Article
Cost-effectiveness of extending cervical cancer screening intervals among women with prior normal pap tests.
Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, USA.
Obstetrics and Gynecology (impact factor:
4.73).
03/2006;
107(2 Pt 1):321-8.
DOI:10.1097/01.AOG.0000196500.50044.ce
pp.321-8
Source: PubMed
-
Citations (0)
- Cited In (3)
-
Article: Cost-effectiveness of human papillomavirus vaccination in the United States.
[show abstract] [hide abstract]
ABSTRACT: We describe a simplified model, based on the current economic and health effects of human papillomavirus (HPV), to estimate the cost-effectiveness of HPV vaccination of 12-year-old girls in the United States. Under base-case parameter values, the estimated cost per quality-adjusted life year gained by vaccination in the context of current cervical cancer screening practices in the United States ranged from $3,906 to $14,723 (2005 US dollars), depending on factors such as whether herd immunity effects were assumed; the types of HPV targeted by the vaccine; and whether the benefits of preventing anal, vaginal, vulvar, and oropharyngeal cancers were included. The results of our simplified model were consistent with published studies based on more complex models when key assumptions were similar. This consistency is reassuring because models of varying complexity will be essential tools for policy makers in the development of optimal HPV vaccination strategies.Emerging infectious diseases 03/2008; 14(2):244-51. · 6.17 Impact Factor -
Article: Human papillomavirus testing with Pap triage for cervical cancer prevention in Canada: a cost-effectiveness analysis.
[show abstract] [hide abstract]
ABSTRACT: Recently published results from a large randomized trial (Canadian Cervical Cancer Screening Trial study group) suggest that human papillomavirus testing followed by Pap smear-based triage for human papillomavirus positive women may be an effective way to screen women for cervical cancer. We determined the potential cost-effectiveness of including human papillomavirus tests for cervical cancer screening for Canada and three provinces: Alberta, Newfoundland and Ontario. We developed four Markov decision models using data from relevant Canadian and provincial studies and databases. The models were used to determine the number of false positive test results, cancers, lifetime costs and life-expectancy for 27 different screening strategies that varied by age to begin screening (18 or 25 years), screening interval (one, two, three, or five years) and whether the currently recommended strategy (screening every year from age 18 until 21 and then every three years afterwards with conventional Paps) was conducted prior to age 25. Strategies were compared using incremental cost-effectiveness ratios. Screening strategies beginning at age 18 were associated with a substantial increase in the number of false-positive test results but only small differences in the number of cancers compared to the same strategy conducted beginning at age 25. Strategies of human papillomavirus testing first, followed by triage with Pap smears were associated with lower costs and greater increases in life-expectancy than the currently recommended screening strategy in Canada. A strategy of human papillomavirus testing beginning at age 25, with Pap triage for women with positive human papillomavirus results may be more effective at reducing cervical cancer at a lower cost than the current recommended strategy for screening in Canada.BMC Medicine 11/2009; 7:69. · 6.03 Impact Factor -
Article: Chapter 19: Cost-effectiveness of cervical cancer screening.
[show abstract] [hide abstract]
ABSTRACT: In the last two decades, computer-based models of cervical cancer screening have been used to evaluate the cost-effectiveness of different secondary prevention policies. Analyses in countries with existing screening programs have focused on identifying the optimal screening interval, ages for starting and stopping screening, and consideration of enhancements to conventional cytology, such as human papillomavirus (HPV)-DNA testing as a triage for equivocal results or as a primary screening test for women over the age of 30. Analyses in resource-poor settings with infrequent or no screening have focused on strategies that enhance the linkage between screening and treatment, consider noncytologic alternatives such as HPV-DNA testing, and target women between the ages of 35 and 45 for screening one, two, or three times per lifetime. Despite differences in methods and assumptions, this paper identifies the qualitative themes that are consistent among studies, and highlights important methodological challenges and high-priority areas for further work.Vaccine 09/2006; 24 Suppl 3:S3/164-70. · 3.77 Impact Factor
Data provided are for informational purposes only. Although carefully collected, accuracy cannot be guaranteed.
The impact factor represents a rough estimation of the journal's impact factor and does not reflect the actual
current impact factor.
Publisher conditions are provided by RoMEO. Differing provisions from the publisher's actual policy or licence
agreement may be applicable.
Keywords
3+ consecutive prior normal Program tests
Annual cervical cancer screening
annual screening
biennial screening
biopsy-proven cervical neoplasia
Cervical Cancer
Disease Control
estimate cost
final Program Pap test
incremental cost-effectiveness ratios
limited evidence
Prevention National Breast
prior normal Pap tests
prior normal Program tests
prior normal tests
prior tests
quality-adjusted life-year
same-aged women
screening women
validated cost-effectiveness model