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SPECIAL CONTRIBUTIONS
Profiles in Patient Safety: Medication Errors in the
Emergency Department
Pat Croskerry, MD, PhD, Marc Shapiro, MD, Sam Campbell, MB, ChB,
Connie LeBlanc, MD, Douglas Sinclair, MD, Patty Wren, MD, Michael Marcoux, RPh
Abstract
Medication errors are frequent in the emergency department (ED). The unique operating characteristics of the ED
may exacerbate their rate and severity. They are associated
with variable clinical outcomes that range from inconsequential to death. Fifteen adult and pediatric cases are
described here to illustrate a variety of errors. They may
occur at any of the previously described five stages, from
ordering a medication to its delivery. A sixth stage has been
added to emphasize the final part of the medication
administration process in the ED, drawing attention to
considerations that should be made for patients being
CASE 1
A 65-year-old man presented to the ED of a teaching
hospital at 2218 hours with left-sided weakness, which
started at 2040 hours that day. He also complained of
mild pain (a cranial headache) and nausea, both of
which started at the same time as the weakness. He
had no other neurological symptoms and had never
had similar symptoms in the past. The patient and his
family were well known to the emergency physician.
The patients history included lung cancer for which
he was currently undergoing chemotherapy, adultonset diabetes, and hypertension. He had no allergies.
Medications included dexamethasone, ondansetron,
metoprolol, and ranitidine.
Physical Examination. Vital signs at triage were
Glasgow Coma Scale score (GCS) 15; heart rate (HR)
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TABLE 1. Factors Contributing to Medication
Errors in the Emergency Department (ED)*
Patients are usually strangers
Multiple patients being treated concurrently
Frequent reliance on verbal orders
Wide range of drugs in use
Variety of administration routes
Wide variety of dangerous drugs
Time pressures
Interruptions/distractions
Tight coupling
ED dispensing
Physician administration of medication
Team communication problems
Laboratory errors
Croskerry et al.
CASE 2
An 18-year-old female student presented to the ED of
a regional hospital in the early afternoon with
a complaint of urinary frequency and back pain. Her
last menstrual period was normal. She was taking no
medications other than birth control pills. She had no
allergies. She had no prior history of urinary tract
infection. Her medical history was significant for
glucose-6-phosphate dehydrogenase (G6PD) deficiency.
She was a healthy-looking woman, in no distress,
with normal vital signs. Her physical examination
was unremarkable other than some mild suprapubic
tenderness on palpation. A pregnancy test was negative. Her urinalysis showed moderate leukocytes,
nitrites, and bacteria.
She was informed that she had a urinary tract
infection and that it would be treated with an antibiotic. A starting dose of trimethoprim-sulfamethoxazole was ordered in the ED. She indicated she was
aware of problems of some drugs with G6PD deficiency and asked if the antibiotic was safe. The
emergency physician said that it was and she took the
medication. A prescription was given for a course of
the antibiotic.
Approximately one hour later the emergency physician received a call from the patients pharmacy
where she had presented her prescription. The pharmacist was aware of the patients G6PD deficiency and,
on routinely checking the antibiotic, noted a precaution. Sulfonamides may cause hemolysis in patients
with G6PD deficiency, an effect that is frequently
dose-related. The physician ordered a substitution. He
later called the patient at home and explained the
error. She was advised that it was unlikely she would
develop a problem with one dose. Nevertheless, she
was cautioned to seek immediate medical attention if
she appeared to be suffering any adverse effects.
Comment. This is a prescribing error attributable
largely to a knowledge deficiency. In Reasons Generic
Error-Modeling System (GEMS), it is classified as
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CASE 3
A 45-year-old woman was brought to the ED of
a regional hospital by ambulance. She had been found
unresponsive by her boyfriend. It appeared that she
had taken a mixed overdose, including a significant
amount of a tricyclic antidepressant. Her pulse was
130 beats/min and her BP was 105/50 mm Hg. Her
GCS was 7.
She was prepared for rapid sequence intubation.
