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. 2019 Jun 4;365:l1927. doi: 10.1136/bmj.l1927

Intensive care use and mortality among patients with ST elevation myocardial infarction: retrospective cohort study

Theodore J Iwashyna 1 ,2 ,4, Colin R Cooke 1 ,2 ,5, Shashank S Sinha 6 ,7, Andrew M Ryan 2 ,5, Robert W Yeh 8 ,9, Brahmajee K Nallamothu 2 ,4 ,5 ,10, Thomas S Valley 1 ,2 ,3
PMCID: PMC6547840  PMID: 31164326

Abstract

Objective

To evaluate the effect of intensive care unit (ICU) admission on mortality among patients with ST elevation myocardial infarction (STEMI).

Design

Retrospective cohort study.

Setting

1727 acute care hospitals in the United States.

Participants

Medicare beneficiaries (aged 65 years or older) admitted with STEMI to either an ICU or a non-ICU unit (general/telemetry ward or intermediate care) between January 2014 and October 2015.

Main outcome measure

30 day mortality. An instrumental variable analysis was done to account for confounding, using as an instrument the additional distance that a patient with STEMI would need to travel beyond the closest hospital to arrive at a hospital in the top quarter of ICU admission rates for STEMI.

Results

The analysis included 109 375 patients admitted to hospital with STEMI. Hospitals in the top quarter of ICU admission rates admitted 85% or more of STEMI patients to an ICU. Among patients who received ICU care dependent on their proximity to a hospital in the top quarter of ICU admission rates, ICU admission was associated with lower 30 day mortality than non-ICU admission (absolute decrease 6.1 (95% confidence interval −11.9 to −0.3) percentage points). In a separate analysis among patients with non-STEMI, a group for whom evidence suggests that routine ICU care does not improve outcomes, ICU admission was not associated with differences in mortality (absolute increase 1.3 (−0.9 to 3.4) percentage points).

Conclusions

ICU care for STEMI is associated with improved mortality among patients who could be treated in an ICU or non-ICU unit. An urgent need exists to identify which patients with STEMI benefit from ICU admission and what about ICU care is beneficial.

Introduction

Survival after ST elevation myocardial infarction (STEMI) has increased by nearly 20% over the past two decades.1 Complications from STEMI, such as cardiogenic shock or life threatening arrhythmias, have also fallen markedly.2 This improvement is usually attributed to the accessibility and implementation of early reperfusion therapy, which typically occurs before patients are admitted to an intensive or coronary care unit (ICU). Nevertheless, 75% of patients with STEMI in the US are admitted to an ICU.3 The costs of this practice are enormous. ICU admissions are on average 2.5 times more costly than non-ICU admissions, and critical care services now account for almost 1% of the US gross domestic product.4

Whether ICU care for patients with STEMI provides a benefit over lower levels of care, such as general, telemetry, or intermediate care, is poorly understood.5 Guidelines for STEMI care also provide conflicting advice. Recent European guidelines recommended admitting all patients with STEMI to an ICU.6 Previous American guidelines suggested that STEMI patients at low risk may not need ICU level care,7 but recent guideline updates did not specifically discuss the role of ICU care for STEMI.1 This uncertainty is reflected in practice. Wide variation exists among hospitals in the use of ICUs for STEMI, both in the US and worldwide.3 8

In this context, we sought to evaluate the effect of ICU admission on mortality for patients with STEMI in the US. As the decision to use an ICU is inherently linked to a patient’s severity of illness, previous observational studies were limited by confounding by indication.9 To overcome this, we used an instrumental variable analysis to examine the effect of ICU admission on patients with borderline or discretionary ICU needs (that is, those patients who could reasonably receive care in an ICU or non-ICU unit). As mortality after STEMI is declining owing to broader use of reperfusion therapy,10 we hypothesized that ICU admission would not be associated with a mortality benefit.

Methods

Study cohort

We did a retrospective cohort study of all fee-for-service Medicare beneficiaries aged 65 years and older who were admitted to a hospital in the US for STEMI between January 2014 and October 2015. We identified patients with STEMI by using international classification of diseases, ninth revision, clinical modification (ICD-9-CM) primary diagnosis codes for STEMI (supplementary table A).10 We excluded patients with STEMI admitted to hospitals without ICU capabilities or admitted directly (that is, transferred in) from other acute care hospitals. We also excluded patients for whom data necessary for analyses were missing (such as ZIP codes (n=1415), hospital characteristics (n=805), or hospital identifiers (n=2)) (supplementary figure A).

