⚙
Visit Header
Follow-Up Visit Header
ENCOUNTER TYPE: [Telepsychiatry / In-Person] — Follow-Up Psychiatric Medication Management
DATE: [MM/DD/YYYY] | TIME: [HH:MM] – [HH:MM] | DURATION: [## min]
// Telepsychiatry only — include below:
PLATFORM: [Doxy.me / Zoom for Healthcare / Epic MyChart / Other]
PATIENT LOCATION: [City, State — patient confirmed]
PROVIDER LOCATION: [Clinic Name, City, State]
TELEHEALTH CONSENT: Previously obtained and on file / Re-confirmed today
IDENTITY VERIFIED: [DOB / Photo ID]
CONNECTION QUALITY: [Audio: Clear | Video: Clear] / [Audio-only — reason: ___]
PATIENT: [Full Name] | DOB: [MM/DD/YYYY] | MRN: [___]
LAST VISIT: [Date] — [Provider Name, credentials]
VISIT SINCE: [## days / weeks / months since last contact]
ACCOMPANYING: [Alone / With: Name, relationship]
1
Interval History
Document the Interval
The interval history establishes what changed between visits. This is the narrative foundation of your note — summarize changes in symptoms, life circumstances, medications, and treatment compliance. New events (hospitalizations, ER visits, crises) must be captured here and cross-referenced with collateral.
Interval History
INTERVAL HISTORY:
Patient returns for follow-up medication management, [## days/weeks] since last visit.
Overall interval course: [Improved / Stable / Worse / Mixed]
SYMPTOM CHANGES:
[Depression/anxiety/mood/psychosis/etc.] — [improved/worsened/unchanged since last visit]
Patient reports: "[Brief quote from patient re: how they've been doing]"
SIGNIFICANT INTERVAL EVENTS:
[ ] No significant events between visits
[ ] Psychiatric hospitalization: [Date, facility, duration, reason, discharge Rx]
[ ] ER visit (psychiatric): [Date, reason, outcome]
[ ] Crisis line contact: [Date, reason, outcome]
[ ] New medical diagnosis or hospitalization: [___]
[ ] Major life event: [Loss / Relationship change / Job change / Legal issue / Other: ___]
[ ] New medications from another provider: [___]
[ ] Substance use relapse: [Substance, date, context, current status]
THERAPY ATTENDANCE:
[Attending therapy with ___: [Consistently / Inconsistently / Discharged / Not in therapy]
Therapy engagement: [Productive / Struggling / Session count since last visit: ___]
BETWEEN-VISIT CONTACTS:
[No between-visit contacts / Phone triage call [date] re: ___]
[Message via portal [date] re: ___]
2
Medication Adherence & Tolerability Review
Adherence = Efficacy
Non-adherence is the leading cause of treatment failure in psychiatry. Document adherence explicitly — it affects your clinical interpretation of symptom response and drives your treatment decisions. Pill counts, pharmacy refill records, and patient self-report are all valid sources.
Current Medication Review
CURRENT MEDICATIONS:
Medication | Dose | Freq | Adherence | Patient Report
--------------------|------------|--------|-----------------|------------------
[Drug 1] | [dose] | [freq] | [100%/partial] | [Helpful/Tolerated]
[Drug 2] | [dose] | [freq] | [partial/%] | [Side effects: ___]
[Drug 3] | [dose] | [freq] | [Non-adherent] | [Reason: cost/SE/forgot]
ADHERENCE SUMMARY:
Overall adherence: [Good (>80%) / Partial (50-80%) / Poor (<50%) / Non-adherent]
Barriers identified (if applicable):
[ ] Cost / copay burden — addressed: [GoodRx / generic / manufacturer coupon / PAP]
[ ] Side effects — addressed: [Dose adjustment / Timing change / Medication switch]
[ ] Forgetting — addressed: [Pillbox / Phone reminder / Once-daily formulation]
[ ] Stigma — addressed: [Psychoeducation provided]
[ ] Lack of perceived benefit — addressed: [___]
[ ] No barriers identified
PRESCRIPTION REFILLS TODAY:
[List medications refilled, quantities, days supply]
[No refills needed at this time]
PHARMACY: [Pharmacy name, address — or patient-confirmed pharmacy on file]
3
Symptom Tracking — Quantitative Scales
Measurement-Based Care
Quantitative symptom tracking (PHQ-9, GAD-7, etc.) improves outcomes, supports billing complexity, provides objective data for prior authorizations, and is the standard of care per APA guidelines. Document scale scores, track trends over time, and use scores to guide clinical decisions.
