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Circles For Sustained Mentoring By Clinical Leaders

One Sheet
July 7, 2023
Mentoring is highly valued among medical thought leaders. As mentees move on, preserving the energy and productivity of initial relationships becomes difficult. Collaboration during subsequent years is valuable for both sides. Circles maintain and expand that value.
Used by providers and industry around the world.Medical thought leaders highly value mentoring young residents, fellows, and medical students. However, as those mentees move on it can be difficult to preserve the energy and productivity of the initial relationships. And collaboration during those subsequent years can be the most valuable for both sides. Circles are the ideal platform to maintain, and indeed expand, that value.Easily collaborate across institutional and national boundaries on study designs for any clinical/scientific topic, any degree of complexityEliminate challenges created by incompatible EMR systems, languages, IRB/MEC policies and individual practice variationsCapture clinical, scientific, and financial value from the real-world evidence generated daily in your and your colleagues' practicesEfficiently develop data-driven conference, educational, website, journal, and social media materialsSecure social media functionality enables active, sustained collaboration, teaching, and learningMore Benefits:Clinical grade, turnkey, integrated, flexible, minimal burdenRCT’s, pragmatic studies, IRB submissions, registries, PROMsOwn and control your datasets. Accessible from any device 24/7Excellent user experience for clinicians and patientsSupport for industry fundingLow cost. High return on investment. Up and running in days. Cancel on 30 days' noticeLarge, growing library of validated observational protocols and outcomes assessment scores. or develop your own Powerful report functionality to generate expected and "serendipitous" correlations Contact us for a demo, or to discuss your requirements.
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Real-World Data And The Business Of Medicine

Post
June 28, 2023
A successful medical practice must also be a successful business. RegenMed partners globally with practioners of generating financial and clinical value from real-world evidence. Investigator fees, honoraria, product discounts, and enhanced patient engagement are examples of such value.
RegenMed has the pleasure of working with independent medical practices around the world. Many of these clients face challenges regarding finance, marketing, IT, personnel management, and other fundamental business elements. This is not surprising since business is rarely taught in medical school, even at an introductory level. Moreover, business courses by themselves do not constitute business experience and judgment. While medical students, residents and fellows benefit from clinical collaboration and mentorship of senior physicians, no analog exists for clinicians dealing with harsh business realities.These business deficits make it difficult for a private practice to reach its full potential – or even survive. The resulting diminishment of independent medical practices is highly regrettable. But its root cause – a lack of preparation for business realities -- has other serious consequences. These include non-physician leadership of medical institutions, inflated healthcare costs, less choice for patients, physician “burn-out” and reduced interest in a medical career among the “best and brightest”.RegenMed Circles are product-agnostic, but certainly not business agnostic. They generate financial as well as clinical value from the enormous amount of real-world data flowing daily through their medical practices each day. Examples of such value include honoraria, product discounts, investigator fees, superior patient engagement, new service lines, and professional advancement.One important approach to any business decision is return on investment. What will I receive and when, in exchange for what I put into a particular initiative? Staff hires, IT licenses, marketing spend, device purchases, rental agreements, ASC partnerships – each should be looked at through an ROI lens. Real-world data remain a major untapped asset of each independent medical practice. The cost and burden of capturing those data are negligible. The returns are manifold and substantial.Contact us to learn more.
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The Medical Trailblazers

Post
June 23, 2023
Medical discoveries are hindered by established knowledge, difficulties in proof development, and self-doubt. Despite this, we live in an exciting time for medicine, where those who possess the scientific rigor and inventiveness of past trailblazers can make advancements. It is not about ...
Medicine advances by questioning standards of care. However, many such standards today are based on expensive and product-specific clinical trials which only well-capitalized for-profit companies can afford.Meanwhile, the need for broader-based improvements in healthcare delivery is becoming more acute. Medicine is increasingly specialized while, paradoxically, the systemic nature of pathologies and treatments alike is increasingly apparent. For the modern clinician, it is easy to be daunted. There is not too little information; there is too much.But we arguably live in the most exciting time in the history of medicine. Those individuals who today combine the courage, inventiveness, persistence, and scientific rigor of past medical trailblazers will stand on their shoulders.It is not a matter of money, nor of access to the latest laboratory equipment, nor of “big data” and complicated algorithms. It is a matter – as it always has been – of careful observation, following one’s informed intuition, scientific methodology and willingness to make mistakes.At RegenMed, we have the honor of working with clinicians and scientists around the world who seek to verify accepted “knowledge”, attempt to make sense of their own observations, believing that they can improve standards of care for their patient panels. They collect and examine real-world evidence, and go where that evidence takes them – whether a tentative confirmation of their hypothesis, a serendipitous correlation or a dead-end. They seek out peers with whom to collaborate. They are willing to publish and otherwise share their hypotheses and data.Circle Members include department chairs, sole practitioners, medical research directors and others. Many, on the basis of their work, began as attendees at medical conferences, and are now invited speakers. Others are receiving industry support while maintaining full control over their studies.To quote Hippocrates, “science begets knowledge; opinion, ignorance.” The building blocks of science are found in the “real world”, where the application of science finds its greatest value. We applaud those modern trailblazers who, using their own powers of observation and professional judgment, strive to advance medicine for the greater good. Modern technology, efficient yet inexpensive, can be a great aid to them.Please contact us to find out more.
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Healthcare Data In The Real World

White Paper
June 7, 2023
A critical step in helping fix “broken healthcare” is re-thinking healthcare data, an important component of which is real world data. These data are found, by definition, at the locus of clinician-patient interactions and patient outcomes assessments. Modern systems technology, and global ...
AbstractA critical step in helping fix “broken healthcare” is re-thinking healthcare data, an important component of which is real world data. These data are found, by definition, at the locus of clinician-patient interactions and patient outcomes assessments.Such real-world data are, in turn, the foundation of real-world evidence, the clinical, scientific, and commercial value of which are widely recognized.Real-world data – the building blocks of real-world evidence – are not to be found in lengthy expensive RCT’s. The severe inclusionary/exclusionary criteria, limited population sizes, length, cost, product specificity and limited data access of those trials result in the antithesis of RWE. However, capturing real-world data in the busy provider environment, and converting it into clinically and statistically significant real-world evidence, pose a number of challenges.This paper argues that modern systems technology, supporting global collaboration among providers and industry, can generate clinical and commercial value for patients, clinicians, and industry alike. Importantly, it can do so in a minimally burdensome, cost-effective manner with excellent user experience. IntroductionThe Status QuoIt is commonly stated that “healthcare is broken”. Costs are rising far faster than most broad health metrics. Physicians are burnt out; patients are frustrated and confused; clinical translation of promising scientific advances is thwarted by lengthy and expensive regulatory hurdles. The two most important groups in the delivery of safe and efficacious healthcare – product manufacturers and providers – find it increasingly difficult to communicate with each other. Healthcare is broken in no small part because healthcare data is “broken”. This is ironic because the world is awash in healthcare data – claims, EMR’s, registries, biosensors, omics analyses, images, thousands of annual conference presentations, and thousands more of journal articles.This enormous amount of data has made clinical decision-making more burdensome, expensive, and confusing. It is far from clear that it has made it better. And of course, this healthcare information “overload” will only accelerate in years to come.The Importance of Real-World EvidenceRWE is a critical component of regulatory compliance, clinical decision-support, value-based medicine, product development/improvement and patient engagement and evidence-based marketing.RWE is not only important support for traditional RCT’s; in many cases it is recognized as superior. It is the basis of many accepted study formats, including pragmatic, n of 1, observational, quality improvement and registries.The power of RWE lies in its large patient population potential, data deriving from everyday clinical interventions, and long-term outcomes capture. Unlike the vast majority of RCT’s sponsored by well-capitalized product companies, RWE is based on data with a much higher degree of clinical relevance.Of course, data are critical for the practitioner. But only the right data, at the right time and with specific clinical relevance. Moreover, data are of