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Influence of physician specialty on outcomes after acute ischemic stroke

The appropriate role of specialists in hospital management of common medical conditions has been vigorously debated.13 Few argue that specialists serve an important role as consultants, but whether patients with specific conditions should be admitted to the care of specialists or generalists is unresolved. This is demonstrated by the large degree of hospital‐to‐hospital variability in the proportion of patients with myocardial infarction admitted to cardiologists,4 patients with asthma exacerbations admitted to pulmonologists,5 and patients with renal failure admitted to nephrologists.6

Stroke is another common diagnosis, with variable rates of admission to specialists and generalists. Several prior studies have suggested that outcomes after ischemic stroke are better if a neurologist is the attending physician.710 However, these observational studies could not rule out the possibility that differences in outcome were a result of prognosis at the time of admission rather than improvements in medical care. Although these studies have controlled for known prognostic variables, it is possible that unknown, unmeasured, or inadequately measured variables were different in the groups admitted to neurologists and the groups admitted to generalists. These differences, in turn, might account for outcome differences rather than specialist care.

This form of selection bias, a type of confounding by indication, is a constant threat to validity in observational studies. Randomized trials avoid it because the randomization process balances all prognostic variables, both known and unknown, in the treatment groups.11 Observational studies cannot guarantee the same balance of unmeasured risk factors.12 Multivariate modeling is meant to account for prognostic differences between groups in observational studies, but confounding by indication may remain if all the factors that determine prognosis are not accurately measured. We developed a method to avoid confounding by indication by evaluating individual outcome differences associated with practice variability.13 This technique, termed grouped‐treatment (GT) analysis, is related to the instrumental variable approach developed by economists and occasionally applied to health services research.14

In multivariate GT analyses, the institutional proportion of cases admitted to the care of a neurologist is used as a predictor of outcomes rather than whether an individual patient was admitted to neurology. For example, at a hospital where three‐fourths of acute stroke patients are admitted to neurology, all patients are treated as having a 75% chance of admission to neurology. Rather than denoting whether each patient's specialist attending was a neurologist or a generalist, the 0.75 probability of admission to neurology is used for analysis. If admission to an attending neurologist improves ischemic stroke care, then GT analysis should demonstrate that hospitals admitting higher proportions of stroke patients to neurologists have improved outcomes regardless of whether there is selection bias at the individual patient level. In this way, the method bypasses unmeasured confounders at the individual level in its estimates of treatment effects. The method is susceptible to confounding at the group level; that is, unmeasured prognostic differences in patients admitted to hospitals that rely more heavily on neurologists could bias the GT estimate of treatment effect. The GT estimates are accurate if it can be assumed that a hospital's rate of treatment is not associated (in an unmeasured way) with its patient population's intrinsic, pretreatment prognosis. However, practice variability is very common between hospitals and is generally poorly associated with systematic differences in prognosis of treated patients,15, 16 and in this setting GT provides an independent assessment of treatment effect that may either confirm or refute an association found at the individual level, where confounding is nearly always an important issue.

In this study, we evaluated the impact of admission to a neurologist or generalist on outcomes of ischemic stroke patients treated at academic medical centers throughout the United States. We also compared traditional analysis to GT analysis. In doing so, we demonstrate the influence of unmeasured confounders on observational assessments of specialist care and may provide a more accurate measure of the impact of care by a neurologist on outcomes after ischemic stroke.

MATERIALS AND METHODS

We used the University HealthSystem Consortium (UHC) administrative database, which contained patient information from 84 large academic health centers and their 39 associate hospitals, with more than 2.1 million discharges each year.17 We obtained UHC discharge abstracts for all ischemic stroke patients admitted through emergency departments from 1997 through 1999. Discharge abstracts included patient demographics, urgency status (emergent, urgent, elective), illness severity class, admitting and discharge specialties, discharge diagnoses, procedure codes, in‐hospital mortality, length of stay, and total hospital charges. Patients were identified using International Classification of Diseases, Ninth Revision (ICD‐9) codes that were previously recognized as specific indicators of acute ischemic stroke (ICD‐9 433.01, 433.11, 433.21, 433.31, 433.81, 433.91, 434.01, 434.11, 434.91, 436).1820 We limited the cohort to emergency department admissions in order to reduce the likelihood of referral bias.

Variables in the discharge database were validated by comparison with a detailed medical record review. Between June and December 1999, 42 institutions participating in a quality improvement project identified 30 consecutive ischemic stroke cases. Trained analysts or clinicians abstracted information on demographics, medical history, and treatment. Kappa statistics have been previously reported for all individual characteristics except hospital charges, for which medical record review data were not available.21 Demographic and clinical variables in the administrative database tended to agree well with medical record review, with agreement ranging from 85% to 100% (kappa 0.581.00). Because the admitting attending likely directed acute stroke management, this was used to define a patient's attending physician specialty in all analyses. Administrative coding of tissue plasminogen activator (tPA) use was imperfect, with a sensitivity of 50% but a specificity of 100%.22

Institutional rate of admission to neurologists versus generalists was calculated as the percentage over the entire study duration. Unadjusted logistic regression was used to compare the distribution of patient pretreatment prognostic factors between institutions above and below the 50th percentile to determine a rate of admission to neurology because generalized estimating equations that could account for clustering were unable to support these models as a result of diverging estimates. We calculated the yearly volume of ischemic strokes treated at an institution from discharge abstracts, including admissions from all sources, because all treated cases would be expected to increase physician experience.

In‐hospital mortality was chosen as the primary outcome because of its frequency, importance, and coding reliability. Univariate predictors of in‐hospital mortality were identified using Pearson's chi‐square and the Wilcoxon rank sum tests.23 Length of stay (LOS), total hospital charges, and receipt of tPA were secondary outcomes. LOS and total hospital charges were compared using the Wilcoxon rank sum test. LOS and total charge calculations included only those patients surviving to discharge so that early mortality would not be confused with more efficient care. Similarly, we compared demographics and clinical variables of patients admitted to the care of neurologists with those of patients admitted to the care of generalists. To evaluate variability between institutions, we determined the proportion of patients with specific characteristics and outcomes at each institution and report median values and the 10th‐ to 90th‐percentile range among the institutions. The correlation between institutional rate of admission and institutional rate of mortality was evaluated.

In standard multivariate analysis, we assessed physician specialty as a predictor of in‐hospital mortality of individual patients after adjustment for demographic characteristics, admission status (emergent, urgent, elective), comorbid illness severity score (range 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness), and annual institutional treatment volume of ischemic stroke. UHC defined severity class to represent an individual's overall calculated risk of illness; its value was dependent on the refinement of the Health Care Facility Administration's diagnosis‐related groups (DRGs) and the Sach's Complication Profiler count of total comorbidities present.24, 25 Effects on LOS and total charges, as well as the ability of physician specialty to predict tPA use in individual patients, were similarly evaluated. Analysis of tPA use was restricted to patients admitted to universities that ever coded tPA use, which increased the sensitivity of the indicator to 57%.22 Residual misclassification error of tPA use would be expected to obscure a true underlying association between its use and physician specialty.

In multivariate GT calculations, we used the institutional proportion of cases admitted to a neurologist as a predictor of outcomes. GT analysis is based on the observation that if a treatment is effective, hospitals that use it more frequently should have better patient outcomes and that this association should persist regardless of whether individual‐level selection bias is present. The method assumes that hospital rates of admission to neurology are independent on the patient population's pretreatment prognosis. Because utilization differences between hospitals likely reflect practice variability rather than differences in patient prognosis,15, 16 the influence of unmeasured confounders at the hospital level is expected to be small. Measured variables that proved significant in univariate analyses or were thought to be responsible for an association between overall patient prognosis and modalities and frequencies of acute stroke treatments used, such as institutional treatment volume, were included in the multivariate GT model in order to isolate the effect of increasing rates of admission to neurologists.

We included both institutional and individual data to more accurately specify individual outcomes and covariates compared with an analysis that simply compared institutions' characteristics and their outcomes.26 Generalized estimating equations (GEE) were used in order to account for institutional clustering of predictor variables and outcomes. GEE is similar to logistic regression but produces broader confidence intervals (CIs) because logistic regression ignores the possibility that individuals at institutions are more similar to each other than would be expected by chance alone. We used a compound symmetry correlation structure, which initiates modeling by assuming a constant correlation between observations within each institution as well as between institutions, and used a logistic link function for binary outcomes in order to mimic logistic regression. The natural log transformations of LOS and hospital charges were modeled to reduce positive skew and approximate a normal distribution, and an identity link function was used in GEE to mimic linear regression for these analyses. To evaluate the impact of adjustment, both unadjusted and adjusted analyses were conducted. Methods to calculate power of GT analysis are not available. The Stata statistical package was used for all analyses (version 8.0; Stata Corporation, College Station, TX).

RESULTS

A total of 26,925 patients with ischemic strokes were admitted to neurologists or generalists through the emergency department at 113 institutions participating in the study. Patients admitted to neurologists rather than generalists (Table 1) were younger and more likely to be male, but less likely to have a serious comorbid illness. Institutions varied widely in the demographics of treated patients as well as in the markers of pretreatment prognosis. Institutional annual case volume of all ischemic strokes ranged from 1 to 741. Mortality rate, mean LOS, and mean hospital charges also varied broadly between institutions (Table 1). Patients treated at institutions whose rate of admissions to a neurologist's care was in the upper 50th percentile were younger and more often male, but did not differ in illness severity class (Table 2).

Individual and Institutional Characteristics of Ischemic Stroke Patients by Attending Specialty
CharacteristicNeurologist (n = 16,287)Generalist (n = 10,638)Institutional (n = 113) median (10th90th percentiles)
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

  • Based on 52 institutions ever coding tPA use for ischemic stroke in 1999. Neurologists, n = 4857; generalists, n = 3351.

