Posts

February 4th, 2013

Selections from Richard Lehman’s Literature Review: February 4th

CardioExchange is pleased to reprint selections from Dr. Richard Lehman’s weekly journal review blog at BMJ.com. Selected summaries are relevant to our audience, but we encourage members to engage with the entire blog.

JAMA Intern Med  28 Jan 2013  Vol 173

Blood Transfusion and Increased Mortality in MI (pg. 132):  One treatment that we are learning to be meaner with is blood transfusion. Several studies in different contexts over the last year have shown that a restrictive transfusion policy is often associated with better survival than a liberal transfusion policy. In this systematic review, the authors look at the literature on transfusion at the time of myocardial infarction. The trials are of variable quality but in terms of all-cause mortality, the message is that less blood is more beneficial.

NEJM  31 Jan 2013  Vol 368

Proteotoxicity and Cardiac Dysfunction (pg. 455):  How nice to read another article about organ failure in old age. Mechanisms of Disease: Proteotoxicity and Cardiac Dysfunction—Alzheimer’s Disease of the Heart? If you trespass beyond the age of 75, your heart may well begin to fail for reasons that are little to do with ischaemia but much to do with stiffening and the general clogging up of cardiomyocytes with defunct protein. At the same time, your brain may be forming plaques and tangles. Bah. Ripe old age means ripe old proteins and time to pack up.
Come Fate with thine abhorrèd shears
And take them to my telomeres.

Lancet  2 Feb 2013  Vol 381

Combined Fitness and Statin Treatment on Mortality Risk in Veterans with Dyslipidaemia (pg. 394):  Ten thousand American veterans with dyslipidaemia in their late fifties were observed for a mean period of 10 years in this cohort study. As expected, those who took a statin had a lower mortality over this period of 9.2% in absolute terms, or in relative terms one third. Fitness, as based on peak metabolic equivalents (MET) achieved during exercise test, demonstrated even larger mortality benefits in this highly selected male population. So although I am not a black American army recruit, I can’t altogether ignore the message that keeps coming back from every observational and interventional study: even quite modest amounts of exercise in older men can lead to big gains in survival.

BMJ   2 Feb 2012  Vol 346

Benefits of β Blockers in Patients with HF and Reduced EF: After the first trials using bisoprolol and carvedilol in heart failure with reduced ejection fraction appeared, great efforts were made to change stable heart failure patients over from other beta-blockers to these particular “evidence-based” agents. I believe this still goes on throughout the UK, consuming the time and effort of numerous heart failure specialist nurses. Desist, dear ladies: several observational studies and now this network meta-analysis have shown that there are probably no mortality differences whatever between different ß-blockers in systolic HF, or if there are, they may even favour atenolol. Nor is the up-titrating of doses based on firm evidence. I have seen no hard data to persuade me that heart failure patients benefit significantly from more than a smallish dose of any ACE inhibitor and a smallish dose of any ß-blocker.

February 2nd, 2013

European Heart Journal Retracts Main Paper of the Kyoto Heart Study

The editors of the European Heart Journal have retracted the 2009 paper reporting the main results of the Kyoto Heart Study, a randomized, open-label study testing the add-on effect of valsartan to conventional therapy for high-risk hypertension. The retraction notice gave no details about the problems that led to the retraction. Here is the full text of the retraction notice:

“This article has been retracted by the journal. Critical problems existed with some of the data reported in the above paper. The editors of the European Heart Journal hereby retract this paper and discourage citations of it.”

For the past year the chief investigator of the Kyoto Heart Study, Hiroaki Matsubara, who had been a prominent cardiologist and researcher at Kyoto Prefectural University in Japan until the recent scandal, has been under fire. Last March, following accusations by independent bloggers in Japan and Germany, the American Heart Association (AHA) issued an Expression of Concern about five papers published in AHA journals coauthored by Matsubara. Then, last month, the editor of Circulation Journal, the official journal of the Japanese Circulation Society (and not to be confused with the American Heart Association’s better known Circulationannounced the retraction of two substudies from the Kyoto Heart Study. The papers, according to the editor, “contain a number of serious errors in data analysis.”

It is worth noting that the Kyoto Heart Study was considered to be an important study with significant clinical implications at the time of its publication. The title of the press release issued by the European Society of Cardiology upon publication of the original study was: “Valsartan reduces morbidity and mortality in Japanese patients with high risk hypertension.”

