Some Factors Influencing the Development of a Voluntary PKU Screening Program
- 15 June 1970
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA
- Vol. 212 (11) , 1835-1842
- https://doi.org/10.1001/jama.1970.03170240039005
Abstract
Mandatory legislation for phenylketonuria (PKU) screening has recently created considerable controversy. This report analyzes three years' experience with a voluntary program in the state of Washington. Sixty-nine percent of newborns were screened in 1967, the last year of the survey reported. The major factor influencing development of screening practice seemed to be physician interrelationships, strongest in the most populous communities, which either favored or hindered the adoption of a screening program. Other medicosociological factors considered had less or no influence. Further observations made that might be considered when planning future mass screening programs were (1) sparsely populated areas and small hospitals need support; (2) the type of testing policy adopted by a hospital staff determines the effectiveness of its program; and (3) screening programs need periodic surveillance to continue to be effective.Keywords
This publication has 4 references indexed in Scilit:
- IATROGENESIS: THE PKU ANXIETY SYNDROMEJournal of the American Academy of Child Psychiatry, 1968
- Phenylketonuria 1967Developmental Medicine and Child Neurology, 1967
- Continuing education and patient care research. Physician response to screening test resultsJAMA, 1967
- Legislation and advances in medical knowledge—acceleration or inhibition?The Journal of Pediatrics, 1966