![]() ![]() Some patients may be implanted with the components that make up a Magnetic Resonance (MR) Conditional system, which allows them to receive an MRI scan if all the requirements for the implanted components and for scanning are met. After defibrillation, confirm the neurostimulation system is still working. External defibrillation can cause induced currents in the lead-extension portion of the neurostimulation system. Safety for use of external defibrillator discharges on a patient receiving neurostimulation has not been established. The safety and efficacy for the treatment of patients who have back pain as the greatest region of pain have not been evaluated.Įxternal defibrillators. The safety and effectiveness of neurostimulation for pediatric use have not been established.īack pain. Safety and effectiveness of neurostimulation for use during pregnancy and nursing have not been established. Implanting physicians should be experienced in the diagnosis and treatment of chronic pain syndromes and have undergone surgical and device implantation training for dorsal root ganglion (DRG) neurostimulation systems. The following warnings apply to this neurostimulation system.Ĭlinician training. Some models of this system are Magnetic Resonance (MR) Conditional, and patients with these devices may be scanned safely with magnetic resonance imaging (MRI) when the conditions for safe scanning are met.įor more information about MR Conditional neurostimulation components and systems, including equipment settings, scanning procedures, and a complete listing of conditionally approved components, refer to the MRI procedures clinician's manual for neurostimulation systems (available online at medical.abbott/manuals).įor more information about MR Conditional products, visit the Abbott Medical product information page at neuromodulation.abbott/us/en/healthcare-professionals/mri-support.html. Patients who failed to receive effective pain relief during trial stimulation are contraindicated to process to the permanent implant procedure. This neurostimulation system is contraindicated for patients who are Changes secondary to neuropathic pain seen in CRPS I (RSD) may be present, but are not a diagnostic requirement for CRPS II (causalgia). Nerve damage may result from traumatic or surgical nerve injury. CRPS II (causalgia) is defined as a painful condition arising from damage to a nerve. **Please note that in 1994, a consensus group of pain medicine experts gathered by the International Association for the Study of Pain (IASP) reviewed diagnostic criteria and agreed to rename reflex sympathetic dystrophy (RSD) and causalgia as complex regional pain syndrome (CRPS) types I and II, respectively. *Study subjects from the ACCURATE clinical study had failed to achieve adequate pain relief from at least two prior pharmacologic treatments from at least two different drug classes and continued their pharmacologic therapy during the clinical study. This neurostimulation system is indicated for spinal column stimulation via epidural and intraspinal lead access to the dorsal root ganglion as an aid in the management of moderate to severe chronic intractable* pain of the lower limbs in adult patients with complex regional pain syndrome (CRPS) types I and II.** The system is intended to be used with leads and associated extensions that are compatible with the system. This neurostimulation system is designed to deliver low-intensity electrical impulses to nerve structures. For specific indications, contraindications, instructions, warnings, precautions, and adverse effects about system components available in your country or region, see the approved clinician's manual for those components. Read this section to gather important prescription and safety information. Be sure to talk to your doctor about the risks associated with the placement of a neurostimulation system.ĭorsal Root Ganglion Therapy (DRG) Therapy Prescription And Safety Information ![]() Complications such as infection, swelling, bruising and possibly the loss of strength in or use of an affected limb or muscle group (i.e., paralysis) are possible. Please note: The placement of the leads is a surgical procedure that exposes you to certain risks. If, at the end of the evaluation period, you and your doctor decide Proclaim™ DRG Neurostimulation is right for you, you can choose to have the system implanted. Improves your ability to perform daily activities.Your pain management doctor will determine if you are a candidate for stimulation therapy with Proclaim™ DRG Technology, and may recommend a temporary evaluation.ĭuring the temporary evaluation, you can see whether the therapy: One of the advantages of the Proclaim™ DRG Neurostimulation System is that you can try it out to see how well it works for you before committing to an implanted system. ![]()
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