92) across Canada who were planning a pregnancy within five years, including those with lifetime or current depression (n = 38), anxiety (n = 55), and comorbidity (n = 104) and those without mental illness (n = 413). Individuals with depression, anxiety, and comorbidity were compared to individuals without mental illness using logistic regression, adjusted for age, sex, and education level.ResultsIndividuals with a lifetime or current mental illness were significantly more likely to have several risk factors for suboptimal reproductive and perinatal outcomes, including increased rates of obesity, stress, fatigue, loneliness, number of chronic health conditions, and medication use. Further, they were more likely to have high-risk health behaviours including increased substance use, internet addiction, poorer eating habits, and decreased physical activity. By assessing depression, anxiety, or both separately, we also determined there was variation in risk factors by mental illness type.ConclusionOur nationwide study is one of the first and largest to examine the preconception care needs of women and men with a lifetime or current mental illness who are pregnancy-planning. We found this population has many important reproductive and perinatal risk factors that are modifiable via preconception interventions which could have a significant positive impact on their health trajectories and those of their future children.
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- 2022
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10. Screen use and internet addiction among parents of young children: A nationwide Canadian cross-sectional survey
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Cindy-Lee Dennis, Sarah Carsley, Sarah Brennenstuhl, Hilary K. Brown, Flavia Marini, Rhonda C. Bell, Ainsley Miller, Saranyah Ravindran, Valerie D’Paiva, Justine Dol, and Catherine S. Birken
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Medicine ,Science - Abstract
Objectives To establish the factorial structure and internal consistency of the Internet Addiction Test (IAT) in parents, the level and correlates of problematic internet use, and patterns and types of screen use. Study design Data were collected through an online questionnaire about preconception health among Canadian women and men with ≥1 child. The questionnaire included the IAT and questions about time spent on screens by device type, use of screens during meals and in the bedroom, and perceptions of overuse. Factor analysis was completed to determine the factorial structure of the IAT, with multivariable linear regression used to determine correlates of the IAT. Results The sample included 1,156 respondents (mean age: 34.3 years; 83.1% female). The IAT had two factors: “impairment in time management” and “impairment in socio-emotional functioning” of which respondents had more impairment in time management than socio-emotional functioning. Based on the original IAT, 19.4% of respondents would be classified as having a mild internet use problem with 3.0% having a moderate or severe issue. In the multivariable model, perceived stress (b = .28, SE = .05, p < .001) and depressive symptoms (b = .24, SE = .10, p = .017) were associated with higher IAT scores. Handheld mobile devices were the most common type of screen used (mean = 3 hours/day) followed by watching television (mean = 2 hours/day). Conclusion Parents spent a significant portion of their time each day using screens, particularly handheld mobile devices. The disruption caused by mobile devices may hinder opportunities for positive parent-child interactions, demonstrating the need for resources to support parents ever-growing use of technologies.
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- 2022
11. Factor structure of the Quality of Children’s Palliative Care Instrument (QCPCI) when completed by parents of children with cancer
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Kimberley Widger, Sarah Brennenstuhl, Jacqueline Duc, Ann Tourangeau, and Adam Rapoport
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Palliative care ,Instrument development ,Pediatrics ,Quality care ,Special situations and conditions ,RC952-1245 - Abstract
Abstract Background Currently available indicators of quality pediatric palliative care tend to focus on care provided during the end-of-life period rather than care provided throughout the disease trajectory. We adapted a previously developed instrument focused on mothers’ perspectives on the quality of end-of-life care and assessed its psychometric properties with mothers and fathers of children with cancer at any stage of the illness. Methods Four subscales were included in the analysis: Connect with Families, Involve Parents, Share Information Among Health Professionals, Support Siblings. The number of items across the four subscales was reduced from 31 to 15. We conducted confirmatory factor analysis, composite reliability, internal consistency, and tests of correlation between the overall scale and subscale totals and a separate question inquiring about overall quality of care. Measurement invariance between mothers and fathers was assessed. Results A total of 533 mothers and fathers completed the survey. The four-factor model was confirmed and there were significant correlations between each subscale score and responses to the overall item on care quality. Cronbach’s alpha was adequate for the scale as a whole and for each subscale ranging from 0.78 to 0.90. We also found the factor structure, means, and intercepts were similar across mothers and fathers, suggesting the tool can be used by both groups. Conclusions There is evidence for a four-factor structure within a new Quality of Children’s Palliative Care Instrument (QCPCI) with demonstrated reliability when used with mothers and fathers of children with cancer. Ongoing assessment of the psychometric properties is needed, including testing in additional populations. However, our initial findings suggest that the QCPCI may be a helpful tool for assessing the quality of palliative care for pediatric patients anywhere along the disease trajectory from the perspective of parents.
