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Nutritional status in cirrhotic patients.
Maedica (Bucur). 2012 Dec; 7(4):284-9.M

Abstract

BACKGROUND

Malnutrition is prevalent in all forms of liver disease: from 20% in compensated liver disease to more than 80% in those patients with decompensated liver disease. Protein-calorie malnutrition (PCM) can be identified in all clinical stages but is easier observed in advanced stages of liver disease. The presence of malnutrition is associated with increased number of complications and increased short and long term mortality.

AIM

to evaluate the nutritional status using of combination of BMI (Body Mass Index), TST (triceps skinfold thickness) and MAMC (mid-arm muscle circumference). Subjective Global Assessment (SGA) of nutritional status was determined for every patient. The features of subjective global assessment are history, physical evaluation and SGA rating. Based on this evaluation, patients were classified into three groups: well, moderately malnourished and severely malnourished.

MATERIAL AND METHODS

Our study was designed as a descriptive prospective analysis of patients with cirrhosis, admitted in Elias Emergency Hospital, Gastroenterology Department, during a year, January 2010-January 2011. The diagnosis of cirrhosis was based on the medical history, physical exa-mination, biochemical findings and imagistic methods (ultrasound and / or computed tomography). A series of 176 hospitalized patients with cirrhosis, 114 (65%) male and 62 (35%) female, median age 52 (range 18-68 years). Etiology of liver disease was alcoholic in 98 (56%), hepatitis B virus in 14 (8%), HCV in 43 (24%), HBV and HDV in 10 (7%), 11 patients have other etiology. The evaluation of nutritional status was made by different methods. A detailed history was recorded with appetite, caloric intake, change in body weight. Subjective Global Assessment (SGA) of nutritional status was determined for every patient.

CONCLUSIONS

Malnutrition was correlated with clinical severity of liver disease. The mild-moderate malnourished patients are 88% Child B, over 58% with viral etiology. 22% from these patients are alcoholic and 11% have Child C score (p<0.01). In severely malnourished group, 43% have alcoholic disease and 31% are Child C classification(p<0.01). Triceps skinfold thickness (mm) and mid-arm circumference(cm) decrease significantly according to the Child score, a positive correlation was found between these two parameters and the severity of cirrhosis.

Authors+Show Affiliations

Clinic of Gastroenterology, Hepatology and Digestive Endoscopy, Elias Emergency University Hospital, Bucharest, Romania.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23483873

Citation

Teiusanu, Adriana, et al. "Nutritional Status in Cirrhotic Patients." Maedica, vol. 7, no. 4, 2012, pp. 284-9.
Teiusanu A, Andrei M, Arbanas T, et al. Nutritional status in cirrhotic patients. Maedica (Bucur). 2012;7(4):284-9.
Teiusanu, A., Andrei, M., Arbanas, T., Nicolaie, T., & Diculescu, M. (2012). Nutritional status in cirrhotic patients. Maedica, 7(4), 284-9.
Teiusanu A, et al. Nutritional Status in Cirrhotic Patients. Maedica (Bucur). 2012;7(4):284-9. PubMed PMID: 23483873.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Nutritional status in cirrhotic patients. AU - Teiusanu,Adriana, AU - Andrei,Mihai, AU - Arbanas,Tudor, AU - Nicolaie,Tudor, AU - Diculescu,Mircea, PY - 2012/07/23/received PY - 2012/10/15/accepted PY - 2013/3/14/entrez PY - 2013/3/14/pubmed PY - 2013/3/14/medline SP - 284 EP - 9 JF - Maedica JO - Maedica (Bucur) VL - 7 IS - 4 N2 - UNLABELLED: BACKGROUND: Malnutrition is prevalent in all forms of liver disease: from 20% in compensated liver disease to more than 80% in those patients with decompensated liver disease. Protein-calorie malnutrition (PCM) can be identified in all clinical stages but is easier observed in advanced stages of liver disease. The presence of malnutrition is associated with increased number of complications and increased short and long term mortality. AIM: to evaluate the nutritional status using of combination of BMI (Body Mass Index), TST (triceps skinfold thickness) and MAMC (mid-arm muscle circumference). Subjective Global Assessment (SGA) of nutritional status was determined for every patient. The features of subjective global assessment are history, physical evaluation and SGA rating. Based on this evaluation, patients were classified into three groups: well, moderately malnourished and severely malnourished. MATERIAL AND METHODS: Our study was designed as a descriptive prospective analysis of patients with cirrhosis, admitted in Elias Emergency Hospital, Gastroenterology Department, during a year, January 2010-January 2011. The diagnosis of cirrhosis was based on the medical history, physical exa-mination, biochemical findings and imagistic methods (ultrasound and / or computed tomography). A series of 176 hospitalized patients with cirrhosis, 114 (65%) male and 62 (35%) female, median age 52 (range 18-68 years). Etiology of liver disease was alcoholic in 98 (56%), hepatitis B virus in 14 (8%), HCV in 43 (24%), HBV and HDV in 10 (7%), 11 patients have other etiology. The evaluation of nutritional status was made by different methods. A detailed history was recorded with appetite, caloric intake, change in body weight. Subjective Global Assessment (SGA) of nutritional status was determined for every patient. CONCLUSIONS: Malnutrition was correlated with clinical severity of liver disease. The mild-moderate malnourished patients are 88% Child B, over 58% with viral etiology. 22% from these patients are alcoholic and 11% have Child C score (p<0.01). In severely malnourished group, 43% have alcoholic disease and 31% are Child C classification(p<0.01). Triceps skinfold thickness (mm) and mid-arm circumference(cm) decrease significantly according to the Child score, a positive correlation was found between these two parameters and the severity of cirrhosis. SN - 1841-9038 UR - https://www.unboundmedicine.com/medline/citation/23483873/full_citation L2 - https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23483873/ DB - PRIME DP - Unbound Medicine ER -