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Critical Pathways for Triage and Treatment Of Chest Pain Patients
in the Emergency Department
Joseph P. Ornato, MD, FACC
Professor of Internal Medicine (Cardiology)
Director of Research
Department of Emergency Medicine
Virginia Commonwealth University/Medical College of Virginia
Richmond, VA
Quick Overview
Introduction
Clinical Pathways "Track" Approach
Preliminary Experience With This Strategy
Conclusion
Introduction
Aggressive intervention, including thrombolytic therapy and mechanical revascularization,
has been demonstrated to reduce mortality and minimize left ventricular
damage consistently when initiated early after the onset of symptoms of
acute myocardial infarction (AMI). (1-6) The need for urgent diagnosis and
intervention has prompted many institutions to explore alternative methods
for rapid screening of patients who present to the emergency department
(ED) with chest pain.
The purpose of this paper is to: (1) describe a process for the multidisciplinary
development of a comprehensive strategy for triage and evaluation of patients
who present to the ED with chest pain; (2) describe a specific strategy
that has evolved at the Medical College of Virginia that incorporates several
different technologies, including standard 12-lead electrocardiography (ECG),
echocardiography, continuous ST-segment monitoring, myocardial markers of
necrosis, and technetium Tc-99m sestamibi; and (3) present preliminary results
on our first 18 months of experience using this strategy.
Clinical Pathways "Track" Approach
The Medical College of Virginia is a 1,080-bed tertiary care academic medical
center. Its 96-bed ED complex is divided into five contiguous subspecialty
treatment units (acute medicine/cardiac, acute surgery/trauma, pediatrics,
obstetrics/gynecology, and episodic primary care). Together, the five units
treat more than 108,000 emergency patients per year.
We have recently implemented a sophisticated Cardiac Emergency Department
approach to the triage and treatment of patients with suspected cardiac
ischemia. (7) The strategy has three basic goals: (1) to rule out AMI; (2)
to rule out unstable angina; and (3) to screen for the presence of clinically
significant coronary artery disease (CAD) in patients who are believed to
be at risk.
All patients with chest pain are brought directly into the treatment unit;
an ECG is begun immediately by nurses or specially trained technicians.
The senior physician in charge of the unit is shown the ECG, takes a brief
history, examines the patient, and makes an immediate triage decision, assigning
the patient to one of five levels or tracks (see Figure 1).
Figure 1
Chest Pain Critical Pathways in the ED
Patients with obvious AMI or unstable angina are treated promptly in
the ED and transferred to the coronary care unit (CCU) or cardiac catheterization
laboratory for further care. Less obvious cases are "fast-tracked"
in the CCU with continuous ST-segment monitoring and accelerated creatine
kinase-MB and myoglobin determinations, followed by a technetium Tc-99m
sestamibi rest and exercise study or cardiac catheterization. Atypical low-risk
cases have technetium Tc-99m sestamibi injected within minutes after arrival
in the ED. A gated single photon emission computed tomography (SPECT) rest
scan is performed directly from the ED. If it demonstrates evidence of cardiac
ischemia or impaired left ventricular function, the patient is admitted
to the CCU on a fast-track rule-out AMI protocol. If both studies are negative,
the patient is sent home and returns the next day for an exercise gated
SPECT technetium Tc-99m sestamibi study.
Quick Overview
Introduction
Clinical Pathways "Track" Approach
Preliminary Experience With This Strategy
Conclusion
Preliminary Experience With This Strategy
To determine the ability of radionuclide imaging to detect significant CAD
in "low-risk" ED patients with chest pain, we compared the results
of resting technetium Tc-99m sestamibi SPECT myocardial perfusion imaging
(MIBI) done in the ED with coronary angiography. ED physicians assigned
all chest pain patients to one of five triage levels based on the clinical
probability of acute cardiac ischemia. They initially judged 433 patients
to be at relatively low risk of acute cardiac ischemia (level 4) because
they had chest pain of less than 30 minutes' duration and nondiagnostic
ECGs. A resting MIBI was performed for all of these patients. The study
population consisted of 49 of the 433 patients (45% M, 55% F, median age
57 years, age range 31 to 86) for whom the CCU attending cardiologist ordered
coronary angiography, either because the resting MIBI was abnormal (n=34)
or because there was other clinical suspicion of acute cardiac ischemia
(n=15).
