After Exposure, Then What? Closing the COVID-19 Prevention Gap - European Medical Journal

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After Exposure, Then What? Closing the COVID-19 Prevention Gap

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Speakers:
Stefan Gravenstein , 1 Lynn McNicoll 1
Disclosure:

Gravenstein has received grant or research support from the CDC, NIH, Genentech, GlaxoSmithKline, Moderna, Pfizer, and Sanofi; consulting, advisory, and speaking fees from AstraZeneca, Genentech, GlaxoSmithKline, Icosavax, Janssen, Moderna, Novavax, Pfizer, and Sanofi. McNicoll has declared no conflicts of interest.

Acknowledgements:

Medical writing assistance provided by Yolande Chalmers, EMJ, London, UK.

Disclaimer:

The opinions expressed in this article belong solely to the named speakers.

Support:

This article was funded by an unrestricted educational grant from Shionogi Inc. (U.S.).

Citation:
Keywords:
COVID-19, exposure prevention, high-exposure settings, high-risk populations, hospitals, households, long-term care facilities (LTCF), post-exposure prophylaxis (PEP), primary care, SARS-CoV-2, vulnerable groups.

Each article is made available under the terms of the Creative Commons Attribution-Non Commercial 4.0 License.

Meeting Summary

During a recent webinar, two leading experts discussed the ongoing impact of COVID-19, including transmission, hospitalizations, and risk to vulnerable populations in high-exposure settings, and highlighted the importance of post-exposure prophylaxis (PEP). They also examined the prevention gap from a primary care workflow perspective, the unmet needs that remain, and how optimal post-exposure care might be implemented.

Successful PEP, they argued, relies on prompt testing and timing. They also stressed the need for simplified prescribing, particularly in vulnerable and/or elderly populations who may already be taking multiple medications. They concluded that future PEP strategies must be simple to implement and prescribe, with clinically robust outcomes in older and/or vulnerable patients, and demonstrably effective at reducing transmission and severe COVID-19 outcomes in the context of real-world care.

Vulnerable People at Direct Risk of SARS-CoV-2 Transmission

In 2026, SARS-CoV-2 transmission and resulting hospitalizations remain a real-world challenge. This is particularly true in high-exposure settings such as households and long-term care facilities (LTCF), including nursing homes, assisted living, and group homes, said Stefan Gravenstein, Professor of Geriatric Medicine and Director of the Division of Geriatrics and Palliative Care, Brown University, Rhode Island, USA; and Lynn McNicoll, Professor of Medicine and Director of Education for the Division of Geriatrics, Brown University, Rhode Island, USA. They highlighted that vulnerable groups, such as older adults, immunocompromised individuals, postoperative patients, patients receiving chemotherapy, and those with underlying comorbidities, are often concentrated in congregate living environments,1 such as assisted living, group homes, and nursing homes. This can create repeated close-contact interactions, thereby multiplying the risk of transmission.

An estimated 75% of adults in the US are considered to be at increased risk of severe COVID-19, having at least one increased-risk condition.2 Those who are at risk and develop COVID-19 are more likely to experience serious outcomes, including hospitalization, ICU admission, intubation or mechanical ventilation, and death.3,4 In addition, SARS-CoV-2 infection in vulnerable patients increases hospitalizations, disrupts chronic care, and worsens overall health outcomes.4,5 Even mild COVID-19 may exacerbate pre-existing chronic conditions, contributing to increased morbidity and mortality.6-13 Key risk factors for severe COVID-19 include age, underlying medical conditions, vaccination status, and sociodemographic factors.2,3 Older age (≥65 years) is a major risk factor, although increased risk is also observed from 50 years onwards.2,3 Clinical risk conditions include cancer, chronic kidney disease, COPD, obesity, serious heart conditions, and Type 2 diabetes.4 Additional high-risk conditions include neurological, respiratory, and cardiovascular disorders, as well as acute kidney injury.6-13 Individuals who are unvaccinated or not up to date on vaccinations are also at increased risk of severe outcomes.3 

Sociodemographic factors, including race, ethnicity, and socioeconomic status, further contribute to disparities in COVID-19 severity.3 Not only are care settings prone to higher risk of transmission, but vulnerable patients in these environments are often also at greater risk of severe outcomes after developing COVID-19.3 

