Introduction
In November 2020, the US Food and Drug Administration issued an emergency use authorization (EUA) for the first evidence-based treatment for outpatients with COVID-19 – bamlanivimab, a neutralizing monoclonal antibody (mAb) therapy [Reference Mahase1] – based on clinical trial data demonstrating efficacy in prevention of hospitalization [Reference Chen, Nirula and Heller2]. While this was a major advance in the fight to mitigate ongoing waves of morbidity and mortality stemming from the COVID-19 pandemic, uptake of the treatment in the US was slow [Reference Toy, Walker and Evans3,4]. Contrary to expectations that high demand would outstrip supply, leading to the need to prioritize only the highest-risk patients for treatment, few people infected with COVID-19 were being treated as outpatients before needing to be hospitalized [4]. By spring of 2021, two additional monoclonal antibody treatments had been granted EUAs – and increasing evidence supported the effectiveness and safety of mAbs as outpatient COVID-19 treatment [Reference Weinreich, Sivapalasingam and Norton5–Reference Dougan, Nirula and Azizad7] - but still fewer than 5% of available doses had been used, despite widespread and ongoing infection, hospitalization, and death [Reference Behr, Maddox, Meara, Epstein, Orav and Barnett8]. To address this problem, federal and state governments, public health departments, and health care systems across the US sought to rapidly enhance access to and use of mAbs for COVID-19 [4]. Yet there was little evidence – and limited infrastructure – to guide these implementation efforts. Furthermore, anticipated challenges related to equitable access to care threatened to exacerbate the already-present disparities in COVID-19 outcomes among certain racial and ethnic groups, frontline health care and other essential workers, and in rural communities [Reference Wiltz, Feehan and Molinari9,Reference Greene, Huber, D’Ambrosio, Thoumi, McClellan, Plescia and Baggett10].
In response to these challenges, in March 2021 the National Center for Advancing Translational Sciences funded the Colorado Clinical & Translational Sciences Institute, in part, to develop and test mAb treatment dissemination and implementation (D&I) strategies. Using methods and theories from the field of D&I science, the “mAb Colorado” team conducted surveys, interviews, and focus groups with community members and health care professionals in the state of Colorado to understand barriers and facilitators to equitable access to mAbs for COVID-19 [Reference Hamer, Alasmar, Kwan, Wynia, Ginde and DeCamp11– Reference Kwan, Sobczak and Gorman13]. In parallel, the team engaged clinicians and community members in co-design of dissemination strategies to enhance awareness of mAb availability, referral, and treatment processes in the state (unpublished data). The multi-level dissemination strategy followed recommendations from Brownson and colleagues [Reference Brownson, Eyler, Harris, Moore and Tabak14] for disseminating public health science. We applied a dissemination framework (diffusion of innovations) [Reference Rogers, Singhal and Quinlan15] and engaged with academic and public partners (community members, policymakers, clinicians) to develop messages and materials useful to those expected to take action [Reference Hamer, Alasmar, Kwan, Wynia, Ginde and DeCamp11–Reference Kwan, Sobczak and Gorman13]. Table 1 summarizes the audience, packaging, and communication channels, and provides example messages for each of the co-designed products. Details about the selection, development, and communication of the comprehensive dissemination strategy are reported elsewhere [Reference Kwan, Sobczak and Begay16]. We launched all main components of the dissemination strategy (newsletters, website, social media, radio) in July 2021 and continued adding and iterating content through December 2021.
Summary of mAb Colorado dissemination strategies
The dissemination strategies we used included community-focused communication campaigns, clinician education and guidance materials, and capacity building through partnerships with health care systems and public health agencies. A key partner in this work was the Colorado Department of Public Health and Environment (CDPHE; the state health department), which had developed a secure, web-based referral system to help clinicians connect patients to mAb treatment sites with available doses. This state system, called “the mAb Connector Tool,” yielded a database of referrals that included patient information, referral date, referring clinician, and referral site. While primarily designed to support clinical care, this database provided a prime source of “real world data” to evaluate the impact of the mAb Colorado dissemination strategies on referral patterns and trajectories statewide.
