60 AI Prompts for IME Physicians Reviewing Medical Records
Practical prompts to accelerate your medical record review while maintaining clinical accuracy and defensibility
Independent Medical Examinations demand precision. You're reviewing hundreds of pages, identifying causation, assessing impairment, and producing a report that will be scrutinized by opposing counsel. AI can accelerate this process—but only if you prompt it correctly.
These 60 prompts are organized by the actual workflow of an IME physician: from initial record triage through causation analysis, impairment rating, and report drafting. Each prompt is designed to extract clinically relevant information while flagging what needs your expert judgment.
Record Triage & Organization
1. Initial Record Assessment
Summarize the volume and types of medical records in this file.
List each provider, date range, and approximate page count.
Identify any obvious gaps in the treatment timeline.
2. Provider Timeline Construction
Create a chronological timeline of all healthcare providers seen by
this claimant. Include: provider name, specialty, first visit date,
last visit date, and primary reason for treatment.
3. Identifying Key Records
Which records in this file are most relevant to the claimed injury
date of [DATE]? List the documents that reference the incident
or immediate post-injury treatment.
4. Missing Records Detection
Based on the treatment timeline, what records appear to be missing?
Consider: referral patterns, typical diagnostic workup for this
injury type, and gaps between provider visits exceeding 30 days.
5. Duplicate Record Identification
Flag any records that appear to be duplicates. Compare: dates,
provider names, visit types, and clinical content. Do NOT flag
records that are true follow-up visits.
6. Pre-Injury Medical History Extraction
Extract all medical records dated BEFORE the claimed injury date.
Summarize: conditions treated, medications prescribed, healthcare
providers seen, and any relevant diagnostic findings.
7. Post-Injury Treatment Summary
Summarize all treatment received AFTER the claimed injury date.
Organize by: acute care (first 72 hours), subacute phase (weeks 1-6),
and chronic phase (beyond 6 weeks).
8. Referral Pattern Analysis
Map the referral pattern: who referred the patient to whom, when,
and for what stated reason? Identify any referrals that seem
clinically unusual or potentially unnecessary.
Clinical Content Extraction
9. Chief Complaint Tracking
Extract the chief complaint from each visit. Track how it evolves
over time. Note any discrepancies between documented complaints
and claimed disability.
10. Symptom Documentation
List every symptom documented in the medical records. Include:
date first reported, frequency of mention, severity descriptors,
and any changes over time.
11. Physical Examination Findings
Extract all physical examination findings. Organize by body system.
Highlight: objective findings (e.g., ROM measurements, reflexes),
subjective findings, and any inconsistencies across providers.
12. Diagnostic Test Results
Compile all diagnostic test results: imaging, lab work, nerve
conduction studies, etc. For each test, note: date, type, findings,
and who interpreted the results.
13. Medication History
Create a complete medication history. For each medication, include:
name, dosage, prescribing provider, start date, end date (if known),
and indication.
14. Procedure and Surgery History
List all procedures and surgeries. For each: date, procedure name,
provider, indication, complications (if any), and outcome.
15. Work Status Documentation
Extract all work status restrictions. Track: date, provider,
restrictions given, duration, and any changes over time. Note
any discrepancies between restrictions and functional capacity.
16. Pain Scale Tracking
Document every pain scale rating in the records. Note: date,
context (rest vs. activity), and any analgesic use at time of
rating. Track trends over time.
Causation Analysis
17. Mechanism of Injury Documentation
Extract all descriptions of the injury mechanism. Note: source
(patient report, witness statement, incident report), date of
documentation, and any inconsistencies between accounts.
18. Temporal Relationship Assessment
Analyze the temporal relationship between the claimed event and
onset of symptoms. Document: first symptom report, time lag
between event and treatment, and any pre-existing symptoms.
19. Pre-Existing Condition Identification
Identify any pre-existing conditions relevant to the claimed injury.
For each: condition name, evidence in pre-injury records, treating
provider, and whether it was symptomatic before the event.
20. Aggravation vs. Exacerbation Analysis
Based on the records, distinguish between: (1) new injury,
(2) aggravation of pre-existing condition, or (3) temporary
exacerbation. Cite specific clinical evidence for your conclusion.
