FDA Adverse Event Injury Summary report: N

SOLETRA

MDR report key: 3397456 · Received October 9, 2013

Report

Report Number
3004209178-2013-17756
Event Type
Injury
Date Received
October 9, 2013
Date of Event
July 17, 2008
Report Date
September 24, 2013
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
MRU
PMA / PMN Number
H020007
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

B.3. THE ACTUAL EVENT DATES WERE NOT PROVIDED. THIS DATE IS BASED ON THE DATE OF PUBLICATION OF THE ARTICLE. IT WAS NOT POSSIBLE TO ASCERTAIN SPECIFIC DEVICE INFORMATION FROM THE ARTICLE OR TO MATCH THE EVENTS REPORTED WITH PREVIOUSLY REPORTED EVENTS. CONCOMITANT: PRODUCT ID 7426 SERIAL# (B)(4) IMPLANTED: (B)(6) 2008 EXPLANTED: (B)(6) 2008 PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR; PRODUCT ID 3387S-40 LOT# V106048 IMPLANTED: (B)(6) 2008 EXPLANTED: (B)(6) 2009 PRODUCT TYPE LEAD; PRODUCT ID 3387S-40 LOT# V106048 IMPLANTED: (B)(6) 2008 EXPLANTED: (B)(6) 2009 PRODUCT TYPE LEAD; PRODUCT ID NEU_UNKNOWN_EXT IMPLANTED: (B)(6) 2008 EXPLANTED: (B)(6) 2008 PRODUCT TYPE EXTENSION; PRODUCT ID NEU_UNKNOWN_EXT IMPLANTED: (B)(6) 2008 EXPLANTED: (B)(6) 2008 PRODUCT TYPE EXTENSION. (B)(4).

Description of Event or Problem · 1

MARKS, W., BAILEY, L., REED, M., POMYKAL, A., MERCER, M., MACOMBER, D., ACOSTA, F., HONEYCUTT, J. PALLIDAL STIMULATION IN CHILDREN: COMPARISON BETWEEN CEREBRAL PALSY AND DYT1 DYSTONIA. JOURNAL OF CHILD NEUROLOGY. 2013;28(7):840-848. DOI:10.1177/0883073813488674 SUMMARY: THE AUTHORS COMPARED THE OUTCOMES OF 17 CHILDREN AGED 7 TO 15 YEARS WITH DYT1 DYSTONIA OR CEREBRAL PALSY FOLLOWING DEEP BRAIN STIMULATION. WHILE PATIENTS WITH CEREBRAL PALSY PRESENTED WITH SIGNIFICANTLY GREATER MOTOR DISABILITY THAN THE DYT1 COHORT AT BASELINE, BOTH GROUPS DEMONSTRATED IMPROVEMENT AT 1 YEAR (CEREBRAL PALSY ¼ 24%; DYT1 ¼ 6%). THE GROUP AS A WHOLE DEMONSTRATED SIGNIFICANT IMPROVEMENT ON THE BARRY-ALBRIGHT DYSTONIA SCALE ACROSS TIME. GAINS IN MOTOR FUNCTION WERE APPARENT IN BOTH AXIAL AND APPENDICULAR DISTRIBUTIONS INVOLVING BOTH UPPER AND LOWER EXTREMITIES. GAINS ACHIEVED BY 6 MONTHS WERE SUSTAINED IN THE CEREBRAL PALSY GROUP, WHEREAS THE DYT1 GROUP DEMONSTRATED CONTINUED IMPROVEMENT WITH ONGOING PALLIDAL STIMULATION BEYOND 18 MONTHS. YOUNG PATIENTS WITH DYSTONIA DUE TO CEREBRAL PALSY RESPONDED COMPARABLY TO PATIENTS WITH DYT1 DYSTONIA. THE SEVERITY OF MOTOR IMPAIRMENT IN PATIENTS WITH CEREBRAL PALSY AT BASELINE AND FOLLOW-UP RAISES THE ISSUE OF EVEN EARLIER INTERVENTION WITH NEUROMODULATION IN THIS POPULATION TO LIMIT LONG-TERM MOTOR IMPAIRMENTS DUE TO DYSTONIA. REPORTED EVENT: AN (B)(6) MALE PATIENT, WHO HAD A BILATERAL DBS IMPLANTED ON (B)(6) 2008, DEVELOPED AN INFECTION EARLY IN THE PROGRAM. THE PATIENT HAD THE PULSE GENERATORS AND EXTENSIONS REMOVED AND AN INCISION AND DRAINAGE OF SCALP INCISIONS ON (B)(6) 2008. IT WAS NOTED THAT THE WOUND CULTURE GREW (B)(6). THIS EVENT WAS PREVIOUSLY REPORTED IN MANUFACTURING REPORT # 3007566237-2013-02622. ANY ADDITIONAL INFORMATION RECEIVED REGARDING TH IS EVENT WILL BE REPORTED USING THE NEW MANUFACTURING REPORT #.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
511733 SOLETRA IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS) MRU MEDTRONIC MED REL MEDTRONIC PUERTO RICO 7426

Patients

Seq Age Sex Outcome Treatment
1 00011 YR Required Intervention