scholarly journals Hypersensitivity reactions to high osmolality Total Parenteral Nutrition: a case report

Author(s):  
Steph A. Pang ◽  
Shaun Eintracht ◽  
Jesse M. Schwartz ◽  
Belinda Lobo ◽  
Elizabeth MacNamara
2019 ◽  
Vol 12 (8) ◽  
pp. e230160
Author(s):  
Jyotsna M Kirtane ◽  
Snehal A Bhange ◽  
Fazal Nabi ◽  
Varshil Shah

This is a case report of a neonate who was antenatally diagnosed with jejunal atresia which turned out to be duodenal atresia with apple peel syndrome. A previous sibling, who also had apple peel but with jejunal atresia, succumbed to sepsis after surgery. The first sibling had jejunal stenosis and had died of sepsis following surgery. Combination of duodenal atresia with apple peel is extremely rare. This coupled with a familial condition is rarer still. This case was challenging due to the short length of the gut and prolonged need for total parenteral nutrition and sepsis in postoperative period.


2019 ◽  
Vol 12 (02) ◽  
pp. 061-065
Author(s):  
Rodrigo Fernandes Weyll Pimentel ◽  
Pedro Carlos Muniz Figueiredo

Abstract Introduction Achondroplasia is the most common form of dwarfism in humans. At the end of the twentieth century, achondroplasia had its natural history investigated and its morbimortality understood. In dwarves, obesity is one of the causes of morbidity, and it is difficult to evaluate it due to the great disproportion among anthropometric data. The characterization of the nutritional needs of these patients represents an interesting dilemma for physicians. In view of these difficulties, the present case report describes an alternative to obtain the ideal weight value of an elderly dwarf in the use of parenteral nutritional therapy. Case Report A 73-year-old male patient, carrier of achondroplastic dwarfism, was admitted for surgical treatment of colon adenocarcinoma. He was submitted to total colectomy with ileum-rectum anastomosis, evolving with abdominal septic shock by suture dehiscence, which was fixed, and a protective ileostomy was installed. Due to the maintenance of prolonged fasting, without the possibility of starting oral or enteral feeding, the patient used total parenteral nutrition. To estimate the total energy expenditure, we chose to ask the patient what his ideal weight was. The patient used total parenteral nutrition for eight days until he was able to meet his caloric needs orally. Conclusion In the absence of indirect calorimetry, the ideal weight mentioned by the patient seems to be a good option for the estimation of the caloric expenditure by simplified equations.


1982 ◽  
Vol 6 (6) ◽  
pp. 534-538 ◽  
Author(s):  
Jacques Di Costanzo ◽  
Jacques Martin ◽  
Noel Cano ◽  
Jean-Claude Mas ◽  
Michel Noirclerc

2015 ◽  
Vol 10 (2) ◽  
pp. 65-68
Author(s):  
Soydan İNCE ◽  
Sefer GÜNAYDIN ◽  
Belgin PETEK BALCI ◽  
Birgül BAŞTAN ◽  
Nihat ÇEVİK ◽  
...  

2011 ◽  
Vol 23 (10) ◽  
pp. 961-963 ◽  
Author(s):  
Abdullah Emre Yildirim ◽  
Reskan Altun ◽  
Sevinç Can ◽  
Serkan Öcal ◽  
Enver Akbaş ◽  
...  

2021 ◽  
Vol 6 (2) ◽  

Purpose, Setting and Subjects: We conducted a case report study of a postoperative pediatric patient on total parenteral nutrition managed by a multidisciplinary team in a tertiary care hospital. In October 2020, data of nutritional status, hypophosphatemia, electrolyte and metabolic imbalance, and the role of thiamine supplement were reviewed. Background: Refeeding Syndrome is usually defined as the possibly lethal maldistribution of fluids and electrolytes that could take place in malnourished patients receiving enteral or parenteral refeeding. This is due to hormonal and metabolic disturbances that may lead to critical clinical deterioration. The biochemical key feature of Refeeding Syndrome is hypophosphatemia. In general, the syndrome is complicated and may also incorporate abnormal electrolytes and fluid balance; changes in serum level of protein, glucose, and the metabolism of fat; thiamine deficiency; hypokalemia; and hypomagnesaemia. Case Report: an ex-preterm 6-year-old boy who underwent major intestinal resection due to necrotizing enterocolitis (NEC) during his stormy neonatal period, presented to ED with constipation for 2 days; the patient was admitted in the pediatric ward under combined care with Pediatric Surgery, as a case of large bowel obstruction for conservative management. He had cachexic appearance, global developmental delay (GDD), and faltering growth. Subsequently and during his PICU stay, he suffered a fluctuating course of electrolytes imbalance a few days after commencing total parenteral nutrition (TPN), and developed altered mental status that responded well to thiamine infusions to resume his baseline sensorium within 48 hours. Conclusions: The role of thiamine in Refeeding Syndrome is extremely underestimated, despite the current evidence of its high efficacy. However, the fussy exclusion mechanism to reach the diagnosis is probably the reason behind the delaying of treatment in most of the cases. A wide range of patients are at risk of developing Refeeding Syndrome, especially malnourished children, as in this case report. Categories: Nutrition, Surgery, Pediatrics, Gastroenterology.


2014 ◽  
Vol 33 ◽  
pp. S237
Author(s):  
J. Behaegel ◽  
E. De Waele ◽  
S. Mattens ◽  
K. Noerens ◽  
P.M. Honoré ◽  
...  

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