quiNIDine gluconate (Rx)
Generic: QuiNIDine gluconate
Brand: not specified
(kwin'i-deen)
Pharmacological Action
Prolongs action potential duration and effective refractory period, thus decreasing myocardial excitability; anticholinergic properties
Therapeutic outcome: Treatment of dysrhythmias
Uses
Wolff-Parkinson-White syndrome, PVST, atrial fibrillation, flutter; paroxysmal atrial tachycardia, ventricular tachycardia, malaria (IV quiNIDine gluconate) Unlabeled uses: Singultus (hiccups)
Contraindications
Hypersensitivity or idiosyncratic response, digoxin toxicity, blood dyscrasias, myasthenia gravis, AV block
Precautions: Pregnancy C, breastfeeding, children, geriatric, renal/hepatic disease, potassium imbalance, CHF, respiratory depression, bradycardia, hypotension, syncope
BLACK BOX WARNING: Cardiac arrhythmias, MI
Dosage & Routes
QuiNIDine sulfate Atrial fibrillation/flutter/PVST/WPW
Adult: PO 200 mg q6-8 hr × 5-8 doses; may increase daily until sinus rhythm is restored; max 4 g/day given only after digitalization; maintenance 200-300 mg tid-qid or 300-600 mg q8-12 hr (EXT REL) Hiccups (unlabeled)
Adult: PO 200 mg qid QuiNIDine gluconate
Adult: PO 324-648 mg q8-12 hr (EXT REL); IM 600 mg, then 400 mg q2 hr; IV give 16 mg/min
Available forms:
Gluconate: ext rel tabs 324, 330 mg; inj gluconate 80 mg/ml; sulfate: tabs 200, 300 mg; ext rel tabs 300 mg
Implementation - Give AV node blocker (digoxin) before starting quiNIDine to avoid increased ventricular rate PO route - Do not break, crush, or chew ext rel tab - Give on an empty stomach with a full glass of water; may be given with meals if GI irritation occurs, absorption will be decreased - Ext rel forms not interchangeable - Tab may be crushed and mixed with fluid or foods for patients with swallowing difficulties IM route - Give IM injection in deltoid, aspirate to avoid intravascular administration Intermittent IV infusion route - Give after diluting 800 mg/50 ml or more D5 W (16 mg/ml); give max 0.25 mg/kg/min, quiNIDine is absorbed by PVC tubing, minimize length; use inf pump
Y-site compatibilities: Alfentanil, amikacin, anidulafungin, ascorbic acid, atenolol, atracurium, atropine, benztropine, bleomycin, bumetanide, buprenorphine, butorphanol, calcium gluconate, caspofungin, chlorproMAZINE, cimetidine, CISplatin, cyanocobalamin, cycloSPORINE, DACTINomycin, digoxin, diltiazem, diphenhydrAMINE, DOBUTamine, DOCEtaxel, DOPamine, doxycycline, enalaprilat, ePHEDrine, EPINEPHrine, epoetin alfa, erythromycin, esmolol, etoposide, famotidine, fenoldopam, fentaNYL, fluconazole, fludarabine, gatifloxacin, gemcitabine, gentamicin, glycopyrrolate, granisetron, HYDROmorphone, IDArubicin, imipenem-cilastatin, irinotecan, isoproterenol, labetalol, lidocaine, linezolid, LORazepam, magnesium sulfate, mannitol, mechlorethamine, meperidine, metaraminol, methoxamine, methyldopate, metoclopramide, metoprolol, metroNIDAZOLE, miconazole, milrinone, mitoXANtrone, morphine, multiple vitamins, mycophenolate, nalbuphine, naloxone, nesiritide, netilmicin, nitroglycerin, norepinephrine, octreotide, ondansetron, oxaliplatin, PACLitaxel, palonosetron, pamidronate, pancuronium, papaverine, pentamidine, pentazocine, phenylephrine, phytonadione, polymyxin B, potassium chloride, procainamide, prochlorperazine, promethazine, propranolol, protamine, pyridoxine, ranitidine, ritodrine, succinylcholine, SUFentanil, tacrolimus, teniposide, theophylline, thiamine, thiotepa, tirofiban, tobramycin, tolazoline, trimetaphan, urokinase, vancomycin, vasopressin, verapamil, vinorelbine, voriconazole, zoledronic acid
Adverse Effects
CNS: Headache, dizziness, involuntary movement, confusion, psychosis, restlessness, irritability, syncope, excitement, depression, ataxia
