THE Q-TRAK SUBCUTANEOUS ELECTRODE
Report
- Report Number
- 2124215-2025-41897
- Event Type
- Injury
- Date Received
- June 25, 2025
- Date of Event
- April 1, 2010
- Report Date
- June 25, 2025
- Manufacturer
- BOSTON SCIENTIFIC CORPORATION
- Product Code
- LWS
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
M. F. EL-CHAMI, B. HARBIEH, M. LEVY, A. R. LEON, AND F. M. MERCHANT, CLINICAL AND ELECTROCARDIOGRAPHIC PREDICTORS OF T WAVE OVERSENSING IN PATIENTS WITH SUBCUTANEOUS ICD, JOURNAL OF ARRHYTHMIA 32 (2016): 181-185.
IT WAS REPORTED PER ARTICLE OF INTEREST LITERATURE REVIEW THAT THE AUTHORS SOUGHT IDENTIFY CLINICAL AND ELECTROCARDIOGRAPHIC PREDICTORS OF T-WAVE OVERSENSING (TWOS) IN A COHORT OF PATIENTS UNDERGOING SUBCUTANEOUS IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (S-ICD). THEY RETROSPECTIVELY IDENTIFIED ALL PATIENTS WHO UNDERWENT S-ICD IMPLANTATION (CAMERON HEALTH MODEL NUMBER 1010 SQ-RX, WITH A SUBCUTANEOUS LEAD-CAMERON HEALTH MODEL 3010) AT THEIR INSTITUTION FROM APRIL 2010 TO JANUARY 2015. NINETY-TWO PATIENTS UNDERWENT S-ICD IMPLANTATION. DURING A MEAN FOLLOW-UP OF 13.1 MONTHS, SIX PATIENTS HAD TWOS RESULTING IN INAPPROPRIATE SHOCKS. IN THE GROUP WITHOUT TWOS, TWO PATIENTS EXPERIENCED INAPPROPRIATE SHOCKS FOR NON-TWOS ETIOLOGIES: ONE FOR SUPRAVENTRICULAR RHYTHM AND ONE FOR ELECTROMAGNETIC INTERFERENCE. CASE 6: A 50-YEAR-OLD MAN WITH HYPERTENSIVE HEART DISEASE PRESENTED WITH SYNCOPE AND SUSTAINED VENTRICULAR TACHYCARDIA, WHICH WAS EASILY REPRODUCED WITH AN ELECTROPHYSIOLOGY STUDY AND POORLY TOLERATED. VENOGRAMS DEMONSTRATED BILATERAL SUBCLAVIAN STENOSIS, ATTRIBUTED TO A HISTORY OF END-STAGE RENAL DISEASE (ESRD), AND SO HE WAS IMPLANTED WITH AN S-ICD. ONE MONTH AFTER IMPLANTATION HE PRESENTED WITH FIVE INAPPROPRIATE SHOCKS DUE TO TWOS IN THE SETTING OF LIGHT ACTIVITY. DESPITE EXTENSIVE DISCUSSIONS REGARDING MANAGEMENT OPTIONS, THE PATIENT ADAMANTLY REFUSED ANY EFFORTS TO MINIMIZE THE RISK OF INAPPROPRIATE SHOCKS AND INSISTED ON DEVICE EXPLANT, WHICH WAS PERFORMED DURING THAT HOSPITALIZATION. NO ADDITIONAL ADVERSE PATIENT EFFECTS WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2588904 | THE Q-TRAK SUBCUTANEOUS ELECTRODE | IMPLANTABLE LEAD | LWS | BOSTON SCIENTIFIC CORPORATION | 3010 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR | Male | Other| R| H |