little use if they are not easily accessible and verifiable by busy clinicians.The FutureOther segments in the economy are able successfully to define, aggregate and utilize data to achieve their specific objectives. For this to happen in healthcare, the following are needed:All healthcare constituencies must recognize the power of real-world data and evidence. The evidence which is inherent in each patient-clinician interaction, but which is often ignored.Clinical thought leaders should exercise their influence by identifying and disseminating the key clinical/scientific questions facing everyday practitioners in their respective fields.Busy clinicians need to be incentivized to capture real-world data.Modern, cost-effective systems and user experience should be implemented which ensure minimum clinical burden in that capture.The institutional and national boundaries preventing genuine and ongoing collaboration among clinicians with similar practices must be overcome.Communications channels between industry and providers must be created enabling the meaningful and sustained exchange of value generated by real-world evidence.Contemporary, targeted publication modalities – including digital and secure social media formats – must be utilized to maximize the clinical education and training potential arising from real-world evidence.This is what clinically useful healthcare data in the 21st century should look like.The ChallengesImpediments to developing and generating value from real-world evidence include the following:BurdenHealthcare delivery models, combined with shrinking reimbursement, impose a large administrative burden on providers. They leave less time for patient care, let alone the capture and analysis of real-world data.Thus, the “real world” is the busy, already over-burdened environment of clinical interventions. It is the unreported outcomes.Lack of IncentivesMany well-intentioned practitioners spend their evenings entering clinical data into medical society of industry sponsored “registries”. They are rarely compensated, financially or professionally, for these efforts. Moreover, those registries typically sharply curtail data access and ownership, and the ability to generate reports specific to a pressing clinical question is difficult if not impossible.Limited Access To ExpertiseThe first step to generating real-world evidence is asking a few “right” questions for a specific indication/treatment protocol. For the busy clinician, this is often not easy.Medical science is advancing ever more rapidly, and is increasingly complex. Much of what was taught in medical school is out-of-date; nor are CME courses particularly helpful. Clinical medicine is becoming hyper-specialized while, at the same time, there is greater recognition of the systemic nature of pathologies as well as treatments.The enormous volume of journal articles, conference presentations and webinars – often inconsistent in their conclusions – have led to information overload and confusion.The Isolation of a PractitionerEven in large academic medical centers, the busy clinician is more isolated from her peers than ever before. Annual society conferences are a welcome respite, but are a far cry from meaningful, sustained collaboration on clinical issues. This isolation has repercussions not only in terms of “burn-out”, but in terms of education, training, and professional advancement.Data AccessAnonymized (non-PHI) data security, ownership, control, and access are important considerations for real-world evidence. There is often a lack of clarity regarding these issues for the practitioner – together with his patients the primary source of real-world data.IRB/MEC RequirementsReal-world evidence derives by definition from clinician-patient interactions. Provider policies, journal requirements and/or the desire of the practitioners herself may require the involvement of an Institutional Review Board or Medical Ethics Committee. For clinicians collaborating across institutional borders, and developing RWE in a multi-center context, a reputable commercial IRB may be required.This can pose a severe administrative and financial burden.Complexity of Technical SystemsSoftware is supposed to make things easier. In healthcare, IT systems are often expensive, complex and involve poor user experience. In addition, there is generally poor communication among various healthcare software systems, even when used by the same provider. Barriers To PublicationTimely access to relevant evidence is an essential component of its value. Unfortunately, for today’s busy clinician, evidence is often delayed, inaccessible, irrelevant, and/or unverifiable. Paradoxically, the proliferation of articles, societies and other information sources often compounds rather than addresses the problem.The Provider - Industry “Divide”In principle, cooperation between industry and providers should lead to greater efficiencies in achieving and clinically translating medical advances. In practice, however, well-intentioned regulations and institutional policies often thwart that cooperation.A Proposed ApproachFielding The TeamSafe and efficacious healthcare delivery obviously depends heavily on “data”. Those data are required in many different contexts. Here, we are discussing only a single but critical context: providing meaningful clinical decision support to the busy clinician through real-world evidence.As suggested above, “simplifying” the generation of and access to such data is a multifaceted challenge. Addressing this task, as is true for any complex task, begins with assembling and coordinating the right “team”. Here, that team comprises thought leaders, practicing clinicians, industry, medical societies, and patients.Of course, each of these “players” has its own interests and constraints. However, they all benefit in multiple ways from the development of real-world evidence. There is a mutual incentive to work together.