Calcium channel blocker overdose
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Establish acute CCB exposure (intentional, accidental pediatric, therapeutic error); classify the engine as a cardiotoxic-shock toxidrome with delayed-peak SR risk (ACMT 2017)
CCB exposure scenario established and formulation (IR vs SR) noted
Patient inputs (13)
Pediatric "one-pill-can-kill" — a single SR verapamil/diltiazem tablet can kill a toddler; weight drives all antidote dosing
Calcium, HIET, lipid-emulsion dosing are all weight-based (U/kg, mL/kg)
Non-DHP (verapamil/diltiazem) vs DHP (amlodipine/nifedipine); IMMEDIATE- vs SUSTAINED-RELEASE drives delayed/prolonged-toxicity expectation + WBI decision
Time since ingestion + estimated dose; SR products peak 6–18 h with pharmacobezoar — a well-appearing early patient can crash
Beta-blocker, digoxin, antihypertensive co-ingestion compounds bradycardia / shock and changes antidote sequence
HYPERGLYCEMIA is the CCB fingerprint (islet insulin-secretion blockade) — separates CCB from beta-blocker tox and correlates with severity (St-Onge 2017)
Baseline + serial during calcium therapy to avoid dangerous hypercalcemia
HIET drives intracellular K shift — q1h K, replace to keep ≥2.8–3.0 mEq/L; baseline before infusion
Sinus bradycardia, PR prolongation, high-grade AV block, junctional escape, QRS/QT changes; baseline rhythm + monitoring
Bradycardia + AV block (non-DHP) vs reflex tachycardia early then bradycardia (DHP massive); drives calcium/atropine/pacing
Hypotension severity drives calcium → fluids → HIET → vasopressor escalation
AMS reflects cerebral hypoperfusion / impending arrest; airway watch
Tissue hypoperfusion marker; trend guides escalation to mechanical support
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (6)
- informationallife_threateningrefractory_bradycardia_av_blockSymptomatic bradycardia / high-grade or complete AV block unresponsive to atropine + calcium boluses (non-DHP phenotype) (Crit Care 2023)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningrefractory_shock_for_hiet_and_lipidHypotension / cardiogenic shock not corrected by calcium boluses + IV fluids (St-Onge Crit Care Med 2017)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningperiarrest_refractory_to_full_ladderPeri-arrest / shock refractory to calcium + max HIET + ≥2 vasopressors ± lipid/methylene blue (ELSO)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningpediatric_one_pill_can_killPediatric ingestion — a single SR verapamil/diltiazem tablet can be lethal in a toddler (Crit Care 2023)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseveresr_formulation_ingestionSustained-/extended-release verapamil, diltiazem, or amlodipine ingestion (even if currently asymptomatic) (ACMT 2017)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverehyperglycemia_distinguishes_ccbHyperglycemia + shock without DKA — pivots diagnosis to CCB (insulin-secretion blockade) vs beta-blocker (St-Onge Crit Care Med 2017)Trigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
CCB overdose — antidotal ladder (calcium → HIET core inotrope → vasopressor → lipid / methylene blue → mechanical support)- calcium gluconatefirst linecalcium_salt30–60 mL of 10% (3–6 g) IV over 5–10 min; repeat q10–20 min ×3–4 PRN, then infusion 0.6–1.5 mL/kg/h of 10% titrated to ionized calcium / hemodynamics • IV • bolus then continuous infusiontriggers: hypotension, bradycardia, av_block, peripheral_iv_onlyACMT 2017 — first antidote; overcomes channel blockade by raising extracellular calcium gradient. Gluconate preferred when only peripheral access (less caustic on extravasation). Target ionized Ca up to ~2× normal; surveil for hypercalcemia (Crit Care 2023)rxcui 1908
