Is povidone iodine (antiseptic solution) effective for pleurodesis?

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Povidone-Iodine for Pleurodesis: Effective Alternative to Talc

Povidone-iodine is an effective and safe sclerosing agent for pleurodesis in malignant pleural effusions, achieving success rates of 88-98% that are comparable to talc (90-93%), with excellent tolerability and significantly lower cost than bleomycin. 1

Evidence Quality and Guideline Position

The major Western guidelines (British Thoracic Society, American Thoracic Society, European Respiratory Society/EACTS) do not include povidone-iodine in their primary recommendations, listing only talc (90-93% success), bleomycin (61% success), and doxycycline (76-85% success) as established options. 1 However, this omission reflects limited use in the UK and US rather than lack of efficacy, as povidone-iodine demonstrates comparable effectiveness to talc in clinical studies. 1

Efficacy Profile

  • Complete response rates range from 82-90% across multiple studies, with one meta-analysis showing 88-98% success comparable to talc's 90-93%. 1, 2
  • A prospective randomized controlled trial comparing povidone-iodine pleurodesis through thoracostomy tube versus thoracoscopic talc poudrage in 42 breast cancer patients showed no significant difference in recurrence rates (15% vs 9%, p=ns). 3
  • In a direct comparison study of 52 patients, povidone-iodine achieved complete response in 86% (24/28 patients) versus talc's 79% (19/24 patients), with similar partial response and failure rates. 4
  • A tertiary hospital study of 38 consecutive patients achieved 89.5% complete response with no recurrence during mean follow-up of 10.2 months. 5

Administration Protocol

  • Insert a small-bore intercostal catheter (10-14F) and drain pleural fluid completely to ensure full lung re-expansion. 1
  • Confirm complete lung expansion with chest radiograph before instillation. 1
  • Instill 20 mL of 10% povidone-iodine solution (diluted in 80 mL normal saline to make 100 mL total volume) through the chest tube. 4, 5
  • Clamp the chest tube for 1-2 hours after instillation. 4
  • Patient rotation during the clamping period is not definitively established for povidone-iodine, though rotation is not necessary for tetracycline-class agents. 1
  • Reconnect to suction after unclamping and remove chest tube when 24-hour drainage is less than 100-150 mL. 1

Safety Profile and Side Effects

  • Povidone-iodine demonstrates excellent tolerability with no risk of acute respiratory failure, unlike talc which carries a small (<1%) risk of ARDS. 1
  • Chest pain during instillation occurs in 7.9-26.9% of patients, which is lower than talc (18% requiring post-procedure analgesia). 5, 6, 3
  • Fever occurs in approximately 5-13% of patients, comparable to other sclerosing agents. 4, 3
  • Thyroid and renal function changes are not clinically significant, despite theoretical concerns about iodine absorption. 6
  • No deaths occurred in the peri-pleurodesis period across multiple studies. 4, 5

Clinical Advantages Over Standard Agents

  • Significantly lower cost than bleomycin while achieving superior success rates (90.6% vs 61%). 1, 7
  • Readily available and does not require specialized handling like cytotoxic agents (bleomycin). 4, 5
  • Can be administered as a bedside procedure through thoracostomy tube, avoiding need for thoracoscopy. 3
  • Shorter post-procedure hospital stay compared to thoracoscopic talc poudrage (mean difference significant at p=0.009). 3
  • Can be repeated if necessary without increased toxicity concerns. 3

When to Choose Povidone-Iodine

Consider povidone-iodine as first-line when:

  • Talc is unavailable or cost is prohibitive. 1
  • Bedside pleurodesis through small-bore catheter is preferred over thoracoscopy. 3
  • Patient has significant comorbidities that increase risk with talc-related ARDS. 1
  • Resource-constrained settings where cost-effectiveness is paramount. 4, 5

Talc remains superior as first-line when:

  • Thoracoscopy is planned for diagnostic purposes (can perform talc poudrage simultaneously). 8
  • Maximum possible success rate is critical and cost is not limiting. 1
  • Extensive guideline support and institutional familiarity favor talc use. 1

Critical Contraindications and Pitfalls

  • Never attempt pleurodesis without confirming complete lung re-expansion, as trapped lung or bronchial obstruction will result in treatment failure. 8, 1
  • Avoid in patients with known iodine hypersensitivity (use alternative agent). 9
  • Do not use in patients with active thyroid disease without endocrine consultation, though clinical thyroid dysfunction is rare. 6
  • Ensure adequate analgesia before instillation, as 26.9% of patients experience significant chest pain. 6

Management of Treatment Failure

If povidone-iodine pleurodesis fails (recurrence of symptomatic effusion):

  • Repeat instillation with same agent is safe and can be effective. 3
  • Consider thoracoscopic talc poudrage as second-line option. 1
  • Indwelling pleural catheter is preferred for patients with trapped lung or multiple failed attempts. 1

References

Guideline

Pleurodesis Procedure Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Local iodine pleurodesis versus thoracoscopic talc insufflation in recurrent malignant pleural effusion: a prospective randomized control trial.

European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery, 2011

Guideline

Bleomycin for Pleurodesis in Malignant Pleural Effusions

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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