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- 2019
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12. A comparison of educational events for physicians and nurses in Australia sponsored by opioid manufacturers.
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Quinn Grundy, Sasha Mazzarello, Sarah Brennenstuhl, and Emily A Karanges
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Medicine ,Science - Abstract
BackgroundEducational activities for physicians sponsored by opioid manufacturers are implicated in the over- and mis-prescribing of opioids. However, the implications of promotion to nurses are poorly understood. Nurses play a key role in assessing pain, addressing the determinants of pain, and administering opioid medications. We sought to understand the nature and content of pain-related educational events sponsored by opioid manufacturers and to compare events targeting physicians and nurses.MethodsWe conducted a cross sectional, descriptive analysis of pharmaceutical company reports detailing 116,845 sponsored educational events attended by health professionals from 2011 to 2015 in Australia. We included events that were sponsored by manufacturers of prescription opioid analgesics and were pain related. We compared event characteristics across three attendee groups: (a) physicians only; (b) at least one nurse in attendance; and (c) nurses only. We coded the unstructured data using iteratively generated keywords for variables related to location, format, and content focus.ResultsWe identified 3,411 pain-related events sponsored by 3 companies: bioCSL/CSL (n = 15), Janssen (n = 134); and Mundipharma (n = 3,262). Pain-related events were most often multidisciplinary, including at least one nurse (1,964/3,411; 58%); 38% (1,281/3,411) included physicians only, and 5% (166/3,411) nurses only. The majority of events were held in clinical settings (61%) and 43% took the form of a journal club. Chronic pain was the most common event topic (26%) followed by cancer pain and palliative care (18%), and then generic or unspecified references to pain (15%); nearly a third (32%) of event descriptions contained insufficient information to determine the content focus. Nurse-only events were less frequently held in clinical settings (32%; p < .001) and more frequently were product launches (17%; p < .001) and a significantly larger proportion focused on cancer or palliative care (33%; p < .001), generic pain topics (27%; p < .001), and geriatrics (25%; p < .001) than physician-only or multidisciplinary events.DiscussionOpioid promotion via sponsored educational events extends beyond physicians to multidisciplinary teams and specifically, nurses. Despite lack of evidence that opioids improve outcomes for long-term chronic non-cancer pain, hundreds of sponsored educational events focused on chronic pain. Regulators should consider the validity of distinguishing between pharmaceutical companies' "promotional" and "non-promotional" activities.
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- 2021
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13. Carrying the Pain of Abuse: Gender-Specific Findings on the Relationship between Childhood Physical Abuse and Obesity in Adulthood
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Esme Fuller-Thomson, Deborah A. Sinclair, and Sarah Brennenstuhl
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Childhood physical abuse ,Adverse childhood experiences ,Gender ,Health behaviors ,Socioeconomic status ,Mental health ,Nutrition. Foods and food supply ,TX341-641 ,Nutritional diseases. Deficiency diseases ,RC620-627 - Abstract
Background: Childhood abuse has been associated with negative adult health outcomes, including obesity. This study sought to investigate the association between childhood physical abuse and adult obesity, while controlling for five clusters of potentially confounding factors: childhood stressors, socioeconomic indicators, marital status, health behaviors, and mental health. Methods: Representative data from the 2005 Canadian Community Health Survey were selected. The response rate was approximately 84%. Gender-specific logistic regression analyses determined the association between abuse and obesity, while controlling for age and race and five clusters of potentially confounding factors. Of the 12,590 respondents with complete data, 2,787 were obese and 976 reported physical abuse as a child or adolescent by someone close to them. Results: Among women with childhood physical abuse compared to no abuse, the odds of obesity were 35% higher, even when controlling for age, race, and the five clusters of factors (odds ratio (OR) = 1.35; 95% confidence interval (CI) = 1.09, 1.67). Childhood physical abuse was not associated with adult obesity among men (OR = 1.12; 95% CI = 0.82, 1.53). Conclusions: This study provides one of the first population-based, gender-specific analyses of the association between childhood physical abuse and obesity controlling for a wide range of factors. The gender-specific findings require further exploration.
