Artifacts in TMS and TES Technique Flashcards

1
Q

What is the potential issue associated with auditory click during TMS?

A

Auditory click can be noisy, annoying, and distracting, with rhythmic patterns; a solution is to use earplugs, white noise, or similar noise in control conditions.

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2
Q

How can mechanical vibrations on the skull during TMS affect data collection, and what is the suggested solution?

A

Mechanical vibrations allow participants to discriminate intensity and guess the locus of stimulation; shock absorbers and sham stimulation with similar vibration can be used as a solution.

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3
Q

What are the potential side effects of TMS involving cranial nerves or muscles, and how can they be addressed?

A

Pain and twitches can be distracting side effects; solutions include coil orientation change, offline stimulation, and selecting less susceptible subjects.

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4
Q

How can noise in TMS affect data interpretation, and what are suggested control conditions?

A

TMS-induced noise might produce non-specific effects; control conditions include using another cortical site, a baseline task condition, and sham or lower intensity stimulation.

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5
Q

How can sensory side effects during TMS be mitigated, and what is the recommended control for sham TMS?

A

Sham TMS involves positioning the coil to lose power or using a placebo coil; it offers better control than no-TMS condition, but control task/site is recommended.

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6
Q

What is the primary concern regarding heat during TMS, and what are the suggested solutions?

A

The coil warming up is a concern; solutions include changing coils, self-refrigerating coils, or modifying the experimental design if possible.

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7
Q

What are the different methods for locating the target site during TMS, and what is the trade-off between them?

A

Methods include external anatomical landmarks, functional methods, and neuro-navigation; the trade-off is between accuracy and feasibility/speed/cost.

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8
Q

How is the control site selected in TMS, and why is the selection of the homologous region often preferred?

A

Control site selection considers areas without direct connections, not involved in the task, and not too distant; homologous regions are preferred for lateralized functions.

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9
Q

What is the problem associated with the coil warming up during TMS sessions, and what are the possible solutions?

A

The coil warming up can affect the magnetic field; solutions include changing coils, self-refrigerating coils, or modifying the experimental design.

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10
Q

What are the potential side effects of TMS, and what is the most dangerous one reported in certain cases?

A

Possible side effects include seizures (most dangerous, reported in patients), hearing loss, heating of the brain, scalp burns, and effects on cognition and mood.

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11
Q

How can seizures be induced during TMS, and what preventive measures are suggested?

A

Seizures are caused by the spread of excitation; prevention involves monitoring with visual/EMG/EEG and a pre-TMS checklist.

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12
Q

What is the risk associated with hearing during TMS, and how can it be reduced?

A

TMS produces loud clicks; the risk is reduced with earplugs.

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13
Q

What is the potential effect of TMS on mood in healthy subjects, and how does it depend on the site of stimulation?

A

TMS can lead to subtle changes in mood; inhibitory rTMS on the left frontal cortex may worsen mood, while inhibitory rTMS on the right frontal cortex may improve mood.

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14
Q

What are the contraindications for TMS, and why is informed consent necessary?

A

Contraindications include metallic hardware, history of seizures, certain medications, pregnancy, serious head trauma, stroke, brain surgery, and other medical/neurologic conditions; informed consent is necessary to disclose all significant risks.

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15
Q

What are the levels of risk in TMS, and what determines the class of risk?

A

Class I has a direct clinical benefit with moderate risk, Class II has potential but unproven benefit with low risk, and Class III has no expected benefit with stringent safety guidelines.

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16
Q

What is the basic principle behind transcranial electric stimulation (TES), and what are the different types of TES?

A

TES involves the flow of electrical current on the scalp; types include transcranial direct current stimulation (tDCS), transcranial alternating current stimulation (tACS), transcranial random noise stimulation (tRNS), and transcranial pulsed current stimulation (tPCS).

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17
Q

What is the most common TES technique, and what does tDCS modulate without inducing action potentials?

A

Transcranial direct current stimulation (tDCS) is the most common; it modulates excitability of neurons without inducing action potentials.

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18
Q

How does anodal tDCS affect neural excitability, and what are the factors influencing tDCS effects?

A

Anodal tDCS increases neural excitability; factors include intensity, protocol type, task, neural excitability, intra- and inter-individual variability, and electrode montage.

