Chlorthalidone

From Doc Moates Wiki
Revision as of 13:37, 17 June 2026 by Docmoates (talk | contribs) (NCLEX nursing pharmacology monographs — batch import)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

Nursing pharmacology study reference (NCLEX-style monograph). Numeric values are standard teaching ranges for study and must be verified against current manufacturer labeling before clinical use. This is educational content, not prescribing guidance.

Chlorthalidone — Antihypertensive, diuretic; Thiazide-like diuretic.

Identification

  • Therapeutic class: Antihypertensive, diuretic.
  • Pharmacologic class: Thiazide-like diuretic.

Pharmacology

  • Mechanism of action: Same distal tubule action as thiazides with a longer duration.
  • Onset / peak / duration: Onset about 2 hours; peak 2 to 6 hours; duration 24 to 72 hours.
  • Half-life / therapeutic level: Half-life 40 to 60 hours; no routine level.

Clinical use

  • Indications: Hypertension, edema.
  • Usual dose, route, frequency: 12.5 to 25 mg PO once daily.
  • Maximum dose / adjustments: Max about 50 mg/day; greater potassium loss than hydrochlorothiazide.

Safety

  • Contraindications: Anuria, sulfonamide hypersensitivity.
  • Black box warning: None.
  • Interactions: Same as hydrochlorothiazide; digoxin, lithium, NSAIDs.
  • Pregnancy / lactation: Use only if clearly needed.
  • High-alert: No.

Adverse effects

  • Common side effects: Hypokalemia, hyponatremia, increased urination, dizziness.
  • Serious effects to report: Severe electrolyte disturbance, dehydration.
  • Antidote / reversal: None; correct electrolytes.

Nursing process

  • Assessment before administration: Blood pressure, electrolytes, renal function.
  • Interventions during therapy: Morning dosing; monitor potassium closely.
  • Monitor: Electrolytes, blood pressure, glucose, uric acid.
  • Evaluation / expected outcome: Sustained blood pressure reduction.

Patient teaching

  • Patient teaching: Take in the morning; report cramps or weakness.
  • Notify provider if: Muscle weakness, palpitations, severe dizziness.
  • Administration tips: Morning dosing.