NI
Report
- Report Number
- 1226348-2019-10132
- Event Type
- Injury
- Date Received
- February 27, 2019
- Date of Event
- March 1, 2018
- Report Date
- February 5, 2019
- Manufacturer
- CODMAN & SHURTLEFF, INC.
- Product Code
- GWM
- PMA / PMN Number
- NI
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
COMPLAINT SAMPLE WAS NOT RETURNED TO CODMAN AND NO LOT NUMBER INFORMATION HAS BEEN PROVIDED; THEREFORE, AN EVALUATION OF THE DEVICE COULD NOT BE PERFORMED AND MANUFACTURING RECORDS COULD NOT BE REVIEWED. THE CAUSE(S) OF THE DIFFICULTY REPORTED BY THE CUSTOMER COULD NOT BE DETERMINED. IF THE COMPLAINT SAMPLE BECOMES AVAILABLE, THIS COMPLAINT WILL BE REOPENED, AND THE RESPECTIVE EVALUATION PERFORMED. TRENDS WILL BE MONITORED FOR THIS OR SIMILAR COMPLAINTS. AT PRESENT, WE CONSIDER THIS COMPLAINT TO BE CLOSED.
IN THE LITERATURE ARTICLE ¿COMPLICATIONS FOLLOWING INTRACRANIAL PRESSURE MONITORING IN CHILDREN: A 6-YEAR SINGLE-CENTER EXPERIENCE.¿ BY RUICHONG MA, DAVID ROWLAND, ANDREW JUDGE, AMEDEO CALISTO, JAYARATNAM JAYAMOHAN , DAVID JOHNSON, PETER RICHARDS, SHAILENDRA MAGDUM AND STEVEN WALL, PUBLISHED JOURNAL OF NEUROSURGERY: PEDIATRICS. 21 (3) (PP 278-283), 2018, IT WAS REPORTED THAT AFTER USE OF UNKNOWN MICROSENSORS IN 385 CASES, THERE WAS A 3.6% RATE OF LEAKAGE, A 0.5% RATE FOR HEMORRHAGE AND A SINGLE CASE OF INFECTION (0.3%). PER THE ARTICLE: ¿INTRACRANIAL PRESSURE (ICP) MONITORING IS AN IMPORTANT TOOL IN THE NEUROSURGEON'S ARMAMENTARIUM AND IS USED FOR A WIDE RANGE OF INDICATIONS. THERE ARE MANY DIFFERENT ICP MONITORS AVAILABLE, OF WHICH FIBER-OPTIC INTRAPARENCHYMAL DEVICES ARE VERY POPULAR. HERE, THE AUTHORS DOCUMENT THEIR EXPERIENCE PERFORMING ICP MONITORING FROM 2005 TO 2015 AND SPECIFICALLY COMPLICATION RATES FOLLOWING INSERTION OF THE MICROSENSOR ICP MONITOR. METHOD(S): A RETROSPECTIVE CASE SERIES REVIEW OF ALL PATIENTS WHO UNDERWENT ICP MONITORING OVER A 10-YEAR PERIOD FROM 2005 TO 2015 WAS PERFORMED. RESULT(S): THERE WERE 385 SEPARATE OPERATIONS WITH AN OVERALL COMPLICATION RATE OF 8.3% (32 OF 385 CASES).¿ NONE OF THESE PATIENTS REQUIRED FURTHER SURGICAL INTERVENTION. THERE WAS NO MORE SPECIFIC DATA AVAILABLE REGARDING THE REPORTED ADVERSE EVENTS. AT THE TIME OF COMPLAINT ENTRY, NO PATIENT OR DEVICE SPECIFIC INFORMATION, I.E. CATALOGUE/LOT NUMBER. THIS ARTICLE WAS DISCOVERED THROUGH THE MONTHLY LITERATURE SEARCH.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 166433 | NI | NI | GWM | CODMAN & SHURTLEFF, INC. | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |