What should be included in a Medication for Opioid Use Disorder (MOUD) template for follow-ups?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 9, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

MOUD Follow-Up Visit Template

For patients on medication for opioid use disorder (MOUD), conduct initial follow-up within 1-4 weeks of starting treatment or dose changes, then reassess at least every 3 months for stable patients, with more frequent visits (monthly or more often) for high-risk individuals. 1

Visit Frequency and Timing

  • Initial follow-up: Schedule within 1-4 weeks of starting MOUD or any dose escalation to assess early response, side effects, and adherence 2, 1
  • Methadone-specific timing: Consider follow-up within 3 days when starting or increasing methadone due to cardiac risks and delayed peak effects 2
  • Ongoing monitoring: Reassess stable patients at minimum every 3 months 2, 1
  • High-risk patients require monthly or more frequent visits if they have: 2, 1
    • Depression or other mental health conditions
    • History of substance use disorder beyond opioids
    • History of overdose
    • Concurrent benzodiazepine or CNS depressant use
    • Dosage concerns or polysubstance use

Core Assessment Components at Each Visit

Treatment Efficacy Assessment

  • Pain control (if applicable): Ask about average pain levels and whether relief is sustained throughout the dosing interval 1
  • Functional improvement: Use the PEG scale (Pain average, interference with Enjoyment of life, interference with General activity) to quantify functional status 2, 1
  • Progress toward goals: Ask specifically about meaningful activities the patient wanted to resume—work capacity, family responsibilities, social engagement 1
  • Quality of life: Determine if overall well-being has improved since starting treatment 1
  • Critical decision point: Patients without improvement at 1 month are unlikely to benefit at 6 months, making this an essential juncture for continuing therapy 1

Medication Adherence and Use Patterns

  • Self-administration patterns: Ask if the patient takes medication exactly as prescribed or feels the need to take more or take it more frequently 1
  • Dose adequacy: For methadone patients specifically, assess whether the dose adequately controls cravings and withdrawal 1
  • Craving assessment: Directly ask about intensity and frequency of opioid cravings 1

Substance Use Screening

  • Illicit opioid use: Screen for any non-prescribed opioid use, including heroin or diverted prescription opioids 1
  • Other substance use: Assess alcohol, stimulants, benzodiazepines, cannabis, and other substances 1
  • Injection drug use: Specifically ask about injection practices due to infectious disease risks 1

Opioid Use Disorder Symptom Monitoring

Ask directly about DSM-5 criteria manifestations: 1

  • Craving: Intense desire or urge to use opioids
  • Loss of control: Taking larger amounts or for longer than intended
  • Escalating use: Increasing frequency or quantity beyond prescribed
  • Functional impairment: Problems at work, school, or home related to use

Side Effect and Safety Monitoring

Common side effects to screen for: 1

  • Constipation (nearly universal with opioid agonists)
  • Drowsiness or sedation
  • Nausea or vomiting
  • Dry mouth

Warning signs of serious complications requiring immediate action: 1

  • Sedation or slurred speech (overdose risk)
  • Confusion or cognitive impairment
  • Respiratory symptoms (decreased rate or depth)
  • Syncope or seizures

Methadone-specific monitoring: 1

  • Ask about cardiac symptoms (palpitations, syncope, chest pain)
  • Consider ECG monitoring, especially at doses >100mg or with risk factors

Mental Health Assessment

  • Depression screening: Use validated tools (PHQ-9) or direct questioning about depressed mood, anhedonia, suicidal ideation 3
  • Anxiety symptoms: Assess for panic, generalized anxiety, or social anxiety
  • Suicidality: Directly ask about suicidal thoughts, plans, or attempts—particularly important as depression and suicidality have been reported with naltrexone 3
  • Trauma history: Screen for PTSD symptoms if not previously assessed

Social Support and Barriers

  • Family awareness: Does the patient's support system know about their treatment? 1
  • Medication reminders: What systems are in place to ensure adherence? 1
  • Recovery support: Is the patient engaged in counseling, peer support groups, or other psychosocial interventions? 2
  • Logistical barriers: Transportation, childcare, work schedule conflicts, housing instability 1

Prescription Drug Monitoring Program (PDMP) Review

  • Check PDMP data at every visit or at minimum every 3 months to identify: 2
    • Other opioid prescriptions from different providers
    • Benzodiazepine prescriptions
    • Other controlled substances
    • Dangerous combinations or dosages

Urine Drug Testing

  • Baseline testing: Obtain before starting MOUD if not already done 2
  • Ongoing testing: Consider at least annually, or more frequently for high-risk patients 2
  • Test for: Prescribed MOUD medication (to confirm adherence), other prescribed controlled substances, illicit opioids, stimulants, benzodiazepines 2

Physical Examination Elements

  • Vital signs: Blood pressure, pulse, respiratory rate, weight 4
  • Injection site examination: If patient has history of injection use, check for abscesses, cellulitis, or signs of endocarditis
  • Pupil examination: Assess for miosis (opioid effect) or mydriasis (withdrawal)
  • Mental status: Level of alertness, speech patterns, cognitive function