“Small Data”, Not “Big Data”Clinical context is all-important for the development of real-world evidence, as well as for achieving its intended purpose. The clinician must exercise her professional judgment in the context of a specific patient, a specific complaint, a specific number of available treatment protocols. Moreover, she must often do so in a relatively short amount of time, which means limited information.The answer is not more data. Rather it is the right data most relevant to that particular clinical encounter and intervention.Reliable, Accessible DataThe clinician and his patient are entitled to diagnoses and treatments which are based on verifiable data – data which are clinically and statistically significant. If such evidence in fact already exists based on relevant, independent RCT’s, that is of course desirable. But most “standards of care” have no or poor quality of evidentiary support.Moreover, medical science is advancing at an accelerated pace. A busy clinician may see ten or more patients each day. He has far too little time to examine the latest potentially relevant literature. Also, the full data behind most RCT’s is rarely easily or fully accessible.This is the value of real-world evidence. It can be delivered in a timely, accessible, and clinically relevant manner.The Power of Peer-to-Peer CollaborationMedicine is increasingly specialized; clinicians are often isolated. This need not be the case, however. Whatever the clinician’s particular field and practice environment, there are many hundreds of peers around the world facing the same issues, in similar environments.Moreover, there are many clinical and scientific thought-leaders ready to assist in defining the right real-world data questions to ask, and in deriving clinically useful correlations from the resulting datasets.Other sectors of the economy are able to achieve and exploit network effects much more successfully than healthcare. The concept of real-world evidence is a powerful opportunity for clinicians, industry, and patients to collaborate in a manner achieving real value for all.Modern technology allows the individual clinician to benefit from the experience of peers and experts around the world in a secure and productive way.Burden and CostHere again, it is useful to compare healthcare with other complex sectors of the economy (finance, semiconductors, telecommunications, space travel, information technology). Those sectors routinely advance their scientific foundations and improve user experience, while driving down costs.Modern systems allow the collection and aggregation of, and value generation from, real-world evidence in a cost effective, minimally burdensome manner.Ethical Provider-Industry CooperationReal-world evidence potentially represents a legitimate and powerful exchange of value among three major healthcare constituencies – providers, patients, and industry. That value includes:Support for clinician decision-makingReimbursement (value-based medicine)Legal/regulatory submissions/complianceProduct development/improvementNew indicationsResearchPatient engagementJournal articles, conference presentationsExpanded thought leader influenceEducation and trainingDeeper clinical customer engagementA major “safe harbor” for industry interaction with and support of providers is the investigator-initiated development of real-world evidence. Turnkey, Integrated SolutionThe value of real-world evidence will not be attained through piecemeal, uncoordinated solutions. Rather, the busy practitioner needs a turnkey approach which integrates the foregoing elements in an efficient, cost-effective, and burden-free manner.Modern technology and processes make this fully achievable in many sectors of the economy. It is equally possible in healthcare as well.ConclusionAlbert Einstein famously said, “make everything as simple as possible, but not simpler.” In healthcare as elsewhere, it is more difficult to achieve simplicity than complexity. Some data, such as dealing with over 10,000 CPT codes for reimbursement, are unavoidably burdensome and complex. Unfortunately, they are also often clinically unhelpful.Conversely, the busy clinician usually requires only a few critical pieces of evidence to augment his professional judgment in developing a treatment protocol with safe, predictable, and effective outcomes. The elements needed to generate that evidence are not complex in principle:Identify a limited number of specific correlations (evidence) which will provide the most valuable clinical decision support for a given indication and patient cohort.Identify the right question and answer formats, including long-term outcomes, most likely to prove/disprove the posited correlations.Collect, aggregate, and analyze those real-world data inherent in one’s everyday practice which are most likely to prove/disprove the posited correlations, and may also uncover “serendipitous” ones.Iterate and improve based on the real-world data constantly generated through one’s clinical activities.Collaborate closely with peers, domain experts and industry in implementing each of the foregoing steps.The broad technical advances in the 21st century enable the busiest solo practitioner to develop real-world evidence which will make a material difference for her practice, her professional advancement, and her patients. The value for larger provider systems and industry is even more profound.For more information, please contact us.
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PROMS For The Busy Clinician

Post
May 11, 2023
Modern healthcare delivery often feels increasingly “transactional” for the patient and, indeed, for the clinician. Depending on how they are designed and implemented, PROMs – patient-reported outcomes measures -- can either reinforce, or counter, this sensation.
