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714 Chapter 15: New Avenues<br />

physical discomfort to the patients of prolonged aerosol therapy <strong>and</strong> confinement<br />

within a scavenging tent; the adverse effects of aerosolized ribavirin, such as<br />

bronchospasm; the high cost of these drugs as well as the intensive respiratory<br />

therapy needed to safely administer aerosolized ribavirin; <strong>and</strong> the need for hospitalization<br />

with more frequent or prolonged ribavirin dosing regimens. Studies are<br />

underway to define more closely the patients at risk <strong>and</strong> to identify the regimen that<br />

is simplest to administer <strong>and</strong> least costly yet effective.<br />

Although prompt therapy of URIs with antiviral drugs <strong>and</strong>/or immunotherapy<br />

appears to have had a favorable impact on the frequency of pneumonia <strong>and</strong> death,<br />

the morbidity <strong>and</strong> mortality associated with RSV infections in these patients is still<br />

high. The optimal therapy is prevention. Active immunoprophylaxis is not an<br />

option, because an effective vaccine is not currently available. Passive immunoprophylaxis<br />

appears promising in high-risk young children <strong>and</strong> warrants investigation<br />

in immunocompromised patients. In children, the monthly administration of<br />

RSV-IVIG (Respigram, Medimmune), a human polyclonal IgG immune globulin<br />

with high RSV microneutralization titers, has been effective in decreasing the risk<br />

of serious RSV disease, as has the monthly administration of monoclonal RSV<br />

antibody (MEDI-493, Medimmune), a humanized monoclonal antibody. 22-24<br />

Prevention of infection through an aggressive infection control strategy can be<br />

highly effective. 8<br />

At the core of an effective strategy is continuing education of<br />

patients, family members, visitors, <strong>and</strong> staff regarding the potential seriousness of<br />

CRV infections, their epidemiology, their modes of transmission, <strong>and</strong> means of<br />

control. In general, infection control strategies need to be designed to prevent<br />

spreading by several different modes of transmission, since several different CRVs<br />

commonly circulate in the community concurrently <strong>and</strong> since CRVs usually can be<br />

spread by several modes of transmission. These measures may need to be<br />

intensified during community or hospital outbreaks of CRV infections. The<br />

intensity <strong>and</strong> duration of the infection control measures need to be tailored<br />

according to the risk of serious CRV in different subsets of transplant recipients<br />

<strong>and</strong> the needs of the patient <strong>and</strong> quality of life issues.<br />

CONCLUSION<br />

The spectrum of emerging viruses <strong>and</strong> their disease manifestations in <strong>blood</strong> <strong>and</strong><br />

<strong>marrow</strong> transplant recipients has evolved rapidly. In addition, traditional<br />

herpesviruses such as CMV are posing new challenges, particularly in the late<br />

posttransplant period, <strong>and</strong> are becoming the model for a new modality of therapy,<br />

adoptive immunotherapy. 25<br />

' 26<br />

Sophisticated diagnostic research tools are gradually<br />

being integrated into the clinical diagnostic laboratories, <strong>and</strong> clinical investigations<br />

are being undertaken to define the sensitivity <strong>and</strong> specificity of these assays <strong>and</strong> to<br />

distinguish shedding of virus from disease. The need for more effective <strong>and</strong> less

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