Paper Details 
Original Abstract of the Article :
A retrospective single center study was performed to evaluate the safety and efficacy of valacyclovir for prevention of cytomegalovirus (CMV) infection (reactivation) after allogeneic stem cell transplantation (SCT). We compared a group of 31 patients at risk for CMV reactivation (donor, recipient o...See full text at original site
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引用元:
https://doi.org/10.1038/sj.bmt.1703129

データ提供:米国国立医学図書館(NLM)

Valacyclovir: A Shield Against Cytomegalovirus

After a bone marrow transplant, the body's immune system is often weakened, like a fragile oasis in a vast desert. This leaves individuals vulnerable to infections, including cytomegalovirus (CMV). This study explores the effectiveness of valacyclovir, a medication commonly used to treat viral infections, in preventing CMV reactivation after bone marrow transplantation.

The researchers conducted a retrospective study, comparing a group of patients who received valacyclovir for CMV prophylaxis with a control group who did not. They discovered that valacyclovir significantly reduced the incidence of CMV reactivation, both for primary and secondary prophylaxis, suggesting its effectiveness in protecting against CMV infections.

Valacyclovir: A Promising Prophylactic

This study offers valuable insights into the use of valacyclovir for CMV prophylaxis after bone marrow transplantation. It highlights the potential of this medication to prevent CMV reactivation and improve outcomes for patients undergoing transplantation. However, the researchers recommend larger prospective studies to further confirm their findings and explore the long-term benefits of valacyclovir.

Dr.Camel's Conclusion

Valacyclovir, like a sturdy camel caravan, can offer protection against the threat of CMV reactivation after bone marrow transplantation. It provides valuable insights into the potential benefits of prophylactic therapy in maintaining the fragile balance of the immune system after transplantation.

Date :
  1. Date Completed 2002-03-07
  2. Date Revised 2018-11-30
Further Info :

Pubmed ID

11535994

DOI: Digital Object Identifier

10.1038/sj.bmt.1703129

Related Literature

SNS
PICO Info
in preparation
Languages

English

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