Master alcohol withdrawal recognition & management
This isn't a lecture — it's hands-on practice. You'll score patients, make clinical decisions, and get instant feedback as you learn.
⏱ ~30 minutes · 4 modules · Earn XP as you go
Why withdrawal happens
CIWA-Ar scoring
Management & meds
Bedside simulation
50% of patients with alcohol use disorder will experience some withdrawal on cessation.
3–5% of those develop seizures or delirium tremens — which can be fatal.
Jesse et al., 2017
Alcohol is a brake pedal on the brain. With daily heavy use, the brain compensates by slamming the gas pedal (glutamate) harder and harder.
When you suddenly remove the brake (stop alcohol), the gas pedal is still floored — the brain goes into a dangerous excitatory overdrive.
GABA (the brake) → Inhibitory. Chronic alcohol enhances it, so the brain downregulates GABA receptors.
Glutamate (the gas) → Excitatory. Alcohol suppresses it, so the brain upregulates glutamate receptors.
Reduced brakes (↓ GABA) + floored gas (↑ glutamate) = tremor, agitation, tachycardia, hypertension, seizures.
Tap each stage to learn more ↓
Anxiety, tremor, insomnia, sweating, nausea
Visual, auditory, or tactile hallucinations
Generalized tonic-clonic seizures
Confusion, agitation, autonomic storm, fever
Each withdrawal episode can be worse than the last. The brain becomes permanently sensitized. A patient on their 3rd withdrawal may seize when their 1st episode was mild.
Always ask: "Have you ever gone through withdrawal before?"
The Clinical Institute Withdrawal Assessment for Alcohol, Revised — the gold-standard bedside tool for measuring withdrawal severity.
10 domains · Max score: 67 · Takes 2–5 minutes
Sullivan et al., 1989 · Validated across multiple settings
Before: Everyone got the same benzo schedule → over-sedation for some, under-treatment for others.
After (symptom-triggered therapy): Medicate only when the CIWA score says to → 50–70% less medication, treatment time from 68 hours → 9 hours.
| # | Domain | Range | Ask / Observe |
|---|---|---|---|
| 1 | Nausea | 0–7 | "Do you feel sick to your stomach?" |
| 2 | Tremor | 0–7 | Arms out, fingers spread — observe |
| 3 | Sweats | 0–7 | Touch forehead/palms — observe |
| 4 | Anxiety | 0–7 | "Do you feel nervous?" Watch for fidgeting |
| 5 | Agitation | 0–7 | Observe behavior: calm → thrashing |
| 6 | Tactile | 0–7 | "Any itching, burning, bugs crawling?" |
| 7 | Auditory | 0–7 | "Are sounds harsh? Hearing things?" |
| 8 | Visual | 0–7 | "Light too bright? Seeing things?" |
| 9 | Headache | 0–7 | "Band around head?" (NOT dizziness!) |
| 10 | Orientation | 0–4 | "What day? Where are you? Who am I?" |
Headache ≠ Dizziness. The CIWA headache item measures head fullness or band-like pressure. If a patient says "I feel dizzy," that is not scored. Ask: "Does it feel like something is pressing on your head?"
Monitor q4–8h. Supportive care only. Hydration, thiamine, quiet room.
Medicate per protocol. Reassess q1–2h. Consider closer monitoring.
Medicate + notify MD. Reassess q30–60min. Consider ICU.
1. Build rapport first — no one cooperates if they feel judged
2. Use the exact phrasing — it's validated
3. Observe before you ask (tremor, sweats, agitation)
4. Score what you see right now, not an hour ago
5. Document each domain, not just the total
6. Patient must be able to participate — if not, use RASS and call the provider
Use the sliders to score each domain based on the patient presentation. Watch the total update in real time.
The Saitz et al. (1994) trial in JAMA changed everything:
Symptom-triggered avg treatment
Fixed-dose avg treatment
Bottom line: Medicate based on the CIWA score, not the clock. Less medication, shorter stays, fewer ICU transfers.
| CIWA | Medication | Action |
|---|---|---|
| < 10 | None | Monitor q4–8h, thiamine, supportive care |
| 10–18 | Lorazepam 1–2 mg or Chlordiazepoxide 25–50 mg PO | Administer, reassess q1–2h |
| ≥ 19 | Lorazepam 2–4 mg IV may repeat per protocol | Notify MD, reassess q30–60min, consider ICU |
Lorazepam → Safe in liver disease (no hepatic oxidation needed)
Chlordiazepoxide → Smoother taper, but needs a working liver
Thiamine BEFORE glucose. Always. No exceptions.
Glucose burns through thiamine. In a depleted patient, giving glucose first can trigger Wernicke encephalopathy — confusion, ataxia, ophthalmoplegia. Permanent brain damage if missed.
✅ Vitals q1–4h based on severity (include temp!)
✅ Continuous telemetry if CIWA ≥ 19 or cardiac hx
✅ I&O — these patients dehydrate fast
✅ Quiet, well-lit room. Minimize stimulation.
✅ Reorientation: clock, whiteboard, consistent staff
✅ Seizure precautions: bed low, rails padded, suction ready
✅ 1:1 if hallucinating, agitated, or CIWA ≥ 25
✅ Fall risk interventions (tremor + sedating meds = falls)
🔴 CIWA ≥ 20 or scores climbing fast despite meds
🔴 Seizure activity
🔴 Temp > 101°F (DTs? Infection?)
🔴 HR > 120 or BP > 180/__ or < 90/__
🔴 Acute mental status change
🔴 > 3 doses lorazepam in 1 hour, no improvement
🔴 RR < 10 or SpO₂ < 92% (respiratory depression)
🔴 Patient can no longer participate in CIWA
Your CIWA-Ar result: Nausea 2, Tremor 3, Sweats 3, Anxiety 3, Agitation 2, Tactile 0, Auditory 1, Visual 0, Headache 1, Orientation 0 = Total: 15 (Moderate)
Your CIWA-Ar: Nausea 5, Tremor 6, Sweats 6, Anxiety 6, Agitation 6, Tactile 5, Auditory 5, Visual 5, Headache 0, Orientation 4 = Total: 48 (Severe)
8 questions. Score ≥ 75% for competency readiness. Good luck!
You earned 0 XP. Well done.
1. Submit your final assessment score to your unit educator
2. Complete a live CIWA-Ar return demonstration
3. Apply these skills at the bedside — your knowledge saves lives
ASAM (2020). Clinical Practice Guideline on Alcohol Withdrawal Management.
Saitz et al. (1994). JAMA, 272(7), 519–523.
Sullivan et al. (1989). Br J Addiction, 84(11), 1353–1357.
Jesse et al. (2017). Acta Neurol Scand, 135(1), 4–16.
Daeppen et al. (2002). Arch Intern Med, 162(10), 1117–1121.
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