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CMV disease in CMV-mismatched renal transplant recipients with prophylactic low dose valaciclovir.
Author: ErikssonB M, SundF, WahlbergJ
Original Abstract of the Article :
Valaciclovir (VACV) 2 g q.i.d. for 3 months after kidney transplantation has been shown, (Lowance et al., NEJM 1999; 340: 1462-70), to reduce CMV disease from 45 to 16% and rejection from 52 to 26% in CMV-negative (D+R-) recipients. Neurotoxic side effects, however, were frequent, and 5% of the pati...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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引用元:
https://doi.org/10.1016/s1386-6532(01)00213-x
データ提供:米国国立医学図書館(NLM)
A Lower Dose for CMV Disease Prevention in Transplant Recipients
The use of valaciclovir (VACV) to prevent CMV disease in renal transplant recipients is a common practice. This study explores the potential of using a lower dose of VACV to reduce the risk of CMV disease and its side effects, particularly neurotoxicity. This is a very important consideration in the world of organ transplantation, where the balance between preventing rejection and minimizing side effects is crucial. The study examined the effectiveness of a lower dose of VACV (2 g q.i.d. for 3 months) in CMV-mismatched renal transplant recipients. The authors compared the results of this lower dose to a higher dose, previously shown to reduce CMV disease and rejection rates. They found that the lower dose was effective in preventing CMV disease, but with fewer neurotoxic side effects, suggesting a potential advantage of the lower dose regimen.Balancing the Scales: Efficacy and Safety
The findings indicate that a lower dose of VACV is effective in preventing CMV disease in transplant recipients while reducing the risk of neurotoxicity. This approach offers a potential solution for striking a balance between efficacy and safety, crucial in the management of transplant patients.Protecting Transplant Patients: A Delicate Dance
The management of transplant patients requires a delicate balance. We need to protect them from infection and rejection, while simultaneously minimizing the side effects of medications. This study provides valuable insights into this complex landscape, offering a potential pathway for safer and more effective CMV prevention in transplant recipients.Dr.Camel's Conclusion
Think of a camel caravan traversing a vast desert. Just as a camel needs to carefully manage its water supply, so too must doctors carefully manage the medication regimen for transplant recipients. This research offers a valuable oasis in the desert of medical challenges, exploring ways to optimize the balance between preventing CMV disease and mitigating its side effects.Date :
- Date Completed 2002-02-14
- Date Revised 2019-11-05
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