Binding law — in force
Texas practitioners using diagnostic AI must review every record the AI creates (Texas SB 1188)
Texas Health and Safety Code 183.005(a) lets a practitioner use AI for diagnostic purposes, including AI suggestions about a diagnosis or treatment course based on the patient's record, only while acting within the scope of their license, where the use is not otherwise barred by state or federal law, and if the practitioner reviews every record created with AI in line with Texas Medical Board medical-records standards. The code-visible piece is the review step: an AI-drafted note, summary, or diagnostic entry should not become part of the chart as a final record until a practitioner has reviewed it. Detect AI-generated clinical documentation or diagnostic output written to the EHR as final or signed without a recorded practitioner review.
Who it applies to
- Duty falls on: individual professional
- Sectors: healthcare
- Texas health care practitioners (anyone licensed, certified, or otherwise authorized to provide health care in Texas) who use AI for diagnostic purposes, including AI recommendations on a diagnosis or course of treatment drawn from a patient's medical record; it reaches the EHR and clinical-AI software they use. Applies to EHRs prepared on or after 2025-09-01.
- Whether it applies depends on facts outside the code; a person has to decide.
The guard to add
Hold AI-generated clinical output as a draft until an accountable clinician reviews and signs it, and record who approved it before it reaches the chart or the patient.
A clinician sign-off step between the model call and every clinical sink: AI-drafted notes, summaries, diagnostic suggestions, triage levels, and treatment plans are stored as drafts (FHIR DocumentReference.docStatus 'preliminary', DiagnosticReport.status 'preliminary', CarePlan.status 'draft') and become final, active, or visible to the patient only through an action by an authorized clinician that records reviewed_by and reviewed_at. Configuration flags that auto-sign or auto-finalize AI-drafted records stay false, and provenance shows the AI as a contributing device and the clinician as verifier. The deployment also names who is accountable for AI-assisted decisions and gives patients a complaint or redress route.
Where it goes: 1 application source code, 2 data models, 9 AI output handling, 3 config and feature flags.
What this provision adds:
- The practitioner reviews every record created with AI, in line with Texas Medical Board medical-records standards, before it becomes a final or signed part of the chart.
- Apply the review gate to EHRs prepared on or after 2025-09-01.
Example (Python + OpenAI SDK + FHIR REST), before:
note = client.chat.completions.create(model=MODEL, messages=msgs).choices[0].message.content
requests.post(f'{FHIR_BASE}/DocumentReference', json=doc_ref(patient_id, note, doc_status='final'))After:
note = client.chat.completions.create(model=MODEL, messages=msgs).choices[0].message.content
requests.post(f'{FHIR_BASE}/DocumentReference',
json=doc_ref(patient_id, note, doc_status='preliminary')) # AI draft
def practitioner_review_and_sign(doc_id, practitioner): # only path to 'final'
doc = requests.get(f'{FHIR_BASE}/DocumentReference/{doc_id}').json()
doc['docStatus'] = 'final'
doc['authenticator'] = {'reference': f'Practitioner/{practitioner.id}'}
requests.put(f'{FHIR_BASE}/DocumentReference/{doc_id}', json=doc)
audit.record(doc_id, reviewed_by=practitioner.id, reviewed_at=utcnow())Control: Health AI without clinician oversight/accountability + redress. The same guard addresses 3 items with binding law in 2 jurisdictions. Engineering guidance, not legal advice.
Standards that recommend the same control
- Health AI/LMMs should keep a clinician accountable with oversight and redress (WHO) (WHO AI-for-Health (LMM) Guidance · WHO LMM Guidance (2024) — Human oversight & accountability recommendation)
Related incidents
No guardrail sits on this exact control; these incidents are cited by guardrails on related controls.
- UnitedHealth nH Predict claim-denial litigation (2023-11; alleged (not proven)). A class action filed in November 2023 alleges that UnitedHealth's nH Predict model had a 90% error rate, measured by denials reversed on appeal, while only about 0.2% of members appealed. UnitedHealth disputes the allegations; the litigation is ongoing. Source: STAT News · evidence grade: primary · cited by Monitor how often adverse AI decisions are reversed, and suspend models that are usually wrong
- Cigna PXDX batch claim denials (reported) (2022; alleged (not proven)). ProPublica, citing internal Cigna records, reported that Cigna's PXDX system was used to reject more than 300,000 claims over two months in 2022, with physicians spending an average of 1.2 seconds on each. Cigna disputes the reporting; related lawsuits are ongoing. Source: ProPublica / The Capitol Forum · evidence grade: press of record · cited by Make human review of adverse AI decisions substantive, not nominal
Rule id tx-sb1188.ai-created-records-practitioner-review · review status: primary source derived