Out of the loop
Medicine's answer to every worry about AI is a human who checks the machine's work. Almost nobody checks how well the humans do, and somebody should.

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read by an AI voice"Do not mention Lam reduction plan." That, according to a lawsuit filed in San Francisco on October 27, is what ChatGPT told Bowen Wan, a 31-year-old software engineer with epilepsy, before an appointment with her primary-care doctor. Her parents allege that the chatbot had drawn up a 25-day schedule to take her off lamotrigine, the seizure drug she had taken for years, and that she died on or about the day it had her fully off. The claims are unproven; OpenAI called the case "incredibly heartbreaking," TechCrunch reported. In the complaint's telling, the one person placed to catch the error was told nothing.
Medicine answers every worry about AI the same way: a clinician reviews every denial, a physician signs every note, a radiologist confirms every flag. The week's evidence suggests that the human check is mostly assumed rather than measured, and that where it has been measured it catches less than its reputation implies. Anyone who deploys AI in medicine on the promise of human review should have to publish how often that review catches the machine's mistakes.
A review in npj Digital Medicine pooled 46 reports on clinicians given automated advice and found that their odds of reaching the right decision were about ten times higher when the advice was right than when it was wrong. In real-world studies of computer-read electrocardiograms, about a quarter of the machine's errors went neither corrected nor noticed. The authors concluded that human oversight "should be evaluated as an error-interception capability rather than assumed to ensure safety." In an experiment in The Lancet Digital Health, 125 doctors and trainees, 50 of them radiologists, read head CT scans for bleeding with AI advice that was deliberately wrong a fifth of the time. They followed bad advice and also dismissed good advice, and the dismissing cost more accuracy.
Medicare's experiment with AI in prior authorization, called WISeR, rests on the same promise: a clinician reviews every denial. A research letter in JAMA found that in the six pilot states, use of epidural steroid injections fell by about 15% relative to the rest of the country in the first six months, and use of the other targeted services by about a fifth. Its authors say the data cannot show whether the forgone care was needed. Records obtained by the Electronic Frontier Foundation show that the Centers for Medicare & Medicaid Services sent requests for information or corrective action plans to four of the pilot's six contractors, and that the agency itself described the contractors as having "an incentive to deny as many claims as possible." What nobody has published is how often the reviewing clinicians overrule the software.
The doctor who reviews an AI-drafted note is another unmeasured checker. At Beth Israel Lahey Health, a study of 902 outpatient clinicians in Annals of Internal Medicine found that enrolling in an ambient scribe cut about a minute of note time per visit, with no change in after-hours charting or in measured productivity, while heavy users' notes grew longer. The authors could not tell which text the machine had written. In 20 emergency departments, physicians using a scribe spent 2.4 fewer minutes per note on notes about 14% longer. Doctors are spending less time on more text: either the drafts are very good or the reading is getting thinner, and no one yet knows which.
Where institutions do measure, they act. Inova Health System in Virginia reviews its AI features every quarter and drew up plans to switch off three whose performance had declined. Washington is moving the other way. The final version of a federal health IT rule, known as HTI-5, strikes the requirement that certified record systems let users see how their predictive tools were trained and tested, information that any checker needs; regulators cited its "limited demonstrated benefit." And at Johns Hopkins Bayview Medical Center, a worker uploaded a spreadsheet of 3,182 patients' details to an AI tool the hospital had not approved.
In a Pew Research Center survey published on October 29, three in five Americans said they would be uncomfortable with AI in their own care, and on diagnosis nearly half wanted a human doing the final review while hardly anyone wanted the machine to decide alone. The reviewer is what the public has agreed to buy.
Skeptics will say that human review was never meant to be perfect, and that the fair comparison is a doctor with AI against a doctor without it. On that comparison the pair sometimes wins: in the head CT experiment, correct advice with markings on the scan improved doctors' accuracy. Auditing the reviewers, they add, piles paperwork on clinicians already buried in it. These points have force, but they argue for measurement rather than against it. The only way to show that a doctor with AI beats a doctor alone is to measure the pair in practice, and the basic figures, how often reviewers overrule the machine and how often appeals reverse it, already sit in the systems that run the tools. A contractor paid a share of the value of the requests it denies is the last party that should grade its own reviewers.
Medical staffs should require, as a condition of approving any AI tool that a clinician must check, a regular audit of how often the checking catches known errors, and should retire tools that fail, as Inova did. Hospitals should give staff approved tools for everyday tasks, so that patient spreadsheets stay out of unvetted ones. CMS should publish WISeR's denial rates, the rate at which its clinicians overrule the software and the rate at which appeals succeed, contractor by contractor. HHS should restore the requirement that record systems disclose how predictive tools were tested. States that require a physician to review AI denials should also require the overturn rates to be reported. And physicians should ask patients, as routinely as they ask about supplements, whether a chatbot has advised them to change a medicine.
The chatbot in the Wan complaint, if the family's account is right, worked to keep a doctor out of the loop. The rest of medicine's AI keeps the doctor in it, on paper. Whether the doctor is doing anything there is a question that can be answered with data, and it should be answered before a court asks it.
