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Safety Goals
September 8, 2017
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this information consult original source materials and qualified healthcare regulatory counsel for specific guidance in healthcare
reimbursement and regulatory matters.
4
Speaker
Carolyn began her healthcare career as a staff nurse in Intensive
Care. She has worked in a variety of staff, administrative and consulting
roles and has been in her current position as Regional Chief Clinical
Officer with HealthTechS3 for the last fifteen years.
Goal 9: Reduce the risk of patient harm resulting from falls (Nursing Care Center)
Goal 14: Prevent health care-associated pressure ulcers (Nursing Care Center)
Goal 15: The hospital identifies safety risks inherent in its patient population (Hospital
Universal Protocol for Preventing Wrong Site, Wrong Procedure and Wrong Person
Surgery
7
Goal 2: Improve the effectiveness of communication among caregivers Hospital CAH Nursing
Care Center
NPSG.02.03.01 Report critical results of tests and diagnostic procedures on a timely basis. X X
Goal 6: Reduce the harm associated with clinical alarm systems Hospital CAH Nursing
Care Center
NPSG.06.01.01 Reduce the harm associated with clinical alarm systems. X X
Goal 7: Reduce the risk of health care-associated infections Hospital CAH Nursing
Care Center
NPSG.07.01.01 Comply with either the current CDC hand hygiene guidelines or the current X X X
WHO hand hygiene guidelines.
NPSG.07.03.01 Implement evidence-based practices to prevent health care-associated Revised Revised New
infections due to multidrug-resistant organisms. 1/1/18 1/1/18 1/1/18
NPSG.07.04.01 Implement evidence-based practices to prevent central line-associated Revised Revised Revised
bloodstream infections. 1/1/18 1/1/18 1/1/18
NPSG.07.05.01 Implement evidence-based practices for preventing surgical site infections. X X
Goal 14: Prevent health care-associated pressure ulcers (decubitus ulcers) Hospital CAH Nursing
Care Center
NPSG.14.01.01 Assess and periodically reassess each patient’s and resident’s risk for developing X
a pressure ulcer and take action to address any identified risks.
Goal 15: The hospital identifies safety risks inherent in its patient population Hospital CAH Nursing
Care Center
NPSG.15.01.01 Identify patients at risk for suicide. X
Universal Protocol for Preventing Wrong Site, Wrong Procedure, and Wrong Hospital CAH Nursing
Person Surgery Care Center
UP.01.01.01 Conduct a preprocedure verification process. X X
2. Label containers used for blood and other specimens in the presence of the
patient or resident.
• I’ve been in healthcare for 10 years and I’ve never had a patient
identification error.
• I’ve done it my way and it works for me.
• Double checking something when I am already certain is a waste of time.
• Patients feel the service I provide is not personal if I keep asking them to
say their name. They may feel like I keep forgetting.
• If I state the wrong patient’s name, they will correct me.
• The person who brought me the patient, SURELY must have already
identified the patient. Why would I need to double check someone else’s
work?
