For infection surveillance, quantitative CMV antigenemia targeting pp65 was tested using direct immunofluorescence method (CINA Kit system, Argene Biosoft, Varilhes, France) 3 times during the first week after transplantation and then weekly during hospitalization. After discharge, patients were monitored monthly during the first year after LT. CMV qPCR testing (Real-Q assay; BioSewoom, Seoul, South Korea) was performed when the patient had leukopenia, according to the clinician’s judgement.
Monitoring Transplant Patients' Health
For infection surveillance, quantitative CMV antigenemia targeting pp65 was tested using direct immunofluorescence method (CINA Kit system, Argene Biosoft, Varilhes, France) 3 times during the first week after transplantation and then weekly during hospitalization. After discharge, patients were monitored monthly during the first year after LT. CMV qPCR testing (Real-Q assay; BioSewoom, Seoul, South Korea) was performed when the patient had leukopenia, according to the clinician’s judgement.
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Corresponding Organization :
Other organizations : Samsung Medical Center, Sungkyunkwan University
Variable analysis
- Frequency of laboratory tests (CBC and liver function test) after LT
- Timing of CMV antigenemia testing (3 times during the first week after transplantation and then weekly during hospitalization, monthly during the first year after LT)
- Timing of CMV qPCR testing (when the patient had leukopenia, according to the clinician's judgement)
- Laboratory test results (CBC and liver function test)
- CMV antigenemia levels
- CMV viral load (qPCR results)
- Patients undergoing liver transplantation (LT)
- No positive or negative controls were explicitly mentioned in the provided information.
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