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- 2013
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14. Health Characteristics of Solo Grandparent Caregivers and Single Parents: A Comparative Profile Using the Behavior Risk Factor Surveillance Survey
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Deborah M. Whitley, Esme Fuller-Thomson, and Sarah Brennenstuhl
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Geriatrics ,RC952-954.6 - Abstract
Objectives. To describe the health characteristics of solo grandparents raising grandchildren compared with single parents. Methods. Using the 2012 Behavioral Risk Factor Surveillance System, respondents identified as a single grandparent raising a grandchild were categorized as a solo grandparent; grandparent responses were compared with single parents. Descriptive analysis compared health characteristics of 925 solo grandparents with 7,786 single parents. Results. Compared to single parents, grandparents have a higher prevalence of physical health problems (e.g., arthritis). Both parent groups have a high prevalence of lifetime depression. A larger share of grandparents actively smoke and did no recreational physical exercise in the last month. However, grandparents appear to have better access to health services in comparison with single parents. Conclusion. Solo grandparents may be at risk for diminished physical capacity and heightened prevalence of depression. Health professionals can be an important resource to increase grandparents’ physical and emotional capacities.
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- 2015
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15. Migraine and Despair: Factors Associated with Depression and Suicidal Ideation among Canadian Migraineurs in a Population-Based Study
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Esme Fuller-Thomson, Meghan Schrumm, and Sarah Brennenstuhl
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Psychiatry ,RC435-571 ,Psychology ,BF1-990 - Abstract
This study sought to (1) investigate the association between migraine and both depression and suicidal ideation and (2) to identify the factors independently associated with each of these mental health problems among Canadian men and women with migraine. Data were analyzed from the 2005 Canadian Community Health Survey (CCHS). Presence of migraine was assessed by self-report of a health professional diagnosis. Current depression was measured using the CIDI-SF, and suicidal ideation was based on a question about serious consideration of suicide at any point during the respondent's lifetime. Migraineurs were found to have elevated odds of depression (men: OR = 2.02; 95% CI = 1.70, 2.41; women: OR = 1.89; 95% CI = 1.71, 2.10) and suicidal ideation (men: OR = 1.70; 95% CI = 1.55, 1.96; women: OR = 1.72; 95% CI = 1.59, 1.86) even when adjusting for sociodemographic variables and disability status. The odds of depression and suicidal ideation were higher among both genders of migraineurs who were younger, unmarried and had more activity limitations; associations with poverty and race depended on gender and whether the focus was on depression or suicidal ideation. While screening for depression is already recommended for those with migraine, this research helps identify which migraineurs may require more immediate attention, including those who are younger, unmarried, and experiencing limitations in their activities.
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- 2013
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16. Nurses’ Attitudes Toward the Importance of Families in Nursing Care: A Multinational Comparative Study
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Zarina Nahar Kabir, Sarah Brennenstuhl, Simon Ching Lam, Hanne Konradsen, Angela Yee Man Leung, Lisa Cranley, and Anne-Marie Boström
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Community and Home Care ,cross-sectional ,Attitude of Health Personnel ,Research ,Perspective (graphical) ,Nurses ,cross-national comparisons ,nurse attitudes ,Nursing care ,Cross-Sectional Studies ,Nursing ,Multinational corporation ,family-focused care ,Surveys and Questionnaires ,Family Nursing ,Humans ,survey ,Nursing Care ,Family Practice ,Psychology - Abstract
The aim of this study was to examine nurses’ attitudes about the importance of family in nursing care from an international perspective. We used a cross-sectional design. Data were collected online using the Families’ Importance in Nursing Care—Nurses’ Attitudes (FINC-NA) questionnaire from a convenience sample of 740 registered nurses across health care sectors from Sweden, Ontario, Canada, and Hong Kong, China. Mean levels of attitudes were compared across countries using analysis of variance (ANOVA). Multiple regression was used to identify factors associated with nurses’ attitudes and to test for interactions by country. Factors associated with nurse attitudes included country, age, gender, and several practice areas. On average, nurses working in Hong Kong had less positive attitudes compared with Canada and Sweden. The effects of predictors on nurses’ attitudes did not vary by country. Knowledge of nurses’ attitudes could lead to the development of tailored interventions that facilitate nurse-family partnerships in care.
