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Mayo Clinic Proceedings: Innovations, Quality & Outcomes logoLink to Mayo Clinic Proceedings: Innovations, Quality & Outcomes
. 2021 May 26;5(3):596–604. doi: 10.1016/j.mayocpiqo.2021.03.006

Estimated Public Health Impact of the Recombinant Zoster Vaccine

Brandon J Patterson a,, Philip O Buck a, Desmond Curran b, Desirée Van Oorschot b, Justin Carrico c, William L Herring c, Yuanhui Zhang c, Jeffrey J Stoddard a
PMCID: PMC8240325  PMID: 34195552

Abstract

Objective

To investigate the potential public health impact of adult herpes zoster (HZ) vaccination with the adjuvanted recombinant zoster vaccine (RZV) in the United States in the first 15 years after launch.

Methods

We used a publicly available model accounting for national population characteristics and HZ epidemiological data, vaccine characteristics from clinical studies, and anticipated vaccine coverage with RZV after launch in 2018. Two scenarios were modeled: a scenario with RZV implemented with 65% coverage after 15 years and a scenario continuing with zoster vaccine live (ZVL) with coverage increasing 10% over the same period. We estimated the numbers vaccinated, and the clinical outcomes and health care use avoided yearly, from January 1, 2018, to December 31, 2032. We varied RZV coverage and investigated the associated impact on HZ cases, complications, and health care resource use.

Results

With RZV adoption, the numbers of individuals affected by HZ was predicted to progressively decline with an additional 4.6 million cumulative cases avoided if 65% vaccination with RZV was reached within 15 years. In the year 2032, it was predicted that an additional 1.3 million physicians’ visits and 14.4 thousand hospitalizations could be avoided, compared with continuing with ZVL alone. These numbers could be reached 2 to 5 years earlier with 15% higher RZV vaccination rates.

Conclusion

Substantial personal and health care burden can be alleviated when vaccination with RZV is adopted. The predicted numbers of HZ cases, complications, physicians’ visits, and hospitalizations avoided, compared with continued ZVL vaccination, depends upon the RZV vaccination coverage achieved.

Abbreviations and Acronyms: CDC, Centers for Disease Control and Prevention; HZ, herpes zoster; PCP, primary care physician; PHN, postherpetic neuralgia; RZV, adjuvanted recombinant zoster vaccine; ZVL, zoster vaccine live


Herpes zoster (HZ) or shingles results from the reactivation of the varicella zoster virus, which lies dormant in basal root ganglia of individuals who have had varicella, commonly known as chickenpox.1 Varicella zoster virus–specific T-cell immunity wanes with aging or due to immunosuppressing illnesses or medications, with the result that approximately one-third of the population experiences shingles at some time in their lives.2,3 The risk of HZ increases substantially with age over 50 years; and as the population ages and people live longer, the burden on individuals and health care providers is projected to increase.4,5

Shingles begins with prodromal pain, followed by a unilateral dermatomal rash most commonly affecting the trunk or face. The skin lesions and pain usually resolve within 4 to 6 weeks,6 but in around 10% to 50% of individuals (depending upon the precise definition and patient age) the pain persists after the rash has resolved, a complication termed postherpetic neuralgia (PHN).1 PHN is the most common complication of HZ; it can be particularly debilitating, slow to resolve, and difficult to relieve by analgesia.6 Other complications are rarer such as HZ ophthalmicus (eye complications including keratitis, uveitis/iritis, conjunctivitis, and loss of vision3,7); more recently HZ has been associated with an increased vascular risk particularly affecting younger HZ sufferers,8 with the increased risk of stroke or cardiovascular event diminishing gradually according to age and length of time after the HZ episode.9

HZ has a significant burden on quality of life, with 90% of patients reporting pain as the predominant symptom.10 In the United States it is estimated that 1 million people suffer an episode of HZ annually, with higher rates of recurrence in older or immunocompromised adults, and as many as 3% of individuals can be hospitalized.11 Physician, emergency department, and outpatient visits and inpatient hospitals stays all contribute to the health care burden associated with the treatment and management of HZ cases and associated complications.12 It has been estimated that HZ costs the US health care system $1.3 billion annually,13,14 with this burden projected to increase with population aging.15