Age (years), mean (SD)66.2 (14.7)69.3 (15.2)67.7 (62.174.8)
Female, n (%)8291 (51)5904 (56)54% (46%67%)
Ethnicity
African American, n (%)4516 (28)3335 (31)19% (0%71%)
Asian American, n (%)570 (4)201 (2)0.7% (0%8%)
Hispanic, n (%)906 (6)458 (4)0.7% (0%16%)
Native American, Eskimo, n (%)48 (0)21 (0)0% (0%1%)
White, n (%)9012 (55)5851 (55)65% (10%95%)
Other ethnicity, n (%)398 (2)157 (1)0.3% (0%4%)
Unknown, n (%)837 (5)615 (6)0.1% (0%9%)
Comorbid illness severity score,* median (interquartile range)1 (01)1 (01)0.83 (0.650.95)
Treatment and outcome
tPA administered, n (%)132 (3)51 (2)1.9% (0.6%6.5%)
In‐hospital deaths, n (%)755 (5)1005 (9)6.1% (3%10%)
Discharges to home, n (%)9504 (59)5235 (49)52% (38%72%)
Length of stay (days), mean (SD)6.6 (7.2)7.9 (9.9)6.6 (4.210.0)
Total charges$16,600 ($20,500)$18,700 ($26,300)$15,000 ($9000$30,000)
Comparison of Patient Pretreatment Prognostic Factors at Institutions with Rate of Admission to Neurologists Above the 50th Percentile with Those with Rate of Admission Below the 50th Percentile
Characteristic<50th percentile>50th percentileP value
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

Age (years), mean (SD)66.7 (15.2)69.4 (14.3)<.001
Female, n (%)5288 (54)8907 (52).001
Comorbid illness severity score*, median (interquartile range)1 (01)1 (01).87

There were 1760 in‐hospital deaths (7.0%). In univariate analysis, older age (P < .001), white ethnicity (P < .001), emergent stroke (P < .001), and increased illness severity (P < .001) were associated with greater risk of death, whereas African‐American (P < .001) and Hispanic (P = .007) ethnicities were protective. No other patient characteristics were important, and institutional annual case volume showed no association with mortality risk.

Overall, 60% of patients with ischemic stroke were admitted to a neurologist's care. In univariate analysis (Table 3), a lower risk of in‐hospital mortality was observed in cases admitted to neurologists (4.6%) compared with those admitted to generalists (9.5%; P < .001). After adjustment in standard multivariable models, the association between neurologist admission and lower risk of death persisted (OR 0.60; 95% CI, 0.500.72; P < .001).

Physician Specialty, In‐Hospital Mortality, and tPA Use in Ischemic Stroke (n = 26,925)*
CharacteristicsUnadjustedAdjusted
Odds ratio (95% CI)P valueOdds ratio (95% CI)P value
  • tPA, tissue plasminogen activator.

  • Analysis limited to 1999 and to 52 institutions ever coding tPA use for ischemic stroke in 1999 (n = 8208).

  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

Mortality
Attending neurologist0.32 (0.260.39)<.0010.60 (0.500.72)<.001
Proportion of admissions to neurology1.05 (0.851.31).641.02 (0.791.30).90
tPA Use
Attending neurologist1.87 (1.302.69).0012.56 (1.723.78)<.001
Proportion of admissions to neurology2.32 (0.985.49).062.47 (1.085.65).03

The institutional rate of admission of ischemic stroke patients to neurologists ranged from 0% to 90%, and higher rates were seen at hospitals with higher institutional case volumes (P < .001). There was no correlation between the institutional rate of admission to neurology and the institutional mortality rate (0.33; P = .73). At the individual‐level, greater rates of admission to neurologists had no significant impact on mortality (OR 1.05; 95% CI, 0.851.31; P = .64; Table 3) in unadjusted analysis. After adjustment for patient demographics, comorbid illness severity score, urgency status, and institutional case volume in GT analysis, there remained no association between death and proportion of ischemic stroke cases admitted to neurologists (OR 1.02; 95% CI, 0.791.30; P = .90), consistent with the absence of an association between neurologist care and in‐hospital mortality.

Patients treated by neurologists were likely to have shorter stays (P < .001) and lower charges (P = .01) in univariate analysis (Table 4). In traditional adjusted multivariable analysis, the same associations were seen for LOS (P < .001) and charges (P = .05). However, in adjusted GT analyses, increased institutional rate of admission to neurologists was not associated with briefer LOS (P = .36) and was associated with greater hospital charges (P = .044).

Physician Specialty and Secondary Outcomes of Ischemic Stroke
CharacteristicUnadjusted AnalysisAdjusted ratio*
NeurologistGeneralistP valueRatio (95% CI)P value
  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

LOS (days), n = 25,094
Standard analysis6.68.0<.0010.92 (0.880.96)<.001
Group‐treatment analysis7.27.1.801.06 (0.941.19).35
Total Charges, n = 21,812
Standard analysis$16,600$18,700.010.95 (0.911.00).05
Group‐treatment analysis$17,800$16,900<.0011.26 (1.011.57).04

In 1999, 190 (2.2%) ischemic stroke patients received tPA at the 64 universities that had ever coded tPA use. In univariate analysis, patients admitted to a neurologist were more likely to have received tPA (P = .001; Table 3), and this association persisted after adjustment (P < .001). In adjusted GT analysis, institutions admitting a higher proportion of ischemic stroke patients to neurologists also treated patients with tPA more frequently (P = .033).

DISCUSSION

Several prior studies found that ischemic stroke outcomes were better when an attending neurologist was responsible for patient care.710 Traditional analyses of our data also indicate that care by a neurologist lowers inpatient mortality, LOS, and total charges. By contrast, a GT analysis that bypasses selection bias at the patient level suggests there is no independent benefit of neurologist care on mortality or LOS and actually shows higher associated charges.

The discrepancy between standard and GT analyses suggests that healthier patients may have been preferentially admitted to the care of neurologists. Measured pretreatment prognostic factors in our data present a mixed picture. Patients admitted to a neurologist's care were younger, more often male, more often emergently admitted, and less likely to have serious comorbid illnesses. These patient factors were controlled for in all adjusted analyses. Although traditional multivariate analysis attempts to adjust for variations between the 2 patient populations, it cannot adjust for inaccurately measured or unmeasured differences. Using the institutional proportion of admissions to neurologists as a predictor of patient outcomes, we were better able to control for the selection bias associated with differential distribution of patients to teams led by attending neurologists versus generalists.13, 14

Petty et al.7 studied 299 ischemic stroke patients and showed equivalent survival among stroke patients admitted to neurology inpatient teams versus generalist teams with neurologic consultation. However, patients cared for by generalist teams without neurologic consultation fared worse. Their subjects were treated at both academic and community hospitals. In our study, contributing hospitals were solely academic institutions. Because specialty cross talk may be more frequent at university‐based hospitals, academic‐based generalist physicians may be more familiar with recent stroke literature and guidelines than are their community‐based peers. Further, restricting analysis to academic centers in our study should have reduced the potential confounding influences of differences between other aspects of institutional care. Although no information was available on neurologist consultation in our database, informal consultation is believed to play a large but hidden role at academic medical centers. Thus, the inclusion of a formal consultation variable may be misleading at academic medical centers.

Analyzing claims data on 44,099 Medicare beneficiaries with acute ischemic strokes cared for at both academic and community hospitals, Smith et al.10 also recently reported a 10% lower risk of 30‐day mortality and 12% lower risk of rehospitalization for infections and aspiration pneumonitis among patients admitted to the care of neurologists compared with those admitted to the care of generalists. However, the upper 95% confidence interval limits for these 2 findings nearly crossed 1 (ranging from 0.9980.999). The study also concluded that patients cared for collaboratively by generalists and neurologists had a 16% lower 30‐day mortality risk (hazard ratio 0.84; 95% CI, 0.790.90) than those cared for by generalists alone but simultaneously noted that patients admitted to generalists only had more comorbidities than either the collaborative care or neurologist‐only patient groups. If sicker patients were triaged to generalist admission, as occurs in confounding by indication (also known as channeling bias), then incomplete adjustment for comorbid disease may bias outcomes in favor of neurologist involvement. The GT analysis we employed is specifically designed to overcome this exact type of selection bias.

In our study, patients admitted to neurologists received tPA significantly more often than those admitted to generalists. GT analysis also found that hospitals admitting a higher proportion of strokes to neurologists treated more patients with tPA. This result is consistent with a prior study demonstrating that academic institutions employing a vascular neurologist had significantly higher odds of administering tPA.21 Since tPA must be administered within 3 hours of symptom onset,27 it is commonly delivered in the emergency department prior to admission. Thus, patients may be preferentially selected for admission to neurologic services because of their receipt of tPA, rather than that this association reflects an actual increased use of tPA by neurologists over generalists. Alternatively, institutions with a higher rate of stroke admissions to neurology may simply be more familiar with tPA protocols. Importantly, the poor sensitivity of our data for actual tPA administration may affect the analysis of its use by physician specialty; however, the failure to administratively code tPA use is unlikely to be differentially biased based on physician specialty. Thus, undercoding of tPA use would be expected to bias these analyses toward the null.

The potential advantage and efficacy of stroke centers, stroke units, stroke services, and other institutional processes of care are not addressed by our data. Previously, among academic hospitals, we found that acute ischemic stroke mortality was lower at hospitals employing a vascular neurologist and at those whose guidelines allowed only neurologists to administer tPA.21 A later analysis evaluated the impact of all elements of stroke center care supported by the original Brain Attack Coalition consensus28 and found that no single element improved mortality.29 However, recent studies have found significant mortality benefit associated with stroke units30, 31 and stroke services.32 Clearly, the debate continues over these important questions.