PHQ-9 — Patient Health Questionnaire (Depression)
Score 0-3 for each item: 0=Not at all, 1=Several days, 2=More than half the days, 3=Nearly every day
1
Little interest or pleasure in doing things: [___]2
Feeling down, depressed, or hopeless: [___]3
Trouble sleeping or sleeping too much: [___]4
Feeling tired or having little energy: [___]5
Poor appetite or overeating: [___]6
Feeling bad about yourself: [___]7
Trouble concentrating on things: [___]8
Moving/speaking slowly, or being fidgety/restless: [___]9
Thoughts of being better off dead or hurting yourself: [___]
TOTAL: [___/27] |
1-4: Minimal | 5-9: Mild | 10-14: Moderate | 15-19: Moderately Severe | 20-27: Severe
Prior score: [___] ([Date]) — Change: [+/-## points — improved/worsened/stable]
Prior score: [___] ([Date]) — Change: [+/-## points — improved/worsened/stable]
GAD-7 — Generalized Anxiety Disorder Scale
Score 0-3: 0=Not at all, 1=Several days, 2=More than half the days, 3=Nearly every day
1
Feeling nervous, anxious, or on edge: [___]2
Not being able to stop or control worrying: [___]3
Worrying too much about different things: [___]4
Trouble relaxing: [___]5
Being so restless it's hard to sit still: [___]6
Becoming easily annoyed or irritable: [___]7
Feeling afraid something awful might happen: [___]
TOTAL: [___/21] |
0-4: Minimal | 5-9: Mild | 10-14: Moderate | 15-21: Severe
Prior score: [___] ([Date]) — Change: [+/-## points]
Prior score: [___] ([Date]) — Change: [+/-## points]
Additional / Alternate Scales
// Use as clinically appropriate — select applicable scales
YMRS (Young Mania Rating Scale — for Bipolar monitoring):
Total Score: [___/60] Interpretation: [Minimal / Mild / Moderate / Severe]
Prior: [___] ([Date]) Change: [___]
PANSS (Positive and Negative Syndrome Scale — for Psychosis):
Positive: [___] Negative: [___] General: [___] Total: [___]
Prior: [___] ([Date])
ASRS-v1.1 (ADHD Self-Report — for ADHD monitoring):
Part A: [___/24] Interpretation: [Positive screen / Negative]
DAST-10 (Drug Abuse Screening Test):
Score: [___/10] Interpretation: [Low/Moderate/Substantial/Severe]
AUDIT-C (Alcohol Use — brief screen):
Score: [___/12] Prior: [___]
PCL-5 (PTSD Checklist DSM-5):
Score: [___/80] Prior: [___] Cutoff: [≥33 = probable PTSD]
CGI-S (Clinical Global Impression — Severity):
Rating: [1=Normal / 2=Borderline / 3=Mildly ill / 4=Moderately ill / 5=Markedly ill / 6=Severely ill / 7=Extremely ill]
Prior: [___] CGI-I (Improvement): [1=Very much improved … 7=Very much worse]
CUSTOM TRACKING:
[Provider-specific tracking metric: ___ = ___]
4
Side Effect Review
Systematic Review Prevents Missing Problems
Patients often don't volunteer side effects unless asked directly. A structured, medication-class-specific side effect review demonstrates thoroughness, catches problems early, and documents that you evaluated safety — critical for controlled substances and high-risk medications.