Data source

We linked inpatient claims from the Medicare Provider Analysis and Review File to mortality data in the Medicare Beneficiary Summary File.11 Characteristics of hospitals came from the American Hospital Association’s Annual Surveys and the Healthcare Cost Reporting Information Systems.12 13 We obtained population and geographic information by linking the patient’s ZIP code of residence to 2010 US census data.

Patient and public involvement

Patients were not involved in the development of the research question, study design, or outcome measures. Patients were not involved in the recruitment, conduct, or interpretation of the study. There are no specific plans to disseminate the results of the research to study participants or to relevant patients beyond the usual channels of publication.

Exposure variable, outcome variable, and covariate definitions

We used room and board charges for each Medicare beneficiary to establish the level of care for which the patient was billed. Thus, we relied on the US Centers for Medicare and Medicaid Services’ definition of an ICU, which is based on two criteria.14 Firstly, an ICU must have lifesaving equipment available for immediate use and be geographically and identifiably separate from general routine care areas. Secondly, a single nurse must take care of no more than two patients, and nursing staff cannot be shared between an ICU and other units that provide lower levels of care.

The exposure variable was admission to ICU (the presence of an ICU or coronary care unit (CCU) revenue center code in the administrative billing record).15 We defined non-ICU admission as any admission to a general/telemetry (the lack of any ICU or CCU revenue center code) or intermediate care ward (the presence of an intermediate ICU or intermediate CCU revenue center code).16 The primary study outcome was 30 day all cause mortality, measured from the time of hospital admission.

To account for differences between patients admitted to ICU or non-ICU units, we used patients’ characteristics such as age, sex, race/ethnicity, comorbid illness,17 severity of illness, cardiac procedures performed during the hospital admission, median household income, and urbanicity for adjustment. We captured severity of illness through secondary ICD-9-CM diagnosis and procedural codes for acute organ dysfunction or mechanical ventilation (supplementary table A).18 19 We identified percutaneous coronary intervention, coronary artery bypass graft procedure, and thrombolytics by using ICD-9-CM procedural codes.20 21 Median household income was based on the patient’s ZIP code of residence, using 2010 US census data. Urbanicity was defined by the National Center for Health Statistics Urban-Rural Classification Scheme.22 We also used characteristics of hospitals, including geographic region, teaching hospital status by resident to hospital bed ratio, hospital size by number of beds, ICU size by proportion of total hospital beds, proportion of Medicaid patients among all admitted patients, nursing ratio (nursing full time equivalents per 1000 patient days averaged over the entire hospital), and annual hospital STEMI case volume, for adjustment.

Instrumental variable analysis

Because admission to an ICU is likely to be correlated with severity of illness (that is, sicker patients are admitted to an ICU and are also more likely to die) and observational data often lack all variables needed for adjustment, standard multivariable regression is likely to be biased through confounding by indication.9 We found that a multivariable adjusted model yielded biased estimates relative to those from an instrumental variable model using the Wooldridge’s score test of endogeneity (F1,1726=5.1; P=0.02).23 Therefore, we used an instrumental variable analysis to account for confounding.

In an instrumental variable analysis, an instrument is used to adjust a patient’s likelihood of receiving the treatment. In this study, we used differential distance as the instrument. It has been used previously in myocardial infarction by McClellan and colleagues to examine the effect of cardiac catheterization on mortality.24 Conceptually, distance to a hospital acts as an instrument because, in general, most people choose their residence for reasons unrelated to nearby hospitals. However, when a person has a STEMI or other acute illness, they are likely to be taken to the nearest hospital.

Differential distance represents the additional distance that a patient would need to travel, beyond the closest hospital, to arrive at a hospital in the top quarter of ICU admission rates for STEMI. We calculated differential distance as the difference between the distance from a patient’s residence to the nearest high ICU use hospital (that is, a hospital in the top quarter of ICU admission rates for STEMI) and the distance from a patient’s residence to the nearest hospital of any type. Distances were measured by using the linear arc distance function, which calculates the distance between the geographic coordinates of the hospital and the centroid of the patient’s residential ZIP code. The median differential distance to a high ICU use hospital was 6.8 miles.

