Adam J Stark, Caleb J Han, Jarrod J Eisma, Alexander K Song, Maria E Garza, Leah G Mann, Daniel O Claassen, Manus J Donahue
{"title":"常规解剖和功能磁共振成像序列在3特斯拉下的脑电图电极和放大器温度变化。","authors":"Adam J Stark, Caleb J Han, Jarrod J Eisma, Alexander K Song, Maria E Garza, Leah G Mann, Daniel O Claassen, Manus J Donahue","doi":"10.1177/15500594251320294","DOIUrl":null,"url":null,"abstract":"<p><p>Magnetic resonance imaging (MRI) sequences commonly used in simultaneous electroencephalogram (EEG)-MRI studies include blood oxygenation level-dependent (BOLD) and anatomical T<sub>1</sub>-weighted MRI. Safety and electrode heating profiles for these sequences have been well-characterized. However, recent improvements in EEG design may allow for additional sequences to be performed with similar expectations of heating safety, which would expand the EEG-MRI infrastructure for quantitative physiological studies. We evaluated temperature changes ex vivo and in vivo over a wider range of preparation and readout modules with differing specific absorption rate (SAR). A 32-channel EEG cap was used at 3 T and ex vivo heating was assessed for 2D- and 3D-pseudo-continuous-arterial-spin-labeling, 2D-cine, 2D-phase-contrast, 2D T<sub>2</sub>-Relaxation-Under-Spin-Tagging, 32-direction <i>b </i>= 1000 s/mm<sup>2</sup> and <i>b </i>= 2000 s/mm<sup>2</sup> 2D-diffusion tensor imaging, multiband-BOLD, 3D-T1 MPRAGE, 3D-FLAIR, and 3D-T2. Temperature was monitored with a fiberoptic probe system and plotted over six different electrodes, the amplifier, and battery pack. In vivo assessments were conducted in three participants with the same system. A further in vivo supplemental cohort (n = 10) was used to further evaluate qualitative self-reported heating. Device integrity was evaluated by the manufacturer following experiments. Peak temperature and maximum temperature increases were 23.0°C and 0.4°C respectively ex vivo, and 37.6°C and 0.7°C respectively in vivo. Temperatures did not approach the safety heating threshold of 40°C (defined as a conservative threshold based on manufacturer recommendations and burn injury data). Participants completed in vivo scans without adverse events. No manufacturer-reported device damage was identified. Overall, the tested scans induced heating below critical limits at the clinical field strength of 3 T.</p>","PeriodicalId":93940,"journal":{"name":"Clinical EEG and neuroscience","volume":" ","pages":"15500594251320294"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electroencephalogram Electrode and Amplifier Temperature Changes During Routine Anatomical and Functional Magnetic Resonance Imaging Sequences at 3 Tesla.\",\"authors\":\"Adam J Stark, Caleb J Han, Jarrod J Eisma, Alexander K Song, Maria E Garza, Leah G Mann, Daniel O Claassen, Manus J Donahue\",\"doi\":\"10.1177/15500594251320294\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Magnetic resonance imaging (MRI) sequences commonly used in simultaneous electroencephalogram (EEG)-MRI studies include blood oxygenation level-dependent (BOLD) and anatomical T<sub>1</sub>-weighted MRI. Safety and electrode heating profiles for these sequences have been well-characterized. However, recent improvements in EEG design may allow for additional sequences to be performed with similar expectations of heating safety, which would expand the EEG-MRI infrastructure for quantitative physiological studies. We evaluated temperature changes ex vivo and in vivo over a wider range of preparation and readout modules with differing specific absorption rate (SAR). A 32-channel EEG cap was used at 3 T and ex vivo heating was assessed for 2D- and 3D-pseudo-continuous-arterial-spin-labeling, 2D-cine, 2D-phase-contrast, 2D T<sub>2</sub>-Relaxation-Under-Spin-Tagging, 32-direction <i>b </i>= 1000 s/mm<sup>2</sup> and <i>b </i>= 2000 s/mm<sup>2</sup> 2D-diffusion tensor imaging, multiband-BOLD, 3D-T1 MPRAGE, 3D-FLAIR, and 3D-T2. Temperature was monitored with a fiberoptic probe system and plotted over six different electrodes, the amplifier, and battery pack. In vivo assessments were conducted in three participants with the same system. A further in vivo supplemental cohort (n = 10) was used to further evaluate qualitative self-reported heating. Device integrity was evaluated by the manufacturer following experiments. Peak temperature and maximum temperature increases were 23.0°C and 0.4°C respectively ex vivo, and 37.6°C and 0.7°C respectively in vivo. Temperatures did not approach the safety heating threshold of 40°C (defined as a conservative threshold based on manufacturer recommendations and burn injury data). Participants completed in vivo scans without adverse events. No manufacturer-reported device damage was identified. Overall, the tested scans induced heating below critical limits at the clinical field strength of 3 T.</p>\",\"PeriodicalId\":93940,\"journal\":{\"name\":\"Clinical EEG and neuroscience\",\"volume\":\" \",\"pages\":\"15500594251320294\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-02-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical EEG and neuroscience\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/15500594251320294\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical EEG and neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/15500594251320294","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Electroencephalogram Electrode and Amplifier Temperature Changes During Routine Anatomical and Functional Magnetic Resonance Imaging Sequences at 3 Tesla.
Magnetic resonance imaging (MRI) sequences commonly used in simultaneous electroencephalogram (EEG)-MRI studies include blood oxygenation level-dependent (BOLD) and anatomical T1-weighted MRI. Safety and electrode heating profiles for these sequences have been well-characterized. However, recent improvements in EEG design may allow for additional sequences to be performed with similar expectations of heating safety, which would expand the EEG-MRI infrastructure for quantitative physiological studies. We evaluated temperature changes ex vivo and in vivo over a wider range of preparation and readout modules with differing specific absorption rate (SAR). A 32-channel EEG cap was used at 3 T and ex vivo heating was assessed for 2D- and 3D-pseudo-continuous-arterial-spin-labeling, 2D-cine, 2D-phase-contrast, 2D T2-Relaxation-Under-Spin-Tagging, 32-direction b = 1000 s/mm2 and b = 2000 s/mm2 2D-diffusion tensor imaging, multiband-BOLD, 3D-T1 MPRAGE, 3D-FLAIR, and 3D-T2. Temperature was monitored with a fiberoptic probe system and plotted over six different electrodes, the amplifier, and battery pack. In vivo assessments were conducted in three participants with the same system. A further in vivo supplemental cohort (n = 10) was used to further evaluate qualitative self-reported heating. Device integrity was evaluated by the manufacturer following experiments. Peak temperature and maximum temperature increases were 23.0°C and 0.4°C respectively ex vivo, and 37.6°C and 0.7°C respectively in vivo. Temperatures did not approach the safety heating threshold of 40°C (defined as a conservative threshold based on manufacturer recommendations and burn injury data). Participants completed in vivo scans without adverse events. No manufacturer-reported device damage was identified. Overall, the tested scans induced heating below critical limits at the clinical field strength of 3 T.