A lesson from Cystic Fibrosis and Anesthesia: Perioperative Management Strategies

CF Postoperative Care

Postoperative care of the CF patient should focus on returning the patient to preoperative baseline status.  Care must include aggressive pulmonary toileting to ensure a complete and adequate clearance of secretions.   The quicker the patient can increase activity, cough vigorously, take vital capacity breaths, and use an incentive spirometer, the sooner active clearance of pulmonary secretions will occur.   The head of the patient’s bed should be elevated to a minimum of 30 degrees to support continued expectoration of secretions.  Supplemental oxygen should be humidified for the CF patient.  

The CF patient continues to be at risk for pulmonary complications, including respiratory depression, pneumothorax, pneumonia, atelectasis, and obstruction of the airway.  If possible, the CF patient should recover in a respiratory ICU instead of a surgical ICU to facilitate the rapid return of full pulmonary function.  Close postoperative monitoring is imperative to ensure a full recovery.  The CF patient must be continually assessed for proper hydration, airway management, pain control, nutritional requirements, and aggressive pulmonary toileting.

ElementTarget or consideration
Secretion clearanceAggressive pulmonary toileting for complete clearance of secretions
Patient activityEarly increase in activity, vigorous coughing, vital capacity breaths and incentive spirometer use
PositioningHead of bed elevated to at least 30 degrees to support expectoration
OxygenSupplemental oxygen, humidified
Recovery locationRespiratory ICU rather than surgical ICU when possible
Ongoing assessmentHydration, airway management, pain control, nutritional requirements and pulmonary toileting
Complications to watchRespiratory depression, pneumothorax, pneumonia, atelectasis and airway obstruction

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