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SBP measurement below goal (ARR, 1.74; 95% CI, 1.07-2.83; P = .03), adjusting for adherence counseling (ARR, 1.49; 95% CI, 1.10-2.04; P = .01) and excluding patients with DM with SBP 140 mm Hg or lower (ARR, 1.49; 95% CI, 0.99-2.23; P = .06). Discussion | Among patients with uncontrolled hypertension, clinical inertia was more likely in those with a diagnosis of depression. Hence, clinical inertia may be 1 mechanism by which depressed patients have worse cardiovascular outcomes. Research has shown that patients with mental illness receive less intensive medical care, such as coronary revascularization6; our study extends this literature by demonstrating differences in clinician behavior with respect to cardiovascular risk factor management in this population. Future studies should explore the underlying processes that affect clinician treatment practices when managing a patient with depression. In the meantime, PCPs should be cautious about undertreating cardiovascular risk factors among patients identified as having depression. Nathalie Moise, MD Karina W. Davidson, PhD William Chaplin, PhD Steven Shea, MD, MS Ian Kronish, MD, MPH Author Affiliations: Center for Behavioral and Cardiovascular Health, Division of General Medicine, Columbia University Medical Center, New York, New York (Moise, Davidson, Chaplin, Shea, Kronish); Department of Psychiatry, Columbia University Medical Center, New York, New York (Davidson); Department of Psychology, St John’s University, Queens, New York (Chaplin); Department of Epidemiology, Joseph Mailman School of Public Health, Columbia University, New York, New York (Shea). Corresponding Author: Nathalie Moise, MD, Division of General Medicine, Columbia University Medical Center, 622 W 168th St, PH9 Center, Room 320, New York, NY 10032 ([email protected]). Published Online: March 10, 2014. doi:10.1001/jamainternmed.2014.115. Author Contributions: Dr Moise had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Moise, Davidson, Kronish. Acquisition of data: Moise, Shea, Kronish. Analysis and interpretation of data: Moise, Chaplin, Shea, Kronish. Drafting of the manuscript: Moise, Kronish. Critical revision of the manuscript for important intellectual content: All authors. Statistical analysis: Moise, Chaplin, Shea, Kronish. Obtained funding: Davidson, Kronish. Administrative, technical, and material support: Kronish. Study supervision: Davidson, Shea, Kronish. Conflict of Interest Disclosures: Dr Kronish received an honoraria from Integritas Communications Group for speaking at a continuing medical education conference. No other disclosures are reported. Funding/Support: This work was supported by funds from the National Heart, Lung, and Blood Institute (K23 HL-098359), the American Heart Association (SDG 10SDG2600321), and the Health Resources and Services Administration (T32HP10260). Role of the Sponsor: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. 1. Lett HS, Blumenthal JA, Babyak MA, et al. Depression as a risk factor for coronary artery disease: evidence, mechanisms, and treatment. Psychosom Med. 2004;66(3):305-315. jamainternalmedicine.com

2. Burg MM, Edmondson D, Shimbo D, et al. The “perfect storm” and acute coronary syndrome onset: do psychosocial factors play a role? Prog Cardiovasc Dis. 2013;55(6):601-610. 3. O'Connor PJ, Sperl-Hillen JAM, Johnson PE, Rush WA, Biltz G. Clinical Inertia and Outpatient Medical Errors Advances in Patient Safety: From Research to Implementation. Rockville, MD: Agency for Healthcare Research and Quality; 2005. Vol 2. Concepts and Methodology. 4. Heisler M, Hogan MM, Hofer TP, Schmittdiel JA, Pladevall M, Kerr EA. When more is not better: treatment intensification among hypertensive patients with poor medication adherence. Circulation. 2008;117(22):2884-2892. 5. Kerr EA, Zikmund-Fisher BJ, Klamerus ML, Subramanian U, Hogan MM, Hofer TP. The role of clinical uncertainty in treatment decisions for diabetic patients with uncontrolled blood pressure. Ann Intern Med. 2008;148(10):717-727. 6. Druss BG, Bradford DW, Rosenheck RA, Radford MJ, Krumholz HM. Mental disorders and use of cardiovascular procedures after myocardial infarction. JAMA. 2000;283(4):506-511.

