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      Comment on: clinical impact of systematic nutritional care in adults submitted to allogeneic hematopoietic stem cell transplantation

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          Abstract

          Allogeneic hematopoietic stem cell transplantation (alloHSCT) is an established form of treatment for many patients with severe disorders of the hematopoietic system. Although it is still associated with substantial morbidity and mortality, the results of alloHSCT have improved considerably over the last decades due to a better understanding of stem cell biology, the development of molecular techniques that improve donor and patient compatibility and supportive care measures(1). Transplantation is a complex and expensive procedure that should involve an interdisciplinary team with a wide range of professionals cooperating to improve the results. In this issue, an article entitled "Clinical impact of systematic nutritional care in adults submitted to allogeneic hematopoietic stem cell transplantation" attempts to demonstrate the impact of a systematic clinical protocol of nutrition care on the outcomes of transplanted patients in a single Brazilian institution(2). Although the authors compare the intervention with a historical group, the patients are similar in nutritional and clinical profiles and the results point to benefits in reducing the total parenteral nutrition (TPN) period by up to almost a week. The authors conclude that the implementation of a follow up protocol and nutritional therapy in adult patients submitted to alloHSCT decreased the length of parental nutrition and this may have an impact on hospitalization costs and potentially on the occurrence of medical complications. Patients undergoing alloHSCT are at increased risk for malnutrition during the transplant period. Multiple factors, such as gastrointestinal toxicity related to radiation and chemotherapeutic agents, as well as graft-versus-host disease (GVHD) decrease absorption in addition to increasing metabolic requirements that contribute to the malnourished state. Nutritional requirements are increased due to catabolic stress, which may also be induced by cytoreductive therapy, GVHD, and blood count reconstitution. Nutritional needs in the alloHSCT population increase by as much as 150% of the estimated basal energy expenditure(3). Poor nutritional status before hematopoietic stem cell transplantation (HSCT) has been shown to prolong hospital stay and increase patient morbidity and mortality(4). Moreover, the effects of alloHSCT continue long after transplantation with nearly 50% of patients not returning to their pre-transplant weight one year after the procedure(5). The use of TPN in alloHSCT has shown reductions in hospital stay by as much as 7 days, and poor oral intake after transplant also predisposes the patient to develop severe acute GVHD(6). TPN is utilized as adjunctive therapy during transplant in up to 92% of patients and has demonstrated to improve long-term survival in transplant recipients. Despite published information outlining nutrition support in these patients, there are no clear recommendations on the best time to start TPN nor the best composition of nutritional substrates and supplements(7,8). Also, the protocols for nutrition assessment, other nutrition support modalities such as the prophylactic use of low-microbial diets, vitamins and supplements, cultural and regional habits and the use of enteral nutrition vary in the literature and in clinical practice(9). In this scenario, systematic nutritional care tailored for regional characteristics might prevent or decrease severity of the most common debilitating complications of alloHSCT and optimize resources. Further studies are welcome to define more evidence-based approaches for nutrition care and to link them with immunology and physiology in alloHSCT science.

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          Most cited references18

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          ESPEN Guidelines on Parenteral Nutrition: non-surgical oncology.

          Parenteral nutrition offers the possibility of increasing or ensuring nutrient intake in patients in whom normal food intake is inadequate and enteral nutrition is not feasible, is contraindicated or is not accepted by the patient. These guidelines are intended to provide evidence-based recommendations for the use of parenteral nutrition in cancer patients. They were developed by an interdisciplinary expert group in accordance with accepted standards, are based on the most relevant publications of the last 30 years and share many of the conclusions of the ESPEN guidelines on enteral nutrition in oncology. Under-nutrition and cachexia occur frequently in cancer patients and are indicators of poor prognosis and, per se, responsible for excess morbidity and mortality. Many indications for parenteral nutrition parallel those for enteral nutrition (weight loss or reduction in food intake for more than 7-10 days), but only those who, for whatever reason cannot be fed orally or enterally, are candidates to receive parenteral nutrition. A standard nutritional regimen may be recommended for short-term parenteral nutrition, while in cachectic patients receiving intravenous feeding for several weeks a high fat-to-glucose ratio may be advised because these patients maintain a high capacity to metabolize fats. The limited nutritional response to the parenteral nutrition reflects more the presence of metabolic derangements which are characteristic of the cachexia syndrome (or merely the short duration of the nutritional support) rather than the inadequacy of the nutritional regimen. Perioperative parenteral nutrition is only recommended in malnourished patients if enteral nutrition is not feasible. In non-surgical well-nourished oncologic patients routine parenteral nutrition is not recommended because it has proved to offer no advantage and is associated with increased morbidity. A benefit, however, is reported in patients undergoing hematopoietic stem cell transplantation. Short-term parenteral nutrition is however commonly accepted in patients with acute gastrointestinal complications from chemotherapy and radiotherapy, and long-term (home) parenteral nutrition will sometimes be a life-saving maneuver in patients with sub acute/chronic radiation enteropathy. In incurable cancer patients home parenteral nutrition may be recommended in hypophagic/(sub)obstructed patients (if there is an acceptable performance status) if they are expected to die from starvation/under nutrition prior to tumor spread.
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            Poor nutritional status prior to peripheral blood stem cell transplantation is associated with increased length of hospital stay.