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- 2021
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17. COVID-19 Pandemic Impact and Response in Canadian Pediatric Chronic Pain Care: A National Survey of Medical Directors and Pain Professionals
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Lauren Harris, Jennifer Stinson, Pablo Ingelmo, Chitra Lalloo, Andrew M. Smith, Anaïs Lacasse, Patricia A. Poulin, Lise Dassieu, Justina Marianayagam, Manon Choinière, Sarah Brennenstuhl, Samina Ali, Fiona Campbell, Marco Battaglia, Vina Mohabir, M. Gabrielle Pagé, Isabel Jordan, Melanie Noel, Tieghan Killackey, Kathryn A. Birnie, and Myles Benayon
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medicine.medical_specialty ,2019-20 coronavirus outbreak ,Medicine (General) ,Coronavirus disease 2019 (COVID-19) ,telehealth ,Telehealth ,RM1-950 ,pediatric pain ,03 medical and health sciences ,0302 clinical medicine ,R5-920 ,Pandemic ,Medicine ,030212 general & internal medicine ,business.industry ,pain clinics ,Public health ,Chronic pain ,COVID-19 ,medicine.disease ,3. Good health ,Anesthesiology and Pain Medicine ,Pain Clinics ,Family medicine ,Pediatric pain ,distance treatments ,e-health ,Therapeutics. Pharmacology ,business ,030217 neurology & neurosurgery ,Research Article - Abstract
Background: The COVID-19 pandemic presents one of the greatest threats to pediatric pain care seen in generations. Due to public health restrictions, many pediatric pain clinics halted in-person appointments, delaying and disrupting access to care. There is no existing research on the impacts of COVID-19 on pediatric chronic pain care in Canada or the challenges experienced by health care professionals and pain clinics. Aims: The aim of this study was to evaluate the impact of COVID-19 on Canadian pediatric chronic pain care by documenting how health care professionals provided care during the first six months of the pandemic. Methods: Two Canadian online cross-sectional surveys were conducted: one among Canadian pediatric pain clinic directors (Study 1) and another among multidisciplinary pediatric pain health care professionals (Study 2). Results: Responses from 13/13 Canadian pediatric pain clinics/rehabilitation programs indicated that all clinics provided virtual care during the pandemic. No significant changes were reported on the frequency of appointment requests. Most clinics reported no perceived change in patient pain levels (n = 9/13, 69%) or occurrence of pain flares (n = 10/13, 77%). Results from 151 individual health care professionals indicated that the majority (90%) of non–emergency department respondents were providing virtual care. The main challenges of virtual care included technological barriers, financial concerns, infrastructure and logistics, privacy, and clinical challenges. Conclusions: This study documented the impact of the COVID-19 pandemic on pediatric chronic pain care in Canada and highlighted the rapid shift to using virtual solutions. Simultaneously, respondents outlined current challenges and potential solutions to consider in the development of virtual care guidelines and policy in Canada.
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- 2021
18. Health of mothers of young children in Canada: identifying dimensions of inequality based on socio-economic position, partnership status, race, and region
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Sarah Brennenstuhl
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Adult ,medicine.medical_specialty ,Canada ,Inequality ,media_common.quotation_subject ,Mothers ,Logistic regression ,Odds ,Decile ,03 medical and health sciences ,Race (biology) ,Young Adult ,0302 clinical medicine ,Risk Factors ,medicine ,Humans ,030212 general & internal medicine ,media_common ,Social policy ,Marital Status ,030503 health policy & services ,Public health ,Racial Groups ,Public Health, Environmental and Occupational Health ,Infant ,General Medicine ,Health Status Disparities ,Middle Aged ,Health Surveys ,Religion ,Social Class ,Child, Preschool ,Community health ,Female ,Quantitative Research ,0305 other medical science ,Psychology ,Demography - Abstract
OBJECTIVES: Little is known about the nature of health inequalities present among women who are mothers of young children in Canada. Therefore, the purpose of the study is to identify dimensions of inequalities based on socio-economic position, race, partner status, and region and determine whether each type of inequality is independent of another. METHODS: Data are from the 2014 Canadian Community Health Survey. Women identifying as a parent living with a child ≤ 5 years, with complete data on the variables of interest, were selected (n = 2656). Poor health was defined as the presence of two or more chronic conditions. Exposures included partner status, education level, race, income, and region (Québec vs. rest of Canada). Logistic regression was used to estimate the odds of poor health according to each exposure unadjusted and adjusted for all other exposures. All analyses controlled for age and employment status. RESULTS: In the fully adjusted model, among mothers of young children, the odds of poor health were significantly higher among non-white identifying (OR = 1.72; 95% CI = 1.34–2.21) and lone mothers (OR = 1.80; 95% CI = 1.35–2.39), but were significantly lower among those with higher incomes (OR[per decile] = 0.86; 95% CI = 0.82–0.90) and those from Québec (vs. the rest of Canada; OR = 0.50; 95% CI = 0.38–0.67). CONCLUSIONS: Living in Québec compared to elsewhere in Canada appears to protect against poor health among mothers of young children. Regardless of region, health inequalities exist by socio-economic position, race, and partnership status. These findings have implications for public health programs and policies, such as universal child care. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.17269/s41997-018-0038-5) contains supplementary material, which is available to authorized users.
