All posts by Darryl S. Weiman, M.D., J.D.

Who Should Direct the CVICU?

By Darryl Weiman, M.D., J.D.

Introduction

The model for taking care of the patient who has had a cardiovascular and/or thoracic procedure is changing. Many hospitals now recognize that the physician directing or co-directing the care of the post-operative cardiothoracic surgical patient should have the knowledge, education, training, and experience to understand the anatomic, developmental, physiologic, and pathophysiologic basis for cardiovascular and pulmonary disease processes. Many universities now believe that this person should be a cardiothoracic surgeon.

Most medical center cardiovascular intensive care units (CVICU) use a multi-disciplinary approach for patient management. They use a hybrid ICU format. Members of the team include critical care nurses, surgeons, cardiologists, pulmonary-critical care, pharmacists, respiratory therapists, social workers, and case managers. The goal of this integrated team is to provide high quality care and minimize adverse events. They all strive for efficient resource management and a seamless patient transition out of the intensive care setting. The one thing this approach lacks is a leader who can oversee the overall management of the patient, especially when the surgeons are focused elsewhere.

The physician taking care of the post-operative cardiac patient should have adequate “hands on” experience in the operative management of such diseases so it is reasonable to have a cardiothoracic surgeon with intensive care experience to lead the multidisciplinary team in the Cardiovascular Intensive Care Unit. This should not result in a turf war as there is a recognized need to have one person oversee the overall care of the individual patient.

Benefits for the Patient

There is no debate that cardiothoracic surgery patients are different from other patients in the intensive care unit. They are generally older, sicker, and frail. Their management has become increasingly complex; even non-operative candidates are undergoing high risk procedures such as (T)rans-catheter Aortic valve replacements (TAVR) and endovascular graft placements in the descending aorta (TEVAR).

More complex tools are being used in the CVICU such as left ventricular assist devices (LVAD) (Intra-aortic balloon pump, Impella, and other LVADs) and vascular access now requires knowledge of Doppler Ultrasound. The knowledge and skills needed to manage these devices is increasing at an exponential rate.

Cardiac arrest in the post-operative cardiac surgical patient shows higher survival rates if the chest is reopened in an expeditious manner. Studies affirm that the chest should be reopened for ventricular fibrillation or ventricular tachycardia that has not responded to 3 DC shocks and amiodarone. Studies have also shown increased survival if the chest is reopened for asystole or severe bradycardia that does not respond to atropine. The chest should also be reopened for pulseless electrical activity (PEA). Cardiac surgeons have the knowledge, experience, and skills needed to open the chest; techniques vary as to the type of closure involved—plates, wires, or a combination of plates and wires.

A study done in 2008 showed that 61% (212/347) of post op coronary revascularization deaths were related to events in the ICU. The reasons given were related to failures of

  1. Diagnosis of life threatening events;
  2. Response of nurse and/or physician;
  3. Patient monitoring;
  4. Decision for timing of reoperation;
  5. Medication dosage and administration;
  6. Communication. 1

A CVICU Director, who is a trained surgeon, should be able to intervene and save some of these patients.

A study done at Stanford University recently concluded that “[i]n its first 2 years, the surgeon-led cardiovascular intensive care unit demonstrated comparable outcomes to the traditional cardiovascular intensive care unit with significant improvements in total length of stay, postoperative transfusions in the cardiovascular intensive care unit, and vasopressor use.”2

Other studies support having a cardiothoracic surgeon manage the postoperative care in the intensive care unit. For example, Whitman, et al showed a decreased length of stay and decreased cost of drugs used postoperatively in a CVICU managed with a cardiothoracic surgeon.3

In an editorial, Hisham Sherif argued strongly that the CVICU should be run by surgeons.

“Deficiencies in the broad-based education, abbreviated clinical training and limited skill sets of non-surgeons seriously impair their situational/environmental awareness and processing of information, their decision-making process and the implementation of decisions, as in the proposed ‘emergent resternotomy in the ICU’ protocol—an often challenging situation for experienced CTS surgeons. Therefore, non-surgeons are not properly qualified to be the primary decision- maker in the high-risk environment of cardiothoracic surgical critical care.”4

Use of the Society of Thoracic Surgeons Data Base

The Society of Thoracic Surgeons continues to monitor quality performance measures in the areas of adult cardiac and general thoracic surgery. These measures are being used by the Centers for Medicare and Medicaid Services (CMS) in their Merit-Based Payment System. These measures are also endorsed by the National Quality Forum. A surgeon well-versed in

these measures can help in seeing that these measures are being followed. He can also help with the checklists needed to document that these measures are being met.

Anti-platelet medication at discharge, Beta blockade at discharge and perioperatively, anti-lipid treatment at discharge, and selection and duration of antibiotic prophylaxis are just a few of the examples of the measures being used in the STS data base.

For Medical Centers that participate in the STS Data base, a surgeon directing the CVICU can help make sure the quality measures are being met, and the data is being captured appropriately by the coders.

Cardiac Surgeons as Intensivists

The American Board of Thoracic Surgery (ABTS) has recognized that critical care has always been a core component of ABTS certification. “Our (D)iplomats have been trained in critical care management of thoracic surgical patients and they have successfully completed both written and oral examinations which cover the critical care aspects of surgical patient management”5

In fact, the ABTS will write a letter on behalf of the Diplomat requesting ICU privileges to the specific credentials committee…to affirm the Diplomat is trained to take care of patients in the intensive care unit.6

The cardiac surgeon is uniquely qualified to:

(1) Ensure proper surgical care of chest tubes, surgical wounds, vascular access devices, and placement of invasive lines and tubes (arterial lines, Pulmonary Artery catheters, bladder catheters, nasogastric tubes and endotracheal tubes);

(2) Ensure disease diagnosis and treatment for arrhythmias, blood pressure abnormalities, and bleeding disorders;

(3) Order the proper tests for diagnosis;

(4) Refer to the appropriate specialists as necessary (pulmonary, cardiology, endocrine, infectious disease, other surgical subspecialties);

(5) Institute and monitor order sets which have become best practices (ventilator bundles, sepsis protocols, sedation protocols, line placement protocols, enteral feeding protocols, renal protection protocols);

(6) Provide for needed bedside surgical procedures such as placement of arterial lines, placement of central lines, chest tube insertion, placement of bladder catheters, placement of endotracheal tubes or a surgical airway, and bronchoscopy for diagnosis and treatment.

Education of Nonphysician Providers, Residents, and Medical Students

The director of the CVICU must encourage a culture of continuous quality improvement and continuing medical education. The director must maintain his own fund of knowledge that keeps up with the new advances now on the cutting edge of surgical critical care.

The CVICU director should be the educator of those working in the unit. Critical care training can be improved with daily teaching rounds incorporated into multidisciplinary work rounds. Improvements in physical exams, formation of differential diagnoses, order sets, procedures, and medical management can all be realized. An experienced cardiothoracic surgeon leading those rounds has become standard at many universities (Johns Hopkins, University of Michigan) and this would be a significant step for any medical center looking to maintain its leadership in Cardiac care in its community.

The emphasis on education is essential in nurse training and a surgeon committed to education would be important in both recruiting and retaining those nurses interested in cardiovascular intensive care.

Research Activity in the CVICU

The CVICU is an excellent place to conduct research pertinent to the care of the critically ill surgical patient. Models for the study of myocardial dysfunction, post-operative bleeding, transfusion management, end-organ dysfunction and the potential for studying genomic markers, new devices, and the creation of new databases for data extraction are all areas ripe for focused research; this research can be led by a surgeon with a research background.

Financial Justification for a Surgeon CVICU Director

Besides providing optimal care for the post-operative patient, the cardiothoracic CVICU intensivist can be a financial benefit for the hospital.

Any procedures done can be billed so long as the proper documentation is shown.

