Digibind
Review and revised 11 July 2014
OVERVIEW
- Digibind is the trade name for a digoxin antidote containing Digoxin-specific antibody Fab fragments
- there is often a reluctance to give digibind due to cost and underestimating the mortality associated with digoxin toxicity, however it is prudent to administer digibind based on a considered risk assessment and before the life-threatening manifestations of digoxin toxicity develop
- digoxin levels cannot be accurately measured for about 3 weeks after administration of digibind, as they will be artefactually high given that most serum digoxin assays measure both free and digibind-bound digoxin in the circulation (some laboratories may be able to measure free digoxin levels specifically)
- supplies of digibind should be available on site in the emergency department, and in severe toxicities early steps to source more may be necessary
CLASS
- Digoxin-specific antibody Fab fragments
MECHANISM OF ACTION
- digibind has a much higher affinity (high affinity (109–1010 L/mol) for digoxin than the Na+/K+ ATPase digoxin receptor site
- binds to digoxin in the extracellular spaces preventing digoxin binding to the Na+/K+ ATPase
- creates a concentration gradient that extracts digoxin from the intracellular space
- bound digoxin is then renally eliminated with digibind
PHARMACEUTICS
- powder
- contains 38mg of digoxin-specific Fab fragments
- reconstitute with sterile water
DOSE
- each 38mg vial will bind about 0.5mg of digoxin
- give over 30min or bolus if in an arrest
- improvement in symptoms usually within 30 min, with maximal effect by 4 hours
Acute digoxin toxicity
- Known dose:
- number of vials = Ingested dose (mg) x 0.8 (bioavailability) x 2 (note that 0.8 represents the 80% oral bioavailability of digoxin)
- Unknown dose:
- Give 5 vials initially if the patient is hemodynamically stable
- Give 10 vials initially if the patient is hemodynamically unstable
- Repeat doses of 5 ampoules should be given every 30 minutes until reversal of digoxin toxicity is achieved
- In cardiac arrest give 20 vials (760 mg), or as many vials as are available if <20 stocked
Chronic digoxin toxicity
- Known level: number of vials required = post-distribution serum digoxin concentration (nanogram/mL) x weight (kg)/100 (multiply by 0.78 if SI units are used for post-distribution serum digoxin concentration)
- empiric dosing: give 2 ampoules and observe for clinical response, if toxicity remains after 30 minutes give a further 2 ampoules
- a source of confusion is the units of measurement used by laboratories: many laboratories measurs serum digoxin levels in nmols/L. The conversion factor is ng/ml x 1.28 = nmols/L
Endpoints
- resolution of nausa and vomiting
- resolution of dysrhythmia
- complete binding of total body digoxin is usually not necessary to control digoxin toxicity
INDICATIONS
Acute digoxin toxicity
- cardiac arrest
- life-threatening dysrhythmia
- K >5mM
- >10mg ingested (adult), >4mg ingested (child)
- >15 nM level (>12ng/mL)
Chronic digoxin toxicity
- cardiac arrest
- life-threatening dysrhythmia
- dysrhythmia or increased automaticity unlikely to be tolerated for a prolonged period
- significant gastrointestinal symptoms
- symptoms of digoxin toxicity and coexistent renal failure
Other life-threatening cardiac glycoside toxicities:
- oleander poisoning
- cane toad poisoning (bufotoxin)
- Chinese medicines (e.g. Chan Su, Dan Shen and Lu-Shen-Wan)
No absolute contraindications
ADVERSE EFFECTS
- anaphylaxis (rare)
- effects from withdrawal of digoxin: AF, heart failure (negative inotropy), hypokalemia
PHARMACOKINETICS
- Absorption – IV administration, from the end of infusion initial response is 20 minutes (0 to 60 min) and maximal response is at 90 minutes (30-360 min)
- Distribution – large Vd
- Metabolism – nil
- Elimination – urinary, t ½ = 11 hrs; bound digoxin has an elimination t1/2 of 16-30h
References and Links
CCC Pharmacology Series
Respiratory: Bosentan, Delivery of B2 Agonists in Intubated Patients, Nitric Oxide, Oxygen, Prostacyclin, Sildenafil
Cardiovascular: Adenosine, Adrenaline (Epinephrine), Amiodarone, Classification of Vasoactive drugs, Clevidipine, Digoxin, Dobutamine, Dopamine, Levosimendan, Levosimendan vs Dobutamine, Milrinone, Noradrenaline, Phenylephrine, Sodium Nitroprusside (SNiP), Sotalol, Vasopressin
Neurological: Dexmedetomidine, Ketamine, Levetiracetam, Lignocaine, Lithium, Midazolam, Physostigmine, Propofol, Sodium Valproate, Sugammadex, Thiopentone
Endocrine: Desmopressin, Glucagon Therapy, Medications and Thyroid Function
Gastrointestinal: Octreotide, Omeprazole, Ranitidine, Sucralfate, Terlipressin
Genitourinary: Furosemide, Mannitol, Spironolactone
Haematological: Activated Protein C, Alteplase, Aprotinin, Aspirin, Clopidogrel, Dipyridamole, DOACs, Factor VIIa, Heparin, LMW Heparin, Protamine, Prothrombinex, Tenecteplase, Tirofiban, Tranexamic Acid (TXA), Warfarin
Antimicrobial: Antimicrobial Dosing and Kill Characteristics, Benzylpenicillin, Ceftriaxone, Ciprofloxacin, Co-trimoxazole / Bactrim, Fluconazole, Gentamicin, Imipenem, Linezolid, Meropenem, Piperacillin-Tazobactam, Rifampicin, Vancomycin
Analgesic: Alfentanil, Celecoxib, COX II Inhibitors, Ketamine, Lignocaine, Morphine, NSAIDs, Opioids, Paracetamol (Acetaminophen), Paracetamol in Critical Illness, Tramadol
Miscellaneous: Activated Charcoal, Adverse Drug Reactions, Alkali Therapies, Drug Absorption in Critical Illness, Drug Infusion Doses, Epidural Complications, Epidural vs Opioids in Rib Fractures, Magnesium, Methylene Blue, Pharmacology and Critical Illness, PK and Obesity, PK and ECMO, Sodium Bicarbonate Use, Statins in Critical Illness, Therapeutic Drug Monitoring, Weights in Pharmacology
Toxicology: Digibind, Flumazenil, Glucagon Therapy, Intralipid, N-Acetylcysteine, Naloxone, Propofol Infusion Syndrome
CCC Toxicology Series
General
Approach to acute poisoning, ECGs in Tox, Evidenced-based Tox, Toxicology literature summaries, Does anti-venom work?