- calcium chloridefirst linecalcium_salt10–20 mL of 10% (1–2 g) IV via CENTRAL line over 5–10 min; repeat q10–20 min PRN then infusion • IV (central) • bolus then continuous infusiontriggers: central_line_available, severe_shock_needs_3x_calcium_per_volume3× elemental calcium per mL vs gluconate — preferred in severe shock when central access exists; vesicant, central line mandatory (ACMT 2017)rxcui 1901
- whole-bowel irrigation (polyethylene glycol)add ongi_decontaminationPEG-ELS 1–2 L/h (adult) / 25 mL/kg/h (peds) NG until rectal effluent clear • PO/NG • continuous until effluent cleartriggers: sustained_release_formulation, large_ingestion_within_window, protected_airway_if_AMSACMT 2017 — SR verapamil/diltiazem form pharmacobezoars; WBI limits ongoing absorption. Activated charcoal 1 g/kg if early and airway protected. Hold if ileus / unprotected airway (Crit Care 2023)
ed playbook — drug actions (6)
- 1. calcium gluconate (or chloride if central)Gluconate 30–60 mL 10% IV over 5–10 min, repeat q10–20 min ×3–4; chloride 10–20 mL 10% central • IV • bolus then infusiontrigger: Hypotension / bradycardia / AV blockFirst antidote — raise extracellular calcium gradient (ACMT 2017)
- 2. HIET (regular insulin)1 U/kg IV bolus then 0.5–1 U/kg/h, titrate to 10 U/kg/h • IV • bolus then infusiontrigger: Shock not rapidly corrected by calcium + fluids — start EARLYCore inotrope, not last resort (St-Onge Crit Care Med 2017)
- 3. dextrose + potassiumD50 25–50 g PRN then D10–25 infusion; KCl to keep K ≥2.8–3.0 • IV • titrated, q30min glucose / q1h Ktrigger: HIET runningPrevent HIET hypoglycemia / intracellular hypokalemia (Crit Care 2023)
- 4. norepinephrine ± epinephrineNE 0.05–0.5 mcg/kg/min titrate to MAP ≥65; add epi for mixed shock • IV (central) • continuoustrigger: MAP <65 despite calcium + HIETPhenotype-guided pressor (Crit Care 2023)
- 5. atropine (adjunct)0.5–1 mg IV q3–5 min, max 3 mg • IV • PRN bradycardiatrigger: Symptomatic bradycardiaOften ineffective — do not delay calcium/HIET/pacing (ACMT 2017)
- 6. IV lipid emulsion 20% (rescue)1.5 mL/kg bolus, repeat ×1–2 for arrest, then 0.25 mL/kg/min • IV • bolus then infusiontrigger: Peri-arrest / refractory lipophilic CCBRefractory rescue (AACT/ACMT lipid workgroup)
Auto-drafted A&P note
edSubjective
- Possible entry pathways: Reported / suspected verapamil, diltiazem, amlodipine, nifedipine ingestion (ACMT 2017); Bradycardia + hypotension in a patient on or with access to a CCB (Crit Care 2023); Hyperglycemia + shock without diabetic ketoacidosis — CCB until proven otherwise (St-Onge Crit Care Med 2017).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Calcium channel blocker overdose** (tox.calcium-channel-blocker-overdose.core.v1). Phenotype framing: Beta-blocker overdose (hypoglycemia not hyperglycemia), digoxin toxicity, clonidine/central alpha-2, organophosphate, hyperkalemia, sick sinus / inferior MI with shock, sepsis, other sympatholytic toxidromes (St-Onge 2017) Scope: Establish acute CCB exposure (intentional, accidental pediatric, therapeutic error); classify the engine as a cardiotoxic-shock toxidrome with delayed-peak SR risk (ACMT 2017) No severity triggers fired against current inputs.
