Estimating the future global dose demand for measles-rubella microarray patches.


Journal

Frontiers in public health
ISSN: 2296-2565
Titre abrégé: Front Public Health
Pays: Switzerland
ID NLM: 101616579

Informations de publication

Date de publication:
2022
Historique:
received: 05 09 2022
accepted: 26 12 2022
entrez: 2 2 2023
pubmed: 3 2 2023
medline: 4 2 2023
Statut: epublish

Résumé

Progress toward measles and rubella (MR) elimination has stagnated as countries are unable to reach the required 95% vaccine coverage. Microarray patches (MAPs) are anticipated to offer significant programmatic advantages to needle and syringe (N/S) presentation and increase MR vaccination coverage. A demand forecast analysis of the programmatic doses required (PDR) could accelerate MR-MAP development by informing the size and return of the investment required to manufacture MAPs. Unconstrained global MR-MAP demand for 2030-2040 was estimated for three scenarios, for groups of countries with similar characteristics (archetypes), and four types of uses of MR-MAPs (use cases). The base scenario 1 assumed that MR-MAPs would replace a share of MR doses delivered by N/S, and that MAPs can reach a proportion of previously unimmunised populations. Scenario 2 assumed that MR-MAPs would be piloted in selected countries in each region of the World Health Organization (WHO); and scenario 3 explored introduction of MR-MAPs earlier in countries with the lowest measles vaccine coverage and highest MR disease burden. We conducted sensitivity analyses to measure the impact of data uncertainty. For the base scenario (1), the estimated global PDR for MR-MAPs was forecasted at 30 million doses in 2030 and increased to 220 million doses by 2040. Compared to scenario 1, scenario 2 resulted in an overall decrease in PDR of 18%, and scenario 3 resulted in a 21% increase in PDR between 2030 and 2040. Sensitivity analyses revealed that assumptions around the anticipated reach or coverage of MR-MAPs, particularly in the hard-to-reach and MOV populations, and the market penetration of MR-MAPs significantly impacted the estimated PDR. Significant demand is expected for MR-MAPs between 2030 and 2040, however, efforts are required to address remaining data quality, uncertainties and gaps that underpin the assumptions in this analysis.

Sections du résumé

Background
Progress toward measles and rubella (MR) elimination has stagnated as countries are unable to reach the required 95% vaccine coverage. Microarray patches (MAPs) are anticipated to offer significant programmatic advantages to needle and syringe (N/S) presentation and increase MR vaccination coverage. A demand forecast analysis of the programmatic doses required (PDR) could accelerate MR-MAP development by informing the size and return of the investment required to manufacture MAPs.
Methods
Unconstrained global MR-MAP demand for 2030-2040 was estimated for three scenarios, for groups of countries with similar characteristics (archetypes), and four types of uses of MR-MAPs (use cases). The base scenario 1 assumed that MR-MAPs would replace a share of MR doses delivered by N/S, and that MAPs can reach a proportion of previously unimmunised populations. Scenario 2 assumed that MR-MAPs would be piloted in selected countries in each region of the World Health Organization (WHO); and scenario 3 explored introduction of MR-MAPs earlier in countries with the lowest measles vaccine coverage and highest MR disease burden. We conducted sensitivity analyses to measure the impact of data uncertainty.
Results
For the base scenario (1), the estimated global PDR for MR-MAPs was forecasted at 30 million doses in 2030 and increased to 220 million doses by 2040. Compared to scenario 1, scenario 2 resulted in an overall decrease in PDR of 18%, and scenario 3 resulted in a 21% increase in PDR between 2030 and 2040. Sensitivity analyses revealed that assumptions around the anticipated reach or coverage of MR-MAPs, particularly in the hard-to-reach and MOV populations, and the market penetration of MR-MAPs significantly impacted the estimated PDR.
Conclusions
Significant demand is expected for MR-MAPs between 2030 and 2040, however, efforts are required to address remaining data quality, uncertainties and gaps that underpin the assumptions in this analysis.

Identifiants

pubmed: 36726626
doi: 10.3389/fpubh.2022.1037157
pmc: PMC9885039
doi:

Substances chimiques

Rubella Vaccine 0
Measles Vaccine 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1037157

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

Copyright © 2023 Ko, Malvolti, Cherian, Mantel, Biellik, Jarrahian, Menozzi-Arnaud, Amorij, Christiansen, Papania, Meltzer, Masresha, Pastor, Durrheim, Giersing and Hasso-Agopsowicz.

Déclaration de conflit d'intérêts

MK, SM, TC, and CM are employed by MMGH Consulting GmbH. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Nat Med. 2021 Mar;27(3):360-361
pubmed: 33589823
Front Public Health. 2022 Mar 02;10:809675
pubmed: 35309224
Wkly Epidemiol Rec. ;92(17):205-27
pubmed: 28459148
Vaccine. 2016 Feb 3;34(6):723-34
pubmed: 26706274
Vaccine. 2017 Dec 4;35(48 Pt B):6676-6684
pubmed: 29074201
Vaccine. 2022 Apr 20;40(18):2525-2527
pubmed: 35341648
MMWR Morb Mortal Wkly Rep. 2021 Nov 12;70(45):1563-1569
pubmed: 34758014

Auteurs

Melissa Ko (M)

MMGH Consulting GmbH, Geneva, Switzerland.

Stefano Malvolti (S)

MMGH Consulting GmbH, Zurich, Switzerland.

Thomas Cherian (T)

MMGH Consulting GmbH, Geneva, Switzerland.

Carsten Mantel (C)

MMGH Consulting GmbH, Zurich, Switzerland.

Robin Biellik (R)

Independent Consultant, La Rippe, Switzerland.

Courtney Jarrahian (C)

PATH, Seattle, WA, United States.

Marion Menozzi-Arnaud (M)

Gavi, The Vaccine Alliance, Geneva, Switzerland.

Jean-Pierre Amorij (JP)

Supply Division, Vaccine Centre, UNICEF, Copenhagen, Denmark.

Hans Christiansen (H)

Supply Division, Vaccine Centre, UNICEF, Copenhagen, Denmark.

Mark J Papania (MJ)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Martin I Meltzer (MI)

Division of Preparedness and Emerging Infections, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Balcha Girma Masresha (BG)

Vaccine Preventable Diseases, World Health Organization Regional Office for Africa (AFRO/WHO), Harare, Zimbabwe.

Desiree Pastor (D)

Immunization Unit, Pan American Health Organization (PAHO), Washington, DC, United States.

David N Durrheim (DN)

Medicine and Public Health, University of Newcastle, Callaghan, NSW, Australia.

Birgitte Giersing (B)

Immunization, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.

Mateusz Hasso-Agopsowicz (M)

Immunization, Vaccines and Biologicals, World Health Organization, Geneva, Switzerland.

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