FDA Adverse Event Injury Summary report: N

UNK DEEP BRAIN STIMULATOR

MDR report key: 1895248 · Received November 8, 2010

Report

Report Number
3007566237-2010-09062
Event Type
Injury
Date Received
November 8, 2010
Date of Event
April 1, 2010
Report Date
October 6, 2010
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). AT THIS TIME, NO ADDITIONAL INFORMATION WAS AVAILABLE. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Description of Event or Problem · 1

LITERATURE: VERGANI F, LANDI A, PIRILLO D, CILIA R, ANTONINI A, SGANZERLA EP. SURGICAL, MEDICAL, AND HARDWARE ADVERSE EVENTS IN A SERIES OF 141 PATIENTS UNDERGOING SUBTHALAMIC DEEP BRAIN STIMULATION FOR PARKINSON DISEASE. WORLD NEUROSURG. APR 2010;73(4):338-344. SUMMARY: THE AUTHORS REPORTED A SINGLE CENTER, RETROSPECTIVE ANALYSIS OF COMPLICATIONS IN A LARGE POPULATION OF PARKINSONIAN PATIENTS WITH A LONG-TERM FOLLOW-UP (MEAN, 4.6 YEARS). A TOTAL OF 141 PATIENTS UNDERWENT BILATERAL SUBTHALAMIC NUCLEUS (STN) DEEP BRAIN STIMULATION (DBS) BETWEEN (B)(6) 1998 AND (B)(6) 2007. IN THIS SERIES, NEITHER SEIZURES NOR EXTRADURAL/SUBDURAL HEMATOMAS WERE OBSERVED. REPORTABLE EVENT: ONE PATIENT PRESENTED WITH A MINOR INFECTION DUE TO S. EPIDERMIDIS; THE INFECTION WAS SUPERFICIAL, AT THE LEVEL OF THE IPG IMPLANTATION, AND RESOLVED AFTER PROLONGED ANTIBIOTIC THERAPY. REMOVAL OF THE DEVICE WAS NOT NECESSARY. THIS COMPLICATION REQUIRED A LONGER IN-HOSPITAL STAY FOR THE PATIENT; HOWEVER, THE PATIENT DID NOT SHOW SIGNIFICANT COMORBIDITY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 59 YR Hospitalization PROGRAMMER: MODEL PROGRAMMER, LOT #UNK| IMPLANTED:| EXPLANTED:| LEAD: MODEL 3389, LOT #UNK