The intensivist, who is acting within his scope of practice, can independently report his professional services. There are numerous CPT Codes that can come into play. Examples are as follows:

(1) Airway management

Bronchoscopic procedures using flexible fiberoptic bronchoscopy (31622, 31624, 31625-29)

Tracheostomy (31600, 31601, 31603-05)

(2) Vascular access

Arterial lines (36620, 36625)

Central lines (36555, 36556)

(3) Mediastinal exploration for bleeding

Take-backs to the OR for post-op bleeding (39000-39010, 60505)

(4) Drainage of wound infections

I&D for superficial infections (35820)

Sternal debridement for deep infections (21627)

Re-wiring for sternal dehiscence (21740-21742, 21750)

(5) Drainage of pleural effusions

Percutaneous (32556)

VATS for evacuation and pleurodesis (32551, 32650)

VATS for decortication (32035, 32036)

(6) Drainage of pericardial effusions

Pericardial window; subxiphoid or thoracotomy (32659, 33025, 33020, 33017-19, 33016)

(7) Pacemaker placement and management (33206-33208)

(8) Swan-Ganz catheter placement (93503)

(9) Thoracostomy tube placement (32551)7

The above are just some of the areas where the surgeon intensivist can help lessen the workload of the main operative cardiothoracic surgeons.

In summary, endoscopic procedures, procedures on the lungs and pleura (VATS), pericardial procedures, temporary pacemakers, implantation of hemodynamic monitors, extracorporeal membrane oxygenation support devices, central venous and arterial access, are examples of procedures that can be done by the surgeon CVICU intensivist.

The generated billings of the CVICU surgeon director who is seeing patients in consultation can easily meet the costs associated with his salary and benefits. Billing accrued from tests ordered, notes written, and procedures done will further justify this position.

Conclusion

In conclusion, a cardiothoracic surgeon helping manage the CVICU is the “right operator, with the right information, making the right decision to use the right tool to perform the right task at the right time in the right manner.”8

“…[A]dvances have not been in improved hemodynamic monitoring, pharmacologic therapy, or understanding of the pathophysiology of the diseases unique to our patients, but rather improvements in the system of medical care delivery such as checklists and improving teamwork” has led to better results.9

Having a Cardiothoracic surgeon directing the CVICU is the national trend, and the time is right for medical centers that do cardiac and thoracic surgery to take this next step in maintaining surgical excellence in cardiovascular and thoracic care.


1 Guru V et al. Circulation, 117; 2969-2976, (2008). 2 Choi PS, Pines KC, Swaminathan A, et al. Diversifying cardiac intensive care unit models: Successful example of an operating surgeon led unit. (JTCVS Open 2023; 16, 524-31). 3 Whitman GJR, Haddad M, Hirose H, Allen JG, et al. Cardiothoracic Surgeon Management of Postoperative Cardiac Critical Care. Arch Surg/Vol 146 (No. 11) Nov 2011, 1253-60. 4 Sherif HMF: After-hours coverage of cardiothoracic critical care units by non-surgeons: process and value issues. European Journal of Cardio-Thoracic Surgery 46 (2014) 507. 5 Baumgartner W, Calhoon JH, Shemin RJ, Allen MS: Critical care: American Board of Thoracic Surgery update. The Journal of Thoracic and Cardiovascular Surgery, 145(6), 1448-9, (2013). 6 Id. 7 CPT 2024 Professional Edition. 8 Sharif HMF. Developing a curriculum for cardiothoracic surgical critical care: impetus and goals. Journal of Thoracic and Cardiovascular Surgery, 143(4), 804-8, (2012). 9 Shake JG, Pronovost PJ, Whitman G. Cardiac surgical ICU care: eliminating “preventable” complications. Journal of Cardiac Surgery, 28(4), 406-13, (2013).

Artificial Intelligence and its Role in Surgical Creativity

Darryl S. Weiman, M.D., J.D.
Associate Program Director, General Surgery Residency
Baptist Memorial Medical Education
Baptist Health Sciences University

Stephen W. Behrman, M.D.
Professor of Surgery and Chair
Baptist Memorial Medical Education
Baptist Health Sciences University

Department of Surgery, Baptist Medical Center, Memphis, TN

“It is tough to make predictions, especially about the future.” Yogi Berra, hall of fame catcher for the New York Yankees

              Based on numerous recent news accounts and several publications in the surgical literature, it is clear that “artificial intelligence” (AI) is positioned to make significant contributions in surgical care and training. AI uses algorithms which then allow computers to make predictions i.e., solve problems based on recognized words, clues seen on images, data collected, and applied statistics.

              Several companies are investing billions of dollars to solidify their spot in the AI market. Microsoft, Apple, Nvidia, Google (Alphabet Inc.), OpenAI, Amazon (Alexa), IBM, and xAI (Grok) are just a few of the companies that have made significant investments as the potential financial return is tremendous.

              The programming of the algorithms used in AI is not known and it is unlikely that they will be made available for review as this intellectual property is very valuable. Absent a change in the United States Constitution, these algorithms will be protected for some time.[1]

              What do we know about AI? It seems that the powerful computers in the AI realm absorb data from huge databases and use these databases to formulate predictions. But sometimes, the answers provided (predictions?) are not true. It may be that the databases used are faulty and thus the computers predictions are faulty. Garbage in, garbage out, so to speak.

              There are several articles that confirm AI platforms are making mistakes. Hiltzik described AI that provided lawyers with false precedents which the lawyers used in supporting their cases. When the judges found the precedents had not been checked by the lawyers, fines and other punishments were levied.[2] Also, a Texas professor recently flunked his whole class when an AI program erroneously accused all the students of plagiarism.[3]

              AI has already proven useful in diagnostic specialties where it can learn to recognize patterns and detect things by analyzing vast libraries of visual images and videos. Specialties such as radiology, pathology, and dermatology have shown that AI can review images and pick up on things that the physician may have missed. Could AI eventually be used to replace human physicians?

              This question was recently raised with a retired IBM executive. This executive assured us that Watson, the IBM AI representative, is meant to help us do our job better.[4] In the diagnostic specialties, this seemed to be a reasonable answer. We then asked if a computer could ever affect a surgeon’s creativity due to an overreliance on the AI direction? She was reluctant to make predictions on AI creativity.

              We then asked this question to Google, and this was the answer we were given:

                             “Concerns that AI could stifle a surgeon’s creative training by removing complex problem-solving are valid, though current research suggests a more nuanced outcome. AI is expected to serve as a supplementary tool in surgical training, automated standard tasks and providing realistic simulations, which can help accelerate skill acquisition. However, the human aspects of surgical creativity—including the ability to respond to unexpected intraoperative events and innovate new techniques—will remain critical for developing a surgeon’s full expertise.”[5]

              This issue of AI harming the knowledge, creativity, and skills of a surgeon was recently raised by Abiodun Adegbesan et. al. In this letter to the editor, this group states, “there is a danger that surgeons may become passive operators which can potentially lead to a reduction in their surgical dexterity, clinical expertise and overall problem-solving abilities.”[6] 

              ChatGPT is an advanced AI language model developed by OpenAI. It is a Generative Pre-trained Transformer that “learns” from internet data to perform tasks such as answering questions, summarizing information, and writing papers.

In a recent article by Keith Naunheim and Mark Ferguson, four popular chatbots were tested against 21 board-certified thoracic surgeons on ten clinical scenarios. The surgeons performed at a significantly higher level than the chatbots. In this study, the authors concluded that “[a]lthough they are becoming increasingly sophisticated, chatbots do not yet perform at the level of a practicing thoracic surgeon when faced with complex clinical scenarios.”[7] It would be interesting to see how the chatbots perform against thoracic surgical residents who have not yet garnered the experience of the certified surgeons.

In a world which has already seen computers beat human opponents at Jeopardy (IBM’s Watson)[8] and Grand Masters at Chess (IBM’s Deep Blue)[9], it is somewhat surprising that several chatbots were not able to outperform the board-certified thoracic surgeons in vignettes relating to well-known clinical scenarios. It is just a matter of time before the computer can surpass surgeons in making diagnoses and formulating treatment plans. But can the computer work with a robot to do operations independent of human control?

At this time, it is unlikely that a robot can be programmed to do operations as well as surgeons because robot arms and graspers are limited in their physical ability. Human hands are superior to any known robot platforms, but this difference is being challenged. At Northwestern University’s Center for Robotics and Biosystems, researchers are working on improving tactile sensing and flexibility of robotic hands.

Kevin Lynch, who leads Northwestern’s team working on robotic hands says, “the team has set a 10-year goal to achieve dexterity sufficient for basic humanlike tasks.”[10]

Engineers at Tesla are also working to improve their humanoid robot, Optimus, so that it will be capable of “performing the small, precise motions that define most skilled labor.”[11] As Elon Musk told the Wall Street Journal, “In order to have a useful generalized robot, you do need an incredible hand.”[12]

But what about the creativity element that is essential for any surgeon who may face a rapidly changing and challenging environment in the operating room? Can creativity be programmed into the AI platform?