To show its validity, an instrument must meet two conditions.25 Firstly, the instrument must be associated with the treatment. Secondly, the instrument should have no relation with the outcome, except through the treatment. As an example, in a randomized trial, the randomization tool may act as the perfect instrument, increasing or decreasing the probability that a person receives a given treatment while also being otherwise unrelated to the study outcome.

In this study, we showed the strength of the instrument in three ways. Firstly, differential distance was highly correlated with ICU admission (partial F1,1726=64; P<0.001). An F statistic greater than 10 generally indicates that an instrument is strongly associated with the treatment.25 Secondly, for every 10 mile increase in differential distance, the probability of ICU admission decreased by 1.8%. Thirdly, more patients who lived close to a high ICU use hospital were admitted to an ICU than patients who lived far from a high ICU use hospital: 73.8% (40 354/54 691 patients) who lived less than the median (6.8 miles) were admitted to an ICU compared with 63.8% (34 873/54 684 patients) whose differential distance was more than 6.8 miles (table 1).

Table 1.

Patients’ characteristics by median differential distance to high intensive care unit (ICU) hospital*. Values are numbers (percentages) unless stated otherwise

Characteristics Differential distance Standardized difference
<6.8 miles ≥6.8 miles
Patients 54 691 (50.0) 54 684 (50.0) -
ICU admission 40 354 (73.8) 34 873 (63.8) 0.22
Intermediate care admission 8330 (15.2) 12 610 (23.1) 0.20
Mean (SD) age, years 76.1 (7.9) 76.0 (7.9) 0.01
Age group, years: 0.01
 65-74 26 857 (49.1) 27 129 (49.6)
 75-84 17 519 (32.0) 17 471 (32.0)
 ≥85 10 315 (18.9) 10 084 (18.4)
Sex: 0.03
 Male 31 686 (57.9) 32 358 (59.2)
 Female 23 005 (42.1) 22 326 (40.8)
Race/ethnicity: 0.16
 White 46 105 (84.3) 48 960 (89.5)
 Black 4650 (8.5) 2897 (5.3)
 Other 3936 (7.2) 2827 (5.2)
Urbanicity: 0.41
 Large central metropolitan 16 659 (30.5) 8594 (15.7)
 Large suburban metropolitan 12 741 (23.3) 12 235 (22.4)
 Medium metropolitan 11 316 (20.7) 12 938 (23.7)
 Small metropolitan 4454 (8.1) 8149 (14.9)
 Micropolitan 5098 (9.3) 7522 (13.8)
 Non-core 4423 (8.1) 5246 (9.6)
Median household income
by ZIP code, $:
0.07
 <40 000 12 269 (22.4) 13 312 (24.3)
 40 000-100 000 39 236 (71.7) 38 824 (71.0)
 >100 000 3186 (5.8) 2548 (4.7)
Mean (SD) Elixhauser comorbidities count 2.2 (1.0) 2.2 (1.0) 0.03
Hospital diagnoses:
 Respiratory failure 9042 (16.5) 8770 (16.0) 0.01
 Shock 8955 (16.4) 8655 (15.8) 0.01
 Cardiac arrest 10 658 (19.5) 10 426 (19.1) 0.01
Procedures performed during hospital admission:
 Percutaneous coronary intervention 46 212 (84.5) 45 815 (83.8) 0.02
 Coronary artery bypass grafting 3506 (6.4) 3352 (6.1) 0.01
 Thrombolytics 958 (1.8) 1116 (2.0) 0.02
 Mechanical ventilation 7981 (14.6) 7561 (13.8) 0.02
 Renal replacement therapy 590 (1.1) 529 (1.0) 0.01
 Mechanical cardiac support§ 5868 (10.7) 5248 (9.6) 0.04
 Targeted temperature management 308 (0.6) 344 (0.6) 0.01
Angus organ failure score: 0.03
 0 32 584 (59.6) 33 377 (61.0)
 ≥1 22 107 (40.4) 21 307 (39.0)
Billing encounter for palliative care 9784 (17.9) 9308 (17.0) 0.02
*

Hospital in top quarter of ICU admission rates for ST elevation myocardial infarction.

Instrument used for this study, representing additional distance patient would need to travel beyond nearest hospital to arrive at high ICU use hospital. Median differential distance was 6.8 miles.

Absolute standardized difference of ≥0.10 generally indicates that covariates are imbalanced between groups.26

§

Percutaneous ventricular assist device or intra-aortic balloon pump.

