Sentinel Event Report
Sentinel Event Report
Sentinel Event Report
Accessibility If you would like to receive this publication in an accessible format, please phone (03) 9096 7201 using the National Relay Service 13 36 77 if required or email sentinel.events@dhs.vic.gov.au This document is also available in PDF format on the Internet at www.health.vic.gov.au/clinrisk
Published by Department of Health, Melbourne, Victoria Copyright, State of Victoria, Department of Health, 2009 This publication is copyright. No part may be reproduced by any process except in accordance with the provisions of the Copyright Act 1968. Authorised by the State Government of Victoria, 50 Lonsdale Street, Melbourne. This document published on www.health.vic.gov.au/clinrisk Printed by Print Dynamics, 25 Lionel Rd, Mount Waverley, VIC 3149. November 2009 rcc_091110
Contents
Foreword Acknowledgements Summary Victorian health care sector sentinel event data Themes emerging from the program in 200809 What are we doing to make health care safer in Victoria? Victorian clinical governance policy framework Open disclosure Victorian health incident management system Infection control and cleaning Clinical engagement program Patient safety initiatives Patient safety monitoring Engaging consumers in care Educating the health care sector Glossary 1 2 6 10 23 23 23 23 25 26 28 29 31 34 35
Foreword
The Victorian Government is committed to ensuring the delivery of high-quality, safe health care within the Victorian health system. Review of errors is an important part to this, particularly those events deemed to be sentinel. In depth investigation of these events identies breakdowns in the often complex health systems in place, and allows health services to identify risk and develop ways to reduce or eliminate the risk of reoccurrence. Working collaboratively between the Department of Health, health services, clinicians and consumers has resulted in a strong culture of reporting when things go wrong. A good safety culture encourages reporting; only when we are aware of something not working can we act to change this. This is the seventh annual public report of the sentinel event program and it presents information on the 68 sentinel events reported within Victorian health services during 200809. The focus of the program remains on lessons learnt in order to prevent similar sentinel events in the future, and will continue in 200910.
Building foundations to support patient safety: Annual report of the 200809 Sentinel event program 1
Acknowledgements
The Department of Health (the department) thanks Victorias public health services, hospitals and participating private facilities for their ongoing contribution to the sentinel event program. The department acknowledges the Clinical risk management reference group, the consultative councils and expert advisory groups that work closely with the department to provide recommendations to health services on system issues. The department also acknowledges the patients and their carers who have experienced adverse patient outcomes.
2 Building foundations to support patient safety: Annual report of the 200809 Sentinel event program
Summary
The Victorian sentinel event program supports a learning environment within Victorias health care system. By examining sentinel events and the settings in which they occur and identifying system changes required, our aim is to reduce, or remove where possible, the likelihood of similar occurrence in the future. The information on sentinel events received by the department is de-identied to preserve the privacy of patients, practitioners and organisations involved. The department shares the learnings from these events throughout the health care sector through: the Risk Watch newsletter1 (available online at http://www.health.vic.gov.au/clinrisk/ publications/riskwatch.htm) alerts for signicant events sentinel event annual report (this document) recommendations to individual health services and the sector. In 200809 the department was notied of 80 sentinel events. Twelve events were withdrawn either because they resulted from known complications of the patients condition or required procedure, or because no system or process issues could be identied. Thus 68 sentinel events were notied with 67 reports analysed, one report was unavailable for full analysis at the time of writing this report.