This paper describes the real-world data methods used to assess changes in Colorado’s mAb referral rates before and after launch of the mAb Colorado multi-level dissemination strategy. In combination with publicly available data on COVID-19 infection and hospitalization rates and population demographics, we conducted a retrospective cohort study using mAb Connector Tool referral data to evaluate: 1) total mAb referrals; 2) number of unique referring clinicians; and 3) COVID-19 hospitalization rates (per 100,000 population) to assess the population-level impact of the mAb Colorado dissemination strategies in terms of behavior change (referrals and referring providers) and outcomes from having received treatment (hospitalization rates). These outcomes were selected from the available comprehensive, real-world data collected by the state health department and used to measure population-level effects. We assess the equitable impact of the mAb Colorado dissemination strategies by examining differences in the outcomes among communities specifically prioritized by these efforts. Communities experiencing disproportionately high burden imposed by COVID-19 (e.g., rural/frontier vs. urban counties, counties with high proportions of Hispanic/Latinx residents) were a focal point of the mAb Colorado dissemination strategies.
Materials and methods
Study design
In this retrospective cohort study of real-world data, we used mAb referral records provided by CDPHE, county COVID-19 hospitalization data, and demographic data on county population composition to address the study objectives of demonstrating the impact of the mAb Colorado dissemination strategies on mAb access, outcomes, and equity. We limited the timeframe of our analysis to November 2020–December 2021, when one or more mAbs were authorized and available for high-risk outpatients with COVID-19 in Colorado. In January 2022, the EUAs were revoked for two of three mAb products that had been available due to demonstrated lack of efficacy against the then-dominant omicron variant [Reference Aggarwal, Beaty and Bennett17]. Low supply of sotrovimab, the remaining effective mAb with an EUA, and availability of alternative treatments meant that doses were allocated and distributed in ways that differed from most of 2021.
Data sources
We compiled data from multiple sources and aggregated observations at the county-level each week from November 29, 2020 to December 26, 2021. Counts of mAb referrals over time came from CDPHE’s mAb Connector Tool, a HIPAA-compliant, REDCap-based form submission tool to enable clinicians to refer patients for mAb treatment. The connector tool form gathered patient-level qualifying information (mAb eligibility criteria), desired mAb treatment site, and a clinician identifier. The tool also included a list and a map of all treatment sites operating in the state (including both intravenous infusion sites and sites offering subcutaneous injection) that wished to be listed. Form submissions were automatically directed to the designated contact at the specified treatment location. This system served as a registry of referrals but did not track actual receipt of treatment. CDPHE personnel prepared a data extract for the study team consisting of weekly counts of referrals and unique referring clinicians for each treatment site. County-level hospitalization rates came from the US Department of Health and Human Services and are reported as the sum of the average number of reported patients currently hospitalized in an inpatient bed who have suspected or confirmed COVID-19 reported during the 7-day period in each hospital per county per 100,000 population [18]. COVID-19 case rates and counts came from the CDPHE COVID-19 County-Level Open Data Repository [19].
We explored multiple model specifications that included many different population-level characteristics as covariates, many of which were highly collinear. Due to small sample sizes and highly correlated covariates introducing noise or diluting/inflating the observed outcomes, the final model includes a limited number of covariates that conceptually were most likely to be associated with mAb referrals and that reflected the priority populations of the mAb Colorado dissemination strategies. These included county type (urban/rural/frontier), share of the population over age 65, by racial/ethnic group, and voting for the Republican presidential candidate in 2020. Fixed (time-invariant) county demographics came from the Colorado Department of Local Affairs, State Demography Office, and County Population Estimates (including urban/rural/frontier county designation). County voting patterns came from the 2020 Presidential Election Results from the Colorado Secretary of State [20,Reference Sehgal, Yue, Pope, Wang and Roby21].
