Risk factors for death in children during inpatient treatment of severe acute malnutrition: a prospective cohort study

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Risk factors for death in children during inpatient treatment of severe acute malnutrition : a prospective cohort study. / Rytter, Maren Johanne Heilskov; Babirekere-Iriso, Esther; Namusoke, Hanifa; Christensen, Vibeke Bak; Michaelsen, Kim F.; Ritz, Christian; Mortensen, Charlotte Gylling; Mupere, Ezekiel; Friis, Henrik.

I: American Journal of Clinical Nutrition, Bind 105, Nr. 2, 2017, s. 494-502.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Rytter, MJH, Babirekere-Iriso, E, Namusoke, H, Christensen, VB, Michaelsen, KF, Ritz, C, Mortensen, CG, Mupere, E & Friis, H 2017, 'Risk factors for death in children during inpatient treatment of severe acute malnutrition: a prospective cohort study', American Journal of Clinical Nutrition, bind 105, nr. 2, s. 494-502. https://doi.org/10.3945/ajcn.116.140822

APA

Rytter, M. J. H., Babirekere-Iriso, E., Namusoke, H., Christensen, V. B., Michaelsen, K. F., Ritz, C., Mortensen, C. G., Mupere, E., & Friis, H. (2017). Risk factors for death in children during inpatient treatment of severe acute malnutrition: a prospective cohort study. American Journal of Clinical Nutrition, 105(2), 494-502. https://doi.org/10.3945/ajcn.116.140822

Vancouver

Rytter MJH, Babirekere-Iriso E, Namusoke H, Christensen VB, Michaelsen KF, Ritz C o.a. Risk factors for death in children during inpatient treatment of severe acute malnutrition: a prospective cohort study. American Journal of Clinical Nutrition. 2017;105(2):494-502. https://doi.org/10.3945/ajcn.116.140822

Author

Rytter, Maren Johanne Heilskov ; Babirekere-Iriso, Esther ; Namusoke, Hanifa ; Christensen, Vibeke Bak ; Michaelsen, Kim F. ; Ritz, Christian ; Mortensen, Charlotte Gylling ; Mupere, Ezekiel ; Friis, Henrik. / Risk factors for death in children during inpatient treatment of severe acute malnutrition : a prospective cohort study. I: American Journal of Clinical Nutrition. 2017 ; Bind 105, Nr. 2. s. 494-502.

Bibtex

@article{aef68ce180914645903910e2483af963,
title = "Risk factors for death in children during inpatient treatment of severe acute malnutrition: a prospective cohort study",
abstract = "BACKGROUND: Children who receive in-hospital treatment of severe acute malnutrition often have high mortality rates, and the reasons are not well understood.OBJECTIVE: We assessed risk factors for death in children who were treated for malnutrition in a hospital.DESIGN: In a prospective observational study of 120 children who were receiving in-hospital treatment of severe acute malnutrition in Uganda with therapeutic formulas F-75 and F-100, we collected data on symptoms, clinical findings, plasma markers of refeeding syndrome (electrolytes and phosphate), and acute phase reactants, and recorded the nutritional therapy given in hospital.RESULTS: Seventeen children (14%) died. Clinical risk factors for death were the presence of oral thrush (HR: 5.0; 95% CI: 1.6, 15.2), a caretaker-reported severity of illness on a visual analog scale (HR: 1.7; 95% CI: 1.1, 2.6), impaired consciousness (HR: 16.7; 95% CI: 3.1, 90.4), and a capillary refill time >2 s (HR: 3.9; 95% CI: 1.4, 11.3). HIV infection was not associated with mortality (HR: 3.0; 95% CI: 0.7, 12.4), which was most likely due to low power. Biochemical risk factors were a plasma C-reactive protein concentration >15 mg/L on admission and low plasma phosphate that was measured on day 2 (HR: 8.7; 95% CI: 2.5, 30.1), particularly in edematous children. The replacement of F-75 with unfortified rice porridge to ameliorate diarrhea was associated with a higher risk of death, particularly if given during the first 2 d (HR: 5.0; 95% CI: 1.9, 13.3), which was an association that remained after adjustment for potential confounders (HR: 69.5; 95% CI: 7.0, 694.6).CONCLUSIONS: Refeeding syndrome may occur in children who are treated for malnutrition, even with moderately low plasma phosphate, and, in particular, in children with edematous malnutrition. The replacement of F-75 with unfortified rice porridge is associated with increased risk of death, which is possibly mediated by lowering plasma phosphate. The identified clinical risk factors may potentially improve the triage of children with malnutrition. This trial was registered at www.isrctn.com as ISRCTN55092738.",
keywords = "Faculty of Science, Edema, Electrolytes, HIV, Hypophosphatemia, Infections, Kwashiorkor, Malnutrition, Marasmus, Mortality, Refeeding syndrome",
author = "Rytter, {Maren Johanne Heilskov} and Esther Babirekere-Iriso and Hanifa Namusoke and Christensen, {Vibeke Bak} and Michaelsen, {Kim F.} and Christian Ritz and Mortensen, {Charlotte Gylling} and Ezekiel Mupere and Henrik Friis",
note = "CURIS 2017 NEXS 021",
year = "2017",
doi = "10.3945/ajcn.116.140822",
language = "English",
volume = "105",
pages = "494--502",
journal = "American Journal of Clinical Nutrition",
issn = "0002-9165",
publisher = "American Society for Nutrition",
number = "2",

}

RIS

TY - JOUR

T1 - Risk factors for death in children during inpatient treatment of severe acute malnutrition

T2 - a prospective cohort study

AU - Rytter, Maren Johanne Heilskov

AU - Babirekere-Iriso, Esther

AU - Namusoke, Hanifa

AU - Christensen, Vibeke Bak

AU - Michaelsen, Kim F.