Surgeons are not the only ones worried that AI may be harmful in training people whose creativity is paramount for job performance. In a military context, war gaming is essential in training intelligence professionals. A quote by President Dwight Eisenhower is on point, “Plans are worthless, but planning is everything.”[13]

              In a recent article from the Combating Terrorism Center at West Point, Nicholas Clark raised the issue that artificial intelligence may result in overreliance by Special Operators who need to be creative and quickly responsive to sudden changes on the battlefield. “While generative AI may assist in automating routine tasks, it lacks the capacity for nuanced judgment, uncertainty quantification, and dynamic responsiveness critical to effective CT work.”[14]

              “The use of generative AI for operational planning may, in fact, make our planners worse by removing the real benefits of the planning process and limit the CT forces’ ability to respond dynamically to branches and sequels.”[15]

              A recent study looked at brain activity when ChatGPT was used.  The study found that users of ChatGPT for helping to write papers became more dependent on the computer as the study progressed. As the users of ChatGPT became more dependent on the computer, the final papers became a copy and paste exercise.[16] There was no more creative input by the humans in writing the papers.

              Surgeons are very much like Special Operators. They must be studying and training constantly to keep up with the specialty; it is a learned profession. The main difference between Special Operators and surgeons is the surgeon knows he is likely to go home alive later in the day.

              But what about doing operations without human control. Could the surgical robots with AI platforms be programmed to do operations by themselves? Robotic operations are being done by humans around the world daily. The operations are being done with surgeons at a console, controlling the robot arms. So far, the critical difference is that the surgeon controls the robot arms and has hands which the robot does not. If things go bad, the surgeon can abort the robotic procedure and can open the patient and do the operation in the conventional way. But that difference may be changing.

              Can the computer be programmed to learn when it is over its head and abandon the robotic procedure? If faced with circumstances that are not answerable with the database provided (i.e. aberrant anatomy, arterial bleeding, hollow viscus injury, etc.), could the computer be creative and provide a solution? How can creativity be programmed? This is a difficult question because we do not know how to define “creativity”, and we do not understand the process of being creative in the first place.

              “ChatGPT runs on something called an artificial neural network, which is a type of AI modeled on the human brain. Instead of having a bunch of rules explicitly coded in like a traditional computer program, this kind of AI learns to detect and predict patterns over time…[But] because systems like this essentially teach themselves, it’s difficult to explain precisely how they work or what they’ll do. Which can lead to unpredictable and even risky scenarios as these programs become more ubiquitous…[AI is] trained…by basically doing autocomplete.”[17]

              When circumstances in the operating room change, the surgeon (at least now) generally has the knowledge, education, experience, and skills to adjust appropriately. He may need to call in a colleague and that is part of being a professional. Could AI act professionally and be creative if the circumstance calls for it? At our present state of knowledge, if creativity is required, it is unlikely that a computer can replace a human surgeon. However, as AI platforms continue to improve, they may enhance simulation exercises, but this should be extrapolated to live surgery with caution. As the retired IBM executive stated, AI computers are meant to help us, not replace us.

              Medical education and surgery are growing at a rapid pace. Being creative and using judgment to adapt to rapidly changing circumstances is often the difference between life and death. AI should only be used when its’ strengths outweigh its weaknesses. We must continue to train our surgeons to be creative and resourceful to better help our profession grow and keep us, at least one step ahead of AI and robots.

              The only part of this article that was AI generated was the answer to the question asked of Google above.



1 United States Constitution, Article I, Section 8, Clause 8. The Congress shall have Power…To promote the Progress of Science and useful Arts, by securing for limited Times to Authors and Inventors the exclusive Right to their respective Writings and Discoveries[.]

[2] Runco MA. AI can only produce artificial creativity. Journal of Creativity 33 (2023) 100063.

[3] Id.

[4] Personal communication with IBM executive (anonymous).

[5] Response given by Google AI to the question on surgeon’s creativity being hampered by overreliance on AI.

[6] Adegbesan A, Akingbola A, Aremu O, et. al. From Scalpels to Algorithms: The Risk of Dependence on Artificial Intelligence in Surgery. Journal of Medicine, Surgery, and Public Health 3 (2024) 100140.

[7] Bryan DS, Platz JJ, Naunheim KS, Ferguson MK. How soon will surgeons become mere technicians? Chatbot performance in managing clinical scenarios. The Journal of Thoracic and Cardiovascular Surgery. Volume 170, number 4 1179-1184, 2025.

[8] Watson beat Brad Rutter and Ken Jennings to win a $1 million prize in 2011.

[9]  Deep Blue beat Gary Kasparov in 1997. Kasparov felt that cheating was involved since some of the computer’s moves were non-sensical. It turned out there were flaws in the programming which have since been fixed. Even with the programming errors, the computer still won.

[10] Jacobs S. Engineering the perfect robotic hand could unlock a $5 trillion humanoid market. Wall Street Journal, October 26, 2025.

[11] Id.

[12] Id.

[13] Eisenhower, D. Remarks at the National Defense Executive Reserve Conference, November 14, 1957.

[14] Clark N. Commentary: The Dangers of Overreliance on Generative AI in the CT Fight. CTC Sentinel, p. 15-19, August 2025.

[15] Id. p. 16.

[16] Nataliya Kosmyna et al., “Your brain on Chat GPT: Accumulation of cognitive debt when using an AI assistant for essay writing task,” arXiv.org, June 10, 2025.

[17] Runco MA Id. p. 5.

Medical Malpractice Legal Requirements May Be Changing

Darryl Weiman, M.D., J.D.

The American Law Institute (ALI) is a group of lawyers, judges, and other legal scholars whose mission is to improve, modernize, and clarify the law to promote the administration of justice. Established in1923, it is a private, independent, non-profit and their writings have great weight in the legal community. The ALI publishes Restatements of the Law, Principles of the Law, and Model Codes, to “express the law as it should be.”

In 2024, the American Law Institute (ALI) wrote new guidelines for medical malpractice which shifted from the “reasonable physician” to a more patient-centered standard which relied more on evidence-based practice guidelines. As mentioned above, these new standards have considerable respect in the legal community, and it is reasonable to conclude that some state legislatures and supreme courts will follow the recommendations to incorporate “evidence-based medicine” into malpractice law. This is a significant shift which may cause major legal problems for physicians.

Medical malpractice is currently predicated on the “reasonable practitioner” standard. Although there is variability among the states, a practitioner would not be liable for malpractice so long as their actions complied with what a reasonable provider would do if faced with the same or similar circumstances.

Here is an example of what might happen with the ALI recommended changes. I was at a continuing legal education meeting where the speaker, a well-known plaintiff’s attorney, stated that deviations from practice guidelines should be construed as medical malpractice. He used the example of the Advanced Cardiac Life Support (ACLS) acronym for the acute coronary syndrome. The acronym is MONA, which stands for morphine, oxygen, nitrates, and aspirin. According to this attorney, a physician who did not follow these guidelines is liable for malpractice if the patient was harmed.

As physicians, we all know not to give morphine to a patient with an allergy to that drug, and we may not be willing to give it to a patient with low blood pressure. We may be reluctant to start oxygen on a patient with severe chronic obstructive pulmonary disease, as the oxygen saturation may be his driver of respiration and providing oxygen may lead him to stop breathing. With similar reasoning, we may not give aspirin to a patient who is allergic to the drug or if gastrointestinal bleeding is an issue. Also, we know not to give nitrates to a patient who is taking Viagra or Cialis because, as the commercials warn us, this can cause a precipitous drop in blood pressure.

With current medical malpractice law, the burden of proof is on the plaintiff who must show, with a preponderance of the evidence standard, that the practitioner did not do what a “reasonable practitioner” would do if faced with the same or similar circumstances. If the recommendations of the ALI are to be used, the burden of proof would shift to the practitioner

who would need to convince the jury that the guidelines should not be applied in his case. This is a significant shift in burden.

Granted, the guidelines have disclaimers, usually at the beginning of the publication, which acknowledge that the guidelines are written for the ideal patient presenting with that disease entity and it is up the physician taking care of the patient to decide whether to use the guidelines. Plaintiffs are likely to downplay or ignore these disclaimers. The result will be to shift the burden of proof to the physician to convince a jury that following guidelines written by experts in the field was the wrong thing to do in his case. Good luck with that.