Toxins / Overdose
Amphetamines, Barbituates, Benzylpiperazine, Beta Blockers, Calcium Channel Blocker, Carbamazepine, Carbon Monoxide, Ciguatera, Citrate, Clenbuterol, Cocaine, Corrosive ingestion, Cyanide, Digoxin, Ethanol, Ethylene Glycol, Iron, Isoniazid, Lithium, Local anaesthetic, Methanol, Monoamine oxidase inhibitor (MAOI), Mushrooms (non-hallucinogenic), Opioids, Organophosphate, Paracetamol, Paraquat, Plants, Polonium, Salicylate, Scombroid, Sodium channel blockers, Sodium valproate, Theophylline, Toxic alcohols, Tricyclic antidepressants (TCA)
Envenomation
Marine, Snakebite, Spider, Tick paralysis
Syndromes
Alcohol withdrawal, Anticholinergic syndrome, Cholinergic syndrome, Drug withdrawals in ICU, Hyperthermia associated toxidromes, Malignant hyperthermia (MH), Neuroleptic malignant syndrome (NMS), Opioid withdrawal, Propofol Infusion Syndrome (PrIS) Sedative toxidrome, Serotonin syndrome, Sympatholytic toxidrome, Sympathomimetic toxidrome
Decontamination
Activated Charcoal, Gastric lavage, GI Decontamination
Enhanced Elimination
Enhanced elimination, Hyperbaric therapy for CO
Antidotes
Antidote summary, Digibind, Glucagon, Flumazenil, HIET – High dose euglycaemic therapy, Intralipid, Methylene Blue, N-Acetylcysteine (NAC), Naloxone
Miscellaneous
Cocaine chest pain, Digoxin and stone heart theory, Hyperbaric oxygen, Hypoxaemia in tox, Liver failure in tox, Liver transplant for paracetamol, Methaemoglobinaemia, Urine drug screen
LITFL
- ECG library – Digoxin Effect
- ECG library – Digoxin Toxicity
- CCC – Calcium, Digoxin Toxicity and ‘Stone Heart’ Theory
Journal articles and textbooks
- Antman EM, Wenger TL, Butler VP Jr, Haber E, Smith TW. Treatment of 150 cases of life-threatening digitalis intoxication with digoxin-specific Fab antibody fragments. Final report of a multicenter study. Circulation. 1990 Jun;81(6):1744-52
- McMillin GA, Owen WE, Lambert TL, De BK, Frank EL, Bach PR, Annesley TM, Roberts WL. Comparable effects of DIGIBIND and DigiFab in thirteen digoxin immunoassays. Clin Chem. 2002 Sep;48(9):1580-4.
- Ip D, Syed H, Cohen M. Digoxin specific antibody fragments (Digibind) in digoxin toxicity. BMJ. 2009 Sep 3;339:b2884
- Pincus M. Management of digoxin toxicity. Aust Prescr. 2016 Feb;39(1):18-20. doi: 10.18773/austprescr.2016.006.
Critical Care
Compendium
Chris is an Intensivist and ECMO specialist at The Alfred ICU, where he is Deputy Director (Education). He is a Clinical Adjunct Associate Professor at Monash University, the Lead for the Clinician Educator Incubator programme, and a CICM First Part Examiner.
He is an internationally recognised Clinician Educator with a passion for helping clinicians learn and for improving the clinical performance of individuals and collectives. He was one of the founders of the FOAM movement (Free Open-Access Medical education) has been recognised for his contributions to education with awards from ANZICS, ANZAHPE, and ACEM.
His one great achievement is being the father of three amazing children.
On Bluesky, he is @precordialthump.bsky.social and on the site that Elon has screwed up, he is @precordialthump.
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