FDA Adverse Event Death Summary report: N

UNKNOWN DEEP BRAIN STIMULATOR

MDR report key: 1564648 · Received December 18, 2009

Report

Report Number
3007566237-2009-09480
Event Type
Death
Date Received
December 18, 2009
Date of Event
November 30, 2009
Report Date
December 8, 2009
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

.

Description of Event or Problem · 1

LITERATURE: DENHEYER M, KISS ZH, HAFFENDEN AM, BEHAVIORAL EFFECTS OF SUBTHALAMIC DEEP BRAIN STIMULATION IN PARKINSON'S DISEASE. NEUROPSYCHOLOGIA. 2009; 47(14): 3203-9. SUMMARY: THIS ARTICLE PRESENTS A REVIEW OF 16 PTS WITH IDIOPATHIC PARKINSON'S DISEASE WHO UNDERWENT BILATERAL STN DBS BETWEEN 2002 AND 2006. POSTOPERATIVELY, THE PTS WERE ASSES WITH THE FRONTAL SYSTEMS BEHAVIOR SCALE (FRSBE) TO PROVIDE A QUANTITATIVE ASSESSMENT OF POST-OPERATIVE BEHAVIORAL FUNCTIONING. THE PRIMARY OBJECTIVE WAS TO EXPLORE THE UTILITY OF THE FRSBE IN CHARACTERIZING BEHAVIOR DISTURBANCE. SECONDLY, THE STUDY SOUGHT TO EXAMINE THE RELATIONSHIP BETWEEN FRSBE SCORES, MOOD, MOTOR FUNCTION, AND COGNITIVE MEASURES. FINALLY, THE STUDY SOUGHT TO DETERMINE THE RELATIONSHIP BETWEEN SELF- AND FAMILY REPORTS OF BEHAVIOR. REPORTABLE EVENT: THREE PTS WERE EXCLUDED FROM THE STUDY, DUE TO DEATH UNRELATED TO THE IMPLANT SURGERY. NO CAUSE OF DEATH OR RELATIONSHIP OF THE PT'S DEATH TO THE DEEP BRAIN STIMULATION THERAPY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNKNOWN DEEP BRAIN STIMULATOR MHY MEDTRONIC NEUROMODULATION UNK NA

Patients

Seq Age Sex Outcome Treatment
1 Death IMPLANTED:| IMPLANTED:| EXPLANTED:| EXPALNTED:| EXPLANTED:| EXTENSION: MODEL UNK, LOT # UNK| IMPLANTED:| EXPLANTED| IMPLANTED:| EXTENSION: MODEL UNK, LOT # UNK| LEAD: MODEL UNK, LOT # UNK| LEAD: MODEL UNK, LOT # UNK