ANRS201 Pharmacology ATI-Style Exam Two Flashcards

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Comprehensive 100-card vocabulary study set covering thyroid disorders, diabetes mellitus, insulins, diuretics, antihypertensives, antianginals, and antilipidemic medications from the ANRS201 Exam Two lecture review.

263 Terms

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Hyperthyroidism

A hypermetabolic clinical state characterized by heat intolerance, sweating, weight loss despite appetite, tachycardia, palpitations, anxiety, tremor, frequent stools, and insomnia.

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Hypothyroidism

A hypometabolic clinical state characterized by cold intolerance, fatigue, weight gain, dry skin, constipation, bradycardia, slowed thinking or depression, and possible facial puffiness.

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Levothyroxine

A synthetic T4T_4 thyroid hormone replacement medication indicated for the management of hypothyroidism.

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Levothyroxine Administration Timing

Administered consistently on an empty stomach with a full glass of water, usually 30–60 minutes30\text{--}60\,\text{minutes} before breakfast.

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Levothyroxine Mineral Separation Rule

The instruction to separate levothyroxine administration from calcium, iron, and certain antacids by approximately 4 hours4\,\text{hours} to prevent reduced drug absorption.

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Levothyroxine Full Therapeutic Latency

The multi-week time period required for levothyroxine to achieve its full clinical and laboratory therapeutic response.

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Levothyroxine Overdose Manifestations

Hyperthyroid-like signs and symptoms resulting from excessive replacement dosing, including chest pain, palpitations, tremor, insomnia, sweating, and heat intolerance.

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Levothyroxine Dosing in Geriatric or Cardiac Patients

A cautious prescribing approach where therapy is initiated at a low dose and titrated slowly to avoid precipitation of myocardial ischemia or dysrhythmias.

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Methimazole

An oral thionamide antithyroid drug commonly preferred for many patients with hyperthyroidism to inhibit thyroid hormone synthesis.

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Propylthiouracil (PTU)

A thionamide antithyroid agent indicated during the first trimester of pregnancy and in thyroid storm protocols.

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PTU Mechanism on Peripheral Conversion

The distinct pharmacologic property of propylthiouracil whereby it inhibits the peripheral deiodination of T4T_4 to the more active T3T_3, in addition to blocking thyroid hormone synthesis.

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Antithyroid-Induced Agranulocytosis

A dangerous hematologic adverse effect of methimazole and PTU presenting clinically as sudden fever or sore throat that demands urgent evaluation and CBC testing.

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Antithyroid Drug Hepatotoxicity

Liver injury associated with thionamide therapy presenting clinically with jaundice, dark urine, or severe abdominal discomfort requiring prompt provider evaluation.

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Thyroid Storm

A life-threatening, decompensated form of severe thyrotoxicosis characterized by high fever, marked tachycardia, agitation, confusion, vomiting, diarrhea, and potential heart failure.

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Thyroid Storm Emergency Regimen

An urgent clinical protocol involving beta-blockers, a thionamide, iodine administered after the thionamide, glucocorticoids, cooling measures, IV fluids, and treatment of the underlying trigger.

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Graves Disease

An autoimmune etiology of hyperthyroidism that presents with diffuse goiter, exophthalmos (eye changes), heat intolerance, tremors, and tachycardia.

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Radioactive Iodine (131I^{131}\text{I})

An oral radioactive therapeutic modality that destroys hyperfunctioning thyroid tissue, frequently culminating in permanent hypothyroidism requiring lifelong levothyroxine.

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Radioactive Iodine Contraindications

Absolute contraindications to radioactive iodine therapy consisting of pregnancy and breastfeeding.

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Radioactive Iodine Radiation Precautions

Safety instructions post-treatment that mandate temporary avoidance of close contact with children and pregnant individuals, alongside meticulous hygiene practices.

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Type 1 Diabetes Mellitus

An endocrine disease resulting from autoimmune destruction of pancreatic beta cells, causing absolute insulin deficiency that requires exogenous insulin replacement.

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Type 2 Diabetes Mellitus

A metabolic disorder characterized by peripheral insulin resistance coupled with progressive beta-cell secretory dysfunction.

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Chronic Complications of Diabetes

Long-term end-organ microvascular and macrovascular consequences of hyperglycemia involving the blood vessels, kidneys, eyes, nerves, and wound healing.

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Rapid-Acting Insulins

Insulin formulations—including insulin lispro, insulin aspart, and insulin glulisine—utilized to cover prandial glycemic rises.

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Rapid-Acting Insulin Pharmacokinetics

Action profile featuring an onset of 10–15 minutes10\text{--}15\,\text{minutes}, a peak of approximately 1 hour1\,\text{hour}, and a duration of 3–5 hours3\text{--}5\,\text{hours}.

