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Alexandre Trigano

Publications and source records attributed to Alexandre Trigano.

7 recordsLinked to original sources

Clinical testing of cellular phone ringing interference with automated external defibrillators.

OBJECTIVE: This study examined cellular phone ringing interference with automated external defibrillators (AED). METHODS: The phone systems tested were two single band handheld telephones: (1) a Global System for Mobile Communication (GSM) receiver; and (2) a Personal Communication Services (PCS) receiver. The ringing phase of a digital cellular phone includes a brief burst of peak-emitted power. The GSM had a maximum power output of 2 W, operating on a 900 MHz carrier frequency, and the PCS had a maximum output of 1 W, operating on a 1800 MHz carrier frequency. During AED monitoring, the digital cellular telephone was placed successively in three positions: (1) on the AED; (2) on the patient's chest between the electrodes; and (3) on the connector between the electrodes and the AED cable. After positioning the cellular phone, calls were placed during the AED analyzing phase. RESULTS: Three AED models were tested using their original electrodes: (1) LifePak 20 monitor/defibrillator device; (2) Lifepak 20 P monitor/defibrillator/stimulator (Medtronic Emergency Response Systems, Redmond, WA, USA); and (3) HeartStart XL M4735A monitor/defibrillator (Philips Medical Systems, Andover, MA, USA). The first two devices had Quik-Combo electrodes and the third device had Adults Plus multifunction electrodes. Ninety-one tests were performed on 13 patients. The only disturbance provoked by testing was noise emitted by the AED speaker when the receiver was close to the device. The noise began 2-4 s before the first audible ringing tone and persisted throughout the ringing phase. The distance at which this effect could be prevented was 15 cm. CONCLUSION: Clinical testing during ECG monitoring by an AED during call from a cellular phone did not show any analysis dysfunction during unshockable rhythms and provoked only transient dysfunction of the speaker device.

Aged↗

Activity-based rate-adaptive pacemakers under hyperbaric conditions.

OBJECTIVES: The aim of this study was to test a variety of currently available activity-based rate-adaptive pacemakers under hyperbaric conditions. BACKGROUND: Sports divers with pacemakers can dive under certain circumstances. The rate response of activity-sensing pacing under hyperbaric conditions has rarely been evaluated. MATERIALS AND METHODS: We manufactured a miniaturized hyperbaric chamber. A pacemaker inside was kept close to the corresponding telemetry wand placed on top of the chamber. An inflation device for coronary balloon angioplasty was used to create hydraulic pressure. Group I pacemakers were exposed to a 30 msw/98 fsw/4 ATA and after a 1-month waiting period to 60 msw/197 fsw-depth/7 ATA. Group II was exposed to only one dive to 60 msw. The electrogram and event marker telemetry were used to monitor the pacing stimuli and measurements were made for case distortion. RESULTS: The baseline pacing rate did not change in 27 tests. Return to baseline was shown during 18 tests after transient sensor-driven rate. There was a sensor rate response to manual brief shaking during and following testing. A case distortion was shown in 15 of 29 tests at 60 m. CONCLUSIONS: Modern accelerometers showed no sensitivity to pressure on the pacemaker can at 30 msw/98 fsw and 60 msw/197 fsw but in some devices responded to pressure changes. There was no pacing dysfunction or suppression of the sensor response despite the high incidence of case distortion at 60 msw/197 fsw. As a general rule, diving should not be allowed at depths greater than 20 msw/65 fsw.

Diving↗

Risk of cellular phone interference with an implantable loop recorder.