Editor's Note

Multimorbidity, Guidelines, and Clinical Inertia Many guidelines and performance measures for chronic conditions, such as hypertension, seem to assume that patients come neatly packaged with only 1 problem. But patients’ conditions are often more complicated, and many patients have more than 1 condition. We know little about the impact that this multimorbidity has on care for common conditions like hypertension. The Research Letter by Moise et al is novel because it clearly demonstrates that co-occurrence of depression has a significant impact on the treatment of hypertension. Specifically, patients who had a blood pressure higher than 140/90 mm Hg were less likely to have their hypertension medications intensified if they also had depression. Moise et al refer to this as clinical inertia. But is clinical inertia always bad? The answer is not clear. In some cases, clinicians may have thought that their patients’ depression was more pressing than their hypertension. Especially if the blood pressure elevation was modest, over the long-term, management of the hypertension may be best optimized by first managing depression. When a patient has multiple problems, it is challenging to prioritize what needs to be done “this visit” and what is best managed over a longer time horizon. The study by Moise et al demonstrates that we need to think hard about the best management strategies for patients with multiple medical problems. Kenneth E. Covinsky, MD

HEALTH CARE REFORM

Headaches and Neuroimaging: High Utilization and Costs Despite Guidelines While most headaches are attributable to benign conditions, patients and physicians are often concerned about intracranial pathologic conditions. However, the yield of significant abnormalities on neuroimaging in patients with chronic headaches is 1% to 3%. 1-3 Editor's Note page 821 Given the comparable yield in patients without headaches, multiple guidelines have recommended against routine headache neuroimaging,4-6 and efJAMA Internal Medicine May 2014 Volume 174, Number 5

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Table. Neuroimaging Utilization and Associated Costs From 2007 Through 2010 Using Different Definitions of a Headache Visit Total Visits, No. (95% CI) (in Millions)

MRI

CT

MRI or CT

Imaging Payments, US $ (95% CI) (in Millions)

All headache

51.1 (43.2-58.9)

7.6 (6.1-9.4)

5.1 (3.7-6.9)

12.4 (10.5-14.7)

3910 (3020-4800)

All migraine

25.4 (19.6-31.2)

6.0 (4.4-8.2)

3.8 (2.1-6.8)

9.8 (7.4-12.9)

1530 (976-2080)

Primary headache

29.2 (23.8-34.6)

10.1 (7.9-12.9)

6.2 (4.2-9.0)

15.9 (13.1-19.1)

2940 (2180-3710)

Primary migraine

16.1 (11.6-20.6)

7.2 (4.9-10.5)

4.5 (2.2-9.1)

11.7 (8.4-16.0)

1160 (670-1660)

Diagnoses

Visits, % (95% CI)

Abbreviations: CT, computed tomography; MRI, magnetic resonance imaging.

Figure. Trends in Neuroimaging Utilization for the Entire Headache Population From 1995 Through 2000 and 2005 Through 2010 25

% Receiving MRI or CT

20

15

10

5

0 1995

1996

1997

1998

1999

2000

2005

2006

2007

2008

2009

2010

Year

forts to improve the efficiency of health care utilization, such as the Choosing Wisely campaign (ABIM [American Board of Internal Medicine] Foundation; http://www.choosingwisely .org), have identified these tests as a target. However, little is known about recent headache neuroimaging utilization, associated expenditures, and temporal trends in the United States. Methods | Institutional review board exemption was obtained from the University of Michigan Health System. We utilized the National Ambulatory Medical Care Survey (NAMCS), a nationally representative survey that uses a 3-stage sampling design (geographic regions, physician practices stratified within specialties, and patient visits within practices) to characterize all outpatient office-based care in the United States. We analyzed all headache visits for patients 18 years or older identified using the Healthcare Cost and Utilization Project (HCUP) Single-level Clinical Classification System (CCS) (International Classification of Diseases, Ninth Revision, Clinical Modification [ICD-9-CM] codes 339.xx, 784.0x, 346.xx, and 307.81). For migraine, ICD-9-CM codes 346.xx were used. To characterize recent headache neuroimaging utilization, the proportion of headache visits with computed tomography (CT) or magnetic resonance imaging (MRI) ordered from 2007 through 2010 was estimated using descriptive statistics 820

