Creates structured dental procedure notes with tooth-specific documentation and material specifications. Use when documenting dental procedures, recording treatment details, or creating dental records.
Standardmäßig ist der Prompt ausgewählt, der zuerst die Quelle prüft. Sie können zu einem direkten Befehl wechseln oder eine lokale Kopie herunterladen.
Quelldateien prüfen
Lesen Sie SKILL.md und alle von SkillsMP angezeigten Begleitdateien, bevor Sie sich für eine Installation entscheiden.
Mit Codex oder Claude installieren Kopieren Sie diesen Prompt, fügen Sie ihn in Codex, Claude oder einen anderen Assistant ein und lassen Sie die Skill-Seite prüfen und installieren.
Ein direkter Befehl überspringt den Prüf-Prompt. Prüfen Sie die Quelle, bevor Sie ihn ausführen.
Creates structured dental procedure notes with tooth-specific documentation and material specifications. Use when documenting dental procedures, recording treatment details, or creating dental records.
Creates structured dental procedure notes with tooth-specific documentation, material specifications, CDT code justification, and medicolegal defensibility per ADA record-keeping standards.
Why This Skill Exists
Dental procedure documentation is simultaneously a clinical communication tool, a legal record, and an insurance billing justification. Incomplete notes—missing anesthetic type, omitting material lot numbers, failing to record intraoperative complications—result in claim denials, failed peer review audits, and indefensible malpractice positions. This skill enforces procedure-specific documentation standards that satisfy clinical, legal, and third-party payer requirements, ensuring every note could withstand a chart audit, insurance review, or legal discovery request.
Checkpoint A — Pre-Documentation Verification
Required Inputs
Approved treatment plan with CDT code and tooth/surface designation for the procedure
Current medical history reviewed and confirmed on the day of service
Informed consent signed for the specific procedure
Anesthetic record (type, concentration, vasoconstrictor, cartridges administered, aspiration result)
Material specifications available (composite shade, cement type, implant system and lot number)
Intake Questions
Has the patient confirmed no changes to medical history or medications since last review?
Is the signed informed consent form for this specific procedure in the chart?
Are pre-operative radiographs current and available for reference?
Has the treatment plan CDT code been verified against the actual procedure to be performed?
Are all materials and their lot numbers available for documentation?
For sedation cases, has the pre-sedation assessment been completed?
Step 1 — Procedure Header
Every procedure note begins with standardized header elements.
Date of service: Full date (MM/DD/YYYY) with appointment start and end time
Provider identification: Treating dentist name, license number, and supervising dentist if performed by a hygienist or assistant under supervision
Tooth identification: Universal numbering (1–32 or A–T); specify surface(s) using MODBL convention
CDT code: Current-year code with full descriptor; if narrative is required for the code, include it
Diagnosis justification: Link the procedure to the diagnosis from the treatment plan (e.g., "D2391 — posterior composite, tooth #30 MOD, for diagnosis of caries extending into dentin on mesial and distal surfaces")
Pre-operative condition: Document the tooth's condition before treatment (e.g., "existing DO amalgam with recurrent caries at distal margin, tooth vital, no symptoms")
Step 2 — Anesthesia Documentation
Record anesthetic administration in standardized format.
Anesthetic type and concentration: e.g., 2% lidocaine with 1:100,000 epinephrine, 4% articaine with 1:100,000 epinephrine, 3% mepivacaine (plain)
Volume: Number of cartridges (1.7 mL or 1.8 mL per cartridge) and total mL administered
Injection technique: Inferior alveolar nerve block (IANB), posterior superior alveolar (PSA), middle superior alveolar (MSA), anterior superior alveolar (ASA), infiltration, intraligamentary, intrapulpal
Aspiration result: Positive or negative; if positive, document repositioning and re-aspiration
Topical anesthetic: Type and location of application (e.g., 20% benzocaine gel applied to buccal mucosa adjacent to #30)
Step 3 — Procedure Narrative
Document the step-by-step execution of the clinical procedure.
Isolation method: Rubber dam (record anchor tooth and clamp type), Isolite, cotton roll isolation, dry angles
Preparation details: For restorative — cavity preparation dimensions, caries removal technique (conventional rotary, air abrasion, chemo-mechanical), pulp proximity, liner/base placement (material and reason)
Material specification: Product name, manufacturer, shade (e.g., Vita A2), lot number, expiration date for implants and bone grafts per FDA tracking requirements
Technique details: Layering technique for composites, bonding system (total-etch, self-etch, universal), light curing time and unit, cement type for crowns, suture material and pattern for surgical cases
Intraoperative findings: Caries deeper than anticipated, pulp exposure (size, bleeding, treatment), crack propagation, unexpected anatomy, bone quality during implant placement
Intraoperative decisions: Document any deviation from the treatment plan and clinical rationale (e.g., "planned MO composite; extended to MOD due to distal marginal ridge caries found during preparation")
Hemostasis: Method and result for surgical procedures (direct pressure, electrocautery, hemostatic agents, suturing)
Step 4 — Post-Operative Documentation
Record completion status and immediate post-procedure findings.