At the time of the initial publication of the Kyoto Heart Study, hypertension researchers Franz Messerli, Sripal Bangalore, and Frank Ruschitzka wrote an editorial that raised some questions about the study. Responding to today’s news of the retraction of the main study, Messerli said:

 “…in our editorial we use terms like ‘somewhat surprisingly’, ‘due to chance’ and ‘somewhat difficult to believe’ to describe the findings of the Kyoto Heart Study. This clearly shows that we had difficulties in reconciling the data  with existing evidence from other studies. I am therefore not  surprised that the veracity of main results also turned out to be questionable.

Screen Shot 2013-02-02 at 11.50.51 AM

February 1st, 2013

Reflections on Our Profession: Dr. James Fang Named Chief of Cardiology at the University of Utah

and

Dr. James Fang, MD, has recently accepted the position of Chief of Cardiology at the University of Utah in Salt Lake City, and he’ll officially start later this spring. Dr. John Ryan, who also recently took a position at the University of Utah, took this opportunity to ask Dr. Fang about his new job and to reflect on the profession as part of a new feature on CardioExchange.

Dr. Ryan: What moment or person influenced your career the most to date?

Dr. Fang: The most prominent person has been Pat O’Gara. However, I would be remiss if I didn’t also mention Peter Ganz, Lynne Stevenson, and Dan Simon. To me, they represent the pinnacle of academic medicine and personal integrity.

Dr. Ryan: Why do you want to be Chief of Cardiology?

Dr. Fang: I was once asked why would I want to lead any group; the simple answer is to help good people do good things; in this case, I recognized there were wonderful folks at Utah that were looking for someone to help lead them to accomplish their goals. I also saw an opportunity to grow an academic division in an institution that was willing to consider other organizational models in a historically collaborative environment. However, there is no doubt the modern CV division has many challenges in trying to balance fiscal responsibility and clinical productivity with the academic missions of education and research. The challenge becomes even more acute within the current healthcare mandate. I also hope to be able to use my position to direct clinical behaviors that reward quality rather than simple diagnostic and procedural volumes.

Dr. Ryan: How do you think the role of Academic Cardiology Divisions will change over the next 5-10 years?

Dr. Fang: Academic medical centers will evolve into institutes where the clinical, teaching, and research missions will be organized by disease states rather than by the traditional divisions into medicine, surgery, and radiology. This change will mean that Academic CV divisions will be integrated into Cardiovascular Institutes or Service Lines where their missions can be conducted with greater efficiency and collaboration. Traditional divisions of surgery and medicine will need to be absorbed into a singular mission to advance the field of CV medicine, whether from a medical, surgical, or endovascular approach. This approach already exists at many medical centers in a virtual way; I anticipate that fiscal and political integration will continue.

Dr Ryan: What steps should we take to ensure the survival of the physician investigator? Or is that even a worthwhile goal?

Dr. Fang: Survival of the physician investigator is an absolute necessity. Advances in medicine only occur with such committed individuals and institutions. But this takes resources and academic medical centers are complex institutions that often have multiple priorities. In order to assure their survival, the first step is to solidify the commitment of hospital leadership to supporting this mission. Increasingly, academic affiliated hospitals must commit their fiscal resources, that are derived from downstream technical revenues, to be re-invested into the drive to discovery. “Protected time” will continue to be a critical part of this equation.

February 1st, 2013

Your Blog, Your CV, and Academic Promotion

“Doctor, could we have a copy of your most recent CV?”

“Sure,” I said, realizing it hadn’t been updated recently.

It is interesting how I approach my academic pursuits now.  It used to be that it was “publish or perish” in the world of academic medicine.  Of course, even now the only “publishing” that counts to the academic world is that of conventional peer-reviewed journals with high impact factors (or grant applications that bring in dollars).  But publishing for the sake of publishing may have its limits, too, since some researchers chose to publish the same research data in many publications and in different formats just to pad their curriculum vitae (CV).

We’re seeing a new era of complete disruption in medicine.  Scientific publishing is no different.  Peer-reviewed journals, while still considered most “scientific” by the academic community, are finding their relatively long turn-around times and paywalls competing against more nimble peer-reviewed open access journals that foster and promote broad commentary across disciplines for free.  Blogs, too, encourage open, free communication and, because they are often syndicated using RSS feed, can have a significant “impact factor” to not only the public, but more conventional main stream media.

