Ethambutol
Ethambutol
Generic Name
Ethambutol
Mechanism
- Inhibits peptide‑transferase 1 (Alr) involved in arabinyl‑transferase activity.
- Impedes synthesis of the mycobacterial arabinogalactan component of the cell wall, leading to weakened cell integrity and bacterial death.
- Active primarily against *slow‑growing* mycobacterial species; less effective as a monotherapy.
Pharmacokinetics
- Absorption: Rapid oral uptake; peak plasma levels in 30–60 min.
- Distribution: Good penetration into most tissues, including lungs; limited distribution to the CNS.
- Metabolism: Mainly renally excreted unchanged (~95% in urine).
- Half‑life: 4–5 h in adults with normal renal function.
- Renal adjustment: Requires dose reduction in decreased eGFR or dialysis.
Indications
- First‑line treatment of active pulmonary and extrapulmonary tuberculosis.
- Component of RIPE regimen (rifampin, isoniazid, pyrazinamide, ethambutol).
- Used for drug‑resistant TB in combination regimens in select cases.
Contraindications
- Contraindicated in patients with pre‑existing optic neuropathy or severe visual impairment.
- Warnings:
- Ocular toxicity (visual acuity loss, red‑green color discrimination).
- Hepatotoxicity rare but possible—monitor liver enzymes.
- Renal impairment necessitates dose adjustment.
Dosing
| Setting | Dose | Schedule | Notes |
| *Adults* with normal renal function | 15 mg/kg (max 1 g) | QID (every 6 h) | 4–6 weeks, then 2–3 weeks if combined with *isoniazid* only. |
| *Renal decline* (eGFR 30–60 mL/min) | 15 mg/kg | QID | Monitor eGFR & visual acuity every 2 weeks. |
| *Dialysis patients* | 15 mg/kg | QD | Post‑dialysis dosing. |
• Route: Oral.
• Administration tips: Take with food to reduce GI upset; avoid splitting tablets if dose >1 g.
Adverse Effects
- Common (≥5%)
- Visual disturbances (color vision, central scotoma).
- Rash, arthralgia.
- Gastrointestinal upset (nausea, diarrhea).
- Serious (≤1%)
- Permanent optic neuropathy → stop immediately.
- Hepatotoxicity; liver function tests required.
- Renal failure in very high doses.
Monitoring
- Visual acuity & color vision: baseline, 2–4 weeks, then every 4–6 weeks.
- Kidney function: serum creatinine, eGFR at baseline & every 2–4 weeks.
- Liver enzymes (ALT/AST) at baseline and periodically.
- Drug interaction checks: e.g., rifampin may lower ethambutol levels; adjust if needed.
Clinical Pearls
1. Early Ocular Cues – Red‑green color confusion often precedes full visual loss; patients should report any color perception changes immediately.
2. “QID” Is Key – Ethambutol’s short half‑life necessitates four times daily dosing; missed doses drastically reduce efficacy.
3. Renal Safety Net – Because 95 % excreted unchanged, a simple eGFR calculation suffices for dose adjustment; avoid over‑correction which may increase toxicity.
4. Combined Pharmacodynamic Synergy – In RIPE, ethambutol’s non‑mycolic‑acid inhibition complements rifampin’s RNA polymerase blockade, lowering resistance emergence.
5. Patient Education – Emphasize routine vision checks; instruct caregivers to monitor children’s reading and recognition tasks.
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• *Ethambutol* is a cornerstone anti‑tuberculosis agent; when used correctly and monitored meticulously, it offers high efficacy with an acceptable safety profile.