1 Department of Health, Risk Watch, State Government of Victoria, Melbourne. Available at www.health.vic.gov.au/clinrisk. 2 Department of Health Your Hospitals: July2008 to June 2009 3 Workforce Survey data, Service and Workforce Planning, Department Health 4 Department of Health Your Hospitals: July2008 to June 2009
Building foundations to support patient safety: Annual report of the 200809 Sentinel event program 3
4 Building foundations to support patient safety: Annual report of the 200809 Sentinel event program
Building foundations to support patient safety: Annual report of the 200809 Sentinel event program 5
6 Building foundations to support patient safety: Annual report of the 200809 Sentinel event program
5 9
1 8
4 5
7 6
11 8
7 11
7 3
0 3
1 4
1 1
0 2
1 3
2 2
1 1
4 0 0 42 79
2 0 0 55 85
9 0 0 77 122
2 0 0 49 91
2 0 0 37 82
6 0 0 37 102
3 0 0 53 68
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ISR 1: severe (including death); ISR 2: moderate; ISR 3: mild; ISR 4: No harm (includes near miss); Indeterminate: Unable to be determined at this time
8 Building foundations to support patient safety: Annual report of the 200809 Sentinel event program
Figure 4: Breakdown of reported other catastrophic events including near miss, 200809
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Table 2 illustrates the range of events reported under the other catastrophic event category and compares the frequency of these sub-categories across the past six reports.
Table 2: Comparisons between reported other catastrophic events including near miss 200203 to 200809
Event Complication of emergency management Complication of anaesthetic management Complication of surgical management Foetal complication of delivery Complication of inpatient fall (death or serious morbidity) Complication of fall (not resulting in death or serious morbidity) Patient absconding from inpatient unit with adverse outcome Infection control breach Hospital process issue Medication error (not resulting in death) Misdiagnosis and subsequent management Communication of test results Other mental health management Other unspecied A good catch/near miss Procedure involving the wrong patient or body part not resulting in permanent loss or death Total # # # # 200203 9 * 9 3 2 * 200304 11 6 10 0 10 * 200405 6 1 6 1 11 18 200506 4 0 5 2 4 1 200607 2 0 3 2 5 0 200708 1 0 6 0 7 0 200809 4 2 5 2 5 0
6 9 * * * * 2
7 7 * * * * 3
8 0 9 4 3 4 5
3 6 7 3 1 3 8
2 0 3 3 0 6 8 3 #
2 3 5 1 0 7 4 0 #
2 0 1 2 1 6 1 0 21
42
55
77
49
37
37
53
*New catastrophic event classications used in the 200405 data analysis #Procedure involving the wrong patient included in 200809
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Contributing factors
Table 3: Factors contributing to sentinel events expressed as a percentage, 200203 to 200809
Contributing factor Percentage of contributing factor 200203 Number of contributing factors = 210 Procedures/ guidelines Human resources Communication Health information Equipment Physical environment Facilities management Patient behaviour* Course of disease* Other Total 32 17 16 7 7 9 6 6 100 200304 Number of contributing factors = 283 41 17 17 9 7 6 3 0 100 200405 Number of contributing factors = 291 31 24 27 4 4 6 1 3 100 200506 Number of contributing factors = 337 43 14 20 2 5 4 3 5 3 1 100 200607 Number of contributing factors = 305 32 15 18 12 4 6 2 6 1 4 100 200708 Number of contributing factors = 302 43 18 16 9 7 2 2 3 0 0 100 200809 Number of contributing factors = 332 36 15 20 8 8 3 3 7 0 0 100
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Appraisals Recruitment
Patient identication
Patient identication is one of the nine priority program areas of the commission and Victoria is participating in the inter-jurisdictional working party on patient identication. One of the rst areas to be addressed is standardising patient identication bands. In 2008 the Australian Health Ministers Conference (AHMC) endorsed the specications for a national patient ID band. Design work is currently being undertaken and then implementation of the specications will be rolled out. The department supports this patient safety initiative and ask that health services utilise the standard in developing patient identication bands within their health service. Although there is no timeline attached to this initiative it is anticipated the standard will be used consistently throughout all health services by 2010. Links to the standard and specications can be found at: http://www.safetyandquality.gov.au, under the programs tab on the web page. Further work in patient identication is being developed by the commission and the department will keep you informed of progress and outcomes.
