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. Author manuscript; available in PMC: 2015 Jul 9.
Published in final edited form as: Front Public Health Serv Syst Res. 2015;4(4):45–50. doi: 10.13023/FPHSSR.0403.02

A Cost Analysis of the 1-2-3 Pap Intervention

Kristina M Rabarison 1, Rui Li 2, Connie L Bish 3, Robin C Vanderpool 4, Richard A Crosby 5, Mehran S Massoudi 6
PMCID: PMC4497949  NIHMSID: NIHMS704693  PMID: 26167424

Abstract

Background

Cervical cancer places a substantial economic burden on our healthcare system. The three-dose human papillomavirus (HPV) vaccine series is a cost-effective intervention to prevent HPV infection and resultant cervical cancer. Despite its efficacy, completion rates are low in young women aged 18 through 26 years. 1-2-3 Pap is a video intervention tested and proven to increase HPV vaccination completion rates.

Purpose

To provide the full scope of available evidence for 1-2-3 Pap, this study adds economic evidence to the intervention's efficacy. This study tested the economies of scale hypothesis that the cost of 1-2-3 Pap intervention per number of completed HPV vaccine series would decrease when offered to more women in the target population.

Methods

Using cost and efficacy data from the Rural Cancer Prevention Center, a cost analysis was done through a hypothetical adaptation scenario in rural Kentucky.

Results

Assuming the same success rate as in the efficacy study, the 1-2-3 Pap adaptation scenario would cover 1000 additional women aged 18 through 26 years (344 in efficacy study; 1346 in adaptation scenario), and almost three times as many completed series (130 in efficacy study; 412 in adaptation scenario) as in the original 1-2-3 Pap efficacy study.

Implications

Determination of the costs of implementing 1-2-3 Pap is vital for program expansion. This study provides practitioners and decision makers with objective measures for scalability.

Keywords: HPV vaccine, cervical cancer, prevention research center, cost analysis, economic evaluation


Cervical cancer, 91% of which is attributable to human papillomavirus (HPV), places a substantial economic burden on our healthcare system.1,2 Estimated direct medical care costs for HPV-associated diseases (e.g., cervical cancer screening and treatment) are $8 billion annually (2010 USD).1 The three-dose HPV vaccine series through age 26 years is a cost-effective intervention to prevent HPV infection and resultant cervical cancer.3 Despite its effectiveness, completion rates are low in women aged 18 through 26 years, especially for those living in underserved areas such as Appalachian Kentucky.4,5 Improving HPV vaccine completion rates, defined as the rate of receiving the third dose, is important and women aged 18 through 26 years are an identified target population.4,5 1-2-3 Pap is a video-based intervention created and tested by the Rural Cancer Prevention Center (RCPC) to increase HPV vaccination completion rates among women aged 18 through 26 years, residing in the eight-county Kentucky River Area Development District (KRADD) who already received the first dose.5

Determining the cost of implementing 1-2-3 Pap is vital for program expansion. This study tested the economies-of-scale hypothesis that the cost of 1-2-3 Pap intervention per number of completed HPV vaccine series would decrease when offered to more women in the KRADD.

METHODS

The 1-2-3 Pap efficacy study, which has been described elsewhere,5 was composed of 344 women who received the first dose of the HPV vaccine series (initiation dose). Results showed that women who watched the video were 2.44 more likely to complete the HPV vaccine series than those who did not.5

To test the intervention's scalability, a cost analysis was conducted using expenditure reports from the RCPC. Subsequently, cost changes were assessed for 1-2-3 Pap through a hypothetical adaptation scenario within the KRADD. Institutional review board approval was not needed because data were obtained from federal reporting documents used to monitor the Centers for Disease Control Prevention Research Centers program. Costs included in the study were for resources used to recruit the original 1-2-3 Pap efficacy study participants, to create and disseminate the video, and to administer HPV vaccine doses.

The adaptation scenario sample size was estimated by multiplying the number of women aged 18 through 26 years in the KRADD (N = 5930; 2010 U.S. Decennial Census) with the national HPV vaccination initiation rate (22.7%).4 This resulted in an estimated 1346 women who would watch the video when receiving the first dose. During the efficacy study, the adherence (Dose 2) and completion (Dose 3) rates among those who watched the 1-2-3 Pap video were 61.2% and 43.3%, respectively.5 Specific adherence and completion rates for rural Kentucky are not available. Therefore, for the adaptation scenario, the national adherence and completion rates were used for women aged 18 through 26 years (17.6% and 12.7%, respectively).4 Assuming that the intervention is as effective in the adaptation scenario as it was in the efficacy study, the adherence (43.6%) and completion (30.6%) rate differences between the 1-2-3 Pap efficacy study and the national rates were used to estimate the adaptation scenario uptake rates.4,5

Perspectives

Costs were estimated from a provider perspective, which includes only the direct costs.

