CROSSING THE CHASM: ENGAGING NURSES IN QUALITY IMPROVEMENT AND EVIDENCE BASED PRACTICE

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CROSSING THE CHASM: ENGAGING NURSES IN QUALITY IMPROVEMENT AND EVIDENCE BASED PRACTICE Joy Goebel RN MN PhD Associate Professor of Nursing California State University Long Beach

Objectives Discuss similarities and differences between EBP, research, and quality improvement (QI) Identify actionable QI targets in your setting Apply the Plan-Do-Study-Act model to a clinical issue in your setting

Improving Care Improving care requires a systematic process of defining problems in order to identify potential causes with the goal of developing strategies to improve care. This process requires being able to measure care.

Quality Improvement Purpose Improve patient care Methods PDCA, FADE, Six Sigma Level Unit Institution Evidence Based Practice Change practice/ implement best practice Numerous models Levels of evidence Individual practitioner Institution Population Research Generate new knowledge Qualitative Quantitative Mixed methods Representative sample Change of: Process Practice Understanding Participant consent Not usually needed Dissemination Usually internal (unit, agency) May be published Sometimes Yes May be internal (unit agency)or external (publication or presentation) Often incorporated into clinical guidelines Usually external (publications or research presentations)

Quality Improvement (Shirley et al 2011) QI improves internal processes and practices with a specific patient group or organization QI protocols are less formal and rigorous and may change QI data collection is usually rapid cycle uses minimal to moderate time and resources

Quality Improvement Tools There are numerous tools to examine care processes. These tools guide the collection of data in order to identify possible problems. Tools provide a way to display data.

Cause-and-Effect / Fishbone Diagram A cause-and-effect or fishbone diagram helps to organize a lot of information that may relate to a problem. A benefit of this diagram is that different levels of cause can be identified. There generally are categories of cause such as people, processes, management, equipment, and environment.

People Processes Equipment Regulation Management Environment

PEOPLE Insufficient staffing in facilities Current facilities are inadequate to meet demand Poor role definition among health care workers Inadequate education, knowledge, and skills among facility-based health workers Insufficient medicines PROCESS/ POLICY Limited opportunities for education Lack of coordination between levels of health facilities Overcrowding in emergency departments Poor or no referral system Too few facilities available POOR QUALITY OF CARE EQUIPMENT/ SUPPLIES ENVIRONMENT

Control Charts Control charts are useful to show the variation that occurs with a particular quality measure of interest. Control charts show how the subject of interest changes over time and whether a process is stable and in control. A control chart has an upper limit of control, a lower limit, and a line that represents an average. Data are plotted in real time and a nurse can tell if the number of events is heading toward or exceeding either the upper or the lower control line in order to make adjustments in care.

9.0 Nurse to Patient Ratios Average Daily Imperfections Sample Mean Lower Control Limit Upper Control Limit 8.0 7.0 6.0 5.0 4.0 3.0 2.0 1.0 0.0 1/1/2009 1/2/2009 1/3/2009 1/4/2009 1/5/2009 1/6/2009 1/7/2009 1/8/2009 1/9/2009 1/10/2009 1/11/2009 1/12/2009 1/13/2009 1/14/2009 1/15/2009 1/16/2009 1/17/2009 1/18/2009 1/19/2009 1/20/2009 1/21/2009 1/22/2009 1/23/2009 1/24/2009 1/25/2009 1/26/2009 1/27/2009 1/28/2009 1/29/2009 1/30/2009 1/31/2009

Histograms A histogram provides a function similar to the control chart in displaying the frequency of events..

PC-NCT Multi-Site Aggregate Report Spiritual Concerns

Multi-Site Report Symptoms Domain Assessed Using PC-NCT in 2012 0 50 100 150 200 250 300 350 400 450 500 Dyspnea None Mild Moderate Severe 0 50 100 150 200 250 300 350 400 450 500 Pain None Mild Moderate Severe 0 50 100 150 200 250 300 350 400 450 500 Number of Visits

Characteristics of Measures Clinically relevant Actionable http://as800.chcr.brown.edu/pcoc/ http://prc.coh.org/res_inst.asp

Types of Measures Process measure -- what you do to the patient-- e.g..., Did the nurse ask about whether you have pain? Outcome measure -- benefit to the patient Did the care you received from the palliative care team improve your pain? http://as800.chcr.brown.edu/pcoc/

Purpose Measurement for Research To discover new knowledge Measurement for Learning and Process Improvement To bring new knowledge into daily practice Tests One large "blind" test Many sequential, observable tests Biases Data Control for as many biases as possible Gather as much data as possible, "just in case" Stabilize the biases from test to test Gather "just enough" data to learn and complete another cycle Duration Can take long periods of time to obtain results "Small tests of significant changes" accelerates the rate of improvement

Institutional Review Board Will your project require IRB review? Is it research? Does it involve human subjects? Federal Common Rule Research is defined as "a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge."

