Current practice in nutrition after allogeneic hematopoietic stem cell transplantation - Results from a survey among hematopoietic stem cell transplant centers.


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
04 2021
Historique:
received: 04 11 2020
revised: 18 02 2021
accepted: 19 02 2021
pubmed: 22 3 2021
medline: 25 8 2021
entrez: 21 3 2021
Statut: ppublish

Résumé

Allogeneic hematopoietic stem cell transplantation (alloHSCT) is frequently associated with impaired oral intake and malnutrition, which potentially increases morbidity and mortality. Therefore, nutrition is one of the major challenges in the post-transplant period. To document the current clinical approach in nutritional treatment, we designed a questionnaire concerning the current practice in nutrition after alloHSCT and distributed it to German speaking centers performing alloHSCT in Germany, Austria and Switzerland between November 2018 and March 2020. Twenty-eight (39%) of 72 contacted centers completed the survey, 23 from Germany, two from Austria and three from Switzerland, representing 50% of alloHSCT activity within the participating countries in 2018. All centers reported having nutritional guidelines for patients undergoing alloHSCT, whereby 86% (n = 24) provided a low-microbial diet during the neutropenic phase. The criteria to start parenteral nutrition (PN) directly after alloHSCT seemed to be consistent, 75% (n = 21) of the corresponding centers started PN if the oral nutritional intake or the bodyweight dropped below a certain limit. In the setting of intestinal graft-versus-host disease (GvHD) the current practice appeared to be more heterogenous. About 64% (n = 18) of the centers followed a special diet, added food stepwise modulated by GvHD symptoms, while only four centers regularly stopped oral intake completely (intestinal GvHD grade >1). Half of the centers (54%, n = 15) applied a lactose-free diet, followed by 43% (n = 12) which provided fat- and 18% (n = 5) gluten-free food in patients with intestinal GvHD. Supplementation of micronutrients in acute intestinal GvHD patients was performed by 54% (n = 15) of the centers, whereas vitamin D (89%, n = 25) and vitamin B The survey documented a general consensus about the need for nutritional guidelines for patients undergoing alloHSCT. However, the nutritional treatment in clinical practice (i.e. lactose-, gluten- or fat-free in intestinal GvHD) as well as the use of food supplements was very heterogeneous. In line with current general recommendations the centers seemed to focus on safe food handling practice rather than providing a strict neutropenic diet. More high-quality data are required to provide evidence-based nutrition to patients during and after alloHSCT.

Sections du résumé

BACKGROUND
Allogeneic hematopoietic stem cell transplantation (alloHSCT) is frequently associated with impaired oral intake and malnutrition, which potentially increases morbidity and mortality. Therefore, nutrition is one of the major challenges in the post-transplant period.
METHODS
To document the current clinical approach in nutritional treatment, we designed a questionnaire concerning the current practice in nutrition after alloHSCT and distributed it to German speaking centers performing alloHSCT in Germany, Austria and Switzerland between November 2018 and March 2020. Twenty-eight (39%) of 72 contacted centers completed the survey, 23 from Germany, two from Austria and three from Switzerland, representing 50% of alloHSCT activity within the participating countries in 2018.
RESULTS
All centers reported having nutritional guidelines for patients undergoing alloHSCT, whereby 86% (n = 24) provided a low-microbial diet during the neutropenic phase. The criteria to start parenteral nutrition (PN) directly after alloHSCT seemed to be consistent, 75% (n = 21) of the corresponding centers started PN if the oral nutritional intake or the bodyweight dropped below a certain limit. In the setting of intestinal graft-versus-host disease (GvHD) the current practice appeared to be more heterogenous. About 64% (n = 18) of the centers followed a special diet, added food stepwise modulated by GvHD symptoms, while only four centers regularly stopped oral intake completely (intestinal GvHD grade >1). Half of the centers (54%, n = 15) applied a lactose-free diet, followed by 43% (n = 12) which provided fat- and 18% (n = 5) gluten-free food in patients with intestinal GvHD. Supplementation of micronutrients in acute intestinal GvHD patients was performed by 54% (n = 15) of the centers, whereas vitamin D (89%, n = 25) and vitamin B
CONCLUSION
The survey documented a general consensus about the need for nutritional guidelines for patients undergoing alloHSCT. However, the nutritional treatment in clinical practice (i.e. lactose-, gluten- or fat-free in intestinal GvHD) as well as the use of food supplements was very heterogeneous. In line with current general recommendations the centers seemed to focus on safe food handling practice rather than providing a strict neutropenic diet. More high-quality data are required to provide evidence-based nutrition to patients during and after alloHSCT.

