TABLE 2.
Characteristic |
RSVPreF3 OA N = 27 |
Placebo N = 95 |
LSMean difference (95% CI) | p value |
---|---|---|---|---|
FLU‐PRO total score | ||||
N with data | 24 | 76 | ||
Baseline a | 0.23 | 0.21 | ||
During episode | 0.76 | 0.81 | −0.05 (−0.30, 0.20) | 0.6956 |
SF‐12 physical functioning score | ||||
N with data | 20 | 69 | ||
Baseline | 74.15 | 76.58 | ||
During episode | 72.16 | 65.16 | 7.00 (−9.86, 23.85) | 0.4125 |
EQ‐5D utility score | ||||
N with data | 19 | 69 | ||
Baseline | 0.8616 | 0.8586 | ||
During episode | 0.8896 | 0.8109 | 0.0786 (−0.0340, 0.1913) | 0.1695 |
Note: A higher FLU‐PRO score indicates a higher level of symptom severity. A higher SF‐12 or EQ‐5D score indicates a higher level of functioning/quality of life.
Abbreviations: CI, confidence interval; EQ‐5D, EuroQol‐5 Dimension; FLU‐PRO, InFLUenza Patient‐Reported Outcome; LSMeans, least squares means, mES, modified exposed set; N, number of first RT‐PCR‐confirmed RSV‐ARI episodes; Placebo, participants receiving placebo; RSV‐ARI, respiratory syncytial virus–acute respiratory infection; RSVPreF3 OA, participants receiving RSVPreF3 OA vaccine; RT‐PCR, reverse transcription polymerase chain reaction; SF‐12 PF, Short Form‐12 physical functioning.
Mean score of the assessments at baseline.