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  Vol. 152 No. 5, May 1998 TABLE OF CONTENTS
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Families' Recommendations for Improving Services for Children With Chronic Conditions

Ann W. Garwick, PhD; Claire Kohrman, PhD; Clara Wolman, PhD; Robert W. Blum, MD, PhD

Arch Pediatr Adolesc Med. 1998;152:440-448.

Background  Little research has been done on services and programs for children with chronic conditions and their families from the perspective of family caregivers from diverse cultural backgrounds.

Objective  To identify recommendations that urban caregiving families from 3 major ethnocultural backgrounds have for improving the care of children with chronic conditions (ie, chronic illnesses and disabilities involving physical health impairments).

Design  Qualitative, community-based study.

Setting  General community.

Participants  The volunteer convenience sample included 21 African American, 20 Hispanic, and 22 European American families from 2 midwestern cities who care for school-aged children with chronic conditions.

Methods  In-home semistructured interviews were conducted with each child's family caregivers. Content analytic techniques were used to identify and classify 275 recommendations from 63 families.

Results  Families focused on the following 4 topics: (1) improving the quality of health care services; (2) decreasing barriers to services and programs; (3) improving the training that health care professionals, families, and the public receive about chronic conditions and their management; and (4) improving the quality and availability of community-based services. Families from all 3 ethnic groups had similar recommendations for improving services and programs; however, several African American and Hispanic families also suggested making information more culturally relevant and resources more accessible to families from diverse cultural backgrounds.

Conclusions  The findings indicate that further work needs to be done to deliver care that is, indeed, family centered and culturally sensitive. Families' recommendations provide information that health care professionals and policymakers can use to transform rhetoric about family-centered care into action.


From the University of Minnesota, School of Public Health, Maternal and Child Health Program (Dr Garwick), and the School of Medicine, Division of General Pediatrics and Adolescent Health (Dr Blum), Minneapolis, Minn; the University of Chicago, Department of Pediatrics, Chicago, Ill (Dr Kohrman); and Barry University, School of Education, Miami Shores, Fla (Dr Wolman).



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