Respiratory syncytial virus (RSV) poses a significant health threat to older adults—particularly those with underlying conditions such as chronic lung disease, heart disease, or weakened immune function— increasing their risk of severe complications, hospitalization, and death.1 The U.S. Food & Drug Administration (FDA) recently approved an RSV vaccine, offering a new preventive measure to reduce these risks.1 The Centers for Disease Control and Prevention (CDC) currently recommends RSV vaccination for adults aged 60 to 74 with risk factors for severe RSV, as well as all adults aged 75 or older, to prevent infection and hospitalization.2
To evaluate the vaccine’s effectiveness, we studied 348,376 patients tested for RSV between May 2023 and December 2024. These patients were either 75 or older or aged 60 to 74 and at increased risk. We adjusted for patient age, geographic region, rural or urban status, social vulnerability, history of influenza vaccination, smoking history, and BMI. For patients 75 or older, we also adjusted for an increased risk of a severe RSV infection. All patients had an RSV lab result. We matched each patient with an RSV vaccine to four patients who did not get an RSV vaccine, were tested for RSV in the same month, and were the same age as the vaccinated patient.
We found that patients aged 60 to 74 who received the RSV vaccine were 73% less likely to have a medically attended RSV infection, 75% less likely to have an RSV-related ED visit, and 75% less likely to be admitted for RSV compared to those who did not receive the RSV vaccine. We also found similar rates of effectiveness in the 75 and older group, as shown in Figure 1.
A sensitivity analysis of patients with RSV-like symptoms or an RSV diagnosis showed similar results.