• Nutr Hosp · Dec 2014

    [Percutaneous endoscopic gastrostomy in a myotrophic lateral sclerosis. Experience in a district general hospital].

    • Inmaculada Prior-Sánchez, Aura Dulcinea Herrera-Martínez, Carmen Tenorio Jiménez, María José Molina Puerta, Alfonso Jesús Calañas Continente, Gregorio Manzano García, and María Ángeles Gálvez Moreno.
    • UGC Endocrinología y Nutrición. Hospital Universitario Reina Sofía, Córdoba. España.. inmapri@hotmail.com.
    • Nutr Hosp. 2014 Dec 1; 30 (6): 1289-94.

    BackgroundAmyotrophic Lateral Sclerosis (ALS) is a degenerative disorder that affects the pyramidal tract, producing progressive motor dysfunctions leading to paralysis. These patients can present with dysphagia, requiring nutritional support with a nasogastric tube or Percutaneous Endoscopic Gastrostomy (PEG). PEG is associated with increased survival rates. However, the timing of PEG placement remains a significant issue for clinicians.ObjectiveTo analyse the characteristics of ALS patients at the moment of PEG placement and their progression.Methods And MaterialsDescriptive retrospective study including patients diagnosed with ALS and PEG who were assessed during the 2005-2014 period in our hospital. Nutritional parameters and respiratory function were assessed for all patients, as well as their progression. The data was analysed using SPSS15.Results37 patients were included (56.8% men, 43.2% women) with an average age of 60 at diagnosis, and an average age of 63.1 at PEG placement. 48.6% started with spinal affection and 51.4%, with bulbar affection. 43.2% of the patients received oral nutritional supplements prior to PEG placement for a mean period of 11.3 months. The mean forced vital capacity at diagnosis was 65.45±13.67%, with a negative progression up to 39.47±14.69% at the moment of PEG placement. 86.5% of patients required non-invasive positive-pressure ventilation. 86.5% presented with dysphagia, 64.9% with weight loss > 5-10% from their usual weight, 8.1% with low Body Mass Index, 27% with malnutrition and 73% with aworsened breathing function; therefore, 100% met the criteria for PEG placement according to our protocol. The period on enteral feeding was extended for 10.1 months with a mortality of 50% during the first 6 months from PEG placement.ConclusionsThere is evidence of a 3-year delay between diagnosis and PEG placement, with a survival rate of 50% at 6 months from PEG insertion. Further studies are required to establish whether an earlier placement might increase survival rates.Copyright AULA MEDICA EDICIONES 2014. Published by AULA MEDICA. All rights reserved.

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