Patient Case Studies

Patient Case Studies

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Initial History

  • Right reverse obliquity subtrochanteric femur fracture

11 Months Post-injury

  • CT scan shows persistent hypertronphic nonunion
  • Hardware and fracture stable
  • EXOGEN prescribed

Post-Op

  • Post-op locked cephalomedullary nailing
  • Persistent pain/lack of healing
  • Underwent nail dynamization at 9 months post-injury

3 Months of EXOGEN Use, 14 Months Post-injury

  • Nonunion healed
  • Symptoms resolved
  • Additional surgery avoided

3 Months

  • No progression of healing
  • Nonunoin diagnosis
  • EXOGEN prescribed
  • Remained in long-leg cast

7 Months

  • Nonunion healed
  • Addiotional bone healing evident
  • Surgery avoided

5 Months

  • Progressed to short-legged walking cast
  • Significant bony healing

3 Months Post-Op

  • No progression with healing, nonunion diagnosis
  • Screw from prior surgery in bending
  • EXOGEN prescribed
  • Boot with weight bearing continued

8 Months Post-Op

  • Patient returned to football

7 Months Post-Op, 17 Weeks of EXOGEN Use

  • Complete union noted 17 weeks after initiating EXOGEN
  • Patient asymptomatic
  • Additional surgery avoided

Summary of Indications for Use
EXOGEN is indicated for the non-invasive treatment of osseous defects (excluding vertebra and skull) that includes the treatment of delayed unions, nonunions,* stress fractures and joint fusion. EXOGEN is also indicated for the acceleration of fresh fracture heal time, repair following osteotomy, repair in bone transport procedures and repair in distraction osteogenesis procedures.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clotting problems. Some patients may be sensitive to the ultrasound gel.

Full prescribing information can be found in product labeling, at EXOGEN.com, or by calling Bioventus Customer Service.

*A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.


Physician @Home Experience

EXOGEN @Home Experience

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Easy and convenient. Delivering proven bone healing.

The EXOGEN @Home Experience provides virtual placement of the EXOGEN device. Patients will receive EXOGEN delivered directly to their home by mail. Once the patient receives the device, a dedicated team member will guide them on how to use the device.

X marks the spot

To give your patients a better understanding of their exact fracture location, explore our interactive digital Fracture Locator!

Explore Our NEW Fracture Locator
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EXOGEN @Home Experience is as easy as 1-2-3

The EXOGEN @Home Experience has a portfolio of tools available to assist with fracture treatment.

Mechanism of Action
Provides an in-depth look at how EXOGEN stimulates bone healing.

   Watch video

Post-Market Data App

Provides real-world patient outcomes by fracture age, location, and comorbidity.

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Casting Application Guide
Provides step-by-step instructions on how to build a cast for use with EXOGEN.

   Watch video

Weighted Applicator Strap
Provides instructions on how to assemble and use the weighted applicator strap.

   Watch video

Summary of Indications for Use
The EXOGEN Ultrasound Bone Healing System is indicated for the non-invasive treatment of established nonunions* excluding skull and vertebra. The EXOGEN device has also been reported as effective as an adjunctive non-invasive treatment of established nonunions in patients:

  • With internal or external fracture fixation hardware present. EXOGEN cannot penetrate metal and therefore should not be applied directly over hardware.
  • Undergoing treatment for infection at the fracture site. EXOGEN is not intended to treat the infection.
  • Believed to have diminished bone quality. EXOGEN is not intended to treat diminished bone quality.

In addition, EXOGEN is indicated for accelerating the time to a healed fracture for fresh, closed, posteriorly displaced distal radius fractures and fresh, closed or Grade I open tibial diaphysis fractures in skeletally mature individuals when these fractures are orthopedically managed by closed reduction and cast immobilization.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clotting problems. Some patients may be sensitive to the ultrasound gel.

*A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.

Full prescribing information can be found in product labelling, at EXOGEN.com, or by calling Customer Service at 1-800-836-4080.


