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Treatment of cholestatic pruritus in children
Jeffrey J Cies1, John N Giamalis
1Department of Pharmacy, Temple University Children's Medical Center, Philadelphia, PA 19140, USA. jeffrey.cies@tuhs.temple.edu
Insights
Treating cholestatic pruritus in children requires individualized approaches, as antihistamines are often ineffective. Agents like ursodiol and cholestyramine show promise, with combination therapy potentially offering synergistic benefits for managing this debilitating symptom.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Pharmacology
Background:
- Cholestasis involves bile substance accumulation, leading to pruritus, a severe symptom in pediatric chronic liver disease.
- Standard antihistamines are generally insufficient for managing cholestatic pruritus in children.
- Various agents like rifampin, phenobarbital, ursodiol, opioid antagonists, and bile-binding resins are used, with varying efficacy.
Purpose of the Study:
- To review the treatment of cholestatic pruritus in children.
- To evaluate the efficacy of different therapeutic agents for pediatric cholestatic pruritus.
Main Methods:
- Review of existing literature on the treatment of cholestatic pruritus in pediatric populations.
- Analysis of the efficacy and safety profiles of various pharmacological agents.
- Discussion of therapeutic strategies based on underlying cholestasis type (intrahepatic vs. extrahepatic).
Main Results:
- No established guidelines exist for managing pediatric cholestatic pruritus, necessitating individualized treatment selection.
- Cholestyramine and ursodiol are safe, affordable, and effective options for pediatric cholestatic pruritus.
- Phenobarbital, ursodiol, bile sequestering agents, and opioid antagonists are effective for intrahepatic cholestasis-related pruritus.
- Rifampin is noted for efficacy in treating pruritus associated with extrahepatic cholestasis.
Conclusions:
- Treatment selection for cholestatic pruritus in children should consider concurrent diseases and medication regimens.
- Combination therapy targeting multiple pruritus mechanisms may enhance treatment outcomes.
- Future research may explore novel agents like serotonin antagonists and leukotriene antagonists for improved management.
Purpose:
The treatment of cholestatic pruritus in children is reviewed.
Summary:
Cholestasis is characterized by an accumulation of substances that are normally secreted in the bile. Pruritus is a well-known feature of chronic cholestasis in both adults and children and has been reported as the most incapacitating symptom in children with chronic liver disease. Traditional agents, such as antihistamines, are typically ineffective as monotherapy in controlling cholestatic pruritus. As a result, clinicians have looked to other agents, such as rifampin, phenobarbital, ursodiol, opioid antagonists, and bile-binding resins, for attaining better control of pruritic symptoms. Each agent demonstrates different levels of efficacy in pediatric and adult literature. There are no guidelines or algorithms to guide therapy with these agents for children. As a result, an agent should be selected based on the patient's concurrent diseases and current medication regimen. Cholestyramine and ursodiol are both safe and inexpensive, with documented efficacy for cholestatic pruritus in children. Because cholestatic pruritus is likely a result of multiple mechanisms, combination therapy with agents that have differing mechanisms of action might be beneficial and could capitalize on potential synergy between the agents used. Future therapy for cholestatic pruritus may include serotonin antagonists, selective serotonin-reuptake inhibitors, and leukotriene antagonists.
Conclusion:
Depending on the underlying disease state resulting in cholestasis, phenobarbital, ursodiol, bile sequestering agents, and opioid antagonists appear to be most effective for treating pruritus related to intrahepatic cholestasis. Alternatively, rifampin appears to be the only agent with reported treatment efficacy for pruritus related to extrahepatic cholestasis.
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