AU - Ritz, Christian

AU - Mortensen, Charlotte Gylling

AU - Mupere, Ezekiel

AU - Friis, Henrik

N1 - CURIS 2017 NEXS 021

PY - 2017

Y1 - 2017

N2 - BACKGROUND: Children who receive in-hospital treatment of severe acute malnutrition often have high mortality rates, and the reasons are not well understood.OBJECTIVE: We assessed risk factors for death in children who were treated for malnutrition in a hospital.DESIGN: In a prospective observational study of 120 children who were receiving in-hospital treatment of severe acute malnutrition in Uganda with therapeutic formulas F-75 and F-100, we collected data on symptoms, clinical findings, plasma markers of refeeding syndrome (electrolytes and phosphate), and acute phase reactants, and recorded the nutritional therapy given in hospital.RESULTS: Seventeen children (14%) died. Clinical risk factors for death were the presence of oral thrush (HR: 5.0; 95% CI: 1.6, 15.2), a caretaker-reported severity of illness on a visual analog scale (HR: 1.7; 95% CI: 1.1, 2.6), impaired consciousness (HR: 16.7; 95% CI: 3.1, 90.4), and a capillary refill time >2 s (HR: 3.9; 95% CI: 1.4, 11.3). HIV infection was not associated with mortality (HR: 3.0; 95% CI: 0.7, 12.4), which was most likely due to low power. Biochemical risk factors were a plasma C-reactive protein concentration >15 mg/L on admission and low plasma phosphate that was measured on day 2 (HR: 8.7; 95% CI: 2.5, 30.1), particularly in edematous children. The replacement of F-75 with unfortified rice porridge to ameliorate diarrhea was associated with a higher risk of death, particularly if given during the first 2 d (HR: 5.0; 95% CI: 1.9, 13.3), which was an association that remained after adjustment for potential confounders (HR: 69.5; 95% CI: 7.0, 694.6).CONCLUSIONS: Refeeding syndrome may occur in children who are treated for malnutrition, even with moderately low plasma phosphate, and, in particular, in children with edematous malnutrition. The replacement of F-75 with unfortified rice porridge is associated with increased risk of death, which is possibly mediated by lowering plasma phosphate. The identified clinical risk factors may potentially improve the triage of children with malnutrition. This trial was registered at www.isrctn.com as ISRCTN55092738.

AB - BACKGROUND: Children who receive in-hospital treatment of severe acute malnutrition often have high mortality rates, and the reasons are not well understood.OBJECTIVE: We assessed risk factors for death in children who were treated for malnutrition in a hospital.DESIGN: In a prospective observational study of 120 children who were receiving in-hospital treatment of severe acute malnutrition in Uganda with therapeutic formulas F-75 and F-100, we collected data on symptoms, clinical findings, plasma markers of refeeding syndrome (electrolytes and phosphate), and acute phase reactants, and recorded the nutritional therapy given in hospital.RESULTS: Seventeen children (14%) died. Clinical risk factors for death were the presence of oral thrush (HR: 5.0; 95% CI: 1.6, 15.2), a caretaker-reported severity of illness on a visual analog scale (HR: 1.7; 95% CI: 1.1, 2.6), impaired consciousness (HR: 16.7; 95% CI: 3.1, 90.4), and a capillary refill time >2 s (HR: 3.9; 95% CI: 1.4, 11.3). HIV infection was not associated with mortality (HR: 3.0; 95% CI: 0.7, 12.4), which was most likely due to low power. Biochemical risk factors were a plasma C-reactive protein concentration >15 mg/L on admission and low plasma phosphate that was measured on day 2 (HR: 8.7; 95% CI: 2.5, 30.1), particularly in edematous children. The replacement of F-75 with unfortified rice porridge to ameliorate diarrhea was associated with a higher risk of death, particularly if given during the first 2 d (HR: 5.0; 95% CI: 1.9, 13.3), which was an association that remained after adjustment for potential confounders (HR: 69.5; 95% CI: 7.0, 694.6).CONCLUSIONS: Refeeding syndrome may occur in children who are treated for malnutrition, even with moderately low plasma phosphate, and, in particular, in children with edematous malnutrition. The replacement of F-75 with unfortified rice porridge is associated with increased risk of death, which is possibly mediated by lowering plasma phosphate. The identified clinical risk factors may potentially improve the triage of children with malnutrition. This trial was registered at www.isrctn.com as ISRCTN55092738.

KW - Faculty of Science

KW - Edema

KW - Electrolytes

KW - HIV

KW - Hypophosphatemia

KW - Infections

KW - Kwashiorkor

KW - Malnutrition

KW - Marasmus

KW - Mortality

KW - Refeeding syndrome

U2 - 10.3945/ajcn.116.140822

DO - 10.3945/ajcn.116.140822

M3 - Journal article

C2 - 28031190

VL - 105

SP - 494

EP - 502

JO - American Journal of Clinical Nutrition

JF - American Journal of Clinical Nutrition

SN - 0002-9165

IS - 2

ER -

ID: 170801202