No empiric method exists to show that the instrument is not associated with the outcome other than through the treatment.25 The recommended way of evaluating this condition is to stratify observed characteristics by the instrument and then carefully examine balance.25 27 Balance of observed characteristics across the instrument provides confidence that unobserved characteristics are similarly balanced. We examined whether patients’ characteristics were balanced across the distribution of the instrument by using standardized differences (table 1). Generally, standardized differences less than 0.1 indicate balance,26 and we showed reasonable balance between the two groups, except for race/ethnicity and urbanicity. Imbalances in race/ethnicity and urbanicity are recognized to be inherent to the use of distance instruments.27

Interpretation of instrumental variable results

The results of a standard regression represent the treatment effect for the average patient. The results of an instrumental variable analysis represent the treatment effect for the statistically marginal patient.28 Marginal patients represent those whose likelihood of receiving the treatment depended on the instrument. A patient in a randomized trial might only receive an experimental treatment if randomized to it, and a marginal patient in this study received ICU care only because they lived close to a hospital with a high ICU admission rate for STEMI. Thus, statistically marginal patients might be considered clinically to have borderline or discretionary ICU needs—they might receive care in an ICU or outside of an ICU depending on the hospital to which they are admitted because different providers might reasonably disagree about the best location for the patient’s care.

Marginal patients cannot be identified within an instrumental variable analysis.28 However, we estimated the size of the marginal population of patients and their population level characteristics by using the method of Angrist and Pischke.29 The statistical code for these estimates is given in the supplementary methods.

Statistical analysis

To account for characteristics of patients and hospitals, we used multivariable logistic regression models. In the instrumental variable analysis, we used two stage least squares regression with adjustment for the same patient and hospital characteristics. To overcome the imbalances in race/ethnicity and urbanicity when using a distance instrument, we specifically included these characteristics in all adjusted models, including the instrumental variable analysis.27 We used predictive margins to estimate adjusted absolute differences in outcomes. All models estimated robust standard errors with clustering at the hospital level.

Subgroup, sensitivity, and falsification analyses

To test whether the results were consistent for specific target populations, to assess for effect measure modification, and to examine mechanisms for identified differences, we did several subgroup, sensitivity, and falsification analyses. Firstly, to evaluate whether severely ill patients could be driving the association between ICU admission and mortality, instrumental variable analyses were stratified by organ failure score and also repeated after exclusion of patients with ICD-9-CM diagnosis or procedural codes for respiratory failure or shock. Secondly, given the imbalance in race/ethnicity and urbanicity when using a distance instrument, we did separate subgroup analyses with these characteristics.

Thirdly, to examine whether patients with life limiting treatment preferences could influence the results, we did separate instrumental variable analyses stratified by whether or not patients were aged 80 years or older, excluding patients who received a billing code for palliative care,30 or excluding patients who did not receive percutaneous coronary intervention, coronary artery bypass graft, or thrombolytics. To ensure that differences in outcomes based on age were not missed by dichotomizing a continuous variable, we did a non-linear two stage residual inclusion instrumental variable analysis and then used predictive margins to estimate adjusted absolute differences in 30 day mortality at 5 year age intervals.

Fourthly, to assess whether particular hospital capabilities could be influencing the results, we did separate subgroup analyses excluding hospitals without percutaneous coronary intervention capabilities or intermediate care. Fifthly, to assess the consistency of the results to the modeling method, we repeated the instrumental variable analysis using a non-linear two stage residual inclusion model.31 Confidence intervals for the two stage residual inclusion model were based on 3000 non-parametric bootstrap samples with replacement. Finally, as a falsification test, we repeated the instrumental variable analysis for non-STEMI patients, a group for which increasing data suggest that routine ICU care does not improve outcomes.32

We used SAS 9.3 and Stata 14.2 for data management and analyses. The analytic code is included in the supplementary methods. All tests were two sided with a P value less than 0.05 considered significant.

