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Chest is a peer-reviewed medical journal covering chest diseases and related issues, including pulmonology, cardiology, thoracic surgery, transplantation, breathing, airway diseases, and emergency medicine. The journal was established in 1935. It is the official journal of the American College of Chest Physicians which publishes
Biological Abstracts is a database produced by Clarivate Analytics. It includes abstracts from peer-reviewed academic journal articles in the fields of biology , biochemistry , biotechnology , botany , pre-clinical and experimental medicine , pharmacology , zoology , agriculture , and veterinary medicine , and has been published since 1926.
PubMed Central (PMC) is a free digital repository that archives open access full-text scholarly articles that have been published in biomedical and life sciences journals. As one of the major research databases developed by the National Center for Biotechnology Information (NCBI), PubMed Central is more than a document repository.
Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot of that product may be recalled.
This is accomplished with access to indexed journal content from Biological Abstracts, and supplemental indexed non-journal content from Biological Abstracts/Reports, Reviews, Meetings (BA/RRM or Biological Abstracts/RRM) and the major publications of BIOSIS. This coverage includes literature in pre-clinical and experimental research, methods ...
Abstract submission involves the authors in preparing their abstracts and sending them to the conference organisers through an online form. The abstracts are either uploaded as documents (typically Microsoft Word, PDF or LaTeX) or, where graphics and tables are not required, they may simply be entered into the form as plain text. The software ...
This article needs to be updated.The reason given is: the section related to E.U. needs further updates (esp. in sections 3.2 and 4.2.2) as the directives 93/42/EEC on medical devices and 90/385/EEC on active implantable medical devices have been fully repealed on 26 May 2021 by Regulation (EU) no. 2017/745 (MDR); furthermore, Brexit triggers updates in these sections (U.K. developed their own ...
The LUCAS device delivers high-quality compressions at a continuous rate, while up to a third of manual compressions can be incorrect. [9] In 2013, a 68-year-old male made a complete recovery, including no intellectual or neurological deficits, after an out-of-hospital cardiac arrest after 59 minutes of mechanical compressions on a LUCAS device.