Occlusal adjustment: Verified with articulating paper; premature contacts eliminated in centric and excursive movements
Post-operative radiograph: Taken when indicated (endodontic fill quality, implant position, extraction socket assessment); describe findings
Margins and contacts: Restoration margins evaluated with explorer; interproximal contacts verified with floss (acceptable resistance)
Patient condition at dismissal: Alert, oriented, vital signs stable (for sedation cases); bleeding controlled; no immediate complications
Complications: Document any that occurred; patient notification documented; management steps taken
Step 5 — Post-Operative Instructions and Follow-Up
Document instructions given and follow-up plan.
Instructions provided: Written post-operative instructions given to patient covering pain management, diet, activity, wound care, and warning signs requiring emergency contact
Prescriptions: Medication name, dose, frequency, quantity, refills; document rationale (e.g., "amoxicillin 500 mg TID × 7 days for post-surgical infection prophylaxis")
Follow-up appointment: Date and purpose (e.g., "return in 2 weeks for suture removal and healing assessment")
Referrals: If procedure revealed need for specialist consultation, document referral with urgency and clinical rationale
Restrictions: Specific limitations (e.g., "no chewing on right side for 24 hours," "soft diet for 1 week following surgery")
Step 6 — CDT Code Reconciliation
Verify that the documented procedure matches the billed code.
Code-procedure match: Confirm the CDT code accurately reflects what was clinically performed, not what was treatment-planned if a deviation occurred
Narrative support: For codes requiring narrative (pre-authorizations, appeals), confirm the note contains sufficient clinical detail
Bundling compliance: Verify no unbundling violations (e.g., separate billing for liner included in restoration code, separate billing for hemostasis included in surgical code)
Modifier or alternate codes: Document if procedure was started but not completed, if additional complexity justified an upgraded code, or if a planned procedure was converted to a different procedure
Checkpoint B — Documentation Completeness Review
Before signing the note, verify:
Tooth number, surface(s), and CDT code are correct and consistent throughout the note
Anesthetic type, volume, technique, and aspiration documented
Materials documented with product names and lot numbers (where required)
Intraoperative findings and any deviations from treatment plan documented with rationale
Post-operative condition and any complications recorded
Post-operative instructions documented as given to patient
Prescriptions recorded with dose, frequency, quantity, and rationale
Follow-up plan documented with date and purpose
CDT code matches the procedure actually performed
Note is signed with provider name, credentials, date, and time
Quality Audit
#
Audit Item
Pass Criteria
1
Procedure identification
Tooth number, surfaces, and CDT code present and consistent
2
Consent documented
Signed consent for this specific procedure in chart
3
Anesthesia complete
Type, volume, technique, and aspiration all recorded
4
Materials tracked
Product name, manufacturer, lot number documented for trackable materials
5
Intraoperative narrative
Step-by-step procedure documented, not just outcome
6
Complications addressed
Any complications documented with management and patient notification
7
Post-op instructions
Written instructions given and documented in note
8
CDT code accuracy
Billed code matches documented procedure
9
Follow-up scheduled
Next appointment date and purpose documented
10
Signature complete
Provider name, credentials, license number, date, and time
Guidelines
Document procedure notes on the same day as the service; never defer to the next business day
Use ADA-standard tooth numbering (Universal 1–32, A–T) and surface notation (MODBL) throughout
Material lot numbers are mandatory for implants, bone grafts, membranes, and any FDA Class II/III devices per 21 CFR Part 821
Every deviation from the treatment plan must be documented with clinical rationale at the point of deviation
Do not use abbreviations that are ambiguous or non-standard; maintain an office-approved abbreviation list per ADA recommendation
For procedures performed under supervision, document the supervising dentist's name, level of supervision (direct, indirect, general), and supervisory review
Informed consent must be procedure-specific; a general consent-to-treat does not substitute for procedure-specific consent for invasive procedures
If a patient declines recommended treatment or leaves against advice, document using direct patient quotes and [PATIENT DECLINED] tag
Notes must be legible, unalterable after signing (EHR audit trail), and available for peer review, legal discovery, or insurance audit within the retention period required by state law (typically 7–10 years, longer for minors)