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Effects of a novel method for enteral nutrition infusion involving a viscosity-regulating pectin solution: A multicenter randomized controlled trial.
Tabei, Isao; Tsuchida, Shigeru; Akashi, Tetsuro; Ookubo, Katsuichiro; Hosoda, Satoru; Furukawa, Yoshiyuki; Tanabe, Yoshiaki; Tamura, Yoshiko.
Afiliação
  • Tabei I; Department of Surgery, The Jikei University School of Medicine Daisan Hospital, Komae, Tokyo, Japan. Electronic address: tabei@jikei.ac.jp.
  • Tsuchida S; Tsuchida Hospital, Sapporo, Hokkaido, Japan.
  • Akashi T; Department of Internal Medicine, Saiseikai Fukuoka General Hospital, Fukuoka, Japan.
  • Ookubo K; Department of General Practice, Ushiku Aiwa General Hospital, Ushiku, Ibaraki, Japan.
  • Hosoda S; Department of Rehabilitation, Ota Hospital, Ota, Tokyo, Japan.
  • Furukawa Y; Department of Surgery, Chiba Kashiwa Tanaka Hospital, Kashiwa, Chiba, Japan.
  • Tanabe Y; Department of Surgery, Shin-Yurigaoka General Hospital, Kawasaki, Kanagawa, Japan.
  • Tamura Y; R&D Division, Kewpie Corporation, Chofu, Tokyo, Japan.
Clin Nutr ESPEN ; 23: 34-40, 2018 02.
Article em En | MEDLINE | ID: mdl-29460811
BACKGROUND & AIMS: The initial complications associated with infusion of enteral nutrition (EN) for clinical and nutritional care are vomiting, aspiration pneumonia, and diarrhea. There are many recommendations to prevent these complications. A novel method involving a viscosity-regulating pectin solution has been demonstrated. In Japan, this method along with the other so-called "semi-solid EN" approaches has been widely used in practice. However, there has been no randomized clinical trial to prove the efficiency and safety of a viscosity-regulating pectin solution in EN management. Therefore, we planned and initiated a multicenter randomized controlled trial to determine the efficiency and safety. METHODS: This study included 34 patients from 7 medical institutions who participated. Institutional review board (IRB) approval was obtained from all participating institutions. Patients who required EN management were enrolled and randomly assigned to the viscosity regulation of enteral feeding (VREF) group and control group. The VREF group (n = 15) was managed with the addition of a viscosity-regulating pectin solution. The control group (n = 12) was managed with conventional EN administration, usually in a gradual step-up method. Daily clinical symptoms of pneumonia, fever, vomiting, and diarrhea; defecation frequency; and stool form were observed in the 2 week trial period. The dose of EN and duration of infusion were also examined. RESULTS: A favorable trend for clinical symptoms was noticed in the VREF group. No significant differences were observed in episodes of pneumonia, fever, vomiting, and diarrhea between the 2 groups. An apparent reduction in infusion duration and hardening of stool form were noted in the VREF group. CONCLUSIONS: The novel method involving a viscosity-regulating pectin solution with EN administration can be clinically performed safely and efficiently, similar to the conventional method. Moreover, there were benefits, such as improvement in stool form, a short time for EN infusion, and a reduction in vomiting episodes, with the use of the novel method. This indicates some potential advantages in the quality of life among patients receiving this novel method.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Vômito / Nutrição Enteral / Diarreia / Soluções de Nutrição Parenteral / Febre Tipo de estudo: Clinical_trials / Guideline / Incidence_studies / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Vômito / Nutrição Enteral / Diarreia / Soluções de Nutrição Parenteral / Febre Tipo de estudo: Clinical_trials / Guideline / Incidence_studies / Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2018 Tipo de documento: Article