Results

Between January 2014 and October 2015, 109 375 patients with STEMI were admitted to 1727 hospitals (supplementary figure A). Among these patients, 75 227 (68.8%) were admitted to an ICU. Patients admitted to an ICU were more likely to be younger, to be male, and to be sicker by the number of organ failures than non-ICU patients, although both had a similar number of Elixhauser comorbidities (table 2). ICU patients were also more likely to receive procedures such as percutaneous coronary intervention, coronary artery bypass graft, or thrombolytics, as well as other procedures such as renal replacement therapy,33 mechanical cardiac support,34 cardiac arrest,35 or targeted temperature management (table 2).35 STEMI patients from the south were more likely to be admitted to an ICU than were other patients. Differences were appropriately balanced by the instrument, except for race/ethnicity and urbanicity (table 1). We identified 431 (25%) hospitals as having high ICU use for STEMI, with ICU admission rates of 85% or greater (fig 1). High ICU use hospitals had lower rates of intermediate care use and were more likely to have fewer than 100 hospital beds and a higher proportion of hospital beds that were ICU beds (table 3).

Table 2.

Patients’ characteristics by intensive care unit (ICU) admission. Values are numbers (percentages) unless stated otherwise

Characteristics ICU Non-ICU
Patients 75 227 (68.8) 34 148 (31.2)
Mean (SD) age, years 75.6 (7.6) 77.1 (8.3)
Age group, years:
 65-74 38 598 (51.3) 15 388 (45.1)
 75-84 24 485 (32.6) 10 505 (30.8)
 ≥85 12 144 (16.1) 8255 (24.2)
Sex:
 Male 45 352 (60.3) 18 692 (54.7)
 Female 29 875 (39.7) 15 456 (45.3)
Race/ethnicity:
 White 65 279 (86.8) 29 786 (87.2)
 Black 5279 (7.0) 2268 (6.6)
 Other 4669 (6.2) 2094 (6.1)
Urbanicity:
 Large central metropolitan 17 146 (22.8) 8107 (23.7)
 Large suburban metropolitan 17 217 (22.9) 7759 (22.7)
 Medium metropolitan 16 498 (21.9) 7756 (22.7)
 Small metropolitan 8514 (11.3) 4089 (12.0)
 Micropolitan 8991 (12.0) 3629 (10.6)
 Non-core 6861 (9.1) 2808 (8.2)
Median household income by ZIP code, $:
 <40 000 18 057 (24.0) 7524 (22.0)
 40 000-100 000 53 260 (70.8) 24 800 (72.6)
 >100 000 3910 (5.2) 1824 (5.3)
Mean (SD) Elixhauser comorbidities count 3.0 (1.9) 2.9 (1.9)
Hospital diagnoses:
 Respiratory failure 15 001 (19.9) 2811 (8.2)
 Shock 15 413 (20.5) 2197 (6.4)
 Cardiac arrest 16 758 (22.3) 4326 (12.7)
Procedures performed during hospital admission:
 Percutaneous coronary intervention 65 970 (87.7) 26 057 (76.3)
 Coronary artery bypass grafting 6013 (8.0) 845 (2.5)
 Thrombolytics 1555 (2.1) 519 (1.5)
 Mechanical ventilation 13 767 (18.3) 1775 (5.2)
 Renal replacement therapy 993 (1.3) 126 (0.4)
 Mechanical cardiac support* 10 075 (13.4) 1041 (3.1)
 Targeted temperature management 614 (0.8) 38 (0.1)
Angus organ failure score:
 0 41 742 (55.5) 24 219 (70.9)
 ≥1 33 485 (44.5) 9929 (29.1)
Billing encounter for palliative care 4136 (5.5) 1863 (5.5)
Median (interquartile range) length of index hospital admission, days 3 (2-6) 3 (2-4)
Discharge destination of index hospital admission:
 Home 52 124 (69.3) 25 604 (75.0)
 Rehabilitation or nursing facility 8567 (11.4) 3714 (10.9)
 Other 3789 (5.0) 1987 (5.8)
In-hospital mortality 10 747 (14.3) 2843 (8.3)
*

Percutaneous ventricular assist device or intra-aortic balloon pump.

Fig 1.

Fig 1

Distribution of intensive care unit (ICU) admission rates for ST elevation myocardial infarction (STEMI). Each circle represents an individual hospital, based on its ICU admission rate for STEMI and then ranked by its ICU admission rate for STEMI

Table 3.