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Case study
A patient presented to a day procedure unit for an elective knee arthroscopy. The written consent stated left knee and was signed by the surgeon and the patient. The orthopaedic registrar checked the patient consent and marked the correct leg, as identied on the consent form. On transfer into the theatre room, the orthopaedic registrar was informed that he was not required for the surgery and took no further part in the procedure. The patient was transferred into the theatre where the anaesthetist checked the wristband of the patient and asked the patient to state their name and what leg was being operated on. The patient stated their name and that it was their right knee, this answer was not checked against the consent form. The anaesthetist inserted the IV cannula in the non dominant hand and set up for a right knee arthroscopy. The theatre staff indicated that they sighted a consent form, but could not recall checking what was written on the consent form with the patient. As is normal practice, a time out occurred, but the surgeon was not present as they were running late. The patient was anaesthetised prior to the surgeons arrival into the theatre, who then donned surgical apparel and commenced the procedure on the right leg. The patient was transferred to the recovery room where the nurse checked the patients legs and noted that the marked leg was not the leg that had been operated on. The nurse then checked the consent form that identied the procedure had occurred to the wrong leg. The recovery nurse informed theatre staff of the error. Prior to being booked for the elective surgery the patient visited the surgeons rooms and discussed that both knees required the same operation. It was decided that the sorest knee would be done rst (left knee consented). How did the health service address the issues identied? the existing procedure for verifying the correct patient, site, side (Time out) for surgical/invasive procedures to be reviewed conduct random audits of the compliance with Time out procedure conduct education sessions for staff in the Time out procedure to develop a culture of adherence a staff member is designated to sign the Time out document rather than just be ticked a letter to all surgeons and anaesthetists advising that a designated person is now responsible for the coordination of Time out. What are some actions other health services have undertaken when a similar event was identied in their health service? Introduce pre theatre group meetings prior to the commencement of the theatre list. Documenting the names of the individuals participating in the time out procedure for each procedure.
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What is happening at the national level? The commission is to expand the Ensuring correct patient, correct site, correct procedure protocol to other therapeutic areas. The commission has nalised the protocols and they have been endorsed by the commissioners. These protocols are available from the commissions website at: http://www.safetyandquality.gov.au. What is happening at an International level? In 2008 the World Health Organization released a surgical safety checklist as part of the Safe Surgery Saves Lives Global Patient Safety Challenge. The Surgical Safety Checklist includes a core set of safety checks for use in any operating theatre environment. It is designed to improve safety by focussing on anaesthetic safety practice, ensuring correct site surgery, avoiding surgical site infection and improving communication within the operating team. The Surgical Safety Checklist combines a range of clinical and administrative processes that are necessary for safe surgery and has been the subject of rigorous international study; the results of which have been published in a premier peer-reviewed journal, the New England Journal of Medicine5. The Royal Australasian College of Surgeons and the commission support this initiative, to nd out more about the World Health Organisation surgical safety checklist visit: http://www.who.int/patientsafety/safesurgery/ss_checklist/en/index.html.