It is no secret that I have published MUCH more on this blog’s pages than I ever would have via peer reviewed journals.  After all, it can be enjoyable and there is virtually no barrier to entering a discussion here.  I have enjoyed the to and fro commentary here and found there are many insightful individuals that greatly enrich not only this blog’s content, but my perspective.  In effect, writer and reader both learn here.

Fantastic.

But there’s another interesting thing I’ve come to find as a result of my work to publish here that academic centers who want to influence discussions should know: I am certain that several topics I have covered in these pages have had MUCH more influence on my chosen field than they they would have had I published just in a closed access, peer-reviewed journal.  Hyperlinks can substantiate claims.  As such, blogs can be change agents and influence action.  In return, I find the process of researching and publishing in this forum increasingly worthwhile professionally.  Writing here can also keep me sane when I need it most.

Sure, there are legal risks to publishing a blog.  HIPAA rules, the permanence of this record, the need to avoid defamation, etc. are critical aspects of working in this public space.  But opinions and unique perspectives that are freely searchable on the internet can spark other ideas or areas for analysis not previously considered in the fixed black-and-white world of print media.  Discussion threads, while now more commonplace behind journal paywalls, remain restrictive to public discovery and review there.

Currently, a link to my blog exists on my curriculum vitae.  I realize it may never be reviewed by the academic medical world nor might it facilitate my academic promotion.  For me, I won’t be crushed if that’s the case.  But for younger doctors just getting started, their efforts at maintaining a well-written scientific blog should be rewarded academically in my view, just like a scientific paper.  After all, a good blog can contribute to important scientific and educational discussions.

Perhaps it’s time academic centers routinely include social media contributions as a regular part of their academic promotion criteria.  It’s not everything, certainly.  But careful, thoughtful, and responsible online writing and interactions should be valued and promoted formally by academic centers in this internet age.

January 30th, 2013

Small Study Suggests Yoga May Benefit AF Patients

A study published online in the Journal of the American College of Cardiology suggests that yoga may benefit people who have atrial fibrillation. The study, which the authors describe as “a small, proof-of-concept study,” is the first of its kind. The findings raise the possibility that yoga may reduce AF symptoms and arrhythmia burden. Other physiological and quality-of-life (QOL) benefits were also observed. But, the authors caution, large randomized trials will be required to confirm the finding.

Dhanunjaya Lakkireddy and colleagues studied 52 consecutive patients with persistent paroxysmal AF  and stable medical therapy at the University of Kansas Medical Center. After an initial 3-month control period, patients received three months of yoga training.

Compared with the end of the control period, the end of the yoga period showed a significant reduction in the number of symptomatic AF episodes, symptomatic non-AF episodes, and asymptomatic AF episodes. Some 22% of patients who had an AF episode in the control period had no episodes during the yoga period.

In addition, at the end of the yoga period there were significant improvements in several QOL measures (physical functioning, general health, vitality, social functioning, and mental health), as well as significant reductions in heart rate and blood pressure.

The authors wrote that their findings “underscore the therapeutic value of a low-cost noninvasive therapy such as yoga to effectively complement the conventional treatment strategies in improving AF patient care. Given the high prevalence of AF and costs of conventional therapy, the public health relevance of these findings is very pertinent.”

The authors speculated that yoga may achieve its effects via several mechanisms of action. Among others, yoga may decrease systemic stress and increase baseline parasympathetic tone. More generally, they write,

the benefit from the emotionally supportive atmosphere at yoga training centers, and the positive impact by the caring relationships, change in diet and life style modification associated with yoga practice on physiological parameters cannot be underestimated.

 

January 30th, 2013

How Insurance Status Affects Treatment for Patients with CAD

, and

In a new study published in the Journal of the American College of Cardiology, Smolderen et al examine the association between insurance status and physicians’ patterns of prescribing evidence-based therapies for coronary artery disease (CAD).

Analyzing the Practice Innovation and Clinical Excellence (PINNACLE) Registry of the National Cardiovascular Data Registry (NCDR), the authors found that: (1) uninsured patients with CAD were 9%, 12%, and 6% less likely to receive treatment with a beta-blocker, an angiotensin-converting enzyme (ACE) inhibitor/angiotensin II receptor blocker (ARB), and lipid-lowering therapy, respectively, than were privately insured patients; (2) patients with public insurance were 9% less likely to be prescribed ACE inhibitor/ARB therapy; and (3) most differences by insurance status were attenuated after adjusting for the site providing care. CardioExchange’s John Ryan interviewed authors Kim Smolderen and Paul Chan about these findings.

