Showing posts with label Chronic Care. Show all posts
Showing posts with label Chronic Care. Show all posts

Thursday, May 7, 2009

The Week in Review - May 7, 2009

AHRQ reports on "Innovations in Using Health IT for Chronic Disease Management" across a portfolio of health IT applications including clinical decision support, health information exchange, telehealth and hospital information systems. "We found no dominant technology application... The portfolio demonstrates that a variety of health IT applications have the potential to transform the quality and safety of care for some of the Nation’s most severely ill patients. Despite several challenges associated with developing and implementing health IT for chronic disease management, information technology can be used to improve clinical processes. Technology also can facilitate better knowledge sharing and support improved communication and coordination across care settings."

NCVHS hears from leaders on the definition of meaningful use including physicians, the Markle Foundation (and 60 supporting organizations), Agency for Healthcare Research and Quality (AHRQ), College of Healthcare Information Management Executives (CHIME), American Medical Informatics Association (AMIA), HIMSS and a broad range of other industry leaders. Carolyn Clancy, AHRQ Director, says that healthcare organizations should prepare now by using health registries to manage the health information of patients with chronic diseases.

Wall Street Journal reports on an "affordable fix for modernizing medical records", the VA's Vista system.

Dr. David Blumenthal, National Coordinator for Health IT, believes that healthcare technology has not advanced sufficiently "when left exclusively to the private sector, so there is a public role."

American Public Media's Markeplace reports that investment in "health care information technology is holding its own. Investors are following the $20 billion in President Obama's stimulus plan to upgrade and modernize health records."

The Use of Health IT in Crisis Control interviews Dr. Nathaniel Hupert, Director of The Preparedness Modeling Unit for The Centers for Disease Control and Prevention (CDC) and Associate Professor of public health and medicine at Weill Cornell Medical College.


Coordination of Care by Primary Care Practices: Strategies, Lessons and Implications reports that "while there was no single recipe for coordination ... some cross-cutting lessons were identified, such as the value of a commitment to interpersonal continuity of care as a foundation for coordination." Medical home initiatives "if aligned with payment incentives ... have the potential to increase quality and satisfaction among patients and providers by helping to move the health care delivery system toward better coordinated care."

Archives of Internal Medicine reports that "computerized medication reconciliation tool and process redesign were associated with a decrease in unintentional medication discrepancies with potential for patient harm. Software integration issues are likely important for successful implementation of computerized medication reconciliation tools."

Health Care Policy and Marketplace Review has maintained a laser focus on the need for healthcare reform to result in real savings. In his latest post, Bob Laszewski contends that "health care reform means fixing the system so we stop spending/wasting so much more than every other industrial nation on health care thereby making our system more affordable and effective." In earlier posts, he referenced two December 2008 CBO reports on the potential savings associated with various reform programs: Key Issues in Analyzing Major Health Insurance Proposals and Budget Options Volume 1 Health Care. "If the CBO just rolls over and lets Congress make up excuses just to spend more for health care we will not have reform--we will only have a bigger fiscal disaster on our hands. How do you reform entitlements by pretending?"

The AMA announces initial partner agreements to provide a secure AMA portal offering a variety of practice management services.

Computer modeling predicts the spread of swine flu. One of the algorithms is rooted in human contact models derived from Where's George? which tracks the passage of one dollar bills from person to person.

HealthMap provides a global disease alert map, including tracking of swine

Tuesday, May 5, 2009

Chronic Care: Best Practices for Care Coordination

The New York Academy of Medicine and the National Coalition on Care Coordination (N3C) have released their report on the Promise of Care Coordination. Lead author Dr. Randall Brown reviewed best practices among 20 care coordination programs nationally focusing on the chronically ill. His work on care coordination and disease management includes leading two recent evaluations of demonstrations funded by the Centers for Medicare & Medicaid Services, resulting in four reports to congress on these programs’ effects on service use, costs, quality of care, and patients’ and physicians’ satisfaction with care.