Intervention
Our intervention consisted of a multi-level, comprehensive dissemination strategy with materials and messages designed for community and clinician audiences. The project also supported enhanced system capacity for mAb treatment through partnerships with health systems and influencing statewide policy change. For instance, the study team advocated to the state to implement mobile buses and enable self-referral, which was implemented in September 2021. These activities were designed in response to community and clinician feedback [Reference Hamer, Alasmar, Kwan, Wynia, Ginde and DeCamp11–Reference Kwan, Sobczak and Gorman13] and in partnership with local and state entities and departments of public health. Using community engagement studio methods [Reference Joosten, Israel and Williams22], we co-designed community-focused messages and materials for five key audiences: general community members, community members living in rural areas, community members with lower literacy, members of American Indian/Alaskan Native communities in Colorado, and Spanish-speaking community members [Reference Lin, Paykin, Halpern, Martinez-Cardoso and Kolak23–Reference Raine, Liu, Mintz, Wahood, Huntley and Haffizulla25]. These messages and materials were disseminated through the project website (www.mabcolorado.org), social media (both paid and unpaid), radio, postcards, flyers in local primary care clinics and emergency departments, and through Google search optimization. We also co-designed clinician-focused messages and materials, including a quick reference patient eligibility and referral checklist, an implementation blueprint, and PowerPoint presentations describing the strength of evidence and referral and implementation guidelines. These materials were distributed through a newsletter that reached more than 300 subscribers across the state, paper delivery to clinics by regional health connectors, and presentations to clinician audiences statewide including several well-attended webinars in partnership with ECHO Colorado [26]. Members of the mAb Colorado team conducted multiple state and national interviews with television and newspaper outlets, many of which were coordinated through the University of Colorado communication office. These dissemination activities launched in July 2021 and continued through fall of 2021.
Setting
To evaluate the overall impact of these dissemination strategies, we define a post-period (July 2021 and later) when the mAb project activities were actively being disseminated, though not always at regular intervals. Our cohort was defined as the 23 counties in Colorado with at least one mAb treatment site documented as active during the study period. In the comparative analyses of COVID-19 hospitalization rates, the comparison group consisted of the 41 Colorado counties without a mAb treatment site at any point during the study period.
Outcomes
We estimated models for multiple outcomes to address our study objectives: total mAb referrals, number of unique referring clinicians, and COVID-19 hospitalization rate (per 100,000 population). Total referrals and number of unique referring providers were direct indicators of the effectiveness of our dissemination strategies and are likely to have been affected by patient-, clinician-, and health-system-facing materials. Absent statewide patient-level data, we used county-level hospitalization rate as a proxy for population-level impact. Hospitalization rate is a distal measure of the effectiveness of having received treatment, one which we expect to have decreased as a result of the mAb Colorado efforts. To address questions of equity and examine communities prioritized by mAb Colorado dissemination strategies, we stratified on county and population characteristics. To examine differences by urbanicity, we stratified into urban versus rural and frontier counties combined (due to small numbers). To examine differences by race/ethnicity, we stratified on the share of the population identifying as Hispanic/Latinx, using 20.6% (the observed mean population share) as the threshold for high- versus low-Hispanic/Latinx population share.
