Ad
related to: bmj open guidelines for nurses practice manual
Search results
Results From The WOW.Com Content Network
BMJ Best Practice is an online decision-support tool made for clinical decision making support. It was created in 2009 by BMJ. [1] Development
BMJ Open is a peer-reviewed open access medical journal that is dedicated to publishing medical research from all disciplines and therapeutic areas. [1] It is published by BMJ and considers all research study types, from protocols through phase I trials to meta-analyses, including small, specialist studies, and negative studies.
Plates vi & vii of the Edwin Smith Papyrus (around the 17th century BC), among the earliest medical guidelines. A medical guideline (also called a clinical guideline, standard treatment guideline, or clinical practice guideline) is a document with the aim of guiding decisions and criteria regarding diagnosis, management, and treatment in specific areas of healthcare.
The PRISMA flow diagram, depicting the flow of information through the different phases of a systematic review. PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) is an evidence-based minimum set of items aimed at helping scientific authors to report a wide array of systematic reviews and meta-analyses, primarily used to assess the benefits and harms of a health care ...
The NGC aimed to provide physicians, nurses, and other health professionals, health care providers, health plans, integrated delivery systems, purchasers and others an accessible mechanism for obtaining objective, detailed information on clinical practice guidelines and to further their dissemination, implementation and use.
Biomedical information must be based on reliable, third-party published secondary sources, and must accurately reflect current knowledge.This guideline supports the general sourcing policy with specific attention to what is appropriate for medical content in any Wikipedia article, including those on alternative medicine.
A similar guideline for clinical trials of medical devices is the international standard ISO 14155, which is valid in the European Union as a harmonized standard. These standards for clinical trials are sometimes referred to as ICH-GCP or ISO-GCP to differentiate between the two and the lowest grade of recommendation in clinical guidelines.
A 2005 systematic review found "Decision support systems significantly improved clinical practice in 68% of trials."' The CDSS features associated with success included integration into the clinical workflow rather than as a separate log-in or screen, electronic rather than paper-based templates, providing decision support at the time and ...