Our study had several limitations. First, generalizability may be lessened because only academic medical centers contributed data and only admissions through the ED were included. However, limiting the study population to academic centers provided a homogenous study population and greatly reduced the potential for confounding at the institutional level. Although the selection of ED cases mitigated the effects of referral bias and the use of only academic hospitals minimized interinstitutional differences, institutions whose rate of admissions to neurology was above the 50th percentile differed from those whose rate admissions to neurology was below the 50th percentile. However, this difference did not consistently result in patients with worse pretreatment prognostic factors being cared for at hospitals with higher rates of admission to neurology. Second, there are important limitations to using administrative data. In our study, patients were selected based on diagnostic coding of records analysts at discharge, and the diagnostic accuracy of such coding for stroke is imperfect.33 Furthermore, missing or incomplete information could have impaired adjustments for patient differences. Third, details of patient treatment were limited. The lack of information about formal and informal consultations may have obscured a true difference in outcomes among specialties.7 Additionally, academic institutions may use systematized care plans more often than do community hospitals, potentially minimizing differences between specialties. Fourth, at the time of our study, tPA had been recently introduced into stroke care. Current rates of tPA use among neurologists and generalists may be more similar. Fifth, the ability of in‐hospital mortality to adequately assess quality of care is limited, and longer‐term and functional outcomes would be better measures and more clinically relevant.

After controlling for selection bias using GT analysis, we found stroke outcomes to be similar regardless of whether a neurologist or a generalist was the admitting physician. This result contrasts with the findings of several previous studies that suggested admitting stroke patients to a neurologist resulted in better clinical outcomes.710 Because only 1 neurologist is employed for approximately every 19.8 generalists in the United States34 and 40% of acute strokes were cared for by generalists, even in this sample entirely restricted to university hospitals, such findings would suggest that many U.S. stroke patients receive inferior care. Because the role of the neurologist as consultant rather than as attending physician is significantly more feasible in most practice settings, the demonstration of equivalent outcomes by both types of physicians is reassuring and certainly reinforces the important role that unmeasured confounders may play in observational studies.

However, these results do imply that it is vital that generalists remain fully trained in the current best practices of acute stroke management in order to maintain the equivalence of care suggested here. Given how common acute stroke is, any proposed future hospitalist training, certification, and recertification programs should include a focus on acute stroke management.

References
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Journal of Hospital Medicine - 3(3)
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ischemic stroke, outcomes measurement, quality improvement
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The appropriate role of specialists in hospital management of common medical conditions has been vigorously debated.13 Few argue that specialists serve an important role as consultants, but whether patients with specific conditions should be admitted to the care of specialists or generalists is unresolved. This is demonstrated by the large degree of hospital‐to‐hospital variability in the proportion of patients with myocardial infarction admitted to cardiologists,4 patients with asthma exacerbations admitted to pulmonologists,5 and patients with renal failure admitted to nephrologists.6

Stroke is another common diagnosis, with variable rates of admission to specialists and generalists. Several prior studies have suggested that outcomes after ischemic stroke are better if a neurologist is the attending physician.710 However, these observational studies could not rule out the possibility that differences in outcome were a result of prognosis at the time of admission rather than improvements in medical care. Although these studies have controlled for known prognostic variables, it is possible that unknown, unmeasured, or inadequately measured variables were different in the groups admitted to neurologists and the groups admitted to generalists. These differences, in turn, might account for outcome differences rather than specialist care.

This form of selection bias, a type of confounding by indication, is a constant threat to validity in observational studies. Randomized trials avoid it because the randomization process balances all prognostic variables, both known and unknown, in the treatment groups.11 Observational studies cannot guarantee the same balance of unmeasured risk factors.12 Multivariate modeling is meant to account for prognostic differences between groups in observational studies, but confounding by indication may remain if all the factors that determine prognosis are not accurately measured. We developed a method to avoid confounding by indication by evaluating individual outcome differences associated with practice variability.13 This technique, termed grouped‐treatment (GT) analysis, is related to the instrumental variable approach developed by economists and occasionally applied to health services research.14

In multivariate GT analyses, the institutional proportion of cases admitted to the care of a neurologist is used as a predictor of outcomes rather than whether an individual patient was admitted to neurology. For example, at a hospital where three‐fourths of acute stroke patients are admitted to neurology, all patients are treated as having a 75% chance of admission to neurology. Rather than denoting whether each patient's specialist attending was a neurologist or a generalist, the 0.75 probability of admission to neurology is used for analysis. If admission to an attending neurologist improves ischemic stroke care, then GT analysis should demonstrate that hospitals admitting higher proportions of stroke patients to neurologists have improved outcomes regardless of whether there is selection bias at the individual patient level. In this way, the method bypasses unmeasured confounders at the individual level in its estimates of treatment effects. The method is susceptible to confounding at the group level; that is, unmeasured prognostic differences in patients admitted to hospitals that rely more heavily on neurologists could bias the GT estimate of treatment effect. The GT estimates are accurate if it can be assumed that a hospital's rate of treatment is not associated (in an unmeasured way) with its patient population's intrinsic, pretreatment prognosis. However, practice variability is very common between hospitals and is generally poorly associated with systematic differences in prognosis of treated patients,15, 16 and in this setting GT provides an independent assessment of treatment effect that may either confirm or refute an association found at the individual level, where confounding is nearly always an important issue.

In this study, we evaluated the impact of admission to a neurologist or generalist on outcomes of ischemic stroke patients treated at academic medical centers throughout the United States. We also compared traditional analysis to GT analysis. In doing so, we demonstrate the influence of unmeasured confounders on observational assessments of specialist care and may provide a more accurate measure of the impact of care by a neurologist on outcomes after ischemic stroke.

MATERIALS AND METHODS

We used the University HealthSystem Consortium (UHC) administrative database, which contained patient information from 84 large academic health centers and their 39 associate hospitals, with more than 2.1 million discharges each year.17 We obtained UHC discharge abstracts for all ischemic stroke patients admitted through emergency departments from 1997 through 1999. Discharge abstracts included patient demographics, urgency status (emergent, urgent, elective), illness severity class, admitting and discharge specialties, discharge diagnoses, procedure codes, in‐hospital mortality, length of stay, and total hospital charges. Patients were identified using International Classification of Diseases, Ninth Revision (ICD‐9) codes that were previously recognized as specific indicators of acute ischemic stroke (ICD‐9 433.01, 433.11, 433.21, 433.31, 433.81, 433.91, 434.01, 434.11, 434.91, 436).1820 We limited the cohort to emergency department admissions in order to reduce the likelihood of referral bias.

Variables in the discharge database were validated by comparison with a detailed medical record review. Between June and December 1999, 42 institutions participating in a quality improvement project identified 30 consecutive ischemic stroke cases. Trained analysts or clinicians abstracted information on demographics, medical history, and treatment. Kappa statistics have been previously reported for all individual characteristics except hospital charges, for which medical record review data were not available.21 Demographic and clinical variables in the administrative database tended to agree well with medical record review, with agreement ranging from 85% to 100% (kappa 0.581.00). Because the admitting attending likely directed acute stroke management, this was used to define a patient's attending physician specialty in all analyses. Administrative coding of tissue plasminogen activator (tPA) use was imperfect, with a sensitivity of 50% but a specificity of 100%.22

Institutional rate of admission to neurologists versus generalists was calculated as the percentage over the entire study duration. Unadjusted logistic regression was used to compare the distribution of patient pretreatment prognostic factors between institutions above and below the 50th percentile to determine a rate of admission to neurology because generalized estimating equations that could account for clustering were unable to support these models as a result of diverging estimates. We calculated the yearly volume of ischemic strokes treated at an institution from discharge abstracts, including admissions from all sources, because all treated cases would be expected to increase physician experience.

In‐hospital mortality was chosen as the primary outcome because of its frequency, importance, and coding reliability. Univariate predictors of in‐hospital mortality were identified using Pearson's chi‐square and the Wilcoxon rank sum tests.23 Length of stay (LOS), total hospital charges, and receipt of tPA were secondary outcomes. LOS and total hospital charges were compared using the Wilcoxon rank sum test. LOS and total charge calculations included only those patients surviving to discharge so that early mortality would not be confused with more efficient care. Similarly, we compared demographics and clinical variables of patients admitted to the care of neurologists with those of patients admitted to the care of generalists. To evaluate variability between institutions, we determined the proportion of patients with specific characteristics and outcomes at each institution and report median values and the 10th‐ to 90th‐percentile range among the institutions. The correlation between institutional rate of admission and institutional rate of mortality was evaluated.

In standard multivariate analysis, we assessed physician specialty as a predictor of in‐hospital mortality of individual patients after adjustment for demographic characteristics, admission status (emergent, urgent, elective), comorbid illness severity score (range 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness), and annual institutional treatment volume of ischemic stroke. UHC defined severity class to represent an individual's overall calculated risk of illness; its value was dependent on the refinement of the Health Care Facility Administration's diagnosis‐related groups (DRGs) and the Sach's Complication Profiler count of total comorbidities present.24, 25 Effects on LOS and total charges, as well as the ability of physician specialty to predict tPA use in individual patients, were similarly evaluated. Analysis of tPA use was restricted to patients admitted to universities that ever coded tPA use, which increased the sensitivity of the indicator to 57%.22 Residual misclassification error of tPA use would be expected to obscure a true underlying association between its use and physician specialty.