5 Haynes AB et al A Surgical Safety Checklist to reduce morbidity and mortality in a global population, N Engl J Med 2009, 360:491-499 6 Victorian Department of Human Services, Mental Health Branch
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Case study
A patient with a number of underlying medical conditions was given an incorrect oral medication by a nurse whilst they were arranging the transfer of the patient to another hospital for further investigations. When organising the medication due prior to transfer, the nurse had mistaken the medication prescribed for a look alike sound alike medication. The medication was checked with a newly medication endorsed division 2 nurse. During transport the patient became lethargic, drowsy and developed a low blood pressure, after medical review at the receiving hospital, the patient was referred to a tertiary hospital. The patient responded to reversal of the incorrect medication, though remained physically unwell, on x-ray a left lung consolidation was detected, the patients observations continued to deteriorate. After discussion with the family, and given the medical condition of the patient, they were deemed not for resuscitation and later died. How did the health service address the issues identied? Review of adherence to medication administration procedures. Review of processes for clinical handover particularly in relation to interhospital transfers. What medication safety measures may further minimise the risk of this error? Introduction of strategies to minimise risk for look alike sound alike medications. For example: - use of both generic and brand names on prescriptions - use of Tallman lettering - completion of the indication eld on the national inpatient medication chart - use of alert stickers on packaging and storage labels. Create a culture of safety to produce an environment where practitioners and senior leaders can learn together about how to create safer systems of care. What further information is available to address this patient safety issue? Reducing risks associated with look-alike, sound-alike medication names is one of the nine patient safety solutions developed by the World Health Organisation Collaborating Center for Patient Safety. Strategies for reducing risks are included in an information leaet which can be found at: http://www.ccforpatientsafety.org/common/pdfs/fpdf/Presskit/PS-Solution1.pdf
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Clinical handover is an area of potential high risk and may often occur in a time pressured environment. The Victorian Quality Council (VQC) and the commission have collated information and tools on clinical handover and Inter-hospital transfer which may provide useful information for hospitals reviewing this process; these can be accessed from: http://www.health.vic.gov.au/qualitycouncil/activities/handover.htm. http://www. safetyandquality.gov.au/internet/safety/publishing.nsf/content/PriorityProgram-05#Tools). The Quality Use Of Medicines Program provides leadership to improve the quality use of medicines (QUM) within Victoria. QUM means selecting management options wisely, choosing suitable medicines if a medicine is considered necessary and using medicines safely and effectively to get the best possible results. High-risk medicines High-risk medicines are those that have a heightened risk of causing signicant or catastrophic harm, should an error in their use occur. The acronym PINCHS is used to raise awareness of: potassium insulin narcotics (such as morphine) chemotherapy heparin (and other medicines that effect blood clotting) systems (such as avoiding wrong route errors). VMACs High-risk Medicines Working Party has worked to reduce the hazards from these medicines. A well-recognised method to raise awareness of medication safety issues is via the distribution of an alert. Following research to determine best practice, several alerts regarding high-risk medicines and systems have been developed. These include: insulin (subcutaneous administration) heparin wrong route administration of oral liquid medicines. Audit tools were also developed to accompany the alert tools. These were designed to help health services improve processes to reduce risks. Further information about alerts and audit tools can be found at: http://www.health.vic.gov.au/qum/initiatives/hrm.htm. In July 2009, an on-line survey was conducted amongst Victorian health professionals to nd out whether the alerts had been helpful in changing practices and to identify barriers and future priorities. A full report of the survey will be available later this year on the QUM website under high risk medicines. Key ndings from the survey were that health services found the alerts facilitated changes to charts, stock management, policies and education and orientation programs. Perceived barriers included resources and processes for changing policies and procedures. Health services indicated that they would value further safety information on insulin infusions, intravenous pumps, cytotoxic agents, allergy recording, omission of medicines and opioids.
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National inpatient medication chart A key project undertaken by VMAC was the implementation of the national inpatient medication chart across all Victorian hospitals. This meant that clinicians could be trained to use one system, whichever health service they were working at, thus reducing error due to lack of familiarity with the chart. Recent developments include the availability of a standardised: paediatric chart long stay chart format for a printable A4 chart. Information about these charts, together with supporting information and a national audit tool may be found at: http://www.health.vic.gov.au/qum/initiatives/nimc/index.htm. Quality Use of Medicines indicator initiative The use of indicators has been shown to effectively drive improvements in quality by demonstrating areas for improvement. The QUM indicator initiative encourages Victorian health services to measure and benchmark performance in medication safety systems. The tools promoted for uptake are the Medication safety self assessment (MSSA)7 for Australian hospitals tools and the Indicators for quality use of medicines in Australian hospitals. The MSSA and MSSA-AT (for antithrombotic therapy) tools focus on safe structures and processes for medications, while the indicators for QUM measure the outcomes of processes. Both the MSSA and MSSA-AT (for antithrombotic therapy) tools were developed with a web based tool that allows hospitals to enter their audit information and generate reports. Following the launch of the QUM indicator initiative and training workshops in metropolitan and regional areas, 27 Victorian hospitals have recorded their participation in the MSSA audit which is a great achievement. Further information about the tools and information to support their implementation can be found at http://www.health.vic.gov.au/qum/initiatives/qum_indicators.htm.