Frequently Asked Questions

Frequently Asked Questions

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Indications for Use

EXOGEN is indicated for the non-invasive treatment of osseous defects (excluding vertebra and skull) that includes the treatment of delayed unions, nonunions,* stress fractures and joint fusion. EXOGEN is also indicated for the acceleration of fresh fracture heal time, repair following osteotomy, repair in bone transport procedures and repair in distraction osteogenesis procedures.

EXOGEN has no known contraindications.

Fracture Treatment

Yes, the biological effect of the ultrasound beam goes around the entire fracture by shear waves.61

In a clinical evaluation, EXOGEN had an 84.3% success rate in treating nonunions of the femur, suggesting that EXOGEN is an excellent choice for patients with deep fractures.31 It is suggested to use targeting to identify the fracture location.62

EXOGEN ultrasound waves can penetrate through skin and soft tissue for an effective penetration depth of ~10 inches (254 mm).61

Active, implantable devices such as cardiac pacemakers may be adversely affected by close exposure to the EXOGEN device. Patients or other people in close proximity during treatment should be evaluated by a cardiologist or physician before using the EXOGEN device.

Mark the fracture location on your patient. The EXOGEN transducer must be in direct contact with skin, so if your patient needs or currently has a cast, you’ll need to build in a transducer port or create a window. Our trained EXOGEN specialists will assist you with proper placement of the transducer port for casting and use with metals for nonunion fractures. For more information, download the EXOGEN Casting Application Techniques or contact Bioventus Customer Service.

EXOGEN Device & Coverage

The EXOGEN unit consists of the main operating unit and the attached cable with transducer head. Patients also receive an application strap, coupling gel, and battery charger.

Some insurers cover the EXOGEN device. For more information, contact your local EXOGEN representative or contact Bioventus Customer Service.

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Summary of Indications for Use
EXOGEN is indicated for the non-invasive treatment of osseous defects (excluding vertebra and skull) that includes the treatment of delayed unions, nonunions,* stress fractures and joint fusion. EXOGEN is also indicated for the acceleration of fresh fracture heal time, repair following osteotomy, repair in bone transport procedures and repair in distraction osteogenesis procedures.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clotting problems. Some patients may be sensitive to the ultrasound gel.

Full prescribing information can be found in product labeling, at EXOGEN.com, or by calling Bioventus Customer Service.

*A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.


The Science Behind EXOGEN

The Science Behind EXOGEN

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The EXOGEN Bone Healing System uses safe, painless, low-intensity ultrasound waves to amplify your patient’s natural bone repair processes.

EXOGEN Mechanism of Action

Mechanism of Action

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Stimulation32

EXOGEN sends ultrasound waves through skin and surrounding soft tissue to reach the site of the bone fracture.
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Activation33

The ultrasound waves activate certain cell receptors, setting off a series of reactions, referred to as a cascade.
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Upregulation34

EXOGEN ultrasound increases upregulation of the processes critical to bone repair.
Check out Patient Case Studies

EXOGEN has multiple Level 1 and 2 clinical studies*1-3,5,13-31

*These studies, which reflect the body of evidence of the bone stimulator EXOGEN, include evaluations of applications outside the approved label. Assignment of evidence levels was based on the updated level of evidence rating system in the Oxford Level of Evidence Criteria.

Indications for Use

EXOGEN is indicated for the non-invasive treatment of osseous defects (excluding vertebra and skull) that includes the treatment of delayed unions, nonunions, stress fractures and joint fusion. EXOGEN is also indicated for the acceleration of fresh fracture heal time, repair following osteotomy, repair in bone transport procedures and repair in distraction osteogenesis procedures.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clothing problems. Some patients may be sensitive to the ultrasound gel.

Full prescribing information can be found in product labeling, at https://www.exogen.com/, or by calling Bioventus Customer Service.

A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.

*The clinical relevance of in vivo findings is unknown

Summary of Indications for Use
EXOGEN is indicated for the non-invasive treatment of osseous defects (excluding vertebra and skull) that includes the treatment of delayed unions, nonunions,* stress fractures and joint fusion. EXOGEN is also indicated for the acceleration of fresh fracture heal time, repair following osteotomy, repair in bone transport procedures and repair in distraction osteogenesis procedures.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clotting problems. Some patients may be sensitive to the ultrasound gel.

