# COVID-19 clinical rebound after treatment with nirmatrelvir/ritonavir

**Authors:** Daniel Camp, Matthew Caputo, Fabiola Moreno Echevarria, Chad J. Achenbach

PMC · DOI: 10.21203/rs.3.rs-4497916/v1 · 2024-06-21

## TL;DR

Some people experience a return of symptoms after taking nirmatrelvir/ritonavir for mild-to-moderate COVID-19, but the rebound is generally mild.

## Contribution

This study quantifies the frequency and characteristics of clinical rebound after NM/r treatment in routine clinical care.

## Key findings

- 6% of patients experienced a clinical rebound after NM/r treatment.
- Clinical rebound occurred a median of 11 days after starting treatment.
- Rebound was generally mild, with only one patient requiring hospitalization.

## Abstract

Nirmatrelvir/ritonavir (NM/r) is a safe and effective oral antiviral therapeutic used for treatment of mild-to-moderate COVID-19. Case reports described a clinical rebound syndrome whereby individuals experience a relapse of symptoms shortly after completing successful treatment. There is a lack of information on frequency of COVID-19 rebound after NM/r in routine clinical care, contributing factors, and clinical outcomes.

We reviewed electronic medical records to verify COVID-19 diagnosis, symptoms, and treatment with NM/r from January-June 2022. We defined COVID-19 clinical rebound as clear improvement in symptoms followed by recurrence or worsening of symptoms within 30 days of a five-day course of NM/r.

We studied 268 adults with median age 57 (IQR 47, 68), 80% White race, 85% non-Hispanic ethnicity, 55% female, 80% vaccinated and boosted against SARS-CoV-2, and 68% with any co-morbidity. Sixteen (6.0%) of studied patients were determined to have COVID-19 clinical rebound. The median time from starting NM/r to rebound was 11 days (IQR 9, 13). Notable demographic and clinical factors with higher proportion (not statistically significant) among COVID-19 rebound patients were female sex (75% rebound vs 54.5% no rebound), Black race (12.5% rebound vs 4.9% no rebound), presence of at least one co-morbidity (81.3% rebound vs 67.5% no rebound), and lack of prior SARS-CoV-2 infection (100% rebound vs 92.9% no rebound). Only one patient (6.25%) was hospitalized after COVID-19 rebound.

COVID-19 clinical rebound after treatment with NM/r is mild with favorable outcomes and more common than previously reported from real-world clinical care studies.

## Linked entities

- **Chemicals:** nirmatrelvir (PubChem CID 155903259), ritonavir (PubChem CID 5076)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** COVID-19 (MESH:D000086382)
- **Chemicals:** NM/r (MESH:C000719967)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11213215/full.md

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Source: https://tomesphere.com/paper/PMC11213215