Antidepressant Side Effects (SSRI/SNRI/Other)
ANTIDEPRESSANT SIDE EFFECTS: Drug: [___________]
GI symptoms (nausea, diarrhea, constipation): [None / Present: ___]
Sexual dysfunction (libido, arousal, orgasm): [None / Present: ___] // Ask directly
Weight change: Current weight [___] vs. last [___] = [+/-___] lbs over [___] months
Sleep effects (insomnia or sedation): [None / Present: ___]
Activation/agitation (especially early): [None / Present: ___]
Headache: [None / Present: ___]
Sweating: [None / Present: ___]
Tremor: [None / Present: ___]
Hyponatremia symptoms (confusion, lethargy): [None / Present: ___] // Especially elderly
Serotonin syndrome signs (if poly-serotonergic): [None / Present: ___]
Symptoms: [fever, clonus, agitation, diaphoresis, tachycardia, diarrhea]
Discontinuation symptoms (if recently stopped): [None / Present: ___]
// Bupropion-specific:
Seizure history review: [None new / ___]
BP (if on SNRI/venlafaxine): [___] — prior: [___]
Urine retention (duloxetine): [None / Present]
Antipsychotic Side Effects
ANTIPSYCHOTIC SIDE EFFECTS: Drug: [___________]
Metabolic:
Weight: [___] vs last [___] = [+/-] lbs | BMI: [___]
Glucose (HbA1c if applicable): [___]
Lipids (if applicable): [___]
Metabolic syndrome screen: [BP/waist circumference/glucose/lipids — reviewed]
Movement disorders:
EPS (akathisia, parkinsonism, rigidity): [None / Present: ___]
Tardive dyskinesia (AIMS): [None / Present: ___]
AIMS score: [___] — prior: [___]
Akathisia (inner restlessness): [None / Present — Barnes scale: ___]
Sedation/cognitive:
Daytime sedation: [None / Mild / Significant]
Cognitive dulling: [None / Present: ___]
Endocrine:
Prolactin effects (galactorrhea, amenorrhea, sexual dysfunction): [None / ___]
QTc prolongation risk (especially ziprasidone, haloperidol):
Last ECG: [Date / Not obtained / QTc: ___ms]
Autonomic:
Orthostatic hypotension (dizziness on standing): [None / Present]
BP: [Sitting ___] / [Standing ___]
Anticholinergic (dry mouth, urinary retention, constipation): [None / Present: ___]
// Clozapine-specific:
ANC: [___] Last CBC: [Date] — Monitoring: [Weekly/biweekly/monthly per protocol]
Hypersalivation: [None / Present] Seizures: [None / Present]
Myocarditis symptoms (if new patient or dose change): [Chest pain/dyspnea/fever — None / ___]
Mood Stabilizer Side Effects
MOOD STABILIZER SIDE EFFECTS: Drug: [___________]
// LITHIUM:
Level: [___ mEq/L] drawn [date] — Therapeutic range: 0.6-1.2 mEq/L (acute 0.8-1.2)
Toxicity symptoms: [None — polyuria/polydipsia/tremor/confusion/GI reviewed]
Tremor: [None / Present — fine/coarse, at rest/intention]
Thyroid (TSH): [___] Renal (Cr/eGFR): [___]
Cognitive/memory: [No change / Reported: ___]
Edema: [None / Present] Acne/psoriasis: [None / Present]
Weight: [___] vs last [___]
// VALPROATE (Depakote):
Level: [___ mcg/mL] — Therapeutic: 50-125 mcg/mL
LFTs: [___] Date: [___] CBC (thrombocytopenia): [___]
Tremor: [None / Present] Hair thinning: [None / Present]
GI tolerability: [Good / Poor — nausea/vomiting]
Weight gain: [None / +___ lbs]
Reproductive-age female: Polycystic ovary syndrome risk discussed: [Y/N]
Neural tube defect risk if pregnant counseled: [Y/N / N/A]
// LAMOTRIGINE (Lamictal):
Current dose: [___ mg/day] — Titration on schedule: [Y/N]
Rash monitoring: [None — educate every visit re: SJS/TEN risk]
New rash: [None / Present — action taken: ___]
Dizziness/diplopia: [None / Present]
Drug interactions checked (OCPs, valproate): [Y/N]
// CARBAMAZEPINE (Tegretol):
Level: [___ mcg/mL] CBC (agranulocytosis): [___] LFTs: [___]
Hyponatremia: [Na: ___] Drug interactions reviewed: [Y/N]
Stimulant Side Effects (ADHD Medications)
STIMULANT SIDE EFFECTS: Drug: [___________]
Cardiovascular:
BP: [___/___] — prior: [___/___] HR: [___] — prior: [___]
Palpitations: [None / Present] Chest pain: [None / Present]
Cardiac symptoms reviewed (per FDA guidelines): [Normal / Concerns: ___]
Appetite/weight:
