Betadine
Betadine®
Generic Name
Betadine®
Mechanism
- Disruption of microbial cell membranes through I₂ released from PVP‑I, forming iodo‑species that oxidize and iodinate cellular components (proteins, nucleic acids) → microbial death.
- Inhibition of enzyme systems critical to bacterial and fungal metabolism.
- The complex protects iodine from rapid volatilization, allowing sustained release and activity over a broad pH range (2–7).
- Activity remains high against Gram‑positive and Gram‑negative bacteria, fungi, spores, and enveloped viruses (e.g., HSV, HIV, influenza).
Pharmacokinetics
| Parameter | Findings |
| Absorption | Minimal systemic absorption when used topically; significant absorption only with extensive burns or large surface area application. |
| Distribution | Systemic distribution occurs when absorbed → iodine bound to serum proteins (mainly thyroid‑associated proteins). |
| Metabolism | Involves deiodination to free iodine and hepatic conjugation. |
| Elimination | Mainly renal; iodine is excreted in urine. |
| Half‑life | Free iodine 2 hrs topically, ensuring prolonged antiseptic effect. |
Indications
- Pre‑operative skin preparation for general, cardiac, and ophthalmic surgery.
- Wound irrigation and disinfection of superficial wounds, lacerations, and abrasions.
- Burn care (especially superficial burns) to reduce infection risk.
- Oral and nasal mucosa rinsing for pre‑operative de‑colonization.
- Ophthalmic use (concentration 0.5–1.25%) for infections such as blepharitis and conjunctivitis.
- Infection prevention in invasive device insertion (e.g., catheter line sites, surgical drains).
- Field medicine for quick disinfection in austere environments.
Contraindications
- Contraindicated in patients with *iodine allergy* or *thyroid disorders* (hyperthyroidism, Hashimoto's thyroiditis) due to potential iodine overload.
- Caution in *pregnant* or *lactating* patients; topical use is generally safe but avoid intra‑ocular application.
- Avoid on *extensive burns*, *corrosive injuries*, or *ulcerative lesions* where systemic absorption risks increase.
- Do not use simultaneously with other iodine products or topical antibiotics that release iodine.
- Risk of systemic hypothyroidism if used >1 % with large surface area or prolonged periods.
Dosing
| Situation | Dose | Duration | Application Notes |
| Skin prep | 10–15 mL of 10 % PVP‑I solution | Single application pre‑op | Use cotton pad; wash off with sterile water after 5–10 min. |
| Wound disinfection | 1–5 % PVP‑I solution | Repeat 2–3 times daily | Do not irrigate wounds >1 cm depth; avoid over‑spraying. |
| Eye drops | 0.5–1.25 % PVP‑I | 5–10 drops, 1‑2 times daily | Use preservative‑free formulation if available. |
| Burns | 0.5–1 % solution | Every 4–6 hr | Keep away from moist dressings unless as recommended. |
• Preparation: Use sterile containers; avoid contact with glass (iodine can leach).
• Contact time: Minimum 30 s for optimal activity; longer contact improves efficacy (>5 min).
• Adjuncts: Use in combination with sterile gauze or antiseptic‑adherent dressings for prolonged contact.
Adverse Effects
- Local: Skin irritation, erythema, dryness, desquamation, hyperpigmentation, or contact dermatitis.
- Systemic:
- Allergic reaction: rash, urticaria, anaphylaxis in iodine‑allergic patients.
- Thyroid dysfunction: transient hypothyroidism, hyperthyroidism, or thyrotoxicosis after extensive use or in susceptible individuals.
- Methemoglobinemia: rare with topical use, but possible with high concentrations or intravenous preparations.
- Ophthalmic: Iodine irritation, blurred vision, corneal epithelium damage if used at >1.25 %.
Monitoring
- Thyroid function tests (TSH, free T₄, total T₃) if prolonged or extensive topical use is anticipated.
- Serum iodine levels in high‑risk patients (e.g., pregnant women, patients with renal impairment).
- Skin assessment: Look for signs of contact dermatitis or delayed wound healing.
- Visual acuity and slit‑lamp exam if used intra‑ocular or peri‑ocular.
Clinical Pearls
- “PVP‑I is not an antibiotic”: It prevents infection but does not treat bacterial superinfection. Reserve antibiotics for clinically infected wounds.
- Use a “pre‑operative chlorhexidine‑plus‑povidone‑iodine” strategy: For heavily contaminated skin, a double‑step prep (chlorhexidine first, rinse, then PVP‑I) can reduce bacterial load more than either agent alone.
- Avoid PVP‑I on eschar: Because iodine penetrates poorly through non‑breathing tissue, eschar debridement or alternative antiseptics (e.g., chlorhexidine) are preferred.
- Burns: For first‑degree or superficial partial‑thickness burns, 1 % PVP‑I rinses can decrease infection; for deeper burns, use sterile gauze soaked in saline or specialized burn wound solutions.
- Ophthalmology: A 0.25–0.5 % solution is safe for short‑term pre‑operative ocular prep; avoid for long‑term therapy due to corneal toxicity.
- In pregnancy: Topical povidone‑iodine is classified as “Category C” but is frequently used because systemic absorption is minimal; still, apply only on the surgical site and avoid eye exposure.
- Thyro‑toxic patients: If using Betadine post‑operatively, consider oral levothyroxine or T₄ supplements; routine monitoring is essential.
- Product storage: Keep in opaque containers at 2–8 °C; avoid sunlight to prevent iodine degradation.
--
• *All information is intended for educational purposes and should be cross‑verified with the latest clinical guidelines and the product’s labeling.*