13
Procedure Example - Armband in Place
Step 2: Step 2:
• Read back out loud the patients first • Read back out loud the patients first
and last name and DOB from the and last name and DOB from the
verifying document, (e.g. request, verifying document, (e.g. request,
label, MAR, Order, etc.) and ensure it label, MAR, Order, etc.) and ensure it
matches the armband matches the armband
14
Procedure Example - Armband NOT in Place
If patient is willing and able to participate: If patient is NOT willing or able to participate:
Step 1: Step 1:
• Ask, “For your safety will you please • Confirm patient’s first and last name and
state your name and your date of birth?” DOB with a photo in EMR or a photo ID
As the patient is responding, confirm
from the verifying document (request, Step 2:
label, MAR, order, Med label or photo ID)
that name and DOB are accurate. • Read back out loud the patients first and
last name and DOB from the request,
label, MAR, order, Med label or photo
Step 2: ID and ensure it matches the armband
• Read back out loud the patient’s first
and last name and DOB from the
request, label, MAR, order, Med label
or photo ID and ensure it matches the
armband
Final Check Toolkit
http://www.thefinalcheck.org/toolkit/ 15
16
Label Specimen in the Presence of the Patient / Resident
The incidence of patient identification errors, including mislabeled and misidentified specimens,
is much too high in clinical laboratories. The best data on errors in U.S. laboratories is derived
from three separate College of American Pathologists (CAP) Q-Probe studies, in which the
reported rates of mislabeled specimens were
• 0.39/1000 in 120 institutions (2006)
• 0.92/1000 in 147 clinical labs (2008), and
• 1.12% of blood bank specimens in 122 clinical labs (2010)
Source: Fixing the Problem of Mislabeled Specimens in Clinical Labs - Some Practical Suggestions—and One High Tech Solution. Author:
Charles D. Hawker, PhD, MBA, FACB and Bonnie L. Messinger, CMQ/OE (ASQ), CPHQ. Date: APR.1.2014 Source: Clinical Laboratory News
17
Label Specimen in the Presence of the Patient / Resident
Typical interventions to reduce mislabeling, from weakest to strongest, are:
• Weak: Retrain the phlebotomist and nurse regarding following the proper policy
and procedure for blood collection.
• Weak, but slightly stronger: Retrain the phlebotomist and nurse and monitor their
behavior.
• Intermediate: Retrain all phlebotomists and nurses and monitor their behavior.
Source: AHRQ: Right Patient, Wrong Sample. Commentary by Michael Astion, MD, PhD
Goal 1: Improve the accuracy of patient and resident identification
NPSG.01.03.01: Eliminate transfusion errors related to patient
18
misidentification
2. When using a two-person verification process, one individual conducting the identification verification is the
qualified transfusionist who will administer the blood or blood components to the patient.
3. When using a two-person verification process, the second individual conducing the identification verification is
qualified to participate in the process, as determined by the organization.
1. Review to make sure your blood administration policy is the same as your
EMR documentation template (many times they are different)
2. If your lab isn’t staffed 24 hours - what is the process for accessing blood
afterhours?
1. Develop written procedures for managing the critical results of tests and diagnostic procedures that
address the following:
– The definition of critical results of tests and diagnostic procedures
– By whom and to whom critical results of tests and diagnostic procedures are reported
– The acceptable length of time between the availability and reporting of critical results of tests
and diagnostic procedures
2. Implement the procedures for managing the critical results of tests and diagnostic procedures.
3. Evaluate the timeliness of reporting the critical results of tests and diagnostic procedures.
• Is timeliness measured and reported internally for ALL critical test results in all
departments? Consider:
– Order to test – especially if STAT
– Test to result
– Result to Nurse and Nurse to Provider (if that’s your process)
OR Clinician to Provider
Goal 3: Improve the safety of using medications
NPSG.03.04.01: Label all medications, medication containers, and other solutions on and 23
off the sterile field in perioperative and other procedural settings
1. In perioperative and other procedural settings both 4. Verify all medication or solution labels both verbally
on and off the sterile field, label medications and and visually. Verification is done by two individuals
solutions that are not immediately administered. qualified to participate in the procedure whenever
This applies even if there is only one medication the person preparing the medication or solution is
being used. not the person who will be administering it.
2. In perioperative and other procedural settings both 5. Label each medication or solution as soon as it is
on and off the sterile field, labeling occurs when any prepared unless immediately administered.
medication or solution is transferred from the
original packaging to another container. 6. Immediately discard any medications or solutions
found unlabeled.
3. In perioperative and other procedural settings both
on, and off the sterile field, medication or solution 7. Remove all labeled containers on the sterile field
labels include the following: and discard their contents at the conclusion of the
– Medication or solution procedure.
– Strength
– Amount of medication or solution containing 8. All medications and solutions both on and off the
medication (if not apparent from container) sterile field and their labels are reviewed by entering
– Diluent name and volume (if not apparent from and exiting staff responsible for the management of
container) medications.