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19
Q

What are the tools required for tDCS, and how can electrode montage be done according to the 10/20 EEG system?

A

Tools include a stimulator, electrodes/pads, and electro-conductive gel; electrode montage is based on the 10/20 EEG system, with anode on a proxy position on the scalp.

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20
Q

What is the purpose of sham tDCS, and what safety issues should be considered?

A

Sham tDCS is an ineffective form used as a control condition; safety issues include age restrictions, metal in the head, history of seizures, medications, medical conditions, headaches, neck aches, hearing changes, syncope, and pregnancy.

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21
Q

What is the most common method for electrode montage in tDCS, and where is the cathode typically positioned?

A

Electrode montage is often based on the 10/20 EEG system; the cathode’s position depends on the area to stimulate/inhibit, with no need for neuro-navigation.

22
Q

What are the different subgroups of tDCS montages, and how does electrode size affect spatial resolution and focality?

A

Subgroups include unilateral monopolar, bilateral bipolar, midline monopolar, and more; larger electrode sizes negatively affect spatial resolution and focality of tDCS effects.

23
Q

What are the advantages of high-density tDCS, and how does it compare to TMS in terms of spatial resolution?

A

High-density tDCS involves one center ring electrode over the target cortical region surrounded by return electrodes, providing higher spatial resolution than TMS.

24
Q

What is the primary difference between tDCS and TMS in terms of portability, cost, and sensory stimulation?

A

tDCS is more portable, cheaper, and lacks noise and tactile/somatosensory stimulation compared to TMS.

25
Q

How does tDCS allow for causal inferences, and in what contexts is it widely used?

A

tDCS allows causal inferences and is widely used in basic research, clinical trials, rehabilitation programs, and potentially neurodoping.

26
Q

What is sham tDCS, and why is it employed as a control condition in experiments?

A

Sham tDCS is an ineffective form of stimulation used as a control condition to account for placebo effects.

27
Q

What are the age restrictions and common contraindications for undergoing tDCS?

A

Age restrictions include 18 and above; contraindications involve metal in the head, history of seizures, certain medications, medical conditions, headaches, neck aches, hearing changes, syncope, and pregnancy.

28
Q

What is the purpose of administering a follow-up questionnaire after tDCS, and what side effects are typically monitored?

A

A follow-up questionnaire monitors side effects like headache, discomfort, burning sensation, itching, tingling, and metallic taste.

29
Q

How does tDCS compare to TMS in terms of side effects, and what conclusion did the review by Fertonani, Ferrari & Miniussi (2015) reach?

A

TDCS rarely has strong effects by itself; the review found that larger electrodes induce stronger side effects, and no serious side effects were ever found for tDCS.

30
Q

What are the factors influencing the effects of tDCS, and how does the intensity of stimulation impact its outcomes?

A

Factors include intensity, protocol type, task, neural excitability, intra- and inter-individual variability, and electrode montage; low-intensity shows differential effects, while higher intensity (> 2mA) increases excitability from both anodal and cathodal polarity.

31
Q

What is the primary concern associated with seizures in TMS, and what measures are suggested for prevention?

A

Seizures are caused by the spread of excitation; prevention involves monitoring with visual/EMG/EEG, a pre-TMS checklist, and vigilance for after-discharges.

32
Q

How does tDCS interact with the brain’s oscillatory rhythms in tACS, and what characterizes the stimulation in tRNS?

A

tACS involves time-dependent stimulation following a sinusoidal shape; tRNS features randomly varied alternating current inducing random activity.

33
Q

How does tPCS differ from tDCS in terms of current direction, and what role did animal models play in its study?

A

tPCS involves unidirectional pulsatile current, typically anodal, to regulate cortical excitability; some animal studies used tPCS to show an intermediate role of astrocytes in cortical plasticity.

34
Q

What is the basic principle behind transcranial electric stimulation (TES), and what historical treatment involved electrical shock?

A

TES involves the flow of electrical current on the scalp; historical treatment involved using electrical shock, such as the shock treatment from a torpedo fish by Hippocrates and Galen.

35
Q

How does tDCS affect neural excitability without inducing action potentials, and what neurotransmitter changes are associated with anodal and cathodal stimulation?

