Amyotrophic lateral sclerosis: update on clinical management

被引:54
作者
Norris, Simone P. [1 ]
Likanje, Marie-France N. [1 ]
Andrews, Jinsy A. [1 ]
机构
[1] Columbia Univ, Irving Med Ctr, Neurol Inst, Dept Neurol,Eleanor & Lou Gehrig ALS Ctr, 710 W 168th St,NI-3, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
amyotrophic lateral sclerosis; clinical management; genetics; staging; treatment; STAGING SYSTEM; ALS; DEGENERATION; MUTATIONS; DIAGNOSIS; CRITERIA; REPEAT;
D O I
10.1097/WCO.0000000000000864
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of review The current review will provide recent updates in the clinical management of amyotrophic lateral sclerosis (ALS). Recent findings Although there is no cure for ALS, there are new treatments, growing knowledge of genetics, development of clinical staging systems, and the recent coronavirus disease 2019 pandemic that have recently impacted the clinical management of ALS. Increased understanding of genetics has helped provide insights into pathophysiology, the staging systems and clinical measures help to provide tools for monitoring disease clinically, and the recent coronavirus disease 2019 pandemic has provided opportunities to develop telemedicine and remote monitoring of disease thereby increasing accessibility to care and reducing burden of travel to centers for people living with the disease and their caregivers. ALS is a progressive neurodegenerative disease that causes degeneration of the motor neurons which leads to paralysis and respiratory failure. Despite the lack of a cure, multidisciplinary care, proactive respiratory management, nutritional care and management of symptoms as well as pharmacological interventions that can improve quality of life and survival.
引用
收藏
页码:641 / 648
页数:8
相关论文
共 52 条
  • [1] Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial
    Abe, Koji
    Aoki, Masashi
    Tsuji, Shoji
    Itoyama, Yasuto
    Sobue, Gen
    Togo, Masanori
    Hamada, Chikuma
    Tanaka, Masahiko
    Akimoto, Makoto
    Nakamura, Kazue
    Takahashi, Fumihiro
    Kondo, Kazuoki
    Yoshino, Hiide
    [J]. LANCET NEUROLOGY, 2017, 16 (07) : 505 - 512
  • [2] Amyotrophic lateral sclerosis: Clinical management and research update
    Andrews, Jinsy
    [J]. CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2009, 9 (01) : 59 - 68
  • [3] Real-world evidence of riluzole effectiveness in treating amyotrophic lateral sclerosis
    Andrews, Jinsy A.
    Jackson, Carlayne E.
    Heiman-Patterson, Terry D.
    Bettica, Paolo
    Brooks, Benjamin Rix
    Pioro, Erik P.
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2020, 21 (7-8) : 509 - 518
  • [4] Amyotrophic lateral sclerosis care and research in the United States during the COVID-19 pandemic: Challenges and opportunities
    Andrews, Jinsy A.
    Berry, James D.
    Baloh, Robert H.
    Carberry, Nathan
    Cudkowicz, Merit E.
    Dedi, Brixhilda
    Glass, Jonathan
    Maragakis, Nicholas J.
    Miller, Timothy M.
    Paganoni, Sabrina
    Rothstein, Jeffrey D.
    Shefner, Jeremy M.
    Simmons, Zachary
    Weiss, Michael D.
    Bedlack, Richard S.
    [J]. MUSCLE & NERVE, 2020, 62 (02) : 182 - 186
  • [5] Association Between Decline in Slow Vital Capacity and Respiratory Insufficiency, Use of Assisted Ventilation, Tracheostomy, or Death in Patients With Amyotrophic Lateral Sclerosis
    Andrews, Jinsy A.
    Meng, Lisa
    Kulke, Sarah F.
    Rudnicki, Stacy A.
    Wolff, Andrew A.
    Bozik, Michael E.
    Malik, Fady I.
    Shefner, Jeremy M.
    [J]. JAMA NEUROLOGY, 2018, 75 (01) : 58 - 64
  • [6] PROGRESSIVE HEMIPARESIS (MILLS SYNDROME) WITH APHASIA IN AMYOTROPHIC LATERAL SCLEROSIS
    Baeumer, Dirk
    Butterworth, Richard
    Menke, Ricarda A. L.
    Talbot, Kevin
    Hofer, Monika
    Turner, Martin R.
    [J]. NEUROLOGY, 2014, 82 (05) : 457 - 458
  • [7] Nutritional prognostic factors for survival in amyotrophic lateral sclerosis patients undergone percutaneous endoscopic gastrostomy placement
    Barone, Michele
    Viggiani, Maria Teresa
    Introna, Alessandro
    D'Errico, Eustachio
    Scarafino, Antonio
    Iannone, Andrea
    Di Leo, Alfredo
    Simone, Isabella Laura
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2019, 20 (7-8) : 490 - 496
  • [8] Responding to requests for physician-assisted suicide - "These are uncharted waters for both of us. ... "
    Bascom, PB
    Tolle, SW
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (01): : 91 - 98
  • [9] A CONTROLLED TRIAL OF RILUZOLE IN AMYOTROPHIC-LATERAL-SCLEROSIS
    BENSIMON, G
    LACOMBLEZ, L
    MEININGER, V
    BOUCHE, P
    DELWAIDE, C
    COURATIER, P
    BLIN, O
    VIADER, F
    PEYROSTPAUL, H
    DAVID, J
    MALOTEAUX, JM
    HUGON, J
    LATERRE, EC
    RASCOL, A
    CLANET, M
    VALLAT, JM
    DUMAS, A
    SERRATRICE, G
    LECHEVALLIER, B
    PEUCH, AJ
    NGUYEN, T
    SHU, C
    BASTIEN, P
    PAPILLON, C
    DURRLEMAN, S
    LOUVEL, E
    GUILLET, P
    LEDOUX, L
    ORVOENFRIJA, E
    DIB, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (09) : 585 - 591
  • [10] Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS
    Bosco, Daryl A.
    Morfini, Gerardo
    Karabacak, N. Murat
    Song, Yuyu
    Gros-Louis, Francois
    Pasinelli, Piera
    Goolsby, Holly
    Fontaine, Benjamin A.
    Lemay, Nathan
    McKenna-Yasek, Diane
    Frosch, Matthew P.
    Agar, Jeffrey N.
    Julien, Jean-Pierre
    Brady, Scott T.
    Brown, Robert H., Jr.
    [J]. NATURE NEUROSCIENCE, 2010, 13 (11) : 1396 - U133