In multivariate GT calculations, we used the institutional proportion of cases admitted to a neurologist as a predictor of outcomes. GT analysis is based on the observation that if a treatment is effective, hospitals that use it more frequently should have better patient outcomes and that this association should persist regardless of whether individual‐level selection bias is present. The method assumes that hospital rates of admission to neurology are independent on the patient population's pretreatment prognosis. Because utilization differences between hospitals likely reflect practice variability rather than differences in patient prognosis,15, 16 the influence of unmeasured confounders at the hospital level is expected to be small. Measured variables that proved significant in univariate analyses or were thought to be responsible for an association between overall patient prognosis and modalities and frequencies of acute stroke treatments used, such as institutional treatment volume, were included in the multivariate GT model in order to isolate the effect of increasing rates of admission to neurologists.

We included both institutional and individual data to more accurately specify individual outcomes and covariates compared with an analysis that simply compared institutions' characteristics and their outcomes.26 Generalized estimating equations (GEE) were used in order to account for institutional clustering of predictor variables and outcomes. GEE is similar to logistic regression but produces broader confidence intervals (CIs) because logistic regression ignores the possibility that individuals at institutions are more similar to each other than would be expected by chance alone. We used a compound symmetry correlation structure, which initiates modeling by assuming a constant correlation between observations within each institution as well as between institutions, and used a logistic link function for binary outcomes in order to mimic logistic regression. The natural log transformations of LOS and hospital charges were modeled to reduce positive skew and approximate a normal distribution, and an identity link function was used in GEE to mimic linear regression for these analyses. To evaluate the impact of adjustment, both unadjusted and adjusted analyses were conducted. Methods to calculate power of GT analysis are not available. The Stata statistical package was used for all analyses (version 8.0; Stata Corporation, College Station, TX).

RESULTS

A total of 26,925 patients with ischemic strokes were admitted to neurologists or generalists through the emergency department at 113 institutions participating in the study. Patients admitted to neurologists rather than generalists (Table 1) were younger and more likely to be male, but less likely to have a serious comorbid illness. Institutions varied widely in the demographics of treated patients as well as in the markers of pretreatment prognosis. Institutional annual case volume of all ischemic strokes ranged from 1 to 741. Mortality rate, mean LOS, and mean hospital charges also varied broadly between institutions (Table 1). Patients treated at institutions whose rate of admissions to a neurologist's care was in the upper 50th percentile were younger and more often male, but did not differ in illness severity class (Table 2).

Individual and Institutional Characteristics of Ischemic Stroke Patients by Attending Specialty
CharacteristicNeurologist (n = 16,287)Generalist (n = 10,638)Institutional (n = 113) median (10th90th percentiles)
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

  • Based on 52 institutions ever coding tPA use for ischemic stroke in 1999. Neurologists, n = 4857; generalists, n = 3351.

Age (years), mean (SD)66.2 (14.7)69.3 (15.2)67.7 (62.174.8)
Female, n (%)8291 (51)5904 (56)54% (46%67%)
Ethnicity
African American, n (%)4516 (28)3335 (31)19% (0%71%)
Asian American, n (%)570 (4)201 (2)0.7% (0%8%)
Hispanic, n (%)906 (6)458 (4)0.7% (0%16%)
Native American, Eskimo, n (%)48 (0)21 (0)0% (0%1%)
White, n (%)9012 (55)5851 (55)65% (10%95%)
Other ethnicity, n (%)398 (2)157 (1)0.3% (0%4%)
Unknown, n (%)837 (5)615 (6)0.1% (0%9%)
Comorbid illness severity score,* median (interquartile range)1 (01)1 (01)0.83 (0.650.95)
Treatment and outcome
tPA administered, n (%)132 (3)51 (2)1.9% (0.6%6.5%)
In‐hospital deaths, n (%)755 (5)1005 (9)6.1% (3%10%)
Discharges to home, n (%)9504 (59)5235 (49)52% (38%72%)
Length of stay (days), mean (SD)6.6 (7.2)7.9 (9.9)6.6 (4.210.0)
Total charges$16,600 ($20,500)$18,700 ($26,300)$15,000 ($9000$30,000)
Comparison of Patient Pretreatment Prognostic Factors at Institutions with Rate of Admission to Neurologists Above the 50th Percentile with Those with Rate of Admission Below the 50th Percentile
Characteristic<50th percentile>50th percentileP value
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

Age (years), mean (SD)66.7 (15.2)69.4 (14.3)<.001
Female, n (%)5288 (54)8907 (52).001
Comorbid illness severity score*, median (interquartile range)1 (01)1 (01).87

There were 1760 in‐hospital deaths (7.0%). In univariate analysis, older age (P < .001), white ethnicity (P < .001), emergent stroke (P < .001), and increased illness severity (P < .001) were associated with greater risk of death, whereas African‐American (P < .001) and Hispanic (P = .007) ethnicities were protective. No other patient characteristics were important, and institutional annual case volume showed no association with mortality risk.

Overall, 60% of patients with ischemic stroke were admitted to a neurologist's care. In univariate analysis (Table 3), a lower risk of in‐hospital mortality was observed in cases admitted to neurologists (4.6%) compared with those admitted to generalists (9.5%; P < .001). After adjustment in standard multivariable models, the association between neurologist admission and lower risk of death persisted (OR 0.60; 95% CI, 0.500.72; P < .001).

Physician Specialty, In‐Hospital Mortality, and tPA Use in Ischemic Stroke (n = 26,925)*
CharacteristicsUnadjustedAdjusted
Odds ratio (95% CI)P valueOdds ratio (95% CI)P value
  • tPA, tissue plasminogen activator.

  • Analysis limited to 1999 and to 52 institutions ever coding tPA use for ischemic stroke in 1999 (n = 8208).

  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

Mortality
Attending neurologist0.32 (0.260.39)<.0010.60 (0.500.72)<.001
Proportion of admissions to neurology1.05 (0.851.31).641.02 (0.791.30).90
tPA Use
Attending neurologist1.87 (1.302.69).0012.56 (1.723.78)<.001
Proportion of admissions to neurology2.32 (0.985.49).062.47 (1.085.65).03

The institutional rate of admission of ischemic stroke patients to neurologists ranged from 0% to 90%, and higher rates were seen at hospitals with higher institutional case volumes (P < .001). There was no correlation between the institutional rate of admission to neurology and the institutional mortality rate (0.33; P = .73). At the individual‐level, greater rates of admission to neurologists had no significant impact on mortality (OR 1.05; 95% CI, 0.851.31; P = .64; Table 3) in unadjusted analysis. After adjustment for patient demographics, comorbid illness severity score, urgency status, and institutional case volume in GT analysis, there remained no association between death and proportion of ischemic stroke cases admitted to neurologists (OR 1.02; 95% CI, 0.791.30; P = .90), consistent with the absence of an association between neurologist care and in‐hospital mortality.

Patients treated by neurologists were likely to have shorter stays (P < .001) and lower charges (P = .01) in univariate analysis (Table 4). In traditional adjusted multivariable analysis, the same associations were seen for LOS (P < .001) and charges (P = .05). However, in adjusted GT analyses, increased institutional rate of admission to neurologists was not associated with briefer LOS (P = .36) and was associated with greater hospital charges (P = .044).

Physician Specialty and Secondary Outcomes of Ischemic Stroke
CharacteristicUnadjusted AnalysisAdjusted ratio*
NeurologistGeneralistP valueRatio (95% CI)P value
  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

LOS (days), n = 25,094
Standard analysis6.68.0<.0010.92 (0.880.96)<.001
Group‐treatment analysis7.27.1.801.06 (0.941.19).35
Total Charges, n = 21,812
Standard analysis$16,600$18,700.010.95 (0.911.00).05
Group‐treatment analysis$17,800$16,900<.0011.26 (1.011.57).04

In 1999, 190 (2.2%) ischemic stroke patients received tPA at the 64 universities that had ever coded tPA use. In univariate analysis, patients admitted to a neurologist were more likely to have received tPA (P = .001; Table 3), and this association persisted after adjustment (P < .001). In adjusted GT analysis, institutions admitting a higher proportion of ischemic stroke patients to neurologists also treated patients with tPA more frequently (P = .033).

DISCUSSION

Several prior studies found that ischemic stroke outcomes were better when an attending neurologist was responsible for patient care.710 Traditional analyses of our data also indicate that care by a neurologist lowers inpatient mortality, LOS, and total charges. By contrast, a GT analysis that bypasses selection bias at the patient level suggests there is no independent benefit of neurologist care on mortality or LOS and actually shows higher associated charges.

The discrepancy between standard and GT analyses suggests that healthier patients may have been preferentially admitted to the care of neurologists. Measured pretreatment prognostic factors in our data present a mixed picture. Patients admitted to a neurologist's care were younger, more often male, more often emergently admitted, and less likely to have serious comorbid illnesses. These patient factors were controlled for in all adjusted analyses. Although traditional multivariate analysis attempts to adjust for variations between the 2 patient populations, it cannot adjust for inaccurately measured or unmeasured differences. Using the institutional proportion of admissions to neurologists as a predictor of patient outcomes, we were better able to control for the selection bias associated with differential distribution of patients to teams led by attending neurologists versus generalists.13, 14

Petty et al.7 studied 299 ischemic stroke patients and showed equivalent survival among stroke patients admitted to neurology inpatient teams versus generalist teams with neurologic consultation. However, patients cared for by generalist teams without neurologic consultation fared worse. Their subjects were treated at both academic and community hospitals. In our study, contributing hospitals were solely academic institutions. Because specialty cross talk may be more frequent at university‐based hospitals, academic‐based generalist physicians may be more familiar with recent stroke literature and guidelines than are their community‐based peers. Further, restricting analysis to academic centers in our study should have reduced the potential confounding influences of differences between other aspects of institutional care. Although no information was available on neurologist consultation in our database, informal consultation is believed to play a large but hidden role at academic medical centers. Thus, the inclusion of a formal consultation variable may be misleading at academic medical centers.