SARS-CoV-2 Transmission: Indirect Risk

McNicoll emphasized that the transmission risk of SARS-CoV-2 extends beyond vulnerable patients. Intimate, prolonged contact between patients/residents and caregivers, such as around-the-clock care, bathing, and feeding, increases the likelihood of caregivers acquiring and spreading SARS-CoV-2, including to other LTCF residents and their own families. Gravenstein added that in nursing homes, staff members providing care to multiple residents can further amplify the transmission risk. Moreover, up to four in 10 household contacts experience a SARS-CoV-2 infection, with household secondary attack rates at 43–47%.14,15 This in turn fuels transmission to the wider community, explained the speakers. Early intervention is, therefore, critical to protect high-risk populations as well as those around them. Recognizing both those at direct risk and those likely to transmit infection in the primary care setting is essential to identifying appropriate candidates for PEP.

Evolving Strains and Increased Transmissibility

Both experts noted that evolving variants of SARS-CoV-2, particularly Omicron, have higher transmissibility and reinfection rates.14,15 Omicron has a reported higher household secondary attack rate (42.7%), compared to the earlier alpha variant (36.4%).14,15 Omicron is also associated with 1.8 times higher hospitalization rates compared with the earlier delta strain, even while causing milder illness, due to the higher number of infections caused.16    The variable incubation period of Omicron, which is commonly 3–5 days depending on the strain, creates a narrow critical window for optimal intervention,17,18 Gravenstein emphasized. He explained that this makes prompt assessment and diagnosis critical for PEP to be effective, with optimal timing varying depending on the antiviral agent used. He highlighted the rapid evolution of SARS-CoV-2, particularly within the Omicron lineage, noting the emergence of the Omicron sublineage BA.3.2 in late 2024. By February 2026, BA.3.2 had been detected in wastewater samples from 25 US states and had been reported in at least 23 countries.19 Experts concluded that the overarching message should be to remain vigilant. Early identification and post-exposure intervention are crucial to prevent spread and reduce transmission risk and disease burden, they said.

The Importance of Early Intervention: Post-exposure Prophylaxis

Both experts emphasized the importance of early PEP intervention in those exposed to SARS-CoV-2, with the aim of protecting vulnerable populations and reducing transmission in high-risk settings.20-22 Utilization of oral antiviral PEP in the early stages of COVID-19 may reduce the viral load, duration of symptoms experienced, and risk of developing severe illness and long COVID, offering meaningful clinical benefit and reduced risk of transmission.23-34 

Both experts agreed they had observed a shift in the attitudes of patients contracting SARS-CoV-2 from the start of the pandemic to today, including a reduced urgency around COVID-19 results and delays to testing and seeking treatment, with individuals not considering reaching out to their primary care doctors. As a result, people with suspected infection may delay testing or not test at all when symptoms develop. They noted that this prevention gap is a practical, real-world challenge, particularly important for those in high-contact settings and households.

After exposure to SARS-CoV-2, as with other respiratory diseases such as influenza, there is a critical period early in the viral replication cycle in which interventions such as antivirals are most effective and may reduce transmission (Figure 1).35-37 The experts noted that this is of particular importance to prevent outbreaks in high-exposure settings, which are associated with high-risk populations.38 Through early intervention in pre-symptomatic patients, primary care physicians may be able to protect vulnerable patients.

Figure 1: Antiviral intervention is most effective early in the viral replication cycle.35-37
PEP: post-exposure prophylaxis.

 

In a similar context of influenza, PEP administered immediately after exposure may suppress viral load,39 reduce secondary household transmission, and slow community spread.40,41 

Overcoming Barriers to Prompt Treatment in Primary Care

While primary care practitioners may not necessarily come into contact with high-risk patients on a regular basis, they are more likely to encounter members of households or caregivers who are likely to be in contact with those individuals. Therefore, experts noted it is imperative that they focus on identifying candidates for PEP to help manage the risk of further exposure and transmission.