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Rapid-Acting Insulin Prandial Coordination

The nursing safety requirement to ensure the patient has an available meal and consumes food immediately following or during the administration of rapid-acting insulin.

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Short-Acting Regular Insulin

An unmodified crystalline insulin formulation administered subcutaneously around 30 minutes30\,\text{minutes} prior to meals or intravenously for glycemic emergencies.

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Regular Insulin Pharmacokinetics

Subcutaneous profile characterized by an onset of 30–60 minutes30\text{--}60\,\text{minutes}, a peak of 2–4 hours2\text{--}4\,\text{hours}, and a total duration of 5–8 hours5\text{--}8\,\text{hours}.

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Regular Insulin IV Indication

The sole standard human insulin preparation approved for continuous intravenous infusion during the management of diabetic ketoacidosis (DKA).

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Intermediate NPH Insulin

Neutral Protamine Hagedorn insulin, an intermediate-acting cloudy suspension that provides basal-type coverage but carries a distinct peak and associated hypoglycemia risk.

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NPH Insulin Pharmacokinetics

Action curve featuring an onset of 1–2 hours1\text{--}2\,\text{hours}, a pronounced peak of 4–12 hours4\text{--}12\,\text{hours}, and a duration of roughly 12–18 hours12\text{--}18\,\text{hours}.

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NPH Physical Appearance

The inherently cloudy, turbid suspension appearance characteristic of Neutral Protamine Hagedorn insulin.

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Long-Acting Basal Insulins

Formulations including insulin glargine and insulin detemir that provide steady background glycemic coverage with little to no pronounced peak.

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Long-Acting Insulin Duration

The extended pharmacologic duration of insulin glargine and detemir lasting approximately 20–24 hours20\text{--}24\,\text{hours}.

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Insulin Degludec

An ultra-long-acting basal insulin analogue that provides flat glycemic coverage lasting longer than 24 hours24\,\text{hours}.

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Basal Insulin Perioperative Protocol

The clinical rule stating that basal insulin should never be automatically discontinued when a patient is made NPO for surgery, requiring provider dose adjustment instead.

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Clear Before Cloudy Rule

The precise sequence for drawing up combined insulins in a single syringe, where clear regular insulin is drawn up prior to cloudy NPH insulin.

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Insulin Glargine Syringe Mixing Rule

The strict manufacturer and clinical contraindication prohibiting the mixing of insulin glargine with any other insulin product in the same syringe.

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NPH 70/30 Premix

A commercially premixed insulin formulation containing 70%70\% NPH intermediate-acting insulin and 30%30\% regular short-acting insulin.

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Diabetic Ketoacidosis (DKA) Triggers

Precipitating clinical events for DKA including missed insulin doses, infections or acute illness, new-onset type 1 diabetes, and physiologic stress.

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Diabetic Ketoacidosis (DKA) Clinical Findings

Hallmark presentation comprising polyuria, polydipsia, dehydration, nausea, vomiting, abdominal pain, weakness, fruity breath, Kussmaul respirations, and high-anion-gap metabolic acidosis.

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Kussmaul Respirations

A deep, rapid compensatory breathing pattern characteristic of severe metabolic acidosis seen in diabetic ketoacidosis.

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DKA Priority Initial Treatment

The immediate administration of intravenous isotonic fluids followed by baseline evaluation of potassium, renal function, blood glucose, and acid-base parameters.

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DKA Pre-Insulin Potassium Assessment

The vital safety requirement to obtain and verify serum potassium concentration before initiating intravenous regular insulin therapy.

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DKA Potassium Threshold for Delaying Insulin

A serum potassium level below 3.3 mEq/L3.3\,\text{mEq/L}, which mandates administering potassium repletion and delaying insulin infusion until hypokalemia is corrected.

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Insulin-Induced Potassium Shift

The cellular physiological action where insulin drives extracellular potassium ions into intracellular spaces, risking sudden, severe hypokalemia.

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Hypoglycemia Definition

A clinical and laboratory state defined as a blood glucose concentration falling below 70 mg/dL70\,\text{mg/dL}.

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Mild-to-Moderate Hypoglycemia Symptoms

Neurogenic and early neuroglycopenic manifestations including sweating, shakiness, hunger, headache, palpitations, irritability, and confusion.

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Severe Hypoglycemia Findings

Advanced neuroglycopenic clinical crisis characterized by seizures, loss of consciousness, or inability to swallow.

