Care Plan for Cystic Fibrosis
Category: Respiratory
Assessment
Patient presents with chronic cough, frequent lung infections, and poor weight gain.
Diagnosis
Ineffective airway clearance related to thick mucus production.
Goals
Patient will maintain clear airways as evidenced by normal breath sounds and absence of respiratory distress. Patient will achieve and maintain a healthy weight.
Interventions
Administer prescribed mucolytics and bronchodilators. Educate patient on chest physiotherapy techniques to clear mucus. Monitor respiratory status and oxygen saturation regularly. Provide high-calorie, high-protein diet to support nutritional needs.
Rationale
These interventions help maintain airway patency, improve gas exchange, and support nutritional status in patients with cystic fibrosis.
Evaluation
Patient's respiratory status and weight will be monitored to evaluate the effectiveness of interventions.
⚠️ 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.