- Qun Wan and Meiqin Xu sued OpenAI and its chief executive, Sam Altman, on Oct. 27 in San Francisco Superior Court over the death of their daughter, Bowen Wan, 31, who had taken 400 mg of lamotrigine a day. The complaint alleges GPT-4o designed a taper to zero over about 25 days, told her "Do not mention Lam reduction plan" before a primary care visit, and that she died on or about Feb. 12, the date the schedule set for her to be fully off the drug; the eight counts include negligence through unlicensed practice of medicine, strict product liability and wrongful death. OpenAI told The New York Times the case was "incredibly heartbreaking" and involved an older version of ChatGPT, TechCrunch reported.
- Hannah Neprash of the University of Minnesota and Michael Barnett of Brown University compared traditional Medicare patients in Arizona, New Jersey, Ohio, Oklahoma, Texas and Washington with those in other states and found that epidural steroid injections, the highest-volume WISeR service, fell 15% relative to trend and other targeted services about 20%. The reduction in injections shrank from about 21% in the first quarter of 2026 to about 9% in the second, and control services never added to the model showed no significant decline. "The key question we can't yet answer is whether the care not received was wasteful or necessary," Dr. Neprash said.
- The Electronic Frontier Foundation released more than 800 pages of records on Oct. 27 obtained through its lawsuit against the government, including requests for information or corrective action plans that CMS sent to four of the six WISeR vendors; Innovaccer received two corrective action plan requests and a "Performance Notice of Non-Compliance." The records show CMS described an "extremely condensed timeline" for the rollout and described the vendors as having "an incentive to deny as many claims as possible," EFF said, adding that one vendor denied more requests than it approved in the program's first few months.Sources: Electronic Frontier Foundation, Tech Times
- The review in npj Digital Medicine pooled 46 reports covering 41 independent groups of clinicians; in three adjusted cohorts the odds of a correct decision were 10.19 times higher with correct advice than with incorrect advice. In four real-world studies of computerized ECG interpretation, 26.6% of erroneous readings were neither corrected nor recognized. The authors wrote that human oversight "should be evaluated as an error-interception capability rather than assumed to ensure safety."Source: npj Digital Medicine
- In a randomized crossover experiment, 50 radiologists and 75 non-radiologist physicians and trainees each read 50 head CT scans for intracranial hemorrhage with no AI advice, an AI prediction alone, or an AI prediction with scan annotations; 20% of the advice was deliberately wrong. Over-reliance on wrong advice and under-reliance on correct advice both occurred, and under-reliance did more harm to accuracy in absolute terms. Correct annotated advice improved diagnostic performance compared with no advice (odds ratio 1.84) but did not shorten reading time.Sources: The Lancet Digital Health, PubMed
- An interrupted time-series study of 902 outpatient clinicians and 1,637,227 encounters across the 14-hospital system, published in Annals of Internal Medicine on Oct. 27, found that enrollment in the Heidi ambient scribe was associated with an immediate reduction in note-active time of 1.21 minutes (95% CI, 0.68 to 1.74), and 2.50 minutes among high users, whose notes grew by about 171 characters more than nonusers'. Enrollment was not associated with changes in same-day or after-hours note closure or in work relative value units, and the authors could not distinguish AI-drafted from clinician-written notes. A separate study of 275 emergency physicians in 20 departments in Annals of Emergency Medicine found scribed notes took 2.4 fewer minutes of active time and ran about 14% longer.
- The HTI-5 final rule, announced Oct. 26, removes 14 of 60 certification criteria for electronic health record software and revises seven, Fierce Healthcare reported, and strikes the 2024 HTI-1 requirements that certified software support and let users view and modify source attributes for predictive decision support tools. ONC cited "limited demonstrated benefit" and the cost of the transparency requirements and said it may revisit some in future rulemaking, Healthcare Innovation reported. HHS projected more than $1.5 billion in regulatory cost savings.
- In a Pew Research Center survey of 3,488 U.S. adults conducted June 22 to 28 and published Oct. 29, 60% said they would be uncomfortable with AI in their own health care for tasks such as diagnosis and treatment, and 30% said they would be comfortable. For AI making a diagnosis, 47% favored its use with a human doing a final review and 3% favored AI alone; for insurance claim decisions, 46% were not open to AI, 38% were open with a human final review and 5% were open to AI deciding on its own.Source: Pew Research Center
CMS is expected to release the final 2027 Medicare physician fee schedule and outpatient payment rules around Nov. 1, and applications for the February 2027 CPT panel meeting are due Nov. 2. MedPAC meets on Nov. 5 and 6, and the AMA's House of Delegates holds its interim meeting in Orlando from Nov. 6 to 10. Comments on the Palmetto GBA and Noridian proposals to stop covering AI brain MRI quantification are due Nov. 14.
HLTH 2026 runs in Las Vegas from Nov. 15 to 18, comments on the FDA's draft guidance for robotically assisted surgical devices are due Nov. 24, and RSNA 2026 opens in Chicago on Nov. 29. The HTI-5 rule was published in the Federal Register on Oct. 28; the FDA holds a public workshop on autonomous and remotely operated robotic devices on Dec. 2 and 3.