7 Acknowledgements: The MSSA tools were originally developed by the Institute of Safe Medication Practice (ISMP) in the United States and have been adapted for use in Australia by the New South Wales Therapeutic Advisory Group (NSWTAG) (copyright is retained by NSWTAG)
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Case study
Patient Smith presented with symptomatic anaemia requiring the administration of two units of red blood cells (RBC). The rst unit was commenced in the emergency department then patient Smith was transferred to the short stay observation unit, where two registered agency nurses were both rostered to work. Upon completion of the rst unit of blood the patient services assistant (PSA) was requested to collect the second unit of blood from blood bank. The transfusion request form for patient Jones was taken from the central desk and given to the PSA, who then collected the blood and gave it to the registered nurse. The transfusion report form and RBC unit for patient Jones was checked at the central desk by two registered nurses. The RBC unit for patient Jones was then taken to the bedside of patient Smith and commenced without a bedside patient and blood component identication check being performed. Patient Smith developed signs and symptoms of an acute haemolytic transfusion reaction which was initially not recognised but eventually managed and required admission to hospital. Patient Smith did not sustain signicant injury however the patient did subsequently form Rh(D) antibodies, this means the patient is limited to only having Rh(D) negative blood for any future transfusions. How did the health service address the issues identied? Reinforce patient identication protocol within the unit. Placing current admission documents relating to the administration of blood components and products at the patients bedside. Implementation of beds that have fold up tables/trays at the base to facilitate checking and documentation practices at the bedside. Implementation of ring bound folders to securely fasten patient admission documents, and the introduction of a labelling system for admission folders that identies the patient. The cancelling of all pending/outstanding requests or medical orders by the medical ofcer to be incorporated into the admission criteria document/protocol. Prerequisite that one of the staff members allocated to a department is a permanent staff member.
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What are some actions other health services have undertaken when a similar event was identied in their health service? Pre transfusion processes in place on the ward are brought into alignment with the organisations procedures and best practice. The ward and divisional management staff continue to work on strategies to increase skill mix and availability of staff within the ward. This includes initiatives to assist senior nursing staff to prioritise the myriad of clinical demands that may arise at periods of high activity. What activities are being undertaken at a state level to address these patient safety issues? The departments Blood matters: better safer transfusion program, has developed a statewide collection tool for monitoring serious transfusion incidents; part of the role of the group that oversees this program is to make recommendations for patient safety in such cases as above. Suggested recommendations with this event were: Compliance with bedside identity check all staff should be familiar with the requirement to review the wristband of a patient and/or verbal conrmation of the patient details prior to administering any blood product and this should match the product and the paperwork exactly prior to transfusion proceeding. Training of staff in transfusion administration. It is recommended that the health service address training and assessment for staff involved in transfusions in awareness of and adherence to guidelines for administration of blood products. That prohibiting transfusion from short stay observational unit may not be necessary if important elements relating to staff members training and adherence to protocol can be implemented, ensuring the health service has maximum use of this unit. What is happening at the national level? Blood safety A review of The Australian and New Zealand Blood Transfusion Society and Royal College of Nursing Blood Administration guidelines that outline all steps in the administration of blood products developed in 2004, and for release in 2009. The South Australian Department of Health, BloodSafe program, has developed a national blood safety training initiative. This e-learning program has been designed to provide clinical staff with an opportunity to develop their knowledge of blood and to encourage safe transfusion practice and the appropriate use of blood components. Further details are available at: https://www.bloodsafelearning.org.au. The National Blood Authority is developing the reporting and governance frameworks for a voluntary haemovigilance program for Australia. It will report on serious transfusion related adverse events occurring in public and private hospitals. This initiative will contribute to our understanding of peri-transfusion errors, incrementally improve safety and quality, and ultimately deliver better transfusion outcomes. Further information is available at: http://www.nba.gov.au/haemovigilance/index.html.
