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. 2023 Jul 24;12(8):2087–2102. doi: 10.1007/s40121-023-00845-7

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 2 — Kaplan–Meier charts of all-cause 28-day mortality for the main cohort (A) and the PSM cohort (B), risk of progressing to a critical condition for the main cohort (C) and the PSM cohort (D), and T_FNANC for the main cohort (E) and the PSM cohort (F) of azvudine recipients versus nirmatrelvir-ritonavir recipients. PSM propensity-score matching; T_FNANC time to first nucleic-acid negative conversion