Model specification
We estimated separate models to evaluate the multiple outcomes of interest. To evaluate the association between mAb Colorado dissemination strategies and total mAb referrals and unique referring clinicians by week, we used zero-inflated negative binomial models due to conditional overdispersion and the large number of zeros observed for the count outcomes [Reference Hardin and Hilbe27]. The zero-inflated model assumes two mechanisms, and thus two distinct groups of counties, with a zero value for the outcome. Specifically, there is one group of counties whose zero mAb referrals and referring clinicians are generated by the standard negative binomial distribution, and a second group of counties that were “always zeros” because they have zero probability of a mAb referral or a referring clinician count greater than zero; observations of zero mAb referrals or referring clinicians may come from either group. The always zeros here refer to counties with zero COVID-19 cases reported in a given week. These counties are distinct from those with COVID-19 cases but no referrals for mAbs. Zero-inflated negative binomial regression estimates the outcome in two parts that account for the generation of a zero through the two separate mechanisms. The final model specification was selected based on BIC. We favored a more parsimonious model to improve explainability and because of relatively small sample sizes.
For the comparative estimation of association between mAb Colorado dissemination strategies and COVID-19 hospitalization rates, we used a zero-inflated negative binomial model. The final model specification was selected on BIC. To allow for heterogeneous effects by time, we modeled “T” post-periods representing each week in July 2021 and later when the mAb Colorado strategies were being disseminated. The model was of the form:
$$\begin{gathered}{Y_{it}} = {\beta _0} + {\beta _1}Has\_sit{e_i} + \sum\limits_{j = 1}^T {{\beta _j}} Pos{t_{jt}} + \sum\limits_{j = 1}^T {{\lambda _j}} {\left( {Has\_site*Pos{t_j}} \right)_t} \\ \!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!\!+ {{X'}_i}\beta + {\eta _{it}} \\ \end{gathered}$$
where i indexed county at time t, Has_site is an indicator for presence of a mAb treatment site and Post is an indicator for each week in the post-period from July to December 2021. The effects of the mAb Colorado dissemination strategies by time are given by the coefficients λj. Thus, the treatment effect by time is a comparison of expected outcomes in each post-period j = 1 to T relative to the combined pre-period (November 2020–June 2021). X’ i represents a vector of time-invariant county characteristics (county urbanicity, key population demographics); η denotes cluster robust standard errors at the county-level. Because the coefficients from the negative binomial models are not directly interpretable, we used predictive margins to obtain the predicted number of events for the cohort and comparison groups each week. We calculate the relative effect in the cohort counties by subtracting pre- from post-estimates for each county group, then taking the difference of those values (i.e., the within- and between-group differences for each week in the post-period). We account for the observation of hospitalization to be delayed after COVID-19 infection and treatment by including a 2-week lag for this outcome.
This study was approved as non-human subjects research (all data were either publicly available or aggregated at the county and week level) by the Colorado Multiple Institutional Review Board (#21-2872). All analyses were conducted using Stata v.16 (College Station, TX). We considered statistical significance at the p = 0.05 level using 2-sided tests of significance.
Results
Among the 64 Colorado counties, 23 (35.9%) had at least one mAb treatment site during the study period (Table 2). Compared to counties without a mAb treatment site, counties with a treatment site had larger populations (p = 0.002) and were more likely to be urban (39.1% vs. 19.5%, p = 0.015). Population characteristics were otherwise similar in terms of age, racial and ethnic group distribution, poverty, and socio-political context (measured by county-level share of Republican candidate votes in the 2020 presidential election) (all p > 0.05). The average absolute number of COVID-19 cases per week was higher in the counties with a mAb treatment site (381.9 vs. 69.9, p < 0.001), though the COVID-19 case rate per 100,000 people was similar (224.3 vs. 219.3, p = 0.65). By the end of 2021, COVID-19 vaccine series completion among people aged 12 years and older was higher in counties with a mAb treatment site (67.3% vs. 58.2%, p = 0.05).
Characteristics of Colorado counties, overall and by presence of mAb treatment sites
Note: T-tests were used to compare group means for continuous variables; Pearson X 2 tests were used to compare categorical variables. Abbreviations: mAb: neutralizing monoclonal antibodies; SD: standard deviation; FPL: Federal poverty level.