AbstractPatient Reported Outcomes Measures (PROMs) have been used since the 1960’s, with some of the earliest in the field of mental illness. Today, there is a large and increasing number of PROMs across virtually all medical specialties.PROMs continue to be used principally for research purposes. However, there is growing recognition of their potential to assist in clinical decision making, value-based medicine and sustained patient engagement. PROMs can thus be a useful vehicle for addressing some of the larger challenges in modern healthcare.However, the design and use of PROMs present serious challenges for the busy clinician. These include selecting or designing the PROMs most relevant to a specific practice, execution, cost, personal health information protection, patient enrollment and continuing engagement, data verification and audit trail, adequate data to generate statistically significant correlations.Fortunately, modern tools now allow clinical groups of any size to generate clinical and financial value from PROMs.PROMs: The Theory And The RealityCapturing longitudinal outcomes data is essential to evidence-based medicine. Thus, standardizing PROMs constructs and scoring systems for all categories of clinical interventions and patient cohorts is a worthy goal. Many medical societies, for example, develop PROMs in the context of their registries. Other organizations publish free and licensed PROM’s. Other groups analyze the strengths and weaknesses of various PROMs.On the one hand, there typically exist multiple PROMs for any pathology. On the other hand, the busy clinician will find it daunting to select PROMs which drive clinical and other value in his particular context. Moreover, PROMs for the same condition can be in part contradictory, duplicative, incomplete and/or confusing. Well intentioned attempts at standardization of PROMs have been unavailing.PROMs As Tools In The Clinical SettingPROMs can play an important role in two major trends in modern healthcare — value-based medicine and clinical decision-making.Value-Based MedicineAs stated in the New England Journal of Medicine:Value-based healthcare is a healthcare delivery model in which providers, including hospitals and physicians, are paid based on patient health outcomes. Under value-based care agreements, providers are rewarded for helping patients improve their health, reduce the effects and incidence of chronic disease, and live healthier lives in an evidence-based way.This approach is found in accountable care organizations, narrow networks, and many other clinical intervention revenue models. Capturing and analyzing outcomes in a systematic, longitudinal manner are essential elements of value-based medicine.However, efforts to derive useful correlations for value-based medicine from EMRs, claims databases, patient registries, and other traditional data sources have been disappointing. These sources often reflect only partial data, poor clinical context, challenges in verifiability, and other weaknesses. Of particular note, there is usually a paucity of outcomes data, and wide variation and discrepancies in what little exists.Meeting these challenges with respect to PROMs begins at the clinic. The treating clinician must select/design the proper PROM construct for each patient cohort. For example, what exactly is the PROM intended to measure – pain, function, quality of life etc. – in the context of a particular class of clinical intervention? Only then, will the outcomes data truly support value-based medicine.Clinical Decision MakingMedical science is advancing ever more quickly. Clinicians must learn to deal with concepts not even mentioned during medical school, as well as new equipment, medications, and diagnostic tests. Modern communications channels offer practitioners and their patients good and bad information on any topic – both good and bad.Despite these oceans of information, or perhaps because of them, the informed judgment of the experienced clinician remains central to accurate diagnoses and safe, efficacious treatment protocols.PROMs As The Foundation of Patient-EngagementAn attractive website, efficient front office, well-lit reception area, testimonials and five-star reviews are only the beginning of patient engagement in the 21st century.Yes, patients are consumers; but they are first and foremost patients. They have a patient story, one or more specific conditions, outcomes objectives, perhaps disappointments with past treatments. Patients have often already researched their conditions and options. They want to be heard, and to be a part of their recovery. Moreover, listening to patients from the initial consult and then throughout their treatment journey can be critical to successful outcomes.PROMs can represent an excellent tool for intermediating the respective “languages” of the patient and the clinician. Properly designed and executed, they make clear to the patient that her doctor is genuinely interested in the success of the long-term outcomes they both are seeking.Removing The Burden; Generating The ValueAs indicated, PROMs have significant potential clinical, patient engagement and financial value. For them to be a realistic part of the active clinician’s armamentarium, however, they must have several key characteristics:Impose minimal burden on the clinician, her staff, and patients.Conform in their constructs to the indications, treatment protocols and other aspects of the clinician’s everyday practice.Comply with patient data privacy and security laws.Real-time mapping of outcomes against a variety of clinician-selected treatment factors.Generate statistically and clinically significant correlations.Allow easy collaboration within peers within and across institutional and national boundaries.Circles enable all of the foregoing. Start or join one today. Or contact us to find out more.
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