HZ can be prevented by vaccination. In the United States, vaccination against HZ was introduced in 2008 for immunocompetent adults aged 60 years and older.11 At the time there was 1 vaccine available, zoster vaccine live (ZVL). Since then vaccination rates have climbed, surpassing the Healthy People 2020 target of 30% coverage.16 However, in 2017 a new vaccine, the adjuvanted recombinant zoster vaccine (RZV) was preferentially recommended by the Advisory Committee on Immunization Practices for immunocompetent adults aged 50 years and older, regardless of prior HZ vaccination history.17 This vaccine has a different clinical profile from that of ZVL. The efficacy of the ZVL vaccine in clinical trials was found to be 38% to 70% dependent upon patient age,18,19 but this decreased over time with ZVL vaccination conferring little or no protection after 9 years.20 By contrast, RZV was found to have higher efficacy (>90%), independent of age at vaccination,21,22 with waning limited and modeled to 1% to 3.6% per year dependent upon age.13,23 It is estimated that to prevent one case of HZ with ZVL, 32 adults would need to be vaccinated, whereas the number needed to vaccinate to prevent one case with RZV is 10.13 Both vaccines have been associated with injection-site reactions, with the rates of grade 3 reactions (severe enough to prevent normal activities) at frequencies of 9.4% for RZV and 0.9% for ZVL17 (although these results might not be directly comparable as discussed by McGirr et al.).24

Previous economic evaluations have assessed the value and affordability of vaccination with RZV in the United States.13,25, 26, 27, 28 These analyses, which were conducted to inform HZ vaccination recommendations and RZV reimbursement decisions, modeled the impact of RZV on hypothetical cohorts of older adults or for specific health plan populations that only represented a portion of the US population. Analyses providing public health stakeholders and other policymakers with broad, population-level estimates of the public health impact of potential RZV coverage levels have not been conducted. With the easing of RZV supply constraints,29,30 and an emphasis on encouraging adult vaccination,31,32 the potential public impact of HZ vaccination with RZV is of great interest. The objective of this study is to predict the public health impact of implementing HZ vaccination with RZV, when reaching coverage levels comparable with the elderly pneumococcal and influenza vaccines of 65%,33 over the next 15 years.

Methods

This analysis is based upon mathematical modeling; therefore, no patients were involved. The model is publicly available and the methodology published.27 The model accounts for national population characteristics (size and age distribution), epidemiological data (incidence of HZ and complications, and HZ recurrence rate), vaccine characteristics from randomized controlled trials and observational studies (efficacy, waning, second dose compliance for RZV, and adverse event rates), and current and anticipated vaccine coverage in the years after RZV launch.

The model, a dynamic, population-level model with underlying Markov disease framework created in Microsoft Excel (Microsoft, Redmond, Washington), considers the US population eligible for vaccination, namely, immunocompetent adults aged 50+ years. As the population ages, individuals leave the model following the natural mortality rate,34 and each year a new cohort aged 50 years joins the model, with figures based upon census data.35 The population can be vaccinated (and if previously vaccinated with ZVL they can be vaccinated with RZV) and the probability of entering one of the health states within the model (HZ, recurrent HZ, PHN, and non-PHN complications) is adjusted accordingly, based on trial data for vaccine efficacy and waning of protection as previously described.13,36 The structure of the model is shown in Figure 1. This model framework, which has been used to estimate the budget impact of RZV vaccination for US health plans,27 is more suitable for calculating the population-level public health impact of HZ vaccination than cohort-level models used in previous cost-effectiveness analyses.

Figure 1.

Figure 1

Population funnel and cohort-level transitions used in the model. An asterisk (∗) indicates immunocompetent adults aged 50 years and older. “HZ” and “recurrent HZ” are modeled as events occurring during years spent in the “No HZ” and “recovered” health states, respectively. “PHN” and “non–PHN complications” are modeled as proportions of overall HZ (or recurrent HZ) cases. All-cause mortality can occur from either the “No HZ” or the “recovered” health states. HZ-related mortality is not included in the model. HZ, herpes zoster; PCP, primary care physician; PHN, postherpetic neuralgia; RZV, adjuvanted recombinant zoster vaccine; ZVL, zoster vaccine live.