Appetite: [Normal / Decreased] Weight: [___] vs last [___] = [+/- ___] lbs
Eating schedule: [Regular / Skipping meals]
Sleep:
Insomnia: [None / Present — timing of last dose: ___]
Sleep quality: [Good / Poor — addressed: ___]
Psychiatric:
Mood/anxiety worsening: [None / Present — concern for substance-induced or predisposed]
Psychosis/paranoia: [None / Present — action: ___]
Irritability: [None / Present]
Rebound effect: [None / Present — timing: ___]
Stimulant misuse/diversion concern:
PDMP reviewed: [Y — findings: ___]
Signs of misuse: [None / Present: ___]
Early refills: [None / Yes — addressed: ___]
Pill count (if clinically indicated): [Not performed / Performed: ___]
Benzodiazepine / Sedative Side Effects
BENZODIAZEPINE / SEDATIVE SIDE EFFECTS: Drug: [___________]
Sedation/cognitive:
Daytime sedation: [None / Mild / Significant]
Cognitive impairment/memory: [None / Present — specify: ___]
Psychomotor impairment (driving concern): [None / Discussed]
Dependence/tolerance:
Escalating dose request: [No / Yes — addressed: ___]
Tolerance (reduced efficacy at same dose): [No / Yes: ___]
Physical dependence: [Likely given: duration ___, dose ___]
Early refill requests: [None / Yes — addressed: ___]
PDMP reviewed for multiple prescribers: [Y — findings: ___]
Falls risk (especially elderly):
Fall history: [None / Yes — ___] Balance/gait: [Normal / Impaired]
Beers Criteria applicable: [Y/N — discussed: ___]
Misuse/diversion:
Alcohol use concurrently: [None / Yes — counseling: ___]
Opioid use concurrently: [None / Yes — COUNSELING CRITICAL — overdose risk]
Signs of misuse: [None / Present: ___]
Tapering plan (if applicable):
Taper goal: [Discontinue / Reduce to minimum effective dose]
Current taper schedule: [___] Tolerance: [Good / Difficult]
Withdrawal symptoms: [None / Present: ___]
5
PDMP Review
PDMP Documentation
PDMP REVIEW:
Date/time accessed: [MM/DD/YYYY HH:MM]
Database: [State PDMP name]
[ ] PDMP accessed — No controlled substance prescriptions outside of expected
Current controlled substance prescribers: [This practice only / List if multiple]
[ ] PDMP accessed — Findings consistent with clinical picture:
[Drug, Dose, Prescriber, Date, Pharmacy — all expected]
[ ] PDMP accessed — Unexpected findings:
Finding: [___]
Clinical response: [Patient education / Referral / Dose adjustment /
Contact other prescriber / No change warranted because: ___]
[ ] PDMP not accessed — Reason: [Patient not receiving controlled substances /
State system unavailable — alternative verification: ___]
// Document even if not prescribing controlled substances — best practice for all patients
// Required before prescribing any new controlled substance in most states
6
UDS Results & Interpretation
UDS Results & Clinical Interpretation
URINE DRUG SCREEN:
TODAY:
[ ] Not ordered today — reason: [___]
[ ] Ordered — point of care / lab send-out — results pending
[ ] Results available (date collected: ___):
RESULTS:
Amphetamines: [Neg / Pos — expected: Y/N] Benzodiazepines: [Neg / Pos — expected: Y/N]
Cannabis (THC):[Neg / Pos — expected: Y/N] Cocaine: [Neg / Pos — expected: Y/N]
Opiates: [Neg / Pos — expected: Y/N] Oxycodone: [Neg / Pos — expected: Y/N]
Fentanyl: [Neg / Pos — expected: Y/N] Buprenorphine: [Neg / Pos — expected: Y/N]
Methamphetamine:[Neg / Pos — expected: Y/N] PCP: [Neg / Pos — expected: Y/N]
Alcohol (EtG): [Neg / Pos — expected: Y/N] Other: [___]
EXPECTED SUBSTANCES: [List patient's prescribed medications that may appear positive]
INTERPRETATION:
[ ] All results consistent with prescription and treatment plan — no action needed
[ ] Prescribed substance absent — discussed: [Non-adherence / Diversion / Delay in testing]
Response: [___]
[ ] Unexpected substance present — discussed: [Not punitive — therapeutic conversation]
Finding: [___] Patient explanation: [___] Clinical response: [___]
// Never interpret a positive result punitively without clinical conversation first