Randy Brown graciously took the time to sit down with Healthcare Technology News to discuss his findings regarding "Models that Decrease Hospitalizations and Improve Outcomes for Medicare Beneficiaries with Chronic Illnesses" (links here to executive summary and full report).

HTN: Many physicians all share one common complaint: that the way care is delivered today is incredibly fragmented. Can you give us some idea of the magnitude of the problem?

Randy Brown: Mai Pham, a colleague of mine at a Mathematica subsidiary, the Center for Health Care Strategies, has done some very interesting work that illustrates the difficult, seemingly impossible, task that physicians face in trying to coordinate the care of their patients. First, she showed that the typical (median) Medicare beneficiary with chronic illnesses saw 7 different physicians during the course of a year. This does not include non-MD medical professionals at skilled nursing facilities or home health agencies who treated the patient. We have done some work of our own and found even higher numbers of physicians seeing a given patient with Congestive Heart Failure (CHF), Coronary Artery Disease (CAD), or diabetes—our estimate was 12 physicians. Gerry Anderson at Hopkins had a similar estimate.

Dr. Pham also looked at it from the doctor’s perspective across the full case load they have and found some startling numbers—her research showed that the median number of different physicians seen by a given physician’s Medicare patients during the course of a year is 229. That means a typical physician would need to coordinate with 229 different physicians during the course of a year (just for their Medicare patients), with many of these requiring multiple contacts because they see the physician’s patients multiple times throughout the year.

These hard data illustrate just how fragmented care is, and what a monumental task it would be for physicians to coordinate it on their own.

HTN: You looked at many different models to coordinate care. What were the keys to success?

Randy Brown: Across a range of rigorous studies we examined or conducted ourselves, we found some common features among the most successful programs. Most of our inferences were drawn from about 20 demonstration programs we have evaluated. Unsuccessful programs also had some of these features, but not all of them, and in some cases didn’t implement them as intensively. Here’s what we found: First, in the successful programs the care coordinators saw patients in-person fairly frequently—about once a month actually—in addition to telephonic contacts. Second, the successful programs targeted people with a substantial risk of hospitalization in the coming year. Third, care coordinators were co-located with the patients’ primary physicians, so they knew and trusted each other, and had frequent opportunities for interacting informally and exchanging information on a patient. Fourth, the successful programs tried to assign the same care coordinator to all of a physician’s patients in the program, to minimize the number of different people the physician had to interact with, and to build trust and familiarity. Fifth, the most effective programs had timely information on when patients were admitted to a hospital, so they could quickly begin working on the new needs the patient would have and capitalize on the learning opportunity presented by the crisis that got them admitted to the hospital. Sixth, the most effective models had the most well-designed and implemented patient education interventions of the programs we evaluated. And last but not least, the two most successful programs were (with one exception) the only ones out of 12 programs for which we had survey data for which the proportion of treatment group patients reporting someone had taught them how to take their medications correctly was significantly higher than the proportion of the corresponding control group reporting they received such guidance.

HTN: What were some of the metrics that defined success?

Randy Brown: We defined “success” as a program that reduced hospitalizations or reduced Medicare expenditures, over a followup period of at least one year. We did not count as successes programs that only improved clinical indicators or patient satisfaction. While these types of improvements are obviously important, settling for only those types of gains would be setting the bar too low. We can and we should reduce the high rate of preventable hospitalizations.

HTN: What innovations did you find in the enabling technologies that seem promising?

Randy Brown: Actually, we found nothing in the way of technologies that distinguished successful from unsuccessful programs. That’s not to say that having EMRs or PHRs would be a waste of money; clearly, it would be helpful for all providers to be able to see a patient’s test results and recent visits and other physicians’ notes about the patient. But it wasn’t the factor that distinguished the successful and unsuccessful programs in our studies or others I’ve seen. That may be because few of the programs really had strong EHRs.

