Therapeutic Plasma Exchange

Use the CRRT machine you trust to deliver mTPE to your patients.

PRISMAX / PRISMAFLEX  Systems offer a simple, efficient and cost-effective alternative to centrifugation-based TPE systems

Expand Your Treatment Offering

  • Studies have shown membrane Plasma Exchange (mTPE) to be similarly safe and effective compared to centrifugation (cTPE)1-6
  • May be significantly more cost effective than contracted mobile apheresis services7
  • THOUSANDS of procedures performed each year in the US7
  • 90% of plasmapheresis treatments are performed by membrane plasma separation in some countries7
tpe set

What is mTPE?

Membrane therapeutic plasma exchange (mTPE) is performed with a highly permeable filter and dialysis equipment. mTPE on a PRISMAFLEX or PRISMAX System is achieved with simultaneous infusion of a replacement solution. Plasma is removed and pumped through the large-pore membrane of the plasma filter, while a colloid solution, such as albumin and/or plasma, or a combination of crystalloid/colloid solution, is infused post-plasma filter to replace the removed plasma.

The disposable TPE 2000 Set is the only extra part needed to run TPE on a PRISMAX or PRISMAFLEX System.

Keeps You in Control

Reduce Delays and Referrals

Initiate therapy rapidly and help maintain control over your patients’ care.

Manage Equipment

Hospitals that already own a PRISMAX System can run TPE without purchasing an additional machine.

Decrease Maintenance

Only one machine to be maintained for multiple therapies, potentially decreasing maintenance costs.

Streamline Training

Set-up and execution is similar to CRRT procedure set-up, so nurses may find training is similar.

Featured Presentation
TPE Part I: Methods, Goals & Guidelines

Therapeutic Plasma Exchange Part I: Methods, Goals & Guidelines

In this 2-part series, Tena Griffin covers apheresis methods and goals of treatment, as well as TPE selection criteria, planning and factors influencing dose and schedule.

Indications and Important Risk Information

PHOXILLUM and PRISMASOL Renal Replacement Solution Indications and Important Risk Information

Indications

PRISMASOL and PHOXILLUM solutions are indicated in pediatric and adult patients for use as a replacement solution in Continuous Renal Replacement Therapy (CRRT) to replace plasma volume removed by ultrafiltration and to correct electrolyte and acid-base imbalances. They may also be used in case of drug poisoning when CRRT is used to remove dialyzable substances

Important Risk Information

PHOXILLUM and PRISMASOL replacement solutions are contraindicated in patients with known hypersensitivities to these products.

PHOXILLUM and PRISMASOL solutions can affect electrolytes and volume and may result in hyperkalemia or hyperphosphatemia. Monitor hemodynamic status and fluid inputs and outputs, potassium, phosphorous, calcium, other electrolytes and acid-base balance throughout the procedure.

PHOXILLUM replacement solutions contain hydrogen phosphate, a weak acid that may increase the risk of metabolic acidosis. 

PRISMASOL and PHOXILLUM replacement solutions can affect blood glucose levels resulting in hypo- or hyper-glycemia depending upon the dextrose content of the replacement solution. Monitor blood glucose levels regularly. 

The following adverse reactions have been identified during post-approval use with these or other similar products and therefore may occur with use of PHOXILLUM or PRISMASOL: Metabolic acidosis, hypotension, acid-based disorders, electrolyte imbalances including calcium ionized increased, hyperphosphatemia, hypophosphatemia, fluid imbalance.

For more information, please see accompanying Full Prescribing Information for PRISMASOL and PHOXILLUM solutions or visit baxterpi.com


MARS Indications

MARS is indicated for the treatment of drug overdose and poisonings. The only requirement is that the drug or chemical be dialyzable (in unbound form) and bound by charcoal and/or ion exchange resins.

MARS is not indicated for the treatment of chronic liver disease conditions or as a bridge to liver transplant. Safety and efficacy has not been demonstrated for those indications in controlled, randomized clinical trials. The effectiveness of the MARS device in patients that are sedated could not be established in clinical studies and therefore cannot be predicted in sedated patients.


The PRISMAFLEX and PRISMAX Systems are intended for:
Continuous Renal Replacement Therapy (CRRT) for patients weighing 20 kilograms or more with acute renal failure and/or fluid overload.

Therapeutic Plasma Exchange (TPE) therapy for patients weighing 20 kilograms or more with diseases where fluid removal of plasma components is indicated.

Rx Only. For safe and proper use of products mentioned herein refer to the appropriate Instructions for Use or Operator's Manual.