Improve Research Reproducibility A Bio-protocol resource
- Home
- Protocols
-
Ask a
question
Favorite
All data were collected retrospectively through the respective electronic patient database system of the ICUs. Each eligible patient was checked for availability of full IBPM at 60 min before and 90 min after each push-dose application of Landiolol (some patients had received several applications with a maximum of four), and in this interval, BP values (every minute) and HR values (prior and post-push-dose) were collected by an information technology specialist.
Copyright and License information: ©2023 by the authors.
Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.
Post a Question0 Q&A