It becomes more problematic when it comes time for the judge to instruct the jury as to what standard of care it should use in deciding the case. Instead of customary care as the standard for reasonableness, the guidelines will be used to define what the law says is “reasonable.” It is foreseeable that the injured plaintiffs will use the guidelines as the best scientific evidence of what the physician should have done.

Expert witnesses for the defense used to opine whether the practitioner did what a reasonable practitioner would do if faced with the same or similar circumstances. That was the law. With the guidelines, by law, now defining the standard of care, defense experts will need to argue that the law should not be followed in this case. Under the “preponderance of the evidence” burden of proof needed in most malpractice actions, this may make it more difficult for the practitioner to win his case; juries instructed to follow the law, are unlikely to ignore that instruction.

Instead of practicing defensive medicine, physicians and other practitioners will be inclined to follow guidelines even though it is rare to find the ideal patient with any disease entity. Knowledge, education, training, experience, and skill will no longer be the lynchpins of medical judgment. Computers may soon be telling us how to take care of our patients. In fact, they already are.

If a practitioner decides not to follow the guidelines, he should document his reasoning in the medical records. With this documentation, the court will be inclined to believe that the physician was doing what he believed to be best for his patient, i.e., he was acting reasonably. This will go a long way in helping him win the case.

The Ethics of Self-Experimentation

By Darryl Weiman, M.D., J.D.

Newsletter from the Standards and Ethics Committee for the Eastern Cardiothoracic Surgical

In 1929, a first-year surgical resident, Werner Forssmann, operating on a dog, was able to insert a urologic catheter through a leg vein into the right atrium. The dog survived. Forssmann hypothesized that the same procedure could be done on humans. With a catheter placed in the right side of the heart, he could then study right sided pressures safely and could evaluate the effects of medicines, such as digoxin, injected directly into the heart.

Forssmann brought his idea to his boss and, not surprisingly, his proposal to place a central catheter in humans was rejected. Forssmann, convinced with the importance of cannulating the central circulation in humans, decided to place a catheter in himself. With the help of an operating room nurse, he obtained sterile instruments and with the nurse—who thought that she was to be the experimental subject—locked themselves into the hospital’s small operating room. Forssmann, then did a cutdown into a left arm vein and threaded a lubricated ureteral catheter 65 centimeters from the arm into his body.

Forssmann probably wanted the nurse to be with him in case something went wrong and probably never intended for her to be the subject of the procedure. Forssmann and the nurse then went to the radiology department where a chest radiograph confirmed the position of the catheter in the heart. The catheter was removed and there were no complications.

The next morning, Forssmann showed the radiograph to his boss who immediately fired him. Forssmann was able to get an unpaid appointment with Ferdinand Sauerbruch at the surgical department at the Charite in Germany. Forssmann’s ideas were ridiculed by his colleagues at Charite so he ended up going to the University Hospital in Mainz where he trained in urology.

From Mainz, he went to the Rudolf Virchow Hospital in Berlin for further training in urology and general surgery. After more training, World War II intervened and Forssmann was never able to fulfill his dream of being an academic surgeon.

Forssmann continued his career as a general practitioner and urologist until 1956 when he was informed that he had been awarded the Nobel Prize. From 1958 to his retirement in 1969, he was the Chair of the surgical division of the Evangelist Hospital in Dusseldorf.

History shows the importance of what Forssmann did to himself on that day in 1929. His Nobel co-recipients Andre Cournand and Dickinson Richards, intrigued by Forssmann’s article of 1929, pioneered the work leading to cardiac catheterization as we know today. Catheterization of the right heart led to study of the left heart and, subsequently, to coronary arteriography.

Percutaneous interventions to the coronary arteries and percutaneous interventions for valves are now being routinely done. Millions of lives have been saved due to the development of cardiac catheterization, but do the results justify the means? In this case, I think they do.

Self-experimentation is not new, and Forssmann is not the only Nobel Prize winner in medicine to do this. Barry Marshall was convinced that H. pylori was a cause of gastritis and ulcers. He drank a broth that contained the bacteria and got gastritis which he then cured with appropriate antibiotics. Marshall’s work changed the treatment of these diseases, and he was awarded the Nobel in 2005.

So what are we to make of those who self-experiment? After all, it is difficult to reconcile between reckless endangerment and heroic self-sacrifice. The ethical principles outlined and defined in the Belmont Report of 1979 are a reasonable starting point.

The three main principles of the Belmont Report are (1) respect for persons (autonomy), (2) beneficence/nonmaleficence, and (3) justice. Can we use these principles as guidelines to determine when self-experimentation is justified?

Under autonomy, it seems obvious that the self-experimenter is exercising his personal liberty, and he has probably given himself informed consent. No vulnerable population seems to be involved, and no person is being coerced. However, bias may lead to an underestimation of the risks. Without external oversight, safeguards may be underestimated or totally absent. Even Forssmann made sure his nurse was present in case something bad happened.

With beneficence/nonmaleficence, the goal is to maximize benefits and minimize risks. The self-experimenter is probably minimizing risk for others but, if the risk to himself is high and the hoped for benefit is low, then the experiment should not be condoned. In fact, if dealing with pathogens e.g., Covid, then risks could spread to the community at large especially if proper safeguards (containment?) are not in place.

Justice requires a fair distribution of research risks and benefits. If the self-experimenter bypasses the IRB review process then ethical standards are not considered which can hurt the justice of the whole research endeavor.

So what are we supposed to do? Pursuit of discovery should be encouraged but recklessness should not. Self-experimentation is a gray zone of modern ethics, and the debate is on-going so do not expect an answer from me. However, safeguards should be placed by the IRB and by journals who may be asked to support and publish the results of the experiment.

Remember, Forssmann was able to publish his experiment, and we can still view the chest radiograph he took in 1929, but that happened long before safeguards for human experimentation were in place. Each IRB and journal should balance the value of the knowledge sought, the risks involved, the safeguards in place, and the effect the experiment is setting for future researchers; these should all be part of the decision-making process.

Journals should only publish reports that can be morally justified. Reports should be judged on a case-by-case basis by ethical review boards and by the journal’s editors. Having a decision-making process already in place will go a long way in justifying publication of a self-experimenter’s report.

Under Oath

Darryl Weiman, M.D., J.D.

Standards and Ethics Committee of the Eastern Cardiothoracic Surgical Society

Ben Franklin said,

“Honesty is the best policy.” When you are under oath, it is the only policy.

During a surgeon’s career, it is likely that he will have to deal with a medical malpractice suit either as a defendant or as an expert witness. In fact, a cardiothoracic surgeon in Tennessee will be named as a defendant, on average, once every three years. During the legal process that will follow, testifying under oath, either at a deposition or at trial, may be required.

Any party in a malpractice action is allowed to take the sworn testimony of any witness, opposing party, or expert expected to be used at the trial by the opposition. This testimony will occur at a deposition. At the deposition, the witness will be put under oath, usually by the court reporter who will also write a word for word transcript of the testimony. There is no judge present at the deposition so any objections will have to be ruled on later. Usually, the objecting attorney will place the objection into the record and then the witness will be allowed to answer the question. If the objection is later sustained, the answer will not be allowed to be used at the trial.

Some depositions are video recorded and that video may be played for the jury if the witness is not able to attend the subsequent trial. This may be more effective than just having someone read the transcript to the jury. The jury can actually see the witness, evaluate his demeanor, the tone of voice and get a sense of the timing of the answers to better judge the witness’s credibility.

As a discovery tool, the deposition will be useful in gathering information that may be sought at trial, and box the witness in as to what they can then say at trial. It is common for the opposing attorney to close his questioning by asking the witness if there are any other issues he will be testifying to at trial. If the witness says “no” then he will not be allowed to bring up new issues at the trial unless the opposing attorney “opens the door” to new testimony by asking a question that he probably should not have asked that was beyond the scope of the deposition testimony.

There is a great deal of strategy that goes into taking and defending depositions. Many experienced attorneys will get right to the heart of the matter and ask as few questions as possible to get the information they need to support their case. This “short and sweet” approach is likely since the witness, if it is the expert witness of the opposition, must be paid by the

deposing attorney’s side. Also, they don’t want to waste time seeking answers that will not make a difference as to the outcome of the cause of action.

