Class
- Neuromuscular drug; skeletal muscle relaxant, direct acting
Dantrolene
Commonly Prescribed for
(FDA approved in bold)
- Chronic spasticity
- Malignant hyperthermia (MT)
- Exercise-induced muscle pain
- Heat stroke
- Neuroleptic malignant syndrome
Dantrolene
How the Drug Works
- Dantrolene produces relaxation by interfering with the release of calcium from the sarcoplasmic reticulum, weakening muscle contraction, and reversing the hypermetabolic process of MT
Dantrolene
How Long Until It Works
- Pain – hours-days
Dantrolene
If It Works
- Discontinue use once MT symptoms remit. For chronic spasticity, continue to use with standard precautions
Dantrolene
If It Doesn’t Work
- For spasticity, increase to highest tolerated dose. If ineffective, stop after 45 days and consider alternative treatments. In MT cases, stop all anesthetics
Dantrolene
Best Augmenting Combos for Partial Response or Treatment-Resistance
- For focal spasticity, i.e., post-stroke spasticity, botulinum toxin is often more effective and is better tolerated
- Use other centrally acting muscle relaxants with caution due to potential synergistic CNS depressant effect
- 100% oxygen, cold gastric lavage, cooling blankets, and cold intravenous fluids may be useful in MT
Dantrolene
Tests
- Obtain baseline liver function studies then do periodically
Adverse Effects (AEs)
Dantrolene
How Drug Causes AEs
- Some are related to CNS depression, others hepatic disease
Dantrolene
Notable AEs
- Fatigue, diarrhea, drowsiness, weakness, rash, labile blood pressure, confusion/depression, abdominal cramps, crystalluria, chills, and fever. Thrombophlebitis
Dantrolene
Life-Threatening or Dangerous AEs
- Hepatotoxicity is not rare even after only short-term use, especially in patients that are females, over 35, taking multiple medications or taking dose greater than 800 mg
- Less common: heart failure, pulmonary edema and hematologic abnormalities have been reported
Dantrolene
Weight Gain
- Unusual
Dantrolene
Sedation
- Problematic
Dantrolene