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. 2013 Apr;54(2):135–145. doi: 10.3325/cmj.2013.54.135

Table 3.

A review of efficacy estimates for live vaccines (PPT– per protocol; ITT – intention to treat).

Author (year of publication) Study design Type of vaccine Control Age of study population Overall vaccine efficacy (VE) Lower confidence interval limit (for overall VE) Upper confidence interval limit (for overall VE)
Belshe (1998)
RCT
Live
Placebo
15-71 months
0.93
0.88
0.96
Belshe (2000)
RCT
Live
Placebo
26-85 months
0.87
0.78
0.93
Beutner (1979)
RCT
Live
Placebo
7-14 years
0.62
0.44
0.87
Clover (1991)
RCT
Live
Placebo
3-18 years
0.65
0.31
1.36
Longini (2000)
RCT
Live
Placebo
15-71 months
1996-97: 0.90
1997-98: 0.85
0.51
0.47
1.59
1.53
Neto (2009)
RCT
Live
Placebo
6 to <36 months
Year 1, similar antigen: 0.74
Year 1, any antigen: 0.72
Year 2, similar antigen: 0.74
Year 2, any antigen: 0.47
0.64
0.62
0.33
0.15
0.81
0.80
0.91
0.67
Tam (2007)
RCT
Live
Placebo
12 to <36 months
Year 1, PPT, similar antigen: 0.73
Year 1, PPT, any antigen: 0.70
Year 1, ITT, similar antigen: 0.70
Year 1, ITT, any antigen: 0.68
Year 2, PPT, similar antigen: 0.84
Year 2, PPT, any antigen: 0.64
0.63
0.61
0.60
0.59
0.70
0.44
0.81
0.77
0.78
0.75
0.92
0.77
Vesikari (2006)
RCT
Live
Placebo
6 to <36 months
Year 1, PPT, similar antigen: 0.85
Year 1, PPT, any antigen: 0.86
Year 1, ITT, similar antigen: 0.84
Year 1, ITT, any antigen: 0.84
Year 2, PPT, similar antigen: 0.89
Year 2, PPT, any antigen: 0.86
Year 2, ITT, similar antigen: 0.89
Year 2, ITT, any antigen: 0.85
0.74
0.76
0.73
0.74
0.82
0.79
0.83
0.78
0.92
0.92
0.91
0.90
0.93
0.91
0.93
0.90
Halloran (2003) Cohort study Live No intervention 1.5-18 years Combined, A (H1N1) and B: 0.91 -0.34 0.99