- Published
- 2018
19. Health Characteristics of Solo Grandparent Caregivers and Single Parents: A Comparative Profile Using the Behavior Risk Factor Surveillance Survey
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Sarah Brennenstuhl, Esme Fuller-Thomson, and Deborah M. Whitley
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Gerontology ,Article Subject ,Descriptive statistics ,Behavioral Risk Factor Surveillance System ,business.industry ,Grandparent ,lcsh:Geriatrics ,Health services ,lcsh:RC952-954.6 ,Grandchild ,Medicine ,Geriatrics and Gerontology ,Risk factor ,business ,Recreation ,Depression (differential diagnoses) ,Research Article - Abstract
Objectives. To describe the health characteristics of solo grandparents raising grandchildren compared with single parents.Methods. Using the 2012 Behavioral Risk Factor Surveillance System, respondents identified as a single grandparent raising a grandchild were categorized as asolo grandparent; grandparent responses were compared with single parents. Descriptive analysis compared health characteristics of 925 solo grandparents with 7,786 single parents.Results. Compared to single parents, grandparents have a higher prevalence of physical health problems (e.g., arthritis). Both parent groups have a high prevalence of lifetime depression. A larger share of grandparents actively smoke and did no recreational physical exercise in the last month. However, grandparents appear to have better access to health services in comparison with single parents.Conclusion. Solo grandparents may be at risk for diminished physical capacity and heightened prevalence of depression. Health professionals can be an important resource to increase grandparents’ physical and emotional capacities.
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- 2015
20. Migraine and Despair: Factors Associated with Depression and Suicidal Ideation among Canadian Migraineurs in a Population-Based Study
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Sarah Brennenstuhl, Esme Fuller-Thomson, and Meghan Schrumm
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medicine.medical_specialty ,Article Subject ,business.industry ,lcsh:RC435-571 ,lcsh:BF1-990 ,Poison control ,medicine.disease ,Mental health ,Suicide prevention ,Occupational safety and health ,Psychiatry and Mental health ,Clinical Psychology ,lcsh:Psychology ,Migraine ,lcsh:Psychiatry ,Injury prevention ,medicine ,medicine.symptom ,Psychiatry ,business ,Suicidal ideation ,Depression (differential diagnoses) ,Research Article - Abstract
This study sought to (1) investigate the association between migraine and both depression and suicidal ideation and (2) to identify the factors independently associated with each of these mental health problems among Canadian men and women with migraine. Data were analyzed from the 2005 Canadian Community Health Survey (CCHS). Presence of migraine was assessed by self-report of a health professional diagnosis. Current depression was measured using the CIDI-SF, and suicidal ideation was based on a question about serious consideration of suicide at any point during the respondent's lifetime. Migraineurs were found to have elevated odds of depression (men: OR = 2.02; 95% CI = 1.70, 2.41; women: OR = 1.89; 95% CI = 1.71, 2.10) and suicidal ideation (men: OR = 1.70; 95% CI = 1.55, 1.96; women: OR = 1.72; 95% CI = 1.59, 1.86) even when adjusting for sociodemographic variables and disability status. The odds of depression and suicidal ideation were higher among both genders of migraineurs who were younger, unmarried and had more activity limitations; associations with poverty and race depended on gender and whether the focus was on depression or suicidal ideation. While screening for depression is already recommended for those with migraine, this research helps identify which migraineurs may require more immediate attention, including those who are younger, unmarried, and experiencing limitations in their activities.
