Care Plan for Phenylketonuria Management
Category: Metabolic Disorders
Assessment
Infant presents with a positive newborn screening for phenylketonuria (PKU).
Diagnosis
Risk for impaired cognitive development related to elevated phenylalanine levels.
Goals
Infant will maintain phenylalanine levels within the target range. Parents will understand the importance of dietary management and regular monitoring.
Interventions
Monitor phenylalanine levels regularly through blood tests. Educate parents on the importance of a low-phenylalanine diet and provide dietary counseling. Provide resources and support for accessing specialized formula and foods. Coordinate care with a metabolic specialist for ongoing management.
Rationale
These interventions aim to manage phenylalanine levels, prevent cognitive impairment, and support parents in managing the condition.
Evaluation
Infant's phenylalanine levels and developmental progress will be monitored regularly.
⚠️ Educational Care Plan Notice
This care plan is for educational purposes only and represents general nursing concepts.
All care plans must be individualized based on:
- Individual patient assessment and current condition
- Healthcare provider orders and facility protocols
- Current evidence-based practice guidelines
- Nursing scope of practice in your jurisdiction
Do not use as direct patient care instructions. Always follow your facility's policies, physician orders, and professional nursing judgment.