Plan
Regimen axis: **CCB overdose — antidotal ladder (calcium → HIET core inotrope → vasopressor → lipid / methylene blue → mechanical support)** — step "Step 1 — IV calcium (bolus → infusion) + GI decontamination". 1. calcium gluconate 30–60 mL of 10% (3–6 g) IV over 5–10 min; repeat q10–20 min ×3–4 PRN, then infusion 0.6–1.5 mL/kg/h of 10% titrated to ionized calcium / hemodynamics IV bolus then continuous infusion (calcium_salt, first line) — ACMT 2017 — first antidote; overcomes channel blockade by raising extracellular calcium gradient. Gluconate preferred when only peripheral access (less caustic on extravasation). Target ionized Ca up to ~2× normal; surveil for hypercalcemia (Crit Care 2023) 2. calcium chloride 10–20 mL of 10% (1–2 g) IV via CENTRAL line over 5–10 min; repeat q10–20 min PRN then infusion IV (central) bolus then continuous infusion (calcium_salt, first line) — 3× elemental calcium per mL vs gluconate — preferred in severe shock when central access exists; vesicant, central line mandatory (ACMT 2017) 3. whole-bowel irrigation (polyethylene glycol) PEG-ELS 1–2 L/h (adult) / 25 mL/kg/h (peds) NG until rectal effluent clear PO/NG continuous until effluent clear (gi_decontamination, add on) — ACMT 2017 — SR verapamil/diltiazem form pharmacobezoars; WBI limits ongoing absorption. Activated charcoal 1 g/kg if early and airway protected. Hold if ileus / unprotected airway (Crit Care 2023) Setting playbook (ed) — Recognize CCB toxidrome (bradycardia/hypotension + hyperglycemia), start calcium + early HIET, decontaminate SR, escalate pressors, and mobilize ICU/ECMO before collapse (ACMT 2017) 4. calcium gluconate (or chloride if central) Gluconate 30–60 mL 10% IV over 5–10 min, repeat q10–20 min ×3–4; chloride 10–20 mL 10% central IV bolus then infusion — Hypotension / bradycardia / AV block (First antidote — raise extracellular calcium gradient (ACMT 2017)) 5. HIET (regular insulin) 1 U/kg IV bolus then 0.5–1 U/kg/h, titrate to 10 U/kg/h IV bolus then infusion — Shock not rapidly corrected by calcium + fluids — start EARLY (Core inotrope, not last resort (St-Onge Crit Care Med 2017)) 6. dextrose + potassium D50 25–50 g PRN then D10–25 infusion; KCl to keep K ≥2.8–3.0 IV titrated, q30min glucose / q1h K — HIET running (Prevent HIET hypoglycemia / intracellular hypokalemia (Crit Care 2023)) 7. norepinephrine ± epinephrine NE 0.05–0.5 mcg/kg/min titrate to MAP ≥65; add epi for mixed shock IV (central) continuous — MAP <65 despite calcium + HIET (Phenotype-guided pressor (Crit Care 2023)) 8. atropine (adjunct) 0.5–1 mg IV q3–5 min, max 3 mg IV PRN bradycardia — Symptomatic bradycardia (Often ineffective — do not delay calcium/HIET/pacing (ACMT 2017)) 9. IV lipid emulsion 20% (rescue) 1.5 mL/kg bolus, repeat ×1–2 for arrest, then 0.25 mL/kg/min IV bolus then infusion — Peri-arrest / refractory lipophilic CCB (Refractory rescue (AACT/ACMT lipid workgroup)) Non-pharmacologic actions: - Whole-bowel irrigation for SR ingestion (PEG-ELS NG) once airway protected (ACMT 2017) - Activated charcoal 1 g/kg if early presentation + airway protected (Crit Care 2023) - Two large-bore IVs + early central line for calcium chloride / pressors (ACMT 2017) - Continuous cardiac + arterial monitoring; transcutaneous pacing pads on (Crit Care 2023) - Notify ICU + ECMO-capable centre EARLY for SR / refractory shock (ELSO) AVOID / contraindication checks: - Calcium chloride central line only — vesicant tissue necrosis on extravasation (ACMT 2017) - Do not delay HIET as a last resort — start early as a core inotrope (St Onge Crit Care Med 2017) - HIET requires q30min glucose and q1h potassium — hypoglycemia and intracellular hypokalemia (Crit Care 2023) - Atropine frequently ineffective in CCB AV block — do not delay calcium/HIET/pacing waiting for it (ACMT 2017) - Methylene blue avoid in G6PD deficiency and with serotonergic agents — serotonin syndrome / hemolysis (Crit Care 2023) - Lipid emulsion may cause fat overload and interfere with lab assays — reserve for refractory/peri arrest (AACT/ACMT lipid workgroup) - Surveil ionized calcium during calcium infusion — avoid dangerous hypercalcemia (Crit Care 2023) - Engage ECMO capable centre early for refractory shock — do not wait for arrest (ELSO)
Monitoring