The emergency physician called for 5 of midazolam,
IV for induction, administering it himself by slow IV
push over 2 minutes, and the patient was successfully
intubated. Shortly afterward, as the record was being
completed, the recording nurse confirmed with the
physician the medication that had been given, specifically that 25 mg of midazolam had been administered.
The physician corrected her, saying that he had given 5
mL of a solution containing 1 mg/mL of midazolam,
for a total of 5 mg. The nurse informed the physician
that, in fact, he had been given a solution containing
5 mg/mL of midazolam and that the patient
had, therefore, received a total of 25 mg. The patient
appeared to suffer no adverse consequences from
the medication overdose. Specifically, there were no
cardiac arrhythmias. She subsequently underwent
stomach lavage, was further stabilized, and was
transferred to the intensive care unit (ICU) where she
made an uneventful and full recovery.
Comment. This is a form of transcription error. It was
an emergent situation and, therefore, a verbal order
was acceptable. The physician assumed that the
concentration of midazolam was 1 mg/mL, believing
that was the only concentration available in the ED.
He was not aware that the alternative higher
concentration was also in stock. The nurse, who was
relatively unfamiliar with the drug and new to the
ED, was also not aware that more than one concentration was available. Nevertheless, the error would
probably have been avoided if the nurse had stated
the concentration of the solution, or if the physician
had verbally confirmed what he understood the
solution strength to be. Subsequently, the higher dose
was removed from ED stock.
CASE 4
An elder woman with type 1 diabetes presented to the
ED of a general hospital feeling weak and dizzy. She
had recently experienced symptoms of a gastrointestinal infection and had not taken her insulin for 24
hours. She had been vomiting and felt dehydrated.
Her glucometer reading in the ED was 24 mmol/L.
Routine blood work was ordered, an IV line was
started for hydration, and the attending physician
wrote an order for 10U insulin to be given intravenously. The nurse read the order as 100 insulin
and proceeded to give it. The patient subsequently
became obtunded. The error was discovered almost
immediately, and a bolus of IV dextrose was given.
The patient was further stabilized in the ED over
several hours, was transferred to the ICU, and made
an uneventful recovery.
Comment. This is a frequently reported transcription
error. The abbreviation U for units is read as a zero
and the dose subsequently magnified by a factor of 10.
To avoid the error, units should be written out in
full and never abbreviated. Furthermore, any unusual
dose should be questioned by the nurse before
administration. Failure to challenge may be due to
authority gradient effects referred to in the Institute of
Medicine (IOM) report9 and discussed by Turnbull.10,11
CASE 5
A 52-year-old woman presented to the ED of a general
hospital with progressive dyspnea over several days.
She had symptoms of an upper respiratory infection.
She had a history of bronchitis, but her medical
history was otherwise unremarkable. She had a mild
fever of 37.58C, and the remainder of her vital signs
were stable. On examination, she had mild inspiratory
and expiratory wheezes and an exudative pharyngitis, with some tender anterior cervical nodes.
She was given a series of bronchodilators by mask,
resulting in an eventual clearing of her chest. A throat
swab was done, and the patient was informed she
would be given a prescription for amoxicillin. The ED
was extremely busy at the time of her presentation,
and the physician had been interrupted several times
during his care of the patient.
The patient returned to the ED three hours later
with facial swelling, nausea, and tightness in her
chest. She said she had filled the prescription on
leaving the ED and had developed the symptoms
after taking the first dose. She was seen by the same
physician who had first seen her, and was immediately treated with subcutaneous epinephrine, bronchodilators by mask, intramuscular diphenhydramine
hydrochloride, and IV methylprednisolone. Her
symptoms resolved over several hours.
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Croskerry et al.
CASE 6
In a busy ED of a tertiary care hospital, an emergency
physician had several patients in various stages of
workup. He had seen and assessed a female patient in
a monitored bed (bed 16), made a diagnosis of migraine
headache, and prescribed prochlorperazine 10 mg/IV.
Another female patient who presented with chest pain
was in an unmonitored bed (bed 12) and being
investigated for a possible acute coronary syndrome.
