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. Author manuscript; available in PMC: 2015 Sep 3.
Published in final edited form as: J Patient Saf. 2011 Jun;7(2):66–71. doi: 10.1097/PTS.0b013e31820c98ba

Table 2.

Results, ranked by final rating, for Rounds 1-3 assessing 19 outpatient ADE triggers for utility of patient interventions

Outpatient ADE Trigger Information Utility of Patient Intervention (1=High, 9=Low)
Name Rule Goal Description Round 1 Round 2 Round 3
N Median
(Range)
N Median
(Range)
N Median
(Range)
Warfarin [Started on warfarin within 14 days AND (International
Normalized Ratio (INR)>3.0 AND INR increased by 1
within 2 days) AND no repeat INR within 2 days]
OR (Started in warfarin longer than 14 days prior AND
INR>4 AND no repeat INR within 2 weeks)
OR (INR>6 AND no repeat INR within 2 days)
Detect rapid or
excessive
anticoagulation to
prevent bleed
Look for over
anticoagulation and no
evidence of rechecking
within reasonable
window
8 1.0
(1-5)
7 1.0
(1-2)
6 1.0
(1-2)
Potassium-
high
[(K+>5.5 and up by >10% since last measurement)
OR (K+>6.0)]
AND (Potassium (K) raiser active OR Potassium reducer
discontinued 1 day to 4 weeks days prior)
AND No new potassium reducer
OR Decrease in potassium raiser within 5 days of
triggering result
Detect hyperkalemia
to prevent further
increase and
arrhythmia
Look for rising
potassium and no
evidence of change
7 1.0
(1-6)
6 1.0
(1-2)
5 1.0
(1-3)
Potassium-
low
Use of potassium (K) reducer
AND [K <3.0 OR (K < 3.5 AND K decreased by >15%)
versus previous measurement]
AND (No new potassium raiser OR decreased potassium
reducer) within 5 days of triggering potassium result
Detect hypokalemia
to prevent further
decline and
arrhythmia
Look for dropping
potassium and no
evidence of change
7 2.0
(1-7)
6 2.0
(1-3)
5 2.0
(1-3)
Delirium Active prescription of sedative hypnotic including
anticholinergic AND Subsequent new diagnosis of
(dementia, fall, delirium)
Detect impairment in
consciousness and
cognition to improve
quality of life
Look for psychotropic
with subsequent decline
in consciousness or
cognition
7 2.0
(1-7)
6 2.0
(1-3)
5 2.0
(1-3)
Bone
Marrow
Toxin
(On bone-marrow-toxic drug with a course more than 2
weeks AND No chemotherapy within 2 weeks)
AND [(white blood cell count (WBCs)<2,500 AND
decrease from before course by more than 2,000) OR
(WBCs<2,000 AND decrease from before course by
more than 1,000) OR (Platelets<50k AND decrease by
75k within 1 week)]
AND (no repeat complete blood count OR no decrease in
drug) within 5 days of triggering result
Detect early signs of
myelo-suppression to
prevent more severe
cases
Look for decrease in
cells after non-cancer
drug and no evidence of
recognition
7 1.0
(1-3)
6 1.0
(1-2)
5 2.0
(1-4)
Hepato-
toxic
Active prescription for hepatotoxic drug
AND aspartate aminotransferase (AST) or alanine
aminotransferase (ALT) levels >150
Detect potential
hepatotoxicity to
prevent serious liver
damage
Look for development of
hepatotoxicity while on
drug that can cause
hepatotoxicity
7 2.0
(1-3)
6 2.0
(1-3)
5 2.0
(1-4)
Thyroid Abnormal thyroid-stimulating hormone (TSH) test on
thyroid replacement and no repeat test or new
prescription of thyroid replacement within 2 months of
triggering value.
Detect out of range
thyroid to prevent
related problems
Look for out-of-range
TSH without evidence of
follow up
8 2.5
(1-7)
7 3.0
(1-4)
6 3.0
(2-4)
Antibiotic Trough levels of antibiotic more than double the
recommended maximum AND at least two days left in
the course
AND no reduction in dose of the antibiotic.
Prevent antibiotic
toxicity (hearing and
renal function)
Look for dangerously
high trough levels
8 2.0
(1-3)
7 2.0
(1-3)
6 3.0
(2-4)
Steroid Long-term prescription of oral glucocorticoid (written for
3-months supply or for 6 months of refills or renewed
after 3 months)
AND at 6 weeks after steroid started no bisphosphonate
prescribed
Detect long-term
steroid course with
inappropriate
monitoring/ treatment
for prevention of
related problems
Look for long term
course of steroid and no
bisphosphonate or no
glucose check
8 3.0
(1-6)
7 3.0
(2-6)
6 3.0
(3-6)
Blood
Pressure
Diagnosis code for (fall, dizziness, orthostatic