Analyzing claims data on 44,099 Medicare beneficiaries with acute ischemic strokes cared for at both academic and community hospitals, Smith et al.10 also recently reported a 10% lower risk of 30‐day mortality and 12% lower risk of rehospitalization for infections and aspiration pneumonitis among patients admitted to the care of neurologists compared with those admitted to the care of generalists. However, the upper 95% confidence interval limits for these 2 findings nearly crossed 1 (ranging from 0.9980.999). The study also concluded that patients cared for collaboratively by generalists and neurologists had a 16% lower 30‐day mortality risk (hazard ratio 0.84; 95% CI, 0.790.90) than those cared for by generalists alone but simultaneously noted that patients admitted to generalists only had more comorbidities than either the collaborative care or neurologist‐only patient groups. If sicker patients were triaged to generalist admission, as occurs in confounding by indication (also known as channeling bias), then incomplete adjustment for comorbid disease may bias outcomes in favor of neurologist involvement. The GT analysis we employed is specifically designed to overcome this exact type of selection bias.

In our study, patients admitted to neurologists received tPA significantly more often than those admitted to generalists. GT analysis also found that hospitals admitting a higher proportion of strokes to neurologists treated more patients with tPA. This result is consistent with a prior study demonstrating that academic institutions employing a vascular neurologist had significantly higher odds of administering tPA.21 Since tPA must be administered within 3 hours of symptom onset,27 it is commonly delivered in the emergency department prior to admission. Thus, patients may be preferentially selected for admission to neurologic services because of their receipt of tPA, rather than that this association reflects an actual increased use of tPA by neurologists over generalists. Alternatively, institutions with a higher rate of stroke admissions to neurology may simply be more familiar with tPA protocols. Importantly, the poor sensitivity of our data for actual tPA administration may affect the analysis of its use by physician specialty; however, the failure to administratively code tPA use is unlikely to be differentially biased based on physician specialty. Thus, undercoding of tPA use would be expected to bias these analyses toward the null.

The potential advantage and efficacy of stroke centers, stroke units, stroke services, and other institutional processes of care are not addressed by our data. Previously, among academic hospitals, we found that acute ischemic stroke mortality was lower at hospitals employing a vascular neurologist and at those whose guidelines allowed only neurologists to administer tPA.21 A later analysis evaluated the impact of all elements of stroke center care supported by the original Brain Attack Coalition consensus28 and found that no single element improved mortality.29 However, recent studies have found significant mortality benefit associated with stroke units30, 31 and stroke services.32 Clearly, the debate continues over these important questions.

Our study had several limitations. First, generalizability may be lessened because only academic medical centers contributed data and only admissions through the ED were included. However, limiting the study population to academic centers provided a homogenous study population and greatly reduced the potential for confounding at the institutional level. Although the selection of ED cases mitigated the effects of referral bias and the use of only academic hospitals minimized interinstitutional differences, institutions whose rate of admissions to neurology was above the 50th percentile differed from those whose rate admissions to neurology was below the 50th percentile. However, this difference did not consistently result in patients with worse pretreatment prognostic factors being cared for at hospitals with higher rates of admission to neurology. Second, there are important limitations to using administrative data. In our study, patients were selected based on diagnostic coding of records analysts at discharge, and the diagnostic accuracy of such coding for stroke is imperfect.33 Furthermore, missing or incomplete information could have impaired adjustments for patient differences. Third, details of patient treatment were limited. The lack of information about formal and informal consultations may have obscured a true difference in outcomes among specialties.7 Additionally, academic institutions may use systematized care plans more often than do community hospitals, potentially minimizing differences between specialties. Fourth, at the time of our study, tPA had been recently introduced into stroke care. Current rates of tPA use among neurologists and generalists may be more similar. Fifth, the ability of in‐hospital mortality to adequately assess quality of care is limited, and longer‐term and functional outcomes would be better measures and more clinically relevant.

After controlling for selection bias using GT analysis, we found stroke outcomes to be similar regardless of whether a neurologist or a generalist was the admitting physician. This result contrasts with the findings of several previous studies that suggested admitting stroke patients to a neurologist resulted in better clinical outcomes.710 Because only 1 neurologist is employed for approximately every 19.8 generalists in the United States34 and 40% of acute strokes were cared for by generalists, even in this sample entirely restricted to university hospitals, such findings would suggest that many U.S. stroke patients receive inferior care. Because the role of the neurologist as consultant rather than as attending physician is significantly more feasible in most practice settings, the demonstration of equivalent outcomes by both types of physicians is reassuring and certainly reinforces the important role that unmeasured confounders may play in observational studies.

However, these results do imply that it is vital that generalists remain fully trained in the current best practices of acute stroke management in order to maintain the equivalence of care suggested here. Given how common acute stroke is, any proposed future hospitalist training, certification, and recertification programs should include a focus on acute stroke management.

The appropriate role of specialists in hospital management of common medical conditions has been vigorously debated.13 Few argue that specialists serve an important role as consultants, but whether patients with specific conditions should be admitted to the care of specialists or generalists is unresolved. This is demonstrated by the large degree of hospital‐to‐hospital variability in the proportion of patients with myocardial infarction admitted to cardiologists,4 patients with asthma exacerbations admitted to pulmonologists,5 and patients with renal failure admitted to nephrologists.6

Stroke is another common diagnosis, with variable rates of admission to specialists and generalists. Several prior studies have suggested that outcomes after ischemic stroke are better if a neurologist is the attending physician.710 However, these observational studies could not rule out the possibility that differences in outcome were a result of prognosis at the time of admission rather than improvements in medical care. Although these studies have controlled for known prognostic variables, it is possible that unknown, unmeasured, or inadequately measured variables were different in the groups admitted to neurologists and the groups admitted to generalists. These differences, in turn, might account for outcome differences rather than specialist care.

This form of selection bias, a type of confounding by indication, is a constant threat to validity in observational studies. Randomized trials avoid it because the randomization process balances all prognostic variables, both known and unknown, in the treatment groups.11 Observational studies cannot guarantee the same balance of unmeasured risk factors.12 Multivariate modeling is meant to account for prognostic differences between groups in observational studies, but confounding by indication may remain if all the factors that determine prognosis are not accurately measured. We developed a method to avoid confounding by indication by evaluating individual outcome differences associated with practice variability.13 This technique, termed grouped‐treatment (GT) analysis, is related to the instrumental variable approach developed by economists and occasionally applied to health services research.14

In multivariate GT analyses, the institutional proportion of cases admitted to the care of a neurologist is used as a predictor of outcomes rather than whether an individual patient was admitted to neurology. For example, at a hospital where three‐fourths of acute stroke patients are admitted to neurology, all patients are treated as having a 75% chance of admission to neurology. Rather than denoting whether each patient's specialist attending was a neurologist or a generalist, the 0.75 probability of admission to neurology is used for analysis. If admission to an attending neurologist improves ischemic stroke care, then GT analysis should demonstrate that hospitals admitting higher proportions of stroke patients to neurologists have improved outcomes regardless of whether there is selection bias at the individual patient level. In this way, the method bypasses unmeasured confounders at the individual level in its estimates of treatment effects. The method is susceptible to confounding at the group level; that is, unmeasured prognostic differences in patients admitted to hospitals that rely more heavily on neurologists could bias the GT estimate of treatment effect. The GT estimates are accurate if it can be assumed that a hospital's rate of treatment is not associated (in an unmeasured way) with its patient population's intrinsic, pretreatment prognosis. However, practice variability is very common between hospitals and is generally poorly associated with systematic differences in prognosis of treated patients,15, 16 and in this setting GT provides an independent assessment of treatment effect that may either confirm or refute an association found at the individual level, where confounding is nearly always an important issue.

In this study, we evaluated the impact of admission to a neurologist or generalist on outcomes of ischemic stroke patients treated at academic medical centers throughout the United States. We also compared traditional analysis to GT analysis. In doing so, we demonstrate the influence of unmeasured confounders on observational assessments of specialist care and may provide a more accurate measure of the impact of care by a neurologist on outcomes after ischemic stroke.

MATERIALS AND METHODS

We used the University HealthSystem Consortium (UHC) administrative database, which contained patient information from 84 large academic health centers and their 39 associate hospitals, with more than 2.1 million discharges each year.17 We obtained UHC discharge abstracts for all ischemic stroke patients admitted through emergency departments from 1997 through 1999. Discharge abstracts included patient demographics, urgency status (emergent, urgent, elective), illness severity class, admitting and discharge specialties, discharge diagnoses, procedure codes, in‐hospital mortality, length of stay, and total hospital charges. Patients were identified using International Classification of Diseases, Ninth Revision (ICD‐9) codes that were previously recognized as specific indicators of acute ischemic stroke (ICD‐9 433.01, 433.11, 433.21, 433.31, 433.81, 433.91, 434.01, 434.11, 434.91, 436).1820 We limited the cohort to emergency department admissions in order to reduce the likelihood of referral bias.

Variables in the discharge database were validated by comparison with a detailed medical record review. Between June and December 1999, 42 institutions participating in a quality improvement project identified 30 consecutive ischemic stroke cases. Trained analysts or clinicians abstracted information on demographics, medical history, and treatment. Kappa statistics have been previously reported for all individual characteristics except hospital charges, for which medical record review data were not available.21 Demographic and clinical variables in the administrative database tended to agree well with medical record review, with agreement ranging from 85% to 100% (kappa 0.581.00). Because the admitting attending likely directed acute stroke management, this was used to define a patient's attending physician specialty in all analyses. Administrative coding of tissue plasminogen activator (tPA) use was imperfect, with a sensitivity of 50% but a specificity of 100%.22

Institutional rate of admission to neurologists versus generalists was calculated as the percentage over the entire study duration. Unadjusted logistic regression was used to compare the distribution of patient pretreatment prognostic factors between institutions above and below the 50th percentile to determine a rate of admission to neurology because generalized estimating equations that could account for clustering were unable to support these models as a result of diverging estimates. We calculated the yearly volume of ischemic strokes treated at an institution from discharge abstracts, including admissions from all sources, because all treated cases would be expected to increase physician experience.

