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Dexmedetomidine

Dexmedetomidine is a sedative used in intensive care settings for sedation of intubated patients for up to 24 hours. It works by selectively agonizing alpha-2 receptors in the brain to produce sedation. Potential side effects include hypotension, bradycardia, and dry mouth. Nurses must continuously monitor the patient's level of sedation and vital signs due to the risk of cardiovascular complications. The drug requires continuous infusion to accurately control the sedation level.

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0% found this document useful (0 votes)
472 views2 pages

Dexmedetomidine

Dexmedetomidine is a sedative used in intensive care settings for sedation of intubated patients for up to 24 hours. It works by selectively agonizing alpha-2 receptors in the brain to produce sedation. Potential side effects include hypotension, bradycardia, and dry mouth. Nurses must continuously monitor the patient's level of sedation and vital signs due to the risk of cardiovascular complications. The drug requires continuous infusion to accurately control the sedation level.

Uploaded by

apt48 ukwms
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Name /bks_53161_deglins_md_disk/dexmedetomidine 02/12/2014 01:21PM Plate # 0-Composite pg 1 # 1

1 Interactions
Drug-Drug: Sedation is enhanced by anesthetics, other sedative/hypnotics, PDF Page #1
dexmedetomidine (dex-me-de-to-mi-deen) and opioid analgesics.
Precedex Drug-Natural Products: Concomitant use of kava-kava, valerian, skullcap,
Classification chamomile, or hops canqCNS depression.
Therapeutic: sedative/hypnotics Route/Dosage
Pregnancy Category C
ICU Sedation
Indications IV (Adults): Loading infusion— 1 mcg/kg over 10 min followed by maintenance
Sedation of initially intubated and mechanically ventilated patients during treatment infusion of 0.2– 0.7 mcg/kg/hr for maximum of 24 hr; rate is adjusted to achieve de-
in an intensive care setting; should not be used for ⬎24 hr. Sedation of non-intubated sired level of sedation.
patients before and/or during surgical and other procedures. IV (Children): Loading infusion-0.5– 1 mcg/kg followed by maintenance infu-
sionof 0.2– 1 mcg/kg/hr. Children ⬍ 1 yr may require higher end of infusion rate.
Action
Acts as a relatively selective alpha-adrenergic agonist with sedative properties. Ther- Procedural Sedation
apeutic Effects: Sedation. IV (Adults): Loading infusion— 1 mcg/kg (0.5 mcg/kg for ophthalmic surgery or
patients ⬎65 yr) over 10 min followed by maintenance infusion of 0.6 mcg/kg/hr;
Pharmacokinetics
rate is adjusted to achieve desired level of sedation (usual range 0.2– 1 mcg/kg/hr)
Absorption: IV administration results in complete bioavailability.
(maintenance infusion of 0.7 mcg/kg/hr recommended for fiberoptic intubation un-
Distribution: Unknown.
til endotracheal tube secured).
Protein Binding: 94%.
Metabolism and Excretion: Mostly metabolized by the liver, some metabolism NURSING IMPLICATIONS
by P450 enzyme system. Metabolites are mostly excreted in urine.
Half-life: 2 hr. Assessment
● Assess level of sedation throughout therapy. Dose is adjusted based on level of se-
TIME/ACTION PROFILE (sedation) dation.
ROUTE ONSET PEAK DURATION ● Monitor ECG and BP continuously throughout therapy. May cause hypo-
IV rapid unknown unknown tension, bradycardia, and sinus arrest.
● Toxicity and Overdose: Atropine IV may be used to modify the vagal tone.
Contraindications/Precautions
Contraindicated in: Hypersensitivity. Potential Nursing Diagnoses
Use Cautiously in: Hepatic impairment (lower doses may be required); Ad- Anxiety (Indications)
vanced heart block; Severe left ventricular dysfunction; Geri:qrisk of bradycardia Implementation
and hypotension (consider dosep); OB, Lactation, Pedi: Safety not established.
● Dexmedetomidine should be administered only in intensive care settings with con-
Adverse Reactions/Side Effects tinuous monitoring.
Resp: hypoxia. CV: BRADYCARDIA, SINUS ARREST, hypotension, transient hyperten- ● A loading dose may not be required when converting patient from another seda-
sion. GI: dry mouth, nausea, vomiting. Hemat: anemia. Misc: fever. tive.
⫽ Canadian drug name. ⫽ Genetic Implication. CAPITALS indicate life-threatening, underlines indicate most frequent. Strikethrough ⫽ Discontinued.
Name /bks_53161_deglins_md_disk/dexmedetomidine 02/12/2014 01:21PM Plate # 0-Composite pg 2 # 2