// Confirm-positive tests with quantitative lab if clinical decision depends on it
// False positives: quinolones → opiates; ibuprofen → cannabis; sertraline → BZD
7
Mental Status Examination
Brief MSE — Follow-Up
MENTAL STATUS EXAMINATION:
Appearance: [Well-groomed / Adequate / Disheveled] | Age: [appropriate / appears older/younger]
Behavior: [Cooperative / Guarded / Agitated / Pleasant]
Psychomotor: [No abnormalities / Agitation / Retardation / Tremor — specify: ___]
Eye contact: [Good / Poor / Avoidant]
Speech: [Rate: Normal/Rapid/Slow | Volume: Normal/Loud/Soft | Rhythm: Normal/Pressured]
Mood (S): "[Patient's own words]"
Affect (O): [Euthymic / Depressed / Anxious / Irritable / Elevated / Labile / Flat]
Range: [Full / Restricted / Blunted] | Congruence: [Congruent / Incongruent]
Thought Process: [Linear, logical, goal-directed / Circumstantial / Tangential / Other: ___]
Thought Content:
SI: [None / Passive / Active — see Risk Assessment]
HI: [None / Present: ___]
Delusions: [None / Present: ___]
Obsessions: [None / Present: ___]
Perceptual: [No hallucinations / AH: ___ / VH: ___ / Other: ___]
Cognition: [Alert and oriented ×4 / Attention intact / Memory intact]
[Any cognitive concerns: ___]
Insight: [Full / Partial / Poor / Absent]
Judgment: [Good / Fair / Poor]
// Compared to last visit: [Improved / Stable / Worse] in: [specific domains]
8
Risk Assessment — Brief
⚠ Document Every Visit
Brief risk assessment must be documented at every psychiatric visit, not just initial evaluations. A single-line statement ("No SI/HI, no safety concerns") is insufficient if a patient presents acutely — document the specifics of what was asked and assessed.
Brief Risk Assessment
RISK ASSESSMENT:
SUICIDALITY:
Current SI: [None / Passive: "I wish I were dead" / Active without plan /
Active with plan: ___]
Since last visit: [No new SI / New SI — addressed: ___]
Current intent: [None / Present — action taken: ___]
If SI present:
Plan: [None / Yes: ___]
Access to means: [No firearms / Firearms — secured: Y/N / Other: ___]
Intent: [None / Uncertain / Clear]
Deterrents: [Family / Children / Fear / Religious beliefs / Other: ___]
SELF-HARM:
Current NSSI: [None / Yes — type: ___, frequency: ___, last occurrence: ___]
HOMICIDALITY:
Current HI: [None / Present — target: ___, plan: ___, action: ___]
Duty to warn assessed: [N/A / Yes — action: ___]
RISK CHANGE FROM LAST VISIT:
[Risk stable / Risk decreased / Risk increased — specify: ___]
RISK LEVEL: Acute: [Low / Moderate / High / Imminent] Chronic: [Low / Moderate / High]
DISPOSITION RATIONALE:
[Patient is appropriate for outpatient management because: ___]
[OR: Patient requires higher level of care because: ___]
SAFETY PLAN:
[Previously established — reviewed today / Updated today / Crisis resources re-provided]
988 Suicide & Crisis Lifeline reviewed: [Y/N]
Patient's crisis contacts: [___]
9
Assessment
Assessment / Diagnostic Impression
ASSESSMENT:
[Patient name] returns for follow-up medication management. [He/She/They] reports
[subjective improvement/worsening/stability] in [target symptoms].
PHQ-9 today [___] vs. prior [___] = [improved/worsened/stable by ## points].
GAD-7 today [___] vs. prior [___] = [improved/worsened/stable].
Medication response: [Responding well / Partial response / Non-response — see plan]
Adherence: [Good / Partial / Poor — see above]
Side effects: [None reported / Manageable / Limiting — see above]
ACTIVE DIAGNOSES:
1. [F32.1] Major Depressive Disorder, [severity] — [improving/stable/exacerbating]
2. [F41.1] Generalized Anxiety Disorder — [status]
3. [F10.20] Alcohol Use Disorder, moderate — [in remission / active]
// Include all active diagnoses with ICD-10 codes at each visit
COMORBID MEDICAL CONDITIONS (relevant):
[List with impact on psychiatric management]
CLINICAL REASONING:
[Narrative summary of why you are making the treatment decisions in the plan below.
What is driving the change? What are you monitoring for? What's the timeline?]
