Clinical Tools

CLINICAL TOOLS

Evidence-Based Tools for the Psychiatric Prescriber

Clinical reference tools for PMHNPs — titration schedules, switching protocols, and interaction checking. All content is reviewed by board-certified PMHNPs and grounded in current clinical guidelines.

๐Ÿ”’ Members Only. These clinical references are intended for Lumina members (licensed prescribers and PMHNP students). Join the waitlist →

โš  Draft — Pending Clinical Review. These tools are in active development. Content is being verified against primary sources and will be marked "Clinically Reviewed" once sign-off is complete. Do not use for patient care decisions until final review is published.

Available Tools

๐Ÿ’Š Drug Interaction Checker

Live lookups powered by the NLM RxNorm database. Enter any medication combination for an instant interaction check with severity rating and clinical summary.

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๐Ÿ“Š Titration Guide

Step-by-step titration schedules for psychiatric medications and MAT agents — Lamotrigine, Lithium, and more.

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๐Ÿ”„ Switching & Withdrawal Protocols

Evidence-based switching guides and withdrawal assessment: SSRI to MAOI washout, antipsychotic cross-taper, CIWA-Ar, COWS, benzodiazepine taper.

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๐Ÿ’Š Drug Interaction Checker

๐Ÿ› ๏ธ

In Development

An interactive tool using the NLM RxNorm/RxNav API will be built here to allow members to enter medication combinations and receive instant interaction checks with severity ratings and clinical summaries. Expected availability: September 2026.


๐Ÿ“Š Titration Guide

Step-by-step titration schedules cross-referenced against FDA prescribing information and current clinical guidelines.

Jump to a medication:

Lamotrigine · Lithium · Quetiapine (coming soon) · Clozapine (coming soon) · Buprenorphine (coming soon) · Naltrexone (coming soon) · Methadone (coming soon)

Lamotrigine (Lamictal) Titration

Indication referenced: Bipolar I maintenance. Not FDA-approved for acute bipolar depression monotherapy; used off-label.

โš  BOXED WARNING — Serious Skin Reactions (SJS/TEN/DRESS).

Risk of life-threatening rash is highest in the first 2–8 weeks. Risk increases with: (1) exceeding recommended starting dose, (2) exceeding recommended dose escalation, and (3) concomitant valproate without dose adjustment. Discontinue at the first sign of rash unless clearly non-drug-related. Pediatric risk is higher than adult.

Standard Adult Schedule (no interacting AEDs)

Week Dose
Weeks 1–2 25 mg PO daily
Weeks 3–4 50 mg PO daily
Week 5 100 mg PO daily
Week 6 200 mg PO daily (target maintenance dose)

With Valproate (VPA inhibits glucuronidation — half dose)

Week Dose
Weeks 1–2 25 mg PO every other day
Weeks 3–4 25 mg PO daily
Week 5 50 mg PO daily
Week 6 100 mg PO daily (target maintenance dose)

With Enzyme Inducers without VPA (CBZ, phenytoin, phenobarbital, primidone, rifampin) — double dose

Week Dose
Weeks 1–2 50 mg PO daily
Weeks 3–4 100 mg PO daily (divided doses)
Week 5 200 mg PO daily (divided doses)
Week 6 300 mg PO daily (divided doses)
Week 7 400 mg PO daily (divided doses) (target maintenance dose)

Missed Doses / Restart Rules

If lamotrigine is discontinued for more than 5 half-lives (approximately 5 days at steady state in a typical adult on monotherapy), the full initial titration must be restarted from Week 1 to avoid serious rash risk.

Key Counseling / Hold Criteria

  • Counsel patient: call immediately for any rash, especially in the first 8 weeks.
  • Hold lamotrigine for: rash with mucosal involvement, fever, lymphadenopathy, facial swelling, eosinophilia, or systemic symptoms (possible DRESS).
  • A benign, non-serious rash may still require discontinuation — err on the side of caution.
  • Hormonal contraceptives (estrogen-containing) and pregnancy can reduce lamotrigine levels ~50% — dose adjustment and therapeutic drug monitoring may be needed.