Both experts highlighted the need for rapid, on-site point-of-care testing in primary practice. Using multiplex PCR, which can distinguish COVID-19 from respiratory syncytial virus or flu, clinicians can act during the visit and administer PEP rather than waiting for delayed lab results from external providers, Gravenstein and McNicoll noted. They emphasized the importance of a prompt response, as delays can increase hospitalizations and mortality.34 Study results suggest that early antiviral treatment, as soon as possible after infection onset, is needed to mitigate transmission, preventing 50% more infections compared to late treatment (started 3–5 days after symptom onset).34

With optimal PEP delivery shown to occur immediately after exposure in influenza studies, McNicoll and Gravenstein emphasized the overarching importance of acting quickly in similar contexts, including for SARS-CoV-2.39-41 They also stressed that ensuring it is simple to prescribe would enable early intervention when it is most effective. Patients in LTCF settings and those interacting with vulnerable individuals should be prioritized, they added.

Real-World Implementation into Clinical Workflow

Rapidity of PEP delivery is reliant on confirmed exposure to SARS-CoV-2, for which the experts recommended a clinic-based nucleic acid amplification test or multiplex testing, with repeated testing if results are negative but suspicion remains. Both experts reiterated that rapid in-clinic testing is preferable to waiting for results from an external center.

Considering real-world use of PEP in geriatric patients, they noted the importance of oral antiviral medications that are suitable for use in frail, older individuals and with minimal drug–drug interactions. They also noted that clinical trials often assess efficacy in younger, healthy individuals, meaning it can be difficult to extrapolate to older patients presenting in clinical practice who may be on a range of drugs. This can sometimes result in prescriber reluctance.

In addition, both experts maintained that the usefulness of non-pharmacologic measures should not be underestimated. Masking, handwashing, general hygiene, and isolation, where feasible, should always be implemented if COVID-19 is suspected, even if tests are negative.

Clinical Profiles of Emerging Post-exposure Prophylaxis

Both experts recognized the promise of emerging oral antivirals to provide protection for at-risk groups, particularly in those where vaccine efficacy may be waning or limited.42 Clinical trials have shown potential, but certain agents are not yet approved in the US for PEP, they noted. McNicoll emphasized that, when evaluating clinical outcomes for COVID-19 PEP, clinicians are interested not only in whether a patient develops COVID-19, but also in disease severity, symptom duration, and the need for hospitalization.18,21,22 

SCORPIO-PEP Study

Ensitrelvir is currently under investigation for the prevention of symptomatic SARS-CoV-2 infection in household contacts of an individual with symptomatic COVID-19.18,43 In the SCORPIO-PEP trial, when treatment was started within 72 hours of symptom onset in the index patient, ensitrelvir was effective in significantly protecting household contacts from COVID-19, including those at high risk. The investigational drug was well tolerated, with no new safety concerns, suggesting potential for other settings with high-risk populations.18,43 

Oral Nirmatrelvir-Ritonavir PEP

Nirmatrelvir/ritonavir has been assessed for efficacy and safety as PEP in asymptomatic household contacts with COVID-19 when administered within 96 hours for 5 or 10 days. In a Phase II-III double-blind trial (n=2,736), PEP with nirmatrelvir/ritonavir for either 5 or 10 days did not significantly reduce confirmed symptomatic COVID-19 compared with placebo.18,21 

Oral Molnupiravir (MOVe-AHEAD) The Phase III household prevention trial with molnupiravir (MOVe-AHEAD) was a randomized, controlled, double-blind Phase III trial comparing molnupiravir with placebo (n=763). The primary efficacy endpoint was the incidence of COVID-19 through Day 14 in modified intent-to-treat participants without detectable COVID-19 at baseline. It was found that molnupiravir was well tolerated, but did not meet the prespecified superiority criterion as a PEP.44 

Conclusion and Future Outlook

COVID-19 continues to pose a significant risk to vulnerable populations, particularly those in congregate living facilities and those with at-risk characteristics. Paired with evolving, more transmissible disease variants and a waning awareness within the general population, it is crucial for primary care physicians to remain vigilant in their practice: vaccination, rapid testing, and masking remain essential to ensure robust management and prevention of the spread of SARS-CoV-2. Recognizing both indirect and direct risk, particularly for those in high-contact care settings, is key to reducing transmission and protecting those most at risk from hospitalization or severe outcomes. Looking ahead, emerging PEP strategies may help address persistent prevention gaps in high-risk settings, subject to further evidence generation and regulatory review.