Time Frame and Analytic Horizon

A 28-month time frame and analytic horizon were assumed, which was the length of the 1-2-3 Pap efficacy study (September 2010–December 2012).5

Direct Costs

Direct costs included 1-2-3 Pap efficacy study participant incentives, video creation and dissemination, and clinical costs associated with administering HPV vaccine doses. The video creation costs included script development, studio time, editing, production services, and local talent fees for six actors.5 The intervention was disseminated via laptop computers and administered by a community health nurse who conducted participant intake interviews during the 1-2-3 Pap efficacy study.5 The clinical costs included vaccine doses two and three, and office visits. The cost of initial doses was excluded because it was a requirement for inclusion in the 1-2-3 Pap program.5 Office visit costs were estimated using the percentage of Kentucky adults with private and Medicaid insurance coverage, the Medicaid physician fee for outpatient services in Kentucky, and the Medicaid-to-private-health-insurance conversion rate (Appendix).

In the adaptation scenario, laptop costs and community health nurse time were excluded because the video would be shared and recommended to women while receiving their initial HPV vaccine dose. Further, the video is available on YouTube, making it easy to share via other social media platforms such as Facebook.

Total Cost

From a provider perspective, the total 1-2-3 Pap efficacy study cost was calculated as the sum of the direct cost. The total 1-2-3 Pap adaptation cost would only include the clinical costs. Total cost per series completed was estimated. Sensitivity analysis was used to estimate the costs if the intervention would be 75% and 50% as effective in adaptation scenario compared to the efficacy study.

RESULTS

The adaptation scenario population had 5930 eligible women aged 18 through 26 years. Among these, assuming the same effectiveness as in the efficacy study, the estimated doses administered were: 1346 initial, 587 adherence, and 412 completion doses.

1-2-3 Pap Efficacy Study Cost

The total 1-2-3 Pap efficacy study cost was $115,655.00 or $890 per series completed (n=130). Table 1.

Table 1.

1-2-3 Pap efficacy study costs per number of 3-dose HPV vaccine series completion, among women aged 18–26 years who watched the video, in rural Kentucky

Cost/Unit ($) (A) N of Units (B) Total Cost ($) (C = A × B)
Trial Participant Incentives
    Gift Cards 26 344 Cards 8,944
    Food - Used to Recruit Participants 5 350 Servings 1,750
Video Creation
    Studio, Editing, and Production Services 27,428 1 Production 27,428
    Local Talent Fees 67 6 Actors 402
Video Dissemination
    Community Health Nurse 48 211 Nurses 10,128
    Laptops (1/4 value) 278 4 Laptops 1,112
Clinical
    Adherence Dose (Dose 2) 137 229 Doses 31,373
    Completion Dose (Dose 3) 137 130 Doses 17,810
    Office Visit - Medicaid 39 122 Visits 4,760
    Office Visit - Private Insurance 52 230 Visits 11,948

Total Intervention Cost 115,655
Intervention Cost per Completed Series 890

1-2-3 Pap Adaptation Cost

The estimated total cost of the adaptation scenario was $160,280, or $389 per series completed (n = 412). Table 2.

Table 2.

Hypothetical adaptation costs per number of 3-dose HPV vaccine series completion, among women aged 18–26 years who watched the video, in rural Kentucky

Estimated Adaptation Cost (N = 1346)
100% Effective a 75% Effective b 50% Effective c
Cost/Unit ($) (A) N of Units (B) Total Cost ($) (C = A × B) N of Units (B) Total Cost ($) (C = A × B) N of Units (B) Total Cost ($) (C = A × B)
Clinical
Adherence Dose (Dose 2) 137 587 80,419 381 52,186 175 23,972
Completion Dose (Dose 3) 137 412 56,444 267 36,512 121 16,596
Office Visit: Medicaid 20 340 6,793 220 4,402 101 2,014
Office Visit: Private Insurance 26 639 16,623 414 10,773 190 4,927
Total Intervention Cost 160,280 103,873 47,509
Intervention Cost per Completed Series 389 390 392
a

Total cost, assuming the adaptation is 100% as effective as the efficacy study

b

Total cost, assuming the adaptation is 75% as effective as the efficacy study

c

Total cost, assuming the adaptation is 50% as effective as the efficacy study

IMPLICATIONS

This analysis provides practitioners and decision makers with objective measures of the costs of implementing 1-2-3 Pap in a larger population. The results supported the hypothesis that 1-2-3 Pap implementation cost would decrease as it is offered to more people. Assuming the same success rate as in the efficacy study, the adaptation scenario would cover 1000 additional women aged 18 through 26 years (344 in efficacy study; 1346 in adaptation scenario), and almost three times as many completed series (130 in efficacy study; 412 in adaptation scenario) as in the original 1-2-3 Pap efficacy study. 1-2-3 Pap's total cost would decrease from $890 to $389 per women completing three doses. Considering that the annual cost of cervical cancer screening and treatment ranges from $30,775 to $52,731 per case (2010 USD),1 the estimated $890 investment per completed series might be worthwhile. Findings likely translate to other rural areas, because local actors and community members were used in the video to ensure cultural relevancies.

