Key result
PCR detects posttransplant CMV pneumonitis ~12 days earlier than standard culture.
Why the study?
Earlier detection of CMV pneumonitis in lung and heart/lung transplant recipients using PCR compared with traditional laboratory criteria was evaluated to improve monitoring and preemptive therapy.
Does PCR amplification of CMV DNA allow earlier detection of CMV pneumonitis compared to traditional laboratory criteria in lung and heart/lung transplant patients?
Observational (n=12)
Does PCR amplification of CMV DNA allow earlier detection of CMV pneumonitis compared to traditional laboratory criteria in lung and heart/lung transplant patients?
Answers are grounded in this paper and cite their sources.
PCR-based testing allows for earlier detection of CMV replication compared to traditional tissue culture and cytology in lung and heart/lung transplant recipients, potentially enabling preemptive therapy.
Polymerase chain reaction (PCR) amplification of CMV DNA recovered from bronchial alveolar lavage (BAL) and peripheral blood samples was compared with tissue culture, cytology, and/or histology for the earlier detection of CMV pneumonitis in 12 recipients of single-lung or heart/lung transplants. In patients with confirmed CMV pneumonitis, cytological evidence of CMV disease in BAL samples was detected 38 +/- 14 days posttransplantation, while tissue culture and PCR-positive results were noted as early as 30 +/- 4.0 days and 18 +/- 4.6 days, respectively. While PCR was positive earlier than culture in a number of cases, culture-positive results were subsequently obtained in each case, consistent with earlier detection of viral replication by PCR as opposed to detection of latent virus. CMV was detected by PCR in 6 of 24 blood samples from patients with confirmed or suspected CMV pneumonitis, while results of all 24 blood samples were negative when assayed by tissue culture. PCR-based testing was more sensitive than traditional tests, allowing detection of viral replication earlier than tissue culture in the posttransplant period. PCR could provide a powerful means of monitoring the immunocompromised patients in whom preemptive therapeutic intervention for CMV disease is desirable.
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Buffone et al. (1993) conducted an observational in CMV pneumonitis (n=12). PCR amplification of CMV DNA vs. Tissue culture, cytology, and/or histology was evaluated on Time to detection of CMV pneumonitis posttransplantation (days). PCR amplification of CMV DNA detected CMV pneumonitis earlier compared to tissue culture and cytology (38 +/- 14 days).
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