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A comprehensive vocabulary review of perioperative medications, analgesics, neurological agents, psychiatric medications, substance use disorders, and respiratory rescue drugs based on the Unit 2 exam study material.
IV Opioid Analgesics Administration
A nursing procedure requiring assessment of respiratory rate, O2 saturation, blood pressure, sedation level, and pain score prior to delivery; doses are held if the respiratory rate is under 12breaths/min, diluted per manufacturer instructions, pushed slowly over 1–5minutes, and kept with naloxone immediately available at the bedside.
Opioid Withdrawal
A syndrome peaking at 1–3days and lasting 5–7days after opioid cessation, characterized by dilated pupils, gooseflesh, sweating, rhinorrhea, lacrimation, yawning, vomiting, diarrhea, insomnia, hypertension, tachycardia, and cravings; managed with clonidine, a methadone taper, buprenorphine, or lofexidine.
Naloxone (Narcan)
An opioid antagonist administered intravenously, intramuscularly, or intranasally and repeated every 2–3minutes as needed to reverse narcotic overdose signs (pinpoint pupils, slow breathing, unresponsiveness); requires ongoing monitoring because its duration of action may be shorter than the opioid.
Tolerance
An expected physiological adaptation to chronic opioid therapy in which an increased amount of drug is required over time to produce the same therapeutic effect, which does not constitute addiction.
Physical Dependence
An expected physiological state produced by chronic opioid therapy that results in withdrawal signs and symptoms if the medication is stopped abruptly, distinct from compulsive psychological addiction.
Pseudoaddiction
A pattern of drug-seeking behavior exhibited by a patient because their pain is undertreated, which resolves once effective pain control is achieved.
Patient-Controlled Analgesia (PCA) Pump
An intravenous delivery system with a programmed lockout to prevent overdose, which must strictly and solely be activated by the patient before pain becomes severe or before physical activity.
Codeine Sulfate
An oral opioid analgesic whose most common adverse effect is constipation; it is contraindicated in pediatric patients under 12years of age and requires restricting total acetaminophen intake below 3–4g/day when prescribed as combination Tylenol #3.
Methadone
A synthetic opioid with a prolonged half-life that accumulates in tissue, creating delayed respiratory depression risks; requires monitoring of respiratory rate (notifying the provider if under 10breaths/min), sedation, intake and output for urinary retention, and electrocardiograms for QT prolongation and torsades de pointes.
Transdermal Fentanyl
A transdermal analgesic patch reserved exclusively for opioid-tolerant clients with chronic or cancer pain, featuring an onset of 12–24hours, a peak effect at 48–72hours, and application changes every 72hours; it must never be cut or exposed to external heat sources.
Spinal Analgesia Adverse Effects
Complications secondary to neuraxial blockade, including hypotension and bradycardia from sympathetic denervation, respiratory depression from epidural opioids, urinary retention, lower-extremity numbness requiring fall precautions, and spinal headache managed by keeping the patient flat and administering fluids and caffeine.
Local Anesthetic Systemic Toxicity (LAST)
A life-threatening systemic complication occurring in an ordered progression: perioral numbness, metallic taste, tinnitus, and agitation, leading to seizures, coma, respiratory arrest, dysrhythmias, and cardiovascular collapse; treated by terminating the injection, administering 100% oxygen, controlling seizures, and infusing 20% lipid emulsion.
Malignant Hyperthermia
An inherited pharmacogenetic reaction triggered by volatile inhaled anesthetics (isoflurane, desflurane, sevoflurane) or succinylcholine, manifesting as masseter muscle rigidity, rapid hypercapnia, tachycardia, extreme pyrexia, metabolic acidosis, and hyperkalemia; managed by stopping the agent, hyperventilating with 100% oxygen, cooling, and infusing intravenous dantrolene.
Scopolamine
An anticholinergic transdermal patch applied to the postauricular area 4hours before travel to prevent motion sickness for 3days; it requires immediate handwashing after handling to avoid pupil dilation, and is contraindicated in narrow-angle glaucoma and benign prostatic hyperplasia.
Carbidopa-Levodopa (Sinemet)
A dopamine replacement combination for Parkinson's disease where levodopa crosses the blood-brain barrier to form dopamine and carbidopa inhibits peripheral breakdown; major adverse effects include orthostatic hypotension, dyskinesias, palpitations, hallucinations, and dark urine or perspiration.
Benztropine
A centrally acting anticholinergic medication used to treat extrapyramidal symptoms and parkinsonism that causes dry mouth, blurred vision, urinary retention, constipation, tachycardia, memory impairment, and anhidrosis with overheating risk; contraindicated in glaucoma.
Phenytoin (Dilantin)
An antiepileptic agent with a therapeutic range of 10–20μg/mL (7.5–20μg/mL per drug guide) that requires monitoring of gingival hyperplasia, Stevens-Johnson syndrome rash, CBC, liver panels, and serum glucose; toxic manifestations progress from nystagmus (above 20μg/mL) to ataxia and slurred speech (above 30μg/mL), followed by lethargy and coma (above 40μg/mL).
Lamotrigine
An antiepileptic and bipolar maintenance drug that requires slow upward dose titration and immediate discontinuation at the first sign of cutaneous rash due to the risk of life-threatening Stevens-Johnson syndrome; serum concentrations are significantly increased by coadministration with valproic acid.
Cyclobenzaprine
A short-term, centrally acting skeletal muscle relaxant related to tricyclic antidepressants that induces sedation, dizziness, dry mouth, constipation, urinary retention, and tachycardia; contraindicated in clients with cardiac disorders, urinary retention, or glaucoma.
