Rapid Pleurodesis Through an Indwelling Pleural Catheter

Patients will be screened throughout the year as part of the clinical referral process to the
Interventional Pulmonology service at the Hospital of the University of Pennsylvania for the
management of a malignant pleural effusion. Patients eligible for inclusion based on the
clinical evaluation will be approached for enrollment. Written consent will be obtained.
Patients will subsequently undergo placement of a IPC under MAC as per standard clinical
practice followed by complete drainage of the pleural space. Patients randomized to the rapid
pleurodesis protocol arm will received 20mL of 10% iodopovidone mixed with 80mL of normal
saline instilled intrapleurally through the IPC. Patients randomized to the standard of care
arm will have 100mL of normal saline (placebo) instilled intrapleurally through the IPC. The
mixture will be allowed to dwell for 2 hours and then completely evacuated through the IPC
and the patient will be discharged home.

After discharge, all patients will continue to drain their IPC on a daily basis for 7 days.
Following this, all patients will continue to drain their IPC on an every-other-day basis
until total IPC output is less than 50ml per session over 3 consecutive sessions. At which
point they will be asked to undergo a clamp trial of no drainage for 7 days followed by a
reattempt at drainage. Patients without return of symptoms over those 7 days and minimal
drainage afterwards (<50ml) will be seen in the office for possible IPC removal. Patients
with return of symptoms during those 7 days or more than minimal drainage afterwards (>50mL)
will be asked to continue drainage until total IPC output is again less than 50mL per session
over 3 sessions.

After a passed clamp trial, patients will be evaluated in the office with a bedside
ultrasound to assess for pleural apposition in 5 of 6 designated points and the absence of
pleural effusions. If all criteria are met, the IPC is removed. If there is evidence of
residual effusion, continued drainage will be advised.

All patients will be evaluated in the office on day 7, day 14, day 30, day 60 and day 90
after IPC placement. On each visit they will be assessed for pleural apposition with
ultrasound. At day 30, 60, and 90 all patients will receive a global health related
questionnaire (EORTC QLQ30) and a symptom questionnaire. At 90 days, complications rate will
be assessed for the entire study period.

Inclusion Criteria:

1. Diagnosis of MPE as defined by

1. A diagnosis a pleural effusion in the setting of known malignancy. AND

2. Confirmed malignant involvement of the pleural space by fluid cytology or pleural
biopsy. OR

3. Evidence of pleural disease on radiographic imaging. OR

4. A recurrent effusion with no other identifiable cause after thorough workup.

2. Symptomatic from the pleural effusions (shortness of breath, cough, or chest pain)

3. Prior thoracentesis with post procedure symptomatic relief

4. Recurrence of symptoms with re-accumulation of pleural effusion

5. Lung re-expansion after thoracentesis on chest imaging within last 30 days

Exclusion Criteria:

1. Malignant pleural effusion due to a hematologic malignancy

2. ECOG >4

3. Any history of trapped lung

4. Prior attempted pleurodesis on the affected site

5. Age <18

6. Pregnant or lactating

7. Known allergy to iodopovidone (Betadine)

8. Unable or unwilling to provide consent

9. Uncorrectable coagulopathy (INR > 1.5, aPTT > 1.5 x the upper limit of normal) or
thrombocytopenia (< 50,000)

10. Anatomic contraindication to IPC (overlying skin abnormalities)

11. Unable or unwilling to care for IPC and adhere to drainage protocol

12. Need for bilateral IPC placement