CT indicates computed tomography; and MRI, magnetic resonance imaging. Error bars indicate 95% confidence interval.

for multiple visit categories: all headache visits, all migraine visits, and visits with a primary diagnosis of headache or migraine. Neuroimaging use (CT or MRI) was directly entered onto the NAMCS survey instrument by physicians or their staff. Neuroimaging payments were determined using the Medicare physician fee schedule. To evaluate for trends over time, we identified headache neuroimaging utilization in years where these tests were directly abstracted onto the NAMCS survey instrument (1995-2000 and 2005-2010) in all headache visits. Survey weights were applied for all analyses. Results | Of all visits, 88% were by patients younger than 65 years and 78% were by female patients. Most visits were to primary care physicians (54.8%), followed by neurologists (20%), other specialists (12.9%), and nonprimary care generalists (12.4%). Over 4 years, a total of 51.1 million headache visits were identified, including 25.4 million migraine visits. Neuroimaging was obtained in 12.4% (95% CI, 10.5-14.7) of all headache visits and 9.8% (95% CI, 7.4-12.9) of migraine visits (Table). Headache neuroimaging utilization was higher if the headache or migraine diagnosis was listed as the primary diagnosis for the visit. Total neuroimaging expenditures were estimated at $3.9 billion over 4 years, including $1.5 billion from migraine visits. Between 1995 and 2010, neuroimaging utilization increased from 5.1% (95% CI, 2.7%-7.5%) to 14.7% (95% CI, 9.4%-20.0%) of all annual headache visits (Figure) (P < .001 for trend).

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Discussion | In the United States, neuroimaging is frequently ordered during outpatient headache visits (12%), contributes substantial cost (nearly $1 billion in annual costs), and is increasing over time. Since 2000, multiple guidelines have recommended against routine neuroimaging in patients with headaches because a serious intracranial pathologic condition is an uncommon cause. 4-6 Consequently, the magnitude of per-visit neuroimaging use found in this study suggests considerable overuse. Perhaps guidelines have not curbed utilization because patients, as opposed to health care providers, may be the primary drivers of utilization. If so, efforts such as the Choosing Wisely campaign, which seeks to empower patients with knowledge regarding unwarranted testing, may be more effective than guidelines alone. Requiring preauthorization of these costly tests and/or value-based insurance designs that shift the cost burden for costly, low-yield tests to patients are alternative strategies. Given that headache neuroimaging is common, costly, and likely substantially overused, interventions to curb utilization of these tests have the potential to substantially reduce health care expenditures while improving guideline concordance. Therefore, optimizing headache neuroimaging practices should be a major national priority. Brian C. Callaghan, MD, MS Kevin A. Kerber, MD, MS Robert J. Pace, MD Lesli E. Skolarus, MD, MS James F. Burke, MD, MS Author Affiliations: Department of Neurology, University of Michigan Health System, Ann Arbor (Callaghan, Kerber, Pace, Skolarus, Burke); Department of Veterans Affairs Center for Clinical Management Research, Ann Arbor, Michigan (Burke). Corresponding Author: Brian C. Callaghan, MD, MS, Department of Neurology, University of Michigan Health System, 109 Zina Pitcher Pl, 4021 BSRB, Ann Arbor, MI 48104 ([email protected]). Published Online: March 17, 2014. doi:10.1001/jamainternmed.2014.173. Author Contributions: Dr Burke had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Callaghan, Kerber, Pace, Burke. Acquisition of data: Pace, Burke. Analysis and interpretation of data: Callaghan, Kerber, Pace, Skolarus, Burke. Drafting of the manuscript: Callaghan, Pace, Burke. Critical revision of the manuscript for important intellectual content: Callaghan, Kerber, Pace, Skolarus. Statistical analysis: Callaghan, Burke. Administrative, technical, and material support: Burke. Study supervision: Pace. Conflict of Interest Disclosures: None reported. Funding/Support: Dr Callaghan is supported by the Katherine Rayner Program, the Taubman Medical Institute, and grant K23NS079417 from the National Institutes of Health, National Institute of Neurological Disorders and Strokes. Dr Kerber is supported by grant R18 HS017690 from the Agency for Healthcare Research and Quality. Dr Skolarus is supported by grant K23NS073685 from the National Institutes of Health, National Institute of Neurological Disorders and Stroke. Dr Burke is supported by grant K08NS082597 from the National Institutes of Health, National Institute of Neurological Disorders and Strokes. Role of the Sponsor: The sponsors had no role in the design and conduct of the study; collection, management, analysis, or interpretation of the data;

