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The aUniversity of California Davis Medical Center, Sacramento, California; the bCleveland Clinic, Cleveland, cThe Ohio State University,
Columbus, and the dUniversity of Cincinnati College of Medicine, Cincinnati, Ohio; the eDuke Clinical Research Institute, Durham, and the fUniversity of North Carolina at Chapel Hill, Chapel Hill, North Carolina; the
g
Pennsylvania Hospital, University of Pennsylvania School of Medicine,
Philadelphia, Pennsylvania; and the hNew York University School of
Medicine, New York, New York. Manuscript received June 30, 2005;
revised manuscript received and accepted September 8, 2005.
CRUSADE is funded by Millennium Pharmaceuticals, Inc., Boston,
Massachusetts, and Schering Corporation, Kenilworth, New Jersey. Bristol-Myers Squibb (New York, New York)/Sanofi Aventis Pharmaceuticals
(Bridgewater, New Jersey) Partnership provides an unrestricted grant in
support of the program.
* Corresponding author: Tel: 916-734-4052; fax: 916-762-8851.
E-mail address: dbdiercks@ucdavis.edu (D.B. Diercks).
0002-9149/06/$ see front matter 2006 Elsevier Inc. All rights reserved.
doi:10.1016/j.amjcard.2005.09.073
occurs in about 40% of patients with nonST-segment elevation (NSTE) acute coronary syndromes (ACSs).1 Although it is intuitive that early identification of NSTE ACS
in patients can facilitate appropriate and timely management, this principle is based on clinical experience without
robust supporting evidence. There are no studies that have
supported a defined time between admission and electrocardiography in the population with NSTE ACS, and it is not
known whether this recommendation is feasible in most
institutions. We evaluated the timing of electrocardiographic (ECG) acquisition in a large, contemporary population of patients with high-risk NSTE ACS to determine
the frequency of ECG acquisition within the recommended
period (10 minutes) according to guidelines of the American College of Cardiology/American Heart Association;
factors associated with a delay in time to ECG acquisition;
and any relation among delays in ECG acquisition, treatment patterns, and clinical outcomes.2
www.AJConline.org
438
Methods
Population: The Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes with
Early Implementation of the American College of Cardiology/American Heart Association Guidelines (CRUSADE)
Quality Improvement Initiative includes patients who are
prospectively identified in the emergency department and
those who are retrospectively identified by discharge diagnosis or procedural logs. Patient inclusion criteria include
ischemic symptoms (lasting for 10 minutes) at rest within
24 hours of presentation and high-risk features such as
ST-segment depression, transient ST-segment elevation,
and/or positive cardiac biomarkers (increased troponin I or
T level and/or creatine kinase-MB level higher than the
upper limit of normal for the local laboratory assay used at
each participating institution).
The CRUSADE Quality Improvement Initiative analyzes
patient records to determine compliance with American
College of Cardiology/American Heart Association guidelines for patients with NSTE ACS.3 Details of this quality
improvement initiative have previously been reported.3 Risk
stratification criteria, such as ECG and biomarker results,
are documented for each patient. Contraindications for recommended NSTE ACS therapies (medication allergy, symptomatic bradycardia, and so forth) are sought to determine
eligibility for guideline-recommended therapies. Timing of
therapies is recorded for medications and for downstream
interventions, such as percutaneous coronary intervention
and coronary artery bypass grafting. Final disposition
(transfer, discharge, or death) is noted for each patient.
All data collection occurs retrospectively and does not
include any patient-identifying information; therefore, informed consent is waived. All participating institutions are
required to comply with local regulatory and privacy guidelines before participation in CRUSADE. Participating institutions are instructed to submit consecutive eligible patients, and data collection occurs by retrospective chart
review after local institutional review board approval of the
initiative. Data are abstracted by trained data collectors
according to standardized definitions. Variables include demographic and clinical information (including age, race,
gender, insurance status, co-morbid illnesses, medical history, clinical presentation, and medical therapies with associated major contraindications), use and timing of cardiac
procedures, laboratory results, and in-hospital outcomes.
Decisions regarding the use of medications and invasive
procedures are made by treating physicians.3
We analyzed the data from patients who were enrolled in
the CRUSADE Quality Improvement Initiative from February 2001 to March 2004. Only patients who presented to
the emergency department were eligible for enrollment;
patients who had transferred directly to the inpatient service
from a non-CRUSADE site were not included. Patients
were excluded if the available time data were incomplete.
