Table 1. Evidence type for efficacy of 4-valent recombinant human papillomavirus vaccination of males aged 16–26 years, summary from ECDC guidance on HPV vaccinationa.
Outcomes | Design | Vaccine efficacy | Risk of bias | Inconsistency | Indirectness | Imprecision | Evidence type (GRADE) | |
---|---|---|---|---|---|---|---|---|
% | 95% CI | |||||||
HPV types 6, 11, 16 and 18 | ||||||||
6MPI | 4-valent recombinant vaccination compared with placebo (one RCT) | 85.6 | 73.4 to 92.9 | Not serious | Not serious | Not serious | Not serious | High |
AIN2/3 | 74.9 | 8.8 to 95.4 | Not serious | Not serious | Not serious | Not serious | High | |
PeIN2/3 | 100.0 | −3 788.2 to 100.0 | Not serious | Not serious | Not serious | Very seriousb | Low | |
Anogenital warts | 89.4 | 65.5 to 97.9 | Not serious | Not serious | Not serious | Not serious | High |
AIN2/3: anal intraepithelial neoplasia grades 2 and 3; CI: confidence interval; ECDC: European Centre for Disease Prevention and Control; GRADE: grading of recommendations, assessment, development and evaluation; HPV: human papillomavirus; PeIN: penile intraepithelial neoplasia; RCT: randomised controlled trial; 6MPI: 6-month persistent infection.
a Based on the ECDC report ‘Guidance on HPV vaccination in EU countries: focus on boys, people living with HIV and 9-valent HPV vaccine introduction’ [14].
b Downgraded by one level for imprecision because of very wide 95% CI.