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. 2023 Jul 26;22:188. doi: 10.1186/s12933-023-01911-7

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Kaplan–Meier curve of the incidence probability for the primary and secondary outcomes. No significant difference was observed in the incidence probability of the primary outcome between new dapagliflozin and empagliflozin users among patients with type 2 diabetes A. The primary outcomes included heart failure-related events, myocardial infarction, ischemic stroke, and cardiovascular death. Regarding the secondary outcomes, the risks of heart failure-related events B, ischemic stroke C, myocardial infarction D, and cardiovascular death E were compared