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preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Additional Contributions: Wade Cooper, MD, University of Michigan, contributed in critical reviewing the manuscript. He received no compensation for his contribution. 1. Clarke CE, Edwards J, Nicholl DJ, Sivaguru A. Imaging results in a consecutive series of 530 new patients in the Birmingham Headache Service. J Neurol. 2010;257(8):1274-1278. 2. Sempere AP, Porta-Etessam J, Medrano V, et al. Neuroimaging in the evaluation of patients with non-acute headache. Cephalalgia. 2005;25(1):30-35. 3. Wang HZ, Simonson TM, Greco WR, Yuh WT. Brain MR imaging in the evaluation of chronic headache in patients without other neurologic symptoms. Acad Radiol. 2001;8(5):405-408. 4. Sandrini G, Friberg L, Coppola G, et al; European Federation of Neurological Sciences. Neurophysiological tests and neuroimaging procedures in non-acute headache (2nd edition). Eur J Neurol. 2011;18(3):373-381. 5. Silberstein SD. Practice parameter: evidence-based guidelines for migraine headache (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2000;55(6):754-762. 6. Strain JD, Strife JL, Kushner DC, et al. Headache: American College of Radiology: ACR appropriateness criteria. Radiology. 2000;215(suppl):855-860.

Editor's Note

Coping With Headaches It is not news that neuroimaging is overordered for patients with headache. In fact, as the authors have alluded to, the American College of Radiology, as part of the Choose Wisely campaign (ABIM [American Board of Internal Medicine] Foundation), has placed “Don’t do imaging for uncomplicated headache” on its top 5 list of things physicians and patients should question. However, because neuroimaging actually increased between 1995 and 2010 despite published guidelines discouraging the ordering of neuroimaging with simple headaches since 2000, the Editors thought the findings of this Research Letter are noteworthy. As the authors demonstrate, the financial costs of neuroimaging for headaches are substantial. But the costs we should care most about as physicians are the unnecessary radiation (in the case of computed tomographic scans) and incidental findings that lead to unnecessary medical procedures and great anxiety on the part of our patients. Because professional guidelines themselves appear to have limited impact on ordering of neuroimaging, we need to focus more on educating our patients about headaches and the dangers of neuroimaging. Headaches are frightening to patients and can conjure thoughts of brain tumors. It is therefore sensible that patients would seek neuroimaging to reassure themselves. Signs to us that the headache does not require further evaluation (ie, no change in the nature of headache for multiple years) may mean to the patient that the headache is serious (ie, it must be serious because I have had these pains for many years). If a physician simply says “you don’t need a scan” patients may think that the physician does not understand how great the pain is, or worse yet, that the physician is saving money for an insurance company. I always begin my evaluation of patients with headache by acknowledging that headaches are frightening and can be disabling and that many people suffer from them their JAMA Internal Medicine May 2014 Volume 174, Number 5

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entire lives. I perform a thorough neurologic examination so that patients know that I take the symptom seriously, and if there are no neurologic deficits, I explain that we need to develop a strategy for dealing with the headaches because they are likely to recur. I explain that I do not want them to have neuroimaging because of the dangers of radiation and incidental findings. Although there will always be patients who will insist on having a test that is not supported by evidence, most patients are reassured when they feel that their physician understands their condition and is working with them to develop a strategy for coping with the problem. Mitchell H. Katz, MD COMMENT & RESPONSE