The model compares a “without RZV” scenario, which is intended to represent a world in which RZV is not available and vaccination with ZVL continues, and a “with RZV” scenario over a time horizon of 15 years. In the “without RZV” scenario, current vaccination rates with ZVL,33 dependent upon age, were assumed to increase by 10% over the 15-year time horizon in alignment with HZ vaccination rate trends before RZV introduction.33 For RZV, the vaccination rate begins at 0% and is assumed to linearly increase to 65% over the corresponding 15 years, which is the coverage achieved for pneumococcal and influenza vaccines in a similar age-group.33 As RZV is a 2-dose vaccine, the second dose compliance was modeled as 76%, consistent with Centers for Disease Control and Prevention (CDC) estimates.37 As described previously,27 model inputs were retrieved based on the best available and most recent nationally representative estimates. These nationally representative values were aligned with the current study’s objective of estimating the population-level public health impact for the United States.

Model outcomes include the number of individuals vaccinated and the number of cases of HZ, PHN, primary care physician (PCP) visits, and hospitalizations avoided when comparing the RZV and ZVL vaccination scenarios. The difference between the two scenarios is presented as the potential incremental benefit of adopting RZV. Target coverage levels for RZV were varied from 30% to 80% in additional scenarios to assess the public health impact of reaching alternative levels of RZV vaccination coverage.

Results

Table 1 shows the modeled number of vaccinees per year for ZVL and RZV over the 15-year time horizon. The predicted cumulative number of RZV vaccine recipients, assuming vaccination coverage reaches 65%, is approximately 94 million (M) over the first 15 years after RZV adoption. The number vaccinated per year varies dependent upon the target RZV vaccination coverage and the number of individuals entering the model each year.

Table 1.

Number of Individuals Vaccinated Each Year (Thousands)a,b

Year
Total
2018 2019 2020 2021 2022 2023 2024 2025 2026 2027 2028 2029 2030 2031 2032
RZV vaccine coverage rate after 15 years (%)
 80 5547 8983 8870 8732 8601 8477 8338 8212 8048 7898 7759 7618 7491 7313 7152 119,038
 70 4687 7700 7607 7492 7384 7282 7167 7062 6927 6802 6686 6569 6463 6315 6181 102,325
 65 4258 7059 6975 6873 6776 6684 6581 6487 6366 6254 6150 6045 5950 5817 5696 93,969
 60 3828 6417 6344 6253 6168 6086 5996 5912 5805 5706 5614 5520 5436 5318 5210 85,613
 50 2969 5134 5081 5014 4951 4891 4824 4763 4683 4610 4541 4472 4409 4320 4239 68,901
 40 2110 3852 3818 3775 3734 3695 3653 3613 3562 3513 3468 3423 3382 3323 3268 52,189
 30 1251 2569 2554 2536 2517 2500 2481 2464 2440 2417 2396 2374 2354 2325 2297 35,477
ZVL vaccine
 2018 coverage rate +10% over 15 years 859 1283 1263 1239 1217 1195 1171 1150 1122 1096 1073 1049 1027 998 971 16,712
a

RZV, (adjuvanted) recombinant zoster vaccine; ZVL, zoster vaccine live.

b

Boldface indicates the base case.

The cumulative number of HZ and PHN cases avoided is shown in Figure 2, comparing increasing RZV coverage to 65% of the eligible US population over 15 years with a 10% increase in ZVL coverage over the corresponding period. The curve shape shows that the cumulative number of cases avoided increases at a higher rate over time, increasing to an estimated 4.6 M HZ cases and 368,000 HZ cases with PHN cases avoided over 15 years.

Figure 2.

Figure 2

The cumulative incremental number of cases avoided when adjuvanted recombinant zoster vaccine (RZV) vaccination is increased to 65% of the eligible population over 15 years. Zoster vaccine live (ZVL) vaccine coverage increased by 10% over the same period. HZ, herpes zoster; PHN, postherpetic neuralgia.

In Figure 3, the corresponding cumulative numbers of PCP visits and hospitalizations avoided are presented, also increasing at a higher rate over time. Assuming the target of 65% coverage is reached in 15 years, in 2032 approximately an additional 1.3 M PCP visits and 14,400 hospitalizations are estimated to be avoided, when comparing the RZV vaccination scenario with ZVL. During the 15-year period, this approximates to a cumulative avoidance of 10.7 M PCP visits and 111,000 hospitalizations beyond what could be expected from a 10% ZVL vaccine coverage increase over the same period.

Figure 3.

Figure 3

The cumulative incremental number of primary care physician (PCP) visits and hospitalizations avoided when adjuvanted recombinant zoster vaccine vaccination coverage is increased to 65% of the eligible population over 15 years. Zoster vaccine live vaccine coverage increased by 10% over the same period. HZ, herpes zoster.

