Draft guidance
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1 Recommendations
1.1 Nirmatrelvir plus ritonavir is recommended as an option for treating COVID-19 in adults, only if they:
have an increased risk for progression to severe COVID-19, as defined in the independent advisory group report commissioned by the Department of Health and Social Care.
Why the committee made this recommendation
This evaluation reviews the clinical and cost effectiveness of nirmatrelvir plus ritonavir for mild COVID-19. Most of the clinical evidence for this treatment is highly uncertain because it comes from studies done before the dominant Omicron variants of SARS-CoV-2 (the virus that causes COVID‑19).
The cost-effectiveness estimates are highly dependent on how well the treatment works compared with standard care, and hospitalisation and mortality rates. Hospitalisation and mortality rates are lower with Omicron variants than earlier variants in the pandemic. They also get lower as the risk of severe COVID-19 decreases. These lower rates increase the cost-effectiveness estimates.
Clinical evidence suggests that nirmatrelvir plus ritonavir is effective at treating mild COVID-19 compared with standard care.
The independent advisory group report commissioned by the Department of Health and Social Care defines people with the highest risk of progression to severe COVID-19. Nirmatrelvir plus ritonavir is recommended for treating COVID-19 in these groups because the likely cost-effectiveness estimates are within what NICE considers an acceptable use of NHS resources.
The Therapeutics Clinical Review Panel modelling group findings on risk of severe COVID-19 outcomes identifies additional groups of people with an increased risk of severe COVID-19. But, the likely cost-effectiveness estimates for nirmatrelvir plus ritonavir in these groups are above what NICE considers an acceptable use of NHS resources.
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