Not intended as a substitute for the provided Patient System Handbook, the Patient Trial Handbook, or the Spinal Cord Stimulator System Information for Patients. The contents of the handbooks must be fully understood before using your Precision Novi System.
The Boston Scientific Spinal Cord Stimulator Systems are indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, Complex Regional Pain Syndrome (CRPS) Types I and II, intractable low back pain and leg pain.
Associated conditions and etiologies may be: radicular pain syndrome, radiculopathies resulting in pain secondary to failed back syndrome or herniated disc, epidural fibrosis, degenerative disc disease (herniated disc pain refractory to conservative and surgical interventions), arachnoiditis, and multiple back surgeries.
Patients contraindicated for permanent SCS therapy are those who:
Unauthorized modification to the medical devices is prohibited. System integrity could be compromised and harm or injury to the patient could occur if the medical devices are subjected to unauthorized modification.
You should not be exposed to Magnetic Resonance Imaging (MRI). Exposure to this diagnostic technology may result in tissue damage, dislodgement of your Stimulator or leads, heating of the Stimulator, severe damage to the Stimulator electronics and/or increased voltage through the leads or Stimulator which can cause an uncomfortable or “jolting” sensation. Precision Novi external components (ie. Remote Control) should not be exposed to MRI. The Precision Novi System has not been evaluated for safety and compatibility in the MR environment. The Precision Novi System components have not been tested for heating or migration in the MR environment. Introducing a patient with this device into an MRI scanner may result in severe patient injury, death, or device malfunction.
Precision Novi external components (Remote Control) are MR Unsafe. They must not be taken into any MR environment such as the MRI scanner room.
The safety and effectiveness of spinal cord stimulation has not been established for pediatric use.
As an SCS patient, you should not have any form of diathermy either as treatment for a medical condition or as part of a surgical procedure. The high energy and heat generated by diathermy can be transferred through your stimulator system, causing tissue damage at the lead site and, possibly, severe injury or death. The Stimulator, whether it is turned on or off, may be damaged.
Spinal cord stimulators may interfere with the operation of implanted sensing stimulators, such as pacemakers and implantable cardiac defibrillators (ICDs). Be sure your physicians are aware of your spinal cord stimulator before going forward with other implantable device therapies so that medical decisions can be made and appropriate safety measures taken.
Burns may result if the pulse generator case is ruptured or pierced and patient tissue is exposed to battery chemicals.
Changes in posture or abrupt movements may cause decreases, or uncomfortable or painful increases in the perceived stimulation level. Keep the Remote Control with you at all times, and turn the stimulation down or off before making posture changes. If unpleasant sensations occur, the stimulation should be turned off immediately.
Strong electromagnetic fields can potentially turn the Stimulator off, or cause uncomfortable or jolting stimulation, or affect wireless communication. Avoid or exercise care around:
If you are near these devices, you may become aware of changing stimulation levels. In rare instances, if the stimulation is on, you could experience an increase in stimulation level to the point that the sensation is uncomfortably strong or possibly “jolting.” If this happens, turn off the Stimulator. If the Stimulator suddenly turns off by itself, first move away from the area. Next, check the stimulation status with the Remote Control by pressing the Unlock button and observing the screen.
Always be aware of your surroundings, particularly near theft detectors/security screeners. Ask for assistance to go around these devices if you feel at all uncomfortable.
Physician training is required.
The following medical therapies or procedures may turn stimulation off or may cause permanent damage to the Stimulator, particularly if used in close proximity to the device:
X-ray and CT scans may damage the Stimulator if stimulation is on. X-Ray and CT Scans are unlikely to damage the Stimulator if stimulation is turned off.
Before having procedures, medical therapies, or diagnostics, have your healthcare professional call our Customer Service department for proper instructions.
Do not operate an automobile, other motorized vehicle, or any potentially dangerous machinery/equipment with therapeutic stimulation switched on. Turn off stimulation first. Sudden stimulation changes, if they occur, may distract you from attentive operation of the vehicle or equipment.
During the two weeks following surgery, it is important to use extreme care so that appropriate healing will secure the implanted components and close the surgical incisions:
Temporarily, there may be some pain in the area of the implant as the incisions heal. If discomfort continues beyond two weeks, contact your physician.
If you notice excessive redness around the wound areas during this time, contact your physician to check for infection and administer proper treatment. In rare cases, adverse tissue reaction to implanted materials can occur during this period.