Despite the availability of mAbs and the presence of COVID-19 cases in the pre-period, there were few referrals for mAbs before July 2021 (Fig. 1). The number of referrals and unique referring clinicians increased after the mAb Colorado dissemination strategies began. In counties with at least one recorded COVID-19 case and mAb treatment site, the weekly average number of mAb referrals increased from 2.99 in the pre-period from November 29, 2020 to June 30, 2021 to 15.47 in the post-period from July 1 to December 30, 2021, a 417.4 percentage point increase. Number of unique referring clinicians increased from a weekly average of 2.20 in the pre-period to 9.73 in the post-period, a 342.3 percentage point increase.
COVID-19 case counts, total mAb referrals, and unique referring providers, December 2020–December 2021. Note: *High case counts in November 2020 and the latter half of December 2021 distort the graph, making trends in mAb referrals and unique referring clinicians indistinguishable. For clarity of presentation, we omit those observations from Fig. 1 (though the observations are included in the analysis). Abbreviations: mAb = neutralizing monoclonal antibodies.
Marginal effects from the zero-inflated negative binomial regression models for the mAb referral and unique referring clinician outcomes are displayed in Figs. 2 and 3 (full regression output reported in Supplemental Table S1 and Table S2). There was a statistically significant increase in the number of mAb referrals each week from July 4 to December 26, 2021, compared to the pre-period average. The magnitude of the increase was variable by time, ranging between 1 and 42 additional mAb referrals per county per week in the post-period (all p < 0.05). Compared to urban counties, there were approximately 10 fewer mAb referrals per week in rural and frontier counties.
Adjusted change in mAb referral counts from baseline (Nov 2020–June 2021), overall and by county type.
Adjusted change in unique referring clinicians from baseline (Nov 2020–June 2021), overall and by county type.
The number of unique referring clinicians increased over the pre-period average beginning in August 2021, approximately five weeks after the mAb Colorado dissemination strategies launched (p < 0.001). There was a variable increase in the number of unique referring clinicians, ranging from 1 to 22 additional clinicians per county per week. Like mAb referrals, there were approximately 6 fewer unique referring clinicians per rural and frontier county per week, compared to urban counties.
In stratified models by urban and rural/frontier designation (rural and frontier combined due to a small number of frontier counties), trends were similar (Fig. 2, Supplemental Table S1). However, the increase in mAb referrals was much greater in urban counties. Population demographics contributed differentially in urban versus rural/frontier counties. In urban counties, a lower number of mAb referrals was observed when there were higher percentages of the population over age 65 (15 fewer referrals for every 1% increase in population over 65, p < 0.001) and higher percentages of Hispanic/Latinx (8.5 fewer mAb referrals per 1% increase, p < 0.001) and Black or African American (5.9 fewer mAb referrals for every 1% increase, p < 0.001) residents. Increased population size of American Indian/ Alaskan Native individuals was associated with more mAb referrals (124.6 more referrals for every 1% increase in share of total population, p < 0.001). There were no corresponding trends in mAb referrals according to population demographics in the rural and frontier counties, which tended to be less racially/ethnically diverse than urban counties. Similar patterns were observed, but to a lesser extent, for the number of unique referring clinicians outcome (Fig. 3, Supplemental Table S2).
In additional models, we stratified by high and low-Hispanic/Latinx population to assess impact on this community, which was an additional priority of the mAb Colorado dissemination strategy (Fig. 2, Supplemental Table S1). There were earlier increases in mAb referrals among low-Hispanic/Latinx population counties (beginning in week 1 post-launch), though counties with higher Hispanic/Latinx populations saw increases in mAb referrals of greater magnitude as time progressed. Rural and frontier counties with low-Hispanic/Latinx populations saw fewer mAb referrals than their urban counterparts (p < 0.05). Further, counties with larger Hispanic/Latinx shares of the population also saw greater mAb referrals as their population share of Black or African American (3.25 more referrals for every 1% increase in population share, p < 0.05) and American Indian/Alaskan Native increased (12.88 more referrals for every 1% increase in population share, p < 0.001). There were few population demographics associated with unique referring clinicians when stratifying by Hispanic/Latinx population share (Fig. 3, Supplemental Table S2).