            The nutritional status of patients prior to peripheral blood stem cell transplantation (PBSCT) and its impact on length of hospital stay is not well described in the literature. The nutritional status of 66 consecutive patients (46 m:20 f); and the mean age 58.7+/-12.0 years was determined a maximum of 2 weeks pre-transplantation using the scored Patient-Generated-Subjective Global Assessment (PG-SGA). According to the global assessment, 73% patients were well nourished, 23% moderately malnourished and 4% severely malnourished. There was a significant difference in post transplant length of stay (mean difference+/-s.e.m. -7.0+/-2.1 days) between well-nourished and malnourished patients and a trend towards higher mortality in the malnourished group (2 vs 20%). Although 89% of patients described no problems eating, two or more nutrition impact symptoms were reported in 30% of patients. From stepwise multiple regression analysis, nutritional status as determined by PG-SGA score was significantly associated with length of stay, accounting for 12% of the variance. In conclusion, malnutrition prior to PBSCT is associated with increased length of stay. Routine nutrition assessment of patients prior to PBSCT should be undertaken.
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              Poor oral nutrition after allogeneic stem cell transplantation correlates significantly with severe graft-versus-host disease.

              It has previously been shown that enteral nutrition has several advantages compared to parenteral nutrition (PN) in critically ill patients. The nutritional history was studied in 231 patients after allogeneic stem cell transplantation (SCT). Parenteral nutrition was given for a median of 10 (0-74) days. Patients with graft-versus-host disease (GVHD) grades III-IV received more PN (median 20, range 0-67) than patients with GVHD grades 0-II (10, 0-74, P=0.016). Eighty-five (37%) patients were not able to eat anything for a median of 4 days (1-37). We found a correlation between the number of days with no oral intake (before the diagnosis of acute GVHD) and the incidence of acute GVHD grades III-IV. In patients with 1-4 days of no oral intake, the incidence of grades III-IV acute GVHD was 6%, in those with 5-9 days it was 17%, and in those with >9 days it was 38%. On multivariate analysis, we found that more than 9 days with no oral intake was associated with acute GVHD grades III-IV (odds ratio 7.66, confidence interval 1.44-40.7, P=0.016). Poor oral intake early after SCT may be associated with an increased risk of developing severe acute GVHD.
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                Author and article information

                Journal
                Rev Bras Hematol Hemoter
                Rev Bras Hematol Hemoter
                Rev Bras Hematol Hemoter
                Revista Brasileira de Hematologia e Hemoterapia
                Associação Brasileira de Hematologia e Hemoterapia
                1516-8484
                1806-0870
                2012
                : 34
                : 5
                : 325-326
                Affiliations
                []Universidade Federal do Rio Grande do Sul - UFRGS, Porto Alegre, RS, Brazil
                Author notes
                Corresponding author: Liane Esteves Daudt Serviço de Hematologia Clínica e TMO Hospital de Clínicas de Porto Alegre Ramiro Barcelos 2350 9º Sul 90.035-903 Porto Alegre, RS, Brazil ldaudt@ 123456hcpa.ufrgs.br
                Article
                10.5581/1516-8484.20120083
                3486817
                23125535
                1c09f85a-f77f-4d4f-b33c-da1a6456136b

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 August 2012
                : 29 August 2012
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                Scientific Comments

                Hematology
                Hematology

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