Clinical guideline development

Sandra S. Zaky, Lisa Bradfield, Caroline D. Patton, Alvin R. Cabrera, Benjamin D. Smith

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Medical societies and government agencies throughout the world create guidelines to optimize patient care based on the latest evidence. Guidelines reduce variability in practice and identify gaps in the evidence. A preliminary literature search is used to determine if a guideline should be written for a specific topic. A task force is then created, and clinical key questions are developed. Next, a systematic review is performed to characterize the existing evidence. Recommendations are developed based on the evidence, and supporting text is written. The quality of evidence and strength of recommendation for each recommendation are assigned using methods predetermined by the sponsoring organization. These steps are important to minimize bias in guideline creation and thereby enhance credibility.

Original languageEnglish (US)
Title of host publicationTranslational Radiation Oncology
PublisherElsevier
Pages537-542
Number of pages6
ISBN (Electronic)9780323884235
ISBN (Print)9780323884242
DOIs
StatePublished - Jan 1 2023

Keywords

  • Conflict of interest
  • Guidelines
  • Key questions
  • PICOTS
  • Quality of evidence
  • Strength of the recommendation

ASJC Scopus subject areas

  • General Agricultural and Biological Sciences
  • General Biochemistry, Genetics and Molecular Biology

Fingerprint

Dive into the research topics of 'Clinical guideline development'. Together they form a unique fingerprint.

Cite this