Medical Staff's Role in Patient Safety
Document Sample


Innovative Techniques for
Physicians to Improve Safety
Tammy Lundstrom, MD
Detroit Medical Center-Wayne State University
VP, Chief Quality and Safety Officer
Improving Patient Safety
means . . .
Reducing medical errors.
Reducing patient harm.
Patient Safety Terminology
Structure Process Outcome
Latent conditions Active failure Adverse event
Root causes Proximate cause Sentinel event
Blunt end Sharp end Patient
Hazards Failures Harm
Overview of a
Comprehensive Program
Detroit Medical Center
13,000 employees
3000 physicians
1000 Graduate Medical Residents
1000 Medical Students
Nursing Students
Pharmacy Students
PA Students
Demonstration of Leadership
Support
Name of System Quality Council changed
to System Quality-Medical Safety Council
Chief Medical Safety Officer named
Medical Safety Committee Established
Monthly reports to the Board
Medical Safety Plan Developed
Value of a Comprehensive
Program
Reduce fear of reporting errors/near
misses, gather more data
Reduce errors through tracking,
trending,analysis, and targeted
improvement projects
Reduce errors through prevention
Comprehensive Program
Comprehensive Medical Safety Program
Medical Safety Committee
Chair- Chief Medical Safety Officer
Employee Safety Patient Safety Environmental Safety
First Steps
Common definitions agreed upon
Common database to enter events
Information flows through each site
Leadership and Performance Improvement
Committee
Information flows from site to system
Critical aspects of safety agreed upon
What is a Safety Culture
And how is it achieved?
Lessons from a Leader
“Safety is not a priority, it’s a
way of life”
Paul O’Neill
CEO Alcoa Steel
Treasury Secretary
Safety Culture Involves Paradigm
Shift
OLD NEW
Who did it? What happened?
Focus on bad event Focus on Near Miss
-Root Cause -FMEA
Top down Bottom up
Punish bad behavior Fix broken processes
Advantage to Focus on near
Misses
No patient harm, therefore no blame
No guilt
Focus on prevention
No fear of litigation
Disclosure of Unanticipated
Outcomes to Patients and
Families
What is an Unanticipated
Outcome?
A negative or unexpected result stemming
from
– A diagnostic test, medical judgment or
treatment, surgical intervention, or
(commission)
– The failure to perform a necessary test,
treatment , or intervention (omission)
Why Disclosure?
We are our patient’s advocates
Literature shows that after an unanticipated
outcome, the patient and family want to
know honestly what happened, and how the
hospital is going to prevent future events
Rebuilds trust
Caregiver/Doctor relationship
Advocating Disclosure
American Society for Healthcare Risk
Managers
JCAHO
AHA
AMA
JCAHO
Standard
RI.1.2.2
Patients and, when appropriate, their
families are informed about the outcomes of
care, including unanticipated outcomes.
AHA
Develop an institutional policy or position statement
on disclosure of unanticipated outcomes
Differentiate between disclosure of an unanticipated
outcome and an admission of liability
Determine who will be responsible for informing
the patient, and, where appropriate, the family
and/or legal representative, about the unanticipated
outcome.
Educate caregivers and staff about your
organization’s policies and procedures covering this
issue, and consider communications training for
those charged with disclosing unanticipated
outcomes
Specify documentation requirements regarding
disclosure
ASHRM
Each Healthcare institution must develop
it’s own policy on management of
unanticipated outcomes
Disclosure of such information to patients
and families must reflect the requirements of
applicable law
Differentiate between unanticipated
outcome and admission of liability
For additional detail
on implementation of
a policy on disclosure
of outcomes,
consistent with the
requirements of this
standard:
AMA
AMA Professional Code of Ethics
Steps to Follow After Event
Care for immediate needs of patient
Preserve evidence (Medical equipment)
Document in the medical record
Report (Risk Management)
Disclose
Documentation
Document only the facts of what occurred
and treatment rendered
NOT
– Blame
– Subjective feelings, opinions
– Speculation
– Reference to “Incident report”
Incident Report
Complete and submit
Notify Risk Management
FDA notification if Medical Device or
Medication
Begin Root Cause/Intensive analysis to
examine process changes that may prevent
future events
Who Will Inform the patient?
The attending physician
May need pre-disclosure conference with
Nursing, Risk Management
All patient questions should be referred to
the attending physician
When Should Disclosure Occur?
As soon as possible after immediate needs
of patient addressed
Gather facts FIRST
May not have all the facts yet, in which case
DON’T SPECULATE! Offer to speak
again as facts become known
How?
Convey compassion
– “I am sorry for your…..” “I am sorry that you…”
Known facts
Privacy
No BLAME on any member of healthcare team
Avoid defensive posture/reaction
Respond to patient complaints (provide forms,
contact patient advocates/ombudsman)
Health Care Worker Involved in
Error
AVOID BLAME
Provide counseling, if needed
Remember: No one goes to work intending
to make a mistake
HCW feel tremendous guilt after event that
harms patient
Examples from the Front
Lines
Physician Leadership is Key
Medication Safety
Why physicians?