Be sure to consult your physician before making lifestyle changes due to decreases in pain.
Never attempt to change the orientation or “flip” (rotate or spin) the implant. Do not “finger” or play with the implant. If you know that the device has turned, contact your physician to arrange an evaluation of the system.
In some cases, the skin over your implant may become very thin over time. If this occurs, contact your physician.
In some instances a lead can move from its original location, and stimulation at the intended pain site can be lost. If this occurs, consult your physician who may be able to restore stimulation by reprogramming the implant in the clinic or re-positioning the lead during another operation.
Implants can fail at any time due to random component failure, loss of battery functionality, or lead breakage. If the device stops working, turn off the Stimulator and contact your physician so that the system can be evaluated.
The operating temperature of the Remote Control is 10–40 °C (50–104 °F).
Do not expose the Remote Control to excessively hot or cold conditions. Do not leave the devices in your car or outdoors for extended periods of time. The sensitive electronics can be damaged by temperature extremes, particularly high heat. If the Remote Control is to be stored for a period of time, be careful that the storage temperature does not exceed -20–60 °C (-4–140 °F).
Handle the system components and accessories with care. Do not drop them or submerge them in water. Avoid all sources of water which can come into contact with the devices. Although reliability testing has been performed to ensure quality manufacturing and performance, dropping the devices on hard surfaces or in water, or other rough handling, can permanently damage the components. Refer to the Limited Warranty for additional information.
Do not dispose of the Remote Control or Charger in fire. The battery in these devices can explode in fire. Dispose of used batteries in accordance with local regulations. The Stimulator should be explanted in the case of cremation, and returned to Boston Scientific. External devices to be disposed of per local regulatory requirements. Please contact your healthcare professional for information.
The Remote Control can be cleaned using a mild detergent applied with a lightly dampened cloth or tissue. Residue from soapy detergents should be removed with a cloth lightly dampened with water. Do not use abrasive cleansers for cleaning.
While we do not anticipate any interference with cell phones, the full effects of interaction with cell phones are unknown at this time. If there is a concern or a problem is encountered, the physician should be contacted.
Potential risks are involved with any surgery. The possible risks of implanting a pulse generator as part of a system to deliver spinal cord stimulation include:
The lead(s) which deliver stimulation may move from their original implanted location, resulting in undesirable changes in stimulation and subsequent reduction in pain relief.
System failure, which can occur at any time due to random failure(s) of the components or the battery. These events, which may include battery leakage, device failure, lead breakage, hardware malfunctions, loose connections, electrical shorts or open circuits and lead insulation breaches, can result in ineffective pain control.
Your body may react negatively to the materials used to manufacture the Stimulator or the leads. You may notice redness, warmth or swelling of the implant area. In some cases, the formation of reactive tissue around the lead in the epidural space can result in delayed onset of spinal cord compression and neurological/sensory deficit, including paralysis. Time to onset is variable, possibly ranging from weeks to years after implant.
The skin over your implant may become thin and increasingly tender over time. A seroma may be formed.
The most common surgical procedural risks are temporary pain at the implant site and infection. However, since the leads are placed in the epidural space, there is a small risk that spinal fluid may leak from the lead insertion site following surgery. Very rarely, you may develop an internal blood clot (hematoma) or blister (seroma); or you may experience epidural hemorrhage or paralysis. Your spinal cord may become compressed.
External sources of electromagnetic interference may cause the device to malfunction and affect stimulation.
MRI. Exposure to magnetic resonance imaging (MRI) can result in noticeable heat near the Stimulator or the leads; may distort or destroy the image needed for diagnosis; and may produce enough electromagnetic interference (EMI) to erase the Stimulator programming, destroy the leads, or cause the leads to move from their intended location.
Undesirable stimulation may occur over time due to cellular changes in tissue around the electrodes, changes in electrode position, loose electrical connections and/or lead failure.
You may experience painful electrical stimulation of your chest wall as a result of stimulation of certain nerve roots several weeks after surgery.
Over time, your implant may move from its original position.
You may experience weakness, clumsiness, numbness or pain below the level of implantation.
You may experience persistent pain at the Stimulator or lead site.
In any event, you should contact your physician and inform him/her.
CAUTION: Federal law restricts this device to the sale, distribution and use by or on the order of a physician.