Ryan: You observe that treatment differences are largely explained by “lower rates of medication treatment at sites with higher proportions of uninsured patients.”  What do you feel is the reason that these sites with large numbers of uninsured patients have lower rates of treatment?

Smolderen and Chan: Although we did not have data within PINNACLE to account for site-level differences in care, there may be several explanations for our findings.  First, clinics with high proportions of uninsured patients are frequently overbooked and inadequately staffed.  As a result, patients at these clinics may have less “face time” (i.e., shorter clinic time slots) with providers than at other practices, thus resulting in less comprehensive care for their CAD.  Second, uninsured patients may not have sufficient funds to acquire some of their CAD medications (including generics), which may indirectly influence physician-prescribing behavior.  And third, uninsured patients often have to contend with other non-medical (e.g., social, psychological, and economic) issues, and physicians may view these as higher priorities for certain patients than meeting established performance measures for CAD.

Ryan: How would you suggest this discrepancy be best addressed?

Smolderen and Chan: We need a restructuring of medical reimbursement in the U.S. health care system.  First, universal access to primary health care for all patients is essential.  The recently passed Affordable Health Care Act is an important step in the right direction, but this law may not go far enough, and many millions will remain uninsured even with its full implementation starting in 2014.  Second, more robust economic incentives (e.g., federal loan repayment) to encourage physicians to work with underserved populations will increase the work force needed in many of these practices with high proportions of uninsured patients.  In doing so, many of these previously under-staffed clinics can now devote adequate time during patient encounters to address the multiple medical needs of their patients.  Third, until such changes are in place, development of strong on-site prescription assistance programs that utilize available federal and state funding and improvement of provider awareness of such programs at their clinics would facilitate more universal patient access to evidence-based medications for CAD.

Ryan: Were you surprised that treatment of patients with public health insurance was similar to those with private insurance?

Smolderen and Chan: Yes, we were surprised.  We had anticipated a graded relationship by insurance status, with treatment rates for publicly insured patients between those of privately and uninsured patients.  The fact that the unadjusted rates of publicly insured patients mirrored those of privately insured patients may suggest that providing any insurance (public or private) translates into better delivery of CAD care.  Our findings would suggest that the mere extension of insurance (through exchanges or Medicaid) for ~10% of the U.S. population in the Affordable Care Act will likely increase rates of evidence-based CAD treatment of previously uninsured patients to the levels of privately insured patients.

Ryan: Based on your work, ACE inhibitors or ARBs were prescribed in 73% of patients with left ventricular systolic dysfunction and/or diabetes mellitus. What do you feel contributes to failure to prescribe ACE inhibitors/ARBs to over a quarter of these patients?

Smolderen and Chan: Medication cost may play a role.  Although generic versions of ACE inhibitors have been available for years, for patients who cannot take these medications, the cost of ARBs may be a barrier, as generic ARBs have not been available until the past year.  It may also be because the evidence supporting the use of ACE inhibitors and ARBs is the most recent, and their current rates reflect the typical time frame for trial evidence to diffuse into routine practice.  Finally, treatment with ACE inhibitor and ARB medications require some monitoring (i.e., electrolytes and renal function), and it is not clear if additional monitoring presents barriers to treatment.

January 29th, 2013

FDA Approves Mipomersen for Homozygous Familial Hypercholesterolemia

The FDA said today that it had granted approval to the novel cholesterol-lowering drug mipomersen sodium for use as an adjunct to diet and drug therapy in patients with homozygous hypercholesterolemia. The drug, which was developed by Isis Pharmaceuticals, will be marketed under the brand name of Kynamro by Genzyme.

Kynamro was approved as an orphan drug, which the FDA describes as meaning it was developed to treat a condition affecting less than 200,000 people. The standard of approval for orphan drugs is less rigorous than other drugs. There has been some confusion about the number of people who have homozygous familial hypercholesterolemia.  The FDA and ISIS/Genzyme said the condition affects about one in every million people.

In December the FDA approved lomitapide (Juxtapid, Aegerion) for the same condition. These are the first drugs specifically developed and approved for familial hypercholesterolemia.

