FDA Adverse Event Injury Summary report: N

INFUSION PUMP

MDR report key: 3849752 · Received June 4, 2014

Report

Report Number
3007566237-2014-01536
Event Type
Injury
Date Received
June 4, 2014
Date of Event
November 4, 2013
Report Date
May 7, 2014
Manufacturer
MEDTRONIC NEUROMODULATION
Product Code
LKK
PMA / PMN Number
P860004
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE REPORTED DATE REFLECTS THE DATE THAT THE ARTICLE WAS ACCEPTED FOR PUBLICATION. IT WAS NOT POSSIBLE TO MATCH THIS EVENT WITH ANY PREVIOUSLY REPORTED EVENT. PRODUCT ID: NEU_UNKNOWN_CATH, LOT# UNKNOWN, PRODUCT TYPE: CATHETER. (B)(4).

Description of Event or Problem · 1

MARGETIS, K., PAPAGEORGIOU, G., GATZONIS, S., POLITIS, K., SIATOUNI, A., SAKAS, D. INTRATHECAL BACLOFEN IMPROVES PSYCHIATRIC SYMPTOMS IN SPASTICITY PATIENTS. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY. 2014. 34. SUMMARY/REPORTED EVENT: THIS REPORT REFERS TO A (B)(6) YEARS-OLD MALE PATIENT (PATIENT 12) WITH TRAUMATIC BRAIN INJURY AND TWO HEMIPARESIS. PRE MODIFIED ASHWORTH (MA) SPASTICITY SCALE WAS REPORTED AS 2. PATIENT RECEIVED BACLOFEN (UNKNOWN MANUFACTURER) PROGRAMMABLE FLOW FOR PSYCHIATRIC SYMPTOM OF SPASTICITY AT A DOSE OF 60 UG/ 24 HOURS THROUGH INTRATHECAL ROUTE, LAMOTRIGINE (UNKNOWN MANUFACTURER) AT A DOSE OF 300 MG, FLUOXETINE (UNKNOWN MANUFACTURER) AT A DOSE OF 20 MG, BACLOFEN (UNKNOWN MANUFACTURER) AT A DOSE OF 15 MG, ORALLY AND AMISULPRIDE (UNKNOWN MANUFACTURER) AT A DOSE OF 100 MG. ON AN UNKNOWN DATE, PATIENT EXPERIENCED CATHETER KINK (REOPERATION). POST MODIFIED ASHWORTH (MA) SPASTICITY SCALE WAS REPORTED AS 0.5 AND PRE BARRY-ALBRIGHT (BA) SCALE WAS 0. THE AUTHORS CONCLUDED THAT THESE RESULTS SUGGEST THAT SPASTICITY PATIENTS WITH PSYCHOLOGICAL DISTRESS SYMPTOMS SHOULD NOT BE DEPRIVED OF THE ITB OPTION AND HIGHLIGHT THE NEED FOR FURTHER INVESTIGATION OF THE ROLE OF ITB ON PSYCHIATRIC SPECTRUM DISORDERS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
327064 INFUSION PUMP PUMP, INFUSION, IMPLANTED, PROGRAMMABLE LKK MEDTRONIC NEUROMODULATION

Patients

Seq Age Sex Outcome Treatment
1 00022 YR Required Intervention