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The Medication Safety Self Assessment (MSSA) for Australian Hospitals 1st Survey @ Kyneton District Health August 2013 What is the MSSA? • Clinical Excellence Commission • Web-based survey tool • allows self assessment of the medication safety practices within a hospital • Heighten awareness of the distinguishing characteristics of a safe hospital medication system • 10 Key Elements, 20 Core Characteristics • 247 questions • create a baseline of Australian hospital efforts to enhance medication safety • identification of improvement opportunities and comparison with the aggregate experience of demographically similar hospitals (based on bed size/public/independent governance/general medical & surgical service/maternity/ENT/paediatrics/rural/internal clinical pharmacy service). • Completed by miniMAC working party Results: individual Results: similar demographics Quality Improvement Plan • Chose items where we scored C or below A= No Activity to implement B= Considered but not implemented C= Partially implemented in some or all areas • 30 targeted actions identified for Quality Improvement off this survey. • Re-survey every 2 years. Standard 4 Medication safety - governance and systems for medication safety 4.2 MSSA AUDIT August 2013 ACTION PLAN Safety Issue Identified + Date Action Required July 2013. VicTAG Safety notice – Neuromuscular Blocking Agents. Discuss at MAC Order warning stickers as per alert Take to UCC working Party for review of current NMBs in UCC & imprest stock of Suxamethonium in Acute. Neuromuscular blocking agents are not available as ward or imprest stock and/or in automated dispensing cabinets (except in operating room/anesthesia stock). If available in critical care units and/or the emergency department, neuromuscular blocking agents are sequestered from other ward or imprest stock medications (including those stocked in automated dispensing cabinets) and labelled with auxiliary warnings to clearly identify the drugs as respiratory paralysing agents that require mechanical ventilation when used. Responsibility + Timeframe Di- by end September 2013 Implementation Progress + Date Started 24/7/13 Draft to miniMAC 19/9/13 -need to expand on feedback & how that works through VHIMS. -new classification of incidents by Standard? -running reports? Discussed @ MAC 4th July. Sticker – listed on Baypac, not listed CH2 18/7/13 Stickers ordered from Baypac, sent to UCCWP agenda, red syringes placed with stock of Sux in Acute & UCC fridge. Stickers obtained 25/7/13. Discussed at UCCWP 8/8/13. Decision to remove all imprest stock except for Theatre. Recommendation made to UCCAC and MAC. Decision revised by MAC, stock of sux to stay in UCC. Safety Notice published in Acute Newsletter 13/9/13, with advice of removal of sux from Acute & availability of red syringes. 10/8/13 from MSSA audit Need to update CPG on Medication Incident Reporting. A clear definition and examples of medication errors and hazardous situations that should be reported have been established and disseminated to PRACTITIONERS. Reportable events include both hazardous situations that could lead to an error and actual errors including those that have been detected and corrected before they reach a patient. Update CPG with VHIMS process. Education to staff once CPG finalised. Di – by October 2013 Before a decision is made to add a drug to the formulary, the potential for error with that drug is investigated in the literature, documented in the drug monograph submitted to the MAC and addressed. To be included in New Formulary Drug Submission Form. Di – October 2013