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Original Abstract of the Article :
The response of serum prednisolone to a single oral dose of 30 mg of prednisone was studied in 12 patients with chronic active hepatitis taking prednisone, and in six healthy volunteers. Five of the 12 patients developed major side effects with prednisone, and seven showed less or no side effects. T...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/6481116
データ提供:米国国立医学図書館(NLM)
Prednisone and its Impact on Chronic Active Hepatitis
The study delves into the fascinating world of prednisone, a corticosteroid commonly used to treat chronic active hepatitis. This research focuses on the pharmacokinetics and serum binding of prednisone in patients with chronic active hepatitis, specifically examining the effects of the medication on patients with varying levels of side effects.A Look at the Intricacies of Prednisone
The researchers discovered that patients experiencing major side effects from prednisone tend to have higher serum bilirubin and lower serum albumin levels. While the peak levels of prednisolone were similar across the groups, the unbound (free) prednisolone was higher in patients experiencing major side effects. This observation suggests that the occurrence of side effects may be linked to altered protein binding of prednisolone, potentially influenced by factors like hypoalbuminemia and hyperbilirubinemia.Navigating Prednisone Therapy
Understanding the relationship between prednisone, serum bilirubin, and albumin levels can be crucial in managing patients with chronic active hepatitis. It highlights the importance of individualizing treatment plans and monitoring patients closely for potential side effects, especially those with compromised liver function.Dr.Camel's Conclusion
The research emphasizes the need for a tailored approach when prescribing prednisone, taking into account individual patient characteristics and potential side effects. This study reminds us that the human body is a complex system, and medications often interact with each other in ways that we are still trying to understand. By continuing to explore these interactions, we can strive to make medication therapy safer and more effective for all.Date :
- Date Completed 1984-11-01
- Date Revised 2014-11-20
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