The next analytical steps are implementation cost estimations for a large urban county and the state of Kentucky, and a cost-effectiveness analysis (CEA). The CEA will provide insight into implementation costs and benefits such as healthcare costs avoided from preventing cervical cancer. The 1-2-3 Pap efficacy study showed that women who watched the video were 2.44 times more likely to complete the series than those who did not. However, initiation rates remain low among this target population, and increased initiation remains a priority.4,5

Summary Box.

What is already known about this topic? The 1-2-3 Pap intervention is an informational and instructional video created and tested to increase HPV vaccination completion rates among women aged 18 through 26 years residing in Appalachian Kentucky who had already received an initiation dose. Women randomized to watch the 1-2-3 Pap video in addition to the standard of care (an educational pamphlet and telephone reminder calls for doses 2 and 3) were 2.44 times more likely to complete the HPV vaccine series than those in the standard-of-care-only group.

What is added by this report? Intervention estimated costs are critical to understanding the full scope of available evidence. This study adds economic evidence of the effectiveness of the 1-2-3 Pap video.

What are the implications for public health practice, policy, and research? Determination of the costs of implementing 1-2-3 Pap is vital for program expansion. This study provides practitioners and decision makers with objective measures for scalability. The results supported the hypothesis that 1-2-3 Pap implementation cost would decrease as it is offered to more people. Findings likely translate to other rural areas, because local actors and community members were used in the video to ensure cultural relevancies.

APPENDIX

APPENDIX

Items Data Sources
Studio, editing, and production services University of Kentucky Rural Cancer Prevention Center
Local talent fees University of Kentucky Rural Cancer Prevention Center
Laptop University of Kentucky Rural Cancer Prevention Center purchased four laptop computers for the efficacy study. Only a fourth of the value was applied to the intervention implementation cost estimation, based on the assumption that the laptops were used for other efficacy study related activities.
Community health nurse University of Kentucky Rural Cancer Prevention Center
HPV vaccine dose cost CDC's HPV Vaccine Information for Young Women (fact sheet) (http://www.cdc.gov/std/hpv/stdfact-hpv-vaccine-young-women.htm)
Office visit, Medicaid Estimated using the outpatient Medicaid reimbursement physician fee in Kentucky - $39 per visit (http://www.chfs.ky.gov/dms/fee.htm)
Office visit, private insurance Estimated using the average private insurance coverage (64%) and Medicaid rates (34%) for Kentucky (http://kff.org/other/state-indicator/adults-19-64/) and the Medicaid to private insurance coverage rate (Private insurance coverage = 0.75 * Medicaid rate) (Ku L. Medical and dental care utilization and expenditures under Medicaid and private health insurance, 2009 [http://mcr.sagepub.com/content/66/4/456.refs])

Footnotes

Recommended Citation

Rabarison KM, Li R, Bish CL, Vanderpool RC, Crosby RA, Massoudi MS. A cost analysis of the 1-2-3 Pap intervention. Front Public Health Serv Sys Res 2015; 4(3):45–50. DOI: 10.13023/FPHSSR.0403.02.

Disclaimer: The findings and conclusions in this paper are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention. Acknowledgments and Disclosures: Centers for Disease Control and Prevention (Kristina M. Rabarison, Rui Li, Connie L. Bish, and Mehran S. Massoudi) do not have any funding sources to report. The authors from the Rural Cancer Prevention Center at the University of Kentucky (Robin C. Vanderpool and Richard A. Crosby) conducted the 1-2-3 Pap efficacy study as part of a project funded by the CDC Prevention Research Centers Program. The authors wish to acknowledge Elisa L. Cohen, Tom Collins, Alicia Heim, Pamela Lilleston, and Margaret McGladrey for abstracting data, reviewing, and commenting on earlier versions of this article.

Contributor Information

Kristina M. Rabarison, Centers for Disease Control and Prevention, krabarison@cdc.gov

Rui Li, Division of Diabetes Translation, Centers for Disease Control and Prevention, RuiLi@cdc.gov.

Connie L. Bish, Division of Population Health, Centers for Disease Control and Prevention, aez2@cdc.gov

Robin C. Vanderpool, University of Kentucky, robin@kcr.uky.edu

Richard A. Crosby, University of Kentucky, richard.crosby@uky.edu

Mehran S. Massoudi, Division of Population Health, Centers for Disease Control and Prevention, mrm8@cdc.gov

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