When the physician reassessed the patient with
headache, he found the response to the initial therapy
to be inadequate. A few minutes later, at the nursing
station, he asked one of the two nurses to Give the
lady in bed 16 one milligram of dihydroergotamine
(DHE). The nurse promptly carried out the verbal
order and administered the drug to the patient in bed
16. However, before he had spoken to the nurse, the
other nurse working in the area had switched the
chest pain patient to bed 16 so that she could be on
a cardiac monitor. The patient with migraine was
moved to the now vacated bed 12. Some 20 minutes
later, when the first nurse asked the physician about
the new treatment for unstable angina, the potentially catastrophic mix-up was discovered.
Fortunately, the chest pain of the patient given DHE
was found to be of a noncardiac origin and she
suffered no ill effects. When informed of the mistake,
she took it cheerfully without complaint. The administration of a vasoconstrictor to a patient with
vaso-occlusive cardiac disease could have caused
significant exacerbation of her condition.
Comment. This case illustrates several errors. First,
there is a dispensing error. The process of dispensing
a medication is to provide it to the person who will
give the drug, a task usually performed by a pharmacist. In this case, however, the nurse dispenses the
medication from the ED herself, ultimately for the
wrong patient. If a pharmacist had been involved in
the transaction, a bed number would not have
sufficed, and a verification process would have
occurred, matching the drug to a particular patient.
Second, there is an administration error in that the
nurse physically administered the drug to the wrong
patient, without verifying the patients identity. Recent Joint Commission on Accreditation of Healthcare
Organizations (JCAHO) recommendations are that
the identity of the patient be doubly confirmed (e.g.,
by asking the patient his or her name as well as
a numeric check [e.g., date of birth]) prior to
administration. Third, this case raises issues around
the use of verbal orders in the ED. Protocols for the
use of verbal orders vary between EDs, some allowing
them only in urgent or emergent situations. In certain
circumstances, however, protocols may be difficult to
apply because physicians may be involved in urgent
or emergent situations with other patients and unable
to leave to write nonurgent orders. Often nurses will
take verbal orders in these nonurgent situations to
maintain patient flow through the department. In this
particular case, the ED did not have a protocol in
place and, therefore, a safety violation did not
technically occur. However, bed switching of patients
is not uncommon in the ED, and the error might have
been avoided if the order had been written on the
patients chart instead of being given verbally.
CASE 7
A 35-year-old woman presented to the ED of a general
hospital with severe flank pain, accompanied by
nausea and vomiting, which had started early in the
morning. A physician was interrupted in his evaluation of another patient to come to assess the patient
because of her level of distress. After a rapid
assessment, the physician determined that the patient
probably had ureteral colic and asked the nurse to
give fentanyl 100 micrograms intravenously and 100
milligrams of indomethacin rectally. He then returned
to his previous patient.
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CASE 8
A 23-year-old woman presented to the ED of a tertiary
care hospital with a complaint of abdominal cramps.
After assessing the patient, the emergency physician
ordered 20 mg hyoscine butylbromide (Buscopan) IV,
saying Ill give her Buscopan. The department was
busy. He asked a nurse to start an IV line, intending to
administer the drug himself to save her from the time-
CASE 9
A 36-year-old man was brought to a teaching hospital
ED by friends. He had collided with another player
and fallen in a rugby game. He complained of an
injury to his right shoulder. He was placed in a bed in
the minor trauma area and an IV line was started. His
vital signs were stable. He was healthy with no
significant medical history. He was seen by a firstpostgraduate-year (PGY1) resident, who suspected
a shoulder dislocation and ordered an x-ray, which
confirmed his diagnosis. The PGY1 resident asked the
nurse to draw up 10 mg diazepam intravenously and
later administered it to the patient. He then went to
discuss the case with the attending physician.