Time to electrocardiography was defined as the time
from hospital arrival to ECG performance. It was assessed
439
Table 1
Demographics, characteristics, and presentation grouped by presentation to electrocardiographic acquisition
Demographic Variables
Total
(n 63,478)
ECG 10 min
(n 22,081)
ECG 10 min
(n 41,397)
p Value
Age (yrs)
Women
White race
Insurance
HMO/private
Medicare
Military
Medicaid
Self/none
Diabetes mellitus
Hypertension
Previous heart failure
Current/recent smoker
Dyslipidemia*
Renal insufficiency
Previous myocardial infarction
Previous coronary angioplasty
Previous coronary bypass
Signs of heart failure
Systolic blood pressure (mm Hg)
Pulse (beats/min)
Increased cardiac markers
ST depression
Transient ST elevation
Off-hours presentation
Academic hospital
No. of beds
Capabilities
No services
Catheterization only
Percutaneous coronary intervention, no surgery
Coronary bypass
69 (5780)
41.9%
78.5%
68 (5779)
36.8%
82.1%
70 (5780)
44.6%
76.5%
0.001
0.001
0.0001
0.001
43.5%
41.2%
0.29%
7.99%
6.0%
33.4%
70.3%
20.8%
25.4%
50.0%
15.1%
31.8%
21.6%
21.1%
25.0%
146 (125, 167)
84 (71, 100)
88.8%
37.9%
7.2%
61.5%
29.2%
377 (251, 518)
45.6%
39.3%
0.2%
7.4%
6.4%
32.0%
69.1%
18.7%
27.3%
48.3%
13.8%
33.4%
24.5%
22.7%
22.8%
146 (126, 168)
84 (70, 100)
88.7%
39.3%
8.3%
64.1%
24.5%
366 (248, 500)
42.4%
42.3%
0.3%
8.3%
5.7%
34.3%
70.9%
22.0%
24.3%
44.7%
15.9%
31.0%
20.2%
20.2%
26.2%
146 (125, 167)
85 (72, 100)
88.9%
37.2%
6.5%
60.2%
31.7%
398 (265, 526)
4.4%
9.6%
6.3%
79.7%
3.8%
8.8%
6.2%
81.2%
4.8%
10.0%
6.4%
78.9%
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.001
0.0001
0.085
0.001
0.48
0.0001
0.0001
0.00001
0.0001
0.0001
Serum creatinine level 2.0 mg/dl, creatinine clearance 30 ml/min, or need for renal dialysis.
Weeknights (5 P.M. to 7 A.M. the next day) and weekends (Friday after 5 P.M. through 7 A.M. Monday morning).
ECG electrocardiography; HMO health maintenance organization.
selected by the investigators, consisted of baseline patient factors (including age, gender, race, insurance status, family history of coronary artery disease, hypertension, diabetes, smoking status, hypercholesterolemia,
previous myocardial infarction, previous percutaneous
coronary intervention, previous coronary artery bypass
grafting, previous congestive heart failure, previous
stroke, positive cardiac biomarker levels, evidence of acute
decompensated congestive heart failure, heart rate, and systolic
blood pressure) and provider and hospital characteristics (physician specialty, total number of hospital beds, facilities
available, region, and whether the hospital was considered
academic or nonacademic).
Acute treatment composite scores were created using a
summation of guideline-recommended pharmacologic treatments for the first 24 hours after presentation.2 To assess a
potential hospital effect, participating institutions were examined in quartiles based on the percentage of patients with
a time 10 minutes to electrocardiography. Acute medica-
Results
Patient characteristics: During the study, 98,571 patients were enrolled in CRUSADE. Of these, 83,581 patients presented to the emergency department, and 18,716
440
Table 2
Factors associated with electrocardiographic acquisition after 10 minutes
Variable
Female gender
Off-hours presentation*
Previous percutaneous
coronary intervention
Nonwhite
Insurance
Self/none (HMO self-pay)
Medicare (HMO self-pay)
Medicaid (HMO self-pay)
Current/recent smoker
Academic (vs nonacademic)
Diabetes mellitus
Previous myocardial infarction
Dyslipidemia
Region
Midwest (vs South)
West (vs South)
Northeast (vs South)
Previous heart failure
Previous coronary bypass
Signs of heart failure
Family history of coronary
artery disease
Adjusted OR
(95% CI)
Chi-square
1.29 (1.251.34)
0.86 (0.830.9)
0.86 (0.820.90)
253.0
50.0
48.2
1.16 (1.101.22)
33.8
29.8
0.88 (0.820.94)
1.06 (1.021.1)
1.07 (1.001.14)
0.91 (0.870.94)
1.39 (1.201.60)
1.07 (1.031.10)
0.94 (0.900.97)
0.94 (0.900.98)
0.79 (0.690.92)
0.87 (0.721.04)
0.94 (0.811.08)
1.08 (1.031.13)
0.94 (0.900.98)
1.07 (1.021.12)
0.95 (0.910.99)
23.3
20.3
14.4
11.0
10.75
9.88
9.07
8.51
7.24
6.93
* Weeknights (5 P.M. to 7 A.M. the next day) and weekends (Friday after
5 P.M. through 7 A.M. Monday morning).
College of Cardiology/American Heart Association guidelines (Table 3). After adjusting for confounders, patients
without delay in ECG acquisition were more likely to receive heparin, glycoprotein IIb/IIIa inhibitors, and clopidogrel within 24 hours of arrival.
