ACTIVA
Report
- Report Number
- 3007566237-2020-00305
- Event Type
- Injury
- Date Received
- March 5, 2020
- Date of Event
- January 8, 2020
- Report Date
- March 5, 2020
- Manufacturer
- MEDTRONIC NEUROMODULATION
- Product Code
- MHY
- PMA / PMN Number
- P960009
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SP
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
OTHER RELEVANT DEVICE(S) ARE: PRODUCT ID: 3387, SERIAL/LOT #: UNKNOWN. 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. THE DEVICE WAS USED FOR AN OFF LABEL INDICATION. CORRIPIO I, ROLDAN A, SARRO S, ET AL. DEEP BRAIN STIMULATION IN TREATMENT RESISTANT SCHIZOPHRENIA: A PILOT RANDOMIZED CROSS-OVER CLINICAL TRIAL. EBIOMEDICINE. 2020;51:102568. 10.1016/J.EBIOM.2019.11.029. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
EIGHT PATIENTS WITH SCHIZOPHRENIA, WHO MET CRITERIA FOR TREATMENT RESISTANCE AND WERE ALSO RESISTANT TO/INTOLERANT OF CLOZAPINE, WERE RANDOMLY ASSIGNED USING CENTRAL ALLOCATION TO RECEIVE DBS IN THE NACC OR SUBGENUAL ACC. AN OPEN STABILIZATION PHASE LASTING AT LEAST SIX MONTHS WAS FOLLOWED BY A RANDOMIZED DOUBLE BLIND CROSSOVER PHASE LASTING 24 WEEKS IN THOSE WHO MET SYMPTOMATIC IMPROVEMENT CRITERIA. THE PRIMARY END-POINT WAS A 25% IMPROVEMENT IN PANSS TOTAL SCORE. REPORTED EVENTS: ONE PATIENT SUFFERED A RIGHT INTERNAL CAPSULE HEMORRHAGE IMMEDIATELY AFTER IMPLANT AND SUBSEQUENTLY DEVELOPED INFECTION IN THE DEVICE WHICH THREATENED TO SPREAD TO THE ELECTRODES. THE PATIENT EXPERIENCED CONFUSION AFTER IMPLANT. AS A RESULT THE INS AND LEADS WERE REMOVED THREE MONTHS AFTER SURGERY. THE PATIENT HAD A LESION IN THE ANTERIOR RIGHT INTERNAL CAPSULE. CORRIPIO I, ROLDAN A, SARRO S, ET AL. DEEP BRAIN STIMULATION IN TREATMENT RESISTANT SCHIZOPHRENIA: A PILOT RANDOMIZED CROSS-OVER CLINICAL TRIAL. EBIOMEDICINE. 2020;51:102568. 10.1016/J.EBIOM.2019.11.029.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 257922 | ACTIVA | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC NEUROMODULATION | 37601 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 37 YR | Required Intervention |