Pain Management: Step-by-Step Guide on How to Write SOAP Notes
Updated January 2026
Pain management documentation is among the most scrutinized in healthcare, requiring meticulous attention to regulatory compliance, risk assessment, and treatment justification. With evolving opioid prescribing guidelines, PDMP requirements, and DEA regulations, pain management SOAP notes must demonstrate clinical reasoning, document informed consent, and support the appropriateness of treatment decisions. This guide provides comprehensive instructions for documenting pain management encounters in compliance with federal and state regulations.
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Unique Aspects of Pain Management Documentation
Pain management documentation differs from other specialties due to heightened regulatory scrutiny and the complexity of chronic pain care:
- Regulatory Compliance: Must align with DEA requirements, state PDMP laws, and CDC opioid prescribing guidelines
- Risk Stratification: Mandatory documentation of opioid risk assessment tools (ORT, SOAPP-R, DIRE)
- PDMP Review: Required documentation of prescription drug monitoring program checks
- Opioid Agreements: Treatment contracts and informed consent for controlled substances
- Urine Drug Testing: Documentation of monitoring protocols and results interpretation
- Multimodal Treatment: Evidence that non-opioid and non-pharmacologic treatments are utilized
- Functional Assessment: Tracking functional improvement, not just pain scores
- Medical Necessity: Clear justification for continued opioid therapy
2026 Regulatory Framework
CDC Clinical Practice Guideline for Prescribing Opioids (2022, Updated)
Per the CDC Opioid Prescribing Guideline:
- Nonpharmacologic and nonopioid therapy are preferred for chronic pain
- Establish treatment goals before starting opioid therapy
- Start low, go slow: Use lowest effective dose
- Evaluate benefits and harms within 1-4 weeks of starting opioids
- Assess risk using validated tools before and during therapy
- Check PDMP before prescribing and periodically during treatment
- Use urine drug testing before starting and at least annually
- Avoid concurrent benzodiazepine prescribing when possible
- Offer naloxone when prescribing opioids to high-risk patients
DEA Controlled Substance Requirements
Per 21 CFR Part 1306 - DEA Prescribing Rules:
- Schedule II prescriptions require written prescription (electronic prescribing for controlled substances - EPCS - is permitted)
- No refills allowed for Schedule II medications
- Legitimate medical purpose and course of professional practice must be documented
- Prescriber must have valid DEA registration
- Patient relationship must be established
CMS 2026 Opioid-Related Requirements
Per CMS 2026 Physician Fee Schedule:
- Pain management services documentation must support medical necessity
- Prior authorization requirements for certain opioid prescriptions
- Opioid treatment program (OTP) documentation requirements
Subjective Section (S)
The Subjective section in pain management requires comprehensive pain characterization, functional impact assessment, and risk factor documentation.
Subjective Section (S) Components
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Chief Complaint:
- Primary pain complaint with duration
- Treatment context (initial evaluation vs. follow-up)
- Example: "Follow-up for chronic low back pain management, 15 years duration"
-
Comprehensive Pain Assessment (PQRST):
- P - Provocative/Palliative: What makes pain worse or better
- Q - Quality: Character of pain (burning, aching, sharp, stabbing, throbbing)
- R - Region/Radiation: Location and radiation pattern
- S - Severity: Current, best, worst, average pain scores (0-10)
- T - Timing: Onset, duration, frequency, constant vs. intermittent
- Example: "Constant aching low back pain, 6/10 currently (worst 9/10, best 4/10), radiating to left posterior thigh, worse with prolonged standing, improved with rest and medication"
-
Functional Impact Assessment:
- Activities of daily living (ADLs)
- Instrumental ADLs (work, driving, housework)
- Sleep quality
- Mood and relationships
- Work/disability status
- Example: "Pain limits standing to 15 minutes, unable to work as electrician, sleeping 4-5 hours/night with frequent awakenings"
-
Current Pain Treatment Regimen:
- All pain medications (opioids, non-opioids, adjuvants)
- Dosages, frequency, adherence
- Effectiveness and side effects
- Example: "Oxycodone 10mg q6h PRN (taking 3-4 tablets daily), gabapentin 300mg TID. Reports 50% pain relief. Mild constipation managed with docusate."
-
Treatment History:
- Prior medications tried and outcomes
- Interventional procedures performed
- Physical therapy and other non-pharmacologic treatments
- Surgical history related to pain condition
- Example: "Failed trials of NSAIDs (GI upset), tramadol (inadequate relief). Completed 12 weeks PT with minimal improvement. L4-L5 laminectomy 2018 with temporary improvement."