There was a significant correlation (n=49; P< .0003) between the MIBI
results and angiographic findings of significant CAD (>75% narrowing
in at least one major epicardial vessel). MIBI results correlated best with
the coronary angiographic findings when the radioisotope was injected during
pain (n=21; P< .0004); however, results also correlated when the radioisotope
was not injected during pain (n=28, P< .01). These findings suggest that
MIBI is of value for detecting significant CAD in "low-risk" ED
chest pain patients.
To determine whether our systematic protocol for triaging ED patients with
chest pain is cost-effective, we compared median hospital length of stay
(LOS) in days and median hospital charges per patient in thousands of dollars
in a sample of CCU patients admitted for evaluation of chest pain before
(1992; n=67) and after (1994; n=31) institution of our comprehensive triage
protocol. In the absence of ECG evidence of AMI or unstable angina, patients
were injected with technetium Tc-99m sestamibi in the ED and a gated SPECT
rest perfusion scan was performed. Scan results were used to stratify patients
for CCU admission. We analyzed the impact of the protocol on a sample of
patients admitted to the CCU who had a final diagnosis of AMI (ICD 410),
unstable angina (ICD 411), and noncardiac chest pain (ICD 786.5) from before
and after institution of the protocol. Distribution of patients in each
category (percentage of CCU admissions for chest pain, LOS, and charges)
is shown in Table 1.

Hospital charges for AMI increased despite a 37% decrease in length of
stay, reflecting inflationary changes from 1992 to 1994 (the protocol was
not designed to alter AMI patient care in any way). For groups impacted
by the protocol (unstable angina and noncardiac chest pain), there has been
a dramatic decrease in length of stay and a modest decrease in hospital
charges (6% and 31%, respectively). The number of ED chest pain patients
admitted to the hospital has decreased by more than 20% since protocol institution.
With the protocol, more unstable angina patients and fewer noncardiac patients
are now admitted to the CCU.
Conclusion
Our experience thus far appears to support the value of a systematic approach
to the triage and treatment of chest pain patients in the ED. The strategy
appears to identify patients with acute coronary syndromes and/or underlying
CAD who might have been overlooked with a more traditional approach. At
our institution, the chest pain critical pathways appear to be highly cost-effective,
primarily by reducing the number of unnecessary hospital admissions and
dramatically reducing the length of hospital stay for many patients.
References
1. Gruppo Italiano per lo Studio della Streptochinasi nell'Infarto
Miocardico (GISSI). Effectiveness of intravenous thrombolytic treatment
in acute myocardial infarction. Lancet. 1986;1:397-402.
2. ISIS (Second International Study of Infarct Survival) Collaborative
Group. Randomized trial of intravenous streptokinase, oral aspirin, both
or neither among 17,187 cases of suspected acute myocardial infarction:
ISIS-2. Lancet. 1988;2:349-360.
3. Wilcox RG, Olsson CG, Skene AM, et al. (for the ASSET Study Group).
Trial of tissue plasminogen activator for mortality reduction in acute myocardial
infarction. Lancet. 1988;2:525-530.
4. AIMS Trial Study Group. Effect of intravenous APSAC on mortality
after acute myocardial infarction: preliminary report of a placebo-controlled
clinical trial. Lancet. 1988;1:545-549.
5. AIMS Trial Study Group. Long-term effects of intravenous anistreptase
in acute myocardial infarction: final report of the AIMS study. Lancet.
1990;335:427-431.
6. The GUSTO Investigators. An international randomized trial comparing
four thrombolytic strategies for acute myocardial infarction. N Engl
J Med. 1993;329:673-682.
7. Tatum JL, Ornato JP, Jesse RL, et al. A diagnostic strategy using
Tc-99m sestamibi for evaluation of patients with chest pain in the emergency
department. Circulation. 1994;90:I367. Abstract.
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