– Expiration date when not used within 24 hours
– Expiration time when expiration occurs in less
than 24 hours
Applies to: Hospital - CAH
24
Mary McClinton
Mary L. McClinton died in 2004. Chlorahexidine, a chemical antiseptic used for skin
preparation, was injected instead of a local injection at Virginia Mason Medical Center in
Seattle, Washington. Both liquids were colorless and clear and the receptacles containing these
liquids were unlabeled.
Carolyn’s Notes 25
2. Applies to all sites of care. The same practices should be adopted throughout the
hospital/clinics, procedural based departments and anesthesia.
1. The only anticoagulant drugs included currently under the requirement are warfarin, unfractionated heparin, and
low molecular weight heparins. Eventually, other anticoagulants may be added to the list in the future. However,
there is nothing that prevents an organization from including any other anticoagulant in their management
program. Such an approach is encouraged but not required.
2. The requirement only applies to patient's receiving "anticoagulation therapy". Thus, it only applies to patients
receiving these drugs for therapeutic purposes, and not for flushes, etc.
3. The term "defined anticoagulant management program" means a program, specified in writing, for individualizing
anticoagulation therapy for each patient that involves the use of standardized practices and patient involvement,
and which is specifically designed to reduce the risk of adverse drug events associated with the use of heparin
(unfractionated), low molecular weight heparin (LMWH), warfarin, and other anticoagulants.
4. NPSG.03.05.01 applies to those situations when anticoagulant is administered therapeutically and not
prophylactically regardless of the medication type (warfarin, heparin, low molecular weight heparin, etc.). However,
if it is usual practice for patients to be kept on therapeutic ranges of anticoagulant for several days as a
prophylactic strategy then NPSG.03.05.01 is applicable.
Goal 3: Improve the safety of using medications
NPSG.03.06.01: Maintain and communicate accurate patient 28
medication information
1. Obtain information on the medications the patient or resident is currently taking when he or she is admitted to the
organization or is seen in an outpatient setting. This information is documented in a list or other format that is
useful to those who manage medications.
2. Define the types of medication information to be collected in non-24 hour settings and different patient
circumstances.
3. Compare the medication information the patient brought to the organization with the medications ordered for the
patient or resident by the organization in order to identify and resolve discrepancies.
4. Provide the patient or resident (or family as needed) with written information on the medication the patient should
be taking when he or she is discharged from the organization’s care or at the end of an outpatient encounter (for
example, name, dose, route, frequency, purpose).
5. Explain the importance of managing medication information to the patient or resident when he or she is leaves
the organization's care or at the end of an outpatient encounter.
• Start by looking at outpatient medical records or a discharge medication list if a patient was recently discharged
from a hospital. If the patient brings his or her own list and it matches with the medical record, or the patient can
explain all discrepancies, the first step is completed.
• More often, patients do not bring their own list or they do not match with other sources, and providers have to
contact the patient's pharmacy to determine what prescriptions have been filled
• If there is still uncertainty, a call to the patient's primary care physician or specialists may be necessary
• A final resource is to ask the family to bring in all the patients' pill bottles from home to confirm the medications the
patient is currently taking
Source: Beckers - Infection Control & Clinical Quality. 4 Steps to Improve Medication Reconciliation. Written by Sabrina Rodak | February 07, 2012
30
Strategy 2 - Risk Stratification
• Each patient's risk level will depend on how many of these factors are present
• High-risk patients will likely need a more in-depth medication history and reconciliation process,
such as having the history and reconciliation completed by a trained clinical pharmacist
Source: Beckers - Infection Control & Clinical Quality. 4 Steps to Improve Medication Reconciliation. Written by Sabrina Rodak | February 07, 2012
31
Strategy 3 - Reconciliation at Discharge
• Reconciliation at discharge is one of the most critical components of a medication reconciliation program
because it can affect the patient's post-hospital safety and health, and thus the chance of readmission.
• Show very clearly how the discharge regimen is different than what the patient was taking prior to
admission.
