FDA Adverse Event Other Summary report: N

DEEP BRAIN STIMULATION LEAD

MDR report key: 1059587 · Received June 6, 2008

Report

Report Number
2182207-2008-03033
Event Type
Other
Date Received
June 6, 2008
Report Date
May 8, 2008
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

JOURNAL REFERENCE: BLOMSTEDT P, HARIZ MI, LEES A, ET AL. ACUTE SEVERE DEPRESSION INDUCED BY INTRAOPERATIVE STIMULATION OF THE SUBSTANTIA NIGRA: A CASE REPORT. PARKINSONISM RELAT DISORD 2008;14(3):253-256. REPORTABLE EVENT: WE PRESENT A MAN WITH PARKINSON'S DISEASE (PD) WHO UNDERWENT BILATERAL STIMULATION IN THE SUBTHALAMIC NUCLEUS (STN). DURING THE INTRAOPERATIVE EVALUATION, STIMULATION THROUGH THE LOWEST CONTACT IN THE RIGHT STN AREA, INDUCED AN ACUTE DEPRESSIVE STATE, DURING WHICH THE PT WAS CRYING AND EXPRESSING THAT HE DID NOT WANT TO LIVE. THE PT RETURNED TO HIS NORMAL STATE OF MOOD WITHIN SECONDS AFTER THE CESSATION OF STIMULATION. REPEATED BLINDED STIMULATIONS RESULTED IN THE SAME RESPONSE. IMMEDIATE POSTOPERATIVE MAGNETIC RESONANCE IMAGING (MRI) REVEALED THAT THE LOWEST CONTACT OF THE RIGHT ELECTRODE WAS LOCATED IN THE SUBSTANTIA NIGRA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DEEP BRAIN STIMULATION LEAD MHY MEDTRONIC NEUROMODULATION 3389 UNK

Patients

Seq Age Sex Outcome Treatment
1 62 YR Other PROGRAMMER: MODEL UNK N=1| IPG: MODEL UNK N=1| EXTENSION: MODEL UNK N=2| LEAD: MODEL 3389 N=1