Some of the programs used heart monitors or home reporting devices for some of their patients. But again, we found no strong association between such innovations and outcomes. Other unpublished work I’ve seen suggests that there may be some potential there, but it remains to be proven in rigorous trials.

HTN: What are the possibilities and limitations of the Patient Centered Medical Home?

Randy Brown:
Medical homes have a number of features that we find are associated with successful care coordination—in-person contacts between care coordinators and patients, co-location of care coordinators and patients’ physicians, and care coordinators potentially having access to timely information on when patients are admitted to a hospital or emergency room. But two issues could limit their effectiveness. First, medical homes will need to reflect some of the other lessons learned about what constitutes effective care coordination as well, like the need for a strong educational intervention (especially around how to take their medications properly), effective monitoring of patients between office visits, a patient-centered focus, teaching patients (and/or their caregivers) how to self-manage their care, effective care planning, and availability of social supports to identify and address problems of depression, isolation, and unmet needs for basic goods and services like transportation or food. Yet these are not required features of a medical home. And even if they were, practices need to know how to implement these factors into their medical home interventions in ways that will be both efficacious and efficient. The second major problem with medical homes as currently designed is targeting. Practices participating in CMS’s medical home demonstration will receive monthly fees for virtually all of their Medicare patients. While all patients should have a usual source of care, many do not need the medical home level of intensity. The diffusion of effort and payment makes it virtually certain that the intervention will not generate net savings, and may not even generate some gross savings in Medicare expenditures before fees. It would seem to be more important to focus efforts and resources on the 20 percent or so of patients who really are at high risk of hospitalization, and really need a medical home level of engagement. That could be made clear to practices by restricting medical home payments to patients who met those criteria (and making that rate higher than the highest of the 4 categories currently planned).

HTN: There are so many physicians practicing in small groups that are challenged to coordinate care. What do they do?

Randy Brown: Good question. About 45 percent of all physicians in the country practice solo or with one other physician. There’s no way they have the scale of operations to meet the criteria to be a medical home on their own, or to provide care coordination services, which are not covered by Medicare. But if a tightly defined care coordination benefit were covered by Medicare, they could get such services for their patients from a local hospital, academic medical center, home health agency, or clinic that decided to offer such a program to any patient in the community who met the eligibility criteria. North Carolina has a program like this.

HTN: Tell us about CMS’s Care Transitions Project.

Randy Brown: This new project was just announced by CMS a few weeks ago, on April 13. Essentially, the QIOs (Quality Improvement Organizations) are tasked with providing assistance to 14 communities around the country to help them reduce their hospital readmission rates, and improve transitions between various types of settings (hospitals, nursing facilities, rehab hospitals, home health care). Nationally, 18% of all Medicare beneficiaries who are admitted to a hospital are readmitted within 30 days after discharge, and three-fourths of these readmits are for preventable reasons. Patients are discharged to home not fully understanding the self-care they are supposed to practice, their new medication regimen, the diet they are supposed to adhere to, what activity level is recommended for them and when they can increase it, symptoms that could indicate a possible problem for which they should be seen immediately, or the importance of making and keeping a followup appointment. At the time they are discharged, they and their family caregivers are confused and bombarded with information, of which they often absorb very little. Transitional care programs, such as those developed by Mary Naylor at University of Pennsylvania school of nursing or Eric Coleman at the University of Colorado, are designed to help patients overcome these problems. They’ve been shown to be very successful in reducing readmissions for patients with chronic illnesses, in well-designed clinical trials.

The idea of the Care Transitions program is to help communities develop solutions that address the factors that lead to high hospital readmissions in their own environment—it’s not a one-size-fits-all solution across the country. The QIO’s will have Care Transitions experts in each of the 14 communities who will organize these efforts. While this idea might not have been too attractive to hospitals in the past, because it would result in lost revenue from those readmissions, President Obama has proposed new rules that would no longer reward hospitals for unplanned readmissions. So the Care Transitions program may be considerably more attractive to hospitals now. You can learn more about it at the Care Transitions website.

