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  1. Article ; Online: Assessing pulmonary function in ALS using electrical impedance tomography.

    Rutkove, Seward B / McIlduff, Courtney E / Stommel, Elijah / Levy, Sean / Smith, Christy / Gutierrez, Hilda / Verga, Sarah / Samaan, Soleil / Yator, Chebet / Nanda, Ajitesh / Pastel, Lisa / Doussan, Allaire / Phipps, Kathy / Murphy, Ethan / Halter, Ryan

    Amyotrophic lateral sclerosis & frontotemporal degeneration

    2024  , Page(s) 1–8

    Abstract: ... ...

    Abstract Objective
    Language English
    Publishing date 2024-04-04
    Publishing country England
    Document type Journal Article
    ZDB-ID 2705049-X
    ISSN 2167-9223 ; 2167-8421
    ISSN (online) 2167-9223
    ISSN 2167-8421
    DOI 10.1080/21678421.2024.2334075
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: A study of flex miniaturized coils for focal nerve magnetic stimulation.

    Colella, Micol / Press, Daniel Z / Laher, Rebecca M / McIlduff, Courtney E / Rutkove, Seward B / Cassarà, Antonino M / Apollonio, Francesca / Pascual-Leone, Alvaro / Liberti, Micaela / Bonmassar, Giorgio

    Medical physics

    2022  Volume 50, Issue 3, Page(s) 1779–1792

    Abstract: ... the performances (e.g., focality and minimal currents) of new generations of mcoil designs. ...

    Abstract Background: Peripheral magnetic stimulation (PMS) is emerging as a complement to standard electrical stimulation (ES) of the peripheral nervous system (PNS). PMS may stimulate sensory and motor nerve fibers without the discomfort associated with the ES used for standard nerve conduction studies. The PMS coils are the same ones used in transcranial magnetic stimulation (TMS) and lack focality and selectiveness in the stimulation.
    Purpose: This study presents a novel coil for PMS, developed using Flexible technologies, and characterized by reduced dimensions for a precise and controlled targeting of peripheral nerves.
    Methods: We performed hybrid electromagnetic (EM) and electrophysiological simulations to study the EM exposure induced by a novel miniaturized coil (or mcoil) in and around the radial nerve of the neuro-functionalized virtual human body model Yoon-Sun, and to estimate the current threshold to induce magnetic stimulation (MS) of the radial nerve. Eleven healthy subjects were studied with the mcoil, which consisted of two 15 mm diameter coils in a figure-of-eight configuration, each with a hundred turns of a 25 μm copper-clad four-layer foil. Sensory nerve action potentials (SNAPs) were measured in each subject using two electrodes and compared with those obtained from standard ES. The SNAPs conduction velocities were estimated as a performance metric.
    Results: The induced electric field was estimated numerically to peak at a maximum intensity of 39 V/m underneath the mcoil fed by 70 A currents. In such conditions, the electrophysiological simulations suggested that the mcoil elicits SNAPs originating at 7 mm from the center of the mcoil. Furthermore, the numerically estimated latencies and waveforms agreed with those obtained during the PMS experiments on healthy subjects, confirming the ability of the mcoil to stimulate the radial nerve sensory fibers.
    Conclusion: Hybrid EM-electrophysiological simulations assisted the development of a miniaturized coil with a small diameter and a high number of turns using flexible electronics. The numerical dosimetric analysis predicted the threshold current amplitudes required for a suprathreshold peripheral nerve sensory stimulation, which was experimentally confirmed. The developed and now validated computational pipeline will be used to improve the performances (e.g., focality and minimal currents) of new generations of mcoil designs.
    MeSH term(s) Humans ; Transcranial Magnetic Stimulation/methods ; Electric Stimulation ; Magnetics ; Electricity ; Nerve Conduction Studies
    Language English
    Publishing date 2022-12-29
    Publishing country United States
    Document type Journal Article
    ZDB-ID 188780-4
    ISSN 2473-4209 ; 0094-2405
    ISSN (online) 2473-4209
    ISSN 0094-2405
    DOI 10.1002/mp.16148
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Optimizing electrical impedance myography of the tongue in amyotrophic lateral sclerosis.