The attending was already discussing a complex
case with another PGY1 resident that took some time
to complete. It was about 20 minutes before the first
PGY1 was able to present his shoulder dislocation
case. The attending discussed the particular case and
then went on to a general discussion of both anterior
and posterior dislocations and their treatment. He
then asked the PGY1 what he thought should be done
in this particular case. The PGY1 responded that the
patient should be sedated and proposed a maneuver
to reduce the shoulder. The attending concurred with
the general plan and asked where the patient was. The
PGY1 gave the location and then said he had already
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Croskerry et al.
CASE 10
A 70-year-old man at a shopping mall experienced
acute onset of shortness of breath and was brought to
a community hospital ED by ambulance. He was
placed in a resuscitation bed. The monitor showed
a wide-complex ventricular tachycardia with a rate of
140 beats/min. The emergency physician was called
and immediately ordered an intravenous bolus of 100
mg lidocaine. Shortly after, an internist assumed the
care of the patient and proceeded to order a bolus
dose of procainamide according to the ED protocol.
The Kardex, opened at the patients bedside, specified
the dose at 100 mg in 10 mL D5W or NaCl.
Procainamide was supplied to the ED in a 10-mL vial
containing 1,000 mg.
There were three nurses in the resuscitation room.
Nurse A, who was unfamiliar with the protocol, drew
up the full 10 mL into a 10-mL syringe. She asked the
internist if he wanted the whole thing. He assumed
he was getting the dose prescribed in the protocol and
said Yes. The patient, therefore, received 1,000 mg
CASE 11
A 41-year-old man presented to the ED of a general
hospital in the early evening complaining of dizziness
and weakness. He stated that he had two seizures the
previous day. When he tried to walk earlier in the day,
he fell onto his face and had a nosebleed. He crawled
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slurred speech, ataxia, nystagmus, and dysarthria.
Later, he was seen to exhibit some choreoathetoid
movements. He was transferred to the ICU. His
phenytoin level peaked at 259 mmol/L at 1310 hours.
The intensivist ordered a repeat phenytoin level on
the first sample that had been taken in the ED, to be
done instead at the laboratory of the local tertiary care
hospital, and this came back at 185 mmol/L. The
patient appeared to suffer no further deterioration.
His neurological status normalized over several days,
and he made an uneventful recovery.
Comment. This case illustrates a variety of errors. The
first is anchoring.7 Both the triage nurse and the
physician appear to accept the patients account of
seizures. Self-reports of seizures and periods of
unwitnessed loss of consciousness are notoriously
unreliable. In fact, it appears clear from the patients
account that the fall was not associated with a seizure
and was probably due to ataxia from phenytoin
toxicity. However, once the physician and nurses had
anchored to the idea that the patient had been having
seizures, then the none detected phenytoin result
would be readily accepted and incorporated into
a prematurely closed diagnosis,7 an example of
confirmation bias.7
The next error occurs in the laboratory. The three
phases of laboratory error are preanalytic, analytic, and
postanalytic (for a recent review, see Bonini et al.19).
The present case is an example of an analytic error (i.e.,
it occurs during the stage of specimen analysis). This is
the phase during which errors are least likely.19
Following the discovery of the error, the laboratory
technician recalled getting a code of ** NR when the
sample was run. The NR refers to No Result and
indicates that the level is outside the dynamic range,
either too low or too high. The procedure then is to
dilute the sample and repeat the test. However, the
code was misunderstood by the technician, read as
not detectable, and reported as such.