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Rule of 15 for Hypoglycemia

The protocol for a conscious patient able to swallow: administer 15 g15\,\text{g} of fast-acting simple carbohydrate, wait 15 minutes15\,\text{minutes}, and recheck capillary blood glucose.

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Unconscious Hypoglycemia Management

The emergency protocol mandating that nothing be given by mouth, requiring parenteral administration of glucagon or IV dextrose per facility protocol.

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Beta-Blocker Masking of Hypoglycemia

The pharmacologic blunting of sympathetic autonomic warning symptoms—specifically tachycardia and tremor—in patients taking beta-adrenergic blockers.

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Persisting Hypoglycemia Sign Under Beta Blockade

Diaphoresis (sweating), which is mediated by sympathetic cholinergic pathways and remains present even when beta blockers conceal tremors and tachycardia.

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Metabolic Syndrome

A constellation of metabolic abnormalities that significantly raises an individual's risk for type 2 diabetes, atherosclerotic cardiovascular disease, and fatty liver disease.

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Metabolic Syndrome Diagnostic Threshold

The requirement that an individual meet at least 33 of the 55 defined clinical criteria to be diagnosed with metabolic syndrome.

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Metabolic Syndrome Abdominal Obesity Criterion

An increased waist circumference exceeding specific sex- and ethnicity-defined clinical thresholds.

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Metabolic Syndrome Triglycerides Criterion

A fasting serum triglyceride level equal to or greater than 150 mg/dL150\,\text{mg/dL} or receiving active drug therapy for hypertriglyceridemia.

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Metabolic Syndrome HDL Criterion

A serum HDL cholesterol level below 40 mg/dL40\,\text{mg/dL} in men or below 50 mg/dL50\,\text{mg/dL} in women, or receiving specific therapy for reduced HDL.

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Metabolic Syndrome Blood Pressure Criterion

A resting blood pressure equal to or exceeding 130/85 mmHg130/85\,\text{mmHg} or receiving ongoing antihypertensive pharmacological therapy.

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Metabolic Syndrome Fasting Glucose Criterion

A fasting plasma glucose concentration equal to or greater than 100 mg/dL100\,\text{mg/dL} or receiving pharmacologic treatment for elevated glucose.

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Loop Diuretics (Furosemide)

The most potent commonly used diuretic class, utilized to treat significant edema, heart failure fluid overload, and pulmonary edema.

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Furosemide Nursing Monitoring

Clinical evaluations including blood pressure, daily body weight, intake and output, renal function tests, and serum levels of potassium, sodium, and magnesium.

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Furosemide Electrolyte Adverse Effects

Severe electrolyte losses caused by loop diuresis, specifically hypokalemia, hyponatremia, and hypomagnesemia.

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Furosemide Ototoxicity

Inner ear sensory impairment manifesting as tinnitus or hearing changes, primarily associated with high intravenous doses or rapid IV push administration.

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Thiazide Diuretics (Hydrochlorothiazide)

A diuretic class working at the distal tubule commonly utilized as foundational therapy for essential hypertension and mild peripheral edema.

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Hydrochlorothiazide Adverse Effects

Metabolic complications including hypokalemia, hyponatremia, dehydration, hyperuricemia (gout attacks), and hyperglycemia.

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Thiazide Effect on Urinary Calcium

The pharmacological property of thiazide diuretics that reduces renal calcium excretion, potentially causing an increase in serum calcium.

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Thiazides in Recurrent Nephrolithiasis

The therapeutic utility of hydrochlorothiazide to diminish urinary calcium excretion in patients prone to calcium-based kidney stones.

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Spironolactone

A potassium-sparing diuretic that competitively blocks mineralocorticoid aldosterone receptors in the renal distal tubule and collecting duct.

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Spironolactone Clinical Indications

Therapeutic uses including congestive heart failure, hyperaldosteronism, liver ascites, and refractory hypertension.

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Spironolactone Major Danger

Hyperkalemia, which carries the high risk of fatal cardiac dysrhythmias and requires strict potassium and renal monitoring.

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Spironolactone Endocrine Side Effects

Steroid-receptor-mediated hormonal side effects including gynecomastia in men, breast tenderness, and menstrual irregularities in women.

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Spironolactone Dietary Precaution

Patient education mandating the strict avoidance of oral potassium supplements and potassium-based salt substitutes.

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Mannitol

An intravenous osmotic diuretic utilized primarily to reduce acutely elevated intracranial pressure and cerebral edema.

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Mannitol Intravascular Expansion Risk

A transient shift of fluid into the vascular bed that can acutely exacerbate pre-existing congestive heart failure and pulmonary edema.

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Mannitol Crystallization

The temperature-dependent physical precipitation of mannitol solution requiring inspection for crystals and the use of an in-line filter before administration.