Source: Beckers - Infection Control & Clinical Quality. 4 Steps to Improve Medication Reconciliation. Written by Sabrina Rodak | February 07, 2012
32
Strategy 4 - Education
• Clinicians need to explain to patients and their families what is different about their medications, why
those changes were made and possible side effects
• In addition, when discharging a patient, hospitals should give discharge instructions to the subsequent
caregiver(s) in both written and verbal forms to ensure comprehension and avoid adverse events
Source: Beckers - Infection Control & Clinical Quality. 4 Steps to Improve Medication Reconciliation. Written by Sabrina Rodak | February 07, 2012
33
Cultural Competency
Cultural Competency in Health Services and Care published by the Washington State
Department of Health outlines six strategies for improving interpersonal communication with
culturally diverse patients or those with limited English proficiency or low health literacy rates:
Source: Washington State Department of Health, Health Systems Quality Assurance. Cultural Competency in Health Services and Care, A Guide for Health
Care Providers. June, 2010
34
Additional Strategies
1. Develop a single medication list ("One Source of Truth"), shared by all disciplines for documenting the patient's current
medications.
2. Clearly define roles and responsibilities for each discipline involved in medication reconciliation.
3. Standardize and simplify the medication reconciliation process throughout the organization, and eliminate unnecessary
redundancies (the flowchart of the current process can help you identify these redundancies).
4. Make the right thing to do the easiest thing to do within the patterns of normal practice.
5. Develop effective prompts or reminders for consistent behavior if true forcing functions (i.e., required reconciliation step presented
to the physician during admission order entry within an electronic health record [EHR] are not possible.
6. Educate patients and their families or caregivers on medication reconciliation and the important role they play in the process.
7. Ensure process design meets all pertinent local laws or regulatory requirements. Linking medication reconciliation to other
strategic goals (e.g., heart failure publicly reported process of care measures related to discharge instructions on medications)
and/or other initiatives (e.g., a hospital project working on improving patient satisfaction related to pain management or patient
communication regarding medications) when appropriate can also strengthen the importance of this process
Source: AHRQ: Medications at Transitions and Clinical Handoffs (MATCH) Toolkit for Medication Reconciliation. Chapter 3. Developing Change: Designing
the Medication Reconciliation Process
“One Source of Truth” 35
• Medication reconciliation process design should center on the concept of a single list to document patient's current medications.
This will be referred to as "one source of truth." This list should be shared and utilized by all physicians, nurses, pharmacists, and
others caring for the patient.
• All disciplines caring for the patient should be working from the same medication list, regardless of the format (electronic or paper-
based).
• The list should be centrally located and easily visible within the patient's medical record.
• This list becomes the reference point for ordering decisions and reconciliation, screening medications to be administered during a
procedure/episode of care, and determining the patient's medication regimen upon discharge.
• Each discipline should have the ability to update the home medications as new or more reliable information becomes available.
• In a paper-based format, old or modified information could be crossed out, new information can be added, and each change can be
dated, timed, and signed.
• In an electronic system, changes would be date and time stamped, and the prescriber's name automatically captured. If the
patient's medication list requires changes at discharge, updated information will remain stored for review and modification for future
admissions.
Source: AHRQ: Medications at Transitions and Clinical Handoffs (MATCH) Toolkit for Medication Reconciliation. Chapter 3. Developing Change: Designing
the Medication Reconciliation Process
Goal 6: Reduce the harm associated with clinical alarm systems
36
NPSG.06.01.01: Improve the safety of clinical alarm systems
2. Identify the most important alarm signals to manage based on the following:
– Input from medical staff and clinical departments
– Risk to patients if the alarm signal is not attended to or if it malfunctions
– Whether specific alarm signals are needed or unnecessarily contribute to alarm noise and alarm fatigue
– Potential for patient harm based on internal incident history
– Published best practices and guidelines
3. Establish policies and procedures for managing the alarms identified in EP2 above that, at a minimum, address the following:
– When alarm signals can be disabled
– When alarm parameters can be changed
– Who in the organization has the authority to set alarm parameters
– Who in the organization has the authority to change alarm parameters
– Who in the organization has the authority to set alarm parameters to “off”
– Monitoring and responding to alarm signals
– Checking individual alarm signals for accurate settings, proper operation, and detectability
4. Educate staff and licensed independent practitioners about the purpose and proper operation of alarm systems for which they are responsible.
