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Malignant Hyperthermia: A Case Report in a Trauma Patient
Ian C Gibbs1, Oluwole Fadahunsi2, Natoya Reid2
1Attending, Yale-New Haven Hospital, New Haven, CT, and Former Resident, Howard University Hospital, Washington, DC.
Malignant hyperthermia is a rare, life-threatening reaction to anesthesia. Early recognition and dantrolene treatment are crucial for patient survival, even with delayed symptoms.
Area of Science:
- Anesthesiology
- Pharmacology
- Genetics
Background:
- Malignant hyperthermia (MH) is a rare, hypermetabolic crisis triggered by volatile anesthetics and succinylcholine in susceptible individuals.
- MH carries a significant mortality rate if not promptly identified and managed.
- Genetic predisposition plays a key role in MH susceptibility.
Observation:
- A 52-year-old male developed signs of MH, including elevated end-tidal carbon dioxide, 70 minutes after anesthesia induction for mandibular fracture repair.
- The patient received succinylcholine and desflurane, known MH triggers.
- A family history of a severe reaction to anesthesia in his sister was discovered post-event.
Findings:
- Delayed onset of MH signs (70 minutes post-induction) complicated initial diagnosis.
- Prompt administration of dantrolene sodium 120 minutes after induction led to symptom resolution within 45 minutes.
- Intraoperative vigilance and monitoring of end-tidal CO2 are critical for early MH detection.
Implications:
- This case highlights the importance of thorough patient history, including family history, for identifying potential MH risk.
- Increased clinical suspicion for MH is warranted with unexplained hypermetabolic signs during anesthesia.
- Awareness and rapid intervention protocols are essential for managing malignant hyperthermia and improving patient outcomes.
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