    Mcilduff, Courtney E / Yim, Sung J / Pacheck, Adam K / Rutkove, Seward B

    Muscle & nerve

    2017  Volume 55, Issue 4, Page(s) 539–543

    Abstract: Introduction: Electrical impedance myography (EIM) can quantify muscle health at a range of frequencies, including that most commonly employed, 50 kHz. However, disease-related changes in EIM data suggest the distinction between normal and patient EIM ... ...

    Abstract Introduction: Electrical impedance myography (EIM) can quantify muscle health at a range of frequencies, including that most commonly employed, 50 kHz. However, disease-related changes in EIM data suggest the distinction between normal and patient EIM values could be more apparent at frequencies of >50 kHz. We investigated at what other selected frequencies tongue EIM may differentiate healthy individuals and amyotrophic lateral sclerosis (ALS) patients, remain reliable, and correlate with a standard metric of bulbar function.
    Methods: Tongue EIM phase data from 30 volunteers and 11 ALS patients were analyzed at 6 discrete frequencies from 50 to 500 kHz.
    Results: Of the frequencies assessed, EIM demonstrated maximal separation and reliability at 100 kHz, where phase value was also significantly correlated with the bulbar subscore on the revised version of the ALS Functional Rating Scale.
    Conclusions: One hundred kilohertz could serve as an optimal frequency at which to measure EIM phase values of the tongue in ALS. Muscle Nerve 55: 539-543, 2017.
    MeSH term(s) Adult ; Aged ; Amyotrophic Lateral Sclerosis/diagnosis ; Amyotrophic Lateral Sclerosis/pathology ; Electric Impedance ; Female ; Humans ; Male ; Middle Aged ; Muscle, Skeletal/physiopathology ; Myography ; Reproducibility of Results ; Tongue/physiopathology ; Young Adult
    Language English
    Publishing date 2017
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.25375
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Critical appraisal of the use of alpha lipoic acid (thioctic acid) in the treatment of symptomatic diabetic polyneuropathy.

    McIlduff, Courtney E / Rutkove, Seward B

    Therapeutics and clinical risk management

    2011  Volume 7, Page(s) 377–385

    Abstract: Background: The most common of the neuropathies associated with diabetes mellitus, diabetic sensorimotor polyneuropathy (DSPN) is a syndrome of diffuse, length-dependent, symmetric nerve dysfunction. The condition is linked with substantial morbidity, ... ...

    Abstract Background: The most common of the neuropathies associated with diabetes mellitus, diabetic sensorimotor polyneuropathy (DSPN) is a syndrome of diffuse, length-dependent, symmetric nerve dysfunction. The condition is linked with substantial morbidity, frequent healthcare utilization, and compromised quality of life due to related discomfort. Correspondingly, antidepressants, anticonvulsants, and opioids are regularly prescribed with the goal of pain control. However, the agents rarely provide complete pain relief and fail to address progression of the disorder. Whereas strict blood glucose control can slow the onset and worsening of DSPN, near-normoglycemia is not easily attainable. Evidence implicating oxidative processes in the pathogenesis of DSPN offers one potentially important therapeutic avenue. Due to its properties as a potent antioxidant, alpha lipoic acid (ALA) could mitigate the development of DSPN and attenuate resultant symptoms and signs. Approved for treatment of DSPN in Germany, the agent is not more widely used due to uncertainty about its efficacy and reported adverse effects. Here we review the effectiveness and tolerability of ALA in the treatment of symptomatic DSPN.
    Methods: The MEDLINE, EMBASE, and Cochrane Library databases were searched for English-language literature on the topic. Randomized, blinded studies comparing parenteral and oral ALA with placebo in the treatment of peripheral neuropathy in diabetic adults were selected. Analysis included studies with a level of evidence of at least 2b.
    Results: The current appraisal summarizes data from 1160 participants in the ALADIN, SYDNEY, ORPIL, SYDNEY 2, and ALADIN III trials. In four of the studies, ALA provided significant improvement in manifestations of DSPN.
    Conclusion: Treatment with ALA 600 mg iv daily for 3 weeks represents a well-tolerated and effective therapy for DSPN. An oral dose of 600 mg daily administered for up to 5 weeks could offer benefits in symptoms and signs of DSPN without significant side effects.
    Language English
    Publishing date 2011-09-05
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2186560-7
    ISSN 1178-203X ; 1176-6336
    ISSN (online) 1178-203X
    ISSN 1176-6336
    DOI 10.2147/TCRM.S11325
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Ultra-focal Magnetic Stimulation Using a µTMS coil: a Computational Study.

