Clinical Application of Variation in Replication Kinetics During Episodes of Post-transplant Cytomegalovirus Infections

Publikation: Bidrag til tidsskriftTidsskriftartikelForskning

  • I P Lodding
  • Henrik Sengeløv
  • C da Cunha-Bang
  • Martin Peter Iversen
  • Allan Rasmussen
  • F Gustafsson
  • J G Downing
  • Jesper Grarup
  • N Kirkby
  • C M Frederiksen
  • A Mocroft
  • S S Sørensen
  • Lundgren, Jens
  • MATCH Programme Study Group

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.

OriginalsprogEngelsk
TidsskriftEBioMedicine
Vol/bind2
Udgave nummer7
Sider (fra-til)699-705
Antal sider7
ISSN2352-3964
DOI
StatusUdgivet - jul. 2015

ID: 162026957