HTN: You make the point that not only are readmissions a problem, but in many cases so are the original admission. How significant an opportunity is there for improvement?

Randy Brown: Many of the hospitalizations for patients with chronic illnesses like CHF, CAD or Chronic Obstructive Pulmonary Disease (COPD) are preventable if patients received better care and more appropriate medications, and adhered better to their physician’s prescribed regimens for diet, exercise, medications and self-care. The proportion of hospitalizations that are preventable (they’re also called ambulatory sensitive conditions, because they are sometimes attributable to inadequate ambulatory care) is high, and varies across conditions. For Congestive Heart Failure, half of all hospital admissions are considered potentially preventable. Efforts to reduce preventable hospitalization across a range of conditions may be especially cost-effective as beneficiaries who had such events accounted for about 17% of all Medicare reimbursement for inpatient, outpatient, and physician services in one 1998 study (Culler, Parchman, and Przybylski). So there is substantial opportunity for reductions in these admissions among patients with serious chronic conditions, without having to wait for one to occur before you intervene. To give you another feel for the potential, we found when looking at the most successful programs in the Medicare Coordinated Care demonstration that hospitalizations for patients with heart disease were reduced by 17 percent, with essentially none of the this reduction being due to lower rates of short term readmissions.

HTN: Does talk of care coordination paper over a deeper problem with our care delivery organization and incentives?

Randy Brown: Yes, it seems pretty clear that our systems are not designed to encourage providers to minimize the need for expensive procedures. Rewards to providers are proportional to the amount of services they provide, rather than the quality and efficiency of the care they deliver. Notice that I said quality and efficiency of care—there are a number of fairly new pay-for-performance efforts out there that reward providers for improved quality, as measured by things like the proportion of their patients receiving preventive care. While improving such indicators is a good thing, it doesn’t focus on coordinating care to reduce the need for hospitalizations, which is the more urgent need and the only focus that is likely to start reducing the rate of growth of medical costs in the near term. And the example I mentioned above concerning hospitals being a bit wary of big efforts to reduce readmissions is another illustration of perverse incentives in our system. Fortunately, incentives can be changed to increase payments to providers whose patients use relatively low levels of expensive services while maintaining or improving the quality of care and patient well-being, and decreasing payments to providers whose patients use relatively high levels of such services. These payments would have to account for differences in severity of illness and comorbidities across providers, but a variety of methods for doing that exist. CMS is funding some research now to lay the groundwork for such payment methods and to disseminate information to physicians about the Medicare cost per episode of care for their own patients relative to that for similar patients seen by other physicians in the same geographic area, and to that of physicians nationally. It will be interesting to see how physicians respond to this information—they’ve never had such feedback before.

We clearly need multiple approaches to address the problems we have; there’s no single magic bullet.

HTN: It seems so obvious that “high touch” methods would be important to patient outcomes. Why is it so rarely used? And how do these best practice high touch methods differ from the services offered by disease management companies?

Randy Brown: High touch care requires a lot of labor, and labor is expensive. The nursing shortage has exacerbated the problem—experienced nurses are hard to find and costly. In our study of 15 Medicare Coordinated Care demonstration programs we found that the programs in which the care coordinators had the most frequent in person contacts tended to be the ones with the largest reductions in hospitalizations. They averaged nearly 1 in person contact per patient per month. That is in stark contrast to the almost solely telephonic contacts by most disease management companies. Those programs have long claimed that they generate large reductions in hospitalizations. Nearly all of those claims are based on deeply flawed studies. When we conducted randomized trials of these disease management programs for Medicare, we found no effects on hospitalizations for any of them. The lack of in person contacts means that the patients tend not to take the care coordinator that seriously, or trust them. It’s just a disembodied voice at the other end of the line. While the patients love the attention, the nurse care coordinator may not be getting their message across. Care coordinators whose only contact with patients is telephonic can’t see the patients’ faces or body language, to see whether they are really grasping the message; they can’t observe loose rugs in the house or the absence of grab bars in the shower or the stock of junk food on the counter or the sallow skin of a decompensating patient; and maybe most importantly, they can’t establish that trust that comes from face to face contact with a medical professional who actually lays hands on them. So the high touch approach is the only one that really seems to be effective, but it isn’t cheap. That’s why one of the biggest challenges for care coordination programs is to learn how to generate more efficiently the favorable impacts we’ve seen in the most effective programs. Since one of our goals has to be to generate some net savings for Medicare and other payers, it isn’t enough to reduce hospitalizations—we have to be able to do it in a cost-effective manner. That will require triaging patients by their level of need for intensive care coordination, and possibly discharging some; using in person contacts enough to produce the savings while not relying too heavily on them over time for all patients; and investigating the use of lower cost staff, such as LPNs and social workers for some of the care coordination work.

