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Whimbey 711<br />

CRVs are a common cause of acute respiratory disease in both allogeneic <strong>and</strong><br />

<strong>autologous</strong> BMT recipients, occurring in a minimum of one-third of hospitalized<br />

BMT transplant recipients with an acute respiratory illness. 3<br />

Although these<br />

infections may occur at any time during the transplant period, either pre- or postengraftment,<br />

the severity of these infections has in some instances been temporally<br />

related to the time of the transplant.<br />

CRV infections in hospitalized <strong>blood</strong> <strong>and</strong> <strong>marrow</strong> transplant recipients are<br />

frequently complicated by life-threatening pneumonias. Approximately 40% of<br />

CRV infections have remained limited to the upper respiratory tract <strong>and</strong> have been<br />

characterized by rhinorrhea, nasal <strong>and</strong> sinus congestion, sore throat, <strong>and</strong> mild<br />

cough. However, 60% of the infections have been complicated by pneumonia,<br />

either primary viral or secondary bacterial/fungal pneumonias, <strong>and</strong> the pneumoniaassociated<br />

mortality has been approximately 50%. An important clue to the<br />

diagnosis of CRV-associated pneumonias has been the finding that 85% of these<br />

pneumonias have been preceded by signs <strong>and</strong> symptoms of a URI, in contrast to<br />

pneumonias due to CMV or Pneumocystis carinii, which are not typically preceded<br />

by a URI. In an era of reasonably effective prophylaxis of CMV disease, CRVassociated<br />

pneumonias have assumed a dominating role in BMT recipients,<br />

occurring four times more frequently than CMV pneumonia <strong>and</strong> accounting for<br />

four times as many deaths. 4<br />

There has been considerable diversity in the frequency <strong>and</strong> severity of CRV<br />

infections observed in different transplant centers. This diversity reflects several<br />

factors, including the intensity of the surveillance; the time of year when the<br />

surveillance was performed <strong>and</strong> the viruses prevalent in the community; the type<br />

<strong>and</strong> degree of immunosuppression of the patients being evaluated; the type of<br />

infection control <strong>and</strong> influenza vaccination policies; the inclusion of potential as<br />

well as actual transplant recipients; the inclusion of outpatients as well as<br />

inpatients; the types of viruses routinely assayed for in the laboratory; the<br />

multiplicity of laboratory methods used to identify different viruses (e.g., culture,<br />

rapid Ag assays, PCR, histopathology); <strong>and</strong> the definition of a case (i.e., confirmed<br />

by culture or by rapid detection assays).<br />

RESPIRATORY SYNCYTIAL VIRUS<br />

RSV is the leading cause of serious lower respiratory tract disease in infants <strong>and</strong><br />

children, causing tracheobronchitis, bronchiolitis, <strong>and</strong> pneumonia. Most persons<br />

are infected during the first years of life. Natural immunity is incomplete, <strong>and</strong> older<br />

children <strong>and</strong> adults experience repeated infections, which are usually manifested as<br />

relatively benign upper respiratory illnesses or tracheobronchitis. In the elderly,<br />

RSV infections are not infrequently associated with lower respiratory tract<br />

syndromes similar to influenza.

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