Budgetary Impact of 20-Valent Pneumococcal Conjugate Vaccine Use for Adult Expatriates Living in Dubai.
Budgetary impact
Immunization
Public health
Streptococcus pneumoniae
Vaccination
Journal
Current therapeutic research, clinical and experimental
ISSN: 0011-393X
Titre abrégé: Curr Ther Res Clin Exp
Pays: United States
ID NLM: 0372621
Informations de publication
Date de publication:
2023
2023
Historique:
received:
28
11
2022
accepted:
06
03
2023
medline:
25
4
2023
pubmed:
25
4
2023
entrez:
25
04
2023
Statut:
epublish
Résumé
Dubai Health Authority currently recommends sequential administration of 13-valent pneumococcal conjugate vaccine (PCV13) followed by (→) 23-valent pneumococcal polysaccharide vaccine (PPV23) to prevent pneumococcal disease among adults at elevated risk of illness. Despite recommendations, disease burden and associated costs remain substantial. A new 20-valent pneumococcal conjugate vaccine (PCV20) recently received regulatory approval in the United Arab Emirates and has the potential to further reduce burden of pneumococcal disease. To evaluate budget impact of use of novel PCV20 compared with current recommendations (ie, PCV13→PPV23) among expatriates in Dubai aged 50 to 99 years and those aged 19 to 49 years with risk factors. A deterministic model depicted 5-year risks and costs of invasive pneumococcal disease and all-cause nonbacteremic pneumonia. Each year of the modeling horizon, persons could be vaccinated with either PCV20 or PCV13→PPV23 or remain unvaccinated; persons vaccinated during the modeling horizon were not eligible for vaccination in subsequent years. Annual vaccine uptake was assumed to be 5% in base cases analyses; higher uptake was considered in scenario analyses. Costs were discounted at 3.5% annually and reported in US dollars. In base case, use of PCV20 alone would prevent an additional 13 cases of invasive pneumococcal disease, 31 cases of inpatient all-cause nonbacteremic pneumonia, 139 cases of outpatient all-cause nonbacteremic pneumonia, and 5 disease-related deaths compared with PCV13→PPV23. Medical care costs would be reduced by $354,000, and total vaccination costs would decrease by $4.4 million. PCV20 would therefore yield net budgetary impact of -$4.8 million, resulting in savings of $2.47 per-person per-year over 5 years. In scenarios with higher vaccine uptake, PCV20 prevented more cases and deaths and yielded greater budget savings (vs PCV13→PPV23). PCV20 would reduce burden and economic costs of pneumococcal disease among expatriates in Dubai compared with PCV13→PPV23 and would therefore be budget saving for private health insurers who cover the majority of this population.
Sections du résumé
Background
UNASSIGNED
Dubai Health Authority currently recommends sequential administration of 13-valent pneumococcal conjugate vaccine (PCV13) followed by (→) 23-valent pneumococcal polysaccharide vaccine (PPV23) to prevent pneumococcal disease among adults at elevated risk of illness. Despite recommendations, disease burden and associated costs remain substantial. A new 20-valent pneumococcal conjugate vaccine (PCV20) recently received regulatory approval in the United Arab Emirates and has the potential to further reduce burden of pneumococcal disease.
Objectives
UNASSIGNED
To evaluate budget impact of use of novel PCV20 compared with current recommendations (ie, PCV13→PPV23) among expatriates in Dubai aged 50 to 99 years and those aged 19 to 49 years with risk factors.
Methods
UNASSIGNED
A deterministic model depicted 5-year risks and costs of invasive pneumococcal disease and all-cause nonbacteremic pneumonia. Each year of the modeling horizon, persons could be vaccinated with either PCV20 or PCV13→PPV23 or remain unvaccinated; persons vaccinated during the modeling horizon were not eligible for vaccination in subsequent years. Annual vaccine uptake was assumed to be 5% in base cases analyses; higher uptake was considered in scenario analyses. Costs were discounted at 3.5% annually and reported in US dollars.
Results
UNASSIGNED
In base case, use of PCV20 alone would prevent an additional 13 cases of invasive pneumococcal disease, 31 cases of inpatient all-cause nonbacteremic pneumonia, 139 cases of outpatient all-cause nonbacteremic pneumonia, and 5 disease-related deaths compared with PCV13→PPV23. Medical care costs would be reduced by $354,000, and total vaccination costs would decrease by $4.4 million. PCV20 would therefore yield net budgetary impact of -$4.8 million, resulting in savings of $2.47 per-person per-year over 5 years. In scenarios with higher vaccine uptake, PCV20 prevented more cases and deaths and yielded greater budget savings (vs PCV13→PPV23).
