Epidemiology and outcomes of early-onset and late-onset adenovirus infections in kidney transplant recipients

J Bruminhent, S Worawichawong… - Open Forum …, 2019 - academic.oup.com
J Bruminhent, S Worawichawong, C Tongsook, E Pasomsub, S Boongird…
Open Forum Infectious Diseases, 2019academic.oup.com
Objective Adenovirus (ADV) infection after kidney transplantation (KT) causes significant
morbidity. Patient characteristics and outcomes of ADV infection in KT recipients were
investigated. Method All adult KT recipients with ADV infection between January 2015 and
June 2019 were included. ADV infection/disease was defined as detection of ADV DNA in
clinical specimens/plus symptoms. Clinical and laboratory findings, treatments, and
outcomes were assessed. Results Adenovirus infection was diagnosed in 24 of 751 (3.2%) …
Objective
Adenovirus (ADV) infection after kidney transplantation (KT) causes significant morbidity. Patient characteristics and outcomes of ADV infection in KT recipients were investigated.
Method
All adult KT recipients with ADV infection between January 2015 and June 2019 were included. ADV infection/disease was defined as detection of ADV DNA in clinical specimens/plus symptoms. Clinical and laboratory findings, treatments, and outcomes were assessed.
Results
Adenovirus infection was diagnosed in 24 of 751 (3.2%) KT recipients. Twenty (83%) were male with a median age of 47 years (interquartile range [IQR], 36–58). Fifteen (63%) underwent deceased donor KT, and 13 (54%) received induction therapy. Twenty-one (88%) and 4 (17%) patients developed hemorrhagic cystitis and disseminated disease, respectively. There were equal distributions of early-onset (EOI) (≤3 months) and late-onset (LOI) (>3 months) infections. Patients who were diagnosed with EOI had lower median absolute lymphocyte counts compared with those with LOI (735/mm3 [IQR, 543–1123] vs 1122/mm3 [IQR, 784–1344], P = .04). All achieved resolution after reduction of their immunosuppression regimen and 13 (54%) received cidofovir therapy. Eighteen (75%) developed allograft dysfunction, of which 67% were transient. One (4%) underwent nephrectomy for allograft failure and 1 (4%) died (non-ADV–related). Patients with EOI were more likely to receive cidofovir therapy (75% vs 33%, P = .04) and develop other opportunistic infections (75% vs 8%, P < .001).
Conclusions
Adenovirus infection after KT typically involves a genitourinary system and transiently impairs an allograft function. Those who developed early infection tend to have more lymphopenia, coinfection, and receive antiviral therapy.
Oxford University Press
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