Medication Safety Flashcards
(90 cards)
Medication error:
is any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is in the control of the healthcare professional, patient or consumer.
-“ This can include errors made in prescribing, order communication, product labeling, and packaging, compounding, dispensing, administration, education or monitoring”.
Medication error are:
- Preventable
Adverse Drug Reactions (ADRs) are:
- Not preventable
- Usually not avoidable
At Risk Behaviors that can compromise patient safety:
Drug and patient-related:
- failure to check/reconcile home medications and doses
- dispensing medications without complete drug knowledge
- Not questioning unusual doses
- Not checking/verifying allergies
Communication:
- not addressing questions/concerns
- rushed communication
Technology:
- overriding computer alerts without proper consideration
not using available technology
Work environment:
- trying to do multiple things vs. focusing on a single complex task
- inadequate supervision and orientation/training
Community Pharmacy:
Use a second patient identifier.
Ask for the patients address or date of birth in addition to the patients name.
Open the bag.
Employ technology. Flag patients with similar names.
Educate patients.
Sentinel event:
is an unexpected occurrence involving death or serious physical injury of a patient.
Errors of Omission- “OMI” like omitted
Something was left out that is needed for safety.
ex. failing to use a pharmacist double check system for chemotherapy orders.
Error of Commission- “Commi” like committed a crime
Something was done incorrectly.
ex. prescribing bupropion to a patient with a history of seizures.
System Based Causes:
- Focus on the system, not the individual. [Instead of placing blame on the individuals, healthcare professionals should find ways to improve the system (“just culture”)]
- Errors will always occur, but the goal is to design systems to prevent medication errors from reaching the patient.
In a just culture, safety is valued, reporting of safety risks is encouraged without penalization, and a clear and transparent process evaluates the errors.
automated dispensing cabinet
- used to reduce medication errors
- reduce pharmacy workload
Response:
A medication error occurred. What should be done?
Take care of the patient.
Immediately report the error.
Document the error.
External notification
Investigation: RCA (Root Cause Analysis)
Improvement
[Telling the patient]
The patient should be told about the error.
- the pharmacist is typically the one to report a medication error
- circumstances leading to the error should be explained completely and honestly
- patient should understand the nature of the error, what effects the error may have, how he or she actively prevent errors in the future.
——————————————————————————————————————–[Telling the physician]
- the physician must be contacted if the error will lead to a side effect.
- the prescriber must be notified if the error will cause an adverse drug reaction.
- the physician must be told if the error will impact the disease being treated.
Response:
Institutions should have a plan in place for responding to medication errors. The plan should address the following:
1)
2)
3)
4)
5)
1) Internal notification
- who should be notified within the institution and within what time frame?
2) External notification
- who should be notified outside of the institution?
3) Disclosure
- What information should be shared with the patient/family? Who will be present when this occurs?
4) Investigation
- What is the process for immediate and long-term internal investigation of an error?
5) Improvement
- What process will ensure that immediate and long-term preventative actions are taken?
Root Cause Analysis:
**- is a retrospective investigation of an event that has already occurred, which includes reviewing the sequence of events that led to the error.
- the information obtained in the analysis is used to design changes that will hopefully prevent future errors.
- What happened primarily, that caused the event to occur.
Reporting:
what should be reported?
- medication errors
- preventable adverse drug reactions
- hazardous conditions
- “close calls” or “near misses”
Should be reported.
-Medication errors are reported so that changes can be made to the system to prevent similar errors in the future. Without reporting, these events may go unrecognized and will likely happen again because others will not learn from the incident.
Reporting:
Community Pharmacy:
- Staff member who discovers the error reports to corporate office (follow designated reporting structure)
OR
- To the owner of an independently owned pharmacy
- Report within 48 hours (state specific) [Document and begin RCA]
- Many states require that the patient and prescriber are also notified as soon as possible
“The fundamental purpose of reporting systems is to learn how to improve the health care delivery process to prevent errors.”
- Many state boards of pharmacy require quality assurance programs to promote pharmacy processes that prevent medication errors.
Reporting:
Hospital:
-** report via Medication Event Reporting System - MERS
- **report to Pharmacy & Therapeutics committee and Medication Safety Committee
Organizations that specialize in error prevention:
- The Patient Safety and Quality Improvement Act of 2005 (Patient Safety Act) authorized the creation of Patient Safety Organizations (PSOs)
- The Agency for Healthcare Reseach and Quality (AHRQ) administers the provisions of the Patient Safety Act and rules for PSOs
- The ISMP National Medication Errors Reporting Program (MERP): confidential national voluntary reporting program
[ISMP- Institute for Safe medication Practices] - On the ISMP website (www.ismp.org), medication errors and close calls can be reported.
- Click on “Report Errors”
- ISMP National (MERP) Medication Errors Reporting Program: is a confidential, voluntary reporting program
- ISMP website (www.ismp.org), medication errors and close calls can be report
Evaluation & Quality Improvement:
Can be performed _______
- prospectivity
- retrospectively
- continuously
Evaluation & Quality Improvement:
Prospective-
prospective analysis
(FMEA) Failure Mode & Effects Analysis:
- is a proactive method used to reduce the frequency and consequences of errors. FMEA is used to analyze the design of a system in order to evaluate the potential for failures and to determine what potential effects could occur when the medication delivery system changes in any substantial way OR if a potentially dangerous new drug will be added to the formulary.
Evaluation & Quality Improvement:
Retrospective-
(RCA) Root Cause Analysis:
- is a retrospective investigation of an event that has already occurred, which includes reviewing the sequence of events that led to the error. The information obtained in the analysis is used to design changes that will hopefully prevent future errors.
RCA
Identify the problem
Define the problem
Understand the problem
Identify the root cause
Corrective action
Monitor the system
Evaluation & Quality Improvement:
Continuous-
(CQI) Continuous Quality Improvement:
- is the goal for most healthcare settings.
- CQI programs improve efficiency, quality, and patient satisfaction while reducing costs.
ex. Lean and Six Sigma, which are often used together. Lean focuses on minimizing waste, while Six Sigma focuses on reducing defects.
Six Sigma uses DMAIC (define, measure, analyze, improve, control) process.
Reporting- Adverse Drug Reactions:
- at MedWatch Food and Drug Administration
Evaluation & Quality Improvement:
A root cause analysis (RCA) retrospective analysis of the sequence of events that led to the error.
Identifying the sentinel event: is an unexpected occurrence involving death or serious physical or psychological injury of a patient.
Findings from the RCA are used to improve the system and prevent repeated events.