Evaluation of a Change in CMV Prevention Strategy Following Pediatric SOT
Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Meeting: 2018 American Transplant Congress
Abstract number: C317
Keywords: Cytomeglovirus, Pediatric, Prophylaxis
Session Information
Session Name: Poster Session C: Transplant Infectious Diseases
Session Type: Poster Session
Date: Monday, June 4, 2018
Session Time: 6:00pm-7:00pm
Presentation Time: 6:00pm-7:00pm
Location: Hall 4EF
Optimal cytomegalovirus(CMV) prevention strategy following solid organ transplantation(SOT) is uncertain. We report on CMV disease with implementation of prophylaxis-based prevention with intensive monitoring.
We retrospectively evaluated the incidence of CMV events(asymptomatic infection/syndrome/disease) after implementation of an evidence-based CMV prevention guideline. Outcomes were recorded from 9/2013-10/2017.
173 pediatric SOT were performed. 37(21%) recipients had CMV events: 22 asymptomatic, 14 syndrome and 1 disease (hepatitis in liver recipient at 121d). Median time to 1st CMV event was 166d(IQR 29-226d). Asymptomatic events occurred during <30, 30-120 and >120d in 9/10, 1/2 and 12/25 CMV events, respectively. After 3 asymptomatic <30d in hearts, prophylaxis dosing was increased for the first 3 weeks with no subsequent events. One liver had asymptomatic CMV at <30d with misclassification of D/R status. Two asymptomatic infections and 1 syndrome occurred with deviations. Kidneys developed CMV only after prophylaxis ended in 6/67(9%). In a similar period(>120d), hearts and livers had 5/36(14%) and 13/70(18%) with scheduled screening.
Invasive end-organ CMV disease is rare with prophylaxis/monitoring. Increased screening resulted in identification of asymptomatic infections, especially early post-transplant. Scheduled screening increased prevalence of late events (heart/liver) and led to early prophylaxis dose change (heart), highlighting its utility.
Organ | Serostatus | Total Tx | CMV Events | 0-30d | 31-120d | >120d |
Heart | D+/R– | 13 | 5 | 5 | ||
D+/R+ | 8 | 4 | 3 | 1 | ||
D–/R+ | 4 | 1 | 1 | |||
D–/R– | 11 | 0 | ||||
Kidney | D+/R– | 21 | 4 | 4 | ||
D+/R+ | 6 | 1 | 1 | |||
D–/R+ | 11 | 1 | 1 | |||
D–/R– | 29 | 0 | ||||
Liver | D+/R– | 17 | 7 | 2 | 5 | |
D+/R+ | 19 | 11 | 1 | 2 | 8 | |
D–/R+ | 13 | 2 | 2 | |||
D–/R– | 21 | 1 | 1 | |||
Total | 173 | 37 | 10 | 2 | 25 |
Table1: CMV by SOT, serostatus, time of 1st event.
CITATION INFORMATION: Pangonis S., Miethke A., Flores F., Schecter M., Kocoshis S., Lazear D., Hemmelgam T., Taylor B., Paulsen G., Danziger-Isakov L. Evaluation of a Change in CMV Prevention Strategy Following Pediatric SOT Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:
Pangonis S, Miethke A, Flores F, Schecter M, Kocoshis S, Lazear D, Hemmelgam T, Taylor B, Paulsen G, Danziger-Isakov L. Evaluation of a Change in CMV Prevention Strategy Following Pediatric SOT [abstract]. https://atcmeetingabstracts.com/abstract/evaluation-of-a-change-in-cmv-prevention-strategy-following-pediatric-sot/. Accessed November 21, 2024.« Back to 2018 American Transplant Congress