[Use of support and relief services for parents of children in need of care: Results of the FamBer observational study]. / Inanspruchnahme von Unterstützungs- und Entlastungsdiensten für Eltern pflegebedürftiger Kinder.

Use of support and relief services for parents of children in need of care: Results of the FamBer observational study Abstract: Background: Parents of children in need of care in Germany can fall back on a variety of relief and support services. So far, however, there has been a lack of systematic studies and quantitative data on the use of such offers at the individual level of parents and other legal guardians. Aim: The study on the compatibility of care and work for parents with a child in need of care (FamBer; funding: Federal Ministry for Family Affairs, Senior Citizens, Women and Youth, Germany) examines the knowledge of relief and support services, their use and the perceived benefits of these offers. Methods: 1070 parents answered a multidimensional online questionnaire in the cross-sectional study that was developed based on the Kindernetzwerk Study 2 from 2013 and the German socio-economic panel (SOEP). In addition to descriptive analyses, group comparisons were carried out using Chi2, Mann-Whitney U or Kruskal-Wallis H tests. Results: 43 to 58% of parents are aware of the respective legal options for taking time off work, but only very few families make use of them. The other support offers differ significantly in terms of the level of knowledge and utilization; these vary primarily with the education of the parents and the care needs of the child. They assessed the used services for consultation and advice as only little helpful. Conclusions: Due to the study design, we cannot rule out that the findings are also based on personal characteristics of the parents and their living conditions. Nevertheless, a large number of problems (e.g. a lack of information, low using, ineffectiveness of support services) can be identified that need to be overcome.

[Care of refugee children and adolescents with chronic diseases and disabilities]. / Versorgung von geflüchteten Kindern und Jugendlichen mit chronischen Erkrankungen und Behinderungen: Anspruch und Möglichkeiten in Deutschland.

Refugee children and adolescents with chronic diseases and disabilities are among the most vulnerable persons as their health and developmental chances are considerably at risk. This article describes the challenges and opportunities in the care of this group of patients from the perspective of different care sectors: initial reception center, public health service, pediatricians in private practice, social pediatric centers and patient organizations. The starting point is a presentation of the rights to optimal healthcare that can be derived from the United Nations (UN) Convention on the Rights of Persons with Disabilities and the UN Convention on the Rights of the Child. It becomes clear that for children and adolescents in the status of asylum seekers there are systematic gaps in the recognition and care of chronic diseases, disabilities and support needs. An expansion of the health examination after arrival, which has so far focused on the detection of communicable diseases, is important and necessary in order to identify individual needs and improve the data situation for this group. A strengthening of the school entry screening by the public health service, especially for older children entering school as lateral entrants, could also significantly improve the nationwide coverage. In contrast to these deficits, which require changes at the political level, there are innovative models of care, especially in local contexts, such as pediatric consultation clinics in initial reception centers, diverse examples of voluntary commitment or the use of social media in patient organizations, which are presented as examples.