Kynamro will carry a boxed warning about the serious risk of liver toxicity. Clinical studies with the drug found that it raised liver enzymes and led to accumulation of fat in the liver. The FDA said this “could lead to progressive liver disease with chronic use.”

Kynamro was approved with a Risk Evaluation and Mitigation Strategy (REMS) which will require certification of prescribers and pharmacies, as well as documentation that the drug is being properly used with each new prescription.

The FDA said the most common adverse reactions with Kynamro were injection site reactions, flu-like symptoms, nausea, headache, and elevations in liver enzymes.

The FDA is requiring the sponsor to perform four postmarketing studies, including a long-term registry of patients to assess the long-term safety of the drug, and an enhanced pharmacovigilance program to monitor potential problems.

“Kynamro is the first systemic antisense drug to reach the market and is the culmination of two decades of work to create a new, more efficient drug technology platform. As evidenced by our robust pipeline, our antisense drug discovery technology is applicable to many different diseases, including the treatment of a chronic and rare disease, like HoFH,” said Stanley Crooke, the chair and CEO of Isis, in a press release.

In October, an FDA advisory panel voted to recommend approval of mipomersen, though the panel expressed considerable caution about the potential for liver damage. In December the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency recommended that the drug not be approved for use in Europe.

January 29th, 2013

Popular Antidepressants May Prolong QT Interval

In August 2011 the FDA issued a safety communication recommending that the extremely popular antidepressant citalopram (Celexa) not be used at doses greater than 40 mg/day because of a potential increased risk for serious cardiac arrhythmias associated with prolongation of the QT interval. Now a study published in BMJ lends support to this warning and suggests that other antidepressants may also prolong the QT interval.

Victor Castro and colleagues, using a pharmacovigilance approach, analyzed data from more than 38,000 patients in the Partners HealthCare system who received an ECG after receiving an antidepressant or methadone prescription. (Methadone, which is known to prolong the QT interval, was used to verify the sensitivity of the study.)

People who used citalopram, escitalopram (Lexapro), and amitriptyline, in addition to methadone, were significantly more likely to have a prolonged QT interval (QTc). By contrast, bupropion was associated with a significant decrease in QTc. The investigators also reported a dose-response relationship. However, the size of the effects observed were small.

The investigators reported that almost 20% of the patients were found to have an abnormal QT interval, but duly noted that “the clinical significance of this prolongation, including the risk of induction of torsades de pointes, is unknown.” The authors write that the question of whether patients who receive antidepressants should receive routine ECGs “before and/or after treatment starts cannot be addressed directly by this study.”

January 29th, 2013

Selections from Richard Lehman’s Literature Review: January 28th

CardioExchange is pleased to reprint selections from Dr. Richard Lehman’s weekly journal review blog at BMJ.com. Selected summaries are relevant to our audience, but we encourage members to engage with the entire blog.

JAMA  23-30 Jan 2013  Vol 309

Hospital Readmission as a Quality Marker? (pg. 381): Readmission is now being looked at routinely as a quality marker for providers in the USA: but does this make any sense? Do we know of any effective means to reduce it? This study of a quality improvement initiative for care transitions by healthcare and social services personnel and Medicare Quality Improvement Organization staff in defined geographic areas was essentially negative. A Viewpoint piece looks at the logic of using 30 day readmission as a quality marker for heart failure care and decides there isn’t any. “Each quality metric should be data driven and patient focused. The 30 day readmission measure does not appear to meet either of these criteria. The important remaining question is whether patients will benefit from this measure. Thus far, it appears that this metric has the potential to result in more harm than benefit for patients with heart failure.”

NEJM  24 Jan 2013  Vol 368

Cardiovascular Safety of Peginesatide in Patients with Anemia Undergoing Hemodialysis (pg. 307): Hmm. Why then did we have the withdrawal of Vioxx and Avandia; why do we still not know if Tamiflu has any useful effect; and why was it so long before there were safety concerns over epoetin? It’s partly because of hidden data, and partly because of inadequate surrogate endpoints. Epoetin is very good at raising haemoglobin levels in renal dialysis patients: the only problem is that those with a “normal” Hb die sooner. Now there is a new kid on the block, called peginesatide, which works as well as epoetin but only needs to be injected monthly. Here is a study (EMERALD 1) which shows that the stuff not only raises Hb but is as safe as epoetin using a composite end-point of all-cause death, myocardial infarction, stroke, or serious cardiac events in dialysis patients.

