PPT-Investigation into Significant Anesthesia Adverse Events during the Post-Op Period

Research by Ryan Dietz RNAI Stephen Both RNAI Gonzaga University Providence Sacred Heart Medical Center March 20 2014 Methodology Retrospective Chart Review At PHSMC Populations Strokes . What is sedation The anesthesia you are given is based on your health history the procedure and your choices Local produces a loss of feeling to a small specific area of the body A shot is given to numb the area Regional produces a loss of feeling t (BEYOND NEWBORN). DANIEL E. LEE, MD PhD. Associate Clinical Professor of Anesthesiology and Pediatrics. University of California, San Diego. PEDIATRIC PERIOPERATIVE RISK. Pediatric . Perioperative. Cardiac Arrest registry (POCA). OBJECTIVES. Describe Adverse Events, Risks and Problems that can Occur in . H. uman . S. ubjects . R. esearch . C. ompliance with Safety . R. eporting . R. egulations in Clinical Research. Identify Current Systems of Patient Care and Patient Safety in Research. . Zarif Jabbar-Lopez, MBBS, MPH. FY2, East of England Deanery. Visiting Research Fellow, Uppsala Monitoring Centre. Disclosure. No conflicts of interest. The . research leading to these results was conducted as part of the PROTECT consortium (. Which Form 4 to Use?. Reason for Reporting Unanticipated Problems. “to assure the protection of the rights and welfare of the human subjects”. UTHSC IRB Submission Forms. 4a: Reportable local adverse events. LOCALIZED I-84 DANBURY IMPROVEMENTS.  . An EA as described in . Section 1508.9 of CEQ's NEPA Regulations. is a concise public document which has three defined functions: . it briefly provides sufficient evidence and analysis for determining whether to prepare an EIS;. regional anesthesia.  that blocks pain in a particular region of the . body. The . goal of an epidural is to provide . analgesia. , or pain . relief. , rather than . anesthesia,.  which leads to total lack of feeling. Epidurals block the nerve impulses from the lower spinal segments. This results in decreased sensation in the lower half of the body.. Reporting Requirements. Protocol References. Section. Title. 7.2. Safety-Related. Data Collection. 7.3. Expedited Adverse Event Reporting. Other References and Resources. 3. Manual for Expedited Reporting of Adverse Events to DAIDS (Version 2.0). S. Percy Ivy, MD. Associate Chief, Senior Investigator. Investigational Drug Branch, National Cancer Institute. ivyp@ctep.nci.nih.gov. . National Cancer Institute. . National Cancer Institute. Clinical and Institutional Disclosure of Adverse Events to Patients Call 1 of 2 Delivered May 21, 2012 updated to reflect directive’s reissue (October 31, 2018) Sponsoring Offices: National Center for Ethics in Health Care MODULE 3 Adverse events following immunizationOverviewUnder recommended conditions all vaccines used in national immunization programmes are safe and e31ective if used correctly In practice however no Problems, and Protocol Deviations. Kathleen O’Malley RN, BSN, CCRP. Manager of Education and Training. Jefferson Clinical Research Institute. Kathleen.omalley@jefferson.edu. 1. Learning Objectives: Adverse Events. : Overview for Healthcare Providers Page 1 of 2 V DH/OEPI/DSI Febr uary 2019 Virginia Department of Health Vaccinia Disease and Vaccinia Adverse Events : Overview for Healthcare Providers Organism Investigator Kick-off Meeting. January 30-31, Clearwater, Florida. Jodie Riley, MISM and Robert Silbergleit. Adverse Events. Adverse Events (AEs) are “. . . any . untoward. medical occurrence in a subject that was not previously identified which does not necessarily have a causal relationship to the study drug…” .