    Colella, Micol / Laher, Rebecca M / Press, Daniel Z / McIlduff, Courtney E / Rutkove, Seward B / Pascual-Leone, Alvaro / Apollonio, Francesca / Liberti, Micaela / Bonmassar, Giorgio

    Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

    2019  Volume 2019, Page(s) 3987–3990

    Abstract: A new miniaturized figure-of-eight coil (μCoil) for TMS applications has been developed taking advantage of the Flex circuit technology. First experiments on volunteers demonstrated the ability of the μCoil to elicit sensorial action potentials of the ... ...

    Abstract A new miniaturized figure-of-eight coil (μCoil) for TMS applications has been developed taking advantage of the Flex circuit technology. First experiments on volunteers demonstrated the ability of the μCoil to elicit sensorial action potentials of the peripheral nervous system. The necessity of reducing the size of standard TMS stimulator arises from the poor spatial resolution of the latter. This study aims to model the μCoil and study the electromagnetic fields induced inside the arm during peripheral nerve stimulation. Results confirmed that the μCoil is capable of inducing a focalized electric field inside the tissues with amplitudes up to 70V/m consistent with the observed peripheral nerve stimulation in healthy volunteers.
    MeSH term(s) Electric Stimulation ; Electricity ; Electromagnetic Fields ; Humans ; Magnetics ; Transcranial Magnetic Stimulation
    Language English
    Publishing date 2019-12-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2694-0604
    ISSN (online) 2694-0604
    DOI 10.1109/EMBC.2019.8857349
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Quantitative ultrasound of muscle can detect corticosteroid effects.

    Martucci, Maria G / McIlduff, Courtney E / Shin, Carmen / Gutierrez, Hilda V / Nam, Joo Yeon / Greenstein, Patricia / Phillips, Kester / Uhlmann, Erik J / Wong, Eric T / Rutkove, Seward B

    Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

    2019  Volume 130, Issue 8, Page(s) 1460–1464

    Abstract: Objectives: In this study, we sought to determine whether quantitative ultrasound (QUS) could detect the impact of corticosteroids on muscle in the absence of frank weakness.: Methods: QUS was performed on selected limb muscles of 20 brain tumor ... ...

