4.1 Review

Percutaneous gastrostomy in amyotrophic lateral sclerosis: a review

Journal

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/21678421.2021.1946089

Keywords

Amyotrophic lateral sclerosis; complications; percutaneous gastrostomy; progression; nutrition; prognostic; survival; therapy

Funding

  1. Fundacao para a Ciencia e a Tecnologia [PTDC/MECNEU/31195/2017]

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This systematic review investigates the role of enteral feeding techniques in ALS patients, concluding that PEG is safe and may prolong survival in non-malnourished patients. Factors such as older age, weight loss, and respiratory dysfunction negatively impact outcomes after PEG insertion. Further research is needed to determine the impact on quality of life and optimal timing of PEG insertion.
Amyotrophic lateral sclerosis (ALS) causes dysphagia and consequent poor nutrition. Sometimes enteral feeding is offered. Percutaneous endoscopic gastrostomy (PEG) is currently the technique of choice for enteral nutrition of these patients. This systematic review addresses the role of PEG and other enteral feeding techniques in maintaining ALS patients' survival and quality of life and in identifying prognostic factors for survival, in order to optimize their usefulness. We also evaluated the mortality of enteral feeding in the first 30 days after each procedure and its complications. Studies were retrieved from Pubmed, Google Scholar, and Cochrane databases, using the relevant keywords, and by hand search. The inclusion criteria were prospective and retrospective designs of studies of people with clinically diagnosed ALS in whom gastrostomy or nasogastric enteral feeding were used in management, published in English. Studies with sample sizes <40, or which focused on a specific gastrostomy technique utilizing less than 30 subjects were excluded in order to avoid small sample bias. We conclude that PEG is safe and probably prolongs survival in non-malnourished ALS patients. However, older age at onset, marked loss of weight or reduced body mass index from symptomatic onset, and marked respiratory dysfunction negatively influence the outcome after PEG insertion. The currently available evidence does not meaningfully address the impact of PEG on quality of life in ALS. The literature about other enteral feeding techniques is insufficient for reliable conclusions. The optimum time for PEG insertion and preferences for specific gastrostomy techniques also require more investigation.

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