Amyotrophic Lateral Sclerosis

ALS

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Assessment and Diagnosis Assessment and Diagnosis ÎScreening for cognitive and behavioral impairment should be considered (B). Screening tests of executive function may be considered to detect cognitive impairment prior to confirmation with formal neuropsychological evaluation (C). However, there are insufficient data to support or refute treatment to optimize communication, treatment of cognitive or behavioral impairment, or the impact of cognitive or behavioral impairment on management of ALS (U). ÎThere is insufficient evidence to support or refute any specific method of disclosing the diagnosis (U). Text in bold = evidence-based Text in italics = consensus-based Figure 2. Algorithm for Nutrition Management Diagnosis: ALS PEG, percutaneous endoscopic gastrostomy Clinic visits every 3 months Early dysphagia detected Nutritional education including PEGb Symptom progressionc or continued weight loss Clinic visits every 3 months Discuss PEG to stabilize weight and possibly prolong survival FVC >50% Low risk for PEG PEG accepted ▶ Oral intake as tolerated ▶ Enteral nutrition via PEG as needed FVC 30-50% Moderate risk ▶ Anesthesia evaluation ▶ Experienced gastroenterologist FVC <30% High risk PEG declined ▶ Respiratory support during PEG if needed ▶ Oral intake as tolerated ▶ Palliative IV hydration ▶ Palliative NG feeding a Bulbar questions in the Amyotrophic Lateral Sclerosis Functional Rating Scale or other instrument. b Percutaneous endoscopic gastrostomy: rule out contraindications. c Prolonged mealtime, ending meal prematurely because of fatigue, accelerated weight loss due to poor caloric intake, family concern about feeding difficulties. Monitor body weight; Dysphagia assessment instrumenta speech therapist referral Nutritionist or respiratory status Monitor

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