    Abstract Objectives: In this study, we sought to determine whether quantitative ultrasound (QUS) could detect the impact of corticosteroids on muscle in the absence of frank weakness.
    Methods: QUS was performed on selected limb muscles of 20 brain tumor patients treated with dexamethasone and 30 healthy controls. Echointensity was quantified using gray scale level (GSL) analysis and compared between groups; correlation to corticosteroid exposure was also performed.
    Results: Average 4-muscle GSL (±standard deviation) was greater in patients compared to controls (35.5 ± 5.61 arbitrary units (AU) versus 30.4 ± 4.17 AU, p = 0.001), with the greatest differences in tibialis anterior. Average muscle GSL also correlated to length of corticosteroid therapy (rho = 0.52, p = 0.01).
    Conclusions: These findings suggest that QUS may be able to quantify skeletal muscle alterations associated with chronic corticosteroid use. Further study of this approach is warranted.
    Significance: The findings of this study may provide a tool to evaluate corticosteroid myopathy.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Antineoplastic Agents, Hormonal/adverse effects ; Antineoplastic Agents, Hormonal/therapeutic use ; Brain Neoplasms/drug therapy ; Dexamethasone/adverse effects ; Dexamethasone/therapeutic use ; Female ; Glucocorticoids/adverse effects ; Glucocorticoids/therapeutic use ; Humans ; Male ; Middle Aged ; Muscle, Skeletal/diagnostic imaging ; Muscle, Skeletal/drug effects ; Muscular Diseases/diagnostic imaging ; Muscular Diseases/etiology ; Ultrasonography/methods
    Chemical Substances Antineoplastic Agents, Hormonal ; Glucocorticoids ; Dexamethasone (7S5I7G3JQL)
    Language English
    Publishing date 2019-05-10
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1463630-x
    ISSN 1872-8952 ; 0921-884X ; 1388-2457
    ISSN (online) 1872-8952
    ISSN 0921-884X ; 1388-2457
    DOI 10.1016/j.clinph.2019.04.709
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Tongue electrical impedance in amyotrophic lateral sclerosis modeled using the finite element method.

    Pacheck, Adam / Mijailovic, Alex / Yim, Sung / Li, Jia / Green, Jordan R / McIlduff, Courtney E / Rutkove, Seward B

    Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology

    2016  Volume 127, Issue 3, Page(s) 1886–1890

    Abstract: Objective: Electrical impedance myography (EIM) of the tongue has demonstrated alterations in patients with amyotrophic lateral sclerosis (ALS) compared to normal subjects. Whether these differences are due to reduced tongue size or diseased-associated ... ...

    Abstract Objective: Electrical impedance myography (EIM) of the tongue has demonstrated alterations in patients with amyotrophic lateral sclerosis (ALS) compared to normal subjects. Whether these differences are due to reduced tongue size or diseased-associated alterations in the electrical characteristics of intrinsic tongue muscles is uncertain.
    Methods: We employed computer simulations using the finite element method, inputting data from healthy and ALS mouse muscle, to help answer that question, comparing our modeled results to human data.
    Results: The models revealed that much of the electrical current flows superficially in the tongue and that tongue thickness only begins to have a major impact on the measured impedance when substantial atrophy is present. Modeled values paralleled the human tongue data.
    Conclusions: These findings suggest that the observed changes in tongue impedance in ALS are mainly due to alterations in the electrical properties of the tongue and are not a mere consequence of tongue volume loss.
    Significance: Further development of EIM for evaluation of bulbar dysfunction in ALS may provide useful information on drug efficacy and could serve as a biomarker in future clinical trials.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Amyotrophic Lateral Sclerosis/diagnosis ; Amyotrophic Lateral Sclerosis/physiopathology ; Animals ; Electric Impedance ; Female ; Finite Element Analysis ; Humans ; Male ; Mice ; Middle Aged ; Models, Biological ; Tongue/physiology ; Young Adult
    Language English
    Publishing date 2016-03
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1463630-x
    ISSN 1872-8952 ; 0921-884X ; 1388-2457
    ISSN (online) 1872-8952
    ISSN 0921-884X ; 1388-2457
    DOI 10.1016/j.clinph.2015.11.046
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Effects of mexiletine on hyperexcitability in sporadic amyotrophic lateral sclerosis: Preliminary findings from a small phase II randomized controlled trial.

    Weiss, Michael D / Macklin, Eric A / McIlduff, Courtney E / Vucic, Steve / Wainger, Brian J / Kiernan, Matthew C / Goutman, Stephen A / Goyal, Namita A / Rutkove, Seward B / Ladha, Shafeeq S / Chen, I-Hweii Amy / Harms, Matthew B / Brannagan, Thomas H / Lacomis, David / Zivkovic, Sasha / Ma, Maxwell / Wang, Leo H / Simmons, Zachary / Rivner, Michael H /
    Shefner, Jeremy M / Cudkowicz, Merit E / Atassi, Nazem

    Muscle & nerve

    2020  Volume 63, Issue 3, Page(s) 371–383

    Abstract: Background: To collect preliminary data on the effects of mexiletine on cortical and axonal hyperexcitability in sporadic amyotrophic lateral sclerosis (ALS) in a phase 2 double-blind randomized controlled trial.: Methods: Twenty ALS subjects were ... ...

