scholarly journals The long-term effects on children and adolescents of a policy providing work supports for low-income parents

2011 ◽  
Vol 30 (4) ◽  
pp. 729-754 ◽  
Author(s):  
Aletha C. Huston ◽  
Anjali E. Gupta ◽  
Jessica Thornton Walker ◽  
Chantelle J. Dowsett ◽  
Sylvia R. Epps ◽  
...  
2009 ◽  
Vol 33 (8) ◽  
pp. 1496-1501 ◽  
Author(s):  
Gaetana Migliardi ◽  
Edoardo Spina ◽  
Concetta D'Arrigo ◽  
Antonella Gagliano ◽  
Eva Germanò ◽  
...  

The Lancet ◽  
2003 ◽  
Vol 362 (9401) ◽  
pp. 2045-2051 ◽  
Author(s):  
Chang-Heok Soh ◽  
James M Oleske ◽  
Michael T Brady ◽  
Stephen A Spector ◽  
William Borkowsky ◽  
...  

2019 ◽  
Vol 4 (4) ◽  
pp. e001475 ◽  
Author(s):  
Adrianna Murphy ◽  
Catherine McGowan ◽  
Martin McKee ◽  
Marc Suhrcke ◽  
Kara Hanson

BackgroundExperiencing illness in low-income and middle-income countries (LMICs) can incur very high out-of-pocket (OOP) payments for healthcare and, while the existing literature typically focuses on levels of expenditure, it rarely examines what happens when households do not have the necessary money. Some will adopt one or more ‘coping strategies’, such as borrowing money, perhaps at exorbitant interest rates, or selling assets, some necessary for their future income, with detrimental long-term effects. This is particularly relevant for chronic illnesses that require consistent, long-term OOP payments. We systematically review the literature on strategies for financing OOP costs of chronic illnesses in LMICs, their correlates and their impacts on households.MethodsWe searched MEDLINE, EconLit, EMBASE, Global Health and Scopus on 22 October 2018 for literature published on or after 1 January 2000. We included qualitative or quantitative studies describing at least one coping strategy for chronic illness OOP payments in a LMIC context. Our narrative review follows Preferred Reporting Items for Systematic Reviews and Meta-Analyses reporting guidelines.ResultsForty-seven papers were included. Studies identified coping strategies for chronic illness costs that are not traditionally addressed in financial risk protection research (eg, taking children out of school, sending them to work, reducing expenditure on food or education, quitting work to give care). Twenty studies reported socioeconomic or other correlates of coping strategies, with poorer households and those with more advanced disease more vulnerable to detrimental strategies. Only six studies (three cross-sectional and three qualitative) included evidence of impacts of coping strategies on households, including increased labour to repay debts and discontinuing treatment.ConclusionsMonitoring of financial risk protection provides an incomplete picture if it fails to capture the effect of coping strategies. This will require qualitative and longitudinal research to understand the long-term effects, especially those associated with chronic illness in LMICs.


PEDIATRICS ◽  
1969 ◽  
Vol 43 (2) ◽  
pp. 160-167
Author(s):  
John H. Kennell ◽  
Eleanor Soroker ◽  
Paula Thomas ◽  
Marvin Wasman

Interviews with 60 parents of children attending a rheumatic fever clinic showed confusion and many unrealistic beliefs about the disease and its long-term effects, about recurrences, and about the rationale for the prophylactic program. The parents' all-pervading anxiety about heart disease and death led them to impose or continue restrictions contrary to medical advice, even on children with normal hearts. The mothers' lack of understanding correlated with their level of education and a number of social and environmental factors. One group of families with a clearly defined pattern of social characteristics-almost entirely Negro, on public assistance, with a low educational level, a very low income, and a high degree of family disorganization-stood out because of its lack of understanding about the disease and about its prophylactic treatment. The responses of Negro mothers on public assistance as well as those with higher educational and income levels were similar in several respects and differed from those of Caucasian mothers. On the basis of what the mothers reported, communication about the disease was remarkably poor between physician and parent, parent and child, and physician and patient.


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