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- 2013
- Full Text
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21. Information needs of early-stage prostate cancer patients: A comparison of nine countries
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Nuno Pimentel, Francis C. J. M. van Gils, Marzena Gawkowska-Suwinska, Deb Feldman-Stewart, Ufuk Abacioglu, Carlo Capirci, Madelon Pijls-Johannesma, Víctor Macías, Clare Moynihan, Sarah Brennenstuhl, Christine Tong, A. Heyda, Herbert Wördehoff, Isabel Monteiro Grillo, Sefik Igdem, Chris Parker, Radiotherapie, and RS: GROW - School for Oncology and Reproduction
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Male ,Health Knowledge, Attitudes, Practice ,Multivariate statistics ,medicine.medical_specialty ,Multivariate analysis ,Stage prostate cancer ,Information needs ,Treatment and control groups ,Surveys and Questionnaires ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Aged ,Retrospective Studies ,Male Genitals ,business.industry ,Prostatic Neoplasms ,Patient information needs ,Hematology ,Variance (accounting) ,Patient education ,Early-stage prostate cancer ,Surgery ,Oncology ,business ,Demography - Abstract
Background and purpose Providing information to patients can improve their medical and psychological outcomes. We sought to identify core information needs common to most early-stage prostate cancer patients in participating countries. Material and methods Convenience samples of patients treated 3–24 months earlier were surveyed in Canada, England, Italy, Germany, Poland, Portugal, Netherlands, Spain, and Turkey. Each participant rated the importance of addressing each of 92 questions in the diagnosis-to-treatment decision interval (essential/desired/no opinion/avoid). Multivariate modelling determined the extent of variance accounted by covariates, and produced an unbiased prediction of the proportion of essential responses for each question. Results Six hundred and fifty-nine patients responded (response rates 45–77%). On average, 35–53 questions were essential within each country; similar questions were essential to most patients in most countries. Beyond cross-country similarities, each country showed wide variability in the number and which questions were essential. Multivariate modelling showed an adjusted R -squared with predictors country, age, education, and treatment group of only 6% of the variance. A core of 20 questions were predicted to be essential to >2/3 of patients. Conclusions Core information can be identified across countries. However, providing the core should only be a first step; each country should then provide information tailored to the needs of the individual patient.
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- 2010
22. Development, Psychometric Assessment, and Predictive Validity of the Postpartum Childcare Stress Checklist.
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Dennis CL, Brown HK, and Brennenstuhl S
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- Adolescent, British Columbia, Child Care standards, Child, Preschool, Depression, Postpartum psychology, Female, Humans, Infant, Longitudinal Studies, Middle Aged, Psychometrics instrumentation, Psychometrics methods, Reproducibility of Results, Stress, Psychological complications, Stress, Psychological psychology, Surveys and Questionnaires, Child Care psychology, Depression, Postpartum etiology, Mothers psychology, Psychometrics standards, Stress, Psychological etiology
- Abstract
Background: Childcare stress has been shown to predict postpartum depression; however, there is little research exploring and validating the dimensions of childcare stress instruments such that preventive interventions can be created., Objectives: The aim of this study was to develop and psychometrically test an instrument to measure parental perceptions of postpartum childcare stress., Methods: Using research based on postpartum stress and childcare stress, the Postpartum Childcare Stress Checklist (PCSC) was developed, and content validity was judged by experts. The PCSC was psychometrically assessed in a cohort of 541 women in a health region near Vancouver, Canada, who were followed to 8 weeks postpartum in 2002. The psychometric assessment analyses comprised internal consistency, exploratory factory analysis, concurrent validity, and predictive validity., Results: The 19-item PCSC had good internal consistency (Kuder-Richardson Formula 20 coefficient: 0.81). Exploratory factor analysis revealed the following dimensions: (a) relationship with the partner, (b) caring for the infant, (c) maternal social interactions, and (d) establishing a new routine. Predictive validity analyses showed that PCSC total and subscale scores at 4 weeks were positively correlated with depressive symptomatology, anxiety, and perceived stress and negatively correlated with global and partner support at 8 weeks postpartum., Discussion: The PCSC is a measure of childcare stress with excellent reliability and validity. Upon further testing, it may be used to identify women and couples in need of greater support, individualize postpartum care, and evaluate the effectiveness of preventive interventions.
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- 2018
- Full Text
- View/download PDF
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