This study examined the risk of cellular phone ringing interference with implantable loop recorders (ILR). The technical manual of ILR warns of potential interference by cellular phone in close proximity to the implanted device, corrupting the data stored in memory or causing inappropriate device operation. The ringing phase of a digital Global System for Mobile Communication (GSM) or Personal Communication Services (PCS) cellular phone includes a brief burst of peak emitted power. To obviate the risk of dysfunction in recipients of implanted ILRs, the testing was performed with externally applied devices. The ILR was positioned in the left parasternal region and the telemetry wand removed after regular programming. Digital cellular telephones were placed over the device at a 1-cm distance and calls were placed. The phone systems tested were single- or dual-band receivers. The GSM used a maximal power output of 2 W, operating on a 900 MHz carrier frequency, and the PCS a maximal output of 1 W, operating on a 1800 MHz carrier frequency. The device activator was used to store the episodes encompassing the tests. Sixty nine tests were performed in 45 patients. In 61 tests, high-frequency polymorphic artifacts were visible on manually activated recordings, beginning a few seconds before the first audible ringing tone and persisting throughout the ringing phase. Cellular phone ringing in close proximity to an externally applied ILR caused bursts of high-frequency signals during electrocardiogram monitoring, without causing permanent device dysfunction or reprogramming. Cellular telephones are a potential source of electrocardiographic artifacts on ILR recordings.

Cell Phone↗

Clinical study of interference with cardiac pacemakers by a magnetic field at power line frequencies.

OBJECTIVES: This study examined the risk of interference by high magnetic flux density with permanent pacemakers. BACKGROUND: Several forms of electromagnetic energy may interfere with the functions of implanted pacemakers. No clinical study has reported specific and relevant information pertaining to magnetic fields near power lines or electrical appliances. METHODS: A total of 250 consecutive tests were performed in 245 recipients of permanent pacemakers during 12-lead electrocardiographic monitoring. A dedicated exposure system generated a 50-Hz frequency and maximum 100-microT flux density, while the electrical field was kept at values on the order of 0.10 V/m. RESULTS: A switch to the asynchronous mode was recorded in three patients with devices programmed in the unipolar sensing configuration. A sustained mode switch was followed by symptomatic pacing inhibition in one patient. No effect on devices programmed in bipolar sensing was observed, except for a single interaction with a specific capture monitoring algorithm. CONCLUSIONS: The overall incidence of interaction by a magnetic field was low in patients tested with a wide variety of conventionally programmed pacemaker models. A magnetic field pulsed at power frequency can cause a mode switch and pacing inhibition in patients with devices programmed in the unipolar sensing configuration. The risk of interference appears negligible in patients with bipolar sensing programming.

Adolescent↗

Interference by cellular telephone with an implantable loop recorder.

We report the observation of interference between an implanted loop recorder and a cellular telephone when the latter was placed over the subcutaneous pocket. The artifact produced during the ringing of the telephone was automatically recorded and stored in the device memory. A similar interference was documented during ex vivo testing.

Adult↗

Reliability of electromagnetic filters of cardiac pacemakers tested by cellular telephone ringing.

BACKGROUND: State-of-the art cardiac pacemakers are protected against radiofrequency signals. Although there have been earlier clinical and in vitro reports of cellular phone interference with implantable devices, only a few studies have been performed in recent years. The ringing phase of digital GSM or PCS cellular phones includes a brief period of peak radiated power. OBJECTIVES: This study tested the protection offered by electromagnetic filters of cardiac pacemakers against cellular phone ringing. METHODS: We performed 330 consecutive tests in 158 patients at the time of routine examination in our pacemaker follow-up clinic. The programmed parameters remained unchanged before testing. During electrocardiographic monitoring, 2 single-band digital cellular phones consecutively placed over the pacemaker pocket each received a call. The phone systems tested were 1) GSM at a maximal power output of 2 W, operating on a 900 MHz carrier frequency, and 2) PCS at a maximal output of 1 W, operating on a 1800 MHz carrier frequency. RESULTS: Interference was noted in only 5 tests, due to interaction by the GSM system with 4 unprotected pacemaker models. The GSM test was negative in 12 other tests of identical pulse generator models. The overall incidence of interference was 1.5% of tests. CONCLUSIONS: Interference by cellular phone ringing occurred only with unprotected pacemaker models. Standard programming of these unprotected models was associated with a low incidence of interference.

Adult↗