dc.creator | Andrade, Pd | |
dc.creator | Fioravanti, Mt | |
dc.creator | Anjos, Ebv | |
dc.creator | De Oliveira, C | |
dc.creator | Albuquerque, Dm | |
dc.creator | Costa, Scb | |
dc.date | 2013 | |
dc.date | 2015-11-27T13:32:27Z | |
dc.date | 2015-11-27T13:32:27Z | |
dc.date.accessioned | 2018-03-29T01:19:01Z | |
dc.date.available | 2018-03-29T01:19:01Z | |
dc.identifier | The Canadian Journal Of Infectious Diseases & Medical Microbiology = Journal Canadien Des Maladies Infectieuses Et De La Microbiologie Médicale / Ammi Canada. v. 24, n. 3, p. e69-74, 2013. | |
dc.identifier | 1712-9532 | |
dc.identifier | | |
dc.identifier | http://www.ncbi.nlm.nih.gov/pubmed/24421834 | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/200947 | |
dc.identifier | 24421834 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1301180 | |
dc.description | Human cytomegalovirus is an important cause of morbidity and mortality in immunocompromised patients. Qualitative polymerase chain reaction (PCR) has proven to be a sensitive and effective technique in defining active cytomegalovirus infection, in addition to having low cost and being a useful test for situations in which there is no need for quantification. Real-time PCR has the advantage of quantification; however, the high cost of this methodology makes it impractical for routine use. To apply a nested PCR assay to serum (sPCR) and to evaluate its efficiency to diagnose active cytomegalovirus infection compared with PCR of peripheral blood leukocytes (L-PCR). Samples of 37 patients were prospectively evaluated. An internal control was created and applied to sPCR to exclude false-negative results. In total, 21 patients (57%) developed active cytomegalovirus infection. After analyzing the two methods for the diagnosis of active infection, higher sensitivity and negative predictive value of the L-PCR versus sPCR (100% versus 62%), and higher specificity and positive predictive value of sPCR versus L-PCR (81% versus 50% and 72%, respectively) were observed. Discordant results were observed in 11 patients who were L-PCR-positive but sPCR-negative for active cytomegalovirus infection, five of whom developed clinical symptoms of cytomegalovirus. Clinical symptoms were observed in 14 patients, 12 of whom were diagnosed with active infection by nested L-PCR (P=0.007) and seven by nested sPCR (P=0.02). Higher specificity and a positive predictive value for sPCR were observed. Nested L-PCR and sPCR were considered to be complementary methods for the diagnosis and management of symptomatic cytomegalovirus infection. | |
dc.description | 24 | |
dc.description | e69-74 | |
dc.language | eng | |
dc.relation | The Canadian Journal Of Infectious Diseases & Medical Microbiology = Journal Canadien Des Maladies Infectieuses Et De La Microbiologie Médicale / Ammi Canada | |
dc.relation | Can J Infect Dis Med Microbiol | |
dc.rights | aberto | |
dc.rights | | |
dc.source | PubMed | |
dc.subject | Cmv | |
dc.subject | Nested Pcr | |
dc.subject | Serum Nested Pcr | |
dc.subject | Transplant | |
dc.title | Peripheral Blood Leukocytes And Serum Nested Polymerase Chain Reaction Are Complementary Methods For Monitoring Active Cytomegalovirus Infection In Transplant Patients. | |
dc.type | Artículos de revistas | |