FDA Adverse Event Injury Summary report: N

ITREL II

MDR report key: 1209908 · Received October 22, 2008

Report

Report Number
2182207-2008-06763
Event Type
Injury
Date Received
October 22, 2008
Report Date
September 25, 2008
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

JOURNAL REFERENCE: LOHER TJ, CAPELLE HH, KAELIN-LANG A, ET AL. DEEP BRAIN STIMULATION FOR DYSTONIA: OUTCOME AT LONG-TERM FOLLOW-UP. J NEUROL. 2008;255(6):881-884. DEEP BRAIN STIMULATION (DBS) HAS EMERGED AS A USEFUL THERAPEUTIC OPTION FOR PTS WITH INSUFFICIENT BENEFIT FROM CONSERVATIVE TREATMENT. NINE PTS HAD UNDERGONE PALLIDAL STIMULATION EXCEPT ONE PT WITH PAROXYSMAL DYSTONIA WHO UNDERWENT THALAMIC STIMULATION. DBS MAINTAINS MARKED LONG-TERM SYMPTOMATIC AND FUNCTIONAL IMPROVEMENT IN THE MAJORITY OF PTS WITH DYSTONIA. REPORTABLE EVENT: IN PT 8, A FEMALE AT IMPLANT, THERE WAS CONTINUED IMPROVEMENT OF ALL COMPONENTS OF DYSTONIA EXCEPT FOR BLEPHAROSPASM BEYOND 3 YEARS FOLLOW-UP, WHICH HAS BEEN WELL CONTROLLED SINCE THEN, HOWEVER, WITH BOTULINUM TOXIN INJECTIONS. SEE MFG REPORT #2182207-2008-06762.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ITREL II MHY MEDTRONIC NEUROMODULATION 7424 NA

Patients

Seq Age Sex Outcome Treatment
1 58 YR Other LEAD MODEL 3387 N=2| EXTENSION MODEL UNK N=2| PROGRAMMER MODEL UNK N=2| IPG ITREL II MODEL 7424 N=1