In‐hospital mortality was chosen as the primary outcome because of its frequency, importance, and coding reliability. Univariate predictors of in‐hospital mortality were identified using Pearson's chi‐square and the Wilcoxon rank sum tests.23 Length of stay (LOS), total hospital charges, and receipt of tPA were secondary outcomes. LOS and total hospital charges were compared using the Wilcoxon rank sum test. LOS and total charge calculations included only those patients surviving to discharge so that early mortality would not be confused with more efficient care. Similarly, we compared demographics and clinical variables of patients admitted to the care of neurologists with those of patients admitted to the care of generalists. To evaluate variability between institutions, we determined the proportion of patients with specific characteristics and outcomes at each institution and report median values and the 10th‐ to 90th‐percentile range among the institutions. The correlation between institutional rate of admission and institutional rate of mortality was evaluated.

In standard multivariate analysis, we assessed physician specialty as a predictor of in‐hospital mortality of individual patients after adjustment for demographic characteristics, admission status (emergent, urgent, elective), comorbid illness severity score (range 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness), and annual institutional treatment volume of ischemic stroke. UHC defined severity class to represent an individual's overall calculated risk of illness; its value was dependent on the refinement of the Health Care Facility Administration's diagnosis‐related groups (DRGs) and the Sach's Complication Profiler count of total comorbidities present.24, 25 Effects on LOS and total charges, as well as the ability of physician specialty to predict tPA use in individual patients, were similarly evaluated. Analysis of tPA use was restricted to patients admitted to universities that ever coded tPA use, which increased the sensitivity of the indicator to 57%.22 Residual misclassification error of tPA use would be expected to obscure a true underlying association between its use and physician specialty.

In multivariate GT calculations, we used the institutional proportion of cases admitted to a neurologist as a predictor of outcomes. GT analysis is based on the observation that if a treatment is effective, hospitals that use it more frequently should have better patient outcomes and that this association should persist regardless of whether individual‐level selection bias is present. The method assumes that hospital rates of admission to neurology are independent on the patient population's pretreatment prognosis. Because utilization differences between hospitals likely reflect practice variability rather than differences in patient prognosis,15, 16 the influence of unmeasured confounders at the hospital level is expected to be small. Measured variables that proved significant in univariate analyses or were thought to be responsible for an association between overall patient prognosis and modalities and frequencies of acute stroke treatments used, such as institutional treatment volume, were included in the multivariate GT model in order to isolate the effect of increasing rates of admission to neurologists.

We included both institutional and individual data to more accurately specify individual outcomes and covariates compared with an analysis that simply compared institutions' characteristics and their outcomes.26 Generalized estimating equations (GEE) were used in order to account for institutional clustering of predictor variables and outcomes. GEE is similar to logistic regression but produces broader confidence intervals (CIs) because logistic regression ignores the possibility that individuals at institutions are more similar to each other than would be expected by chance alone. We used a compound symmetry correlation structure, which initiates modeling by assuming a constant correlation between observations within each institution as well as between institutions, and used a logistic link function for binary outcomes in order to mimic logistic regression. The natural log transformations of LOS and hospital charges were modeled to reduce positive skew and approximate a normal distribution, and an identity link function was used in GEE to mimic linear regression for these analyses. To evaluate the impact of adjustment, both unadjusted and adjusted analyses were conducted. Methods to calculate power of GT analysis are not available. The Stata statistical package was used for all analyses (version 8.0; Stata Corporation, College Station, TX).

RESULTS

A total of 26,925 patients with ischemic strokes were admitted to neurologists or generalists through the emergency department at 113 institutions participating in the study. Patients admitted to neurologists rather than generalists (Table 1) were younger and more likely to be male, but less likely to have a serious comorbid illness. Institutions varied widely in the demographics of treated patients as well as in the markers of pretreatment prognosis. Institutional annual case volume of all ischemic strokes ranged from 1 to 741. Mortality rate, mean LOS, and mean hospital charges also varied broadly between institutions (Table 1). Patients treated at institutions whose rate of admissions to a neurologist's care was in the upper 50th percentile were younger and more often male, but did not differ in illness severity class (Table 2).

Individual and Institutional Characteristics of Ischemic Stroke Patients by Attending Specialty
CharacteristicNeurologist (n = 16,287)Generalist (n = 10,638)Institutional (n = 113) median (10th90th percentiles)
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

  • Based on 52 institutions ever coding tPA use for ischemic stroke in 1999. Neurologists, n = 4857; generalists, n = 3351.

Age (years), mean (SD)66.2 (14.7)69.3 (15.2)67.7 (62.174.8)
Female, n (%)8291 (51)5904 (56)54% (46%67%)
Ethnicity
African American, n (%)4516 (28)3335 (31)19% (0%71%)
Asian American, n (%)570 (4)201 (2)0.7% (0%8%)
Hispanic, n (%)906 (6)458 (4)0.7% (0%16%)
Native American, Eskimo, n (%)48 (0)21 (0)0% (0%1%)
White, n (%)9012 (55)5851 (55)65% (10%95%)
Other ethnicity, n (%)398 (2)157 (1)0.3% (0%4%)
Unknown, n (%)837 (5)615 (6)0.1% (0%9%)
Comorbid illness severity score,* median (interquartile range)1 (01)1 (01)0.83 (0.650.95)
Treatment and outcome
tPA administered, n (%)132 (3)51 (2)1.9% (0.6%6.5%)
In‐hospital deaths, n (%)755 (5)1005 (9)6.1% (3%10%)
Discharges to home, n (%)9504 (59)5235 (49)52% (38%72%)
Length of stay (days), mean (SD)6.6 (7.2)7.9 (9.9)6.6 (4.210.0)
Total charges$16,600 ($20,500)$18,700 ($26,300)$15,000 ($9000$30,000)
Comparison of Patient Pretreatment Prognostic Factors at Institutions with Rate of Admission to Neurologists Above the 50th Percentile with Those with Rate of Admission Below the 50th Percentile
Characteristic<50th percentile>50th percentileP value
  • Comorbid illness severity score range: 04, from 0 = no substantial comorbid illness to 4 = catastrophic comorbid illness.

Age (years), mean (SD)66.7 (15.2)69.4 (14.3)<.001
Female, n (%)5288 (54)8907 (52).001
Comorbid illness severity score*, median (interquartile range)1 (01)1 (01).87

There were 1760 in‐hospital deaths (7.0%). In univariate analysis, older age (P < .001), white ethnicity (P < .001), emergent stroke (P < .001), and increased illness severity (P < .001) were associated with greater risk of death, whereas African‐American (P < .001) and Hispanic (P = .007) ethnicities were protective. No other patient characteristics were important, and institutional annual case volume showed no association with mortality risk.

Overall, 60% of patients with ischemic stroke were admitted to a neurologist's care. In univariate analysis (Table 3), a lower risk of in‐hospital mortality was observed in cases admitted to neurologists (4.6%) compared with those admitted to generalists (9.5%; P < .001). After adjustment in standard multivariable models, the association between neurologist admission and lower risk of death persisted (OR 0.60; 95% CI, 0.500.72; P < .001).

Physician Specialty, In‐Hospital Mortality, and tPA Use in Ischemic Stroke (n = 26,925)*
CharacteristicsUnadjustedAdjusted
Odds ratio (95% CI)P valueOdds ratio (95% CI)P value
  • tPA, tissue plasminogen activator.

  • Analysis limited to 1999 and to 52 institutions ever coding tPA use for ischemic stroke in 1999 (n = 8208).

  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

Mortality
Attending neurologist0.32 (0.260.39)<.0010.60 (0.500.72)<.001
Proportion of admissions to neurology1.05 (0.851.31).641.02 (0.791.30).90
tPA Use
Attending neurologist1.87 (1.302.69).0012.56 (1.723.78)<.001
Proportion of admissions to neurology2.32 (0.985.49).062.47 (1.085.65).03

The institutional rate of admission of ischemic stroke patients to neurologists ranged from 0% to 90%, and higher rates were seen at hospitals with higher institutional case volumes (P < .001). There was no correlation between the institutional rate of admission to neurology and the institutional mortality rate (0.33; P = .73). At the individual‐level, greater rates of admission to neurologists had no significant impact on mortality (OR 1.05; 95% CI, 0.851.31; P = .64; Table 3) in unadjusted analysis. After adjustment for patient demographics, comorbid illness severity score, urgency status, and institutional case volume in GT analysis, there remained no association between death and proportion of ischemic stroke cases admitted to neurologists (OR 1.02; 95% CI, 0.791.30; P = .90), consistent with the absence of an association between neurologist care and in‐hospital mortality.

Patients treated by neurologists were likely to have shorter stays (P < .001) and lower charges (P = .01) in univariate analysis (Table 4). In traditional adjusted multivariable analysis, the same associations were seen for LOS (P < .001) and charges (P = .05). However, in adjusted GT analyses, increased institutional rate of admission to neurologists was not associated with briefer LOS (P = .36) and was associated with greater hospital charges (P = .044).

Physician Specialty and Secondary Outcomes of Ischemic Stroke
CharacteristicUnadjusted AnalysisAdjusted ratio*
NeurologistGeneralistP valueRatio (95% CI)P value
  • Analyses adjusted for age, sex, ethnicity, urgency status, illness severity class, and institutional annual acute stroke case volume.