-
PDMP Review Discussion:
- Acknowledgment that PDMP was reviewed
- Discussion of any concerns identified
- Per state PDMP requirements
- Example: "PDMP reviewed on [date]. Patient receiving controlled substances only from this practice. No concerning patterns identified."
-
Risk Assessment Tools:
- Opioid Risk Tool (ORT) score
- Screener and Opioid Assessment for Patients with Pain (SOAPP-R)
- DIRE Score (if applicable)
- Example: "ORT Score: 7 (moderate risk). SOAPP-R: 12 (low risk)."
-
Substance Use History:
- Current and past alcohol use (quantity, frequency)
- Tobacco use
- Illicit drug use history
- Personal and family history of substance use disorders
- Example: "Denies current illicit drug use. History of alcohol use disorder, in recovery x 8 years. Family history of opioid use disorder (brother)."
-
Mental Health Screening:
- Depression screening (PHQ-2/PHQ-9)
- Anxiety screening (GAD-2/GAD-7)
- History of psychiatric conditions
- Example: "PHQ-9: 8 (mild depression). Reports chronic pain has negatively impacted mood. Seeing therapist monthly."
-
Safety Assessment:
- Suicidal ideation screening
- Access to firearms
- Safe medication storage
- Example: "Denies SI/HI. Medications stored in locked cabinet away from grandchildren."
-
Medication Agreement Compliance:
- Adherence to opioid treatment agreement
- Early refill requests
- Lost/stolen medication reports
- Example: "Compliant with opioid agreement. No early refill requests. Brings pill count to each visit."
Example Subjective Section for Pain Management
Objective Section (O)
The pain management Objective section documents physical examination findings, vital signs, urine drug testing results, and observational assessments for signs of medication misuse.
Objective Section (O) Components
-
Vital Signs:
- Blood pressure (important for pain assessment and medication effects)
- Heart rate
- Weight (for medication dosing and monitoring)
- Pain score (per facility protocol)
- Example: "BP 132/78, HR 72, Weight 195 lbs (stable), Pain 5/10"
-
General Appearance and Behavior:
- Level of distress
- Affect and demeanor
- Signs of sedation or intoxication
- Gait observation
- Example: "Alert, well-groomed, no acute distress. Normal affect. Ambulates with antalgic gait favoring left. No signs of sedation."
-
Pain-Focused Physical Examination:
- Inspection (posture, guarding, swelling)
- Palpation (tenderness, muscle spasm)
- Range of motion (with pain behavior notation)
- Neurological examination (strength, sensation, reflexes)
- Special tests relevant to condition
- Example: "Lumbar spine exam: Tenderness L4-L5 paraspinals bilaterally, left > right. Positive straight leg raise left at 45 degrees. L5 dermatomal hypesthesia left."
-
Functional Assessment:
- Observed functional capacity
- Gait analysis
- Ability to rise from chair, get on exam table
- Example: "Able to walk to exam room without assistance. Uses arms to rise from chair. Can heel-walk and toe-walk with mild difficulty."
-
Signs of Misuse Evaluation:
- Behavioral observations (appropriate vs. concerning)
- Physical signs (pupil size, track marks, coordination)
- Consistency between reported pain and observed behavior
- Document using objective, non-judgmental language
-
Urine Drug Testing Results:
- Specimen validity testing
- Expected medications present
- Unexpected substances (positive or negative)
- Interpretation and action taken
- Example: "UDT (immunoassay): Positive for oxycodone (expected), negative for benzodiazepines, THC, cocaine, amphetamines, opiates. Consistent with prescribed regimen."
-
Pill Count (if performed):
- Number of pills remaining
- Calculation of expected vs. actual
- Example: "Pill count: 24 oxycodone tablets remaining. Prescribed 90 tablets on [date], 28 days ago. Expected remaining: 22-26. CONSISTENT."
-
Review of Imaging/Diagnostics:
- Relevant imaging findings
- EMG/nerve conduction studies
- Laboratory results
Example Objective Section for Pain Management
Assessment Section (A)
The pain management Assessment synthesizes clinical findings, documents risk stratification, evaluates treatment response, and justifies continued therapy.
Assessment Section (A) Components
-
Pain Diagnosis:
- Primary pain diagnosis with ICD-10 code
- Underlying pathology
- Chronicity (acute, subacute, chronic)
-
Opioid Therapy Assessment:
- Indication for opioid therapy
- Treatment response (function, pain, quality of life)
- Tolerance assessment
- Dependence vs. addiction assessment
-
Risk Stratification:
- Current risk level (low, moderate, high)
- Basis for risk assessment
- Changes from prior assessment
-
Treatment Response Evaluation (4 A's):
- Analgesia: Degree of pain relief
- Activity: Functional improvement
- Adverse effects: Side effects and management
- Aberrant behaviors: Any concerning behaviors
-
Benefits vs. Risks Analysis:
- Document ongoing benefit
- Weigh against risks
- Support for continued treatment
Example Assessment Section for Pain Management
Plan Section (P)
The pain management Plan documents multimodal treatment strategies, controlled substance prescribing details, monitoring protocols, and safety planning.