Hospitals’ characteristics by intensive care unit (ICU) use. Values are numbers (percentages) unless stated otherwise

Characteristics High ICU use* Low ICU use*
Hospital 431 (25.0) 1296 (75.0)
Mean (SD) ICU admission rate for STEMI, % 91.7 (4.5) 63.7 (17.6)
Mean (SD) intermediate care admission rate for STEMI, % 3.0 (4.3) 22.8 (20.1)
Median (SD) hospital STEMI annual case volume 47 (23-77) 51 (28-86)
Median (SD) hospital PCI/CABG annual case volume 43 (21-73) 46 (25-81)
Hospital ownership†:
 For profit 94 (22.0) 278 (21.7)
 Not for profit 258 (60.3) 871 (67.9)
 Government 76 (17.8) 133 (10.4)
Medical school affiliated 209 (48.5) 624 (48.2)
Teaching status:
 No residents 312 (72.4) 956 (73.8)
 Minor teaching program (<0.25 residents/bed) 67 (15.6) 211 (16.3)
 Major teaching program (>0.25 residents/bed) 52 (12.1) 129 (10.0)
Hospital beds:
 <100 57 (13.2) 100 (7.7)
 100-199 107 (24.8) 350 (27.0)
 >199 267 (62.0) 846 (65.3)
Percentage of total beds that are ICU beds:
 <% 52 (12.1) 191 (14.7)
 5-10% 117 (27.2) 438 (33.8)
 >10% 262 (60.8) 667 (51.5)
Medicaid patients served:
 <16% 134 (31.1) 442 (34.1)
 16-23% 139 (32.3) 437 (33.7)
 >23% 158 (36.7) 417 (32.2)
Mean (SD) nursing ratio, FTE per 1000 patient days 4.2 (1.3) 4.2 (1.3)
Census regions:
 North east 66 (15.3) 206 (15.9)
 Midwest 114 (26.5) 317 (24.5)
 South 190 (44.1) 498 (38.4)
 West 61 (14.2) 275 (21.2)

CABG=coronary artery bypass graft; FTE=full time equivalents; PCI=percutaneous coronary intervention; STEMI=ST elevation myocardial infarction.

*

High ICU use indicates ICU admission rate for STEMI ≥85.2%. Low ICU use indicates ICU admission rate for STEMI <85.2%.

Ownership information was missing for 17 hospitals.

Patients with STEMI who were admitted to an ICU had higher unadjusted 30 day mortality than STEMI patients admitted to non-ICU units (18.2% for ICU admission versus 13.8% for non-ICU admission) (table 4). In a multivariable regression adjusted for characteristics of patients and hospitals, ICU admission for STEMI was associated with an increase in 30 day mortality compared with non-ICU care (17.0% for ICU admission versus 16.5% for non-ICU admission; absolute increase 0.5 (95% confidence interval 0.3 to 1.0) percentage points).

Table 4.

Association of intensive care unit (ICU) admission with 30 day mortality

Model Absolute 30 day mortality, % (95% CI) P value
Unadjusted results
ICU 18.2 -
Non-ICU 13.8 -
Adjusted model *
ICU 17.0 (16.7 to 17.3) Reference
Non-ICU 16.5 (16.1 to 16.9) 0.04
Instrumental variable model
ICU 14.9 (13.1 to 16.7) Reference
Non-ICU 21.0 (17.1 to 25.0) 0.04
*

Adjusted for characteristics of patients and hospitals in table 2 and table 3. Standard errors adjusted for clustering of patients within hospitals.

Two stage least squares regression of all patients, using differential distance to nearest hospital with high ICU admission rates as instrumental variable, adjusted for characteristics of patients and hospitals in table 2 and table 3. Standard errors adjusted for clustering of patients within hospitals.

We estimated that approximately one in 10 patients in this study had borderline ICU needs (that is, received ICU or non-ICU care dependent only on their proximity to a given hospital) (supplementary table B). The population of patients with borderline ICU needs was more likely to be over the age of 85, have no organ failures, live in the western US, or have a median household income by ZIP code of more than $100 000 (£77 000; €90 000) (supplementary table C).

In the instrumental variable analysis, ICU admission was associated with lower 30 day mortality compared with non-ICU admission (14.9% for ICU admission versus 21.0% for non-ICU admission; P=0.04), with an absolute reduction in 30 day mortality of 6.1 (−11.9 to −0.3) percentage points) (table 4).

Subgroup analyses showed results consistent with the main effect. Point estimates were consistent with the main result for subgroups of race/ethnicity and urbanicity. Point estimates favored a benefit to ICU admission across organ failures and age strata; after exclusion of severely ill patients, patients who received a billing encounter for palliative care, patients who did not receive an intervention for STEMI, or patients admitted to hospitals without percutaneous coronary intervention or intermediate care capabilities; and when the association of ICU admission was estimated using a two stage residual inclusion model. A falsification test in which the instrumental variable analysis was repeated for non-STEMI patients showed no mortality benefit associated with ICU admission (absolute increase 1.3 (−0.9 to 3.4) percentage points) (fig 2; supplementary table D, supplementary figure B).