hypotension)
AND antihypertensive started within 3 months
AND systolic BP below 140
AND no reduction in or new prescription for any
antihypertensive medication
Detect symptomatic
low BP to prevent
further problems
Look for problem
associated with relatively
low BP and no evidence
of addressing the
problem
7 4.0
(1-9)
6 3.0
(1-8)
6 3.0
(1-6)
Anti–
Platelet
Receiving antiplatelet agent
AND platelets < 50,000/m3
AND no repeat complete blood count within 2 weeks
Detect platelet
impairment with
thrombocytopenia to
prevent bleed
Look for low platelets in
a patient receiving an
antiplatelet agent
7 3.0
(1-9)
6 3.0
(1-8)
6 3.0
(2-9)
Creatinine [New order or increase in (direct GFR reducer OR
volume reducer OR nephrotoxin) within (1-5 days OR 1
day to last creatinine measure)
AND (No new trimethoprim within 5 days)]
AND (No decrease in any meds above since the last
creatinine measure OR no repeat order for creatinine)
AND (>25% reduction in creatinine clearance since
initiation or increase of above med AND resulting
creatinine clearance < 50)
Detect decreased
renal function to
prevent reactions
from other drugs that
are renally cleared
Soon after starting a drug
that might decrease
creatinine, look for a
decrease in creatinine
clearance to a concerning
level and make sure that
the new drug has not
been decreased.
7 3.0
(1-9)
5 3.0
(2-9)
6 3.5
(2-7)
Calcium
Channel
Blocker
Weight increased >6 pounds between 2 weeks and 3
months of starting dihydropyridine calcium-channel
blocker (CCB)
AND no diagnosis of congestive heart failure
AND (no discontinuation of CCB OR no new
antihypertensive other than a diuretic)
Detect edema to
mitigate it
Look for rapid weight
gain soon after starting
CCB that may induce LE
edema and no evidence
of recognition
7 3.0
(2-9)
6 3.5
(2-6)
6 4.5
(3-8)
Theo-
phylline
Theophylline level >20 μg/ml
OR Theophylline given for >12 months with no level
measured
Detect potential or
actual dangerous
theophylline level to
prevent dangerous
adverse reactions
Look for high
theophylline level or
inadequate monitoring
7 4.0
(2-8)
6 4.5
(3-8)
5 5.0
(4-8)
Parkin-
sonism
Change from (typical to atypical antipsychotic OR from
any antipsychotic to quetiapine) within 4 weeks of
starting therapy
OR [prescription of dopaminergic medication OR new
diagnosis of (akathisia OR parkinsonism OR tremor)]
within 3 months of starting
Detect drug induced
parkinsonism
Look for early change to
less toxic antipsychotic
or new diagnosis of
common adverse effects
of antipsychotic
medication
7 5.0
(2-9)
6 5.0
(3-9)
5 5.0
(3-8)
ACE
Inhibitor
New order for Angiotensin II Receptor Blockers (ARB)
within 3 months of starting Angiotensin Converting
Enzyme Inhibitor (ACEI)
Detect cough from
ACE inhibitor
Look for switch from
ACE inhibitor to ARB.
7 5.0
(2-9)
6 5.0
(4-9)
6 5.0
(4-9)
C-Diff Prescription of (oral vancomycin or metronidazole OR
Order for Clostridium Difficile culture or toxin OR ICD9
code for C. diff colitis or similar codes) within (1 day
after start AND before 4 weeks after the completion) of
an antibiotic course
OR Prescription of antidiarrheal within (1 day after start
AND before 3 weeks after the completion) of an
antibiotic course
Detect antibiotic-
associated diarrhea
Look for evidence of
clinical suspicion of C.
difficile colitis or regular
antibiotic-associated
diarrhea
8 6.0
(1-9)
7 6.0
(1-9)
6 6.0
(3-7)
Fungal Prescription of an oral or vaginal antifungal between 3
days after start of antibiotic and 10 days after end of
course.
Detect antibiotic-
associated fungal
infection
Look for treatment of
mucosal fungal infection
8 7.0
(3-9)
7 7.0
(3-9)
6 7.0
(3-9)
Anti-
depressant
Within a time frame of 1 day to 6 weeks after the
prescription of an antidepressant, prescription of a
different antidepressant.
Detect any adverse
event from an
antidepressant
Look for new
antidepressant within a
time frame that is more
suggestive of replacing a
prior antidepressant than
augmentation therapy.
7 7.0
(3-9)
6 7.5
(3-9)
6 7.5
(3-8)

ADE=Adverse drug event

N= number of participants who rated the trigger

Highlighted cells indicate triggers that met consensus criteria in Round 2and were selected for testing with patient-level data