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Case study
An elderly patient with a history of falls and a stroke presented to an emergency department (ED) and admitted as an inpatient. They had presented to the ED the previous week following a fall at home resulting in pain, swelling and bruising. In the late evening they were found on the oor near their bed and were noted to have a large facial haematoma. Neurovascular observations were commenced and the CT conrmed a large cerebral haemorrhage with right frontal lobe midline shift. They were intubated and immediately transferred to a metropolitan hospital. How did the health service address the issues identied? Improve the identication of patients at risk of falls at a ward level by disseminating information regarding this event to regular staff meetings and by other means of communication including staff education sessions. Improve patient identication for falls risk at the ward level by ensuring that an electronic alert is generated on the medical record and at nursing handover by including falls risk information. What activities are being undertaken at a state level to address these patient safety issues? To support clinicians in identifying and implementing interventions, the Victorian Quality Council (VQC) has developed an online falls minimisation education package with modules for acute, sub-acute and residential care settings. The objectives of the package are: - to provide standardised education for falls minimisation for the Victorian health sector - to improve patient safety by improving understanding of the link between falls risk factors and the implementation of falls prevention strategies. During the development of this package, feedback from the sector identied the need for organisations to be able to track staff members who had completed the package. In response, the VQC is currently developing a mechanism for returning data from the package to health services. Participants will be required to log in and a summary of their details will be sent to their hosting health service on completion of the package. This functionality is expected to be available in 2010. All Victorian Health Services will be invited to utilise the package in this way. Resources can be found at: http://www.health.vic.gov.au/qualitycouncil/fallsprevention.
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What is happening at the national level? The National Ageing Research Institute was commissioned to summarise the Minimising the risk of falls and fall-related injuries guidelines into an introductory module. An Expert working group was then convened to develop case based scenarios relevant for the various settings. These provide readers with the opportunity to apply learning to practical and relevant examples of patients they are likely to encounter. Information can be found at: http://www.mednwh.unimelb.edu.au/tips_on_ageing/falls.htm.
Case study
Following the end of the days work and clean up; nurse 1 commenced loading the autoclave with the newly cleaned and packaged instruments. Nurse 1 closed the sterilisers door but could not access the on switch as it was blocked by nurse 2 who was lling the water chamber of the benchtop steriliser. Nurse 1 walked away assuming nurse 2 would turn the steriliser on when she had completed her task. However, nurse 2 also walked away without switching on the autoclave. The next day, nurse 3 unloaded the equipment from the autoclave and placed it on the sorting bench. Nurse 3 and nurse 4 took the equipment without checking sterilisation status and commenced setting up the sterile set ups for the clinicians use. These set ups were then used by the clinician in their respective surgeries. The health service identied some causative factors that led to this infection control breach. A shared responsibility for sterilisation duties and lack of communication between the two nurses. Inexperience and pressure to meet workload demand resulted in a failure to follow established procedure, such as checking for sterilisation status. No formal method of assuring that sterility had been achieved. Compliance with Australian standards: As part of their infection control program health services must ensure that they comply with the Australian standards and other relevant guidelines. Standards particular to this incident are: AS/NZS: 4815:2006 Ofce-based health care facilities Reprocessing of reusable medical and surgical instruments and equipment, and maintenance of the associated environment AS/NZS: 4817:2003 Cleaning, disinfecting and sterilizing reusable medical and surgical instruments and equipment, and maintenance of associated environments in health care facilities.
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These two standards provide detail on the requirements for: Maintaining sterilisation cycle records that include date, load number, exposure time and temperature, name/identication of person authorising release of contents, specic contents of the load. Documentation required for the release of processed items either parametric or non parametric.