Medication Safety
Large % medication errors due to
prescribing (20-49%)
For the most part- physicians prescribe
DMC Medication Safety Committee
– Physician Chair
– Review all events
– Review ISMP alerts/External incidents
– Chemotherapy Administration Policy
Medication Safety- Physician
Lead PI
Look-alike Sound-alike Posters and alerts
Define safe medication order writing
policy/pocket card
Promote physician incident entry
Develop delineation of privileges form
related to chemotherapy administration
Dangerous Intended Meaning Misinterpretation Recommendation
Abbreviation
U Units Mistaken as a zero or a four when poorly Use units
written, resulting in overdose. (4U seen as
"40" or 4U seen as "44")
g Micrograms Mistaken for "mg" when handwritten, Use mcg
resulting in overdose
q.o.d. or Every other day Misinterpreted as qd or qid if the "o" is Use every other day or q
Q.O.D. poorly written. 48 hours and time/day to
begin therapy
TIW Three times a week Misinterpreted as "three times a day" or Use three times a week
"twice a week"
cc Cubic centimeters Misread as "u" (units) Use mL
AU Both ears Misinterpreted as "OU", "OS", and "OD". Use both ears, left ear or
AS Left ear right ear
AD Right ear
OU Both eyes Misinterpreted as "AU", "AS', and "AD" Use both eyes, left eye or
OS Left eye right eye
OD Right eye
Physician Education
Physician Led
Board Support
All physicians and trainees will have 3 hours of
mandated compliance and safety education each
credentialing cycle
Failure to complete required education will be
deemed voluntary resignation
Web-based
Continuing Medical Education credits
Required for all new applications to the Medical
Staff
Physician experts develop and approve education
modules
Physician Education Modules
Sexual Harassment
Code of Conduct
Pain Management
Medical Safety and Incident Reporting
Restraint Use
Conscious Sedation
Infection Control
Life Safety
Moderate Sedation
for Physicians and
Licensed Independent Practitioners
Moderate Sedation
Moderate sedation/analgesia describes a drug-
induced depression of consciousness during which
patients respond purposefully to verbal
commands, either alone or accompanied by light
tactile stimulation. No interventions are required
to maintain a patent airway, and spontaneous
ventilation is adequate. Cardiovascular function is
usually maintained.
Moderate Sedation
Patient Evaluation Standards
History and Physical includes:
– abnormalities of major organ systems with specific
focus on the cardiopulmonary history
– pregnancy status
– previous adverse experiences with sedation/analgesia,
as well as anesthetic techniques
– current medications and drug allergies/adverse
reactions
– time and nature of last oral intake of foods, fluids, etc.
– history of tobacco, alcohol, or substance use or abuse
Moderate Sedation
Patient Evaluation Standards
Focused physical exam that minimally includes an
evaluation of the airway and auscultation of the heart and
lungs.
Assignment of ASA Classification of Physical Status
Pre-procedure laboratory and diagnositic testing guided by
the patient’s underlying medical condition.
History and physical examination are valid up to 30 days
prior to the scheduled procedure. Verification and review
of this information is necessary immediately prior to the
provision of moderate sedation.
Moderate Sedation
Monitoring Standards
Level of consciousness
– Monitoring the patient’s response to verbal and/or tactile stimuli
should be routine (unless contraindicated by procedure).
Pulmonary Ventilation
– Ventilatory function is continually monitored by observation
and/or auscultation during the procedure.
Oxygenation
– Continuously monitored by pulse oximetry with appropriate low
limit alarms.
Hemodynamics
– Baseline blood pressure established; measured at regular intervals
intra and post-procedure. Electrocardiograph continuously
monitored.
Moderate Sedation
Emergency Equipment
Pharmacologic Antagonists and resuscitation
drugs
Intravenous access
Supplemental oxygen
Advanced airway equipment
Cardiac defibrillator
Moderate Sedation
Discharge Criteria
Following the provision of moderate sedation, patients are
monitored until they are suitable for discharge:
– Level of consciousness and hemodynamic/respiratory variables
evaluated and no longer at risk for sedation and cardiorespiratory
depression.
– For patients who received pharmacologic antagonists, post-
procedure monitoring should continue for a sufficient period of
time to detect and appropriately treat its recurrence.
Discharge criteria that pertain to the patient population and
specific procedures is developed:
– A qualified physician or registered nurse should be in attendance
until discharge criteria are fulfilled.
Sharps Safety
Why Physicians?
Physician-Performed Testing
Requirements
Dfn: Test personally performed by a
physician in conjunction with the physical
examination or treatment of a patient
PPT
Amniotic fluid pH
Cervical mucous smears for ferning
Fecal leukocytes
Gastric biopsy urease
Nasal smears for eosinophilia
Occult blood, fecal and gastric
Pinworm exam
PPT
Post-coital mucous exam
Potassium hydroxide preparations
Semen analysis, qualitative
Synovial fluid for crystals
Urine dipstick
Urine sediment microscopy
Vaginal wet mount microscopy
What’s required?
Policy- scope of testing for physicians
Procedure manual- specimen handling
QI program
– Quality control, reagents
– Instrument maintenance
– Corrective action equipment/reagent failure
Documented training- test specific
Competency assessment-credentialing
System for reporting results
How will you comply?
Training and documentation
Reagent control
– No bottles in pockets!!
House staff? Other trainees?
Sharps Safety
Physicians perform many procedures
– Forgotten “frontline worker”
Physician sharps injuries under-reported
HIV conversions
– 57 documented conversions
– 6 physicians
Many Safety devices used primarily by physicians
– Safety Scalpels
– Blunted suture needles
Physician Peer review and
Patient Safety
Incident Reports
Incident Occurs
Root Cause Peer Review
-Process -Physician
specific
practice as it
relates to care
of this patient
Goal of Peer Review
Monitor and improve physician care of
patients
Accomplish by:
– Open, non-punitive discussion
– Review and discuss alternatives
– Disseminate to ALL physicians
Monthly Vignettes
Code Blue
Get away from “monitoring Code”
Move towards: review previous 48 hour
record
– Could this event have been prevented?
– Were signs of deterioration missed?
• Elevated BP, dropping BP
• Elevated HR, dropping HR
• Elevated RR
Get documents about "