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Mannitol Nursing Assessments

Ongoing clinical assessments including neurological status, hourly urine output, serum electrolytes, serum osmolality, and auscultation of lung fields.

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Initial Antihypertensive Teaching

Patient education instructing adherence without abrupt discontinuation, slow position changes, regular BP checks, and physician consultation regarding OTC medications.

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Orthostatic Hypotension Prevention

Behavioral guidance advising patients on antihypertensive agents to change positions slowly from lying to sitting to standing to prevent dizziness and falls.

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Hypertension OTC Drug Interactions

Non-prescription medications—specifically NSAIDs and oral decongestants—that can blunt antihypertensive drug effects and elevate systemic vascular resistance.

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Lifestyle Measures for Blood Pressure

Foundational non-pharmacologic interventions including dietary sodium restriction, regular physical activity, body weight management, and moderation of alcohol intake.

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ACE Inhibitors

Antihypertensive agents (e.g., lisinopril, enalapril) that block the conversion of angiotensin I to angiotensin II, decreasing vasoconstriction and aldosterone release.

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Post-MI Benefit of ACE Inhibitors

The pharmacologic reduction of left ventricular afterload and inhibition of maladaptive ventricular remodeling following an acute myocardial infarction.

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Ventricular Remodeling

Pathologic alterations in ventricular size, geometry, and thickness following myocardial injury that dilate the chamber and accelerate systolic heart failure.

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ACE Inhibitor Cough

A persistent, dry, non-productive respiratory side effect resulting from the pulmonary accumulation of bradykinin during ACE inhibitor therapy.

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ACE Inhibitor Adverse Effects

Clinical complications including dry cough, hyperkalemia, profound hypotension, elevated serum creatinine, and potential life-threatening angioedema.

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ACE Inhibitor Contraindications

Absolute clinical contraindications consisting of pregnancy, previous history of ACE-inhibitor-induced angioedema, and bilateral renal artery stenosis.

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Angiotensin II Receptor Blockers (ARBs)

Antihypertensive medications (e.g., valsartan, losartan) that selectively block AT1AT_1 receptors, providing cardiovascular benefits with a lower incidence of dry cough.

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ARB Adverse Effect Profile

Complications including hyperkalemia, hypotension, renal function alterations, and fetal toxicity, with uncommon occurrence of angioedema.

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ACE Inhibitor and ARB Dual Therapy

A prescribing practice generally avoided in routine care due to increased incidence of adverse outcomes without proportional clinical benefit.

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Angioedema

Sudden, dramatic submucosal or subcutaneous edema involving the lips, face, tongue, or pharynx that can produce hoarseness, dysphagia, and fatal airway compromise.

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Angioedema Priority Emergency Action

The immediate discontinuation of the suspected medication, immediate airway assessment, and urgent escalation/activation of emergency rescue protocols.

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Metformin

A first-line oral biguanide antidiabetic medication that inhibits hepatic gluconeogenesis and enhances peripheral insulin sensitivity.

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Metformin Dosing Administration

The administration rule instructing patients to take metformin with or immediately after meals to reduce common gastrointestinal upset.

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Metformin Gastrointestinal Side Effects

Frequent, self-limiting early symptoms consisting of nausea, watery diarrhea, abdominal discomfort, and flatulence.

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Metformin-Associated Lactic Acidosis (MALA)

A rare but life-threatening metabolic emergency precipitated by severe renal failure, tissue hypoxia, severe sepsis, or acute hemodynamic collapse.

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Metformin and Iodinated Radiocontrast

The safety guideline instructing that metformin be temporarily withheld prior to and following procedures using iodinated contrast to prevent contrast-induced nephropathy and lactic acidosis.

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Metformin Long-Term Monitoring

Serial clinical assessments focused primarily on renal function tests (serum creatinine/eGFR) and glycemic control indicators (glucose and HbA1c\text{HbA}_{1\text{c}}).

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Normal Fasting Plasma Glucose

A baseline euglycemic fasting plasma glucose measurement falling within the reference interval of 70–99 mg/dL70\text{--}99\,\text{mg/dL}.

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Diabetic Fasting Glucose Diagnostic Level

A fasting plasma glucose concentration equal to or greater than 126 mg/dL126\,\text{mg/dL} on confirmatory repeat laboratory evaluation.

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Normal Glycated Hemoglobin (HbA1c\text{HbA}_{1\text{c}})

An HbA1c\text{HbA}_{1\text{c}} level reflecting an estimated average blood glucose over the preceding 2–3 months2\text{--}3\,\text{months} of less than 5.7%5.7\%.