6. Alarm settings that are not customized to the individual patient or patient population
7. Inadequate staff training on the proper use and functioning of the equipment
(e.g., inconsistent team training, response, and interpretation of alarm signals)
9. Alarm conditions and settings that are not integrated with other medical devices
Source: TJC Sentinel Alert: Sentinel Event Alert Issue 50: Medical device alarm safety in hospitals. April 8, 2013
39
Strategies
1. Leadership ensures that there is a process for safe alarm management and response in high-risk areas (as identified by
the organization)
2. Prepare an inventory of alarm-equipped medical devices used in high-risk areas and for high-risk clinical conditions, and
identify the default alarm settings and the limits appropriate for each care area
3. Establish guidelines for alarm settings on alarm-equipped medical devices used in high-risk areas and for high-risk clinical
conditions; include identification of situations when alarm signals are not clinically necessary
4. Establish guidelines for tailoring alarm settings and limits for individual patients. The guidelines should address situations
when limits can be modified to minimize alarm signals and the extent to which alarms can be modified to minimize alarm
signals
5. Inspect, check, and maintain alarm-equipped devices to provide for accurate and appropriate alarm settings, proper
operation, and detectability. Base the frequency of these activities on criteria such as manufacturers’ recommendations,
risk levels, and current experience.
Source: TJC Sentinel Alert: Sentinel Event Alert Issue 50: Medical device alarm safety in hospitals. April 8, 2013
40
TJC Sentinel Alert Additional Strategies
8. Assess whether the acoustics in patient care areas allow critical alarm signals to be audible
10. Establish a cross-disciplinary team that includes representation from clinicians, clinical engineering, information technology, and risk management, to
address alarm safety and the potential impact of alarm fatigue in all patient care areas.
– Establish a process for continual improvement and constant optimizing of alarm system policies and configurations.
– Review trends and patterns in alarm-related events to identify opportunities for improving alarm use.
– Implement an alarm system management policy, including the periodic review of alarm coverage processes and systems, and the development of
realistic, implementable strategies to address vulnerabilities.
11. Share information about alarm-related incidents, prevention strategies, and lessons learned with appropriate organizations, such as AAMI, ECRI Institute,
the FDA, and The Joint Commission
Source: TJC Sentinel Alert: Sentinel Event Alert Issue 50: Medical device alarm safety in hospitals. April 8, 2013
41
And A Few More
1. Provide proper skin preparation for electrocardiogram electrodes to improve conductivity and decrease the number
of false alarms
4. Customize delay and threshold settings on oxygen saturation via pulse oximetry (SpO2) monitors
6. Establish interprofessional teams to address issues related to alarms, such as the development of policies and
procedures
Source: American Association of Critical Care Nurses. 7 Alarm Management Strategies for Nurses
Written by Sabrina Rodak | June 21, 2013
Goal 7: Reduce the risk of health care-associated infections
NPSG.07.01.01: Comply with either the current CDC hand hygiene 42
guidelines of the current WHO hand hygiene guidelines
1. Implement a program that follows categories 1A, 1B and 1C of either the current
CDC or the current WHO hand hygiene guidelines.
• Hand hygiene compliance data are not collected or reported accurately or frequently
• Hands full
• Distractions
Source: The Joint Commission Journal on Quality and Patient Safety, January 2015, Volume 41, Number 1. Sustaining and Spreading Improvement in Hand
Hygiene Compliance
44
Strategies
3. Connect the World Health Organization's five moments for hand hygiene to the whole patient journey
Source: Becker’s Hospital Review: 7 ways to improve hand hygiene, from hospital managers Written by Heather Punke (November 21, 2014
World Health Organization – Five Moments 45
Safety culture does not stress hand hygiene at • Make hand hygiene a habit—as automatic as looking both ways when you cross the street or
all levels . fastening your seat belt when you get in your car.
• Ensure commitment of leadership to achieve hand hygiene compliance of 90+%
• Serve as a role model by practicing proper hand hygiene.
• Hold everyone accountable and responsible—physicians, nurses, food service staff,
housekeepers, chaplains, technicians, therapists.
