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The PeritX™ Peritoneal Catheter System is the first and only tunneled catheter* that is indicated for drainage of malignant and non-malignant ascites.
Designed with active vacuum technology to help facilitate the drainage of ascites fluid, the PeritX™ Peritoneal Catheter System allows your patients to manage fluid from malignant and non-malignant ascites at home.
The PleurX™ Peritoneal Catheter System was introduced in 2005 for malignant ascites management. In 2020, the PleurX™ Peritoneal Catheter System received a new, expanded indication for non-malignant ascites. The new, expanded indication will allow you to serve patients who present with ascites that is the direct result of liver disease or other non-malignant origins. With the new, expanded indication, the PleurX™ Peritoneal Catheter System will be rebranded as the PeritX™ Peritoneal Catheter System.
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Vacuum bottle
Active vacuum technology drains quickly and comfortably without the need for gravity. Bottles are available in 500 mL and 1,000 mL sizes
Roller clamp
The roller clamp provides easy control of drainage flow for optimal comfort.
Proprietary safety valve
The valve helps prevent inadvertent passage of air or fluid through the catheter. It also helps to reduce the risk of misconnection that may occur with a standard luer connection.
Polyester cuff
This promotes tissue ingrowth to help reduce infection risk and to hold the catheter securely in place.
Fenestrations
Large, smooth fenestrations promote drainage and help reduce the risk of occlusions.
15.5 Fr silicone catheter
Soft and flexible catheter conforms to the peritoneal space and helps minimize insertion-site discomfort.
Barium stripe
Dark barium stripe provides enhanced visibility under radiography
Patient focus
- Allows patients to manage fluid in the comfort of their home, reducing the need for repeat paracentesis procedures
- Drainage supplies are available through one of the nation’s largest Medicare-certified, HIPAA-compliant suppliers of direct-to-patient disposable medical products
- The App, for use with the PeritX™ Peritoneal Catheter System, helps patients record and track drainage
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*April, 2021
BD-31443
PeritX™ Peritoneal Catheter System
Indications for Use:
The PeritX™ Peritoneal Catheter System is indicated for intermittent, long term drainage of symptomatic, recurrent, malignant and non-malignant ascites that does not respond to medical management of the underlying disease and for the palliation of symptoms related to recurrent ascites. The use of the PeritX™ Peritoneal Catheter for non-malignant ascites is limited to patients who are intolerant or resistant to maximum medical therapy, refractory to large volume paracentesis (LVP) and are not candidates for a trans-jugular intrahepatic portosystemic shunt or LVP. The PeritX™ Peritoneal Catheter is indicated for adults only.
The Lockable Drainage Line is used to drain fluid using standard wall suction, water seal drainage system, vacuum bottle, or other appropriate method.
Warnings:
Do not put anything except the access tip of the Lockable Drainage Line, Catheter Access Kit, or PleurX™ Vacuum Bottles into the catheter valve since any other device could damage the valve. A damaged valve may allow air into the body or let fluid leak out through the valve when not draining.
A diagnostic paracentesis should be performed if the patient shows signs or symptoms of possible spontaneous bacterial peritonitis (SBP) such as fever or abdominal pain. If SBP is present, the patient should be treated per institutional guidelines, including systemic antibiotics and repeat diagnostic paracentesis at the end of the antibiotic regimen. For a patient with resolved SBP, the patient should be treated per institutional guidelines, including prophylactic antibiotics to help in the prevention of refractory or recurrent SBP. In the case of refractory or recurrent infections, the catheter should be removed and reinserted at the discretion of the clinician after the SBP has resolved.
Do not place the PeritX™ Peritoneal Catheter into the pleural space as it could lead to misidentification of the catheter and/or mistreatment of the patient.
Please consult product labels and package inserts for indications, contraindications, hazards, warnings, cautions, and information for use.
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