Table 3.
Potential Mechanisms of Action of Agents Used to Treat Cramps in Cirrhotic Patients
Agent | Mechanism of action | Route of administration (dose studied) | Side effects |
---|---|---|---|
Quinidine sulfate | Increases the muscle refractory period and decreases the excitability of motor end plate to nerve stimulation | Oral (400 mg daily) | Mild diarrhea, thrombocytopenia, cardiac arrhythmias, cinchonism |
Vitamin E | Important antioxidant in the cell membrane that acts to decrease circulating free radicals | Oral (200 mg 3 times daily) | None reported |
Human albumin | Expansion of plasma volume and improvement of hypovolemia and possible subsequent ischemia to neurons | Intravenous (100 mL 25% human albumin solution) | None reported |
Zinc | Unknown | Oral (220 mg twice daily) | Mild diarrhea |
Taurine | Sarcolemma stabilization via calcium channel regulation and conductance | Oral (3 g daily) | None reported |
Eperisone hydrochloride | Centrally acting muscle relaxant | Oral (150–300 mg daily) | Dizziness, fatigue, and epigastric discomfort |
Branched-chain amino acids | Increases serum albumin and taurine production | Oral (4 g granules 3 times daily) | None reported |