Please note: In 2003, the CTF updated its Grades of Recommendations to include an "I Recommendation" for situations where insufficient evidence exists to allow a recommendation to be made.  (Formerly, these situations were captured under a "C Recommendation".)  This change is not retroactive, and all "C Recommendations" made prior to 2003 have not been reevaluated in light of the new "I" recommendation grade.  For a discussion of these recommendation grades, please link to the 2003 article in the Canadian Medical Association Journal here.

Screening for Phenylketonuria

Adapted by William Feldman, MD, FRCPC, Department of Pediatrics, University of Toronto, from the report prepared for the US Preventive Services Task Force by Robert Baldwin, MD and Modena E.H. Wilson, MD, MPH

Objective
To make recommendations for screening pregnant Canadian women and their newborn infants for phenylketonuria (PKU).

Burden of Suffering
Phenylketonuria is an inborn error of phenylalanine metabolism that occurs in 1 out of every 12,000 births in North America.  In the absence of treatment during infancy, most persons with this disorder develop severe, irreversible mental retardation, and may also experience neurobehavioral symptoms such as seizures, tremors, gait disorders, athetoid movements, and psychotic episodes.  Since the legislation of routine screening in the mid 60s, these clinical manifestations have rarely developed in children, resulting in a cohort of health phenylketonuric women entering childbearing age.  Unless dietary restriction of phenylalanine is maintained during pregnancy, these women are at an increased risk of giving birth to a child with mental retardation, microcephaly, congenital heart disease, and low birth weight (incidence of maternal PKU is about 1 in 30,000-40,000 pregnancies).

Options
Screening options include a closed phenylalanine hydroxylase gene probe for prenatal diagnosis and the Guthrie blood determination for infants.  Treatment options include strict adherence to a special low-protein diet for 4 to 8 years or through adolescence or into adulthood. Material dietary treatment may need to be started before conception for women with PKU.

Outcomes
False positive rates and sensitivity for the blood tests. Infants with PKU may have reduced intelligence, cognitive function, and attention and academic difficulties. Maternal hyperphenylketonuria with infants who do not have PKU may develop mental retardation, microcephaly, intrauterine growth retardation, and other birth defects.

Evidence
These recommendations were adapted from a report prepared for the U.S. Preventive Services Task Force.  MEDLINE was searched up to 1993 using the keyword phenylketonuria.

Values
The 13-member Task Force of experts in family medicine, geriatric medicine, pediatrics, psychiatry and epidemiology used an evidence-based method for evaluating the effectiveness of preventive health care interventions. Recommendations were not based on cost-effectiveness of options. Patient preferences were not discussed.

Background papers providing critical appraisal of the evidence and tentative recommendations prepared by the chapter author were pre-circulated to the members. Evidence for this topic was presented and deliberated upon in 1- to 2-day meetings, 2 to 3 times per year from January 1993 to June 1993. Consensus was reached on final recommendations.

Benefits, Harms, and Costs
Using a cut point of 240 micromoles/L, false negative rates associated with the Gurthrie test done on the first day of life ranged from 2% to 31%. These rates decreased on the second day to 0.6% to 2% and on the third day to 0.3%. Flurometric assays have excellent sensitivity and lower false negative rates. The gene probe has not been fully tested. Routine screening of pregnant women has very low yields.

Untreated PKU causes mental retardation. One cohort study in 1953 showed that 85% of untreated children had an intelligent quotient (IQ) < 40 and < 1% had an IQ above 70. Since dietary phenylalanine restriction was introduced > 95% of children with PKU have normal or near-normal intelligence. Diet treatment of at least 4 years (and up to adulthood) showed that treated children have an IQ in the normal range although somewhat less than parents and siblings. Some psychological deficits including perceptual motor dysfunction and attention and academic difficulties have been found.

Maternal hyperphenylalanemia can cause teratogenic effects even in infants without PKU; this effect is proportional to the levels of phenylalanine in the mother. Children born to mothers with PKU may develop mental retardation (>90%), encephalopathy (75%), intrauterine growth retardation (40% to 50%), and other birth defects (10% to 25%). Low phenylalanine diets during pregnancy may lead to poor fetal growth.

Recommendations
Recommendation grade [A, B, C, D, E]  and level of evidence [I, II-1, II-2, II-3, III] are indicated after each recommendation. Citations in support of individual recommendations are identified in the guideline text.

Validation
This report was externally peer reviewed.  All Canadian provinces have universal screening programs and U.S. states have varying regulations. The 1989 United States Preventive Services Task Force recommended that all newborn infants be screened before discharge. For infants discharged before 24 hours, repeat the test at 7 to 14 days. They do not recommend prenatal screening for maternal PKU.  The American Academy of Pediatrics (AAP) and the American Association of Family Physicians recommend universal screening of infants using capillary blood samples taken as close to discharge as possible. Premature infants and other treated infants should be checked at 7 to 14 days. The AAP recommended repeat screening of infants if they are tested before 24 hours of age. The AAP and the American College of Obstetricians and Gynecologists do not recommend maternal screening.

Sponsors
The Canadian Task Force on Preventive Health Care developed this guideline with funding from Health Canada.

Source Document
Feldman W. Screening for phenylketonuria. In: Canadian Task Force on the Periodic Health Examination. Canadian Guide to Clinical Preventive Health Care. Ottawa: Health Canada, 1994;180-8.