LOS (days), n = 25,094
Standard analysis6.68.0<.0010.92 (0.880.96)<.001
Group‐treatment analysis7.27.1.801.06 (0.941.19).35
Total Charges, n = 21,812
Standard analysis$16,600$18,700.010.95 (0.911.00).05
Group‐treatment analysis$17,800$16,900<.0011.26 (1.011.57).04

In 1999, 190 (2.2%) ischemic stroke patients received tPA at the 64 universities that had ever coded tPA use. In univariate analysis, patients admitted to a neurologist were more likely to have received tPA (P = .001; Table 3), and this association persisted after adjustment (P < .001). In adjusted GT analysis, institutions admitting a higher proportion of ischemic stroke patients to neurologists also treated patients with tPA more frequently (P = .033).

DISCUSSION

Several prior studies found that ischemic stroke outcomes were better when an attending neurologist was responsible for patient care.710 Traditional analyses of our data also indicate that care by a neurologist lowers inpatient mortality, LOS, and total charges. By contrast, a GT analysis that bypasses selection bias at the patient level suggests there is no independent benefit of neurologist care on mortality or LOS and actually shows higher associated charges.

The discrepancy between standard and GT analyses suggests that healthier patients may have been preferentially admitted to the care of neurologists. Measured pretreatment prognostic factors in our data present a mixed picture. Patients admitted to a neurologist's care were younger, more often male, more often emergently admitted, and less likely to have serious comorbid illnesses. These patient factors were controlled for in all adjusted analyses. Although traditional multivariate analysis attempts to adjust for variations between the 2 patient populations, it cannot adjust for inaccurately measured or unmeasured differences. Using the institutional proportion of admissions to neurologists as a predictor of patient outcomes, we were better able to control for the selection bias associated with differential distribution of patients to teams led by attending neurologists versus generalists.13, 14

Petty et al.7 studied 299 ischemic stroke patients and showed equivalent survival among stroke patients admitted to neurology inpatient teams versus generalist teams with neurologic consultation. However, patients cared for by generalist teams without neurologic consultation fared worse. Their subjects were treated at both academic and community hospitals. In our study, contributing hospitals were solely academic institutions. Because specialty cross talk may be more frequent at university‐based hospitals, academic‐based generalist physicians may be more familiar with recent stroke literature and guidelines than are their community‐based peers. Further, restricting analysis to academic centers in our study should have reduced the potential confounding influences of differences between other aspects of institutional care. Although no information was available on neurologist consultation in our database, informal consultation is believed to play a large but hidden role at academic medical centers. Thus, the inclusion of a formal consultation variable may be misleading at academic medical centers.

Analyzing claims data on 44,099 Medicare beneficiaries with acute ischemic strokes cared for at both academic and community hospitals, Smith et al.10 also recently reported a 10% lower risk of 30‐day mortality and 12% lower risk of rehospitalization for infections and aspiration pneumonitis among patients admitted to the care of neurologists compared with those admitted to the care of generalists. However, the upper 95% confidence interval limits for these 2 findings nearly crossed 1 (ranging from 0.9980.999). The study also concluded that patients cared for collaboratively by generalists and neurologists had a 16% lower 30‐day mortality risk (hazard ratio 0.84; 95% CI, 0.790.90) than those cared for by generalists alone but simultaneously noted that patients admitted to generalists only had more comorbidities than either the collaborative care or neurologist‐only patient groups. If sicker patients were triaged to generalist admission, as occurs in confounding by indication (also known as channeling bias), then incomplete adjustment for comorbid disease may bias outcomes in favor of neurologist involvement. The GT analysis we employed is specifically designed to overcome this exact type of selection bias.

In our study, patients admitted to neurologists received tPA significantly more often than those admitted to generalists. GT analysis also found that hospitals admitting a higher proportion of strokes to neurologists treated more patients with tPA. This result is consistent with a prior study demonstrating that academic institutions employing a vascular neurologist had significantly higher odds of administering tPA.21 Since tPA must be administered within 3 hours of symptom onset,27 it is commonly delivered in the emergency department prior to admission. Thus, patients may be preferentially selected for admission to neurologic services because of their receipt of tPA, rather than that this association reflects an actual increased use of tPA by neurologists over generalists. Alternatively, institutions with a higher rate of stroke admissions to neurology may simply be more familiar with tPA protocols. Importantly, the poor sensitivity of our data for actual tPA administration may affect the analysis of its use by physician specialty; however, the failure to administratively code tPA use is unlikely to be differentially biased based on physician specialty. Thus, undercoding of tPA use would be expected to bias these analyses toward the null.

The potential advantage and efficacy of stroke centers, stroke units, stroke services, and other institutional processes of care are not addressed by our data. Previously, among academic hospitals, we found that acute ischemic stroke mortality was lower at hospitals employing a vascular neurologist and at those whose guidelines allowed only neurologists to administer tPA.21 A later analysis evaluated the impact of all elements of stroke center care supported by the original Brain Attack Coalition consensus28 and found that no single element improved mortality.29 However, recent studies have found significant mortality benefit associated with stroke units30, 31 and stroke services.32 Clearly, the debate continues over these important questions.

Our study had several limitations. First, generalizability may be lessened because only academic medical centers contributed data and only admissions through the ED were included. However, limiting the study population to academic centers provided a homogenous study population and greatly reduced the potential for confounding at the institutional level. Although the selection of ED cases mitigated the effects of referral bias and the use of only academic hospitals minimized interinstitutional differences, institutions whose rate of admissions to neurology was above the 50th percentile differed from those whose rate admissions to neurology was below the 50th percentile. However, this difference did not consistently result in patients with worse pretreatment prognostic factors being cared for at hospitals with higher rates of admission to neurology. Second, there are important limitations to using administrative data. In our study, patients were selected based on diagnostic coding of records analysts at discharge, and the diagnostic accuracy of such coding for stroke is imperfect.33 Furthermore, missing or incomplete information could have impaired adjustments for patient differences. Third, details of patient treatment were limited. The lack of information about formal and informal consultations may have obscured a true difference in outcomes among specialties.7 Additionally, academic institutions may use systematized care plans more often than do community hospitals, potentially minimizing differences between specialties. Fourth, at the time of our study, tPA had been recently introduced into stroke care. Current rates of tPA use among neurologists and generalists may be more similar. Fifth, the ability of in‐hospital mortality to adequately assess quality of care is limited, and longer‐term and functional outcomes would be better measures and more clinically relevant.

After controlling for selection bias using GT analysis, we found stroke outcomes to be similar regardless of whether a neurologist or a generalist was the admitting physician. This result contrasts with the findings of several previous studies that suggested admitting stroke patients to a neurologist resulted in better clinical outcomes.710 Because only 1 neurologist is employed for approximately every 19.8 generalists in the United States34 and 40% of acute strokes were cared for by generalists, even in this sample entirely restricted to university hospitals, such findings would suggest that many U.S. stroke patients receive inferior care. Because the role of the neurologist as consultant rather than as attending physician is significantly more feasible in most practice settings, the demonstration of equivalent outcomes by both types of physicians is reassuring and certainly reinforces the important role that unmeasured confounders may play in observational studies.

However, these results do imply that it is vital that generalists remain fully trained in the current best practices of acute stroke management in order to maintain the equivalence of care suggested here. Given how common acute stroke is, any proposed future hospitalist training, certification, and recertification programs should include a focus on acute stroke management.