Plan Section (P) Components
-
Multimodal Treatment Plan:
- Pharmacologic interventions (opioid and non-opioid)
- Interventional procedures
- Physical/occupational therapy
- Psychological/behavioral therapies
- Complementary approaches
-
Opioid Prescribing Details:
- Specific medication, dose, quantity, directions
- Rationale for dose (continuation, increase, decrease, rotation)
- MME calculation
- PDMP documentation statement
-
Non-Opioid Medications:
- Adjuvant analgesics
- Medications for side effect management
- Tapering plans if applicable
-
Monitoring Plan:
- UDT frequency
- Pill count schedule
- PDMP review frequency
- Follow-up interval
-
Opioid Agreement Documentation:
- Status of treatment agreement
- Any updates or discussions
-
Safety Planning:
- Naloxone prescription
- Storage instructions
- Overdose prevention education
-
Interventional Procedures:
- Planned procedures with rationale
- Prior authorization status
-
Referrals:
- Specialty referrals
- Behavioral health
- Substance use treatment if needed
Example Plan Section for Pain Management
AI-Assisted Documentation for Pain Management
As of 2025, 66% of healthcare providers utilize AI tools in their practice. AI scribes can significantly reduce documentation burden for pain management providers while maintaining the comprehensive records required for regulatory compliance.
How AI Can Help with Pain Management Documentation
- Pain assessment capture: Documents comprehensive PQRST pain characterization from patient conversation
- Medication reconciliation: Accurately captures complex medication regimens with dosing
- Functional assessment: Documents patient-reported functional status and changes
- Compliance documentation: Assists with standardized monitoring documentation
- Template generation: Creates structured notes with required elements
Controlled Substance Documentation Considerations
Critical Elements AI Must Capture Accurately:
- Medication names and dosages: Verify exact opioid doses, quantities, and directions
- PDMP review documentation: Confirm statement that PDMP was reviewed
- UDT results: Verify interpretation accurately reflects results
- Pill count results: Confirm numbers and calculations
- Risk assessment scores: Verify ORT, SOAPP scores if discussed
- MME calculations: Double-check morphine equivalent dosing
What AI Captures Well:
- Patient-reported pain levels and descriptors
- Functional status descriptions
- Treatment history discussion
- Side effect reporting
- Patient goals and preferences
- Education and counseling provided
What Requires Careful Clinician Review:
- Opioid prescribing details: ALWAYS verify medication, dose, quantity, directions
- PDMP findings: Ensure documented review is accurate
- Risk stratification: Confirm assessment aligns with clinical judgment
- Behavioral observations: Verify observations match your assessment
- Compliance language: Ensure agreement status accurately documented
- MME calculations: Verify morphine equivalent doses
AI Documentation Review Checklist for Pain Management
For more details, see our complete AI-Assisted Documentation Guide.
Telehealth Pain Management Documentation
Telehealth for pain management involving controlled substances requires careful attention to both telehealth documentation requirements and DEA regulations.
DEA Telehealth Prescribing Rules for Controlled Substances
Per DEA Telehealth Prescribing Regulations and the 2024 Telemedicine Final Rule:
Current Framework (as of 2025):
- Establishing Patient Relationship: The DEA requires at least one in-person evaluation for prescribing controlled substances, unless specific exceptions apply
- Telemedicine Exceptions: Special registration may allow prescribing via telemedicine in certain circumstances
- State Laws Apply: Many states have additional restrictions on telehealth prescribing of controlled substances
- Schedule II Limitations: Most stringent requirements apply to Schedule II opioids
Documentation Requirements for Telehealth Controlled Substance Visits:
- In-Person Relationship Documentation: Document date and nature of qualifying in-person evaluation
- Telehealth Platform: HIPAA-compliant, audio-video required for controlled substance discussions
- Patient Identity Verification: Robust verification required
- State Locations: Document both patient and provider state (critical for licensure and prescribing authority)
- Examination Limitations: Clearly document what cannot be assessed via telehealth
- Appropriateness Statement: Justify why telehealth is appropriate for this controlled substance patient
Telehealth Pain Management Documentation Template
State-Specific Considerations
Important: State laws vary significantly regarding telehealth prescribing of controlled substances. Before prescribing:
- Verify prescriber is licensed in patient's state
- Confirm state allows telehealth prescribing of controlled substances
- Document compliance with state-specific requirements
- Some states require more frequent in-person visits
- Some states prohibit initial controlled substance prescriptions via telehealth
For complete telehealth documentation guidance, see our Telehealth SOAP Notes Guide.