Cardiovascular Safety of Peginesatide for Anemia in Patients with CKD Not Receiving Dialysis (pg. 320): However, when you compare peginesatide with darbepoetin in patients with advanced renal failure who are not on dialysis, the picture is less favourable. Cardiovascular end-points are commoner with the new agent. That’s a high price to pay for greater convenience of use, and I’m not convinced we yet know enough about this new agent to license it for general use.

January 29th, 2013

In REGARDS to Depression, MI, and Death in Patients with CHD

In a recent Journal of the American College of Cardiology study, Ye et al explored whether behavioral mechanisms (i.e., alcohol use, smoking, physical inactivity, and medication non-adherence) explain the association between depressive symptoms and myocardial infarction (MI) or death in individuals with coronary heart disease (CHD) enrolled in the REGARDS (REason for Geographic and Racial Differences in Stroke) study. The authors confirmed that elevated depressive symptoms are associated with an increased risk of MI or death, and that, of the behavioral mechanisms assessed, smoking and physical inactivity were the most substantial contributors. CardioExchange’s Dr. John Ryan discusses these findings with the study’s Senior Author, Dr. Monika Safford.

Ryan: Dr. Safford, why did you feel it was important to study the role of behavioral mechanisms in depression and CHD? And why did you choose alcohol use, smoking, physical inactivity, and medication non-adherence? Do you think there are other behavioral mechanisms that play a role?

Safford: Given the well-described association between depressive symptoms and CHD outcomes, we wanted to better understand the mechanisms that may lead to this observation. Understanding these mechanisms points the way to new directions for treating this vulnerable population. The four behavioral mechanisms we chose — alcohol use, smoking, physical activity, and medication non-adherence — all had plausible associations with both depression and CHD and were available in the national, population-based biracial REGARDS cohort study, which was an exciting setting for the study. However, although these four pathways are very important, the situation is likely more complex, and there are probably other important behavioral mechanisms that we were not able to study, including being unable or unwilling to follow up with physicians. Nevertheless, this study is a good first step to better understanding the relationship between depression and CHD outcomes.

Ryan: Do you now think that depression does not have an independent effect on CV risk and only exerts an effect as it is mediated through these risk factors?

Safford: Our results on smoking and physical activity are consistent with findings from the Heart and Soul Study and the Cardiovascular Health Study, so we think these two factors definitely do play a large role in explaining the association between depression and cardiac risk. However, we must be careful when we interpret these results and attribute causality. For instance, are depressed individuals less likely to exercise and are therefore at higher risk for cardiac events, or is it that individuals who don’t exercise are more likely to be depressed, which then confers higher risk? Both scenarios can lead to the results we have shown. In the most rigorous sense of the term, to claim mediation would require us to show that one precedes the other, for which we would need assessments at additional time points. To make the picture even more complex, the causal pathways may also differ between individuals, and these individual variations may be part of the reason why it has  been so difficult to identify successful strategies to treat depression that also reduce cardiac risk in this patient population. Finally, we should note that in our analysis, although the independent effect of depressive symptoms was no longer statistically significant after accounting for behavioral mechanisms, our bootstrap analysis showed that the behavioral mechanisms only explained 36.9% of the overall effect with a fairly wide confidence interval, suggesting that additional risk factors that we did not have available play a role, and that there may be considerable variability in these unmeasured effects.

Ryan: Do CV specialists need to screen for depression? Or should we focus on risk factors, acknowledging that treating depression is good in its own right, but can be left to the primary care provider?

Safford: From the patient’s perspective, depression has a huge impact on quality of life.  Depression is also very common in patients with CHD, so it definitely warrants screening and treatment from that perspective alone. We think our study supports a holistic approach that recognizes that risk factors such as physical inactivity and smoking may be especially prevalent in CHD patients with depressive symptoms, and that it is important to address these problems.  Guidelines such as the AHA Science Advisory on depression and CHD call for CV specialists to screen for depression and provide appropriate referral, which is certainly a reasonable approach given how closely CV specialists often follow CHD patients, though the level of evidence for this recommendation is still mostly expert opinion. We think what is ultimately needed is a more robust evidence base for team-based, collaborative approaches that are now emerging (see Katon WJ et al, N Engl J Med 2010 and Davidson KW et al, Arch Intern Med 2010) to effectively and efficiently treat depression, and in which CV specialists play a prominent role.