Bio
Randall S. Brown (Ph.D. Economics, University of Wisconsin) is a Vice President and Director of Health Research at Mathematica Policy Research in Princeton, NJ. Over the past 25 years, Dr. Brown has designed and led evaluations of some of the nation’s largest demonstration programs in both care coordination and long term care. He is currently leading several ongoing studies of these programs to develop lessons about how to improve outcomes for Medicare beneficiaries with chronic illnesses. In the long term care area, he led the evaluation of the Cash and Counseling Demonstration, for which he and his MPR colleagues won the AcademyHealth 2009 Impact Award. He currently is Principal Investigator for the Money Follows the Person program evaluation. His most prominent earlier work includes leading large-scale evaluations of the Medicare managed care program, the expansion of Medicaid benefits to low-income families, and the National Channeling Demonstration.

Monday, April 27, 2009

Chronic Care: Reducing Socioeconomic Differences in Outcomes

On April 21, the Commonwealth Fund released its report on "Universal Health Care as a Health Disparity Intervention." The study found that universal health insurance and improved access to care helps to reduce socioeconomic differences in chronic disease control.

The report finds that "ensuring that adults under age 65 have health coverage may reduce racial, ethnic, and socioeconomic differences in health outcomes for cardiovascular disease and diabetes."


While overall control of control of diabetes and cardiovascular disease has improved from 1999 to 2006, there are continuing disparities between racial, ethnic and socioeconomic groups. The study found that these disparities were reduced in Medicare-eligible populations. "With near-universal Medicare coverage after age 65 years, differences in systolic blood pressure, hemoglobin A1c levels, or total cholesterol levels reduced substantially. These reductions may substantially decrease racial and socioeconomic differences in mortality as well."

Monday, March 23, 2009

Chronic Care: Improving Patients' Quality of Life

The March 16 edition of the American Journal of Managed Care reports that a "laboratory-based decision support system designed for low cost and easy integration into primary care... showed significant improvements in clinical care and health care utilization." The study was funded in part by the National Institute of Diabetes and Digestive and Kidney Diseases.

Dr. Ben Littenberg (MD, FACP) is the principal investigator for the study. He is the Henry and Carleen Tufo Professor of Medicine, Professor of Nursing and Director of General Internal Medicine for the University of Vermont College of Medicine. He is also CEO of Vermont Clinical Decision Support which distributes the Vermedx® Diabetes Information System (VDIS), the subject of this study.

Dr. Littenberg sat down with Healthcare Technology News to talk about his findings.

HTN: Can you please talk about Wagner's Chronic Care Model and its influence on your work?

Ben Littenberg: The Chronic Care Model is a very influential idea about how to do a good job in taking care of people with ongoing medical problems like high blood pressure, arthritis, and in our case, diabetes. It tells what resources the health care system must have to get the most out of the interaction between the doctor and the patient. These include systems to support clinical decision making, up-to-date and easy-to-use clinical information, reminders, support for patient self-management, and so on. Turning a typical primary care medical office into a fully-functional chronic care model practice is a good thing, but it is complex, expensive and time-consuming. It requires extensive retraining of the physicians, nurses and other staff, installation of comprehensive electronic medical records systems, changes in the way patients and staff interact, and even an overhaul of the way care is paid for. So, very few practices have successfully transformed themselves. When we designed Vermedx(R), we took as much of the chronic care model as we could while still maintaining very low cost per patient, very little disruption of the clinical work-flow, and no requirement that the practice invest money on computers or other fixed costs.

