Atropine Sulphate

Anticholinergic

View Brand Names (2)

Dose and dosage

Swine

0.04 mg/kg IM (Thurmon & Benson 1986)

Dog

As a preanesthetic adjuvant:
a) In geriatric patients: 0.01–0.02 mg/kg IM, IV; do not use anticholinergics indiscriminately in geriatric patients. (Carpenter et al. 2005)
b) 0.074 mg/kg IV, IM or SC (Package Insert; Atropine Injectable, S.A.— Fort Dodge)
c) 0.02–0.04 mg/kg SC, IM or IV (Morgan 1988) For adjunctive treatment of bradycardias, Incomplete AV block, etc.
a) During cardiopulmonary cerebral resuscitation (CPCR) efforts: 0.04 mg/kg IV or IO; can repeat every 3–5 minutes for a maximum of 3 doses. For intra-tracheal (IT) administration: 0.08–0.1 mg/kg; dilute in 5–10 mL of sterile water before administering (Plunkett & McMichael 2008).
b) 0.02–0.04 mg/kg IV or IM (Russell & Rush 1995) To differentiate vagally-mediated bradyarrhythmias from non-vagal bradyarrhythmias (Atropine Response Test): Rishniw Preference: 1) Record ECG at baseline; 2) Administer 0.04 mg/kg atropine IV; 3) Wait 15 minutes; 4) Record ECG for at least 2 minutes (use slow paper speed). If the response is incomplete, repeat steps 2–4. Persistent sinus tachycardia at >140 bpm is expected in most dogs with vagally-mediated bradycardia. Kittleson Preference: 1) Record ECG at baseline; 2) Administer 0.04 mg/kg atropine SQ; 3) Wait 30 minutes; 4) Record ECG for at least 2 minutes (use slow paper speed). Persistent sinus tachycardia at >140 bpm is expected in most dogs with vagally-mediated bradycardia. (Rishniw & Kittleson 2007)
For treatment of cholinergic toxicity:
a) 0.2–0.5 mg/kg; 1/4 of the dose IV and the remainder IM or SC (Firth 2000)
For treatment of bronchoconstriction:
a) 0.02–0.04 mg/kg for a duration of effect of 1–1.5 hours (Papich 1986)

Cat

As a preanesthetic adjuvant:
a) In geriatric patients: 0.01–0.02 mg/kg IM, IV; do not use anticholinergics indiscriminately in geriatric patients. (Carpenter et al. 2005)
b) 0.074 mg/kg IV, IM or SC (Package Insert; Atropine Injectable, S.A.— Fort Dodge)
c) 0.02–0.04 mg/kg SC, IM or IV (Morgan 1988)
For treatment of bradycardias:
a) During cardiopulmonary cerebral resuscitation (CPCR) efforts: 0.04 mg/kg IV or IO; can repeat every 3–5 minutes for a maximum of 3 doses.
For intra-tracheal (IT) administration: 0.08–0.1 mg/kg; dilute in 5–10 mL of sterile water before administering (Plunkett & McMichael 2008).
b) 0.02–0.04 mg/kg SC, IM or IV q4–6h (Miller 1985)
For treatment of cholinergic toxicity:
a) 0.2–2 mg/kg; give ¼th of the dose IV and the remainder SC or IM (Morgan 1988)

Cattle

Note: When used in food animals at doses up to 0.2 mg/kg, FARAD recommends a 28 day meat and 6 day milk withdrawal time. (Haskell et al. 2005)
As a preanesthetic:
a) Because of a lack of extended efficacy and potential adverse reactions, atropine is not used routinely as a preoperative agent in ruminants. If it is desired for use, a dose of 0.06–0.12 mg/kg IM has been suggested.) (Thurmon & Benson 1986) For adjunctive treatment of bovine hypersensitivity disease:
a) 1 gram per cow once daily followed by 0.5 gram/cow in 2–3 days (method of administration not specified) (Manning & Scheidt 1986) For treatment of cholinergic toxicity (organophosphates):
a) 0.5 mg/kg (average dose); give ¼th of the dose IV and the remainder SC or IM; may repeat q3–4h for 1–2 days (Bailey 1986)

Horse

For treatment of bradyarrhythmias due to increased parasympathetic tone:
a) 0.01–0.02 mg/kg IV (Mogg 1999)
b) 0.045 mg/kg parenterally (Hilwig 1987)
As a bronchodilator:
a) 5 mg IV for a 400–500 kg animal (Beech 1987)
b) 5–7 mg/kg IV for a 450 kg horse can serve as a rescue medication in cases with severe airway obstruction, but it has an abbreviated duration of action (0.5–2 hours) and adverse effects (ileus, CNS toxicity, tachycardia, increased mucus secretion, and impaired mucociliary clearance) limit its use to a single rescue dose. (Rush 2006)
For organophosphate poisoning:
a) Approximately 1 mg/kg given to effect, IV (use mydriasis and absence of salivation as therapy endpoints), may repeat every 1.5–2 hours as required subcutaneously (Oehme 1987)
b) 0.22 mg/kg, ¼th of the dose administered IV and the remainder SC or IM (Package Insert; Atropine Injectable, L.A.— Fort Dodge)

