Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
1.
Clin Infect Dis ; 66(3): 339-345, 2018 01 18.
Article in English | MEDLINE | ID: mdl-29029053

ABSTRACT

Background: The long-term effectiveness of the quadrivalent human papillomavirus (qHPV) vaccine was assessed by monitoring the combined incidence of cervical intraepithelial neoplasia (CIN2, CIN3), adenocarcinoma in situ (AIS), and cervical cancer related to HPV16 or HPV18. Methods: Women from Nordic countries of Denmark, Iceland, Norway, and Sweden who received a 3-dose regimen of the qHPV vaccine in the beginning of FUTURE II (Females United to Unilaterally Reduce Endo/Ectocervical Disease; V501-015, base study NCT00092534) are followed through different national registries. Effectiveness analyses were conducted approximately 2 years following completion of the base study and occur approximately every 2 years thereafter for 10 years (ie, 14 years from day 1 of the base study). Vaccine effectiveness against HPV16/18-related CIN2 or worse (CIN2+) was estimated by comparing the observed incidence with the expected incidence of CIN2+ in an unvaccinated cohort using historical registry data. Results: In the per-protocol population (2084 women) analysis of effectiveness after the first 12 years, there were no breakthrough cases of HPV16/18 CIN2+ after 9437 person- years of follow-up. Statistical power was sufficient to conclude that qHPV vaccine effectiveness remains above 90% for at least 10 years. The number of person-years during the follow-up interval of 10-12 years is continuing to accrue and shows a trend toward continuing effectiveness of the vaccine during that period. Conclusion: The qHPV vaccine shows continued protection in women through at least 10 years, with a trend for continued protection through 12 years of follow-up. Clinical Trials Registration: NCT00092534. Study Identification: V501-015.


Subject(s)
Adenocarcinoma in Situ/prevention & control , Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18/therapeutic use , Papillomavirus Infections/prevention & control , Uterine Cervical Dysplasia/prevention & control , Uterine Cervical Neoplasms/prevention & control , Vaccination/statistics & numerical data , Vaccine Potency , Adenocarcinoma in Situ/epidemiology , Adenocarcinoma in Situ/virology , Adult , Cohort Studies , Denmark/epidemiology , Female , Follow-Up Studies , Human papillomavirus 16 , Human papillomavirus 18 , Humans , Iceland/epidemiology , Norway/epidemiology , Papillomavirus Infections/epidemiology , Risk Factors , Sweden/epidemiology , Time Factors , Uterine Cervical Neoplasms/epidemiology , Uterine Cervical Neoplasms/virology , Young Adult , Uterine Cervical Dysplasia/epidemiology , Uterine Cervical Dysplasia/virology
2.
Stat Med ; 26(7): 1579-93, 2007 Mar 30.
Article in English | MEDLINE | ID: mdl-16927249

ABSTRACT

The detection of clusters of events occurring close together both temporally and spatially is important in finding outbreaks of disease within a geographic region. The Knox statistic is often used in epidemiology to test for space-time clustering retrospectively. For quicker detection of epidemics, prospective methods should be used in which observed events in space and time are assessed as they are recorded. The cumulative sum (CUSUM) surveillance method for monitoring the local Knox statistic tests for space-time clustering each time there is an incoming observation. We consider the design of this control chart by determining the in-control average run length (ARL) performance of the CUSUM chart for different space and time closeness thresholds as well as for different control limit values. We also explain the effect of population density and region shape on the in-control ARL and discuss other distributional issues that should be considered when implementing this method.


Subject(s)
Disease Outbreaks , Epidemiologic Methods , Public Health/methods , Space-Time Clustering , Computer Simulation , Humans
SELECTION OF CITATIONS
SEARCH DETAIL