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New Vaccine Development: Establishing Priorities: Volume II, Diseases of Importance in Developing Countries (1986)
Board on Population Health and Public Health Practice (BPH)

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. "7. Calculation and Comparison of the Health Benefits and Differential Costs Associated with Candidate Vaccines." New Vaccine Development: Establishing Priorities: Volume II, Diseases of Importance in Developing Countries. Washington, DC: The National Academies Press, 1986.

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New Vaccine Development: Establishing Priorities, Volume II, Diseases of Importance in Developing Countries

in children 2 years of age or older, but not in infants. It could be argued that the health benefits of an improved pneumococcal vaccine are simply the incremental benefit that could be obtained from extending protection to the child population under 2 years of age who would respond to the conjugated improved vaccine. However, a more reasonable assumption is that the current vaccine would not be used in the developing world for the reason stated above and because the delivery requirement (children 2 years and older) could not conveniently be added to existing vaccination schedules. Additionally, it is doubtful the existing vaccine would be used if the improved version becomes available. Hence, the potential benefits of an improved vaccine are calculated using the entire existing disease burden as a starting point. The proportion of the TDBV that is vaccine preventable is discussed in Appendix D-17.

This analysis does not include calculation of the potential benefits of improving any vaccine that is in widespread use in the developing world. For such calculations it is necessary to estimate the incremental benefits (e.g., in efficacy, disease proportion amenable to vaccine prevention by virtue of effectiveness at younger ages, etc.) or costs associated with its use as compared to the existing vaccine. The analyses of potential benefits for improved influenza and pertussis vaccines presented in the committee’s first report illustrate the approach needed in such calculations (Institute of Medicine, 1985).

RESULTS

The results of the central analysis, presented below, are based on the following assumptions:

  • the probability of successful development and other vaccine characteristics, e.g., efficacy, described in Chapter 5

  • the times to licensure and adoption, and the delay of vaccination benefits, as shown in Tables 5.1 and 7.2

  • a discount rate of 0.05

  • the IME perspective representing the median of values derived from public health professionals in various developing countries (as described in Chapter 4)

  • the uniformity of utilization rates across target populations (Chapter 6)

Health Benefits

Table 7.4 shows values representing the possible health benefits resulting from the development of each vaccine candidate. Total disease burden values represent the burden of illness resulting from the pathogen(s) against which the vaccine is directed.

Vaccine preventable illness values represent the burden of illness that could be averted by delivering a hypothetical vaccine that is 100

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Front Matter (R1-R16)
1. Summary (1-18)
2. Priority Setting for Health-Related Investments: A Review of Methods (19-29)
3. Overview of the Analytic Approach (30-43)
4. Comparison of Disease Burdens (44-62)
5. Predictions of Vaccine Development (63-75)
6. Assessing the Likely Utilization of New Vaccines (76-81)
7. Calculation and Comparison of the Health Benefits and Differential Costs Associated with Candidate Vaccines (82-105)
8. Additional Issues in the Selection of Priorities for Accelerated Vaccine Development (106-120)
9. Findings, Conclusions, and Recommendations (121-142)
Appendix A: Selection of Vaccine Candidates for Accelerated Development (143-148)
Appendix B: The Burden of Disease Resulting from Acute Respiratory Illness (149-158)
Appendix C: The Burden of Disease Resulting from Diarrhea (159-169)
Appendix D-1: The Prospects for Immunizing Against Dengue Virus (170-177)
Appendix D-2: The Prospects for Immunizing Against Escherichia coli (178-185)
Appendix D-3: The Prospects for Immunizing Against Hemophilus influenzae Type b (186-196)
Appendix D-4: The Prospects for Immunizing Against Hepatitis A Virus (197-207)
Appendix D-5: The Prospects for Immunizing Against Hepatitis B Virus (208-222)
Appendix D-6: The Prospects for Immunizing Against Japanese Encephalitis Virus (223-240)
Appendix D-7: The Prospects for Immunizing Against Mycobacterium leprae (241-250)
Appendix D-8: The Prospects for Immunizing Against Neisseria meningitidis (251-266)
Appendix D-9: The Prospects for Immunizing Against Parainfluenza Viruses (267-274)
Appendix D-10: The Prospects for Immunizing Against Plasmodium spp. (275-286)
Appendix D-11: The Prospects for Immunizing Against Rabies Virus (287-298)
Appendix D-12: The Prospects for Immunizing Against Respiratory Syncytial Virus (299-307)
Appendix D-13: The Prospects for Immunizing Against Rotavirus (308-318)
Appendix D-14: The Prospects for Immunizing Against Salmonella typhi (319-328)
Appendix D-15: The Prospects for Immunizing Against Shigella spp. (329-337)
Appendix D-16: The Prospects for Immunizing Against Streptococcus Group A (338-356)
Appendix D-17: The Prospects for Immunizing Against Streptococcus pneumoniae (357-375)
Appendix D-18: The Prospects for Immunizing Against Vibrio cholerae (376-389)
Appendix D-19: The Prospects for Immunizing Against Yellow Fever (390-402)
Appendix E: Questionnaire for Assessing Morbidity-Mortality Trade-Offs (403-411)
Appendix F: Technical Notes (412-412)
Appendix G: Biographical Notes on Committee Members (413-417)
Appendix H: Additional Sources of Advice to the Committee (418-419)
Appendix I: Contents of Supplement to Volume II (420-420)
Appendix J: Preface to Volume I (421-422)
Appendix K: Contents to Volume I (423-423)
Index (424-432)