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Prolonged outbreak of adenovirus A31 in allogeneic stem cell transplant recipients
L Swartling1, A Allard2, J Törlen3
1Division of Infectious Diseases, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Insights
An outbreak of human adenovirus (HAdV) A31 in stem cell transplant patients was difficult to control, leading to significant medical consequences. Continuous transmission may result from unidentified mild cases, necessitating extended patient monitoring.
Area of Science:
- Infectious Diseases
- Virology
- Hematology
Background:
- A human adenovirus (HAdV) A31 outbreak occurred at a stem cell transplantation center from December 2011 to March 2012.
- The study investigated transmission routes and medical outcomes of the HAdV A31 outbreak.
Purpose of the Study:
- To analyze the HAdV A31 outbreak at a stem cell transplantation center.
- To identify transmission routes and assess medical consequences in patients.
Main Methods:
- Retrospective analysis of medical records for patients admitted during the outbreak.
- Phylogenetic analysis of HAdV strains using hexon and E3 gene sequencing.
Main Results:
- Nine cases of HAdV A31 infection were identified, with evidence of nosocomial transmission.
- Hygiene measures were insufficient to halt transmission for two months.
- Transplantation was postponed/cancelled in one patient; five received cidofovir for viremia. Graft-versus-host disease (GVHD) complicated clinical presentation in seven patients.
Conclusions:
- Controlling HAdV outbreaks in hematopoietic stem cell transplantation (HSCT) recipients is challenging.
- Despite no severe initial disease, medical consequences were significant.
- Extended surveillance beyond the last identified case may be crucial for controlling transmission.
Background:
An outbreak of human adenovirus (HAdV) A31 occurred from December 2011 to March 2012 at the Center for Allogeneic Stem Cell Transplantation (CAST), Karolinska University Hospital in Sweden. We analyzed the outbreak, the routes of transmission, and report the medical consequences.
Methods:
The medical records of all patients admitted to CAST during the outbreak period were studied. Phylogenetic analysis of the patient HAdV strains was performed by sequencing the hexon gene and the more variable E3 gene.
Results:
We identified 9 cases of HAdV A31. Hygiene measures were implemented, but transmission continued for 2 months. All 9 patients had been admitted to the ward, but 2 had no connection in time to other known HAdV A31 cases. DNA sequencing of the patient strains strongly suggested nosocomial transmission. Transplantation was postponed and then cancelled in 1 patient, and 5 patients were treated with cidofovir because of high levels of viremia. In 7 patients, concomitant graft-versus-host disease (GVHD) grade II-V complicated the clinical picture, as it was difficult to distinguish symptoms of GVHD from those of HAdV infection.
Conclusion:
An outbreak of HAdV in HSCT recipients can be difficult to control. Although none of the patients had severe disease, the medical consequences were significant. It is possible that unidentified cases with mild symptoms may have caused continuous transmission at the unit. Regular testing of all patients several weeks beyond the last case identified may be an important measure to control transmission.
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