Hospitalization rates were variable over our study period, slightly lagging the trends in COVID-19 cases (Fig. 4). There were no sustained statistically significant differences in COVID-19 hospitalization rates between counties with and without mAb treatment sites (Fig. 5, Supplemental Table S3) after the mAb Colorado dissemination strategies were launched.
COVID-19 case counts and COVID-19 hospitalization rates by county presence of mAb treatment sites, November 2020–December 2021.
Adjusted COVID-19 hospitalization rates, by presence of mAb treatment site(s).
Discussion
Using real-world data, our analyses suggest that launching the mAb Colorado multi-level dissemination strategy (community-, health system-, and public health policy level) was associated with a significant increase in mAb referrals and number of referring clinicians in counties with available mAb treatment sites. Urban American Indian/Alaskan Native populations and communities with higher proportions of historically underrepresented racial and ethnic minority residents (especially Hispanic/Latinx) were priority communities for the mAb Colorado dissemination efforts.
There are both strengths and limitations to conducting a retrospective, observational study using real-world data. While the data suggest an increase in referrals corresponding with the mAb dissemination strategies, several other co-occurring events may have influenced the uptake of mAbs. In spring and early summer of 2021, there was optimism surrounding the freedom afforded by vaccination; case counts were lower. Other data from our study showed clinicians generally saw few, if any patients, with COVID-19 at that time [Reference Kwan, Sobczak and Beaty12]. Yet in late July and early August 2021, there was a new wave of COVID-19 cases stemming from the Delta variant and an increase in vaccine “breakthrough” cases, so overall demand for treatment may have been higher. However, the effects of the dissemination strategy were observed even when adjusting for case counts. Other factors might have included increased national media coverage from other states (e.g., Florida, Texas) where mAbs were being promoted aggressively [28,29]. Yet there was also media coverage of nationally-known politicians who received mAb treatment in the fall and winter of 2020, without the correspondingly high demand when mAbs first became authorized and when vaccines were still not widely available. Availability of mAbs was influenced by changes in the federal mAb allocation policies, such that mAbs were at first allocated by the federal government (Administration for Strategic Preparedness and Response) to the state health departments in limited supply for distribution to healthcare facilities (November 2020 to February 2021), then loosened to allow treatment sites to order product directly from the federal distributor (February 2021 to September 2021), then returned to a more restrictive federal allocation strategy (September 2021 to December 2021) [30].
Even with increased referrals for mAbs, the results did not show a corresponding decrease in COVID-19 hospitalizations after implementing the dissemination strategies. Estimates from this analysis indicate a maximum of about 30–40 additional mAb referrals per week in counties with mAb treatment sites following the launch of dissemination strategies; other real-world effectiveness evidence from the time showed a number needed to treat of 20–30 for mAbs to avert 1 hospitalization and approximately 100 to prevent 1 death [Reference Wynia, Beaty and Bennett31]. Thus, it follows that the increase in mAb referrals after the launch of mAb Colorado dissemination strategies induced no observable difference in hospitalization rates. It is also the case that our data only reports on referrals, rather than actual receipt of treatment. It is not known how many patients with referrals were ultimately able to schedule an appointment and receive treatment promptly to alter their disease course, nor how many may have desired treatment but were unable to access it due to supply shortages. In future pandemic or other large-scale public health emergency scenarios, the importance of early and consistent data collection cannot be understated. Disparate data sources greatly inhibit real-time assessment of communities most affected and make coordinated efforts to direct resources where they are most needed nearly impossible.