Fig 2.

Fig 2

Subgroup, sensitivity, and falsification analyses. All models used an instrumental variable analysis and adjusted for characteristics of patients and hospitals. Error bars represent 95% confidence intervals for absolute 30 day mortality differences (intensive care unit (ICU) v non-ICU care). STEMI=ST elevation myocardial infarction

Discussion

Admission to ICU was associated with an absolute survival benefit of 6.1 percentage points at 30 days for STEMI patients with borderline or discretionary ICU needs. This association persisted in several subgroup and falsification analyses. Contrary to the prespecified hypothesis, we found that ICU care may be underused for certain patients with STEMI. This finding has important implications given the rising costs and use of critical care services globally.

Findings in context

Whether patients with STEMI benefit from ICU care has been uncertain. No randomized trials have evaluated the use of ICU care for STEMI, and guidelines do not offer consistent recommendations about whether to admit STEMI patients to an ICU.1 6 7 As a result, tremendous variation exists in whether ICUs are used for patients with myocardial infarction, both in the US and globally.3 8

This variation is clinically relevant because, despite the decrease in mortality for myocardial infarction over time,10 our ability as clinicians to identify patients at high risk of decompensation has not necessarily improved.36 37 Thus, although inpatient care for STEMI patients may be safer overall, certain populations of patients may continue to be at risk, and efforts to reduce the number of STEMI patients who receive ICU care on average may place these patients at even higher risk in the future.

The results of this study apply specifically to statistically marginal patients and not to those with obvious indications for or against ICU care.28 Marginal patients are those who were admitted (or not admitted) to an ICU solely on the basis of their proximity to a given hospital. Clinically, these patients likely have borderline or discretionary ICU needs. In other words, they may be admitted to an ICU in some but not all hospitals because clinicians may disagree about the optimal location of care. Thus, the borderline patients in this study represent a group of patients for whom there is clinical equipoise and unwarranted variation exists in care.

Instrumental variable analyses are unable to identify individual patients who are “marginal” or “borderline.” Despite this, we were able to identify population level characteristics associated with these patients. For example, we found that the borderline population was more likely to be older than 85 and have no organ failures. This suggests that the population of patients in this study with those characteristics was particularly vulnerable to local hospital practices and, as a result, was more likely to benefit from ICU admission. Future research can use this profile of borderline patients to design a prospective trial to test whether expanded ICU access improves outcomes for patients with STEMI.

What about ICU care might be beneficial to STEMI patients remains unclear.5 Historically, CCUs were developed to monitor for post-infarction complications, such as life threatening ventricular arrhythmias or mechanical sequelae.38 The incidence of these complications has been greatly reduced by early reperfusion therapy,39 and most STEMI patients receive definitive reperfusion therapy before admission to an ICU or CCU. Thus, neither the existing literature nor our study precisely identifies what about ICU care might be particularly beneficial to these patients.

ICUs in the US are primarily defined by their level of nursing care and by their ability to provide aggressive, lifesaving treatment. STEMI patients with borderline ICU needs, compared with other types of myocardial infarction patients, may benefit from the enhanced nursing care available in ICUs, allowing for earlier detection of complications or decompensation.40 The results may also reflect the growing complexity of STEMI patients, who might also present with or develop non-cardiac conditions (for example, pneumonia), for which ICU care may be beneficial.41 42 Finally, ICUs may be capable of providing more timely access to particular treatments or may have more effective protocols to ensure the provision of important care (for example, discharge drugs) than non-ICU units.43 Thus, the results of this study may have more to do with limitations of non-ICU care rather than the direct benefits of ICU care, suggesting that certain hospitals may be better prepared to care for STEMI patients across different units.44

Previous observational studies evaluating the role of ICU care are important to note for two reasons. Firstly, on comparison, the mortality rate in this study may seem unusually high relative to results from recent clinical trials. However, our 30 day mortality rates were consistent with other studies of myocardial infarction among the Medicare population, which is older and at higher risk than the general population.45 46 47 Secondly, most previous studies suggested increased mortality among patients admitted to an ICU, but these studies are at risk for confounding by indication and for estimating average rather than the more clinically relevant marginal treatment effects (that is, the effect on patients who could reasonably be treated in either ICU or non-ICU settings).48 49 50 Our unadjusted and adjusted results also showed increased mortality associated with ICU admission. Other instrumental variable analyses have similarly shown a shift in the effect compared with conventional regression analyses.42 51