A

tDCS modulates excitability without inducing action potentials; anodal stimulation causes depolarization with less GABA, while cathodal stimulation causes hyperpolarization with less Glu involvement.

36
Q

What evidence supports the effects of tDCS on neural excitability, and what do studies on MEPs and BOLD signals indicate?

A

Evidence from MEPs shows increased neural excitability with anodal stimulation and decreased with cathodal; BOLD signals tend to increase with anodal and decrease with cathodal stimulation.

37
Q

What are the various factors influencing the effects of tDCS, and how does intra- and inter-individual variability play a role?

A

Factors include intensity, protocol type, task, neural excitability, and electrode montage; intra- and inter-individual variability contributes to the variation in tDCS outcomes.

38
Q

What is the primary difference between the electrode montage in tDCS and TMS, and how is it done based on the 10/20 EEG system?

A

Electrode montage in tDCS is based on the 10/20 EEG system; the anode is positioned on a proxy position on the scalp, and the cathode’s placement depends on the area to stimulate/inhibit.

39
Q

How does electrode size affect the spatial resolution and focality of tDCS effects, and what are the advantages of high-density tDCS?

A

Larger electrode sizes negatively affect spatial resolution and focality; high-density tDCS with one center ring electrode provides higher spatial resolution.

40
Q

How does tDCS compare to TMS in terms of portability, cost, and sensory stimulation?

A

tDCS is more portable, cheaper, and lacks noise and tactile/somatosensory stimulation compared to TMS.

41
Q

In what contexts is tDCS widely used, and how does it contribute to causal inferences in research?

A

tDCS is widely used in basic research, clinical trials, rehabilitation programs, and possibly neurodoping; it allows for causal inferences.

42
Q

What is the primary purpose of administering sham tDCS, and how is it typically used as a control condition?

A

Sham tDCS is an ineffective form of stimulation used as a control condition to account for placebo effects.

43
Q

What age restrictions and contraindications are associated with undergoing tDCS, and why is a follow-up questionnaire recommended?

A

Age restrictions include 18 and above; contraindications involve metal in the head, history of seizures, certain medications, medical conditions, headaches, neck aches, hearing changes, syncope, and pregnancy. A follow-up questionnaire is recommended to monitor side effects.

44
Q

How does tDCS compare to TMS in terms of side effects, and what conclusion did the review by Fertonani, Ferrari & Miniussi (2015) reach?

A

TDCS rarely has strong effects by itself; the review found that larger electrodes induce stronger side effects, and no serious side effects were ever found for tDCS.

45
Q

What factors influence the effects of tDCS, and how does the intensity of stimulation impact its outcomes?

A

Factors include intensity, protocol type, task, neural excitability, intra- and inter-individual variability, and electrode montage; low-intensity shows differential effects, while higher intensity (> 2mA) increases excitability from both anodal and cathodal polarity.

46
Q

What is the primary concern associated with seizures in TMS, and what measures are suggested for prevention?

A

Seizures are caused by the spread of excitation; prevention involves monitoring with visual/EMG/EEG, a pre-TMS checklist, and vigilance for after-discharges.

47
Q

How does tDCS interact with the brain’s oscillatory rhythms in tACS, and what characterizes the stimulation in tRNS?

A

tACS involves time-dependent stimulation following a sinusoidal shape; tRNS features randomly varied alternating current inducing random activity.

48
Q

How does tPCS differ from tDCS in terms of current direction, and what role did animal models play in its study?

A

tPCS involves unidirectional pulsatile current, typically anodal, to regulate cortical excitability; some animal studies used tPCS to show an intermediate role of astrocytes in cortical plasticity.

49
Q

What is the basic principle behind transcranial electric stimulation (TES), and what historical treatment involved electrical shock?

A

TES involves the flow of electrical current on the scalp; historical treatment involved using electrical shock, such as the shock treatment from a torpedo fish by Hippocrates and Galen.

50
Q

How does tDCS affect neural excitability without inducing action potentials, and what neurotransmitter changes are associated with anodal and cathodal stimulation?

A

tDCS modulates excitability without inducing action potentials; anodal stimulation causes depolarization with less GABA, while cathodal stimulation causes hyperpolarization with less Glu involvement.