Clinical Decision-Making Algorithm

Continue Current Treatment If:

  • Sustained clinically meaningful improvement in function and quality of life 1
  • No serious adverse events or warning signs 1
  • Benefits clearly outweigh risks 1
  • Patient expresses preference to continue given current benefit-to-risk ratio 1

Action: Maintain current dose and monitoring schedule 1

Increase Monitoring Frequency If:

  • New mental health symptoms emerge 2, 1
  • Positive urine drug screen for illicit substances 2
  • PDMP reveals concerning prescriptions 2
  • Patient reports increased cravings or near-relapse episodes 1
  • Social support deteriorates (housing loss, relationship breakdown) 1

Action: Schedule more frequent visits (every 2-4 weeks) and consider intensifying psychosocial support 2

Reduce Dose or Discontinue If:

  • Patient experiences overdose or serious adverse events (hospitalization, disability) 2, 1
  • No sustained improvement in function after adequate trial (>1 month) 1
  • Patient on high-risk regimen (concurrent benzodiazepines) without clear benefit 2, 1
  • Patient requests dose reduction or discontinuation 2, 1
  • Signs of diversion (consistently "lost" medications, early refill requests)

Action: Initiate slow taper (10-50% weekly dose reduction), maximize non-pharmacologic supports, consider pain specialist consultation 2

Coordination of Care

For Patients in Opioid Treatment Programs (OTPs):

  • Obtain signed release to exchange information between prescribers before prescribing any controlled substances 1
  • Communicate regularly with OTP counselors about patient progress and concerns
  • Avoid duplicate prescribing of opioids or benzodiazepines without OTP coordination 2

Psychosocial Treatment Integration:

  • Recommend minimum 52 weeks of MOUD combined with behavioral interventions 2
  • Evidence-based options include: Cognitive Behavioral Therapy, Contingency Management, Motivational Enhancement Therapy 2
  • Refer to community resources: Peer support groups (SMART Recovery, Narcotics Anonymous), vocational rehabilitation, housing assistance 2

Documentation Requirements

Document at each visit: 4

  • Specific symptoms: Craving intensity (0-10 scale), withdrawal symptoms, pain levels
  • Functional status: Work/school attendance, family engagement, self-care activities
  • Medication adherence: Pill counts if available, patient report of missed doses
  • Substance use: Results of urine drug testing, patient-reported use
  • Side effects: Specific symptoms and severity
  • PDMP review: Date checked and findings
  • Clinical decision: Rationale for continuing, adjusting, or discontinuing treatment
  • Treatment plan: Next visit date, any referrals made, patient education provided

Special Populations

Adolescents and Young Adults (Age 16-25):

  • Access barriers: Only 1% of buprenorphine-waivered physicians are pediatricians; less than 2% of adolescents with OUD receive MOUD 2
  • Retention challenges: Adolescents have higher dropout rates than older adults 2
  • Medication preferences: Adolescents more likely to receive buprenorphine-naloxone or naltrexone rather than methadone compared to young adults 2
  • Enhanced screening: Use validated tools (S2BI, CRAFFT v2.0) at every visit 2
  • Developmentally appropriate interventions: Involve family when appropriate, address school/peer issues, provide age-appropriate education 2

Pregnant Patients:

  • Preferred medications: Methadone or buprenorphine (not naltrexone) 5
  • Coordination: Work closely with obstetrics for prenatal care and delivery planning
  • Avoid withdrawal: Do not taper or discontinue MOUD during pregnancy due to relapse and fetal risks

Criminal Justice-Involved Patients:

  • Continuity planning: Ensure MOUD access continues during incarceration and upon release 2
  • High-risk period: First 2 weeks post-release have highest overdose risk 2
  • Mandated treatment: Patients in drug court or probation may need documentation of attendance and compliance

Common Pitfalls to Avoid

  • Premature discontinuation: Patients should be encouraged to continue MOUD indefinitely; discontinuation dramatically increases relapse risk 6, 7
  • Inadequate dose: Underdosing (particularly methadone <80mg or buprenorphine <16mg) leads to breakthrough cravings and relapse 5
  • Ignoring polysubstance use: Concurrent stimulant or alcohol use requires additional intervention, not MOUD discontinuation 2
  • Dismissing pain complaints: Patients on MOUD can have legitimate pain; address with non-opioid multimodal analgesia 2
  • Punitive approach to positive drug screens: Use as opportunity for enhanced support rather than treatment termination 7
  • Neglecting psychosocial treatment: MOUD alone is less effective than MOUD plus behavioral interventions 2, 5
  • Failure to prescribe naloxone: All patients on MOUD should have take-home naloxone for overdose reversal 2, 5

References

Guideline

Opioid Management and Monitoring

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Psychiatric Medication Management Follow-Up Visits

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Medication Treatment of Opioid Use Disorder.

Biological psychiatry, 2020

Research

Opioid Use Disorder: Medical Treatment Options.

American family physician, 2019

Research

Opioid use disorder.

Nature reviews. Disease primers, 2020

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.