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Nexobrid Dosage

Generic name: ANACAULASE-BCDB 158mg in 1g;
Dosage form: kit
Drug class: Topical debriding agents

Medically reviewed by Drugs.com. Last updated on Aug 21, 2024.

Important Administration Information

NEXOBRID is only to be administered by a healthcare provider. Take precautions to avoid exposure to NEXOBRID during preparation and handling (e.g., use gloves, surgical masks, other protective coverings, as needed).

Use pain management as practiced for an extensive dressing change of burn wounds 15 minutes prior to and throughout all NEXOBRID-related procedures.

NEXOBRID is available as:

  • 2 g of lyophilized powder (containing 1.94 grams of anacaulase-bcdb) with a 20 g gel vehicle, for treatment of up to 180 cm2 of burn area after mixing.
  • 5 g lyophilized powder (containing 4.85 grams of anacaulase-bcdb) with a 50 g gel vehicle, for treatment of up to 450 cm2 of burn area after mixing.

NEXOBRID lyophilized powder and gel vehicle must be mixed no more than 15 minutes prior to administration. Discard NEXOBRID if not used within 15 minutes of preparation, as the enzymatic activity of the product decreases progressively following mixing.

Each vial of lyophilized powder, jar of gel vehicle, and the mixed NEXOBRID are for use for only one patient and for one application.

NEXOBRID is for topical use only.

Apply an ointment skin protectant around the treatment area to create an ointment barrier.

Recommended Dosage

Recommended Dosage in Adults
Apply a 3 mm thick layer (approximate thickness of a tongue depressor) of NEXOBRID to a burn wound area of up to 15% body surface area (BSA) in one application in adult patients. Remove NEXOBRID after 4 hours.

A second application of NEXOBRID may be applied 24 hours following the first application to either the same area previously treated with NEXOBRID or to a new area in adult patients. Apply a second application if:

  • The wound area is more than 15% BSA, or
  • Multiple wound areas on different body surfaces require two treatments for logistical reasons such as body position, or
  • The first application's eschar removal was not complete.

For both applications, the total treated area must not exceed 20% BSA.

Recommended Dosage in Pediatric Patients

Pediatric Patients 6 Years of Age and Older

Apply a 3 mm thick layer (approximate thickness of a tongue depressor) of NEXOBRID to a burn wound area of up to 15% BSA in one application in pediatric patients 6 years of age and older. Remove NEXOBRID after 4 hours. A second application of NEXOBRID is not recommended.

Pediatric Patients Less Than 6 Years of Age

Apply a 3 mm thick layer (approximate thickness of a tongue depressor) of NEXOBRID to a burn wound area of up to 10% BSA in one application in pediatric patients less than 6 years of age. Remove NEXOBRID after 4 hours. A second application of NEXOBRID is not recommended.

Preparation of Patient and Burn Wound Treatment Area

Prepare the wound area as follows:

  1. Thoroughly clean the wound to remove any charred tissue, blisters, and any topical products.
  2. Apply a dressing soaked with an antibacterial solution to the treatment area for at least 2 hours.
  3. Ensure the wound bed is clear of any remnants of topical agents (e.g., silver sulfadiazine, povidone iodine).
  4. Apply an ointment skin protectant (e.g., petrolatum) 2 to 3 cm outside of the treatment area to create an ointment barrier. Avoid applying the protectant ointment to the treatment area itself, as this would impede direct contact of NEXOBRID with the eschar.
  5. Protect any other open wounds (e.g., laceration, abraded skin, escharotomy incision) with skin protectant ointments or ointment gauze to prevent possible exposure to NEXOBRID.

Preparation and Application of NEXOBRID

Gather the following sterile supplies prior to NEXOBRID preparation and application:

  • Instrument for mixing (e.g., spatula or tongue depressor)
  • Tongue depressor for NEXOBRID application
  • 0.9% Sodium Chloride Irrigation
  • Occlusive film dressing
  • Loose, thick fluffy dressing and bandage

Preparation
Prepare NEXOBRID at the patient’s bedside within 15 minutes of the intended application.

Using aseptic technique, mix NEXOBRID lyophilized powder and gel vehicle as follows:

  1. Pour the NEXOBRID lyophilized powder into the gel vehicle jar.
  2. Thoroughly mix the NEXOBRID lyophilized powder and gel vehicle using a sterile instrument (e.g., tongue depressor or spatula) until the mixture is uniform. The mixed lyophilized powder and gel vehicle produce NEXOBRID in a final concentration of 8.8% w/w.

DISCARD NEXOBRID IF NOT USED WITHIN 15 MINUTES OF PREPARATION, as the enzymatic activity of NEXOBRID decreases progressively following mixing.

Application
Apply NEXOBRID within 15 minutes of preparation as follows:

  1. Moisten the treatment area by sprinkling sterile 0.9% Sodium Chloride Irrigation onto the burn wound.
  2. Using a sterile tongue depressor, completely cover the moistened burn wound treatment area with the mixed NEXOBRID in a 3 mm thick layer (approximate thickness of a tongue depressor). Ensure NEXOBRID covers the entire target treatment area.
  3. Cover the treated wound with a sterile occlusive film dressing.
  4. Gently press the occlusive film dressing at the area of contact with the ointment barrier to ensure adherence between the occlusive film dressing and the ointment barrier and to achieve complete containment of NEXOBRID on the treatment area. There should be no visible air under the occlusive film dressing.
  5. Cover the occlusive film dressing with a sterile loose, thick, fluffy dressing and secure with a sterile bandage.
  6. Discard any unused portions of NEXOBRID.

Removal of NEXOBRID

Remove NEXOBRID after 4 hours. Gather the following sterile supplies prior to NEXOBRID removal:

  • Blunt-edged instruments (e.g., tongue depressor)
  • Large dry gauze
  • Gauze soaked with 0.9% Sodium Chloride Irrigation
  • Dressing soaked with an antibacterial solution
  1. Remove the occlusive film dressing using aseptic technique.
  2. Remove the ointment barrier using a sterile blunt-edged instrument.
  3. Remove the dissolved eschar from the wound by scraping it away with a sterile blunt-edged instrument.
  4. Wipe the wound thoroughly with a large sterile dry gauze, then wipe with a sterile gauze that has been soaked with sterile 0.9% Sodium Chloride Irrigation. Rub the treated area until the appearance of a clean dermis or subcutaneous tissues with pinpoint bleeding.
  5. To remove remnants of dissolved eschar, apply a dressing soaked with an antibacterial solution for at least 2 hours.

Monitoring

Monitor patients for signs of local or systemic allergic reactions. If a hypersensitivity reaction occurs, remove NEXOBRID (if applicable) from the treatment area and initiate appropriate therapy.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.