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New Vaccine Development: Establishing Priorities: Volume I, Diseases of Importance in the United States (1985)
Board on Population Health and Public Health Practice (BPH)

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. "9. Findings, Conclusions, and Recommendations." New Vaccine Development: Establishing Priorities: Volume I, Diseases of Importance in the United States. Washington, DC: The National Academies Press, 1985.

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New Vaccine Development Establishing Priorities, Volume I: Diseases of Importance in the United States
  1. The mixed public-private vaccination program described in Chapter 7.

  2. Times to licensure and adoption, and delay of vaccination benefits presented in Chapter 7.

  3. Calculations of health benefits and costs as described in Chapters 4 and 7, and Appendixes C through P (including calculation of the incremental benefits from new influenza vaccines and the benefits of an improved pertussis vaccine, i.e., the elimination of current adverse effects).

  4. Use of a 5 percent discount rate for future health benefits and costs.

  5. Adoption, for illustrative purposes only, of the committee median perspective on the undesirability of various morbidity conditions and mortality.

  6. Consideration of the development of each vaccine candidate (for each target population) as an independent project.

  7. Expression of health benefits in units considered equivalent in undesirability to the death of an infant (i.e., infant mortality equivalents, IMEs) (see Chapter 4).

Findings

The results of the central analysis, using the committee median perspective (Chapter 7 and Tables 9.1 and 9.2), have been interpreted for a hypothetical situation in which five vaccines are to be selected for highest priority (with no more than one vaccine per disease/target population combination).

First, we rule out vaccines that are dominated in both benefits and costs by another vaccine against the same disease (Table 9.2, columns 1 and 3). Thus, the RSV glycoprotein vaccine is dominated by the RSV attenuated live virus (ALV) vaccine; the hepatitis A subunit vaccine is dominated by the hepatitis A ALV vaccine; and the human rotavirus ALV vaccine is dominated by the bovine rotavirus ALV vaccine.

Table 9.3 displays the patterns of dominance between the remaining 19 vaccine candidates. Procedures described in Chapter 3 are used to select the desired number of candidates.

Thus, of the remaining 19 vaccines, we can as a second step rule out those that are dominated by at least five other vaccines (see Table 9.3). On this basis, we eliminate from consideration: CMV (all target populations); herpes simplex (all vaccines); B. pertussis; N. gonorrhoeae; hepatitis A; rotavirus (bovine ALV); and Coccidioides immitis.

These two steps leave the following nine vaccines (eight diseases) in contention for the top five positions: hepatitis B; RSV (ALV); Hemophilus influenzae type b; influenza (subunit or ALV); Herpesvirus varicellae (for high-risk individuals); Herpesvirus varicellae (for normals and children); streptococcus group B; parainfluenza viruses. RSV dominates six others, so it must be among the top five, regardless of the weight given to benefits and costs.

The selection of the remaining four vaccines depends on the relative weight of health benefits versus costs. In particular, if the

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Front Matter (R1-R14)
1. Summary (1-16)
2. Priority Setting for Health Related Investments: A Review of Methods (17-27)
3. Overview of the Analytic Approach (28-38)
4. Comparison of Disease Burdens and Costs (39-58)
5. Predictions on Vaccine Development (59-66)
6. Assessing the Likely Utilization of New Vaccines (67-91)
7. Calculation and Comparison of the Health Benefits and Costs Associated with Candidate Vaccines (92-120)
8. Additional Issues in the Selection of Priorities for Accelerated Vaccine Development (121-126)
9. Findings, Conclusions, and Recommendations (127-148)
Appendix A: Some Examples of the Application of Project Selection Method (149-152)
Appendix B: Pathogenic Agents for Which Accelerated Vaccine Development Does Not Appear Appropriate (153-170)
Appendix C: Prospects for Immunizing Against Bordetella pertussis (171-182)
Appendix D: Prospects for Immunizing Against Coccidioidomycosis (183-197)
Appendix E: Prospects for Immunizing Against Cytomegalovirus (198-234)
Appendix F: Prospects for Immunizing Against Hemophilus influenzae type b (235-251)
Appendix G: Prospects for Immunizing Against Hepatitis A Virus (252-260)
Appendix H: Prospects for Immunizing Against Hepatitis B Virus (261-279)
Appendix I: Prospects for Immunizing Against Herpes Simplex Viruses 1 and 2 (280-312)
Appendix J: Prospects for Immunizing Against Herpesvirus varicellae (313-341)
Appendix K: Prospects for Immunizing Against Influenza Viruses A and B (342-364)
Appendix L: Prospects for Immunizing Against Neisseria gonorrhoeae (365-384)
Appendix M: Prospects for Immunizing Against Parainfluenza Viruses (385-396)
Appendix N: Prospects for Immunizing Against Respiratory Syncytial Virus (397-409)
Appendix O: Prospects for Immunizing Against Rotavirus (410-423)
Appendix P: Prospects for Immunizing Against Streptococcus group B (424-439)
Appendix Q: Questionnaire for Assessing Morbidity-Mortality Trade-Offs (440-443)
Appendix R: Technical Notes (444-444)
Appendix S: Biographical Notes on Committee Members (445-449)
Appendix T: Additional Sources of Advice to the Committee (450-452)
Index (453-458)