21. Diagnostic Evidence for Causation
What diagnostic evidence supports or refutes causation? Consider:
imaging findings, objective clinical findings, and whether
diagnostics are consistent with the claimed mechanism.
22. Alternative Causation Hypotheses
Are there alternative explanations for the claimant's condition
besides the claimed event? Consider: degenerative changes,
pre-existing conditions, subsequent injuries, or non-organic factors.
23. Maximum Medical Improvement (MMI) Assessment
Based on the treatment records, when did the claimant reach
MMI? Cite: plateau in improvement, cessation of active treatment,
and any provider statements regarding prognosis.
Functional Capacity & Disability
24. Activities of Daily Living (ADL) Documentation
Extract all documentation of ADL limitations. Include: specific
activities affected, degree of limitation, source of information,
and any objective corroboration.
25. Employment History Analysis
Summarize the claimant's employment history. Include: job titles,
physical demands, dates worked, and reason for leaving each position.
Note any work-related injuries.
26. Functional Capacity Evaluation (FCE) Analysis
If an FCE was performed, summarize: date, type, results, and
validity indicators. Note any discrepancies between FCE findings
and clinical examination.
27. Work Restriction Reasonableness
Are the documented work restrictions clinically reasonable given
the objective findings? Identify any restrictions that lack
clinical justification or appear excessive.
28. Disability Duration Analysis
Calculate total duration of disability. Distinguish between:
total disability, partial disability, and able-to-work periods.
Note any discrepancies with treatment timeline.
29. Secondary Gain Indicators
Flag any potential secondary gain indicators in the records.
Consider: litigation history, disability applications, workers'
comp claims, and inconsistencies in symptom reporting.
Impairment Rating Preparation
30. Impairment Rating Methodology Selection
Based on the jurisdiction and injury type, which impairment rating
guides should be used? (AMA Guides 5th/6th, state-specific, etc.)
Cite the rationale for methodology selection.
31. Objective Findings for Impairment
List all objective clinical findings that can be used for
impairment rating. For each: cite the specific examination finding,
date, and which guide section applies.
32. ROM Measurements Compilation
Compile all range of motion measurements. Include: date, joint,
motion type, degrees, and examiner. Note any significant
variability between measurements.
33. Neurological Deficit Documentation
Document all neurological deficits. Include: type (sensory, motor,
reflex), distribution, severity, and objective evidence (EMG,
clinical exam).
34. Pain-Related Impairment Considerations
If pain is a component of impairment, document: location, severity,
chronicity, and whether it meets criteria for pain-related impairment
under the applicable guides.
35. Pre-Existing Impairment Calculation
Calculate any pre-existing impairment. Use pre-injury records to
establish baseline. Document methodology and apportionment rationale.
36. Maximum Impairment Assessment
What is the maximum impairment rating supported by objective
findings? Cite specific guide sections and clinical evidence.
Note any areas of clinical judgment.
Consistency & Credibility Analysis
37. Symptom-Consistency Check
Are the reported symptoms consistent with the objective findings
and diagnosed condition? Flag any inconsistencies between subjective
complaints and clinical evidence.
38. Cross-Provider Consistency
Compare clinical findings across different providers. Identify:
consistent findings, inconsistent findings, and findings that
appear or disappear without explanation.
39. Waddell Sign Assessment
Document any positive Waddell signs or other non-organic physical
findings. Note: which signs, when observed, by whom, and clinical
context.
40. Symptom Magnification Indicators
Flag any indicators of symptom magnification. Consider:
inconsistent examination findings, disproportionate pain behavior,
and discrepancies between reported and observed function.
41. Treatment Compliance Analysis
Assess treatment compliance. Document: missed appointments,
non-compliance with recommendations, and any patterns of
treatment-seeking behavior.
42. Return-to-Work Barriers
What barriers to return-to-work are documented? Distinguish
between: medical barriers, psychological barriers, and
non-medical barriers (e.g., job availability, employer issues).
Report Drafting Assistance
43. Executive Summary Draft
Draft a one-paragraph executive summary of this IME. Include:
injury date, diagnosis, causation opinion, current functional
status, and impairment rating (if applicable).