To investigate the impact of achieving alternative coverage levels on the potential public health impact of RZV vaccination, in Table 2 (and Supplemental Figure, available at http://www.mayoclinicproceedings.org) the incremental numbers of PCP visits and hospitalizations avoided are presented varying RZV vaccination coverage from a target of 30% to 80% over 15 years. It can be seen with the highest target vaccination rate of 80% for RZV that, after 4 years, the incremental number of PCP visits avoided in 1 year has exceeded that which can be achieved with a target 30% coverage in the 15th year (more than 511,000 vs 436,000, respectively). With the base case 65% target vaccination rate for RZV, after 5 years the incremental number of annual PCP visits avoided surpasses that achieved in the 15th year with a vaccination rate of 30% (476,000 vs 436,000, respectively). Looking at the incremental annual hospitalizations avoided, the highest reduction achieved with a 50% target coverage (9860) is achieved 5 years earlier with a target of 65% RZV coverage.

Table 2.

Incremental Number of PCP Visits and Hospitalizations Avoided Varying Target RZV Coverage From 30% to 80% Over 15 Yearsa,b,c

Vaccine coverage (RZV), % Visits avoided 2018 2019 2020 2021 2022 2023 2024 2025 2026 2027 2028 2029 2030 2031 2032 Cumulative
80 Hosp 988 2129 3160 5461 6533 7463 8138 8,705 12,766 13,196 13,502 13,699 13,842 19,401 19,031 148,013
80 PCP 89,478 219,644 344,202 511,167 631,088 742,256 839,975 929,647 1,133,841 1,217,653 1,291,656 1,353,008 1,408,341 1,600,272 1,625,129 13,937,357
70 Hosp 801 1740 2593 4474 5379 6168 6755 7,253 10,578 10,984 11,285 11,507 11,679 16,203 15,973 123,374
70 PCP 73,323 182,106 286,571 426,141 527,794 622,344 706,002 783,000 955,676 1,029,087 1,094,195 1,148,607 1,197,724 1,363,164 1,387,347 11,783,083
65 Hosp 707 1546 2310 3980 4802 5521 6064 6,527 9483 9879 10,177 10,412 10,597 14,605 14,444 111,054
65 PCP 65,246 163,337 257,756 383,629 476,147 562,388 639,015 709,677 866,594 934,804 995,464 1,046,406 1,092,416 1,244,610 1,268,457 10,705,946
60 Hosp 613 1351 2026 3487 4225 4874 5373 5,802 8389 8773 9069 9316 9516 13,006 12,915 98,734
60 PCP 57,169 144,568 228,941 341,116 424,500 502,433 572,028 636,353 777,511 840,521 896,733 944,205 987,108 1,126,056 1,149,566 9,628,809
50 Hosp 425 962 1459 2500 3070 3579 3991 4,350 6201 6561 6852 7125 7352 9809 9857 74,094
50 PCP 41,014 107,030 171,310 256,091 321,205 382,521 438,055 489,707 599,346 651,955 699,272 739,804 776,491 888,948 911,785 7,474,535
40 Hosp 237 573 893 1513 1916 2285 2609 2,898 4012 4350 4636 4933 5189 6611 6800 49,455
40 PCP 24,860 69,492 113,680 171,066 217,911 262,609 304,081 343,060 421,181 463,389 501,811 535,402 565,874 651,840 674,004 5,320,261
30 Hosp 49 184 326 526 762 990 1227 1,446 1824 2138 2419 2742 3026 3414 3742 24,815
30 PCP 8705 31,954 56,050 86,041 114,616 142,698 170,108 196,413 243,015 274,823 304,349 331,001 355,258 414,732 436,223 3,165,986
a

Hosp, hospital; PCP, primary care physician; RZV, adjuvanted recombinant zoster vaccine.

b

ZVL zoster vaccine live vaccine coverage increased by 10% over the same period.

c

Boldface indicates the base case.

Discussion

Previous economic analyses have shown that RZV is a good value for the money and have estimated the impact of RZV adoption on short-term health care payer budgets. To our knowledge, this study is the first to assess the longer-term potential public health impact of RZV in the United States. Results showed that significant numbers of HZ and PHN cases can be avoided with RZV vaccination, together with the associated PCP visits and hospitalizations, representing a substantial reduction in human suffering and health care burden. The vaccination coverage rate with the RZV vaccine is estimated to have a considerable impact upon the overall public health, with higher vaccination rates accelerating the attainment of vaccination benefits.

