285 lines
8.0 KiB
Markdown
285 lines
8.0 KiB
Markdown
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# Standard Operating Procedure: TMS Treatment Protocol
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| Document ID | SOP-TMS-001 |
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| Title | Transcranial Magnetic Stimulation Treatment Protocol |
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| Revision | 1.0 |
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| Effective Date | [DATE] |
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| Author | [AUTHOR] |
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| Approved By | [APPROVER] |
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| Department | TMS Clinic |
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---
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## 1. Purpose
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To establish standardized procedures for the safe and effective administration of Transcranial Magnetic Stimulation (TMS) therapy in accordance with FDA clearances, manufacturer guidelines, and clinical best practices.
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## 2. Scope
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This procedure applies to all TMS treatments including:
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- Repetitive TMS (rTMS) for Major Depressive Disorder
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- rTMS for Obsessive-Compulsive Disorder
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- Intermittent Theta Burst Stimulation (iTBS)
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- Other FDA-cleared or investigational protocols
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## 3. Responsibilities
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### 3.1 TMS Technician/Operator
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- Position patient and equipment
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- Determine motor threshold
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- Administer treatment per prescription
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- Monitor patient during treatment
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- Document treatment parameters
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### 3.2 Prescribing Physician
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- Evaluate patient eligibility
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- Prescribe treatment protocol
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- Review progress and adjust treatment
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- Manage adverse events
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- Provide medical oversight
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### 3.3 Clinical Coordinator
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- Schedule treatments
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- Track treatment compliance
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- Coordinate patient assessments
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- Maintain equipment logs
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## 4. Definitions
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| Term | Definition |
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|------|------------|
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| MT | Motor Threshold - minimum intensity to produce MEP |
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| MEP | Motor Evoked Potential - observable motor response |
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| rTMS | Repetitive Transcranial Magnetic Stimulation |
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| iTBS | Intermittent Theta Burst Stimulation |
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| DLPFC | Dorsolateral Prefrontal Cortex - common target for depression |
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## 5. Equipment and Materials
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- TMS device (FDA-cleared)
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- Treatment coil (figure-8 or appropriate for indication)
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- Positioning chair or table
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- Ear protection (ear plugs)
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- Treatment cap or head marking system
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- Motor threshold determination tools
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- Emergency equipment (as per emergency SOP)
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## 6. Procedure
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### 6.1 Pre-Treatment Assessment
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#### 6.1.1 Initial Evaluation (First Treatment)
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1. **Verify Prescription**
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- Diagnosis confirmed
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- Treatment protocol specified
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- Contraindications reviewed
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- Informed consent on file
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2. **Safety Screening**
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Confirm absence of contraindications:
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- [ ] No ferromagnetic metal in head/neck
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- [ ] No implanted devices (pacemaker, cochlear implant, DBS)
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- [ ] No history of seizures (unless per protocol)
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- [ ] No unstable medical conditions
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- [ ] Current medications reviewed for seizure threshold effects
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- [ ] Pregnancy test negative (if applicable)
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3. **Baseline Assessments**
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- PHQ-9 or HAM-D (depression)
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- Y-BOCS (OCD, if applicable)
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- Vital signs
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- Cognitive baseline if indicated
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#### 6.1.2 Daily Pre-Treatment Check
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Before each session:
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- [ ] Patient identity verified
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- [ ] Assess for new contraindications
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- [ ] Confirm adequate sleep (>4 hours)
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- [ ] Confirm no alcohol/illicit substances
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- [ ] Confirm no significant medication changes
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- [ ] Assess for current illness
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- [ ] Review previous session tolerance
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### 6.2 Motor Threshold Determination
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**Required at:**
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- First treatment session
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- Any significant change in medications affecting neural excitability
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- If treatment efficacy changes significantly
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- Per physician order
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**Procedure:**
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1. Position patient comfortably
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2. Place coil over motor cortex (M1) contralateral to dominant hand
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3. Begin at 30-40% machine output
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4. Deliver single pulses at 10-second intervals
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5. Observe for thumb/finger movement (APB)
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6. Increase intensity by 5% increments
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7. Record lowest intensity producing 5 MEPs in 10 trials
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8. Document MT and method used
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| MT Parameter | Value |
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|--------------|-------|
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| Date | |
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| Resting Motor Threshold (%) | |
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| Target Muscle | |
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| Number of Trials | |
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| Determined By | |
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### 6.3 Treatment Coil Positioning
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#### 6.3.1 Left DLPFC Targeting (Standard Depression Protocol)
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**5-cm Rule Method:**
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1. Identify motor hotspot (from MT determination)
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2. Measure 5 cm anteriorly along scalp surface
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3. Mark position on treatment cap
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4. Verify coil angle (45° to midline)
