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

Overview of attention for article published in Nutrición Hospitalaria, December 2014
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Title
Percutaneous endoscopic gastrostomy in a myotrophic lateral sclerosis. Experience in a district general hospital.
Published in
Nutrición Hospitalaria, December 2014
DOI 10.3305/nh.2014.30.6.7808
Pubmed ID
Authors

Inmaculada Prior-Sánchez, Aura Dulcinea Herrera-Martínez, Carmen Tenorio Jiménez, María José Molina Puerta, Alfonso Jesús Calañas Continente, Gregorio Manzano García, María Ángeles Gálvez Moreno

Abstract

Amyotrophic 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.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 4%
Unknown 22 96%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 22%
Student > Bachelor 4 17%
Student > Doctoral Student 3 13%
Professor > Associate Professor 2 9%
Lecturer 1 4%
Other 4 17%
Unknown 4 17%
Readers by discipline Count As %
Nursing and Health Professions 9 39%
Medicine and Dentistry 5 22%
Biochemistry, Genetics and Molecular Biology 1 4%
Arts and Humanities 1 4%
Psychology 1 4%
Other 1 4%
Unknown 5 22%