Current adult vaccination rates in the United States are suboptimal, with HZ vaccination coverage around 30%, significantly lower than the 65% coverage rate achieved with pneumococcal and influenza vaccination of older adults.33 Recommendations in favor of HZ vaccination by public health bodies, such as the CDC, have been shown to significantly increase interest in HZ vaccination, according to Google search data38; however, the CDC recommendation has failed to translate into sustained higher HZ vaccination rates. Several investigators have suggested an explanation, citing out-of-pocket costs as an obvious financial barrier (compared with pneumococcal and influenza vaccines) and recommending that in order to increase HZ vaccination, copayments should be eliminated or, at least, reduced.39,40

One attempt to increase adult vaccination rates has involved the public and private sectors developing adult immunization performance measures (including zoster vaccination) and adding these to the 2019 Healthcare Effectiveness Data and Information Set, a widely used set of performance measures reportable by private US health plans.41 Additional initiatives have involved professional associations recommending to members to vaccinate and providing guidance for various patient groups. Among these are the American College of Rheumatologists42 and the National Psoriasis Foundation.43

However, even with recommendations and targets in place, it is clear that the strongest influencers for vaccination are the patients’ physicians. The key reason for a patient being vaccinated is them having received a recommendation from a health care provider.44 Therefore, PCPs must know the vaccination policy, agree with the policy, recommend vaccination, and then ideally have the office systems to facilitate vaccination, such as standing orders and immunization reminder systems.45 Additionally, pharmacies can play a part by improving patient awareness and education45 and by providing vaccination outside office hours, thereby increasing access and convenience for patients.46 In summary, coordination of efforts across all health care professionals regardless of role is essential to create an environment for ensuring access to and use of vaccines.47

Study Limitations

The limitations of the model and data used for this analysis, including the generalizability of vaccine efficacy from clinical trial populations to a real-world setting, have been discussed previously. Target coverage levels considered for RZV in this study were projections based on coverage levels observed for other older adult vaccines and may not reflect real-world uptake of RZV vaccination. The vaccine efficacy and safety estimates were obtained from clinical trial data and may differ from real-world settings. Early real-world effectiveness data for RZV are beginning to emerge,48,49 and future modeling exercises incorporating robust estimates for effectiveness and coverage will allow for better validation of the outcomes projected in this study.

The analysis has several strengths: the modeling approach has been published previously; the input parameters are based on the best available national data; the model is publicly available and has a user-friendly interface, and the inputs, calculations, and assumptions are transparent.

Conclusion

This modeling analysis predicts the public health impact of HZ vaccination, with a focus on RZV adoption post launch. Results show that the potential public health impact of vaccinating with RZV is dependent on the vaccine coverage achieved, with higher vaccination rates providing larger and earlier reductions in the number of HZ cases and the associated health care burden. A concerted effort across all health care providers is required to improve HZ vaccination rates to maximize the public health impact possible through RZV vaccination.

Acknowledgments

The authors thank Lijoy Varghese (former GSK employee) for his help in developing the original model; the Business & Decision Life Sciences platform for editorial assistance and manuscript coordination, on behalf of GSK; Amandine Radziejwoski for coordinating manuscript development and editorial support; and Rachel Emerson (Business & Decision Life Sciences, on behalf of GSK) for providing medical writing support. The work described was performed in accordance to ICMJE recommendations for conduct, reporting, editing, and publications of scholarly work in medical journals.

Footnotes

Potential Competing Interests: D.v.O. and D.C. are employees of the GSK group of companies and hold shares in the GSK group of companies. B.J.P., P.O.B., and J.J.S. were employees of the GSK group of companies at the time the study was conducted. W.L.H. and J.C. are employees of RTI Health Solutions, which received funding via a contractual agreement with the GSK group of companies to perform the work contributing to this research. Y.Z. was an employee of RTI Health Solutions at the time the study was conducted.

Grant Support:GlaxoSmithKline Biologicals SA funded this study (GSK study identifier: HO-16-18001) and was involved in all stages of study conduct, including analysis of the data. GlaxoSmithKline Biologicals SA also paid all costs associated with the development and publication of this manuscript.

Supplemental material can be found online at http://www.mayoclinicproceedings.org. Supplemental material attached to journal articles has not been edited, and the authors take responsibility for the accuracy of all data.

Supplemental Online Material

Supplemental Figure 1
mmc1.pdf (1.4MB, pdf)

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