Strengths and limitations of study

The quality of an instrumental variable analysis depends on the validity of the instrument.25 We showed that differential distance was strongly correlated with ICU admission, showed balance of observed patients’ characteristics as a result of the instrument, and did several analyses to evaluate for residual confounding. We used the instrument to look at a separate condition for which ICU care may not be beneficial—non-STEMI—and found no association between ICU admission and mortality.32

This study should be considered in the context of several limitations. Firstly, we used administrative data. Thus, certain clinically relevant variables such as infarct size, blood pressure, left ventricular ejection fraction, Killip class,52 culprit vessel, or time to reperfusion were unavailable. Residual confounding based on these factors cannot be ruled out. However, the excellent balance shown by the instrument suggests that unmeasured differences may be balanced as well. In addition, we did several subgroup and falsification analyses, which showed consistent results. Collectively, these results suggest that the effect of differential distance on the outcome operated through changes in the use of ICU care and not through other potential confounders. Secondly, the study’s cohort consisted of US Medicare beneficiaries and may not generalize to STEMI patients younger than 65 or to non-US STEMI patients. Thirdly, this study treated intensive care and coronary care units as the same. In many real world settings, these units are often combined to care for critically ill patients; differences between the two units at some hospitals may affect patient care and should be considered in future work. Similarly, key differences may exist between intermediate and general ward/telemetry care that were not assessed in this study. Finally, most hospitals in this study were non-teaching hospitals, and whether clinical outcomes for STEMI patients may differ between teaching and non-teaching hospitals remains controversial.53 54 55

Implications and conclusions

This study has important implications for clinicians and health system leaders. Conventional wisdom in the US suggests that ICU care is generally overused and that efforts must be made to reduce the number of patients receiving ICU care.5 56 However, this study, in combination with others,42 57 indicates instead that ICU care may often be misdirected, with some patients experiencing underuse while others experience overuse.

ICU admission for STEMI patients with borderline or discretionary ICU needs was associated with improved survival at 30 days. Methods to identify STEMI patients who might benefit from ICU care are needed and should be followed by randomized trials to test the effect of expanded access to ICU and the mechanisms that result in benefit from ICU care.

What is already known on this topic

  • On average, 75% of patients with ST elevation myocardial infarction (STEMI) in the US are admitted to an intensive or coronary care unit (ICU)

  • Most patients with STEMI receive definitive reperfusion treatment before ICU admission

  • Whether ICU admission is beneficial for STEMI patients in contemporary practice is unknown

What this study adds

  • This study suggests that ICU admission improves mortality for STEMI patients who could be treated in an ICU or non-ICU unit

  • STEMI patients who might benefit from ICU care should be identified, and the effect of expanded ICU access for these patients should be tested

Web extra.

Extra material supplied by authors

Supplementary materials

valt048284.ww1.pdf (747.4KB, pdf)

Contributors: TSV and BKN were responsible for study concept and design. TSV obtained funding. TSV and CRC acquired the data, and all authors were involved in analysis and interpretation of data. TSV and BKN drafted the manuscript, and all authors revised it critically for important intellectual content. The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted. TSV is the guarantor.

Funding: This work was supported by NIH K23 HL140165 (TSV), K12 HL138039 (TJI), and R01 HL137816 (CRC). The funding organizations had no role in the design and conduct of the study; in the collection, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript.

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare: no support from any organization for the submitted work other than that described above; no financial relationships with any organizations that might have an interest in the submitted work in the previous three years; and no other relationships or activities that could appear to have influenced the submitted work.

Ethical approval: The Institutional Review Board for the University of Michigan approved the study and provided a waiver of consent (HUM00053488).

Data sharing: The statistical code for the analyses is included in the supplementary materials. Additional code can be obtained from the corresponding author on request. Medicare data are not publicly available but can be obtained through the Center for Medicare and Medicaid Services.

Transparency: The lead author affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.

Disclaimer: This manuscript does not necessarily represent the views of the US Government or the Department of Veterans Affairs.

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Supplementary materials

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