References
McMichael TM et al. Epidemiology of COVID-19 in a long-term care facility in King County, Washington. N Engl J Med. 2020;382(21):2005-11. Ajufo E et al. U.S. population at increased risk of severe illness from COVID-19. Am J Prev Cardiol. 2021;6:100156. Centers for Disease Control and Prevention (CDC). Underlying conditions and the higher risk for severe COVID-19. Available at: https://www.cdc.gov/covid/hcp/clinical-care/underlyingconditions.html. Last accessed: April 13 2026. Li Y et al. Impact of SARS-CoV-2 infection on clinical characteristics, antibody levels, and immune responses in patients with malignant hematological tumors. J Chemother. 2026;38(1):54-65. Hanson HA et al. A systematic review: impact of SARS-CoV-2 infection on morbidity, mortality, and viral suppression in patients living with HIV. SN Compr Clin Med. 2023;5(1):144. Centers for Disease Control and Prevention (CDC). Long COVID or Post-COVID conditions. Available at: https://www.cdc.gov/covid/long-term-effects/index.html. Last accessed: April 14 2026. Marsters CM et al. Increased frequency and mortality in persons with neurological disorders during COVID-19. Brain. 2024;147(7):2542-51. Conway SE et al. COVID-19 severity is associated with worsened neurological outcomes in multiple sclerosis and related disorders. Mult Scler Relat Disord. 2022;63:103946. Di Iorio M et al. DMARD disruption, rheumatic disease flare, and prolonged COVID-19 symptom duration after acute COVID-19 among patients with rheumatic disease: a prospective study. Semin Arthritis Rheum. 2022;55:152025. Chiner-Vives E et al. Short and long-term impact of COVID-19 infection on previous respiratory diseases. Arch Bronconeumol. 2022;58(Suppl 1):39-50. Pepera G et al. Epidemiology, risk factors and prognosis of cardiovascular disease in the coronavirus disease 2019 (COVID-19) pandemic era: a systematic review. Rev Cardiovasc Med. 2022;23(1):28. Nugent J et al. Assessment of acute kidney injury and longitudinal kidney function after hospital discharge among patients with and without COVID-19. JAMA Netw Open. 2021;4(3):e211095. Sarin SK et al. Pre-existing liver disease is associated with poor outcome in patients with SARS CoV2 infection; the APCOLIS study (APASL COVID-19 Liver Injury Spectrum Study). Hepatol Int. 2020;14(5):690-700. Baker JM et al. Household transmission of SARS-CoV-2 in five US jurisdictions: comparison of delta and omicron variants. PLoS One. 2025;20:e0313680. Madewell ZJ et al. Household secondary attack rates of SARS-CoV-2 by variant and vaccination status: an updated systematic review and meta-analysis. JAMA Netw Open. 2022;5:e229317. Iuliano AD et al. Trends in disease severity and health care utilization during the early omicron variant period compared with previous SARS-CoV-2 high transmission periods — United States, December 2020–January 2022. MMWR Morb Mortal Wkly Rep. 2022;71:146-52. Del Águila-Mejía J et al. Secondary attack rate, transmission and incubation periods, and serial interval of SARS-CoV-2 omicron variant, Spain. Emerg Infect Dis. 2022;28(6):1224-8. Hayden FG et al. Ensitrelvir to prevent COVID-19 in households: SCORPIO-PEP Phase 3 placebo-controlled trial results. Abstract 200. CROI, March 9-12, 2025. Shakya M et al. Centers for Disease Control and Prevention (CDC) Morbidity and Mortality Weekly Report (MMWR). Early Detection and Surveillance of the SARS-CoV-2 Variant BA.3.2 — Worldwide, November 2024–February 2026. 2026. Available at: https://www.cdc.gov/mmwr/volumes/75/wr/mm7510a1.htm#:~:text=Abstract,by%20at%20least%2023%20countries. Last accessed: April 12 2026. Mitjà O, Clotet B. Use of antiviral drugs to reduce COVID-19 transmission. Lancet Glob Health. 