A lesson from Cystic Fibrosis and Anesthesia: Perioperative Management Strategies

Anesthesia Induction in Cystic Fibrosis: Preoxygenation, RSI, and Airway Planning

Induction of the CF patient must be carried out safely and effectively to help ensure a positive postoperative recovery.  If thoughtfully completed, a comprehensive preoperative assessment will adequately prepare the anesthesia provider for the induction of the adult CF patient.  Preoxygenation should be performed for a full three to five minutes. The high incidence of gastroesophageal reflux suggests that a rapid sequence induction (RSI) technique should be utilized.  The experienced provider can sometimes use a modified RSI or standard intravenous or inhalation induction.  If an inhalation induction is the chosen method, the anesthesia provider must consider the CF patient’s decreased tidal volume, decreased functional residual capacity, and the ventilation to perfusion mismatch that will slow inhalation induction times.  This approach may need to be augmented by intravenous agents, avoiding agents that can irritate the airway, since bronchospasm should be avoided. 

Propofol is a safe intravenous induction agent because it has a short half-life and lacks histamine release.   Ketamine should be avoided for induction.  Ketamine is associated with increased sympathetic activity and bronchial secretions, which could compromise the patient’s stability. 

Succinylcholine is the best choice for a paralytic agent when an intravenous induction and endotracheal intubation are warranted due to the patient’s high aspiration risk.   If the procedure requires paralysis, nondepolarizing neuromuscular blocking agents associated with rapid clearance should be used.   Mivacurium should be considered because it has a short duration of action.   Other intermediate-acting, nondepolarizing neuromuscular-blocking agents such as rocuronium and cisatracurium are also acceptable.

Endotracheal intubation is recommended for most surgical procedures.

This approach allows for adequate and proper ventilation control.   This is important in the adult CF population because these patients require higher carbon dioxide levels to maintain their respiration drive.   Caution must be used during nasal intubation due to the high incidence of nasal polyps in CF patients.   If the placement of an endotracheal tube is not possible, using a laryngeal mask airway (LMA) is an option.  Routine use of an LMA is not the best choice for surgical procedures because there is an increased risk of aspiration and an inability to remove viscous secretions.  The use of the LMA has also been associated with gas trapping and pneumothorax in CF patients.

Agent or deviceUse in CFRationale
PropofolSafe induction agentShort half-life and no histamine release
KetamineAvoidIncreased sympathetic activity and bronchial secretions could compromise stability
SuccinylcholineBest paralytic with intravenous induction and intubationHigh aspiration risk favors rapid sequence technique
MivacuriumConsider when paralysis is requiredShort duration of action
Rocuronium, cisatracuriumAcceptable alternativesIntermediate-acting nondepolarizers with rapid clearance
Endotracheal tubeRecommended for most proceduresAllows ventilation control; use caution with nasal intubation given frequent nasal polyps
Laryngeal mask airwayFallback only when an endotracheal tube cannot be placedIncreased aspiration risk, inability to remove viscous secretions, gas trapping and pneumothorax

Free lesson

This lesson is part of “Cystic Fibrosis and Anesthesia: Perioperative Management Strategies”

Lesson 4 of 11

Unlock all 11 lessons, the quiz, and 1.5 Class A credits.

More free lessons from this module