Author: Mel Harris

Next Generation Physicians are Using Augmented Intelligence: Is the Law Ready? 

What if a physician working alone at night in a rural hospital could summon a tireless “Dr. House” with every difficult case; a trained medical diagnostician that is always awake, ever ready, and rarely hallucinates?

Interactive artificial intelligence (AI) diagnostic models are rapidly evolving beyond ChatGPT and traditional “black box” systems that opaquely analyze radiology scans or lab values to higher-order transparent language models capable of intelligent explanation and diagnosis of complex illnesses. Researchers at Harvard Medical School recently developed an AI system named “Dr. CaBot” that will eventually function as a digital peer capable of generating differential diagnoses and detailed reasoning processes. As medical schools from Harvard to the University of Miami train tomorrow’s physicians to problem solve using science, clinical judgment, pattern recognition, and logic, educators are embracing a novel resource to strengthen their students’ skills. The American Medical Association (AMA) uses the phrase “augmented intelligence” as a way to conceptualize AI’s assistive role, emphasizing the way the tools enhance human intelligence rather than replace it. 

Technology and medicine are moving quickly, and the legal field has yet to catch up; innovation, in many cases, has spread faster than stare decisis. While attorneys await new rules, advancements in AI and machine learning pose greater risks and rewards for the healthcare sector than many other applications, rivaled only by risks incurred by the defense industry. 

Evolving Liability Frameworks 

As patients navigate an increasingly automated health care ecosystem where many insurance determinations are made by algorithms and 66% of clinicians integrate Artificial Intelligence/Machine Learning (AI/ML) tools—new questions around liability and standards of care will emerge. When harm occurs as a result, does the law look to the software developer who wrote the code, the healthcare system that deployed it, or the physician who ultimately incorporated the technology into their clinical decision making? Is the use of assistive-AI any different than orthostatic vital signs in the hands of a skilled practitioner who interpreted the readings correctly vs. incorrectly?

The incorporation of advanced AI diagnostics into patient care has created a patchwork of legal and regulatory challenges across the nation. Currently, the FDA classifies AI/ML technologies in healthcare settings under “Software as a Medical Device (SaMD)” guidance in an attempt to bring AI tools under medical device and products liability regulations. However, a framework intended for the development of a static medical device that may suffer manufacturing, design, or warning defects was not created for a quickly moving target such as an AI tool which can learn and evolve over time. 

The SaMD classification gives AI/ML diagnostic tools a form of FDA preemption that complicates malpractice and products liability claims under state law. For example, when a legacy device, such as an insulin pump or glucometer for a diabetic patient, receives FDA clearance under the 21 U.S.C. § 360k, the manufacturer may introduce a new product to the market, subject to certain risk-mitigation measures. In Dickson v. Dexcom, for example, a “Class II: De Novo” authorization shielded the manufacturer from tort liability when a continuous glucose monitor failed to warn a patient of hypoglycemia, which led to a motor vehicle accident. Many AI diagnostic tools are entering the market under this same “device” classification, making it critical for doctors and administrators to understand the regulatory landscape and potential exposure before deployment.

Duty to Disclose in Clinical Practice 

In addition to understanding state and federal liability frameworks, there is growing discussion around disclosure and transparency related to the use of AI in diagnostic processes. Because the use of AI/ML is closely associated with protected health information (PHI) and broader risks, California, Colorado, and Utah, have created laws that mandate disclosure in clinical treatment. For providers, and the attorneys who represent them, this is often a state-specific discussion: Texas laws require providers to disclose AI use in clinical care, whereas Nevada prohibits providers from utilizing AI systems in behavioral health contexts. 

Where state law is silent on the issue, physicians should remain vigilant around efforts to obtain valid informed consent regarding use of AI in clinical settings, as state medical boards ultimately hold physicians accountable for disclosures and outcomes related to the integration of novel tools into diagnosis and treatment plans.

Regardless of jurisdiction, research shows that patients value connection with physicians, and when visiting a healthcare practice, they expect to consult with a doctor. Few people expect their provider to sidebar with ChatGPT or even a purpose-built OpenAI language model that can rule out hundreds of mystery illnesses sans implicit bias—although Augmented Intelligence may ultimately solve the problem. Similarly, when harm occurs, current medical malpractice remedies were built around the assumption of human negligence instead of errors arising from machine learning misinformation.

Moving Forward

Legal scholars stand at the nexus of healthcare liability and AI/ML diagnostics where case law is yet to be written. Can plaintiffs’ attorneys establish vicarious or joint and several liability when claims involve an AI developer and a health system? What remedy exists when a physician outsources clinical judgment to a trained language model or fails to scrutinize results? As a net benefit, will the predictive powers of AI diagnostic models decrease both primary care-to-specialist patient wait times, and the risk of human error?