HTN: What is the current state of technology to assist in the management of diabetes?

Ben Littenberg: Drugs for diabetes have gotten much better in the last 20 years. Also, we know a lot now about how to prevent the complications of diabetes - heart attacks, strokes, kidney failure, blindness, amputations, and so on. However, it takes a lot of very careful attention to lots and lots of data. How high is the blood sugar? When was it measured? When should the cholesterol be tested again? How close is the patient to goal? Office systems have failed to keep up with the needs of the patients and providers. Paper records just don't work well in this setting. A typical laboratory report shows the numeric value of the result and a so-called "normal" range, but it doesn't tell you what the test means or what to do about it.

Most offices have no organized method for keeping track of all the blood and urine tests used in diabetes, let alone a system that reminds the patient when a test is due and even advises the doctor on what to do.

HTN: How is VDIS different?

Ben Littenberg: Vermedx automatically collects the laboratory test results on diabetic patients and reports them to the doctor (or other health care provider). It puts the test results into context, shows trends over time, and suggests actions. It also takes action when a test should have been done, but wasn't. It sends reminders to the practice and letters (from the providers) to the patients encouraging them to get into care. If the test results are very high, it also notifies the patient to get back to the practice to change the care plan. Vermedx also provides a population view of the doctor's entire panel of diabetic patients: who is doing well, who needs help, and how the practice is doing compared to others.

HTN: Your study found a sustained continuing decrease in utilization that is striking. Please tell us about the results.

Ben Littenberg: With NIH funding, we conducted a long-term randomized study of VDIS in community primary care. Over 7,000 patients in 64 practices participated. The patients in that study who received VDIS reported far fewer trips to the Emergency Room, unscheduled hospital admissions and doctor visits than patients who didn't get VDIS. The problem was that we didn't have access to the medical bills in that study. The recent study in the American Journal of Managed Care looked at patients getting Vermedx as part of their usual care and was able to compare the insurance claims paid to other diabetic adults who did not have Vermedx. Before VDIS was available, both groups had steadily rising costs month-by-month. The control patients' claims kept going up, but less than a year after turning on the system, the VDIS patients' claims started going down. The savings were $504 per patient in the first year, went up to $3,563 in year 4, and kept getting better!

HTN: For the VDIS patients, what were the differences in health outcomes?

Ben Littenberg: VDIS patients are much more likely to get their laboratory tests on time. Although they are no more likely to reach goals for blood sugar or cholesterol, they spend less time in the Emergency Room and hospital, which indicates a substantial improvement in quality of life.

HTN: Understanding that your study does not suggest causality between VDIS and utilization, what is your hypothesis about the relationship?

Ben Littenberg: Actually, the first study was randomized and therefore, does provide good evidence of causality. However, nobody is entirely certain how it works. Since the blood test results aren't different, it probably doesn't work by preventing complications. One theory is that improved communications give patients confidence - they know that they will be back in touch with the doctor and don't need to call for every little issue. It's like those reminder postcards to get your car's oil changed. You know you're going to bring the car in soon, so you might be less anxious about getting service right away for some funny noise under the dashboard. Of course, you're also being seen on a schedule - before you have an emergency!

HTN: VDIS sends alerts to both physicians and patients. What is your view of the relative effectiveness of focus on the physician or focus on patient self-management?

Ben Littenberg: They both seem to be valuable. The core idea behind the Chronic Care Model is to activate the patient to get involved in their care AND prepare the practice to meet that patient's needs. Working on both ends of the relationship is much more effective than either one alone.