Allen SM. Gender differences in spousal caregiving and unmet need for care. J Gerontol (1994 Jul) 49(4):S187-95.

1995 ◽  
Vol 13 (3) ◽  
pp. 24-25
2019 ◽  
Vol 22 (3) ◽  
pp. 255-261 ◽  
Author(s):  
Rebecca Miller ◽  
Dmitry Tumin ◽  
Don Hayes ◽  
Joshua C. Uffman ◽  
Vidya T. Raman ◽  
...  

2011 ◽  
Vol 101 (3) ◽  
pp. 640-644 ◽  
Author(s):  
Sharon K Long ◽  
Karen Stockley ◽  
Shanna Shulman

Under its health reform legislation, Massachusetts has achieved near universal insurance coverage, along with significant gains in health care access and affordability. This paper examines the impacts of health reform in Massachusetts on differences in coverage, access, and affordability for women and men. We find that both women and men gained under health reform, with the gender gap in insurance coverage narrowed as men's coverage increased relative to that of women. However, the gaps in access and affordability of care have not narrowed—women in Massachusetts continue to report more unmet need for care and problems affording care than men.


2014 ◽  
Vol 65 (6) ◽  
pp. 774-780 ◽  
Author(s):  
Jordan E. DeVylder ◽  
Hans Y. Oh ◽  
Cheryl M. Corcoran ◽  
Ellen P. Lukens

Author(s):  
D. G. M. Eijgermans ◽  
H. Raat ◽  
P. W. Jansen ◽  
E. Blok ◽  
M. H. J. Hillegers ◽  
...  

AbstractApproximately, 15% of children in Western countries suffer from emotional and behavioural problems. However, not all children receive the psychosocial care they need, especially children with a non-Western background experience an unmet need for care. This might be because parents of non-Western children report a lower need for care than parents of Western children, unrelated to the actual need. This study examined the association between teacher-reported problems and psychosocial care use, independent of mother-reported problems. Further, the role of ethnic background in this association was investigated. The study sample of 9-year-old children was retrieved from the Generation R Study (N = 3084), a prospective, population-based cohort of children born in Rotterdam, the Netherlands. Teacher- and mother-reported problems were measured via questionnaire when the children were  6/7 years old. Psychosocial care use was mother-reported at the research centre when children were 9 years old (8.1%). Hierarchical logistic regressions showed significant positive associations between teacher-reported total, externalising and internalising problems and later psychosocial care use. These associations were independent of mother-reported problems. Children with a non-Western background used less care, but ethnic background did not moderate the association between teacher-reported problems and care use. Our findings suggest that teachers might have an important role, next to parents, in the identification of problems and children’s access to care. This may be particularly important for non-Western children, as they use less psychosocial care than Western children, despite other research showing that they generally display higher levels of problems. Directions for future research and implications are discussed.


2009 ◽  
Vol 64B (1) ◽  
pp. 147-156 ◽  
Author(s):  
K. Sugiura ◽  
M. Ito ◽  
M. Kutsumi ◽  
H. Mikami

2019 ◽  
Vol 22 (3-4) ◽  
pp. 109-116 ◽  
Author(s):  
Vini Singh ◽  
Melanie Pinkett-Davis ◽  
Luther G. Kalb ◽  
Gazi Azad ◽  
Jason Neely ◽  
...  

Introduction Parents of children with autism spectrum disorder often experience high levels of stress and challenges when organizing medical and behavioral services for their child. Care coordination could alleviate these challenges, however little is known about the effectiveness of this service. This study examined the need, feasibility, and acceptability of a care coordination program. Methods Families of 176 children with autism, seen at a multidisciplinary autism clinic in the United States, participated in a prospective observational study. Families received a three-month structured care coordination program and completed pre- and post-program questionnaires that probed parents’ beliefs about the need and acceptability of the program through structured and open-ended questions. Results Most (≥90%) parents reported both a need for care coordination and satisfaction with the program. Qualitative themes identified valuable aspects and ways to improve the program. Discussion Parents raising a child with autism spectrum disorder experience an unmet need for care coordination. When provided, parents’ demonstrated high uptake of service and high levels of satisfaction with the program.


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