# Effectiveness of nirmatrelvir/ritonavir and molnupiravir in reducing the risk of short-term and long-term cardiovascular complications of COVID-19: a target trial emulation study

**Authors:** Zihao Guo, Yuchen Wei, Guozhang Lin, Katherine Min Jia, Christopher Boyer, Huwen Wang, Conglu Li, Chi Tim Hung, Carrie Ho Kwan Yam, Tsz Yu Chow, Shi Zhao, Kehang Li, Aimin Yang, Chris Ka Pun Mok, David SC Hui, Eng Kiong Yeoh, Ka Chun Chong

PMC · DOI: 10.1038/s41467-025-67776-4 · Nature Communications · 2025-12-21

## TL;DR

This study shows that nirmatrelvir/ritonavir reduces both short- and long-term cardiovascular risks from COVID-19 better than molnupiravir in hospitalized patients.

## Contribution

Demonstrates the long-term cardiovascular benefits of nirmatrelvir/ritonavir over molnupiravir in real-world hospitalized patients.

## Key findings

- Nirmatrelvir/ritonavir significantly lowers one-year cardiovascular mortality and complications.
- Molnupiravir reduces short-term cardiovascular risks but has limited long-term benefits.
- Nirmatrelvir/ritonavir is more effective than molnupiravir in preventing long-term cardiac issues.

## Abstract

While treatment with nirmatrelvir/ritonavir or molnupiravir is effective in lowering the rate of severe COVID-19, the effectiveness of these antivirals in reducing the risk of cardiovascular outcomes, especially among the hospitalized population, remains largely unknown. In this study, we assessed the real-world effectiveness of nirmatrelvir/ritonavir and molnupiravir on short- and long-term cardiovascular complications of COVID-19 using a target trial emulation design. Two target trials of COVID-19 antivirals were emulated by using a territory-wide, population-based, retrospective cohort of hospitalized patients in Hong Kong. Nine cardiovascular outcomes were evaluated in both short-term (day 0–21) and long-term (day 22–365) post-SARS-CoV-2 infection. Compared with the control group, the use of nirmatrelvir/ritonavir was associated with a significantly lower one-year risk of cardiovascular mortality, composite cardiovascular complications, major adverse cardiac events, cerebrovascular disorders, dysrhythmia, ischemic heart disease, and other cardiac disorders following infection. Molnupiravir use was associated with a short-term risk reduction in cardiovascular complications, but only a marginal risk reduction in long-term cardiovascular mortality among other complications. This study demonstrated the effectiveness of nirmatrelvir/ritonavir in reducing the risks of short- and long-term cardiovascular complications following a SARS-CoV-2 infection among the hospitalized population. Our findings suggested health-related benefits of prescribing nirmatrelvir/ritonavir over molnupiravir against severe cardiovascular post-acute sequelae of COVID-19 in the long term.

While antivirals like nirmatrelvir/ritonavir and molnupiravir are known to reduce severe COVID-19, their impact on cardiovascular outcomes is unclear. Here, the authors use a target trial emulation design to show that nirmatrelvir/ritonavir significantly lowers long-term cardiovascular risks among hospitalized patients, highlighting its potentials over molnupiravir for mitigating post-COVID-19 cardiovascular complications.

## Linked entities

- **Chemicals:** nirmatrelvir (PubChem CID 155903259), ritonavir (PubChem CID 5076), molnupiravir (PubChem CID 145996610)
- **Diseases:** COVID-19 (MONDO:0100096), ischemic heart disease (MONDO:0024644)

## Full-text entities

- **Diseases:** cardiac disorders (MESH:D006331), cardiovascular complications (MESH:D002318), dysrhythmia (MESH:D001145), cerebrovascular disorders (MESH:D002561), ischemic heart disease (MESH:D017202), cardiovascular post-acute sequelae of COVID-19 (MESH:D000094024), short-term and long-term cardiovascular complications of COVID-19 (MESH:D000088562), infection (MESH:D007239), COVID-19 (MESH:D000086382)
- **Chemicals:** Molnupiravir (MESH:C000656703), nirmatrelvir/ritonavir (MESH:C000719967)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12847700/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12847700/full.md

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Source: https://tomesphere.com/paper/PMC12847700