Identifiants

pubmed: 33744601
pii: S0261-5614(21)00118-7
doi: 10.1016/j.clnu.2021.02.030
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1571-1577

Informations de copyright

Copyright © 2021 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest R.T. received a research grant from Bayer AG, travel support from Falk-Pharma and serves as consultant for Bayer AG. D.W. received honoraria from Falk-Pharma. R.T., H.G., A.L., J.H., A.B., A.S., J.A., P.J., J.M., I.H., S.K., E.M. W-D., C.S., G.B. and D.W. did not receive payment or services from a third party for any aspect of the submitted work and have nothing further to declare.

Auteurs

R Toenges (R)

Department of Medicine, Hematology/Oncology, Goethe-University, 60590 Frankfurt, Germany. Electronic address: Rosa.Toenges@kgu.de.

H Greinix (H)

Division of Hematology, Medical University of Graz, Austria. Electronic address: Hildegard.Greinix@klinikum-graz.at.

A Lawitschka (A)

St. Anna Children's Hospital, Vienna, Austria. Electronic address: Anita.Lawitschka@stanna.at.

J Halter (J)

Dept. of Hematology, University Hospital Basel, Switzerland. Electronic address: Joerg.Halter@usb.ch.

A Baumgartner (A)

Dept. of Endocrinology, Medical University Klinik Kantonsspital Aarau, Aarau, Switzerland. Electronic address: Annic.Baumgartner@ksa.ch.

A Simon (A)

Pediatric Oncology and Hematology, Saarland University Hospital, Saar, Homburg, Germany. Electronic address: Arne.Simon@uks.eu.

J Arends (J)

Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany. Electronic address: Jann.Arends@uniklinik-freiburg.de.

P Jäger (P)

Department of Hematology, Oncology and Clinical Immunology, University Hospital Duesseldorf, Medical Faculty, Duesseldorf, Germany. Electronic address: PaulSebastian.Jaeger@med.uni-duesseldorf.de.

M Middeke (M)

Dept. of Internal Medicine I, University Hospital Dresden, Dresden, Germany. Electronic address: JanMoritz.Middeke@uniklinikum-dresden.de.

I Hilgendorf (I)

Universitätsklinikum Jena, Klinik für Innere Medizin II, Abteilung für Hämatologie und Internistische Onkologie, Jena, Germany. Electronic address: Inken.Hilgendorf@med.uni-jena.de.

S Klein (S)

III. Medizinische Klinik Hämatologie und Onkologie Universitätsmedizin Mannheim, Mannheim, Germany. Electronic address: Stefan.Klein@umm.de.

E M Wagner-Drouet (EM)

3rd Medical Dept., Hematology, Oncology and Pneumology, University Medical Center Mainz, Germany. Electronic address: Eva.Wagner@unimedizin-mainz.de.

C Schmid (C)

Department of Hematology and Oncology, Universitätsklinikum Augsburg, Augsburg, Germany. Electronic address: christoph.schmid@uk-augsburg.de.

G Bug (G)

Department of Medicine, Hematology/Oncology, Goethe-University, 60590 Frankfurt, Germany. Electronic address: Gesine.Bug@kgu.de.

D Wolff (D)

Dept. of Internal Medicine III, University Hospital, Regensburg, Germany. Electronic address: Daniel.Wolff@klinik.uni-regensburg.de.

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