Free Pain Management SOAP Note Templates
Chronic Pain Follow-Up Template
Opioid Treatment Agreement Documentation Template
Related Resources
- Telehealth SOAP Notes Guide
- AI-Assisted Documentation Guide
- Psychiatry SOAP Notes
- Physical Therapy SOAP Notes
- Free SOAP Note Templates
Official Resources and References
Federal Agencies
- CDC Clinical Practice Guideline for Prescribing Opioids for Pain
- DEA Prescribing Requirements (21 CFR 1306)
- DEA Telemedicine Prescribing
- CMS 2026 Physician Fee Schedule
- SAMHSA Opioid Treatment Resources
Professional Organizations
- AMA Opioid Resources
- American Academy of Pain Medicine
- PDMP TTAC (Training and Technical Assistance Center)
Frequently Asked Questions
DEA compliance requires documentation of: (1) legitimate medical purpose for prescribing, (2) established patient-provider relationship, (3) valid DEA registration, (4) proper prescription format with patient identifiers, date, drug name, strength, quantity, directions, and prescriber signature, (5) Schedule II prescriptions cannot include refills, and (6) for electronic prescribing of controlled substances (EPCS), the system must meet DEA certification requirements. Document all elements in your SOAP note to demonstrate compliance with 21 CFR Part 1306.
Per CDC guidelines and most state laws, PDMP should be checked before initiating opioid therapy and periodically during treatment. Most states require PDMP checks every 1-3 months for stable patients, with many mandating checks before every Schedule II prescription. Document each PDMP review with the date, findings (consistent vs. concerns), and any action taken. This documentation is critical for demonstrating due diligence in controlled substance prescribing.
The 4 A's is a validated framework for assessing opioid therapy effectiveness: Analgesia (pain relief achieved), Activity (functional improvement), Adverse effects (side effects and management), and Aberrant behaviors (signs of misuse or diversion). Document each element at every visit, using objective measures when possible. For example: 'Analgesia: 50% pain relief. Activity: Walking tolerance improved from 1/2 block to 1 block. Adverse effects: Mild constipation, managed with docusate. Aberrant behaviors: None observed, UDT consistent, pill count accurate.'
Document UDT comprehensively including: specimen validity (temperature, creatinine, pH), expected medications (should be positive for prescribed opioids), unexpected positives or negatives, and your clinical interpretation. When results are inconsistent, document your discussion with the patient, their explanation, whether confirmatory testing was ordered, and the action plan. Use objective, non-judgmental language. Example: 'UDT: Oxycodone positive (expected), THC positive (unexpected). Patient reports CBD oil use. Confirmatory GC/MS ordered. Counseled on THC avoidance per opioid agreement.'
Document the specific MME calculation using CDC conversion factors, compare to risk thresholds (50 MME/day and 90 MME/day), and provide clinical justification for doses exceeding thresholds. Example documentation: 'Current regimen: Oxycodone 10mg QID = 40mg/day = 60 MME/day. Below 90 MME threshold. Dose justified by documented functional improvement, failure of lower doses, and stable monitoring parameters.' Also document naloxone co-prescription for patients at higher risk.
Document that the opioid treatment agreement was reviewed, signed, and understood by the patient. Include: date of original agreement, date of any renewals, key elements discussed (single prescriber/pharmacy, no early refills, UDT requirements, medication storage, grounds for discontinuation), patient acknowledgment of risks and benefits, and alternatives discussed. Note patient compliance status at each visit. Example: 'Opioid treatment agreement on file (signed 6/2025, reviewed today). Patient compliant with all terms. Risks of long-term opioid therapy reviewed including addiction, overdose, and tolerance.'
Yes, SOAPNoteAI.com offers AI-assisted documentation specifically designed for healthcare providers, including pain management specialists. The platform is fully HIPAA-compliant with a signed Business Associate Agreement (BAA), ensuring patient data protection. It works on iPhone, iPad, and web browsers, allowing you to dictate or input patient encounters and receive properly formatted SOAP notes with pain management-specific elements like PDMP documentation, UDT interpretation, MME calculations, and 4 A's assessments. The AI understands controlled substance documentation requirements and helps ensure regulatory compliance while significantly reducing documentation time.
Medical Disclaimer: This content is for educational purposes only and should not replace professional medical judgment. Always consult current clinical guidelines and your institution's policies.