Gender Income Disparities Can Be Explained by Alternative Factors To the Editor In response to the Research Letter titled “Trends in Earnings of Male and Female Health Care Professionals in the United States, 1987-2010” and the accompanying Invited Commentary, the decision by Seabury et al1 and Cooke2 to control for variables such as demographic characteristics, state, work hours, and tenure is well-constructed and laudable. However, their conclusion that gender inequities in compensation are “persistent” is premature. Neither Seabury et al1 nor Cooke2 present data on clinical collections, relative value units, or benefit packages, all of which can be critical elements of total compensation. Years of experience and practice location type (private practice, satellite clinic vs hospital based, multiphysician office vs solo) are completely ignored, when such factors contribute materially in terms of productivity, entrepreneurship, and risk. Extramural research funding and philanthropic or investment fundraising are also neglected. A recent study commissioned by the US Department of Labor states “Research indicates that women may value non-wage benefits more than men do, and as a result prefer to take a greater portion of their compensation in the form of health insurance and other fringe benefits.”3(p2) In summary, this letter and commentary do not control for many relevant, nondiscriminatory, and potentially explanatory variables in physician compensation. Balamurali Ambati, MD, PhD, MBA Author Affiliation: Department of Ophthalmology, University of Utah, Salt Lake City (Ambati). Corresponding Author: Balamurali Ambati, MD, PhD, MBA, Department of Ophthalmology, University of Utah, 65 Mario Capecchi Dr, Salt Lake City, UT 84132 ([email protected]). Conflict of Interest Disclosures: None reported. 1. Seabury SA, Chandra A, Jena AB. Trends in the earnings of male and female health care professionals in the United States, 1987 to 2010. JAMA Intern Med. 2013;173(18):1748-1750. 2. Cooke M. Persistent earnings inequities for female physicians: still the same old story. JAMA Intern Med. 2013;173(18):1750-1751. 3. CONSAD Research Corporation. An analysis of the reasons for the disparity in wages between men and women: final report. 2009. http://www.consad.com /content/reports/Gender%20Wage%20Gap%20Final%20Report.pdf. Accessed March 7, 2014.

822

In Reply The purpose of our study1 was to assess whether differences in income between male and female physicians present in the late 1980s are still present today. We found that gender differences in physician earnings have not substantively changed in 25 years. Dr Ambati notes that physician earnings come from a number of sources (eg, relative value units, benefit packages), which is true. However, our estimates of income from the Current Population Survey (CPS) (https://www .census.gov/cps/data/) were designed to capture all sources of labor earnings. While the CPS does not break down labor earnings by source, most if not all of these sources should be included. And if any were missing, we have no reason to suspect that any items that are not reported differ systematically by gender in ways that could explain the persistent malefemale earnings gap. Dr Ambati also correctly identifies that at any given point in time a number of factors may “explain” why male physicians earn more than female physicians, and our data were not rich enough to allow us to study these factors. Some of these factors could reflect differences in preferences between male and female physicians (as suggested in research quoted by Dr Ambati). It is certainly true that the mere existence of an earnings gap is not evidence of discrimination. But it is important to understand that one must be thoughtful about which factors to “adjust for” in statistical analysis. For example, if female medical school graduates are more likely than male medical school graduates to enter historically lower paying fields such as family medicine or pediatrics, one should carefully consider whether to adjust for specialty choice in the analysis. If there are barriers to entry for women in higher-paying specialties, one should not adjust for specialty because differences in average earnings between male and female physicians reflect these barriers to entry. If, instead, these choices are made with equal opportunity, it would be important to adjust for specialty choice. The same logic extends to the types of practices that female physicians choose. If female physicians work in lower-volume practices that are more conducive to lifestyle, do choices reflect barriers to entry into these practices (eg, difficulties being hired into highervolume practices) or preferences of female physicians for better lifestyle? Ultimately, research on gender differences in physician earnings should attempt to understand the contribution of factors that are preference based vs those that reflect barriers to earnings. Doing so will require new data that include information on not only specialty and practice patterns but also stated preferences of male and female physicians for both of these contributors to earnings. Seth A. Seabury, PhD Amitabh Chandra, PhD Anupam B. Jena, MD, PhD Author Affiliations: Department of Emergency Medicine and Leonard D. Schaeffer Center for Health Policy and Economics, University of Southern California, Los Angeles (Seabury); Harvard Kennedy School of Government, Harvard University, Cambridge, Massachusetts (Chandra); Department of Health Care Policy, Harvard Medical School, Boston, Massachusetts (Jena); Department of Medicine, Massachusetts General Hospital, Boston (Jena).

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Headaches and neuroimaging: high utilization and costs despite guidelines.

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