44. History of Present Illness Section
Draft the History of Present Illness section. Include: mechanism
of injury, immediate symptoms, treatment timeline, and current
status. Cite specific records for each fact.
45. Past Medical History Summary
Summarize the Past Medical History. Organize by: relevant
pre-existing conditions, prior injuries, surgeries, and current
medications. Note relevance to claimed injury.
46. Physical Examination Findings Section
Draft the Physical Examination Findings section. Include:
general appearance, vital signs, and system-specific findings.
Distinguish between objective and subjective findings.
47. Diagnostic Studies Summary
Summarize all diagnostic studies. For each: date, type, findings,
and clinical significance. Note any studies that were recommended
but not performed.
48. Causation Opinion Formulation
Draft the causation opinion section. State: whether the condition
was caused by, aggravated by, or unrelated to the claimed event.
Cite specific evidence supporting this opinion.
49. Functional Capacity Opinion
Draft the functional capacity opinion. State: current work
capacity, specific restrictions (if any), and whether restrictions
are temporary or permanent.
50. Impairment Rating Explanation
Draft the impairment rating explanation. Include: methodology used,
specific findings rated, calculations, and final whole person
impairment percentage.
51. Prognosis Statement
Draft the prognosis statement. Include: expected course, potential
for further improvement, anticipated treatment needs, and any
factors affecting prognosis.
52. Recommendations Section
Draft the recommendations section. Include: further diagnostic
studies, treatment recommendations, work restrictions, and
follow-up timeline.
Quality Assurance & Review
53. Citation Verification
Verify that every clinical statement in the draft report has a
corresponding citation to the medical records. Flag any
uncited statements.
54. Opinion Consistency Check
Review the draft report for internal consistency. Check: do the
opinions align with the documented findings? Are there any
contradictions between sections?
55. Defensibility Review
Review the draft report for defensibility. Consider: Are all
opinions supported by evidence? Are alternative explanations
addressed? Is the reasoning clear?
56. Missing Information Flag
What critical information is missing from the records that would
strengthen or clarify the IME opinion? List specific documents
or diagnostic studies needed.
57. Cross-Examination Preparation
Prepare for potential cross-examination questions. Identify:
weak points in the opinion, alternative interpretations of the
evidence, and areas where clinical judgment was required.
58. Peer Review Checklist
Generate a peer review checklist for this IME report. Include:
methodology verification, citation accuracy, opinion support,
and compliance with standards.
59. Report Completeness Audit
Audit the report for completeness. Check: all required sections
present, all records reviewed cited, all opinions stated, and
all recommendations clear.
60. Final Quality Check
Perform a final quality check. Verify: spelling of claimant name,
accuracy of dates, correct impairment calculations, and consistency
of terminology throughout the report.
How to Use These Prompts Effectively
Best Practices:
- Start with Triage — Use prompts 1-8 to organize the file before diving into clinical analysis
- Extract Systematically — Work through prompts 9-16 to build your clinical foundation
- Apply Clinical Judgment — Prompts are tools, not replacements for your expertise
- Verify Everything — Always cross-check AI output against the original records
- Document Your Reasoning — Use prompts 43-52 to draft, then refine with your clinical voice
What AI Cannot Do:
- Replace your clinical examination of the claimant
- Make the final causation determination
- Apply clinical judgment to borderline findings
- Assess credibility during the face-to-face interview
- Sign the report and take professional responsibility
What AI Does Well:
- Rapid extraction of clinical data
- Pattern recognition across large record sets
- Timeline construction and gap identification
- Drafting structured report sections
- Citation verification and cross-referencing
The Bottom Line
These prompts accelerate the mechanical aspects of IME record review—extracting data, organizing timelines, and drafting structured sections. But the core of an IME remains your clinical expertise: examining the claimant, interpreting findings in context, and rendering opinions you can defend under cross-examination.
Use AI as a force multiplier, not a replacement. Your signature on that report means you stand behind every word.
Need help implementing AI in your IME practice? Contact us to discuss workflow integration that maintains clinical accuracy and defensibility.
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