2008
DOI: 10.1227/01.neu.0000311085.73519.b4
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Reversible Neurological Symptoms Caused by Diathermy in a Patient With Deep Brain Stimulators

Abstract: This is the first reported case of reversible injury from diathermy in a patient with DBS implants. Neurosurgeons must continue to emphasize to their patients and to other practitioners treating this population that diathermy is contraindicated for those with DBS implants.

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Cited by 37 publications
(18 citation statements)
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“…One agreed and lifethreatening risk of MW is its use in proximity to indwelling stimulators or electronic equipment. 2,61,62 The use of US away from such sites is erroneously also often contraindicated because its biophysical properties are misunderstood. 61 Both MW and US can cause superficial burning under certain conditions.…”
Section: Discussionmentioning
confidence: 99%
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“…One agreed and lifethreatening risk of MW is its use in proximity to indwelling stimulators or electronic equipment. 2,61,62 The use of US away from such sites is erroneously also often contraindicated because its biophysical properties are misunderstood. 61 Both MW and US can cause superficial burning under certain conditions.…”
Section: Discussionmentioning
confidence: 99%
“…2,61,62 The use of US away from such sites is erroneously also often contraindicated because its biophysical properties are misunderstood. 61 Both MW and US can cause superficial burning under certain conditions. However, most adverse incidents reported with MW are secondary to its use in warming hot packs or damp cloths for superficial heating.…”
Section: Discussionmentioning
confidence: 99%
“…Any environmental sources of electromagnetic interference such as cardiac pacemakers, implantable or external cardiac defibrillators, magnetic resonance imaging (MRI), and security checkpoints pose a potential risk of causing the DBS to change settings or turn off, according to the manufacturer's online manual . Cases of adventitious current or heat at the electrode site induced by MRI, diathermy, and cardioversion leading to severe neurologic injury have been reported . If MRI is to be used for a DBS patient, only scanners that are equipped with 1.5 Tesla horizontal bores, transmit–receive head coils, average head‐specific absorption rates below 0.1 watts/kg, and dB/dt gradients of 20 Tesla/sec or less are permitted according to manufacturer's warnings .…”
Section: Introductionmentioning
confidence: 99%
“…In the European Union, however, St. Jude Medical has received Conformité Européenne (CE) approval for its DBS device [3] , and Boston Scientific is conducting a clinical trial on its Vercise System [4] , aimed at obtaining CE approval. In the USA, the efficacy of DBS for both treatment-resistant depression and for epilepsy is currently under investigation, raising the possibility that an even greater proportion of patients will soon be implanted with DBS devices [5] .…”
Section: Introductionmentioning
confidence: 99%