Solutions Targeted to the Main Causes of Hand Hygiene Failures47
Source: The Joint Commission Journal on Quality and Patient Safety, January 2015, Volume 41, Number 1. Sustaining and Spreading Improvement in Hand
Hygiene Compliance
49
Methods for Measuring Handwashing Compliance
• Direct observation
– This method involves monitoring the actual hand hygiene actions of staff. It can be done manually — with an actual
person doing the monitoring — or it can be done with the assistance of technology such as smartphone apps. The
smartphone apps can improve the likelihood of making covert observations and reduce the instances of Hawthorne
effect, which is a social occurrence in which individuals alter or improve their behavior in response to their awareness of
being observed.
• Electronic monitoring
– Several different types of sensors are now available to measure handwashing compliance. While they can be expensive, a major
benefit of electronic monitoring is it can provide administrators with real-time feedback on compliance prior to a healthcare worker's
interaction with patients.
Compliance with environmental hygiene can be measured by direct observation, fluorescent markers, ATP or environmental culture.
There are advantages and disadvantages for each of these measures, but according to the CDC Toolkit: Options to Evaluate
Environmental Hygiene, the goal is to optimize high touch surface cleaning using an objective monitoring and feedback method.
Carolyn’s View 50
• Observe
– Wound debridement
– PICC Line Insertion
– IV insertion
– Medication Administration
– Compounding
– Delivering meal trays
– Isolation
– Respiratory treatments
– Invasive procedures
Goal 9: Reduce the risk of patient harm resulting from falls (Nursing Care Center)
Goal 14: Prevent health care-associated pressure ulcers (Nursing Care Center)
Goal 15: The hospital identifies safety risks inherent in its patient population (Hospital
Universal Protocol for Preventing Wrong Site, Wrong Procedure and Wrong Person
Surgery
52
Page 53
TJC 2017/2018 National Patient Safety Goals
Goal 1: Improve the accuracy of patient and resident identification YES! Maybe NO
NPSG.01.01.01 Use at least two patient identifiers when providing care, treatment, and
services.
NPSG.01.03.01 Eliminate transfusion errors related to patient misidentification.
NPSG.02.03.01 Report critical results of tests and diagnostic procedures on a timely basis.
NPSG.03,04.01 Label all medications, medication containers, and other solutions on and off the
sterile field in perioperative and other procedural settings.
NPSG.03.05.01 Reduce the likelihood of patient harm associated with the use of anticoagulant
therapy.
NPSG.03.06.01 Maintain and communicate accurate patient and resident medication
information.
Page 54
TJC 2017/2018 National Patient Safety Goals
Goal 6: Reduce the harm associated with clinical alarm systems YES! Maybe NO
NPSG.07.01.01 Comply with either the current CDC hand hygiene guidelines or the current
WHO hand hygiene guidelines.
NPSG.07.03.01 Implement evidence-based practices to prevent health care-associated
infections due to multidrug-resistant organisms.
NPSG.07.04.01 Implement evidence-based practices to prevent central line-associated
bloodstream infections.
NPSG.07.05.01 Implement evidence-based practices for preventing surgical site infections.
Goal 14: Prevent health care-associated pressure ulcers (decubitus ulcers) YES! Maybe NO
NPSG.14.01.01 Assess and periodically reassess each patient’s and resident’s risk for developing
a pressure ulcer and take action to address any identified risks.
Goal 15: The hospital identifies safety risks inherent in its patient population YES! Maybe NO
Universal Protocol for Preventing Wrong Site, Wrong Procedure, and Wrong YES! Maybe NO
Person Surgery
UP.01.01.01 Conduct a preprocedure verification process.
The New Health Care Innovation Model: National Patient Safety Goals – Part 2
Is It All Hocum? Carolyn St.Charles, Regional Chief
Diane Bradley, Regional Chief Clinical Clinical Officer
Officer October 13, 12:00pm Central
September 22, 12:00pm Central https://attendee.gotowebinar.com/register
http://bit.ly/2sDNKvF /1133422051074822145
58
Thank you! 58