Intrathecal baclofen therapy business plan

The last study, however, did not provide data that could be reliably analyzed.

Intrathecal Baclofen Therapy

Patients will be assessed 3, 6 and 12 months post pump insertion to determine the affect of ITB therapy and if the patients goals have been achieved. Signs of overdose may appear suddenly or insidiously. If the pump alarm goes off.

This keeps side effects to a minimum. When you have insufficient spasticity control using other options. Trial of weaning is done to assess the ongoing need for ITB therapy.

In most cases, symptoms of withdrawal appeared within hours to a few days following interruption of baclofen therapy. In cases reported to date, overdose has generally been related to pump malfunction, inadvertent subcutaneous injection, or dosing error.

When the patient is booked for theatre the hardware needs to be ordered from Medtronic and the booking discussed with the paediatric team who will need to be available for the re-programming at implantation.

What other health conditions do you have that could be affected by your treatment choice? Direct injection into this catheter access port or inadvertent injection into the subcutaneous tissue may cause a life-threatening overdose.

This type of treatment, called intrathecal baclofen ITBcan help people who have a hard time with side effects of the pill form. All patients receiving intrathecal baclofen therapy are potentially at risk for withdrawal.

One patient, a 44 year old male with MS, died in hospital on the second day following pump implantation. This patient population includes those with refractory spasticity secondary to a variety of etiologies, such as spinal cord injury, cerebral palsy, multiple sclerosis, and familial spasticity syndrome.

Intrathecal Baclofen Pump

Product technical manuals and the appropriate drug labeling must be reviewed prior to use for detailed disclosure. This system delivers baclofen directly to where it is needed—into the intrathecal space inside the spinal canal that contains the fluid that bathes the spinal cord.

Oral or enteral baclofen alone should not be relied upon to halt the progression of intrathecal baclofen withdrawal. Effectiveness Intrathecal baclofen is generally very effective at reducing spasticity in the spinal cord injured population.

Baclofen is a white to off-white, odorless or practically odorless crystalline powder, with a molecular weight of Because of the risks associated with the screening procedure and the adjustment of dosage following pump implantation, these phases must be conducted in a medically supervised and adequately equipped environment following the instructions outlined in the Dosage and Administration section.

A second patient, a 52 year old woman with MS and a history of an inferior wall myocardial infarction, was found dead in bed 12 days after pump implantation, 2 hours after having had documented normal vital signs.

You will be monitored for four to six hours to see if you get any side effects, Your spasticity will be tested, preferably using functional assessments and not just moving your legs and arms around. What are the potential side effects?

A second cross-over study was conducted in 11 patients with spasticity arising from brain injury. Peak spasmolytic effect is seen at approximately four hours after dosing and effects may last four to eight hours.

Concentration in your system varies according to how recently you took your last dose, and this may cause peaks and valleys in spasticity control. Furthermore, in the literature, the infection rate reportedly ranges from 0.

The suggested treatment for intrathecal baclofen withdrawal is the restoration of intrathecal baclofen at or near the same dosage as before therapy was interrupted. In people, as well as in animals, baclofen has been shown to have general CNS depressant properties as indicated by the production of sedation with tolerance, somnolence, ataxia, and respiratory and cardiovascular depression.

The pump is computer-controlled for automatic dosage and the reservoir in the pump can be replenished by percutaneous injection. In the event that technical support is required for the management of ITB therapy. Special attention should be given to patients at apparent risk e.Intrathecal Baclofen Pump Baclofen is a muscle relaxant medicine commonly used to decrease spasticity related to multiple sclerosis, spinal cord injuries, or other neurological diseases.

An intrathecal delivery system, which provides the baclofen right to the target site in the spinal cord, is an effective way to deliver the medicine. Baclofen Pump Therapy for the Treatment of Spasticity A Guide for Patients and Families If you are considering baclofen pump therapy call your insurance company The trial will check if the spasticity responds to intrathecal baclofen and identify - 6.

May 01,  · Intrathecal Baclofen Pump for Spasticity. The London Health Sciences Centre Business Plan reported that the number of treatable patients with spasticity associated with ABI is rare.

communication and nutritional status of children with spasticity of cerebral origin during intrathecal baclofen therapy (Level 3 evidence). One. Intrathecal baclofen therapy MichaeL D Partington MD, FAAP, FAANS Gillette Children’s Specialty Healthcare Have a plan for weaning/stopping oral baclofen (not seen in baclofen therapy, usually in mixed drugs).

Multiple Sclerosis and Baclofen Therapy. What Is Intrathecal Baclofen? All of these professionals work together to check your spasticity symptoms and to set a treatment plan that fits your.

Baclofen, sold under the brand name Lioresal among others, is a medication used to treat spasticity. It is used as a central nervous system depressant and skeletal muscle relaxant.

Intrathecal baclofen therapy for spasticity: A compliance-based study to indicate effectiveness

It is also used in topical creams to help with pain.

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Intrathecal baclofen therapy business plan
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