Table 2.
Pathogen | Mode of transmission | Usual time of presentation | Presenting features | Diagnosis | Treatment |
---|---|---|---|---|---|
HHV-6 | Reactivation of latent infection | Commonest in first 2–4 weeks, may occur up to 2 years | Fever, rash, myelosuppression, hepatitis, pneumonitis, encephalitis ↑ risk of CMV and opportunistic infections | PCR | Ganciclovir |
HHV-7 | Transmission from donor | Histopathology | Cidofovir Foscarnate | ||
Adenovirus | Reactivation, nosocomial transmission | Commonest in first 3 months, may occur until several years | Interstitial nephritis, hemorrhagic cystitis, pneumonitis | Immunohistochemistry PCR in plasma | IVIG Cidofovir |
West Nile virus | Transmission from donor,blood transfusion, environmental exposure | Fever, meningoencephalitis,hyporeflexic paralysis | PCR (short viremic phase)Serology (may be delayed) IgM antibody in CSF | IVIG | |
LCM | Transmission from donor, | First 4 weeks | Fever, diarrhea, asepticmeningitis, interstitial pneumonia, hepatitis, multisystem failure | Cerebrospinal fluid PCR, serology | |
Parainfluenza and metapneumovirus | Environmental and nosocomial transmission | After 1 year illness, pneumonia | Fever, upper respiratory | PCR Antigen detection on respiratory secretions | Ribavirin |
Parvovirus B19 | Transmission from donor | First year | Fever, joint pain, pure redcell aplasia, hepatitis, pneumonitis | PCR Bone marrow examination | IVIG |
Respiratory syncytial virus | Nosocomial transmission | Any time | Upper respiratory tract infection, interstitial pneumonia | PCR Antigen testing on respiratory secretions | Ribacirin IVIG |
Rotavirus | Environmental transmission | Any time | Self-limiting diarrhea, lowergastrointestinal bleeding | None |
HHV: human herpesvirus; LCM: lymphocyte choriomeningitis virus, CSF: cerebrospinal fl uid, IVIG: intravenous immunoglobulin; PCR: polymerase chain reaction