Table 1.
Summary of Respiratory Syncytial Virus Epidemiologic Gaps
| Epidemiologic Gap | Summary |
|---|---|
| Surveillance for burden estimates | • Needed for all age groups, with finer age strata for extremes of age |
| • Include MAARI and hospitalizations | |
| • Include high-risk populations, including preterm infants, children, and adults with underlying heart and lung disease, neurologic diseases, immunocompromised, Alaska Natives, American Indians, pregnant women, and residents of congregate settings (eg, long-term-care facilities) | |
| • Ensure design of surveillance platforms: | |
| -Can test for multiple respiratory pathogens | |
| -Avoid influenza-like illness and severe acute respiratory infection definitions | |
| RSV-associated mortality | • Collect hospital and community-associated RSV deaths in all age groups |
| Short- and long-term outcomes of RSV infection | • Investigate effects of RSV on recurrent wheezing and asthma, particularly long-term effects |
| • Conduct studies in pregnant women to determine impact of maternal RSV disease on pregnancy and neonatal outcomes | |
| • Assess impact on frailty in older adults | |
| Correlates of protection | • Assess durability of respiratory mucosal antibodies and role in protection |
| • Study correlation of neutralization and viral protein– or epitope-specific antibodies with disease protection | |
| • Investigate role of cellular immunity in RSV disease outcome | |
| Cost-effectiveness | • Costs and benefits of vaccine introduction in target populations, which will need up-to-date burden estimates, indirect and out-of-pocket costs associated with RSV- associated MAARI, hospitalizations, and deaths |
| Assessing RSV diagnostic practices | • Needed to document potential underestimation of disease burden due to testing behaviors |
| Surveillance once vaccine is introduced | • Adverse events |
| • Genomic sequencing of breakthrough infections to document changes in the virus |
Abbreviation: RSV, respiratory syncytial virus.