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Driving Performance Through Effective Data Management Kimberly Reints RN, BSN, PHN, CNOR Objectives: 1. Identify the difference between a proactive and a reactive performance improvement study 2. Describe at least three types of data that can be captured in performance improvement studies 3. Explain at least two methods of data collection 4. Discuss one method to utilize results of a performance improvement study. Definitions of Proactive and Reactive Performance Improvement Studies Proactive Reactive Controlling a situation by making things happen or by preparing for possible future problems. Doing something in response to a problem or situation. Reacting to problems when they occur instead of doing something to prevent them from happening. Proactive Performance Improvement Studies • Requires planning ahead and investigating • Goal oriented • Usually based on stakeholder motivations or quality • • • • initiatives An assessment of risks and vulnerabilities Foresighted and visionary Prioritizes data collection Sets priorities (Prioritization Matrix) Reactive Performance Improvement Studies • Something that “must be fixed” • Response to an incident or near miss • Response to unexpected or adverse patient outcomes • Failed processes that were relied upon and trusted • Breaches in acceptable standards of practice, standards of care or regulatory requirements • Puts future patients at risk for adverse outcomes • Requires intensive analysis and cannot be ignored • Focuses on the S – K - I What is S-K-I? • Systems or processes that are deficient or defective • Knowledge that is insufficient and competency can be the issue • Individual performance or behavior that is inappropriate or non-compliant Data, Information and Knowledge The D-R-I-P Concept: D Data R Rich I Information P Poor • Data is comprised of facts • Information is data that has become and is meaningful or useful • Knowledge involves managing and utilizing information to predict and the control the future performance of processes for optimal outcomes Three Types of Data Captured in Performance Improvement Studies • Internal benchmarks or current organizational standards • • • If organizational processes in control • • • • What is the data telling us? Where do we stand? What is our current baseline? Are there small random variations in standards of care or documentation? Are trends in data positive? Is there compliance with CMS regulations and accreditation standards? If organizational processes out of control • • • Are there major fluctuations or variations in standards or care or documentation? Are trends in data negative? Is there lack of compliance with CMS regulations and accreditation standards? Prioritization of Performance Improvement Studies by Standards Three Types of Standards • • • The organizational standard • Is our current organizational standard in line with current standards? • What is our internal benchmark or compliance rate? The empirical standard • The external benchmark comparison • The compliance rate compared with a regulation or evidence based practice standard The absolute or normative standard • Usually determined by clinical trials typically referred to as evidence based medicine • Can be referred to as best practices • Can include “Consensus Conference” which draws from health care professional opinions – often referred to as the GOBSAT phenomenon GOBSAT PHENOMENON G – Good O – Old B – Boys S – Sitting A – Around T - Talking Reactive Performance Improvement Sources • Adverse Events (AE) – an incident resulting in harm to the patient • CMS Metrics • • • • • • • • Falls Burns Hospital Transfers / Admissions Wrongs –Wrong Site, Patient, Procedure or Implant Health Care Acquired Infection Medication Errors Return to the operating room or procedure room Breaches in cleaning and sterilization processes and/or high-level disinfection process Reactive Performance Improvement Sources Cont’d • Procedures or processes that place the patient at risk when • • • • • • not performed Procedures or processes performed when not indicated Procedures or processes not performed when indicated Problem prone procedures or processes such as procedures with complications High Cost Procedures Patient injury of any kind Safe Injection practices – one needle, one syringe, on patient, one time (Immediately reportable by SA & AO) Proactive Performance Improvement Sources • Patient Satisfaction Survey Results • Corporate benchmarks • Clinical Salaries per procedure • Clinical Hours per procedure • Drug Expenses per procedure • Linen Expense per procedure • Office supplies expense per procedure • Salaries and benefits per procedure • Maintenance costs of instrumentation • Supply expense per procedure Proactive Performance Improvement Sources Cont’d • • • • • • • • • Retrospective chart audits Medication tracers against written orders for medications Verbal order tracers against medications given and authenticated History and physical completion tracers Increase in the number of procedures for a low volume problem prone procedure Narcotics signed out, used, documented & wasted with witness The 5 moments of Hand Hygiene compliance Pathology reports are not being sent to ASC or reviewed for abnormal tissue in a timely manner Near miss sharps injuries Contributing Factors of No-Harm Incidents 1. 