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Open disclosure
Open disclosure refers to the process of open communication with patients and their families following an adverse event. This process not only facilitates communications among health care professionals but also between health care professionals and patients. It is fundamental to continuing to develop trust and accountability within Victorias health care system. Building on from the work undertaken in previous years the department provided open disclosure education and training to a broad range of metropolitan and regional health service staff. Over 700 people attended from a wide range of professional backgrounds and included the support from the Victorian Managed Insurance Authority (VMIA) to assist hospitals promote active engagement with patients. The most signicant challenges for the participants appeared to be the challenge of the term open disclosure it has been suggested they use the term open explanation, in the context of an information continuum. Acknowledging the harm to a patient in a way that is honest and frank, but not at odds with their insurance policy requirements continues to remain a challenge for most organisations. More information can be found at: http://www.health.vic.gov.au/clinrisk/opendisc.htm.
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VHIMS in scope health services include: 88 public health services and all other services running under their auspices 39 funded (stand-alone) community health services Ambulance Victoria Royal District Nursing Service Ballarat District Nursing Service and Healthcare 14 bush nursing centres Forensicare 5 public sector incorporated residential aged care services. The following incident types are within the scope of the VHIMS project: clinical incidents Events or circumstances which could have, or did lead to unintended and/or unnecessary harm to a person receiving care. This includes adverse events and near misses consumer feedback (including complaints, compliments and enquiries) occupational health and safety incidents (staff incidents) incidents of all severity levels, including near misses (incidents that dont cause harm).
Implementation
The department will commence a three month lead implementation in October 2009 with six health services. Following an evaluation in January 2010 a phased statewide implementation will commence. Implementation has been planned in waves to extend over a 12 month period. Timing of the phases outlined below is subject to change by the VHIMS project board: wave one, February to April 2010 wave two, May to July 2010 wave three, August to October 2010 wave four, November 2010 to February 2011. Implementation will be supported by education and training of health service based project ofcers, these positions will be backlled by the department for 12 weeks. The project ofcers will act as project leads for their health service in planning for transition, coordinating education and implementation. Generic education materials are being developed by the department in a train the trainer framework. These materials will form the basis for the health services education programs. There will be exibility within the toolkits for services to include their local policies and governance processes.
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Overall HH Compliance for the State has improved as follows: November, 2007: March, 2008: August, 2008: 48% (95% CI 47%-48%) 59% (95% CI 58%-59%) 66% (95% CI 65%-66%) November, 2008: March, 2009: September, 2009: 69% (95% CI 69%-70%) 71% (95% CI 70%-71%) 71% (95% CI 70%-71%).
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The rate of MRSA bacteraemia has been reduced from 0.0157 per 100 separations to 0.0106 per 100. This is equivalent to 108 fewer patients developing MRSA bacteraemia in the states hospitals over the past two years. From 1 January 2010 all hospitals in Victoria will submit all Staphylococcus aureus bacteraemia (SAB) data not just the subset MRSA, as the aim is to reduce all SAB infections in health services to 2 per 10,000 bed days by 2011. Surveillance The Victorian hospital-acquired infection surveillance system (VICNISS) has been funded by the department since 2002 to collect, analyse and report data, and will commence benchmarking with other jurisdictions in the future.
Hospital cleaning
Following a comprehensive statewide review, the cleaning standards for Victorian health facilities were released in February 2009. New reporting requirements come into effect in 2010 when acute public hospitals and health services will be required to submit results of three external cleaning standards per annum. To support the changes in reporting requirements a course in cleaning standards auditing has been approved by the Victorian registration and qualications authority and will be offered by Registered training organisations in the metropolitan and rural regions across Victoria.