Some attorneys try to wear the witness out in hopes that he will make a mistake as he gets tired. You should be able to figure out the strategy being used but answering truthfully is still required. If the opposing attorney can show that you are lying, your credibility will be destroyed, and you will probably be punished by the court.

Besides answering truthfully, there are other things to keep in mind while testifying. Always be professional and polite. Testifying is stressful but you must maintain your cool and answer to the best of your ability. The judge and jury (if you go to trial), know that you are stressed and they will respect you more if they see you are being courteous—even to your adversary. Dress appropriately and be on time. Do not try to be funny or sarcastic with opposing counsel. Every word you say is recorded by the court reporter and if your testimony will be read back at trial, you want to be sure that your words were appropriate.

If you are asked a question and you don’t remember the answer, it is alright to say you “don’t remember” or “don’t recall.” It is rare for a person to recall what they were thinking at a particular time many years ago. It is also not a good idea to guess what you might have been thinking. The opposing attorney may ask you to review the medical record and then ask if that may have refreshed your memory so that you could now try to answer his question. It is unlikely that the chart review will allow you to remember what you were thinking back then so you may want to point out that a review of the chart won’t be enough to recreate the thought pattern you might have had during that time.

The opposing attorney may persist and present you with a hypothetical patient that is like the plaintiff and then ask your opinions as to diagnosis and treatment. As a physician, it is fair to point out that the presence of the patient—one that you can talk to and examine—is critical to making a diagnosis and treatment plan and without such patient, you are reluctant to answer based on limited knowledge.

If your case involves a missed diagnosis which led to harm to the patient, some attorneys will persist in trying to get you to admit to a mistake. They will do this by posing a theoretical question dealing with the signs and symptoms of the plaintiff and ask for a differential diagnosis. For example, let’s say the patient had an aortic dissection and the diagnosis was not made until he was already dead. The attorney may ask for a differential diagnosis for a patient who presents with substernal chest pain, shortness of breath, and tachycardia.

Faced with this scenario, the inclination is to say, “it could be an aortic dissection.” This is especially true because you know that this is what the plaintiff had. It would be truthful and better for your case if you do not jump ahead. Provide the attorney with a list of conditions which meet the proposed criteria so that the judge and jury can see that the case is not as simple as the plaintiff attorney is trying to portray. In this example, the list could include myocardial

infarction, pulmonary embolus, aortic dissection, pneumonia, pancreatitis, a duodenal or gastric ulcer with perforation, costochondritis, and perhaps a sternal or rib fracture, etc.

Do not start offering opinions without examining the theoretical patient. Do not let the opposing attorney force you to make suppositions as to what the patient might have had since you are only being given limited information which was not the situation when you were taking care of the patient.

It is wise to only answer the question you’ve been asked. Many defendants feel the need to give a long, detailed explanation that goes beyond the scope of the question. Their goal is to educate the attorney as to their thought process and make him realize that they were thoughtful and reasonable. This is unlikely to happen and may even hurt your case. The more information you provide to plaintiff’s attorney will just give him more material with which to ask questions.

If you are asked a “yes” or “no” question, you don’t need to provide explanations. For example, if you are asked if you remember seeing the patient on a particular day when there is no note by you or a member of your team, then “no” is the answer. If you say, “No, but it could have been one or two times and I just didn’t document it,” you will be opening yourself up to another line of questioning dealing with your documentation habits. Do not volunteer information.

Your lawyer may advise you to use medical terms in your answer to force the opposing attorney to look to you for help. This may be risky. Instead, it would be best to answer in a way that would be understandable to a member of the jury. Remember, your testimony may be read to the jury at trial. The jury would appreciate it if they perceived that you are not talking down to them.

Some opposing attorneys may be threatening and try to coerce you into providing them with more favorable testimony. If you are telling the truth, you should not be intimidated.

Remember, as a physician, you will be more knowledgeable about patient care than any attorney. Use your knowledge, education, training, experience, and skills to your advantage.

PATH Audits and Other Rules That Affect Resident Autonomy

Newsletter for the Standards and Ethics Committee
Eastern Cardiothoracic Surgical Society

By Darryl Weiman, M.D., J.D.

In June 1996, the Office of the Inspector General (OIG) initiated a plan to audit teaching hospitals (the PATH audits). The OIG wrote, “[t]his initiative grows out of the extensive work performed by the OIG at a major East Coast University.”1 The focus of the review was compliance with intermediary Letter 372 (IL-372). This letter explained the Medicare rule affecting payment for physician services provided by residents. The review found that the university hospital was not in compliance with the rule.

The university in question was the University of Pennsylvania where it was alleged that the attending surgeons were billing for services provided by the residents and there was improper “upcoding” of the level of services provided to maximize Medicare reimbursement. The rule in question would allow for billing of the resident services so long as there was proper documentation for attending supervision. The rule required documentation with specificity and, if the documentation was inadequate, the services could not be billed for.

Prior to this audit, it was customary for chief residents to function independently, especially at night, and the attendings did not come in unless requested by the chief resident. With the new rule, which most (if not all) of the attendings were not aware of, the lack of documented supervision put the university at risk for a False Claims Act violation and that is exactly what happened.

The University of Pennsylvania was found to be billing despite “inadequate documentation” and there were 1.4 million claims submitted during the audit period. The Hospital for the University of Pennsylvania calculated that even if only 2% of the records had inadequate documentation, they would be at risk for statutory penalties of $280 million under the False Claims Act (not including treble damages for overpayments). The OIG did not want to bankrupt one of the premier teaching hospitals, so they agreed to a settlement of $30 million.

The University of Washington was the next target and that university agreed to a $35 million dollar settlement. This case was complicated by a neurosurgeon who tried to suborn perjury by having his residents say he was in the operating room when the bills were generated.

The Dartmouth Hitchcock Medical Center was found to have only a minimal billing error ($778) but it cost them $1.7 million to defend against the audit. The costs were high even with a victory.

With these financial victories, the OIG was looking to do more. Attorneys in the OIG found the audits to be a great way to advance their careers and it was no surprise that they planned to audit all teaching hospitals. Of course, the teaching hospitals fought back as their financial viability was on the line. Lobbying efforts by the universities and teaching hospitals led to Congressional hearings. The hearings led to a moratorium on the PATH audits, but this moratorium was not permanent. In fact, a recent audit led to a settlement at the University of Pittsburgh.

Since those PATH audits, teaching hospitals have worked hard to remain in compliance with the requirements for resident supervision at all levels, but an unintended consequence was a detrimental effect on resident training. As RVUs became more important in deciding attending salary, attendings were less likely to let residents do cases independently. The RVU issue was a result of the Omnibus Budget Reconciliation Act of 1989 which pushed surgeons to do more to increase their own operative load; this, of course decreased the resident involvement with the case.

Other laws and regulations on point were the 1997 CME (Coding and Medical Encounter Documentation) modifiers for billing involving resident doing cases and the 2002 CMS Mandates requiring the attending to be present for critical portions of the case. Although these laws and regulations led to a decrease in resident experience, the Libby Zion case probably had the most significance in reducing the “hands on” exposure in the operating room, wards, and clinics.

The Libby Zion case led to the Bell Commission in New York. This led to an 80-hour work week restriction for residents in that state. Other states soon followed the New York example and the ACGME bought in to the 80-hour work week restriction which affected all residencies.

It is now no surprise that up to 60% of general surgery residents finishing training are concerned that they may not be able to function independently, especially in the operating room. In fact, up to 80% of graduating general surgery residents go on to do a fellowship as they hope the added training will allow them to be safe and clinically competitive.2

If your practice is hiring new graduates, it may be prudent to mentor them as they may need to acquire the confidence needed to function safely and independently. It’s not their fault that the states and ACGME decided that residents in training needed more time off. I’m sure the new graduates will appreciate your help.


1Ruth SoRelle, Tracking a Tangled PATH, Circulation, 1998; 97:2191. 2 Yeo H, Viola K, Berg D, et al. Attitudes, training experiences, and professional expectations of US general surgery residents: a national survey. JAMA 2009; 302:1301-1308.

