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Factors associated with the speed and scope of diffusion of COVID-19 therapeutics in a nationwide healthcare setting: a mixed-methods investigation.
La, Jennifer; Fillmore, Nathanael R; Do, Nhan V; Brophy, Mary; Monach, Paul A; Branch-Elliman, Westyn.
  • La J; VA Boston Cooperative Studies Program, Boston, MA, United States of America.
  • Fillmore NR; VA Boston Cooperative Studies Program, Boston, MA, United States of America.
  • Do NV; Department of Medicine, VA Boston Healthcare System, 1400 VFW Parkway, West Roxbury, Boston, MA, 02132, United States of America.
  • Brophy M; Dana Farber Cancer Institute, Boston, MA, United States of America.
  • Monach PA; Harvard Medical School, Boston, MA, United States of America.
  • Branch-Elliman W; VA Boston Cooperative Studies Program, Boston, MA, United States of America.
Health Res Policy Syst ; 20(1): 134, 2022 Dec 14.
Article in English | MEDLINE | ID: covidwho-2162378
ABSTRACT

BACKGROUND:

The global COVID-19 pandemic is an opportunity to evaluate factors associated with high levels of adoption of different therapeutics in a real-world setting. The aim of this nationwide, retrospective cohort study was to evaluate the diffusion and adoption of novel therapeutics with an emerging evidence basis and to identify factors that influenced physicians' treatment decisions.

METHODS:

Cohort creation A cohort of Veteran patients with a microbiologically confirmed diagnosis of SARS-CoV2 were identified, and cases were classified by disease severity (outpatient, inpatient with mild and severe disease, intensive care unit ICU]). After classification of disease severity, the proportion of cases (outpatients) and admissions (inpatients) in each category receiving each type of medication were plotted as a function of time. Identification of milestones and guidance changes Key medications used for the management of COVID-19 milestones in the release of primary research results in various forms (e.g. via press release, preprint or publication in a traditional medical journal), policy events and dates of key guidelines were identified and plotted as a timeline. After a timeline was created, time points were compared to changes in medication use, and factors potentially impacting the magnitude (i.e. proportion of patients who received the treatment) and the speed (i.e. the slope of the change in use) of practice changes were evaluated.

RESULTS:

Dexamethasone and remdesivir, the first two medications with clinical trial data to support their use, underwent the most rapid, complete and sustained diffusion and adoption; the majority of practice changes occurred after press releases and preprints were available and prior to guideline changes, although some additional uptake occurred following guideline updates. Medications that were not "first in class", that were identified later in the pandemic, and that had higher perceived risk had slower and less complete uptake regardless of the strength and quality of the evidence supporting the intervention.

CONCLUSIONS:

Our findings suggest that traditional and social media platforms and preprint releases were major catalysts of practice change, particularly prior to the identification of effective treatments. The "first available treatment in class" impact appeared to be the single most important factor determining the speed and scope of diffusion.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Health Res Policy Syst Year: 2022 Document Type: Article Affiliation country: S12961-022-00935-x

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Humans Language: English Journal: Health Res Policy Syst Year: 2022 Document Type: Article Affiliation country: S12961-022-00935-x