    Abstract Background: To collect preliminary data on the effects of mexiletine on cortical and axonal hyperexcitability in sporadic amyotrophic lateral sclerosis (ALS) in a phase 2 double-blind randomized controlled trial.
    Methods: Twenty ALS subjects were randomized to placebo and mexiletine 300 or 600 mg daily for 4 wk and assessed by transcranial magnetic stimulation and axonal excitability studies. The primary endpoint was change in resting motor threshold (RMT).
    Results: RMT was unchanged with 4 wk of mexiletine (combined active therapies) as compared to placebo, which showed a significant increase (P = .039). Reductions of motor evoked potential (MEP) amplitude (P = .013) and accommodation half-time (P = .002), secondary outcome measures of cortical and axonal excitability, respectively, were also evident at 4 wk on mexiletine.
    Conclusions: The relative stabilization of RMT in the treated subjects was unexpected and could be attributed to unaccounted sources of error or chance. However, a possible alternative cause is neuromodulation preventing an increase. The change in MEP amplitude and accommodation half-time supports the reduction of cortical and axonal hyperexcitability with mexiletine.
    MeSH term(s) Adult ; Aged ; Amyotrophic Lateral Sclerosis/drug therapy ; Amyotrophic Lateral Sclerosis/physiopathology ; Axons ; Cortical Excitability ; Double-Blind Method ; Electrodiagnosis ; Electromyography ; Evoked Potentials, Motor/physiology ; Female ; Humans ; Male ; Median Nerve/physiopathology ; Mexiletine/therapeutic use ; Middle Aged ; Neural Conduction/physiology ; Preliminary Data ; Transcranial Magnetic Stimulation ; Voltage-Gated Sodium Channel Blockers/therapeutic use
    Chemical Substances Voltage-Gated Sodium Channel Blockers ; Mexiletine (1U511HHV4Z)
    Language English
    Publishing date 2020-12-31
    Publishing country United States
    Document type Clinical Trial, Phase II ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.27146
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Critical appraisal of the use of alpha lipoic acid (thioctic acid) in the treatment of symptomatic diabetic polyneuropathy

    McIlduff CE / Rutkove SB

    Therapeutics and Clinical Risk Management, Vol 2011, Iss default, Pp 377-

    2011  Volume 385

    Abstract: Courtney E McIlduff, Seward B RutkoveDepartment of Neurology, Beth Israel Deaconess Medical Center ...

    Abstract Courtney E McIlduff, Seward B RutkoveDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USABackground: The most common of the neuropathies associated with diabetes mellitus, diabetic sensorimotor polyneuropathy (DSPN) is a syndrome of diffuse, length-dependent, symmetric nerve dysfunction. The condition is linked with substantial morbidity, frequent healthcare utilization, and compromised quality of life due to related discomfort. Correspondingly, antidepressants, anticonvulsants, and opioids are regularly prescribed with the goal of pain control. However, the agents rarely provide complete pain relief and fail to address progression of the disorder. Whereas strict blood glucose control can slow the onset and worsening of DSPN, near-normoglycemia is not easily attainable. Evidence implicating oxidative processes in the pathogenesis of DSPN offers one potentially important therapeutic avenue. Due to its properties as a potent antioxidant, alpha lipoic acid (ALA) could mitigate the development of DSPN and attenuate resultant symptoms and signs. Approved for treatment of DSPN in Germany, the agent is not more widely used due to uncertainty about its efficacy and reported adverse effects. Here we review the effectiveness and tolerability of ALA in the treatment of symptomatic DSPN.Methods: The MEDLINE, EMBASE, and Cochrane Library databases were searched for English-language literature on the topic. Randomized, blinded studies comparing parenteral and oral ALA with placebo in the treatment of peripheral neuropathy in diabetic adults were selected. Analysis included studies with a level of evidence of at least 2b.Results: The current appraisal summarizes data from 1160 participants in the ALADIN, SYDNEY, ORPIL, SYDNEY 2, and ALADIN III trials. In four of the studies, ALA provided significant improvement in manifestations of DSPN.Conclusion: Treatment with ALA 600 mg iv daily for 3 weeks represents a well-tolerated and effective therapy for DSPN. An oral dose of 600 mg daily administered for up to 5 weeks could offer benefits in symptoms and signs of DSPN without significant side effects.Keywords: alpha lipoic acid, antioxidant, diabetes mellitus, neuropathy, thioctic acid
    Keywords Medicine (General) ; R5-920
    Subject code 610
    Language English
    Publishing date 2011-09-01T00:00:00Z
    Publisher Dove Medical Press
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Provisional best practices guidelines for the evaluation of bulbar dysfunction in amyotrophic lateral sclerosis.

