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Background: Neighborhood and caregiver characteristics have each been linked to children's asthma outcomes, but less is known about how caregiver psychosocial functioning may explain the link between neighborhood characteristics and asthma outcomes.
Objective: To examine associations between neighborhood safety, caregiver stress and depressive symptoms, and children's asthma outcomes, and to evaluate whether caregiver stress and depressive symptoms mediate the relationship between neighborhood safety and asthma outcomes.
Methods: We analyzed baseline data from a prospective cohort study of the effects of a housing mobility program on children's asthma-related outcomes. Age- and sex-adjusted models evaluated associations of neighborhood safety, and caregiver stress and depressive symptoms, with children's asthma symptoms and exacerbations.
Results: Participants were 140 low-income children with persistent asthma (98% Black participants; 53% males; mean age, 9.0 years) with an average of 7.1 ± 5.3 maximum symptom days per 2 weeks. Lower neighborhood safety, and higher caregiver stress and depressive symptoms, were associated with higher asthma symptoms, but not exacerbations, in adjusted models (eg, for neighborhood safety, maximum symptom days: odds ratio, 1.41; 95% CI, 1.07-1.88; for caregiver stress, maximum symptom days: odds ratio, 1.08; 95% CI, 1.01-1.15; for depressive symptoms, maximum symptom days: odds ratio, 1.05; 95% CI, 1.00-1.11). Exploratory analyses suggested that caregiver stress partially mediated associations between neighborhood safety and asthma symptoms for children in unsafe neighborhoods.
Conclusions: Neighborhood safety was associated with children's asthma symptoms independent from caregiver stress and depressive symptoms, although for children in unsafe neighborhoods, caregiver stress may partially mediate this association. Findings suggest the importance of targeting multiple systems to improve children's asthma outcomes.
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http://dx.doi.org/10.1016/j.jaip.2021.08.043 | DOI Listing |
Rev Infirm
September 2025
Faculté des sciences infirmières, Pavillon Ferdinand-Vandry, local 3463, Université Laval, Québec, G1V 0A6, Canada. Electronic address:
While we work with patients when they are victims of an adverse event in their care, we too often ignore the fact that the caregiver also experiences the consequences of this event. Some of these events lengthen hospital stays, aggravate health problems and can even lead to death. For the caregivers involved, as well as for the health-care teams, the effects are far from negligible in terms of affect and psychological suffering.
View Article and Find Full Text PDFDementia (London)
September 2025
International Observatory on End of Life Care, Lancaster University, UK.
As the prevalence of dementia rises exponentially globally, instituting practices to support the dying process of people affected by dementia is a public health priority. However, end-of-life quality indicators such as place of death provide limited information about the totality of the dying process. Hence, this study's aim was to identify factors affecting the relatively understudied concept of final place of care (where care was received in the last three days of life i.
View Article and Find Full Text PDFPediatr Transplant
November 2025
BC Children's and Women's Hospital, Vancouver, British Columbia, Canada.
Background: Many children and adolescents who undergo solid organ transplants (SOT) develop post-traumatic stress (PTS) symptoms. Despite its prevalence and strong association with long-term impairments in quality of life, PTS is often overlooked as a major co-morbidity in many transplant programs. To address this unmet need, the purpose of this study was to explore the factors that impede or facilitate awareness of PTS, access to resources, and readiness to engage with mental health services.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, County Clinic Hospital, Calea Bucuresti 25-27 Street, 500037 Brasov; Faculty of Medicine, Transilvania University, Balcescu Street 56, 500040 Brasov, Romania.
Shifting away from the traditional perspective on parkisonism, which focused only on the motor state of the patients, recent research proves the importance of early recognition and treatment of non-motor symptoms. Patients with parkinsonism, who suffer from various sleep disturbances, such as excessive daytime sleepiness (EDS), experience lower quality of life, a negative impact on activities of daily living, and possible exposure to life-threatening situations. Implementing the routine use of subjective and objective means of diagnosing EDS, into clinical practice, allows for a personalised management plan, in scope of efficiently decreasing disease burden for both the patient and the caregiver.
View Article and Find Full Text PDFSleep Med Clin
September 2025
Department of Neurology, National Institute of Mental Health & Neuro Sciences (NIMHANS), Hosur Road, Bengaluru 560029, Karnataka, India. Electronic address:
Sleep dysfunction is a significant component of the non-motor symptom profile in Parkinson's disease (PD). Patients with early onset PD (EOPD) are a unique challenge and may present with specific patterns of sleep disturbances, which tend to be related to the underlying genetic causes. Furthermore, owing to the younger age of patients with EOPD, sleep disturbances significantly impact multiple domains including employment, ability to drive, social interactions, caregiver burden, and so forth.
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