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Next steps
The Statewide Quality Branch has a suite of projects currently underway to enhance clinical engagement, working closely with senior medical staff and health services to further policy implementation and facilitation of safe, high quality health care. These include: Commissioning DLA Phillips Fox, in association with SACS Consulting and the Royal Australasian College of Medical Administrators, to develop a performance appraisal and support process for senior medical staff in Victorias public health services, due for completion at the end of 2009. The development of an understanding clinical practice toolkit which will deliver a practical guide for clinicians and managers to support the implementation of the clinical governance framework, the credentialling and scope of practice policy, and the performance appraisal and support process. A formative evaluation of the policy to determine the impact of the implementation of the policy on selected health services. The results will inform a summative evaluation of the policy scheduled for 2012. The department sees this work as an opportunity to build on the outstanding work organisations are doing to strengthen their credentialling and dening scope of practice processes and the skilful clinical work being performed by Victorian senior medical staff.
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The strength of the indicators is in their use as screening tools to identify apparent changes in performance rather than absolute event rates. These tools appropriately support the targeting of effort rather than providing an absolute measure of performance. The department is the rst Australian body to undertake this work of translation and renement for Australian use and places the department at the forefront in this area. The indicator set will ultimately be widely available for use with any administrative dataset. The patient safety monitoring indicator set includes: death in low mortality diagnostic groups complications of anaesthesia in-hospital fracture postoperative haemorrhage or haematoma postoperative deep vein thrombosis/pulmonary embolus obstetric trauma vaginal or caesarean delivery stroke in-hospital mortality heart failure in-hospital mortality AMI (heart attack) in-hospital mortality pneumonia in-hospital mortality hip fracture in-hospital mortality.
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Glossary
The following terms are used frequently in this report. The department acknowledges that their usage varies and that a number of denitions are used in the literature.
adverse event an unintended injury or complication that results in disability, death or prolongation of hospital stay and is caused by health care management rather than the patients disease a system for classifying human blood based on the antigenic components of blood cells and their corresponding antibodies processes involved in establishing a patients cognitive state, particularly whether the patient is at risk of wandering, absconding or causing harm to staff any policy, procedure or guidelines concerning the processes involved in the clinical management of patients an approach to improving quality in health care that places special emphasis on identifying circumstances that put patients at risk of harm and then acting to prevent or control those risks a health service boards accountability for ensuring a framework and rigorous systems are established so health care safety and quality are monitored, evaluated and continuously improved a treatment regime agreed by consensus that includes all the elements of care, regardless of the effect on patient outcomes direct and indirect activities involving a negative impact, including injury, death, increased length of stay, time loss, money loss, service disruption, and reputation, political and intangible losses death, disease, injury, harm, suffering or disability experienced by a person a source of potential harm or a situation with a potential to cause loss an event or circumstance resulting from health care that could have, or did, lead to unintended or unnecessary harm to a person and/or a complaint, loss or damage a method to quantify the actual or potential consequences of an incident or near miss to check, supervise, observe critically or record the progress of an activity or system on a regular basis to identify change an incident that did not cause harm the chance of something happening that will have an impact on objectives; it is measured in terms of consequence and likelihood the overall process of risk analysis and risk evaluation the process used to determine risk-management priorities by comparing the level of risk against predetermined standards, target risk levels or other criteria the culture, processes and structures that are directed to the effective management of potential opportunities and adverse effects a signicant factor that contributed to an incident
ABO blood group behavioural assessment clinical guidelines clinical risk management clinical governance
harm hazard incident incident severity rating (ISR) monitor near miss risk risk assessment risk evaluation risk management root cause
36 Building foundations to support patient safety: Annual report of the 200809 Sentinel event program
a systematic process where the factors that contributed to an incident are identied strategies required to reduce the risk of similar adverse patient outcomes occurring in the future a relatively infrequent, clear-cut event that occurs independently of a patients condition; it commonly reects hospital system and process deciencies, and results in unnecessary outcomes for the patient the systems or process cause that allows for the proximate cause of an event to occur Victorian Admitted Episodes Data Set