CV: Hypotension, bradycardia, PVCs, heart block, cardiovascular collapse, arrest, torsades de pointes, widening QRS complex, ventricular tachycardia
EENT:
Cinchonism: tinnitus, blurred vision, hearing loss, mydriasis, disturbed color vision
GI: Nausea, vomiting, anorexia, diarrhea, hepatotoxicity, abdominal pain
HEMA: Thrombocytopenia, hemolytic anemia, agranulocytosis, hypoprothrombinemia
INTEG: Rash, urticaria, angioedema, swelling, photosensitivity, flushing with severe pruritus
RESP: Dyspnea, respiratory depression
Pharmacokinetics
Absorption: Well absorbed (PO, IM), slowly absorbed (sus rel)
Distribution: Widely distributed, crosses placenta, protein binding 80%-90%
Metabolism: Liver
Excretion: Kidney unchanged, 10%-50% breast milk
Half-life: 6-7 hr (prolonged in geriatrics, cirrhosis, CHF)
Pharmacodynamics
PO (SULFATE): Onset ½ hr, Peak 1-6 hr, Duration 6-8 hr PO EXT
REL: Onset Unknown, Peak 4 hr, Duration 8-12 hr PO (GLUCONATE): Onset Unknown, Peak 4 hr, Duration 6-8 hr
IM: Onset ½ hr, Peak ½-1½ hr, Duration 6-8 hr
IV: Onset 5 min, Peak Unknown, Duration 6-8 hr
Interactions
Individual drugs
Amiodarone, cimetidine,
NIFEdipine: increased quiNIDine level
Digoxin: increased digoxin level NIFEdipine, sodium bicarbonate, verapamil: increased quiNIDine effect Phenytoin, rifampin, sucralfate: decreased effects of quiNIDine
Propranolol: increased effect of propranolol
Reserpine: increased cardiac depression
Warfarin: increased levels of warfarin
Drug classifications
Antacids, carbonic anhydrase inhibitors, hydroxide suspensions: increased effects of quiNIDine Anticholinergic blockers: increased vagolytic effects Anticoagulants (oral): increased levels of anticoagulant Antidepressants (tricyclics): increased effect of antidepressant
Antidysrhythmics: increased cardiac depression Barbiturates, cholinergics: decreased effects of quiNIDine Neuromuscular blockers: increased neuromuscular blocking
Phenothiazines: increased cardiac depression
Drug/herb
Hawthorn: increased quiNIDine effect
Drug/food
Grapefruit juice: decreased absorption, decreased metabolism
Drug/lab test
Increased: CPK
Interference: triamterene therapy interferes with quiNIDine test levels
Nursing Considerations
Assessment - Monitor ECG continuously to determine product effectiveness, measure PR, QRS, QT intervals, check for PVCs, other dysrhythmias; monitor B/P continuously for hypo/hypertension; for rebound hypertension after 1-2 hr; check for dehydration or hypovolemia - Monitor blood levels (therapeutic level 2-7 mcg/ml) -
Cinchonism: assess for tinnitus, headache, nausea, dizziness, fever, vertigo, tremor, may lead to hearing loss - Monitor • I&O ratio, electrolytes (potassium, sodium, chloride); check weight daily; check for signs of CHF or pulmonary toxicity: dyspnea, fatigue, cough, fever, chest pain; if these occur, product should be discontinued - Monitor liver function tests: AST, ALT, bilirubin, alkaline phosphatase - Assess for CNS symptoms: confusion, psychosis, numbness, depression, involuntary movements; if these occur, product should be discontinued - Monitor cardiac rate, respiration: rate, rhythm, character, chest pain; watch for ventricular tachycardia, supraventricular tachycardia, or fibrillation that indicates toxicity Patient/family education - Instruct patient to report adverse effects immediately to prescriber - Caution patient that sunglasses may be needed for photophobia; to use sunscreen, protective clothing, or stay out of sun to prevent burns - Instruct patient to complete follow-up appointments with health care provider including pulmonary function tests, chest x-ray, ophth and otoscopic exams - Advise patients to report signs of cinchonism, diarrhea, anorexia, decreased B/P - Avoid grapefruit
Evaluation
Positive therapeutic outcome: Resolution of dysrhythmias
Reference
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