The laboratory error is further compounded by
assumptions and subsequent events in the ED. The
patient had told both the triage nurse and the
physician that he had taken his usual dose of
phenytoin (3 3 100 mg) that day. Thus, when the
phenytoin result was reported as none detected, it
should have been questioned immediately. (In fact,
the patient had actually overdosed on phenytoin
before presenting to the ED). If another patient simply
had presented with a seizure disorder despite taking
antiseizure medication, the laboratory value would
not have gone unchallenged. However, this patients
psychiatric diagnosis of personality disorder, coupled
with the inconsistent history, resulted in the laboratory values being given more credence, and he
subsequently received a loading dose of phenytoin
on top of an already toxic phenytoin state. Credibility
of the patient is one of a number of errors uniquely
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CASE 12
A 62-year-old man was brought to a community
hospital by ambulance. About an hour earlier he had
developed severe midline chest pain radiating between his shoulder blades. It was associated with
numbness in both arms, dyspnea, diaphoresis, and
vomiting. He was taken immediately to the cardiac
room where vital signs, blood work, and a 12-lead
electrocardiogram (ECG) were done. A second IV line
was started. His blood pressure was 180/100 mm Hg,
pulse 110 beats/min, and respiratory rate 22 breaths/
min. The ECG showed significant ST-segment elevation in several leads. The cardiac nurse took it to the
physician, a family practitioner who did regular shifts
in the ED. The nurse asked whether she should start
mixing the thrombolytic. The physician agreed and
went to assess the patient.
The patient was in significant distress. He was pale
and sweaty. He was taking no medications other than
antihypertensives and had no cardiac history. The
nurses had prepared the patient for thrombolysis and
asked for permission to proceed. The physican had
thrombolysed a patient only twice before and asked
for a call to be placed to the cardiologist on call. He
ordered morphine for the patient. The cardiologist,
who was out of hospital, responded promptly and
discussed the case with the physician. On the basis of
the history he was given, and a description of the ECG
findings, he advised that the patient was likely
experiencing an acute myocardial infarct and the ED
could go ahead with thrombolysis or wait until the
cardiologist arrived in about 30 minutes. The physician decided to go ahead.
The cardiologist arrived in about 25 minutes, by
which time a bolus of thrombolytic had been given,
and an infusion started. A portable chest x-ray was
done but the results were not yet available. While he
was reviewing the ECG, the patient experienced
cardiac arrest. All efforts at cardiopulmonary resuscitation failed and he was declared dead. The
CASE 13
A 6-month-old female with no significant medical or
surgical history was brought to the ED with a fever
(maximum body temperature 1028F), overnight irritability for two nights, and having vomited once that
day. On examination, a bulging fontanel was noted, as
well as a new flat, blanching rash. In the ED, the
patients temperature was 101.48F (rectal), pulse was
160 beats/min, and respiratory rate was 40 breaths/
min. A lumbar puncture was ordered to rule out
meningitis. The patients weight on the ED record was
listed as 15.6 kg, so the patient was given acetaminophen 240 mg rectally and ceftriaxone 1.5 g intravenously.
It was subsequently discovered that the patients
weight of 15.6 that was entered in the space marked
for kilograms was actually pounds. The patients
actual weight was 7.1 kg. This error resulted in
a twofold dosing error of both acetaminophen and
ceftriaxone. The patient appeared to suffer no adverse
effects from these two overdoses.
Comment. The pediatric chart in this ED had a box
for the childs weight in kilograms only. However, the
weighing scales had the option for weighing in either
pounds or kilograms. In this case, the nurse weighed
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CASE 14
A 40-year-old man with no significant medical history
and taking no medications came to the ED complaining of right-sided chest wall pain intermittently
for one week. The pain was exacerbated by deep
inspirations and sometimes by light activity. No
shortness of breath, retractions, or nasal flaring was
noted, and the monitor showed normal sinus rhythm.
Blood pressure was 140/80 mm Hg, pulse 84 beats/
min, respiratory rate 16 breaths/min, and pulse
oximetry 99%. Tests included complete blood count
(CBC), Chem 7, liver function tests (LFTs), chest x-ray,
ECG, and ventilation-perfusion (V-Q).
The laboratory later called to report a critical result
of a blood glucose of 39 mg/dL. The patient was
immediately given 1 ampule of 50% dextrose (25 g in
50 mL). Approximately one hour later, the laboratory
notified the ED that the result previously reported
was for the wrong patient. This patients correct
glucose value was 94 mg/dL. No adverse effects
resulted from the error.
Comment. This is an example of a postanalytic
laboratory error, involving patient identification. Postanalytic errors constitute a relatively small proportion
of all laboratory errors,19 but ED personnel should be
vigilant for them. In this case, the erroneous laboratory
value is accepted uncritically by the ED and acted on.