Full prescribing information can be found in product labeling, at EXOGEN.com, or by calling Bioventus Customer Service.

*A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.


For Providers

Many patients have difficult-to-heal fractures or fractures they want to heal more quickly. EXOGEN offers a non-surgical option that helps to heal nonunion fractures and accelerates indicated acute fractures, so your patients can resume active lifestyles.*1-3

Get in touch with an EXOGEN Representative

EXOGEN is a low-intensity pulsed ultrasound (LIPUS) bone stimulator with over 25 years of proven non-invasive bone healing. Prescribed by more than 10,000 physicians annually to help over a million patients worldwide, EXOGEN has an 86% nonunion heal rate and accelerates the healing of indicated acute fractures by 38%.1-4,12

EXOGEN makes treatment compliance tracking convenient for your patients and verifiable for you, with a built-in treatment tracking calendar.

0
-min
daily treatment

Getting Started is Easy

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See the Results in the Data

The EXOGEN Ultrasound Bone Healing System is like no other. It is the only FDA-approved device with 38% accelerated healing of indicated acute fractures.1,2

Outcomes with EXOGEN:

Accelerated healing in cortical and cancellous bone:

  • 58 days and 37 days faster, respectively1,2
  • Fracture healing promoted 41% to 51% faster in patients who smoke9

Accelerated healing of indicated fresh tibia fractures in younger and older patients1,48

  • 42 days and 84 days faster, respectively1,48

Discover the noninvasive choice for resolution of nonunions. In clinical studies, low-intensity pulsed ultrasound waves helped heal nonunion fractures.

EXOGEN is effective:

  • In chronic nonunion fractures that failed to heal at least one year prior to treatment – 86% heal rate3
  • In atrophic, hypertrophic, or infected nonunions25,37,49
  • With challenging, established nonunions – 86% heal rate3
  • With high-energy nonunion fractures – 89% heal rate7
  • For use on nonunions with an interfragment gap up to 10 mm and stable osteosynthesis15

Heal rate of common fractures at risk for nonunions8

In many cases, EXOGEN may prevent the need for further surgery.

Humerus- 69.1% heal rate50
Clavicle- 83.3% heal rate51
Scaphoid- 90.7% heal rate52
Radius/Ulna- 83.9% heal rate53
Femur- 76.1% heal rate54
Hand/wrist- 88.5% heal rate55
Ankle- 71.0% heal rate56
Tibia/Fibula- 87%57
Metatarsal- 90% heal rate58
Foot- 83.9% heal rate59

Heal rates based on fractures ages between 181-365 days.50-59

Includes metacarpal, carpal and hamate
§Includes talus, calcaneus, tarsal navicular, cuboid and cuneiform

**These studies, which reflect the body of evidence of the bone stimulator EXOGEN, include evaluations of applications outside the approved label. Assignment of evidence levels was based on the updated level of evidence rating system in the Oxford Level of Evidence Criteria.

*Summary of Indications for Use

The EXOGEN Ultrasound Bone Healing System is indicated for the non-invasive treatment of established nonunions excluding skull and vertebra. The EXOGEN device has also been reported as effective as an adjunctive non-invasive treatment of established nonunions in patients:

  • With internal or external fracture fixation hardware present. EXOGEN cannot penetrate metal and therefore should not be applied directly over hardware.
  • Undergoing treatment for infection at the fracture site. EXOGEN is not intended to treat the infection.
  • Believed to have diminished bone quality. EXOGEN is not intended to treat diminished bone quality.

In addition, EXOGEN is indicated for accelerating the time to a healed fracture for fresh, closed, posteriorly displaced distal radius fractures and fresh, closed or Grade I open tibial diaphysis fractures in skeletally mature individuals when these fractures are orthopedically managed by closed reduction and cast immobilization.

There are no known contraindications for the EXOGEN device. Safety and effectiveness have not been established for individuals lacking skeletal maturity, pregnant or nursing women, patients with cardiac pacemakers, on fractures due to bone cancer, or on patients with poor blood circulation or clotting problems. Some patients may be sensitive to the ultrasound gel.

A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.

Full prescribing information can be found in product labelling, at EXOGEN.com, or by calling Customer Service at 1-800-836-4080.