2 sodium acetate, sodium bicarbonate, sodium phosphates, succinylcholine, sufen-


tanil, tacrolimus, teniposide, theophylline, thiopental, thiotepa, ticarcillin/clavu-
● Continuous Infusion: Diluent: To prepare infusion, withdraw 2 mL of dexme- lanate, tigecycline, tirofiban, tobramycin, topotecan, trimrthoprim/sulfamethox- PDF Page #2
detomidine and add to 48 mL of 0.9 NaCl for a total of 50 mL. Concentration: 4 azole, vancomycin, vasopressin, vecuronium, verapamil, vinblastine, vincristine,
mcg/mL. Shake gently. Solution should be clear; do not administer solutions that vinorelbine, voriconazole, zidovudine, zoledronic acid.
are discolored or contain particulate matter. Ampules and vials are for single use ● Y-Site Incompatibility: amphotericin B colloidal, amphotericin B lipid com-
only. Rate: Administer loading infusion over 10 minutes, followed by mainte- plex, blood, diazepam, irinotecan, pantoprazole, plasma, phenytoin.
nance infusion of 0.2– 0.7 mcg/kg/hr for ICU sedation and 0.2– 1.0 mcg/kg/hr
for procedural sedation. Adjust dose to achieve desired level of sedation. Adminis- Patient/Family Teaching
ter via infusion pump to ensure accurate rate. ● Explain to patient and family the purpose of the medication.
● Y-Site Compatibility: 0.9% NaCl, 20% mannitol, acyclovir, alfentanil, allopuri-
nol, amifostine, amikacin, aminophylline, amiodarone, amphotericin B liposome, Evaluation/Desired Outcomes
ampicillin, ampicillin/sulbactam, anidulafungin, argatroban, atracurium, atro- ● Sedation for up to 24 hr.
pine, azithromycin, aztreonam, bivalirudin, bleomycin, bumetanide, buprenor- Why was this drug prescribed for your patient?
phine, busulfan, butorphanol, calcium chloride, calcium gluconate, carboplatin,
carmustine, caspofungin, cefazolin, cefepime, cefoperazone, cefotaxime, cefote-
tan, cefoxitin, ceftazidime, ceftriaxone, cefuroxime, chlorpromazine, ciprofloxa-
cin, cisatracurium, cisplatin, clindamycin, cyclophosphamide, cyclosporine, cy-
tarabine, dacarbazine, dactinomycin, daptomycin, daunorubicin hydrochloride,
D5W, dexamethasone, dexrazoxane, digoxin, diltiazem, diphenhydramine, dobu-
tamine, docetaxel, dolasetron, dopamine, doxacurium, doxorubicin hydrochlo-
ride, doxycycline, droperidol, enalaprilat, ephedrine, epinephrine, ertapenem,
erythromycin, esmolol, etomidate, etoposide, etoposide phosphate, famotidine,
fenoldopam, fentanyl, fluconazole, fludarabine, fluorouracil, foscarnet, fospheny-
toin, furosemide, gancyclovir, gemcitabine, gentamicin, glycopyrrolate, granise-
tron, haloperidol, heparin, hydrocortisone, hydromorphone, idarubicin, ifosfam-
ide, imipenem/cilastatin, insulin, isoproterenol, ketorolac, labetalol, leucovorin,
levofloxacin, levorphanol, lidocaine, linezolid, lorazepam, magnesium sulfate,
mannitol, mechlorethamine, meperidine, meropenem, mesna, methohexital,
methotrexate, methylprednisolone, metoclopramide, metoprolol, metronidazole,
midazolam, milrinone, mitomycin, mitoxantrone, morphine, mycophenolate, nal-
buphine, naloxone, nesiritide, nicardipine, nitroglycerin, nitroprusside, norepi-
nephrine, octreotide, ondansetron, oxaliplatin, oxytocin, paclitaxel, palonose-
tron, pancuronium, pemetrexed, pentamidine, pentobarbital, phenobarbital,
phenylephrine, piperacillin/tazobactam, plasma substitute, potassium acetate, po-
tassium chloride, potassium phosphate, prochlorperazine, promethazine, propo-
fol, propranolol, quinapristin/dalfopristin, ranitidine, remifentanil, rocuronium,
䉷 2015 F.A. Davis Company

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