2020;8(5):e639-40. Hammond J et al. Oral nirmatrelvir–ritonavir as postexposure prophylaxis for Covid-19. N Engl J Med. 2024;391(3):224-34. Ohmagari N et al. Efficacy and safety of ensitrelvir for asymptomatic or mild COVID-19: an exploratory analysis of a multicenter, randomized, phase 2b/3 clinical trial. Influenza Other Respir Viruses. 2024;18(6):e13338. Chu WM et al. Comparison of safety and efficacy between Nirmatrelvir-ritonavir and molnupiravir in the treatment of COVID-19 infection in patients with advanced kidney disease: a retrospective observational study. EClinicalMedicine. 2024;72:102620. Wang W et al. Paxlovid use is associated with lower risk of cardiovascular diseases in COVID-19 patients with autoimmune rheumatic diseases: a retrospective cohort study. BMC Med. 2024;22(1):117. Cai H et al. Paxlovid for hospitalized COVID-19 patients with chronic kidney disease. Antiviral Res. 2023;216:105659. Wu J et al. Early antiviral treatment contributes to alleviate the severity and improve the prognosis of patients with novel coronavirus disease (COVID-19). J Intern Med. 2020;288(1):128-38. Platzer M et al. The effect of early remdesivir administration in COVID-19 disease progression in hospitalised patients. Wien Klin Wochenschr. 2024;136(15-16):458-64. Hammond J et al. Oral nirmatrelvir for high-risk, nonhospitalized adults with COVID-19. N Engl J Med. 2022;386(15):1397-408. Colaneri M et al. Impact of early antiviral therapy on SARS-CoV-2 clearance time in high-risk COVID-19 subjects: a propensity score matching study. Int J Infect Dis. 2024;149:107265. Jiang J et al. Early use of oral antiviral drugs and the risk of post COVID-19 syndrome: a systematic review and network meta-analysis. J Infect. 2024;89(2):106190. Drysdale M et al. Impact of treatment of COVID-19 with sotrovimab on post-acute sequelae of COVID-19 (PASC): an analysis of National COVID Cohort Collaborative (N3C) data. Infection. 2025;DOI:10.1007/s15010-025-02505-z. Lin SN et al. Effectiveness of potential antiviral treatments in COVID-19 transmission control: a modelling study. Infect Dis Poverty. 2021;10(1):53. Bai Y et al. Public health impact of paxlovid as treatment for COVID-19, United States. Emerg Infect Dis. 2024;30(2):262-9. Matrajt L et al. Could widespread use of antiviral treatment curb the COVID-19 pandemic? A modeling study. BMC Infect Dis. 2022;22(1):683. Gonçalves A et al. Timing of antiviral treatment initiation is critical to reduce SARS-CoV-2 viral load. CPT Pharmacometrics Syst Pharmacol. 2020;9(9):509-14. Lee N et al. Viral loads and duration of viral shedding in adult patients hospitalized with influenza. J Infect Dis. 2009;200(4):492-500. Puhach O et al. SARS-CoV-2 viral load and shedding kinetics. Nat Rev Microbiol. 2023;21(3):147-61. Ma BHM et al. Clinical outcomes following treatment for COVID-19 with nirmatrelvir/ritonavir and molnupiravir among patients living in nursing homes. JAMA Netw Open. 2023;6(4):e2310887. Zaaraoui H et al. Modelling the effectiveness of antiviral treatment strategies to prevent household transmission of acute respiratory viruses. PLoS Comput Biol. 2024;20(12):e1012573. Germann TC et al. Mitigation strategies for pandemic influenza in the United States. Proc Natl Acad Sci USA. 2006;103(15):5935-40. Ikematsu H et al. Baloxavir marboxil for prophylaxis against influenza in household contacts. N Engl J Med. 2020;383(4):309-20. Chemaitelly H, Abu-Raddad LJ. Waning effectiveness of COVID-19 vaccines. Lancet. 2022;399(10327):771-3. Shionogi. Phase 3 study of S-217622 in prevention of symptomatic SARS-CoV-2 infection (SCORPIO-PEP). NCT05897541. https://clinicaltrials.gov/study/NCT05897541 Alpizar SA et al. Molnupiravir for intra-household prevention of COVID-19: the MOVe-AHEAD randomized, placebo-controlled trial. J Infect. 2023;87(5):392-402.

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