Although there was an increased incidence of unadjusted
in-hospital death in patients with a delayed electrocardiogram (5.4% vs 4.7%, p 0.001), there was no statistically
significant difference in the adjusted risk of death and other
adverse clinical outcomes (Table 4).
Hospital acute treatment patterns and ECG acquisition:
Among hospitals in the lowest quartile of delayed ECG
acquisition, the median acute medication adherence score
was 75.8% (25th to 75th percentile 67.3 to 81.6), whereas
among hospitals in the highest quartile of delayed ECG
acquisition, the median acute medication adherence score
was 71.1% (25th to 75th percentile 63.1 to 79.6).
Discussion
In a large, contemporary population of patients with NSTE
ACS, we have demonstrated that only 33% of patients with
ischemic symptoms at presentation undergo electrocardiography within 10 minutes of hospital presentation as recommended in evidence-based guidelines. We also found that
the factor most strongly associated with ECG delays is
female gender.
The initial standard for time to ECG acquisition was set
by the National Heart Attack Alert Program, when timely
acquisition of an electrocardiogram was demonstrated to be
a critical time point in the management of patients who have
ST-segment elevation myocardial infarction and undergo
fibrinolytic therapy.5 A time-to-ECG goal should arguably
be in place for all patients with chest pain to identify the
presence of ST-segment elevation, which drives treatment
algorithms. Further, at the time of triage of patients with
chest pain, identification of those subsequently found to
have ST-segment elevation myocardial infarction or NSTE
ACS is obviously unknown. However, the temporal effect of
urgent and timely pharmacologic or mechanical interventions
on adverse clinical outcomes continues to be investigated in
patients with NSTE ACS, and we found no link between early
ECG acquisition and adjusted risk of adverse events (in-hospital mortality and recurrent myocardial infarction).
Of significant concern is the increased likelihood of
delay in time to ECG acquisition in women. Although
gender-related disparities in the treatment of NSTE ACS
have been reported previously, we found that, among patient characteristics, female gender was the strongest independent predictor of a delay in ECG acquisition, which far
exceeded the association with other factors.6 This phenomenon has been reported previously in the ST-segment elevation myocardial infarction population.7 Data from the
National Registry of Myocardial Infarction-1 indicate that
441
Table 3
Acute (within 24 hours) medications and invasive procedures*
Variable
Aspirin
Blocker
Heparin, any
Glycoprotein IIb/IIIa inhibitor
Clopidogrel
Cardiac catheterization 24 hours
Cardiac catheterization 48 hours
Percutaneous coronary intervention
Coronary artery bypass grafting
Total
(n 63,478)
Electrocardiogram
10 mins
(n 22,081)
Electrocardiogram
10 mins
(n 41,397)
p Value
Adjusted OR
(95% CI)
91.8%
79.2%
81.9%
33.7%
40.5%
31.3%
49.5%
40.2%
12.2%
92.5%
80.2%
84.6%
39.0%
44.4%
36.6%
55.4%
44.7%
12.9%
91.4%
78.6%
80.4%
30.8%
38.4%
28.3%
46.2%
37.6%
11.8%
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.0001
0.0002
0.95 (0.881.01)
0.96 (0.921.00)
0.87 (0.830.91)
0.80 (0.770.84)
0.88 (0.850.91)
0.78 (0.750.82)
0.81 (0.770.85)
0.85 (0.810.89)
0.98 (0.931.04)
Table 4
Clinical outcomes
Variable
Death
Postadmission myocardial infarction
Death or myocardial infarction
Total
(n 63,478)
ECG 10 min
(n 22,081)
ECG 10 min
(n 41,397)
p Value
Adjusted Risk
(95% CI)
5.2%
2.9%
7.5%
4.7%
2.9%
7.1%
5.4%
2.9%
7.7%
0.0001
0.92
0.004
1.01 (0.941.09)
1.01 (0.901.12)
1.01 (0.941.08)
associated with a delay in ECG acquisition, we noted several limitations. First, we did not adjust for variation in
institutional policies or protocols. Second, we did not collect data on mode of transportation to the emergency department (emergency medical services vs private vehicle),
which has been reported to influence the period between
presentation to electrocardiography. Third, we did not account for other co-existing medical complaints that may
have affected ECG acquisition time and adverse clinical
outcome. Fourth, due to the retrospective nature of quality
improvement initiatives, we could not determine which patients had active pain at the time of presentation, recurrent
pain during evaluation in the emergency department, or an
atypical presentation that may have led to delayed ECG
acquisition. Fifth, we used a dichotomous cut-off time to
electrocardiography. Although this is consistent with
guidelines of the American College of Cardiology/American Heart Association, it assumes that there is no difference between a delay of 11 minutes and a delay of 120
minutes.
Although we were unable to link conclusively a delay in
ECG acquisition with adverse events in this patient population, obtaining a timely electrocardiogram is a critical step
in the evaluation of the undifferentiated population with
chest pain. Future studies need to assess the effect of overcrowding between presentation and ECG acquisition and to
determine whether internal guidelines can decrease the time
to ECG acquisition in patients who present with the complaint of chest pain.
442
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