10
Plan — Risk/Benefit Medication Documentation
The Risk/Benefit Framework
This format — adapted from VA SUDS documentation standards — provides ironclad documentation for every medication decision. It makes explicit: what you're doing, why, what risks you discussed, that the patient understood and agreed. This is your clinical and legal record.
CONTINUE Template
ACTION: CONTINUE [Drug Name] [Dose] [Frequency]
Indication: [Diagnosis] — [FDA-Approved / Off-Label]
Response to date: [Partial response / Good response / Stable on current dose]
Rationale: [Why continue at current dose: ___]
Risk/Benefit: Continuing current regimen. Ongoing risks include [relevant SE for this
patient — e.g., weight gain, sexual dysfunction, metabolic effects].
Benefits of [symptom control / functional improvement] outweigh risks.
Patient [agrees to continue / acknowledges risks].
Monitoring: [Ongoing: weight, BP, labs — next lab due: ___]
Refill: [Qty: ___ | Days supply: ___ | Refills: ___]
START Template
ACTION: START [Drug Name] [Dose] [Frequency]
Indication: [Diagnosis] — [FDA-Approved / Off-Label]
Rationale: [Why this drug? Why now? What drove this decision?
Prior trial failures: ___. Patient factors: ___.
Formulary/cost considerations: ___.]
Risk/Benefit: Discussed risks including [specific side effects relevant to THIS
patient — e.g., "nausea and sexual dysfunction common with SSRIs;
rare risk of serotonin syndrome; black box warning re: suicidality
in patients <25 years old — patient is ___ years old"].
Benefits of [expected therapeutic effect] outweigh risks.
Alternatives discussed: [___]. Patient agreed to start.
Instructions: [Take [with/without food], [time of day], [titration: ___]]
Monitoring: [Follow-up in ## weeks; call if [specific symptoms]]
Starting dose: [___ mg] — titrate to [___ mg] at [timeframe]
Rx: [Qty: ___ | Days supply: ___ | Refills: ___]
CHANGE (Dose Adjust) Template
ACTION: CHANGE [Drug Name] dose from [old dose] to [new dose] [Frequency]
Indication: [Diagnosis] — [FDA-Approved / Off-Label]
Rationale: [Why changing dose? Partial response requiring optimization /
Side effect at current dose / Patient request /
Therapeutic level below range: ___]
Risk/Benefit: Increasing dose carries risk of [dose-dependent side effects: ___].
Decreasing dose carries risk of [symptom return / withdrawal: ___].
Benefits of [rationale for change] outweigh risks.
Patient understood and agreed to dose change.
Monitoring: [Follow-up timeline: ___ | What to monitor: ___]
New Rx: [New Qty: ___ | Days supply: ___ | Refills: ___]
DISCONTINUE / TAPER Template
ACTION: DISCONTINUE [Drug Name] [with taper / abruptly — specify]
Reason: [Ineffective / Intolerable side effects / Patient request /
Drug interaction / No longer indicated / Better alternative started]
Taper plan: [Reduce by [dose] every [timeframe] until [final dose/D/C]
OR: Abrupt discontinuation — rationale: ___]
Discontinuation risk: Discussed potential for [discontinuation syndrome / rebound /
symptom return: ___]. Patient instructed to contact office if [___].