Birds (Other)

For organophosphate poisoning:
a) 0.2 mg/kg IM every 3–4 hours as needed; ¼th the initial dose is administered. Use with pralidoxime (not in raptors) at 10–20 mg/kg IM q8–12h as needed. Do not use pralidoxime in carbamate poisonings. To assist in diagnosing organophosphate poisoning (with history, clinical signs, etc.) in birds presenting with bradycardia: May administer atropine at 0.02 mg/kg IV. If bradycardia does not reverse, may consider organophosphate toxicity. (LaBonde 2006)
As a preanesthetic:
a) 0.04–0.1 mg/kg IM or SC once (Clubb 1986)

Reptiles (Large)

For organophosphate toxicity in most species:
a) 0.1–0.2 mg/kg SC or IM as needed. (Gauvin 1993)
For ptyalism in tortoises:
a) 0.05 mg/kg (50 micrograms/kg) SC or IM once daily (Gauvin 1993)

Small mammals

To treat organophosphate toxicity: 10 mg/kg SC q20 minutes (Ivey & Morrisey 2000)

Ferrets

a) As a premed: 0.05 mg/kg SC or IM (Williams 2000)


Applications: Preanesthetics, bronchoconstriction, Salivation, Seizure, Diarrhea
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The principal veterinary indications for systemic atropine include:

  • Preanesthetic to prevent or reduce secretions of the respiratory tract
  • Treat sinus bradycardia, sinoatrial arrest, and incomplete AV block
  • Differentiate vagally-mediated bradycardia for other causes
  • As an antidote for overdoses of cholinergic agents (e.g., physostigmine, etc.)
  • As an antidote for organophosphate, carbamate, muscarinic mushroom, bluegreen
  • algae intoxication
  • Hypersialism
  • Treatment of bronchoconstrictive disease

Do not use in patients with glaucoma, intestinal ileus, gastroparesis, or tachycardia.

Atropine, like other antimuscarinic agents, competitively inhibits acetylcholine or other cholinergic stimulants at postganglionic parasympathetic neuroeffector sites. High doses may block nicotinic receptors at the autonomic ganglia and at the neuromuscular junction. Pharmacologic effects are dose related. At low doses salivation, bronchial secretions, and sweating (not horses) are inhibited. At moderate systemic doses, atropine dilates and inhibits accommodation of the pupil, and increases heart rate. High doses will decrease GI and urinary tract motility. Very high doses will inhibit gastric secretion.

Atropine sulfate is well absorbed after oral administration, IM injection, inhalation, or endotracheal administration. After IV administration peak effects in heart rates occur within 3–4 minutes. Atropine is well distributed throughout the body and crosses into the CNS, across the placenta, and can distribute into the milk in small quantities

The following drug interactions have either been reported or are theoretical in humans or animals receiving atropine and may be of significance in veterinary patients:
The following drugs may enhance the activity or toxicity of atropine and its derivatives:
AMANTADINE
ANTICHOLINERGIC AGENTS (other)
ANTICHOLINERGIC MUSCLE RELAXANTS
ANTIHISTAMINES (e.g., diphenhydramine)
DISOPYRAMIDE
MEPERIDINE
PHENOTHIAZINES
PROCAINAMIDE
PRIMIDONE

TRICYCLIC ANTIDEPRESSANTS (e.g., amitriptyline, clomipramine)
ALPHA-2 AGONISTS (e.g.,dexmedetomidine, medetomidine): Use of atropine with alpha-2 blockers may significantly increase arterial blood pressure, heart rates and the incidence of arrhythmias (Congdon et al. 2009). Clinical use of atropine or glycopyrrolate to prevent or treat medetomidineor dexmedetomidine-caused bradycardia is controversial and many discourage using together. This may be particularly important when using higher dosages of the alpha-2 agonist.
AMITRAZ: Atropine may aggravate some signs seen with amitraz toxicity; leading to hypertension and further inhibition of peristalsis
ANTACIDS: May decrease PO atropine absorption; give oral atropine at least 1 hour prior to oral antacids
CORTICOSTEROIDS (long-term use): may increase intraocular pressure
DIGOXIN (slow-dissolving): Atropine may increase serum digoxin levels; use regular digoxin tablets or oral liquid
KETOCONAZOLE: Increased gastric pH may decrease GI absorption; administer oral atropine 2 hours after ketoconazole
METOCLOPRAMIDE: Atropine and its derivatives may antagonize the actions of metoclopramide

Side effects include xerostomia, ileus, constipation, tachycardia, and urine retention

Use high doses (e.g., 0.04 mg/kg) cautiously because it increases oxygen demand.