Taking Call Has Risks

By Darryl S. Weiman, M.D., J.D.
Associate Program Director, General Surgery Residency Program
Baptist Medical Center, Memphis, Tennessee

Newsletter submitted on behalf of the Standards and Ethics Committee of the Eastern Cardiothoracic Surgical Society

Can taking call, in and of itself, put you at risk for a malpractice action even if you have never met the patient? After all, a duty owed is one of the elements that must be proven by the plaintiff in order for them to win the suit. If a physician-patient relationship has never been established, then how can a duty be owed? This issue was addressed in Millard v. Corrado.1

On November 5, 1994, 63-year-old Marjorie Millard was involved in a motor vehicle accident (MVA). The emergency medical technicians (EMT) arrived at the scene at 10:28am.2 The accident scene was 14 miles from the Audrain Medical Center (AMC) and 25 miles from the University of Missouri Medical Center. Since the EMTs found no measurable blood pressure or radial pulse, they chose to transport to Audrain.

Dr. Joseph Corrado was the general surgeon on call for Audrain, but he had signed out to Dr. Ben Jolly, an orthopedic surgeon. Dr. Corrado then left town so that he could attend the local American College of Surgeons meeting. Unfortunately, Dr. Jolly did not have general surgery privileges and Dr. Corrado had not notified anyone else that he would be unavailable for emergencies.

Millard arrived at AMC at 11:07am. IV fluids were started and a chest radiograph was obtained. The chest film was consistent with blood in the chest. The emergency room attending examined Millard and he concluded that she was also bleeding into the abdomen.

Dr. Corrado was paged twice but he did not answer. At 12:00pm, air transport was called but they were grounded due to bad weather. At 12:07pm, Dr. Jolly entered the ER and saw the patient. He agreed that she needed an abdominal exploration, but he did not have the privileges or training to do that operation.

At 12:23pm, Dr. Corrado responded to the previous pages. After being told the situation, he agreed that Millard should be transferred to the University of Missouri Medical Center. At 1:45pm, the patient arrived at the University of Missouri where she underwent an abdominal exploration beginning at 2:15pm; this was about four hours after the MVA.

Ms. Millard was found to have broken ribs, a ruptured diaphragm, injuries to the renal artery and vein, and adrenal artery. She presented in hypovolemic shock.3

The left kidney, gall bladder, part of the colon and part of the small bowel had to be removed. Millard brought a malpractice action against Dr. Corrado claiming that “…as a direct and proximate result of the delay in treatment caused by Dr. Corrado’s absence (she) sustained aggravation of the injuries sustained in the accident and additional serious injuries.”4

Dr. Corrado moved for summary judgment arguing that the plaintiff had failed to establish the formation of a physician-patient relationship—a necessary component proving that a duty of care was owed.

The trial court agreed with Dr. Corrado. The motion for summary judgment was granted and a judgment in favor of Dr. Corrado was entered. However, on appeal, the judgment was reversed. The appellate court held that the public policy of Missouri and the foreseeability of harm to patients in the position of the plaintiff support the recognition of a duty flowing from Dr. Corrado to Ms. Millard. By being “on call” the physician owes a duty to reasonably foreseeable emergency patients to, at least, provide notice to the hospital when they will be unable to respond to calls.5

In dictum, the court went on to say that the duty to provide adequate notice should not have a detrimental effect on the ability of the hospital to attract physicians to accept “on-call” assignments. It is now common practice for hospitals to pay physicians to “take call” and many young physicians are anxious to take call to help build their practices.

A concurring opinion summed up the “duty owed” issue very well. “One who undertakes, gratuitously or for consideration, to render services to another which he should recognize as necessary for the protection of a third person or his things, is subject to liability to the third person for physical harm resulting from his failure to exercise reasonable care to protect his undertaking if his failure to exercise reasonable care increases the risk of harm…”6

Since the plaintiff produced substantial evidence that Dr. Corrado’s actions resulted in a delay in obtaining treatment for her injuries, thus increasing the risk of harm, Dr. Corrado lost his summary judgment motion.

As we now know, taking call, in and of itself, will create a duty of care owed to any foreseeable patient who may need our care during that call period. With the advent of the Emergency Medical Treatment and Active Labor Act (EMTALA) of 1986, further legal requirements may be required of us if a patient with an emergency condition is able to make it to our hospital.

Using public policy factors, courts will consider the prevention of future harm, the cost of the conduct, and the ability to spread the risk of loss, and the economic burden upon the actor and the community related to the conduct.

The court in Millard concluded that Corrado did owe a duty of care to Ms. Millard. Also, Corrado had a contractual obligation to AMC to notify them if he would not be able to cover. The court also construed a contractual obligation for the “on-call” physician to respond to being called in a reasonable time frame, i.e., 30 minutes.

The legal requirements of Millard only apply to the state of Missouri, but other states have their own “on-call” laws. Each physician should learn the laws in their state. Ignorance of the law is no excuse if the laws are violated in their malpractice arena.


1 Millard v. Corrado, 14 S.W.3d (Mo. App. E.D. 1999). 2 Id. 3 Id. 4 Id. 5 Id. 6 Id.

Futile Care—Ethical and Legal Considerations

Darryl S. Weiman, M.D., J.D.

Standards and Ethics Committee Newsletter for the ECTSS

What should the health care provider do when the patient or the patient’s family requests that life-prolonging care be started or continued when there is no reasonable expectation that the care would be helpful? These types of demands are not unusual and are based on the ethical principles of autonomy and self-determination. It is legally accepted that patients can refuse treatment; does the law recognize their right to demand care based on the same principles?

“Futile care” is medical care or treatment for a patient when there is no reasonable hope of a cure or benefit. Physicians are sometimes faced with a situation when the patient (or the patient’s family) requests care that the physician believes is futile and may even be harmful. No State requires a physician to provide care that he believes to be futile, but the physician’s judgment may be subject to second guessing, and he may be served with a medical malpractice or wrongful death suit.

There are mainly two reasons that patients and families push for care that is against their physician’s advice. The first rests on religious or cultural reasons where the family believes that everything should be done to preserve life, even if prolonged suffering is the result. In some cases, such as “brain death”, the religion may not recognize the medical definitions. In some religions, death only occurs when the heart and lungs have stopped working. This is why New York and New Jersey have religious exceptions for their “brain death” statutes.

The second reason is related to a lack of understanding as to the limits of medical care. This leads to false beliefs that care given can reverse what the medical professionals know to be an irreversible situation. This scenario is usually managed with regular meetings with the family with discussions as to what reasonable outcomes can be expected. However, even with improved communications, the family may continue to request “futile” care.

Fear of legal ramification usually leads to honoring the family’s request. As a result, cost of care goes up and limits are placed on scarce medical resources.

To help physicians deal with these difficult clinical situations, some states have enacted laws to protect providers who may decide to not honor a family’s request for futile care.

Texas has a model for how to approach this difficult clinical scenario, but not all states have this type of “safe harbor” statute relating to futile care. In Texas, when a patient or family demands care that the physician believes is futile, the law requires the care-giver to get a second opinion from another physician. When this is done, the person providing the second opinion should see and examine the patient and review the medical records. The second opinion should

then be documented in the medical records and the family should be informed as to the opinion. In most cases, the opinion will be consistent with the first physician’s opinion but that may not be the case.

If the second opinion is in agreement with the family or patient, that physician should then take over the care of the patient. If the second opinion agrees that the care requested would be “futile” then the family or patient will either need to change their opinion or continue to request the care in question.

If, after hearing the second opinion, the family still wants the “futile” care to be given, the physician should obtain a consult from the hospital’s Ethics Committee. The committee should then review the medical records and examine the patient. Usually the ethics opinion will agree with the physician. If the family still is pushing for the “futile” care, then the physician and the hospital should offer to try to transfer the patient to another facility which would be willing to provide the care in question. This attempt to transfer the patient is unlikely to be successful as most other hospitals will not want to deal with a “futile care” conflict.

If all of the steps outlined in the Texas statute are done, then the physician will have a “safe harbor” under the law to not provide the requested care; he would even be allowed to withdraw care that he deems to be futile. The family will still be allowed to bring a medical malpractice or wrongful death suit, but they will be unlikely to win.

The underlying intent of the process outlined in the Texas law is to allow the family to come to grips with the gravity of their loved one’s situation. Once they realize that the medical staff is in agreement, they are likely to back off from their demands for further, unwarranted, care.

