Zestril

Zestril

Generic Name

Zestril

Brand Names

for the antihypertensive drug *lisinopril*, a potent, long‑acting ACE inhibitor.

Mechanism

* ACE inhibition – Zestril blocks the conversion of angiotensin I to angiotensin II by inhibiting angiotensin‑converting enzyme (ACE).
* Decreased angiotensin II – leads to vasodilation, lowered aldosterone secretion, and reduced sympathetic tone.
* Increased bradykinin – accumulation of bradykinin contributes to vasodilatory effects and can cause the characteristic ACE‑inhibitor cough.

Pharmacokinetics

ParameterTypical Value (Standard Dose)
AbsorptionOral, peak plasma ~1‑2 h, ~60‑70 % bioavailability
DistributionVd ≈ 15 L; limited protein binding (~10 %)
MetabolismMinimal hepatic metabolism; largely unchanged in plasma
ExcretionRenal (≈80 %) via glomerular filtration and tubular secretion; half‑life ~12 h (shorter in renal impairment)
Special Populations • Renal dysfunction → dose adjustment
• Pregnancy (category D) → avoid
• Elderly → monitor renal function

Indications

* Hypertension – both monotherapy and in combination regimens.
* Heart Failure – improves survival and reduces hospitalizations.
* Post‑myocardial infarction – attenuation of remodeling, cardiovascular mortality benefit.
* Diabetic nephropathy – slows progression of kidney disease in type 2 diabetes.

Contraindications

* Contraindications
• History of angioedema related to previous ACE‑inhibitor or cystic fibrosis.
• Bilateral renal artery stenosis or unilateral kidney removal.
• Pregnancy (avoid; fetal harm).

* Warnings
Renal insufficiency – dose reduction; monitor serum creatinine and potassium.
Hyperkalemia risk – particularly with concomitant potassium‑sparing diuretics, NSAIDs, or potassium supplements.
Hypotension – especially in volume‑depleted patients or when combined with other antihypertensives.
Cough – may progress to refractory cough; consider switching to ARB if persistent.

Dosing

ConditionStarting DoseTitrationMax Dose (allowable)
Hypertension (adult)5 mg PO daily+5 mg every 2‑4 weeks to target BP40 mg/day
Heart Failure5 mg PO daily+5 mg every 2‑4 weeks, usually reaching 20‑40 mg40 mg/day
Post‑MI5 mg PO daily±5 mg every 2‑4 weeks40 mg/day
Type 2 DM nephropathy5 mg PO dailytitrate to 20 mg daily40 mg/day
Renal impairment (CrCl 30‑59 mL/min)2.5 mg daily or 5 mg every 48 htitrate sparingly20 mg/day
PregnancyNone – contraindicated

*Take orally with or without food. Avoid patient‑specific elimination factors (e.g., high diuretic use).*

Adverse Effects

Common
* Dry cough (≈10 %)
* Dizziness/hypotension (5–10 %)
* Headache (5–10 %)
* Ankle edema (≤3 %)

Serious
* Angioedema (rare but life‑threatening)
* Hyperkalemia (esp. with renal impairment or potassium‑sparing agents)
* Acute kidney injury (marked rise in creatinine ≥50 % or oliguria)
* Severe hypotension (especially in volume‑depleted states)

Monitoring

* Baseline and every 4–8 weeks: serum creatinine, BUN, eGFR, serum potassium.
* Blood pressure at each visit.
* After initiation or dose change: monitor for cough, angioedema signs.
* In patients with diabetes: hemoglobin A1c, urinary albumin‑creatinine ratio.

Clinical Pearls

  • ACE‑inhibitor cough – check for hyperkalemia or drug interactions before labeling as “cough”; consider ARB switch (Benazepril or losartan).
  • Renal adjustment – stagger dosing (e.g., 5 mg every other day) in CrCl 30‑50 mL/min rather than immediately lowering dose.
  • Combination with beta‑blockers – can blunt the rise in intrarenal renin, reducing the risk of acute kidney injury.
  • Office vs. home BP – Zestril’s onset is ~4–8 h; advise patients to take the dose at bedtime to match the rhythm of nocturnal BP dips.
  • Pregnancy avoidance – even a single dose in the first trimester can cause fetal renal dysgenesis; patients should be advised to use reliable contraception.
  • Potassium‑sparing diuretics – avoid concurrent use unless absolutely necessary; if unavoidable, close serum potassium checks.
  • Angioedema – if swelling occurs, immediate discontinuation and ENT evaluation; epinephrine & steroids are standard treatment.

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