Whenever an abnormal laboratory value is received
that is inconsistent with the patients clinical assessment, it should always be challenged and, if possible,
repeated before action is taken (e.g., potassium values
that are aberrant due to hemolysis or sampling procedures are not uncommon in EDs).
CASE 15
A 5-week-old female was brought to the ED at 1754
hours with a history of fever since the previous
evening. She had been irritable during the day and
had refused to feed. Her 2-year-old sibling had been
unwell a few days earlier with a presumed viral
respiratory and gastrointestinal illness. The babys
medical history was unremarkable. She had been born
at term by caesarian section because of maternal hip
dislocation. Her birth weight was 3.4 kg.
At triage, she appeared mottled with a full fontanel.
HR was 190 beats/min, respiratory rate 52 breaths/
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min, O2 saturation 99%, and rectal temperature
40.38C. Her weight was 4.7 kg. She was brought into
the department at 1800 hours and seen by a pediatric
PGY2 resident at 1810 hours. On examination she was
irritable. The head and neck examination was normal,
chest clear, cardiovascular examination normal, and
abdomen soft and nontender. She had a fine maculopapular rash over her abdomen. A full septic
workup was performed, including a catheter urine
specimen, blood culture, and lumbar puncture.
Ampicillin 230 mg and gentamicin 35 mg IV were
ordered by the resident. There was no documentation
on the ED record from the staff physician. The
gentamicin was given in the ED at 2025 hours. This
dose was three times the usual dosage. Ampicillin
was not given until the baby arrived on the ward at
2250 hours. The admitting orders were written by
a second PGY4 resident who transcribed the same
doses of antibiotics. The nurse on the ward identified
the error, and a verbal order was received to hold
gentamicin for two doses and to reduce the dose to 12
mg every eight hours. No further gentamicin was
given, and cefotaxime and acyclovir were added to
the treatment.
The medication error was disclosed to the family.
The father, who worked in quality control in the
airline industry, remained very angry throughout the
hospital stay. Hospital quality resources were involved in the case. A final diagnosis of enteroviral
meningitis was made, and the baby made an uneventful recovery. Arrangements were made to follow
her for a potential hearing loss, but it was anticipated
that causality with the medication error might prove
difficult to establish because viral meningitis is also
associated with hearing deficits.
Comment. The primary error is one of dose calculation, which is common in pediatrics, and classified as
a rule-based mistake. In this case, a threefold error
was made because the first resident calculated the
total dose for 24 hours but then wrote it as
gentamicin 35 mg/IV/q8h. For this hospitals
formulary, the recommended total daily dose for this
weight is 7.5 mg/kg/day. The error would have been
less likely if a forcing function had been applied,
requiring this order to be written as total daily dose
of 35 mg, based on 7.5 mg/kg/day, to be given as 12
mg IV q8h. The obvious discrepancy with the childs
weight would then more likely have been detected.
The transcription of the same dose by the second and
more senior resident is a form of copycat error. It may
have been due, in part, to fatigue, which is known to
contribute to error.23 She had been working since 0800
hours and had already been at work for 15 hours when
she wrote the admitting orders. There is also a timedelay error in that with a working diagnosis of meningitis, the first dose of antibiotic was administered
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TABLE 2. The Medication Process, Error-producing Conditions, and Prevention Strategies in the
Emergency Department (ED)*
Stage
Prescribing
.
Transcribing
.
Dispensing
.
Administration
.
Monitoring
.
Discharge drugs
Error-producing Conditions
Prevention Strategies
Verbal orders
Poor penmanship
Team communication errors
Dispensing by nurses
Dispensing by physicians
Patient ID
more than two hours after the patient was first seen
by the resident, and the second antibiotic dose was
not given until more than four hours after. This error
proved inconsequential because the final diagnosis
was viral meningitis.
CONCLUSIONS
This series illustrates a variety of adult and pediatric
medication errors, occurring in each of the five stages
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