There are situations, usually in the trauma scenario, where there is not enough time to meet the requirements of the futile care statute. For example, patients who have sustained blunt chest trauma and present with no cardiac rhythm often get a resuscitative thoracotomy in the emergency department even though the mortality is significant and those who survive have horrible neurologic outcomes (Powell DW, Moore EE, et. al., Journal of the American College of Surgeons, August 2004). The recommendations of the Powell article are to stop doing these thoracotomies for any patient with blunt chest trauma who was getting prehospital cardiopulmonary resuscitation for longer than five minutes even though not doing the thoracotomy may lead to medical malpractice actions related to the “loss of chance” for survival.

Although the “Futile Care” statute will afford some protections to the physician and hospital, they may still have to experience the financial and other expenses of defending their actions. No one wants to be the first case to test the law since it is uncertain if the courts will deem the law to be constitutional or not. It is possible to argue that the law is unconstitutional as it may deprive a person of “life, liberty, or property” without “due process of law.” A further constitutional argument against the law can be based on the “equal protection” clause of the Fourteenth Amendment; if one person is treated, then all can claim the “right” for the same treatment.

New therapies for acute life-threatening illnesses such as ventricular assist devices, organ transplants, coronary and valvular interventions, have led to increases in the need for intensive care (ICU) beds. As a result, there are times where there is not enough ICU beds to meet the demands of the patient population that could benefit from that environment.

To optimize the use of scarce medical resources, there should be a push to educate the public and health care providers about futile care alternatives such as palliative care (keeping the patient comfortable). Education should also focus on reasonable discussions on end of life issues such as “advanced directives” and “power of attorney for health care issues.” It might also be useful to educate health care providers on the ethical, and legal, issues relating to providing, or not providing care which is costly and unlikely to provide a reasonable hope of meaningful recovery.

One of the first things that needs to be done is provide a clear definition of what constitutes “futile care” and what strategies can be done to more effectively use the ICUs or emergency rooms scarce resources.

There are few cases that have gone to court to decide on the “futility” issue. This is probably because few physicians and hospitals are willing to face the costs and possible reputational damage for removing life-sustaining treatment over the protests of the patient or family. Although most judicial rulings have upheld the physicians’ judgment, some have not.

In medicine, it is often said that “when God puts his hands on, take yours off.” This saying is applicable to the situation where the requested care is deemed to be futile. However, withdrawing care is problematic as no one wants the aggravation of defending his actions in courts of law or courts of public opinion.

Health Care Reform: The Laws May Soon Be Changing

Darryl Weiman, M.D., J.D.

Despite the passage of the Affordable Care Act (ACA), people are still paying ever higher prices for, what appears to be, a lesser quality of care. Physicians are also struggling. It has been estimated that 13% of practice expenditures are dealing with insurance billing and reimbursement. It is not surprising that, with republicans now in control of the White House and both the House and Senate that plans are being made to replace many aspects of “Obamacare.”

In fact, under the “One Big Beautiful Bill” recently passed and signed into law, the insurance companies will no longer be able to keep patients in narrow networks with limited choices as to physicians and health care facilities.1 This is the first of what may be far reaching changes for health care.

Both republicans and democrats agree that health care costs are too high and that there are too many people that are not covered by health care insurance. Both the Affordable Care Act passed during the Obama administration and several plans being discussed by the republicans have remarkably similar goals. If the republicans follow through on their promise to “repeal and replace” the Affordable Care Act, then they must carefully tailor their plan to (1) decrease costs of health care, (2) allow everyone to have access to some form of health insurance, (3) allow patients to have choices in tailoring their individual plans, (4) place an emphasis on preventative care so as to keep more patients out of the hospital, and (5) have some medical malpractice tort reform.

There were several good ideas embedded in the Affordable Care Act. For example, pre-existing conditions are no longer used to deny a person health care coverage. Small businesses (defined as a business with less than 50 employees) are given tax credits for up to 50% of employee premiums. The cut-off age for young adults covered by their parents’ insurance was raised to 27. This was especially good for recent college graduates who were finding it difficult to get jobs in the depressed economy.

The ACA also eliminated the “donut hole” for Part D medication expenditures in January 2025. Now, any medication expenditure over $2,000 is covered by Medicare.

Lifetime caps on health insurance expenditures were eliminated by the ACA. Previously, insurers could cut off patients whose bills exceeded a certain amount. With the ACA, insurers had to keep paying for health care so long as the patient was not dead.

Under the ACA, all insurance plans had to include preventative care without co-pays by 2018. Preventative care is important in keeping patients with chronic conditions out of the hospital where the costs are highest.

There are several models being presented as to what might replace the ACA and it is worthwhile looking at some of these ideas. Whichever plan they choose, it would be wise for the Congress to keep the good aspects of the ACA in place if they are to garner broad-based support.

As physicians, we need to keep up with what is being debated in Congress and the White House so we can better support the ideas that would be best for our patients.

Here are some thoughts on what a new health plan might incorporate.

Most republican plans will eliminate the community rating where everyone in a community are charged the same premiums. The community rating was needed to keep premiums down for people with pre-existing conditions, but it forced others to pay higher premiums. Also, mandatory benefits in the ACA health plans forced people to pay for benefits they would never use. The republicans argue that people should not have to pay for plans mandating care for such things as in-vitro fertilization, cosmetic surgery, and abortions. The ACA required this coverage so that the higher premiums could be used to offset the costs of patients who needed these benefits and other benefits that few would use.

There are several other ideas that are being discussed to make health care insurance more affordable. For example, vouchers of $5,000 for the purchase of health insurance with tax-free dollars would allow people to shop for policies that would meet their budget and needs. This would not require a large bureaucracy; it would only require the people to process the forms and police the system for fraud. People would have a vested interest in their health care policy and, hopefully, the free market would decrease the costs. The use of vouchers would be a good way for those with pre-existing conditions to purchase policies without having everyone else pay higher premiums for coverage for things they would never need.

Currently, the states regulate health care insurance. This leads to large cost disparities. If people could cross state lines to buy insurance, then they could shop for the best deals to meet their needs. I believe the Commerce Clause would allow Congress to pass a law to allow for this. This would probably lead to an overall decrease in premiums as the insurers would have to compete with more companies in other states.

Another way to cut health care costs is to put people in charge of their own routine care. One way to do this is to let people set up health savings accounts where tax free dollars are used to pay for routine care. Medical providers will have to compete for these dollars by offering the best service for the lowest price. Once the free market is back in play, drug companies, hospitals, and providers will not be able to raise prices without losing patients.

The health savings accounts should not be used for over-the-counter remedies and there would be tax penalties for those patients who make non-medical withdrawals.

Premiums for health insurance should be tax deductible. If companies can do it (and they can) then individuals should be allowed to do this also. This would allow most of the 176 million enrolled in company owned plans to buy their own insurance and force the companies to compete by offering supplemental tax-free compensation to allow the consumer to buy more

insurance if they see the need. This would be another way to allow those with pre-existing conditions to get coverage without having everyone else pay higher premiums.

Health coverage should be portable. Employees should be able to control their own health plans and should be able to take these plans with them from job to job. This would force employers to treat their workers better since the worker would not be locked into the job for fear of losing their health care insurance.

Health care insurance should be like other insurance i.e., auto, life, home, and fire. The plans would be private property, and they would allow for maximum choice. They should be flexible and creative, allowing the consumer to buy a policy they deem necessary to meet their needs. This would remove big business, labor unions, and politicians from the health insurance business and let the free market control the costs.

Updating Medicare by allowing each senior $250,000 to purchase some form of elder care insurance would encourage older patients and their caregivers to shop for their own health care. Again, it is hoped that the free market would lead to decreased costs as this patient population would be empowered to look for the best deals.

Unfortunately, under the Affordable Care Act, many providers stopped caring for Medicare and Medicaid patients as the costs exceeded the payments the providers were getting for providing this care. If the government would allow charitable care to be tax deductible, health care providers would be more inclined to treat the low income or uninsured patient. This would be much cheaper than having these patients rely on the ER for their primary care. It would also lead to a predictable continuity of care which would be beneficial for the patients and the providers. Providers who have patients for the long term are more likely to reap the benefits of managing chronic conditions in the out-of-hospital setting.

