TY - CHAP M1 - Book, Section TI - Management of Neuromuscular Respiratory Muscle Dysfunction A1 - Bach, John R. A2 - Grippi, Michael A. A2 - Elias, Jack A. A2 - Fishman, Jay A. A2 - Kotloff, Robert M. A2 - Pack, Allan I. A2 - Senior, Robert M. A2 - Siegel, Mark D. Y1 - 2015 N1 - T2 - Fishman's Pulmonary Diseases and Disorders, 5e AB - Patients with ventilatory impairment due to ventilatory muscle dysfunction are often evaluated and managed according to practices developed for patients with chronic lung diseases. However, pulmonary function laboratories, designed primarily for assessment of lung diseases, do not evaluate lung volume recruitment capacities or cough flows that are important in the assessment of patients with inspiratory and expiratory muscle dysfunction. In the setting of ventilatory muscle dysfunction polysomnograms may be misinterpreted as central or obstructive apneas and hypopneas rather than hypoventilation due to inspiratory muscle dysfunction, and continuous positive airway pressure (CPAP) or nocturnal bilevel positive airway pressure (BiPAP) prescribed. In the context of ventilatory muscle dysfunction CPAP does not increase tidal volumes, and may actually reduce them by causing them to approach maximum lung capacity for these patients with severe pulmonary restriction while BiPAP is often used at pressures inadequate to support alveolar ventilation, provide inspiratory muscle rest, or assist in coughing.1 In addition, the patients are often treated with supplemental oxygen to correct hypoxemia when efforts to improve oxygenation should be directed at normalizing alveolar ventilation and clearing airway secretions. With advancing inspiratory and expiratory muscle weakness, the common scenario is that respiratory failure ensues and is treated by mechanical ventilation via endotracheal intubation. When ventilator weaning fails, a tracheostomy is performed and mechanical ventilation is continued indefinitely, often in an institution. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/04/19 UR - accessmedicine.mhmedical.com/content.aspx?aid=1122364284 ER -