References
  1. Harrold LR,Field TS,Gurwitz JH.Knowledge, patterns of care, and outcomes of care for generalists and specialists.J Gen Intern Med.1999;14:499511.
  2. Rosenblatt RA,Hart LG,Baldwin LM,Chan L,Schneeweiss R.The generalist role of specialty physicians: is there a hidden system of primary care?JAMA.1998;279:13641370.
  3. Gabriel SE.Primary care: specialists or generalists.Mayo Clin Proc.1996;71:415419.
  4. Willison DJ,Soumerai SB,McLaughlin TJ, et al.Consultation between cardiologists and generalists in the management of acute myocardial infarction: implications for quality of care.Arch Intern Med.1998;158:17781783.
  5. Wu AW,Young Y,Skinner EA, et al.Quality of care and outcomes of adults with asthma treated by specialists and generalists in managed care.Arch Intern Med.2001;161:25542560.
  6. Avorn J,Bohn RL,Levy E, et al.Nephrologist care and mortality in patients with chronic renal insufficiency.Arch Intern Med.2002;162:20022006.
  7. Petty GW,Brown RD,Whisnant JP,Sick JD,O'Fallon WM,Wiebers DO.Ischemic stroke: outcomes, patient mix, and practice variation for neurologists and generalists in a community.Neurology.1998;50:16991678.
  8. Kaste M,Palomaki H,Sarna S.Where and how should elderly stroke patients be treated? A randomized trial.Stroke.1995;26:249253.
  9. Mitchell J,Ballard D,Whisnant J,Ammering C,Samsa G,Matchar D.What role do neurologists play in determining the costs and outcomes of stroke patients?Stroke.1996;27:19371943.
  10. Smith MA,Liou JI,Frytak JR,Finch MD.30‐Day survival and rehospitalization for stroke patients according to physician specialty.Cerebrovasc Dis.2006;22:2126.
  11. Miettinen OS.The need for randomization in the study of intended effects.Stat Med.1983;2:267271.
  12. Rothman K,Greenland S.Modern Epidemiology.Philadelphia, PA:Lippincott‐Raven;1998.
  13. Johnston SC,Henneman T,McCulloch CE,van der Laan M.Modeling treatment effects on binary outcomes with grouped‐treatment variables and individual covariates.Am J Epidemiol.2002;156:753760.
  14. McClellan M,McNeil BJ,Newhouse JP.Does more intensive treatment of acute myocardial infarction in the elderly reduce mortality? Analysis using instrumental variables.JAMA.1994;272:859866.
  15. McPherson K.The Cochrane Lecture. The best and the enemy of the good: randomised controlled trials, uncertainty, and assessing the role of patient choice in medical decision making.J Epidemiol Community Health.1994;48:615.
  16. Wen SW,Kramer MS.Uses of ecologic studies in the assessment of intended treatment effects.J Clin Epidemiol.1999;52:712.
  17. University HealthSystem Consortium. Available at: http://www.uhc.edu. Accessed April 11,2007.
  18. Ellekjaer H,Holmen J,Kruger O,Terent A.Identification of incident stroke in Norway: hospital discharge data compared with a population‐based stroke register.Stroke.1999;30:5660.
  19. Goldstein L.Accuracy of ICD‐9‐CM coding for the identification of patients with acute ischemic stroke: effect of modifier codes.Stroke.1998;29:16021604.
  20. Leibson C,Naessens J,Brown R,Whisnant J.Accuracy of hospital discharge abstracts for identifying stroke.Stroke.1994;25:23482355.
  21. Gillum LA,Johnston SC.Characteristics of academic medical centers and ischemic stroke outcomes.Stroke.2001;32:21372142.
  22. Johnston SC,Fung LH,Gillum LA, et al.Utilization of intravenous tissue‐type plasminogen activator for ischemic stroke at academic medical centers: the influence of ethnicity.Stroke.2001;32:10611068.
  23. Daniel W.Biostatistics: a Foundation for Analysis in the Health Sciences.New York:John Wiley 1995.
  24. Sachs Group.Sachs Complications Profiler, version 1.0, User's Guide.Evanston, IL,1995.
  25. University HealthSystem Consortium Services Corporation.Clinical information management: risk adjustment of the UHC clinical database.Oak Brook, IL,1997.
  26. Johnston SC.Combining ecological and individual variables to reduce confounding by indication: case study—subarachnoid hemorrhage treatment.J Clin Epidemiol.2000;53:12361241.
  27. The National Institute of Neurological Disorders and Stroke rt‐PA Stroke Study Group.Tissue plasminogen activator for acute ischemic stroke.N Engl J Med.1995;333:15811588.
  28. Alberts MJ,Hademenos G,Latchaw RE, et al.Recommendations for the establishment of primary stroke centers. Brain Attack Coalition.JAMA.2000;283:31023109.
  29. Douglas VC,Tong DC,Gillum LA, et al.Do the Brain Attack Coalition's criteria for stroke centers improve care for ischemic stroke?Neurology.2005;64:422427.
  30. Organised inpatient (stroke unit) care for stroke.Cochrane Database Syst Rev2002:CD000197.
  31. Candelise L,Gattinoni M,Bersano A,Micieli G,Sterzi R,Morabito A.Stroke‐unit care for acute stroke patients: an observational follow‐up study.Lancet.2007;369:299305.
  32. Birbeck GL,Zingmond DS,Cui X,Vickrey BG.Multispecialty stroke services in California hospitals are associated with reduced mortality.Neurology.2006;66:152732.
  33. Benesch C,Witter DM,Wilder AL,Duncan PW,Samsa GP,Matchar DB.Inaccuracy of the International Classification of Diseases (ICD‐9‐CM) in identifying the diagnosis of ischemic cerebrovascular disease.Neurology.1997;49:660664.
  34. Smart D.Physician characteristics and distribution in the US. 2006 ed. In: Department of Data Quality and Measurement, ed. Physician Characteristics and Distribution in the US. Washington, DC: American Medical Association,2006:312.
References
  1. Harrold LR,Field TS,Gurwitz JH.Knowledge, patterns of care, and outcomes of care for generalists and specialists.J Gen Intern Med.1999;14:499511.
  2. Rosenblatt RA,Hart LG,Baldwin LM,Chan L,Schneeweiss R.The generalist role of specialty physicians: is there a hidden system of primary care?JAMA.1998;279:13641370.
  3. Gabriel SE.Primary care: specialists or generalists.Mayo Clin Proc.1996;71:415419.
  4. Willison DJ,Soumerai SB,McLaughlin TJ, et al.Consultation between cardiologists and generalists in the management of acute myocardial infarction: implications for quality of care.Arch Intern Med.1998;158:17781783.
  5. Wu AW,Young Y,Skinner EA, et al.Quality of care and outcomes of adults with asthma treated by specialists and generalists in managed care.Arch Intern Med.2001;161:25542560.
  6. Avorn J,Bohn RL,Levy E, et al.Nephrologist care and mortality in patients with chronic renal insufficiency.Arch Intern Med.2002;162:20022006.
  7. Petty GW,Brown RD,Whisnant JP,Sick JD,O'Fallon WM,Wiebers DO.Ischemic stroke: outcomes, patient mix, and practice variation for neurologists and generalists in a community.Neurology.1998;50:16991678.
  8. Kaste M,Palomaki H,Sarna S.Where and how should elderly stroke patients be treated? A randomized trial.Stroke.1995;26:249253.
  9. Mitchell J,Ballard D,Whisnant J,Ammering C,Samsa G,Matchar D.What role do neurologists play in determining the costs and outcomes of stroke patients?Stroke.1996;27:19371943.
  10. Smith MA,Liou JI,Frytak JR,Finch MD.30‐Day survival and rehospitalization for stroke patients according to physician specialty.Cerebrovasc Dis.2006;22:2126.
  11. Miettinen OS.The need for randomization in the study of intended effects.Stat Med.1983;2:267271.
  12. Rothman K,Greenland S.Modern Epidemiology.Philadelphia, PA:Lippincott‐Raven;1998.
  13. Johnston SC,Henneman T,McCulloch CE,van der Laan M.Modeling treatment effects on binary outcomes with grouped‐treatment variables and individual covariates.Am J Epidemiol.2002;156:753760.
  14. McClellan M,McNeil BJ,Newhouse JP.Does more intensive treatment of acute myocardial infarction in the elderly reduce mortality? Analysis using instrumental variables.JAMA.1994;272:859866.
  15. McPherson K.The Cochrane Lecture. The best and the enemy of the good: randomised controlled trials, uncertainty, and assessing the role of patient choice in medical decision making.J Epidemiol Community Health.1994;48:615.
  16. Wen SW,Kramer MS.Uses of ecologic studies in the assessment of intended treatment effects.J Clin Epidemiol.1999;52:712.
  17. University HealthSystem Consortium. Available at: http://www.uhc.edu. Accessed April 11,2007.
  18. Ellekjaer H,Holmen J,Kruger O,Terent A.Identification of incident stroke in Norway: hospital discharge data compared with a population‐based stroke register.Stroke.1999;30:5660.
  19. Goldstein L.Accuracy of ICD‐9‐CM coding for the identification of patients with acute ischemic stroke: effect of modifier codes.Stroke.1998;29:16021604.
  20. Leibson C,Naessens J,Brown R,Whisnant J.Accuracy of hospital discharge abstracts for identifying stroke.Stroke.1994;25:23482355.
  21. Gillum LA,Johnston SC.Characteristics of academic medical centers and ischemic stroke outcomes.Stroke.2001;32:21372142.
  22. Johnston SC,Fung LH,Gillum LA, et al.Utilization of intravenous tissue‐type plasminogen activator for ischemic stroke at academic medical centers: the influence of ethnicity.Stroke.2001;32:10611068.
  23. Daniel W.Biostatistics: a Foundation for Analysis in the Health Sciences.New York:John Wiley 1995.
  24. Sachs Group.Sachs Complications Profiler, version 1.0, User's Guide.Evanston, IL,1995.
  25. University HealthSystem Consortium Services Corporation.Clinical information management: risk adjustment of the UHC clinical database.Oak Brook, IL,1997.
  26. Johnston SC.Combining ecological and individual variables to reduce confounding by indication: case study—subarachnoid hemorrhage treatment.J Clin Epidemiol.2000;53:12361241.
  27. The National Institute of Neurological Disorders and Stroke rt‐PA Stroke Study Group.Tissue plasminogen activator for acute ischemic stroke.N Engl J Med.1995;333:15811588.
  28. Alberts MJ,Hademenos G,Latchaw RE, et al.Recommendations for the establishment of primary stroke centers. Brain Attack Coalition.JAMA.2000;283:31023109.
  29. Douglas VC,Tong DC,Gillum LA, et al.Do the Brain Attack Coalition's criteria for stroke centers improve care for ischemic stroke?Neurology.2005;64:422427.
  30. Organised inpatient (stroke unit) care for stroke.Cochrane Database Syst Rev2002:CD000197.
  31. Candelise L,Gattinoni M,Bersano A,Micieli G,Sterzi R,Morabito A.Stroke‐unit care for acute stroke patients: an observational follow‐up study.Lancet.2007;369:299305.
  32. Birbeck GL,Zingmond DS,Cui X,Vickrey BG.Multispecialty stroke services in California hospitals are associated with reduced mortality.Neurology.2006;66:152732.
  33. Benesch C,Witter DM,Wilder AL,Duncan PW,Samsa GP,Matchar DB.Inaccuracy of the International Classification of Diseases (ICD‐9‐CM) in identifying the diagnosis of ischemic cerebrovascular disease.Neurology.1997;49:660664.
  34. Smart D.Physician characteristics and distribution in the US. 2006 ed. In: Department of Data Quality and Measurement, ed. Physician Characteristics and Distribution in the US. Washington, DC: American Medical Association,2006:312.
Issue
Journal of Hospital Medicine - 3(3)
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Journal of Hospital Medicine - 3(3)
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184-192
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184-192
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Influence of physician specialty on outcomes after acute ischemic stroke
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Influence of physician specialty on outcomes after acute ischemic stroke
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ischemic stroke, outcomes measurement, quality improvement
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ischemic stroke, outcomes measurement, quality improvement
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