The Affordable Care Act had no provisions pertaining to tort reform. Most republican plans recognize that tort reform is critical if health care costs are to be decreased. Malpractice insurance is costly. For some specialties, premiums can be over $200,000 per year and these costs are transferred to the patients. Defensive medicine as a strategy to defend against potential malpractice claims raises the cost of health care for everyone. Estimated costs for defensive medicine is about $124 billion per year and each year, this estimate is going up.

Some states limit the payment for non-economic damages in a malpractice suit to control malpractice premiums. Some states may soon try to take malpractice claims out of the hands of juries by using alternative forms of resolution such as Health Courts.

Limiting attorneys’ fees is another strategy being looked at to decrease the costs of malpractice premiums, but attorneys are lobbying against this; since many legislators are themselves attorneys, this would be an uphill battle.

The ACA was over 2,000 pages long and was very complex. The republican plan should not try to fix everything at once. They should start with some laws that are understandable and

allow some choice for the patients. The providers also need some protection to keep all the cost cuts from falling on their shoulders.

No matter what elements are incorporated in a republican plan, it looks like they recognize the fundamental fact that optimal health care is a very personal experience between the patient and his provider. This experience must be affordable, and patient centered.

We should study the details of any new health care plan. The patients and their providers should lobby for what is best for them. 1 Bobby Jindal, Wall Street Journal, August 1, 2025.


1 Bobby Jindal, Wall Street Journal, August 1, 2025.

Advice and Consent for Article III Judges

Darryl S. Weiman, M.D., J.D.

Since the re-election of President Trump, several federal district courts have issued national injunctions which have blocked several of his executive orders. The United States Supreme Court finally stepped in and ruled that the federal district courts could not issue national injunctions. Any district court injunction could only apply to the parties involved in that court’s jurisdiction. How did we get to the point that the courts felt they could wield such enormous power?

Article II, section 2 of the United States Constitution states the president “…shall nominate and by and with the Advice and Consent of the Senate, shall appoint…Judges of the supreme court.” Eventually, all Article III judges had to go through a confirmation process in the Senate. Not surprisingly, with the increasing politicization of the courts, the importance of placing judges whose judicial philosophy is consistent with the president’s has become paramount. Issues such as health care, abortion, freedom of religion, political speech, gun control, results of an election, and affirmative action have become so contentious that control of the Supreme Court and the lower federal courts as political tools has taken on critical importance.

It used to be that the legislative powers as defined in Article I of the Constitution were vested in the Congress and the executive power, under Article II, was outlined for the President. Judicial power was defined in Article III and was meant to keep the executive and legislative bodies from extending their designated powers and from taking freedoms designated to the states and the people in the Bill of Rights and subsequent amendments. This was the intent of separation of powers and the concept of federalism.

Over the last few decades, it has become clear that the courts are making more decisions relating to legislation and to executive powers. As such, the politics of judicial appointments have become increasingly contentious with the minority party resorting to the filibuster to block a presidential appointment that they felt would be detrimental for their legislative goals. With the filibuster, the minority party only needed to muster 41 votes to block a nomination instead of a majority of 51.

Since the filibuster is not part of the Constitution, how did this procedural rule come to take on such importance? Dating back to the 1830’s, a simple majority in the Senate was not enough to confirm a judicial appointee. This was due to a senate procedural rule which allowed for a “filibuster”—defined as a “dilatory tactic, esp. prolonged and often irrelevant speechmaking, employed in an attempt to obstruct legislative action” (Black’s Law Dictionary, seventh edition). The Constitution allows the House and Senate to set their own rules, and, in the Senate, a rule was made to allow for a debate to continue for an unlimited time. The only way to end the debate was for passage of a motion for “cloture” which required a three-fifths majority of the senators duly sworn. With the present senate, this meant that 60 senators are required to pass the motion for ending the debate.

In its original form, the filibuster allowed for a group of senators to speak for as long as they could on the senate floor to prevent a cloture vote from ever taking place. This tactic can still be done today; if the vote for cloture is very close, the minority can prevent any voting on an issue if the filibuster is on-going in hopes of garnering more votes for their position.

To keep the senate from becoming completely paralyzed from the one issue being filibustered, subsequent rules allowed for the issue to be tabled if it is obvious that there are not enough votes for cloture. This allowed for other business to be done while the issue generating the filibuster is effectively blocked.

The history of Senate confirmation of Article III judges is interesting and is worth reviewing.

The Constitution does not specify how many votes are needed to confirm a judicial nominee. Numbers for confirmation are enumerated in other areas of the Constitution such as ratifying a treaty (2/3 majority), voting to convict someone who has been impeached (2/3 majority), expelling one of its members (2/3 majority), and concurring on a proposed Constitutional Amendment (2/3 majority). Since no number is specified, the Advice and Consent role is, arguably, met with a simple majority vote.

Over the years, there were several threats to end the filibuster, especially as it related to judicial appointments. The move to end this procedural tool was called the “nuclear option” although many people preferred to call it the “constitutional option” as they claimed the Constitution only required a majority vote to meet the requirements of “advice and consent.”

The first opinion written in support of ending the filibuster was done in 1917 by Thomas Walsh, a Democratic senator from Montana. Walsh argued that each new Senate could write its own procedural rules and did not have to abide by the rules of previous terms. These rules could be put in place with only a majority vote.

In 1957, then Vice President Richard Nixon wrote an opinion stating that the Constitution allows for the presiding officer of the Senate—the Vice President—to override Senate rules with subsequent rules put in place with only a majority vote. No action was taken on this written opinion.

The first Senator to use the term “nuclear option” was Trent Lott, a Republican from Mississippi. Lott coined the term during President George W. Bush’s first term after the Democrats blocked several of the President’s judicial nominees. Lott used the term because he recognized that it was a last resort and would probably result in negative consequences for both sides.

Bill Frist, a former heart surgeon and then senate Majority leader, threatened to use this nuclear option later in 2005 in hopes of ending Democratic filibusters of judicial nominees of

President Bush. A group of seven Democratic and seven Republican Senators, later referred to as the “Gang of 14,” joined to oppose both the nuclear option and the filibusters of judicial nominees except in rare circumstances. The seven Democrats agreed to vote for confirmation of most of the pending nominees and, in turn, the seven Republicans agreed to vote against the nuclear option. The Republicans in the Gang of 14 recognized that the Democrats might someday become the majority party in which case the Republicans would need the filibuster for unacceptable nominees of a Democratic president. Senator Frist agreed to honor this compromise.

Despite the long history looking to end the filibuster, it remained as a procedural option to block a presidential judicial nominee unless at least 60 senators supported him. Things finally changed in November 2013 when Harry Reid let the Senate vote to change the cloture rule. Senator Reid pushed for the nuclear option because of frustration with the Republicans who had blocked three of President Obama’s nominations to the United States Court of Appeals for the District of Columbia. By a 52 to 48 vote, the filibuster cloture requirement was changed for all nominations, except for justices of the Supreme Court, to only require a majority. All Republicans, the minority at that time, and three Democrats voted against the change. The three Democrats recognized that the change could dilute their power when the Republicans became the majority and they were right.

When Antonin Scalia died, President Obama nominated Merrick Garland to replace him on the Supreme Court. The Republicans held off on hearings for the nomination in hopes of winning the 2016 presidential election and then getting their own nominee. The Democrats, believing they would win the election, did not push for the necessary hearings thinking they would get their appointment when Hillary Clinton became president.

With the surprising win of Donald Trump, the Republican strategy turned out to be correct. Neil Gorsuch was nominated for the position and, predictably, the constitutional option was passed so that the Republicans could assure confirmation of the appointment. It was foreseeable that the Republicans would extend the option to include nominations to the Supreme Court when it became obvious they would not get cloture on the threatened filibuster. At least for now, any nomination for a judgeship in an Article III court, even a Supreme Court justice, will only need a majority vote in the Senate for confirmation.

With the politicization of judicial appointments, it is not surprising that some federal judges felt they had the power to block some executive orders and new laws with the injunction power until such time that the cases were litigated and appealed. Since the litigation could take years, they were effectively blocking the laws until a more favorable President could be elected.

This change in confirming justices for the Supreme Court and other Article III judges will have significant importance for health care providers as the constitutional questions of parts of the Affordable Care Act, such as the Independent Payment Advisory Board, and other health care related issues make their way to the Court. All health care providers need to stay informed to be better able to advocate for their patients’ best interest.