TY - CHAP M1 - Book, Section TI - Chapter 66. Neuromuscular Diseases Leading to Respiratory Failure A1 - Marinelli, William A. A1 - Leatherman, James W. A2 - Hall, Jesse B. A2 - Schmidt, Gregory A. A2 - Wood, Lawrence D.H. Y1 - 2005 N1 - T2 - Principles of Critical Care, 3e AB - Neuromuscular disorders (NMDs) in critical care may be divided into those that precipitate admission to the ICU and those that arise during ICU management; the latter are much more common and significantly influence the pace and extent of recovery from critical illness.The maximal inspiratory pressure (MIP), maximal expiratory pressure (MEP), vital capacity (VC), and qualitative judgment of oropharyngeal function are the most important parameters to follow in patients with NMDs.An effective cough is unlikely with a MEP <40 cm H2O or a VC <30 mL/kg.Sleep-related deterioration in hypoventilation and hypoxemia is common in patients with respiratory muscle impairment.Many patients with Guillain-Barré syndrome or myasthenia gravis of sufficient severity to precipitate ICU admission will benefit from treatment with plasmapheresis or intravenous immunoglobulin.Muscle biopsy is useful in the diagnosis of polymyositis, mitochondrial disease, and other myopathies, and should be considered when electrophysiologic and other testing does not offer a clear diagnosis of peripheral neuropathy or myoneural junction diseases.Critical illness myopathy and neuropathy should be considered in all patients with protracted critical illness, particularly when multisystem organ failure has been present; avoidance of paralytics, appropriate correction of the metabolic milieu, early physical therapy, and measures to shorten duration of mechanical ventilation may help ameliorate the impact of these acquired NMDs. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2023/10/04 UR - accessmedicine.mhmedical.com/content.aspx?aid=2293033 ER -