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DOI 10.1080/14660820510035388

Медицинская библиотека · Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases · 2005

Comparison of two percutaneous radiological gastrostomy tubes in the nutritional management of ALS patients.

Rio Alan, Ampong Mary Ann, Turner Martin R, Shaw Ashley S, Al-Chalabi Ammar, Shaw Chris E, Leigh P Nigel, Sidhu Paul S

Клиническое исследованиеСравнительное исследованиеСтатьяПеревод в очереди

Аннотация

Patient care and minimizing complications post gastrostomy have to date received little attention in ALS patients. We compare the complications associated with pigtail and mushroom type percutaneous radiological gastrostomy tubes in this patient group. Patients requiring PRG received either Wills-Oglesby or the skin level Entristar. Retrospective review of the clinical notes was performed capturing demographic data, peristomal infection, tube displacement, tube failure, nutritional status, site of disease onset, and survival. Thirty-five patients (Group 1) had the Wills-Oglesby tube of which 14 (40%) tubes required replacement. The Entristar tube was inserted in 29 patients (Group 2) where 8 (28%) required replacement (NS). The incidence of infection was significantly lower with the Entristar tube, (p<0.001). The mean time to tube removal in Group 2 was 223 days (SD 147; range 71-494 days) due to 'buried bumper syndrome'. We conclude that the Entristar skin level gastrostomy tube is associated with a reduction in peristomal infection, tube failure and blockage compared with the Wills-Oglesby tube.

Для цитирования: Rio Alan, Ampong Mary Ann, Turner Martin R, Shaw Ashley S, Al-Chalabi Ammar, Shaw Chris E, Leigh P Nigel, Sidhu Paul S. Comparison of two percutaneous radiological gastrostomy tubes in the nutritional management of ALS patients.. Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases. 2005. DOI: 10.1080/14660820510035388.

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