2017
DOI: 10.1016/j.bjid.2016.09.016
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Clinical correlates of pp65 antigenemia monitoring in the first months of post kidney transplant in patients undergoing universal prophylaxis or preemptive therapy

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Cited by 4 publications
(10 citation statements)
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References 31 publications
(36 reference statements)
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“…In bone marrow transplanted patients, a single positive cell is enough to be considered as a positive result33. Therefore, routine CMV monitoring in transplantation can be used as a preemptive approach, so that pp65 antigenemia might work as a marker of infection or viral replication, as performed in our group31. In 2013, a study10 reported a cutoff value of 10 cells per 200,000 leukocytes to associate CMV with mortality in autoimmune diseases ( 75% sensitivity and 72.2% specificity).…”
Section: Discussionmentioning
confidence: 89%
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“…In bone marrow transplanted patients, a single positive cell is enough to be considered as a positive result33. Therefore, routine CMV monitoring in transplantation can be used as a preemptive approach, so that pp65 antigenemia might work as a marker of infection or viral replication, as performed in our group31. In 2013, a study10 reported a cutoff value of 10 cells per 200,000 leukocytes to associate CMV with mortality in autoimmune diseases ( 75% sensitivity and 72.2% specificity).…”
Section: Discussionmentioning
confidence: 89%
“…CMV viremia is very prevalent among immunosuppressed patients, and various diagnostic strategies have been commonly used in clinical practice, for example PCR and pp65 antigenemia. Some transplantation centers monitor antigenemia closely, and to prevent CMV complications phisicians start promptly preemptive and /or prophylactic treatment, mostly in the first six months after transplantation31. However, data about CMV monitoring in autoimmune diseases are scarce, as well as protocols about when and how to monitor CMV infection in these autoimmune patients.…”
Section: Discussionmentioning
confidence: 99%
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“…(Figure S1). In patients receiving prophylaxis (5 studies), reported rates of CMV infection during the first year post‐SOT were 5.2%, 30 26.0%, 24 45.4%, 31 50.0%, 22 and 50.2% 32 . According to studies conducted in Brazil, India, and South Korea, infection typically appeared after a median of 1–2 months postkidney or postliver transplantation 8,21,25,27,29,32–39 .…”
Section: Resultsmentioning
confidence: 99%
“…The recipient received thymoglobulin as induction therapy and was maintained on prednisone, mycophenolate sodium, and tacrolimus. She underwent universal prophylaxis for CMV infection with intravenous ganciclovir (5 mg/kg) 5 days after transplant, according to the institutional protocol: 10 twice a day (week 1 and week 2 post-transplant, PT); three times a week (week 3 and week 4 PT); twice a week (week 5 up to week 8 PT), once a week (week 9 up to week 12 PT). The dose of ganciclovir was adjusted for the patient's renal function.…”
Section: Introductionmentioning
confidence: 99%