High Alert Drugs |
Although
most medications have a wide margin of safety, a few have a
risk of causing injury when they are misused. These are termed
"high alert drugs". Although errors may or may not
be more common with these drugs than with others, their consequences
may be more devastating. [Cohen MR, Kilo CM. High- alert medications:
Safeguarding against errors. In Cohen MR, ed. Medication Errors.
American Pharmaceutical Association, Washington, DC, 1999.]
Examples of high alert drugs include heparin,
insulin, chemotherapy, concentrated electrolytes, IV digoxin,
opioid narcotics, neuromuscular blocking agents, and adrenergic
agonists. |
Implement |
Accomplish
or achieve in practice, not just policy, to carry into effect. |
Potentially
Serious Medication Error |
A medication
error that has the potential to cause serious patient harm, but
did not actually reach the patient or did not cause serious harm
if it did reach the patient; a serious "near miss." |
Practitioner |
In this self-assessment
tool, "practitioner" refers to professional staff such
as physicians, pharmacists, nurses, and other licensed healthcare
staff members. |
Age-Specific Medications |
Medications packaged in concentrations or volumes of varying sizes
that are intended for ease of administration and control of waste
for a specific age group (e.g., neonatal, paediatric, adult). |
Error-Prone Abbreviations |
Certain medical abbreviations, symbols, and dose designations
that are considered “dangerous” and have often contributed
to serious medication errors. A sample list can be found on the
ISMP web site (www.ismp.org). |
Failure Mode and Effects
Analysis |
A proactive risk assessment method based on the simultaneous analysis
of possible failure modes, their consequences, and associated
risk factors. |
Human Factors |
The interrelationships between humans, the tools they use, and
the environment in which they work. |
Independent
Double Check |
A process
in which a second practitioner conducts a verification. Such
verification can be performed in the presence or absence of
the first practitioner. In either case, the most critical aspect
is to maximize the independence of the double check by ensuring
that the first practitioner does not communicate what he expects
the second practitioner to see, which would create bias and
reduce the visibility of an error. For example, an error in
calculation is more likely to be detected if the second person
performs all calculations independently, without knowledge of
(without seeing) any prior calculations. |
Interface |
A
direct link between two information systems such that the information
from one system is immediately available to the user of the
second system, and is integrated in a way that supports clinical
decision making (e.g., interfacing the laboratory and pharmacy
computer systems would immediately provide corresponding laboratory
data to the pharmacist while entering or reviewing a specific
medication order). This may or may not include a bi-directional
interface if two systems allow communication in both directions. |
Machine-Readable
Coding |
Any encoded
identifying mark (e.g., bar code) representing data that can be
read with a computerized reading device, such as a scanner or
imager. |
Maximum
Dose |
The dose of
medication that represents the upper limit that is normally found
in the literature or manufacturer’s recommendations. Maximum
doses may vary according to age, weight, or diagnosis. |
Medication
Delivery Devices |
Equipment such
as syringes, tubing, infusion pumps, implantable pumps, patient
controlled analgesia pumps, automated compounding devices, robotics,
and other related devices that are used for medication preparation,
dispensing, and administration. |
Mnemonic |
A limited number
of letters and numbers that are used to represent a specific medication
(e.g., ASA80T may represent aspirin 80 mg tablets). |
Moderate
Sedation |
The administration
of any pharmacological agent, which will likely cause a medically
controlled state of depressed consciousness. This state would
be limited to short periods and utilized for diagnostic and therapeutic
procedures that: 1) allow the protective reflexes to be maintained,
2) retain the patient’s ability to maintain a patent airway,
respiratory rate and rhythm, and 3) permit expected responses
by the patient to physical stimulation and verbal command. |
Pharmacy
and Therapeutics Committee |
An interdisciplinary
committee that convenes on a scheduled basis, or when necessary,
to review the safety, use, efficacy, and monitoring of medications
that will be available for use in the hospital. The committee
also sets policy and procedures regarding the safety of the entire
medication use process, on behalf of the medical staff and hospital
administration. |
Patient-Specific
Medication or Dose |
A ready-to-administer
dose of medication that exactly matches the dose ordered by the
prescriber for a specific patient. This may or may not correspond
to the manufacturer’s unit dose package. |
Root
Cause Analysis |
A retrospective
process for identifying the most basic or causal factors that
underlie the occurrence or possible occurrence of an adverse event. |
Smart
Pump Technology |
An infusion
pump with computer software that is capable of alerting the user
to unsafe dose limits and programming errors if standard concentrations
and dose limits have been programmed into the pump’s library.
Smart pumps may also have the capability to block user over-rides
and be bar code technology compatible. |
TALL-Man
Lettering |
Enhancement
of unique letter characters of drug names by use of upper case
characters, and may include italics, colour background, or a combination
of these elements to improve differentiation of look-alike drug
names. |
Turnaround
Time |
An interval
that represents the period of time it takes for a medication order
to be processed, typically from the time an order is written or
electronically entered into a computer until the medication is
available to a practitioner for administration to a patient. |
Unit
Dose |
A single package
that contains one dose of medication intended for one patient
(e.g., a package with one tablet, one single-use vial of parenteral
medication, 5 mL container holding one dose of liquid medication). |
Unit-of-Use |
A supply of
medication that is intended for several doses of therapy, for
a single patient (e.g., an inhaler, a tube of ointment or a 100
mL bottle of cough syrup). |
WalkRounds™ |
A formal
process in which a core group, including senior executives,
conducts weekly visits to different areas of the hospital to
ask specific questions about adverse events or near misses and
about factors or system issues that lead to these events. [Frankel
A, Graydon-Baker E, Neppl C, Simmonds T, Gustafson M, Gandhi
TK. Patient safety leadership WalkRoundsTM. Jt Comm J Qual Safety.
2003;29:16-26.] |