2. 3. 4. 5. 6. Team factors such as written and verbal communication issues or confusion Task factors such as the availability of facility protocols and/or the availability and use of test results Work environment factors such as the design, availability and maintenance of equipment, staffing levels and skill mix of staff Patient screening factors such as ASA 3’s and ASA 4’s Individual factors such as staff knowledge, skills, physical and mental health Organizational and management factors such as structure, policies, standards and goals of the organization Methods of Data Collection 100% of medical record audits of a specific documentation – preoperative orders for eye medications and eye medications documented as given. 2. Determine your sample size if 100% medical record review is not possible – narrow the population or sample size by doctor, days of the week, patient age, type of procedure, etc. 3. Asking patients and families if there was anything we could have done better of different to improve their facility experience 4. Published evidence based practices in peer reviewed journals as comparison to existing data like benchmarks 1. How Do We Prioritize Our PI Projects? Criteria for Performance Improvement Prioritization 1. 2. 3. 4. 5. IMPACT UPON: Patient Outcomes Patient Safety Cost of Implementation Staffing Efficiency Cost reduction or savings Criteria for Performance Improvement Prioritization 1. 2. 3. 4. APPLICABILITY TO: Perceptions of patient, family and staff High volume procedures High risk procedures Problem prone procedures Criteria for Performance Improvement Prioritization 1. 2. 3. 4. REQUIREMENTS BY: Required by regulations – CMS Required by Accreditation Standard Required by Process Control – internal policy and procedure based on evidence based standard Quality Control required by manufacturer PI Study Prioritization Matrix Parameters 4 3 2 1 0 Impact: On patient outcomes Important improve-ment in patient care Moderate improvement in patient care Little improvement in patient care Questionable improvement in patient care No improvement in patient care Impact: On patient safety Patient safety com- promised at present Patient safety at potential risk Contributing factor to patient safety risk Minimal risk to patient safety No risk to patient safety Impact: On cost of implementation No cost for implementation One time cost <5% of operating budget One time cost 5%-10% of op. budget One time cost >10% of operating cost Ongoing increased costs Impact: On staffing or efficiency Reduction of 1 FTE Reduction of 0-1 FTE Possible reduction in FTE No impact on staffing or efficiency Increase in staffing costs Impact: On cost reductions Measureable reduction > 10% 5% to 10% measure-able reduction 1% to 5% measureable reduction No impact on cost of implementation Increase in operating costs Applicability: Perceptions of patient, family, staff Problems as indicated by surveys, complaints or patient grievances Possible highly positive effect on patient satisfaction Possible moderate effect on patient satisfaction and/or staff satisfaction Possible minimal effect on patient satisfaction or staff satisfaction No effect on patient, family, visitor or staff satisfaction Applicability: High Volume Affects 100% of patients Affects 50% to 75% of patients Affects 25% to 50% of patients Affects 0 to 25% of patients Does not affect patients Applicability: High Risk May cause patient death May cause per- manent serious complication or injury to patient May cause permanent minor / temporary minor patient complication May cause temporary minor complication to patient No risk of complications to the patient Applicability: Problem Prone Process problems with increased risk to patients/staff Process problems with moderate risk to patients or staff Process problems with low risk to patients/staff Process problems with no risk to patients/staff No process problems noted Requirements: Regulatory or required standard Required by CMS Required by another regulatory body Required by accreditation standard NA Not required Requirements: Process Control / Quality control Show significant variation in process Shows moderate variation in process Show minimal variation in process NA No variation noted Total Methods to Utilize the Results of a Performance Improvement Study 1. 2. 3. 4. 5. 6. 7. Report it to the Board and document it in the Board Minutes Make certain that staff (rank and file) know the outcomes of the study and the benefits to the center Implement lasting change Identify opportunities for staff in-services and staff competency training if necessary Utilize data to target other related issues to the original study Utilize data to use for employee performance appraisals At least one study must show improvement from a goal to outcomes in practice - AAAHC