Patient acknowledged: Risk of stopping — [agreed to taper plan / understands risks of abrupt DC]
Last prescription: [Qty for taper / No new prescription written]
Additional Plan Elements
LABS ORDERED:
[CMP / CBC / TSH / Lithium level / Valproate level / Lipids / HbA1c /
Prolactin / LFTs / Other: ___]
[No labs needed today — last drawn [date], results reviewed]
REFERRALS:
[No new referrals / Referred to: ___ for: ___]
[PCP notified of: ___]
THERAPY:
[Continue with current therapist / Referred for therapy: ___]
[Recommended modality change: ___]
LIFESTYLE / NON-PHARMACOLOGICAL:
[Sleep hygiene reinforced / Exercise discussed / Stress management techniques /
Dietary counseling re: medication interactions / Alcohol reduction counseling]
PSYCHOEDUCATION TODAY:
[Medication mechanism / Side effect management / Relapse warning signs /
Diagnosis education / Other: ___]
SUBSTANCE USE:
[No action needed / SBIRT completed / Referred to: ___ / Naloxone: provided/renewed]
CRISIS PLAN:
[Reviewed — no changes / Updated / Crisis line reiterated: 988]
11
Follow-Up Plan
Follow-Up Timing & Instructions
FOLLOW-UP:
Next appointment: [Date / In ## weeks]
Appointment type: [Telepsychiatry / In-Person]
Rationale for timing:
[ ] Stable — routine follow-up in [4-8 weeks]
[ ] New medication started — follow-up in 2-4 weeks to assess response/tolerability
[ ] Dose change — follow-up in 2-4 weeks
[ ] Elevated risk — follow-up in [1-2 weeks / sooner: ___]
[ ] Lab results pending — follow-up in [___] to review
Between-visit instructions:
Contact us for: [Significant side effects / Worsening SI / Medication questions]
After-hours: [Practice after-hours line: ___]
Crisis: [988 Suicide & Crisis Lifeline / Local ER: ___]
RETURN PRECAUTIONS REVIEWED:
Patient instructed to seek emergent care for:
- Active suicidal ideation with plan or intent
- Active homicidal ideation
- Significant medication adverse reaction (rash, chest pain, severe agitation)
- [Condition-specific: severe manic symptoms / psychotic break / other: ___]
Patient verbalized understanding: [Yes / N/A]
12
Billing Complexity Support
Follow-Up Billing Guide: Follow-up medication management visits typically bill 99214 (moderate complexity, 30-39 min) or 99215 (high complexity, 40-54 min). 90833 (add-on for psychotherapy, 16-37 min) or 90836 (38+ min) can be added if therapy was provided alongside medication management.
Billing Documentation
BILLING INFORMATION:
CPT CODE: [99214 / 99215] + [90833 add-on if psychotherapy provided]
TOTAL TIME: [## minutes total face-to-face and/or administrative time]
// If time-based: 99214 = 30-39 min | 99215 = 40-54 min | 99215 = 55+ min
MEDICAL DECISION MAKING:
Problem complexity:
[ ] Chronic illness with exacerbation (moderate-high)
[ ] Multiple chronic conditions addressed (high)
[ ] New problem addressed in addition to chronic (moderate)
[ ] Prescription drug management (moderate)
[ ] Drug requiring intensive monitoring — lithium/clozapine/valproate (high)
Data:
[ ] Reviewed and summarized external records
[ ] Reviewed and ordered diagnostic tests
[ ] Reviewed standardized instruments (PHQ-9, GAD-7, YMRS) — interpreted results
[ ] Independent interpretation of test results
Risk:
[ ] Controlled substance prescription (moderate-high)
[ ] Risk assessment documented with clinical stratification (moderate-high)
[ ] Social determinants of health impacting management (moderate-high)
[ ] Medication change requiring close monitoring (moderate)
PSYCHOTHERAPY ADD-ON (if applicable):
[90833 — 16-37 min interactive complexity psychotherapy]
[90836 — 38-52 min interactive complexity psychotherapy]
Psychotherapy time: [## min] Type: [CBT / Supportive / DBT / Other: ___]
Description: [Brief description of psychotherapy content separate from E&M]
SUPERVISOR (if applicable):
[Collaborating/Supervising Physician: ___, MD/DO]
Supervision: [Present / Chart review and countersignature / Available for consultation]
★
Quick Reference — Scale Interpretation
| Scale | Score Range | Interpretation | Action Trigger |
|---|---|---|---|
| PHQ-9 | 0-4 | Minimal depression | Routine monitoring |
| 5-9 | Mild | Consider watchful waiting or therapy | |
| 10-14 | Moderate | Therapy ± medication | |
| 15-19 | Moderately severe | Active medication management | |
| 20-27 | Severe | Immediate treatment, consider HLoC | |
| GAD-7 | 0-4 | Minimal anxiety | Routine monitoring |
| 5-9 | Mild | Behavioral interventions | |
| 10-14 | Moderate | Consider medication | |
| 15-21 | Severe | Active medication management | |
| AUDIT-C (W) | ≥3 | Positive screen | Full AUDIT, brief intervention |
| AUDIT-C (M) | ≥4 | Positive screen | Full AUDIT, brief intervention |
| PCL-5 | ≥33 | Probable PTSD | Full assessment, trauma-informed care |
| ASRS-v1.1 Part A | ≥4 positive | Probable ADHD | Full evaluation |