Cholinergic Toxicity (SLUDGE)
A toxic syndrome caused by excessive parasympathetic stimulation presenting with Salivation, Lacrimation, Urination, Diarrhea, GI cramps, and Emesis, accompanied by bradycardia and bronchospasm; reversed with intravenous atropine.
Bethanechol
A direct-acting cholinergic agonist utilized postoperatively to treat nonobstructive urinary retention, evidenced as therapeutically effective when the patient voids within approximately 60minutes of administration.
Lithium
A first-line mood stabilizer for bipolar disorder maintaining a therapeutic window of 0.5–1.2mEq/L (or 0.6–1.2mEq/L); early toxicity occurs at 1.5–2.0mEq/L (vomiting, diarrhea, coarse tremor) and severe toxicity occurs above 2.0mEq/L, precipitated by hyponatremia, dehydration, diuretics, ACE inhibitors, and NSAIDs.
Bupropion
A norepinephrine-dopamine reuptake inhibitor (NDRI) indicated for major depression, seasonal affective disorder, and smoking cessation (Zyban); it does not cause sexual dysfunction or weight gain but carries a dose-dependent risk of seizures at dosages exceeding 450mg/day.
Monoamine Oxidase Inhibitors (MAOIs)
Third-line antidepressant agents that prevent the breakdown of norepinephrine, serotonin, and dopamine; carrying severe risks of fatal hypertensive crisis when combined with dietary tyramine or decongestants, and serotonin syndrome when combined with SSRIs without a 14–day washout period.
Tyramine Dietary Restrictions
A strict regimen maintained during and for 2weeks following MAOI therapy that prohibits aged cheeses, cured/smoked/processed meats, pickled or fermented foods, soy sauce, overripe bananas/avocados/raisins/fava beans, beer, and red wine to avoid catastrophic hypertensive crises.
Alprazolam
A short-acting benzodiazepine that enhances the inhibitory action of GABA to treat anxiety disorders; clients must be monitored for sedation, ataxia, respiratory depression, and dependence, avoid alcohol, and undergo gradual tapering to prevent withdrawal seizures.
Moderate Anxiety Teaching Strategy
Educational interventions designed for a patient whose perceptual field is narrowed but who can still learn with guidance, utilizing a calm, quiet environment, staying at the bedside, delivering short, simple instructions one at a time with repetition, providing written materials, and seeking return demonstrations.
Risperidone
A second-generation atypical antipsychotic indicated as a first-line agent for schizophrenia to treat positive and negative symptoms; adverse effects include substantial weight gain, hyperglycemia, dyslipidemia, hyperprolactinemia, orthostatic hypotension, and extrapyramidal symptoms.
Clozapine
A second-generation atypical antipsychotic requiring immediate drug cessation and complete blood count testing if the patient develops signs of infection such as a sore throat or fever, due to the risk of severe agranulocytosis.
Haloperidol
A first-generation antipsychotic and dopamine antagonist used in schizophrenia and Tourette syndrome that commonly induces extrapyramidal symptoms (dystonia, akathisia, pseudoparkinsonism, tardive dyskinesia), neuroleptic malignant syndrome, QT prolongation, orthostatic hypotension, and benign pink or red-brown urine.
CNS Stimulants (ADHD)
First-line sympathomimetic agents (such as methylphenidate and amphetamines) prescribed to manage hyperactivity and inattention; they require monitoring of appetite suppression, weekly weights, growth, sleep patterns, and vitals, and must be scheduled 30–45minutes before meals and at least 6hours before bed.
Medication Abuse Indicators
Clinical and behavioral patterns indicative of substance abuse, including doctor shopping across multiple prescribers or pharmacies, early refills, reporting lost prescriptions, asking for high dosages, behavioral volatility, alongside drug-specific physical findings such as miosis or stimulant-induced mydriasis and insomnia.
Alcohol Withdrawal Timeline
A predictable progression of symptoms following alcohol cessation: mild tremors, anxiety, diaphoresis, and autonomic hyperactivity occur at 6–24hours; withdrawal seizures appear at 12–48hours; and delirium tremens emerges at 48–72hours.
Wernicke Encephalopathy Prophylaxis
A protocol in acute alcohol withdrawal requiring parenteral administration of thiamine before intravenous glucose solutions to avoid precipitating acute neurological damage, followed by benzodiazepine therapy (chlordiazepoxide, lorazepam) for sedation and seizure control.
Anaphylaxis Emergency Management
A prioritized resuscitation sequence beginning with stopping the offending trigger, immediately injecting intramuscular epinephrine (0.3–0.5mg into the anterolateral thigh repeated every 5–15minutes as needed), and providing oxygen, IV fluids, H1/H2 blockers, inhaled albuterol, and systemic corticosteroids.
Sumatriptan
A serotonin 5–HT1 receptor agonist that aborts acute migraines through cranial vasoconstriction; adverse reactions include facial flushing, tingling sensations, elevated blood pressure, and substernal chest tightness or pressure caused by coronary vasospasm.
Ibuprofen vs Naproxen Sodium
Nonsteroidal anti-inflammatory agents differentiated by pharmacokinetics: ibuprofen is short-acting, dosed every 4–6hours, and best suited for acute pain and pyrexia; naproxen sodium is long-acting, dosed every 8–12hours, and preferred for chronic inflammatory conditions such as arthritis and dysmenorrhea.
Albuterol Administration Technique
A stepwise procedure for a short-acting beta-2 agonist rescue inhaler: shake the canister, exhale fully, inhale deeply and slowly while depressing the canister, hold breath for 10seconds, wait 1minute before a second puff, and always administer before inhaled corticosteroid doses.