FDA Adverse Event Injury Summary report: N

DEEP BRAIN STIMULATION LEAD

MDR report key: 978826 · Received January 11, 2008

Report

Report Number
2182207-2008-00179
Event Type
Injury
Date Received
January 11, 2008
Report Date
November 2, 2007
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

JOURNAL REFERENCE: ONDO ET AL. "SUBTHALAMIC DEEP BRAIN STIMULATION IN PATIENTS WITH A PREVIOUS PALLIDOTOMY" MOVEMENT DISORDERS/2006/21/8/1252-1254. THE ARTICLE DESCRIBES THE RESULTS FROM A STUDY THAT INVOLVED A SERIES OF PATIENTS TREATED WITH DEEP DRAIN STIMULATION (DBS) OF THE SUBTHALAMIC NUCLEUS (STN) FOR MGMT OF SYMPTOMS RELATED TO PARKINSONS DISEASE. THE DBS SYSTEMS USED INCLUDED 1 UNILATERAL AND 9 BILATERAL. PRIOR TO THE DBS TREATMENT, THE STUDY PATIENTS HAD ALL RECEIVED UNILATERAL PALLIDOTOMY TREATMENT. THE CONTROL GROUP WAS MADE UP OF 25 PATIENTS TREATED WITH DEEP STIMULATION (DBS) OF THE SUBTHALAMIC NUCLEUS (STN) THAT HAD NOT RECEIVED PALLIDOTOMY TREATMENT. THE STUDY OBJECTIVE INVOLVED THE ASSESSMENT OF THE SAFETY AND EFFICACY OF THE PALLIDOTOMY WITH STN DBS THERAPY. THE ARTICLE INCLUDED A NUMBER OF COMPLICATIONS, FROM BOTH GROUPS, RELATED TO DEEP DRAIN STIMULATION THERAPY. REPORTABLE EVENTS: TWO PATIENTS (LEADS N=2) EXPERIENCED WORSE BALANCE RELATED TO STN STIMULATION FOLLOWING A PALLIDOTOMY. TREATMENT AND OUTCOME INFO WAS NOT PROVIDED.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 UNK YR Other LEAD EXTENSIONS (N=2)| UNILATERAL SYSTEM:| IPG (N=1)| DUAL OUTPUT IPG (N=1)| LEAD EXTENSIONS (N=1)| BILATERAL SYSTEM:| SINGLE OUTPUT IPG (N=2)| SYSTEM NOT SPECIFIED.| DBS LEAD UNK (N=1)