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Breast development in a 7 year old girl with CF treated with ivacaftor: An indication for personalized dosing?
Author: BeekmanJeffrey M, BerkersGitte, HeijermanHarry Gm, JeyaratnamJoshena, van der EntCornelis K, van der MeerRenske
Original Abstract of the Article :
Substantial progress has been made in the treatment of Cystic fibrosis due to introduction of CFTR modulators. However, little is known about the long term side effects of treatment with these drugs. We here present a 7 year old girl with CF who presented with breast development as a rare dose depen...See full text at original site
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引用元:
https://doi.org/10.1016/j.jcf.2021.06.001
データ提供:米国国立医学図書館(NLM)
Breast Development in a 7-Year-Old Girl with Cystic Fibrosis: A Case for Personalized Dosing
The development of [CFTR modulators] has revolutionized the treatment of [Cystic fibrosis (CF)], but the long-term effects of these medications remain largely unknown. This case report describes a [7-year-old girl with CF] who developed [breast development] as a rare side effect of [ivacaftor] treatment. The authors highlight the need for personalized dosing strategies to optimize treatment effectiveness and minimize potential adverse effects. The findings suggest that [ivacaftor] plasma concentrations may vary significantly among patients, emphasizing the importance of individualizing treatment plans to ensure optimal outcomes.
Personalized Dosing: Tailoring Treatment to Individual Needs
This research emphasizes the importance of [personalized dosing] in [CF] treatment. The case report highlights the potential for variability in [ivacaftor] plasma concentrations among patients, underscoring the need for individualized treatment approaches. This could involve adjusting medication dosages based on factors such as [body weight] and [body surface area] to optimize therapeutic effects and minimize potential side effects. The findings suggest that a more personalized approach to [CF] management could lead to improved patient outcomes.
Optimizing CFTR Modulator Therapy
This study calls for a more nuanced approach to [CFTR modulator] therapy, recognizing the importance of individual patient characteristics and the potential for variability in drug response. The authors suggest that a more individualized dosing strategy could optimize treatment outcomes, minimize potential adverse effects, and ultimately improve the quality of life for [CF] patients.
Dr. Camel's Conclusion
This case report provides a valuable reminder of the importance of personalized medicine, particularly in the context of [Cystic fibrosis (CF)] treatment. The findings highlight the need for careful monitoring and adjustment of [ivacaftor] dosages to optimize treatment effectiveness and minimize potential adverse effects, ultimately leading to better patient outcomes.
Date :
- Date Completed 2022-02-07
- Date Revised 2022-02-07
Further Info :
Related Literature
English
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