Regimen monitoring: - continuous telemetry + arterial line (Crit Care 2023) - glucose q30min during HIET titration (St-Onge Crit Care Med 2017) - potassium q1h during HIET — replace to keep K ≥2.8–3.0 mEq/L (Crit Care 2023) - ionized calcium q1–2h during calcium infusion — avoid hypercalcemia (ACMT 2017) - lactate clearance q2–4h as perfusion marker (Crit Care 2023) - MAP / cardiac output (echo or invasive) to phenotype pump vs vasoplegia (ELSO) - prolonged ≥24 h monitoring for SR pharmacobezoar delayed peak (ACMT 2017) - delayed hypoglycemia surveillance for hours after HIET discontinuation (St-Onge 2017) Setting (ed) monitoring: - HR/rhythm + MAP continuous (ACMT 2017) - Glucose q30min during HIET (St-Onge Crit Care Med 2017) - Potassium q1h during HIET (Crit Care 2023) - Ionized calcium q1–2h during calcium infusion (ACMT 2017) - Lactate q2–4h (Crit Care 2023) Follow-up plan: Wean HIET (taper as glucose tolerance falls — risk of hypoglycemia on abrupt stop), de-escalate vasopressors/calcium; psychiatry + safety planning if intentional; medication-safety / lethal-means counselling; pediatric poison-prevention education and Poison Control reporting (AACT/ACMT) - Close-out criterion: Antidotes safely weaned, psych/social disposition complete, prevention education delivered Monitoring phase: Continuous telemetry + arterial line; q30min glucose and q1h K during HIET (intracellular K shift), serial ionized calcium during calcium infusion, lactate clearance, MAP/cardiac output, urine output; prolonged monitoring (≥24 h) for SR pharmacobezoar (ACMT 2017)
Disposition
Current setting: ed — Recognize CCB toxidrome (bradycardia/hypotension + hyperglycemia), start calcium + early HIET, decontaminate SR, escalate pressors, and mobilize ICU/ECMO before collapse (ACMT 2017) Disposition criteria: - ICU: any antidote requirement, any SR product, any symptomatic ingestion, any AV block (Crit Care 2023) - Monitored ward only if asymptomatic IR ingestion with normal serial vitals/ECG + observation window cleared (ACMT 2017) - Transfer to ECMO-capable centre for refractory cardiogenic shock (ELSO) - Psychiatry + safety planning before discharge if intentional (AACT/ACMT) Escalation triggers (move to higher acuity): - Refractory hypotension on calcium + HIET → add vasopressors + ICU now (Crit Care 2023) - High-grade AV block / pre-arrest → pacing + ICU + tox consult (ACMT 2017) - SR product ingestion → admit/observe ≥24 h even if currently well (pharmacobezoar) (ACMT 2017) - Peri-arrest / shock refractory to full ladder → IV lipid + ECMO-centre transfer (ELSO)
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] Symptomatic bradycardia / high-grade or complete AV block unresponsive to atropine + calcium boluses (non-DHP phenotype) (Crit Care 2023) - [LIFE_THREATENING] Hypotension / cardiogenic shock not corrected by calcium boluses + IV fluids (St-Onge Crit Care Med 2017) - [LIFE_THREATENING] Peri-arrest / shock refractory to calcium + max HIET + ≥2 vasopressors ± lipid/methylene blue (ELSO)
Citations
- ACMT 2017 Position Statement: Interim Guidance for the Use of High-Dose Insulin and Lipid Emulsion in CCB/BB Poisoning + St-Onge et al. Crit Care Med 2017 (Experts Consensus / systematic review on CCB-poisoning management) + AACT/ACMT Lipid Emulsion Workgroup + 2023 Critical Care narrative review of CCB/BB toxicity + ELSO ECPR guidance [PMID:27749343](https://pubmed.ncbi.nlm.nih.gov/27749343/) - Cited evidence (PMID 28169558) [PMID:28169558](https://pubmed.ncbi.nlm.nih.gov/28169558/) - Cited evidence (PMID 26059743) [PMID:26059743](https://pubmed.ncbi.nlm.nih.gov/26059743/) - Cited evidence (PMID 37170354) [PMID:37170354](https://pubmed.ncbi.nlm.nih.gov/37170354/) - Cited evidence (PMID 25998059) [PMID:25998059](https://pubmed.ncbi.nlm.nih.gov/25998059/) Last reconciled with current guidelines: 2026-05-16.
- ACMT 2017 Position Statement: Interim Guidance for the Use of High-Dose Insulin and Lipid Emulsion in CCB/BB Poisoning + St-Onge et al. Crit Care Med 2017 (Experts Consensus / systematic review on CCB-poisoning management) + AACT/ACMT Lipid Emulsion Workgroup + 2023 Critical Care narrative review of CCB/BB toxicity + ELSO ECPR guidance — PMID:27749343
- Cited evidence (PMID 28169558) — PMID:28169558
- Cited evidence (PMID 26059743) — PMID:26059743
- Cited evidence (PMID 37170354) — PMID:37170354
- Cited evidence (PMID 25998059) — PMID:25998059