Sudden infant death syndrome: impact on families and a direction for change
Abstract
Until recently, there were no standardized approaches to the diagnosis of sudden infant death syndrome (SIDS), the leading cause of death in the age group of one week to one year in the United States. This has led to confusion among professionals and hardships for parents and families. The Sudden Infant Death Syndrome Act of 1974 provided funding for the dissemination of information, counseling, and education. The author reviews the scope of the SIDS problem, the ways in which it affects families, and mechanisms by which community resources can be mobilized to assist families.
Access content
To read the fulltext, please use one of the options below to sign in or purchase access.- Personal login
- Institutional Login
- Sign in via OpenAthens
- Register for access
-
Please login/register if you wish to pair your device and check access availability.
Not a subscriber?
PsychiatryOnline subscription options offer access to the DSM-5 library, books, journals, CME, and patient resources. This all-in-one virtual library provides psychiatrists and mental health professionals with key resources for diagnosis, treatment, research, and professional development.
Need more help? PsychiatryOnline Customer Service may be reached by emailing [email protected] or by calling 800-368-5777 (in the U.S.) or 703-907-7322 (outside the U.S.).