This study has multiple limitations. Our unit of analysis was the county, with mAb referrals being attributed to the county of treatment/referral, not patient residence. Similarly, not all counties contain a hospital, and patients may travel or be transferred outside their county of residence for the hospital admission. Benefits of mAbs would have been realized in the county of residence, not the county of referral or treatment, meaning that analysis of hospitalization outcomes would be biased toward the null. Thus, we view our findings as conservative estimates of the impact of the mAb Colorado efforts. We are not able to infer causation; while we control for a limited set of county demographics, and there is the possibility of unmeasured or residual confounders that we could not account for. We could not capture heterogeneous effects or more nuanced findings in counties where mAb Colorado dissemination efforts were especially concentrated. Using aggregate referral data, we were unable to capture individual clinician rates (per COVID-19 patient) of mAb referral. We could not distinguish between the possibility of a smaller number of high-volume “mAb referrers” who were central to increasing mAb referrals, or whether increased referrals came from more clinicians referring at similar volumes. We were not able to control for the number of mAb doses available to people in Colorado each week, so we were limited to evaluating total mAb referrals and unable to discern how much of the total state mAb supply this accounted for. Finally, there was little variability in population share of some underrepresented racial and ethnic minority groups to stratify into categories other than those presented in the paper.
In conclusion, our approach represents a pragmatic, efficient strategy to estimate the population impact of a multi-level dissemination strategy, focusing on access to treatment, outcomes, and equity of mAbs for COVID-19. In doing so, we overcame known challenges to evaluating dissemination strategies [Reference Brownson, Eyler, Harris, Moore and Tabak14], which can be limited to assessment of changes in knowledge, intentions to use, or observation of policy change. While descriptive measures of the number and type of materials distributed, the number of website hits, or social media reactions can be useful, these dissemination measures do not reflect health impact or behavior change. By contrast, our use of real-world data collected by the state health department allowed for a population-level assessment of patient and clinician behavior change (referrals, referring clinicians) and patient outcomes (hospitalization rates) resulting from the multi-channel dissemination strategy. Finally, conducting randomized trials of dissemination strategies with primary data collection can be both cost and time prohibitive, and may not always be feasible or ethical [Reference Mazzucca, Tabak and Pilar32] – especially within the context of a rapidly changing pandemic. In this analysis, we demonstrated the use of aggregate real-world data made available by the state health department to evaluate a multi-level dissemination strategy for enhancing equitable access to treatment for COVID-19. While real-world data have been used to assess ongoing mAb treatment effectiveness for COVID-19 [Reference Wynia, Beaty and Bennett31,Reference Aggarwal, Beaty and Bennett33], use to evaluate dissemination impact is innovative. We demonstrated change in two key data points – number of mAb referrals and number of unique referring clinicians – reflecting uptake and adoption of mAb referrals, especially in prioritized populations. Even as the COVID-19 pandemic transitions into an endemic phase, there are other outpatient COVID-19 therapeutics, proposed need for annual COVID-19 vaccine boosters, and future rapidly emerging public health needs that will benefit from equitable, multi-level dissemination strategies to communicate availability and access to effective prevention or treatment approaches for patients who would benefit (and the clinicians who care for them).
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/cts.2023.679.
Acknowledgments
The authors wish to thank Ms. Madelaine Carter and Mr. Matthew Rhodes, both from the University of Colorado Anschutz Medical Campus, for editorial assistance.
Funding statement
This publication was supported by grants from the National Institutes of Health (NIH; https://nih.gov/)/National Center for Advancing Translational Sciences (NCATS; https://ncats.nih.gov/) Colorado CTSA Grant Number UL1-TR002535-03 (PI: Ronald Sokol) and 3UL1TR002535-03S3 / 3UL1TR002535-04S2 (MPI: Ronald Sokol and Adit Ginde) [MKH, CS, LW, RLB, RK, JAB, HDL, AAG, MKW, BMK]. Its contents are the authors’ sole responsibility and do not necessarily represent official NIH views. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests
The authors have no conflicts of interest to disclose.
Open access
