Symptoms, viral loads, and rebound among COVID-19 outpatients treated with nirmatrelvir/ritonavir compared to propensity score matched untreated individuals
Supporting Files
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11 14 2023
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File Language:
English
Details
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Alternative Title:Clin Infect Dis
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Personal Author:Smith-Jeffcoat, Sarah E. ; Biddle, Jessica E. ; Talbot, H. Keipp ; Morrisey, Kerry Grace ; Stockwell, Melissa S. ; Maldonado, Yvonne ; McLean, Huong Q. ; Ellingson, Katherine D. ; Bowman, Natalie M. ; Asturias, Edwin ; Mellis, Alexandra M. ; Johnson, Sheroi ; Kirking, Hannah L. ; Rolfes, Melissa A.R. ; Olivo, Vanessa ; Merrill, Lori ; Battan-Wraith, Steph ; Sano, Ellen ; McLaren, Son H. ; Vargas, Celibell Y. ; Goodman, Sara ; Sarnquist, Clea C. ; Govindaranjan, Prasanthi ; Petrie, Joshua G. ; Belongia, Edward A. ; Ledezma, Karla ; Pryor, Kathleen ; Lutrick, Karen ; Bullock, Ayla ; Yang, Amy ; Haehnel, Quenla ; Rao, Suchitra ; Zhu, Yuwei ; Schmitz, Jonathan ; Hart, Kimberly ; Grijalva, Carlos G. ; Salvatore, Phillip P.
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Description:Background:
Nirmatrelvir/ritonavir (N/R) reduces severe outcomes among patients with COVID-19; however, rebound after treatment has been reported. We compared symptom and viral dynamics in community-based individuals with COVID-19 who completed N/R and similar untreated individuals.
Methods:
We identified symptomatic participants who tested SARS-CoV-2 positive and were N/R eligible from a COVID-19 household transmission study: index cases from ambulatory settings and their households were enrolled, collecting daily symptoms, medication use, and respiratory specimens for quantitative PCR for 10 days, March 2022—May 2023. Participants who completed N/R (treated) were propensity score matched to untreated participants. We compared symptom rebound, viral load (VL) rebound, average daily symptoms, and average daily VL by treatment status measured after N/R completion or, if untreated, seven days after symptom onset.
Results:
Treated (n=130) and untreated participants (n=241) had similar baseline characteristics. After treatment completion, treated participants had greater occurrence of symptom rebound (32% vs 20%; p=0.009) and VL rebound (27% vs 7%; p<0.001). Average daily symptoms were lower among treated participants compared to untreated participants without symptom rebound (1.0 vs 1.6; p<0.01), but not statistically lower with symptom rebound (3.0 vs 3.4; p=0.5). Treated participants had lower average daily VLs without VL rebound (0.9 vs 2.6; p<0.01), but not statistically lower with VL rebound (4.8 vs 5.1; p=0.7).
Conclusions:
Individuals who completed N/R experienced fewer symptoms and lower VL but were more likely to have rebound compared to untreated individuals. Providers should still prescribe N/R, when indicated, and communicate possible increased rebound risk to patients.
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Subjects:
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Source:Clin Infect Dis. 78(5):1175-1184
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Pubmed Central ID:PMC11090981
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Document Type:
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Funding:
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Volume:78
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Issue:5
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Collection(s):
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Main Document Checksum:urn:sha256:a36ec3f032ead5500c55093b9d36fa05c6fa4c1966ce95e44bef55dece6b4ec3
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Download URL:
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File Type:
Supporting Files
File Language:
English
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