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**Neuronavigation Method (if available):**
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1. Register patient to MRI
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2. Identify target coordinates
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3. Position coil using navigation system
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4. Document coordinates and trajectory
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#### 6.3.2 Alternative Targets
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- Right DLPFC (low-frequency protocol)
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- Supplementary Motor Area (OCD)
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- Other per protocol specification
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### 6.4 Treatment Administration
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1. **Patient Preparation**
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- Seat in treatment chair
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- Provide ear protection
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- Position head comfortably
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- Instruct patient on what to expect
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2. **Equipment Setup**
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- Power on device and perform calibration
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- Select prescribed protocol
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- Set treatment parameters:
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| Parameter | Value |
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| Frequency (Hz) | |
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| Intensity (% MT) | |
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| Pulses per train | |
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| Inter-train interval | |
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| Total pulses | |
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| Duration | |
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3. **Treatment Delivery**
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- Position coil at marked location
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- Maintain consistent coil contact
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- Begin treatment delivery
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- Monitor patient continuously
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- Pause if patient reports concerning symptoms
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4. **Patient Monitoring During Treatment**
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Observe for:
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- Facial twitching (may indicate coil drift)
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- Signs of distress
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- Seizure warning signs
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- Excessive discomfort
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### 6.5 Standard Treatment Protocols
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#### Major Depressive Disorder - Standard rTMS
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| Parameter | Left DLPFC |
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| Frequency | 10 Hz |
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| Intensity | 120% MT |
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| Train duration | 4 seconds |
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| Inter-train interval | 26 seconds |
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| Trains per session | 75 |
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| Total pulses | 3,000 |
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| Session duration | ~37.5 minutes |
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| Total sessions | 30-36 |
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#### Major Depressive Disorder - iTBS
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| Parameter | Left DLPFC |
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|-----------|------------|
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| Pattern | 50 Hz bursts at 5 Hz |
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| Intensity | 120% MT |
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| Bursts per train | 10 (30 pulses) |
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| Inter-train interval | 8 seconds |
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| Total pulses | 600 |
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| Session duration | ~3 minutes |
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| Total sessions | 30-36 |
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### 6.6 Post-Treatment
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1. **Immediate Assessment**
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- Ask about side effects
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- Assess for headache, scalp pain
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- Evaluate mental status
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- Confirm safe to leave
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2. **Documentation**
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Complete FRM-TMS-001 Treatment Log:
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- Date and session number
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- Treatment parameters used
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- Coil position
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- Patient tolerance
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- Any adverse effects
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- Operator signature
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3. **Patient Instructions**
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- Mild headache/scalp discomfort common
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- OTC analgesics acceptable
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- Report severe/persistent symptoms
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- Confirm next appointment
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### 6.7 Adverse Event Management
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| Event | Severity | Action |
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| Scalp discomfort | Mild | Adjust position, OTC analgesic |
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| Headache | Mild-Moderate | OTC analgesic, reduce intensity if persistent |
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| Syncope | Moderate | Stop treatment, lie patient down, assess vitals |
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| Seizure | Severe | Stop treatment, protect patient, follow seizure protocol |
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**Seizure Response:**
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1. Stop stimulation immediately
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2. Note time
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3. Protect patient from injury
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4. Do not restrain
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5. Call for help / activate emergency protocol
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6. Monitor airway and breathing
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7. Time seizure duration
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8. Notify physician immediately
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9. Complete incident report
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## 7. Outcome Monitoring
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| Assessment | Timing | Tool |
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| Depression severity | Weekly | PHQ-9 or HAM-D |
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| OCD severity (if applicable) | Weekly | Y-BOCS |
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| Side effects | Each session | TMS side effect checklist |
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| Treatment response | Sessions 10, 20, 30 | Physician evaluation |
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| Remission assessment | End of acute course | Full clinical evaluation |
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## 8. Documentation
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- FRM-TMS-001 TMS Treatment Log
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- FRM-TMS-002 Motor Threshold Record
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- FRM-TMS-003 Side Effect Checklist
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- Outcome assessment forms
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- Equipment maintenance logs
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## 9. References
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- FDA clearance documentation
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- Manufacturer operating manual
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- Clinical practice guidelines (APA, CANMAT)
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- Peer-reviewed TMS literature
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---
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## Revision History
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| Rev | Date | Description | Author |
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|-----|------|-------------|--------|
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| 1.0 | [DATE] | Initial release | [AUTHOR] |
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