It appears that emerging physicians have embraced the next “possibility model” in medicine—and the health law community must respond by establishing guidance to address outstanding questions related to liability, reliability, governance, consent, and privacy. Perhaps tomorrow’s attorneys can ask AI for guidance.

Authors Note: Some healthcare providers and policymakers now prefer the term “misinformation” over “AI hallucination” in an effort to avoid stigmatizing mental health conditions.

A Crisis of Accountability: Medical Neglect and Preventable Deaths in Immigration Detention

On September 14, 2025, Hasan Ali Moh’D Saleh, a lawful permanent resident, was arrested by Immigration and Customs Enforcement (ICE) and transferred to Krome Detention Center in Miami, Florida for removal proceedings. On October 10th, Saleh was transported to Larkin Community Hospital due to a fever; the next day, he was dead.

As immigration raids take place in front of cameras across the country, an unseen crisis has developed behind heavily guarded gates. With the escalation of Immigration and Customs Enforcement-Related Operations (ERO) in the United States under the second Trump Administration, there is mounting public outcry and a flurry of legal challenges concerning the lack of due process regarding the arrests of undocumented migrants, asylum seekers, and green card holders like Mr. Saleh. Conflicting narratives have emerged between advocates and authorities regarding the safety and welfare of individuals detained in ICE-related actions. 

As of September 2025, the Trump Administration is holding nearly 60,000 immigrants in ICE detention facilities around the country, not including those held by local authorities under detainer requests from ICE. Seven in ten people detained have no criminal convictions; the majority are working age adults who deny serious medical complaints at intake. Even so, detainees are dying in custody at record speed, most often due to illness, according to reports made public by ICE. 

The agency maintains that relevant details linked to ERO-related deaths are published on its website within two days. However, the “relevant details” connected to the demise of immigrants like Mr. Ismael Ayala-Uribe at age 39 are often cloudy. According to ICE records, Uribe was arrested on August 17th, 2025. On September 18th, nurses noted that Mr. Uribe was in “10 out of 10 pain” near his anus, so a physician ordered a pain reliever and fiber. By September 21st, he was vomiting, sweating, and his heart rhythm was abnormal, having deteriorated to the point that medical staff needed to transfer him to a local hospital. The ICE press release, replete with an account of Uribe’s crimes, arrests, and his DACA status, states that early on September 22nd, he became unresponsive and died.

In the landmark Supreme Court case, Estelle v. Gamble, the Court found that such unnecessary suffering is inconsistent with contemporary standards of decency, codifying the common law view that “[we are] required to care for the prisoner who cannot by reason of the deprivation of his liberty, care for himself.” Given the inmate’s complete reliance on staff for medical treatment, the Court explained that the “deliberate indifference to serious medical needs” constitutes the infliction of cruel and unusual punishment involving the “unnecessary and wanton infliction of pain” forbidden by the Eighth Amendment. The Court further held that such neglect by prison doctors and guards can result in torture or lingering death, and in less severe instances, cause unnecessary pain and suffering which serves no legitimate penological purpose.

Legislators have worked to gain oversight of detention centers for the purpose of investigating welfare complaints and medical standards in settings where patients do not have the autonomy to make informed decisions about their healthcare. NPR received a rare look inside ICE facilities via inspection reports from experts hired by The Department of Homeland Security. In the findings from 2017-2019, inspectors cited negligent medical care that, in some cases, contributed to detainee deaths. 

One inspection revealed that in the Calhoun County Correctional Center, a man in ICE custody was sent into general population with an open wound from surgery and no bandaging, even though he still had surgical drains in place. Jesse Dean, a detainee at the same facility, was never referred to a physician although he had been unable to eat, lost almost 20 pounds in a short time, and suffered from severe nausea; he died in custody from an undiagnosed gastrointestinal hemorrhage.

A joint study published by American Oversight revealed that the overwhelming majority of incidents such as Dean’s could have been prevented if ICE detention medical staff had provided timely and clinically appropriate medical care to include correct, appropriate, and complete diagnoses for detained immigrants.

After 2020, loss of life in ICE custody attributed to chronic or acute medical conditions declined, and spiked recently in correlation to Trump-mandated mass ERO’s:

As ICE arrests surge, concern continues to grow over rising morbidity and mortality rates in immigration detention centers, along with the absence of accountability or consequences for responsible parties. While an analysis of factors contributing to preventable detainee medical deaths cannot cure those who are no longer alive, an honest post-mortem inquiry into systemic failures is vital in order to safeguard the living.