In 2011, all clinical departments at The Ottawa Hospital (TOH) were encouraged to create a structured process to review and manage quality of care and patient safety matters relevant to each department’s clinical area of focus. The Department of Anesthesiology and Pain Medicine at TOH delivers clinical care for > 30,000 inpatient and outpatient procedures each year across a multi-campus academic health sciences centre setting. The department consists of 83 full-time equivalent staff anesthesiologists, 68 residents/fellows, and 16 anesthesia assistant respiratory therapists (AART).
Use of the existing institution-wide incident reporting system (patient safety learning system [PSLS], Datix Ltd, London, UK), which had been recently introduced at TOH, became a central focus for QPS activities in each department at that time. The PSLS is a hospital-wide, electronic incident reporting platform accessible on TOH computers to all hospital employees, physicians, and trainees. The software uses free text and dropdown menus to characterize and direct the reports accordingly for review. The reports are reviewed by TOH employees/physicians with a QPS role in the department/clinical care area where the report originated. If needed, reviewers from other departments/care areas can be “actioned” or contacted through the PSLS platform to provide a multidisciplinary perspective of the event. The PSLS reviewers are notified by email that a report has been entered in their respective care area. The event reporter (i.e., person who entered the event) receives a notification email that the report has been directed for review and can access the PSLS to follow the progress of the report including any subsequent actions that are derived from the review. The event reporter’s name is available to PSLS reviewers to facilitate further discussion of the event, if needed.
The current CAS Guidelines identify and encourage adverse event reporting systems as one way to monitor quality of anesthetic care throughout the healthcare facility.5 Review of the PSLS reports informs much of our QPS committee’s focus and direction to identify, assess, and manage threats to patient safety at our centre. Reporting patient safety events for review by a predetermined body of peers (such as members of a QPS committee) provides a local granular perspective and interpretation that national and international incident reporting databases may not be able to achieve. It is important, however, to juxtapose and compare one’s local reports with the trends noted elsewhere for a balanced, complimentary view of safety matters in the perioperative domain. In addition, the local reporting system also generates an invaluable source of peer-vetted cases to aid the conduct of morbidity and mortality rounds, another feature of monitoring quality of anesthesia care identified in the Guidelines.5
For anesthesia departments without an established infrastructure for reporting and reviewing events, the recently launched Canadian Anesthetic Incident Reporting System (CAIRS)6 will hopefully foster and facilitate a reporting culture in perioperative medicine to improve systems of care. Like any reporting system, CAIRS is a tool that may provide feedback and information about events to support quality and safety improvement at the department, hospital, and health-system levels of care. Nevertheless, like any tool, its products and outputs should be interpreted, reviewed, and applied by the appropriate healthcare professionals who are knowledgeable about the intricacies of their own local care environment.
At our centre, when a report is entered into the PSLS, a predetermined group of departmental QPS clinical reviewers (who are staff anesthesiologists) receive an email notification that an event is available for review. In the PSLS report, the patient’s medical chart number is listed, enabling the reviewer to access the patient’s electronic medical record for further details of the event and care the patient received. The PSLS clinical reviewers from each TOH campus (two staff anesthesiologists from each inpatient campus and one staff anesthesiologist from the outpatient campus) evaluate the PSLS reports submitted from their respective site. Each case is then considered for presentation and discussion by the committee at the monthly QPS committee meeting. If system and/or cognitive issues are involved in the event, further discussion of the case is warranted at the committee level. Case specifics are further expanded upon as necessary by the clinical reviewer at the monthly QPS committee meeting. During discussion of the PSLS reports, the QPS committee determines next steps and/or actions (if appropriate) for the cases reviewed. Specifically, the QPS committee assesses if a threat to quality/patient safety exists and if remediable actions are feasible to prevent future occurrences. The mode of dissemination of the information learned from case review to perioperative colleagues is also considered. If there are system and/or cognitive issues that merit presentation of the report, the event is added to the list of possible cases for presentation at “QPS rounds” (departmental morbidity and mortality rounds).
The committee selects suitable PSLS cases for “QPS rounds”, presented using the Ottawa Morbidity and Mortality Model (OM3)7 format, which occur every six to twelve weeks within our department’s grand rounds schedule. An overview of PSLS report management via the QPS committee is provided in Fig. 1.
The QPS committee functionality is in keeping with institutional policies and Ontario provincial law8 surrounding collection, use, and disclosure of personal health information (PHI) to improve the quality of healthcare services provided. While our QPS committee model is designed for quality improvement and safety assessment, some of the experiences and learnings derived from our QPS committee reviews and audits may generate novel data worthy of publication. Though detailed explanation of the ethics review process for data derived from QPS-mediated access to PHI is beyond the scope of this article, the Chair of our local Research Ethics Board is consulted on a case-by-case basis about the type of ethics review indicated when disseminating findings external to our centre.