FDA Adverse Event Injury Summary report: N

IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

MDR report key: 5651397 · Received May 12, 2016

Report

Report Number
3007566237-2016-01960
Event Type
Injury
Date Received
May 12, 2016
Date of Event
August 1, 2004
Report Date
May 12, 2016
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MRU
PMA / PMN Number
H020007
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

SEX: THIS VALUE REFLECTS THE GENDER OF THE MAJORITY OF THE PATIENTS REPORTED IN THE ARTICLE AS SPECIFIC PATIENT GENDERS WERE NOT IDENTIFIED. EVENT DATE: PLEASE NOTE THAT THIS DATE IS BASED OFF OF THE MONTH AND YEAR OF PUBLICATION OF THE ARTICLE AS THE EVENT DATES WERE NOT PROVIDED IN THE PUBLISHED LITERATURE.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

COUBES, P., CIF, L., EL FERTIT, H., HEMM, S., VAYSSIERE, N., SERRAT, S., PICOT, M.C., TUFFERY, S., CLAUSTRES, M., ECHENNE, B., FREREBEAU, P. ELECTRICAL STIMULATION OF THE GLOBUS PALLIDUS INTERNUS IN PATIENTS WITH PRIMARY GENERALIZED DYSTONIA: LONG-TERM RESULTS. J NEUROSURG. 2004. 101:189-194. SUMMARY: PRIMARY GENERALIZED DYSTONIA (PGD) IS A MEDICALLY REFRACTORY DISEASE OF THE BRAIN CAUSING TWISTING OR SPASMODIC MOVEMENTS AND ABNORMAL POSTURES. IN MORE THAN 30% OF CASES IT IS ASSOCIATED WITH THE AUTOSOMAL DYT1 MUTATION. CONTINUOUS ELECTRICAL STIMULATION OF THE GLOBUS PALLIDUS INTERNUS (GPI) HAS BEEN USED SUCCESSFULLY IN THE TREATMENT OF PGD. THE AIM OF THIS STUDY WAS TO EXAMINE THE LONG-TERM EFFICACY AND SAFETY OF DEEP BRAIN STIMULATION (DBS) IN THE TREATMENT OF PGD IN CHILDREN AND ADULTS WITH AND WITHOUT THE DYT1 MUTATION. REPORTED EVENTS: ONE (B)(6) PATIENT WITH BILATERAL GLOBUS PALLIDUS INTERNUS (GPI) DEEP BRAIN STIMULATION (DBS) FOR PRIMARY GENERALIZED DYSTONIA, WHO WAS NOTED TO BE BEDRIDDEN, EXPERIENCED A DELAYED UNILATERAL INFECTION OF THE IMPLANTABLE NEUROSTIMULATOR (INS) WITH STAPHYLOCOCCUS EPIDERMIDIS. THE SYSTEM WAS EXPLANTED AND REIMPLANTED 6 MONTHS LATER, RESULTING IN CLINICAL IMPROVEMENT. THE PATIENT'S SYMPTOMS REPORTEDLY RECURRED WITHIN ONE WEEK (OF EXPLANT), BUT DISAPPEARED QUICKLY ON REACTIVATION OF STIMULATION. THE AUTHORS NOTED THAT PATIENTS WERE BILATERALLY IMPLANTED WITH A PAIR OF 3389 ELECTRODES, WHICH WERE CONNECTED TO EITHER AN ITREL II OR III NEUROSTIMULATOR. IT WAS NOT POSSIBLE TO ASCERTAIN SPECIFIC DEVICE INFORMATION FROM THE ARTICLE (SUCH AS SERIAL NUMBERS) OR TO MATCH THE REPORTED EVENT WITH ANY PREVIOUSLY REPORTED EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
304651 IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS) MRU MEDTRONIC NEUROMODULATION NEU_INS_STIMULATOR UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 6 YR Required Intervention