Cytomegalovirus infection and disease in pediatric liver transplantation: Burden of disease under a preemptive therapy approach

• Published in: Pediatric transplantation Vol. 27; no. 1; pp. e14356 - n/a
• Main Authors: Arroyo‐Orvañanos, Jorge, Hernández‐Plata, José‐Alejandro, Erro‐Aboytia, Rosa, Nieto‐Zermeño, Jaime, Reyes‐López, Alfonso, Varela‐Fascinetto, Gustavo
• Format: Journal Article
• Language: English
• Published: Denmark Wiley Subscription Services, Inc 01.02.2023
• Subjects: Antigenemia; Antiviral agents; Antiviral Agents - therapeutic use; Child; CMV; CMV disease; CMV infection; Cost of Illness; Cytomegalovirus; Cytomegalovirus Infections - drug therapy; Cytomegalovirus Infections - epidemiology; Cytomegalovirus Infections - etiology; Disease prevention; Epidemiology; Ganciclovir - therapeutic use; Hepatitis; Humans; Infections; Liver diseases; Liver Transplantation; Liver transplants; Patients; pediatric liver transplant; Pediatrics; Pp65 protein; preemptive therapy; Risk Factors; Side effects; preemptive therapy; pediatric liver transplant; CMV infection; CMV disease; CMV
• ISSN: 1397-3142; 1399-3046
• DOI: 10.1111/petr.14356

Background CMV remains a frequent complication after liver transplantation. Few studies exist in children reporting the epidemiology and outcomes of CMV after LT with current prevention strategies. Our goal is to report the incidence of CMV infection and disease in pediatric LT recipients under preemptive therapy, identify risk factors, complications, and adverse reactions to treatment. Methods All pediatric LT recipients from a single center (1998–2018) were included. Antigenemia pp65 (1998–2003) and QNAT or both were used to inform preemptive therapy. Cutoff value for starting treatment was Agpp65 > 10 + cells/200 000 or QNAT >1500 copies/ml or any value in high‐risk recipients (D+/R−). Results One hundred eighteen LT were analyzed. CMV infection was detected in 67% of patients, only 44 (37%) required treatment, and 5 (4%) developed CMV disease. All patients responded well to treatment, and no graft or patients were lost to CMV effects. There were no differences in mortality, CMV indirect effects, or other complications between those who required treatment and those who did not. Thirty‐two percent of the patients who received antivirals developed an adverse hematological reaction. Risk factors associated with CMV infection requiring treatment were D+/R− (OR 13.9, p = .01) and fulminant hepatitis (OR 4.8, p = .02). Conclusions Preemptive therapy for CMV in children is safe and effective, yields low CMV infection rates that require treatment, and minimal rates of CMV disease, without increasing CMV‐related complications. Using this strategy, 63% of our patients did not receive treatment. Therefore, drug exposure, adverse reactions, and resistance risk were minimized.