    Pattee, Gary L / Plowman, Emily K / Focht Garand, Kendrea L / Costello, John / Brooks, Benjamin Rix / Berry, James D / Smith, Richard A / Atassi, Nazem / Chapin, Jennifer L / Yunusova, Yana / McIlduff, Courtney E / Young, Eufrosina / Macklin, Eric A / Locatelli, Eduardo R / Silani, Vincenzo / Heitzman, Daragh / Wymer, James / Goutman, Stephen A / Gelinas, Deborah F /
    Perry, Bridget / Nalipinski, Paige / Stipancic, Kaila / O'Brien, Meghan / Sullivan, Stacey L / Pioro, Erik P / Gargiulo, Gisella / Green, Jordan R

    Muscle & nerve

    2019  Volume 59, Issue 5, Page(s) 531–536

    Abstract: Introduction: Universally established comprehensive clinical bulbar scales objectively assessing disease progression in amyotrophic lateral sclerosis (ALS) are currently lacking. The goal of this working group project is to design a best practice set of ...

    Abstract Introduction: Universally established comprehensive clinical bulbar scales objectively assessing disease progression in amyotrophic lateral sclerosis (ALS) are currently lacking. The goal of this working group project is to design a best practice set of provisional bulbar ALS guidelines, available for immediate implementation within all ALS clinics.
    Methods: ALS specialists across multiple related disciplines participated in a series of clinical bulbar symposia, intending to identify and summarize the currently accepted best practices for the assessment and management of bulbar dysfunction in ALS Results: Summary group recommendations for individual speech, Augmentative and Alternative Communication (AAC), and swallowing sections were achieved, focusing on the optimal proposed level of care within each domain.
    Discussion: We have identified specific clinical recommendations for each of the 3 domains of bulbar functioning, available for incorporation within all ALS clinics. Future directions will be to establish a formal set of bulbar guidelines through a methodological and evidence-based approach. Muscle Nerve 59:531-531, 2019.
    MeSH term(s) Amyotrophic Lateral Sclerosis/complications ; Amyotrophic Lateral Sclerosis/rehabilitation ; Communication Aids for Disabled ; Deglutition Disorders/diagnosis ; Deglutition Disorders/etiology ; Deglutition Disorders/rehabilitation ; Disease Management ; Humans ; Referral and Consultation ; Speech Disorders/diagnosis ; Speech Disorders/etiology ; Speech Disorders/rehabilitation ; Speech Therapy
    Language English
    Publishing date 2019-01-22
    Publishing country United States
    Document type Journal Article ; Practice Guideline
    ZDB-ID 438353-9
    ISSN 1097-4598 ; 0148-639X
    ISSN (online) 1097-4598
    ISSN 0148-639X
    DOI 10.1002/mus.26408
    Database MEDical Literature Analysis and Retrieval System OnLINE

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