Conclusions
UNASSIGNED
PCV20 would reduce burden and economic costs of pneumococcal disease among expatriates in Dubai compared with PCV13→PPV23 and would therefore be budget saving for private health insurers who cover the majority of this population.
Identifiants
pubmed: 37096181
doi: 10.1016/j.curtheres.2023.100698
pii: S0011-393X(23)00008-5
pmc: PMC10121387
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100698Informations de copyright
© 2023 The Authors.
Déclaration de conflit d'intérêts
Pfizer Gulf FZ LLC provided funding to Policy Analysis Inc for the analysis and reporting of the results, and medical writing/editorial support for the development of the manuscript. Neither honoraria nor payments were made to co-authors for authorship. M. Zayed and J. Joury are employees of Pfizer and may hold stock or stock options. A. Averin and E. Kutrieb are employees of Policy Analysis Inc, which received financial support from Pfizer Gulf FZ LLC for this study (including manuscript preparation). The authors have indicated that they have no other conflicts of interest regarding the content of this article.
Références
Euro Surveill. 2008 Nov 20;13(47):
pubmed: 19021957
Proc Natl Acad Sci U S A. 2020 Dec 1;117(48):30547-30553
pubmed: 33168723
J Infect Dis. 2022 Aug 24;226(2):342-351
pubmed: 35481950
Clin Infect Dis. 2022 Aug 24;75(1):e1154-e1164
pubmed: 34904635
Nat Commun. 2022 May 24;13(1):2884
pubmed: 35610217
Emerg Infect Dis. 2002 Mar;8(3):278-82
pubmed: 11927025
MMWR Morb Mortal Wkly Rep. 2021 Jul 23;70(29):1013-1019
pubmed: 34292924
CMAJ. 2021 Jul 26;193(29):E1140-E1141
pubmed: 34312169
Lancet Digit Health. 2021 Jun;3(6):e360-e370
pubmed: 34045002
Int J Infect Dis. 2019 Aug;85:135-140
pubmed: 31150842
J Microbiol Immunol Infect. 2022 Dec;55(6 Pt 1):1101-1107
pubmed: 34756671
JAMA Netw Open. 2022 Jun 1;5(6):e2218959
pubmed: 35763298
Clin Infect Dis. 2020 Nov 5;71(8):e235-e243
pubmed: 31955196
Clin Infect Dis. 2022 Aug 31;75(3):390-398
pubmed: 34940806
Vaccine. 2018 Nov 26;36(49):7574-7579
pubmed: 30391053
PLoS One. 2017 May 23;12(5):e0177985
pubmed: 28542347
N Engl J Med. 2015 Mar 19;372(12):1114-25
pubmed: 25785969
Front Cell Infect Microbiol. 2016 Sep 21;6:98
pubmed: 27709102
EClinicalMedicine. 2019 Jan 02;6:42-50
pubmed: 31193709
Eur J Clin Microbiol Infect Dis. 2021 Nov;40(11):2389-2395
pubmed: 34347190
Open Forum Infect Dis. 2016 Feb 02;3(1):ofw020
pubmed: 26955644
Lancet Infect Dis. 2018 Nov;18(11):1191-1210
pubmed: 30243584
Antimicrob Agents Chemother. 2006 Nov;50(11):3646-50
pubmed: 16940064
Expert Rev Vaccines. 2022 Sep;21(9):1331-1341
pubmed: 35929956
PLoS One. 2021 Sep 1;16(9):e0256856
pubmed: 34469441
Emerg Microbes Infect. 2021 Dec;10(1):2202-2204
pubmed: 34723783
Lancet Infect Dis. 2019 Jan;19(1):56-66
pubmed: 30409683
PLoS One. 2013;8(4):e60273
pubmed: 23565216
PLoS Med. 2020 Oct 23;17(10):e1003326
pubmed: 33095759
J Antimicrob Chemother. 2018 Jul 1;73(suppl_7):vii12-vii19
pubmed: 29982572
Clin Infect Dis. 2022 Sep 30;75(7):1149-1153
pubmed: 35136983