Sources: Lamotrigine FDA prescribing information (current revision, GlaxoSmithKline). Stahl SM. Prescriber's Guide, 7th ed. Cambridge University Press. Maudsley Prescribing Guidelines in Psychiatry, 14th ed. American Psychiatric Association Practice Guideline for the Treatment of Patients with Bipolar Disorder.

Lithium Carbonate Titration

Indications referenced: Bipolar I (acute mania, maintenance). Narrow therapeutic index.

โš  Toxicity Risk. Lithium toxicity can occur at levels close to therapeutic. Monitor serum levels closely. Risk increases with dehydration, NSAIDs, ACE inhibitors, thiazide diuretics, and low-sodium states.

Pre-Treatment Workup (Baseline)

  • SCr / eGFR, BUN, electrolytes
  • TSH, free T4
  • Calcium (lithium can cause hyperparathyroidism)
  • CBC
  • Urine pregnancy test (Ebstein's anomaly risk — counsel)
  • ECG if age ≥40 or cardiac history
  • Weight / BMI baseline

Starting Dose

  • Typical adult starting dose: 300 mg PO BID or TID (600–900 mg/day total).
  • Elderly or impaired renal function: Start 150 mg BID (300 mg/day) and titrate more slowly.
  • Preferred formulation: immediate-release for initiation; extended-release (Lithobid) can reduce GI side effects and peak-related tremor.

Target Serum Levels (12 hours post-dose, trough)

Indication Target Level (mEq/L)
Acute mania 1.0 – 1.2 mEq/L
Maintenance 0.6 – 1.0 mEq/L
Elderly 0.4 – 0.8 mEq/L (lower end)
Toxicity concern ≥1.5 mEq/L (mild) · ≥2.0 (moderate) · ≥2.5 (severe — medical emergency)

Monitoring Schedule

Parameter Frequency
Lithium level Check 5 days after each dose change (steady state), then every 3 months once stable, then every 6–12 months if stable long-term
SCr / eGFR Every 3 months for first year, then every 6–12 months
TSH Every 6 months
Calcium Annually
Weight, BMI Every visit

Level Timing Rule

Lithium levels must be drawn as a 12-hour trough (exactly 12 hours after the last dose, typically morning draw if patient takes evening dose). Levels drawn at other times are not interpretable for dose adjustment.

Key Drug Interactions

  • NSAIDs (except aspirin, sulindac): can raise lithium levels significantly.
  • Thiazide diuretics: decrease renal clearance, can raise levels.
  • ACE inhibitors / ARBs: can raise levels.
  • Dehydration / low-sodium diet: raises levels.
  • Caffeine withdrawal: can raise levels (caffeine is mildly diuretic).

Sources: Lithium carbonate FDA prescribing information. Stahl SM. Prescriber's Guide, 7th ed. American Psychiatric Association Practice Guideline for the Treatment of Patients with Bipolar Disorder. Maudsley Prescribing Guidelines in Psychiatry, 14th ed. NICE Guideline CG185 (Bipolar Disorder).


๐Ÿ”„ Switching & Withdrawal Protocols

๐Ÿ› ๏ธ

In Development

Switching protocols (SSRI→MAOI washout, antipsychotic cross-taper, valproate→lamotrigine, methadone→buprenorphine Bernese), withdrawal assessment tools (CIWA-Ar, COWS), and benzodiazepine taper frameworks will be drafted here and submitted for clinical review. Expected availability: September 2026.


Clinical Disclaimer

These tools are intended as clinical decision support for licensed prescribers. They do not replace clinical judgment, patient-specific assessment, or current prescribing information. Always verify dosing against FDA-approved labeling, check patient-specific factors (renal/hepatic function, pregnancy status, drug allergies, concomitant medications), and consult current guidelines before making prescribing decisions.

Lumina PMHNP Mentorship does not assume liability for clinical decisions made using these tools.