UNKNOWN DBS LEAD
Report
- Report Number
- 3007566237-2015-03577
- Event Type
- Injury
- Date Received
- December 2, 2015
- Date of Event
- October 6, 2015
- Report Date
- January 25, 2016
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Product Code
- MHY
- PMA / PMN Number
- P960009
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
(B)(4)
THIS VALUE REFLECTS THE GENDER OF THE MAJORITY OF THE PATIENTS REPORTED IN THE "ELDERLY" GROUP IN THE ARTICLE AS SPECIFIC PATIENTS COULD NOT BE IDENTIFIED. PLEASE NOTE THAT THIS DATE IS BASED OFF OF THE DATE OF PUBLICATION OF THE ARTICLE AS THE EVENT DATES WERE NOT PROVIDED IN THE PUBLISHED LITERATURE. IT WAS NOT POSSIBLE TO ASCERTAIN SPECIFIC DEVICE INFORMATION FROM THE ARTICLE OR TO MATCH THE EVENTS REPORTED WITH PREVIOUSLY REPORTED EVENTS. CORRESPONDENCE HAS BEEN SENT TO THE AUTHOR OF THE ARTICLE INQUIRING ABOUT INDIVIDUAL PATIENT INFORMATION AND ADDITIONAL INFORMATION REGARDING THE REPORTED EVENTS. (B)(4).
ADDITIONAL INFORMATION RECEIVED REPORTED THAT CT SCANNING HAD SHOWN THE LARGE INTRA-PARENCHYMAL HEMATOMA. AFTER SIX MONTHS OF REHABILITATION, THE PATIENT RECOVERED FROM HEMIPLEGIA. THE AUTHOR NOTED THAT THE CAUSE WAS LIKELY TO BE A VENOUS INFARCTION. IT WAS NOTED THAT IT WAS NOT POSSIBLE TO IDENTIFY SERIAL/LOT NUMBERS OF THE DEVICES.
LEVI, V., CARRABBA, G., RAMPINI, P., LOCATELLI, M. "SHORT TERM SURGICAL COMPLICATIONS AFTER SUBTHALAMIC DEEP BRAIN STIMULATION FOR PARKINSON'S DISEASE: DOES OLD AGE MATTER?" BMC GERIATRICS. 2015;15(1):116. DOI 10.1186/S12877-015-0112-2 SUMMARY: PATIENTS AGED 65 YEARS AND OLDER ARE NOT TRADITIONALLY CONSIDERED OPTIMAL CANDIDATES FOR SUBTHALAMIC DEEP BRAIN STIMULATION (STN-DBS), MAINLY FOR THEIR PRESUMED INCREASED INCIDENCE OF SURGICAL COMPLICATIONS. THE AIM OF THIS STUDY WAS TO ASSESS STN-DBS SURGERY SAFETY IN RELATION TO AGE. A TOTAL OF 107 CONSECUTIVE PATIENTS UNDERGOING BILATERAL STN-DBS AT OUR INSTITUTION BETWEEN 2002 AND 2014 WERE RETROSPECTIVELY STRATIFIED ACCORDING TO AGE IN TWO GROUPS (YOUNG GROUP <(><<)> 65 YEARS OLD; ELDERLY GROUP = 65 YEARS OLD;). RATE OF SHORT-TERM SURGICAL COMPLICATIONS (WITHIN 90 DAYS) WAS REVIEWED AND COMPARED BETWEEN THE TWO GROUPS. PRE-OPERATIVE BASELINE DATA WERE COMPARABLE BETWEEN THE TWO GROUPS. THE 90-DAYS POST-OPERATIVE MORTALITY RATE WAS 0%. OVERALL INCIDENCE OF COMPLICATIONS RELATED TO SURGERY WAS 6 ,54%. IN THE ELDERLY GROUP WE OBSERVED 3 POST-OPERATIVE INTRA-CEREBRAL HAEMATOMAS (7,89%), 1 REQUIRING URGENT SURGICAL EVACUATION. IN THE YOUNG GROUP WE OBSERVED 2 POST-OPERATIVE ASYMPTOMATIC INTRA-CEREBRAL HAEMATOMAS (2,89%) AND 2 WOUND INFECTIONS (2,89%), 1 REQUIRING SYSTEM REMOVAL. NO OTHERS SURGICAL COMPLICATIONS WERE NOTICED IN BOTH GROUPS. CHRONOLOGICAL AGE = 65 YEARS OLD SHOULD NOT BE CONSIDERED ALONE AS EXCLUSION CRITERIA TO STN-DBS SURGERY. REPORTED EVENTS: ONE (B)(6) YEAR-OLD PATIENT WITH DEEP BRAIN STIMULATION (DBS) FOR PARKINSON'S DISEASE EXPERIENCED POST-OPERATIVE INTRA-CEREBRAL HEMATOMA /HEMORRHAGIC STROKE. THE AUTHOR STATED THAT THE INTRACRANIAL HEMORRHAGE REQUIRED AN URGENT CRANIOTOMY FOR SURGICAL EVACUATION. IT WAS NOTED THAT THE PATIENT HAD AN UNREPORTED HISTORY OF ARTERIAL HYPERTENSION. THE SOURCE LITERATURE INCLUDED THE FOLLOWING DEVICE SPECIFICS: IMPLANTABLE NEUROSTIMULATOR KINETRA OR ACTIVA PC FURTHER INFORMATION HAS BEEN REQUESTED; A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF ADDITIONAL INFORMATION IS RECEIVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 791914 | UNKNOWN DBS LEAD | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC NEUROMODULATION | NEU_UNKNOWN_LEAD | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00070 YR | Required Intervention |