Clinical Application of Variation in Replication Kinetics During Episodes of Post-transplant Cytomegalovirus Infections
I.P. Lodding,
H. Sengeløv,
C. da Cunha-Bang,
M. Iversen,
A. Rasmussen,
F. Gustafsson,
J.G. Downing,
J. Grarup,
N. Kirkby,
C.M. Frederiksen,
A. Mocroft,
S.S. Sørensen,
J.D. Lundgren
Affiliations
I.P. Lodding
Centre for Health and Infectious Disease Research (CHIP), Department of Infectious Diseases and Rheumatology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
H. Sengeløv
Department of Hematology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
C. da Cunha-Bang
Department of Hematology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
M. Iversen
Department of Cardiology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
A. Rasmussen
Department of Surgery C, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
F. Gustafsson
Department of Cardiology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
J.G. Downing
Centre for Health and Infectious Disease Research (CHIP), Department of Infectious Diseases and Rheumatology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
J. Grarup
Centre for Health and Infectious Disease Research (CHIP), Department of Infectious Diseases and Rheumatology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
N. Kirkby
Department of Clinical Microbiology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
C.M. Frederiksen
Centre for Health and Infectious Disease Research (CHIP), Department of Infectious Diseases and Rheumatology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
A. Mocroft
Research Department of Infection and Population Health, University College of London (UCL), Royal Free Hospital Rowland Hill Street London NW3 2PF, United Kingdom
S.S. Sørensen
Department of Nephrology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
J.D. Lundgren
Centre for Health and Infectious Disease Research (CHIP), Department of Infectious Diseases and Rheumatology, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen Ø, Denmark
Background: Cytomegalovirus (CMV) infection in transplant recipients is reported to replicate with a doubling time of 1.2–2 days, and weekly screening is recommended for early diagnosis. We re-evaluated these features in our cohort of transplant recipients. Methods: The CMV doubling time of the first CMV infection in the first year post-transplant could be calculated for 193 recipients of haematopoietic stem cell or solid organ transplantation. Factors determining the proportion of recipients with a high diagnostic CMV viral load (≥18,200 IU/mL) were explored using mathematical simulation. Findings: The overall median doubling time was 4.3 days (IQR 2.5–7.8) and was not influenced by prior CMV immunity, or type of transplantation (p > 0.4). Assuming a fixed doubling time of 1.3 days and screening intervals of 7 or 10 days, 11.1% and 33.3% were projected to have a high CMV viral load at diagnosis, compared to 1.4% and 4.3% if the doubling time varies as observed in our cohort. Consistently, 1.9% of recipients screened weekly had a high diagnostic virus load. Interpretation: Screening intervals can be extended to 10 days in cohorts with comparable CMV doubling time, whereas shorter than 7 days is required in cohorts with shorter doubling times to maintain pre-emptive screening quality.