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Intrathecal baclofen pump: a foreign-body reaction case report and its solution
Benjamin Bernuz1, Haudrey Assier, Helene Bisseriex
1Neurorehabilitation Unit, Leon Berard Hospital, Hyeres, France. bernuzbenjamin@yahoo.fr
Journal of Rehabilitation Medicine
|January 12, 2012
Summary
A rare foreign-body reaction to intrathecal baclofen pumps caused skin issues in a cerebral palsy patient. Replacing the pump with a polyethylene terephthalate-wrapped device resolved symptoms, offering a potential solution for similar cases.
Area of Science:
- Neurology
- Dermatology
- Biomaterials Science
Background:
- Intrathecal baclofen pump (ITB) therapy is effective for managing severe spasticity in conditions like cerebral palsy.
- Complications, though rare, can impact treatment efficacy and patient quality of life.
Observation:
- A patient with cerebral palsy experienced recurrent aseptic skin reactions and partial pump exposure following multiple intrathecal baclofen pump implantations.
- Despite negative skin patch tests and absence of infection signs, symptoms resolved upon pump removal and recurred upon reimplantation.
- Histological examination revealed a foreign-body reaction without signs of contact dermatitis or infection.
Findings:
- A foreign-body reaction to the intrathecal baclofen pump, presenting as skin intolerance, was diagnosed.
- The patient's symptoms resolved completely after reimplantation with a pump coated in polyethylene terephthalate.
- A 3-year follow-up confirmed no recurrence, with improved patient outcomes.
Implications:
- Foreign-body reactions to intrathecal baclofen pumps are a previously unreported complication, even with negative dermatological assessments.
- Suspecting skin intolerance in cases of unexplained local reactions is crucial for timely diagnosis and management.
- Utilizing pumps with inert coatings, such as polyethylene terephthalate, presents a viable and effective solution for patients experiencing such intolerance.
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