TY - JOUR
T1 - Clinical Evaluation of the Safety of Repetitive Intraoperative Defibrillation Threshold Testing
AU - FRAME, ROSEMARY
AU - BRODMAN, RICHARD
AU - FURMAN, SEYMOUR
AU - KIM, SOO G.
AU - ROTH, JAMES
AU - FERRICK, KEVIN
AU - HOLLINGER, INGRID
AU - GROSS, JAY
AU - FISHER, JOHN D.
PY - 1992/6
Y1 - 1992/6
N2 - One goal of the initial implantation procedure for a cardioverter defibrillator is determination of the configuration and patch location with the lowest defibrillation threshold (DFT). To determine the safety of multiple defibrillation tests, an analysis of the intraoperative defibrillation threshold tests (DFTT) in our patients was performed. In 84 patients, the mean number of DFT trials was 5.27; the mean number of joules received was 275.0. The maximum number of shocks in one implant procedure was 50 for a total of 4,895 joules without complications. Four patients received 30 or more DFT shocks without complication. There were two complications related directly to the DFTT: one patient with severe noninflammatory cardiomyopathy developed electromechanical dissociation and was subsequently resuscitated and survived; the second patient with severe triple vessel coronary artery disease suffered an intraoperative myocardial infarction during testing and eventually died 22 days postoperatively. All patients received an ICD unit; six patients had DFTs of > 20 joules. Based on our experience, we followed the clinical status (heart rate, blood pressure, EGG changes, fluid status, total anesthesia time) during the DFTT to determine the extent and duration of our testing protocol. Multiple shocks due to repositioning of the leads in a stable patient should not prohibit extensive testing as adverse consequences do not appear to be cumulative.
AB - One goal of the initial implantation procedure for a cardioverter defibrillator is determination of the configuration and patch location with the lowest defibrillation threshold (DFT). To determine the safety of multiple defibrillation tests, an analysis of the intraoperative defibrillation threshold tests (DFTT) in our patients was performed. In 84 patients, the mean number of DFT trials was 5.27; the mean number of joules received was 275.0. The maximum number of shocks in one implant procedure was 50 for a total of 4,895 joules without complications. Four patients received 30 or more DFT shocks without complication. There were two complications related directly to the DFTT: one patient with severe noninflammatory cardiomyopathy developed electromechanical dissociation and was subsequently resuscitated and survived; the second patient with severe triple vessel coronary artery disease suffered an intraoperative myocardial infarction during testing and eventually died 22 days postoperatively. All patients received an ICD unit; six patients had DFTs of > 20 joules. Based on our experience, we followed the clinical status (heart rate, blood pressure, EGG changes, fluid status, total anesthesia time) during the DFTT to determine the extent and duration of our testing protocol. Multiple shocks due to repositioning of the leads in a stable patient should not prohibit extensive testing as adverse consequences do not appear to be cumulative.
KW - defibrillation threshold testing
KW - implantable cardioverter defibrillator
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U2 - 10.1111/j.1540-8159.1992.tb03077.x
DO - 10.1111/j.1540-8159.1992.tb03077.x
M3 - Article
C2 - 1376899
AN - SCOPUS:0026871028
SN - 0147-8389
VL - 15
SP - 870
EP - 877
JO - PACE - Pacing and Clinical Electrophysiology
JF - PACE - Pacing and Clinical Electrophysiology
IS - 6
ER -