Research Requiring IRB Review Probably requires review Probably does not require review Designed to contribute to generalized knowledge Plan to disseminate beyond the agency Conditions are other than standard care Risks of participation exceed those of usual care Information collected goes beyond routine care Designed to gain knowledge to improve care in a particular setting Plan to disseminate within the agency Conditions are based on standard care with an improvement Risks of participation are the same as usual care Information collected is part of routine care

How to get started? http://www.youtube.com/watch?v=fw8ammcvajq

PDSA The three questions The three questions: What are we trying to accomplish? The aims statement How will we know if the change is an improvement? What changes can we make that will result in improvement?

Plan-Do-Study-Act (PDSA) Plan - the change to be tested or implemented Do - carry out the test or change Study - data before and after the change and reflect on what was learned Act - plan the next change cycle or full implementation

PLAN Determine the clinical issue Search for best practice Accepted clinical guidelines Systematic reviews Other research evidence Develop project proposal Plan location, time, who will be involved, how the change with take place, what data needs to be collected

Plan for whom? Who are you planning for? Yourself, Programmatic, Leadership, Query or mandate What is [stakeholder] most concerned about? Costs, costs, costs? Quality, query or mandate, throughput / access? Do you need to make a business case? Use stakeholder to define other parameters (e.g., time and ROI)

Identify the problem? Is data available? Medical charts, administrative (drugs and procedures), facility surveys What data collection is feasible? Hard and often unrealistic step Can others experience inform how to characterize the problem? Talk to patients / families / clinical teams, look at what is published, especially quality measures (process and outcome)

DO Engage implementation team Collect baseline data Begin practice change Document outcomes Record responses to change

Recruiting an implementation team Who Representation of all parties who will be impacted Nurses RN, On-call, LPN/LVN, CNA Social workers Counselors Medical directors Pharmacy Volunteers Patient/family When Team should be formed during the PLAN stage so they fully understand the implementation plan How Clinical release time Rewards for participation

Tailoring change to organization resources Leadership support Multidisciplinary cooperation Decision-making style Organization size and divisions Location Competition Documentation system Technology

DO Do find out who needs to approve the project Administration Unit managers Practice council Institutional review board

DOs and DON Ts of implementation DO pilot the change with one team, group, unit, etc. Gives you the chance to Tailor the change to your organization Discover implementation issues Determine if the change is beneficial in your setting DON T try to change too much at the same time Too many processes Too much of the organization

Steps for DO Determine implementation team Who will you ask for which role? Begin communication of change Awareness campaign Staff education (who, what, when, where) Tailor to organizational resources Get all appropriate approvals Begin practice change

STUDY Examine the measures, did they measure what we wanted? Compare outcomes after practice change to previous outcomes Determine costs of the change

ACT Decide if outcomes are worth the cost of change What action are you going to take as a result of this cycle (adopt, adapt, abandon)? Describe what modifications to the plan will be made for the next cycle from what you learned.

ACT Make any necessary changes in plan Re-pilot, if necessary Begin cycle again to implement on a wider basis Are we ready to implement the change?

Quality Improvement Resource Center (GLA VA) Development of EHR tools to standardize and improve palliative care EHR tools allows the collection of data to examine for processes over time EHR tools provides an opportunity for QI on patient level, facility level, VISN level or national level

PC-NCT Multi-Site Aggregate Report Moderate & Severe Pain

PC-NCT Multi-Site Aggregate Report Surrogate Decision Maker & Surrogate Documentation Is the surrogate information documented in an advance directive or power of attorney? Has the person authorized under VA policy to make decisions for the incapacitated patient been identified?

PLAN Discuss potential targets for QI in your respective settings Identify the potential merits/barriers Identify stakeholders, people with an interest What/how will you measure

PLAN ACT DO STUDY

DO Anticipate the implement plan To what extent are we following the plan Are we capturing the data as we go Document unexpected findings Begin data analysis

PLAN ACT DO STUDY

STUDY Complete the analysis How will you display the results What does the data from our trial implementation tell us? Summarize what was learned

PLAN ACT DO STUDY

ACT What documentation is required to capture the memory Policy Process flowcharts Supporting documents Who needs to be mentored, trained and coached Establish future plan (what should we be improving next)

Conclusions QI is an integral part of state of the science patient care QI poses challenges and opportunities for clinicians QI is