Screening for Chlamydia trachomatis in Women 15 to 29 Years of Age: A Cost-Effectiveness Analysis

  1. Delphine Hu, MD, MPH;
  2. Edward W. Hook III, MD; and
  3. Sue J. Goldie, MD, MPH
  1. From Harvard School of Public Health, Boston, Massachusetts, and University of Alabama at Birmingham, Birmingham, Alabama.

    Abstract

    Background: Clinical guidelines have traditionally advised annual Chlamydia trachomatis screening for women younger than 25 years of age.

    Objective: To assess the cost-effectiveness of recently proposed strategies for chlamydia screening.

    Design: State transition simulation model; cost-effectiveness analysis.

    Data Sources: Published literature.

    Target Population: Sexually active U.S. women 15 to 29 years of age.

    Time Horizon: Lifetime.

    Perspective: Modified societal.

    Interventions: Four strategies targeted to 3 specific age groups (15 to 19 years, 15 to 24 years, and 15 to 29 years): 1) no screening, 2) annual screening for all women, 3) annual screening followed by 1 repeated test within 3 to 6 months after a positive test result, and 4) annual screening followed by selective semiannual screening for women with a history of infection.

    Outcome Measures: Clinical events (for example, pelvic inflammatory disease, chronic pelvic pain, ectopic pregnancy, and infertility), lifetime costs, quality-adjusted life expectancy, and incremental cost-effectiveness ratios.

    Results of Base-Case Analysis: Annual screening in women 15 to 29 years of age followed by semiannual screening for those with a history of infection was the most effective and cost-effective strategy. It consistently had an incremental cost-effectiveness ratio less than $25 000 per quality-adjusted life-year (QALY) compared with the next most effective strategy. When the indirect transmission effects of a 10-year screening program on the probability of infection in uninfected women (that is, per-susceptible rate of infection) were considered, all strategies became more cost-effective.

    Results of Sensitivity Analysis: Results were sensitive to the annual incidence of chlamydia, probability of persistent infection, screening test costs, and costs of treating long-term complications. Each variable was associated with threshold values beyond which screening became cost-saving. In probabilistic analysis, annual screening in women 15 to 29 years of age followed by semiannual screening for those with a history of infection had an incremental cost-effectiveness ratio less than $50 000 per QALY in 99% of simulations.

    Limitations: Uncertainty about the natural history of chlamydial infection and consideration of only the indirect transmission effects of C. trachomatis screening.

    Conclusions: Annual C. trachomatis screening for all women 15 to 29 years of age and selective targeting of those with a history of infection for semiannual screening is very cost-effective compared with other well-accepted clinical interventions.

    Article and Author Information

    • Acknowledgments: The authors thank Karen Kuntz for guidance on probabilistic sensitivity analysis and Steven Sweet for technical advice and help with manuscript preparation.

    • Grant Support: By Agency for Healthcare Research and Policy Fellowship Award (Dr. Hu).

    • Potential Financial Conflicts of Interest:Consultancies: E.W. Hook (Abbott Laboratories, Gen-Probe); Honoraria: E.W. Hook (Abbott Laboratories, Gen-Probe); Other: E.W. Hook (Abbott Laboratories; Roche Molecular Systems, Inc.; Gen-Probe; Becton, Dickinson, and Co).

    • Requests for Single Reprints: Sue J. Goldie, MD, MPH, Department of Health Policy and Management, Harvard School of Public Health, 718 Huntington Avenue, 2nd Floor, Boston, MA 02115-5924.

    • Current Author Addresses: Drs. Hu and Goldie: Department of Health Policy and Management, Harvard School of Public Health, 718 Huntington Avenue, 2nd Floor, Boston, MA 02115-5924.

    • Dr. Hook: Department of Medicine, University of Alabama at Birmingham, 703 19th Street South ZRB 242, Birmingham, AL 35294-0007.

    • Author Contributions: Conception and design: D. Hu, S.J. Goldie.

    • Analysis and interpretation of the data: D. Hu, E.W. Hook, S.J. Goldie.

    • Drafting of the article: D. Hu, S.J. Goldie.

    • Critical revision of the article for important intellectual content: D. Hu, E.W. Hook, S.J. Goldie.

    • Final approval of the article: D. Hu, E.W. Hook, S.J. Goldie.

    • Statistical expertise: S.J. Goldie.

    • Administrative, technical, or logistic support: S.J. Goldie.

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