Protein Requirements for Critically Ill Patients With Renal and Liver Failure

被引:16
作者
Patel, Jayshil J. [1 ]
McClain, Craig J. [2 ,3 ]
Sarav, Menaka [4 ]
Hamilton-Reeves, Jill [5 ]
Hurt, Ryan T. [6 ]
机构
[1] Med Coll Wisconsin, Dept Med, Div Pulm & Crit Care Med, 9200 West Wisconsin Ave,Suite E5200, Milwaukee, WI 53226 USA
[2] Univ Louisville, Dept Med, Dept Pharmacol & Toxicol, Div Gastroenterol Hepatol & Nutr, Louisville, KY 40292 USA
[3] Robley Rex VA Med Ctr, Louisville, KY USA
[4] Univ Chicago, Dept Med, NorthShore Univ Hosp Hlth Syst, Div Nephrol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[5] Univ Kansas, Med Ctr, Dept Dietet & Nutr, Kansas City, KS 66103 USA
[6] Mayo Clin, Dept Med, Rochester, MN USA
关键词
critical care; acute kidney injury; acute liver failure; decompensated liver cirrhosis; protein requirements; catabolism; amino acids; dietary proteins; CHAIN AMINO-ACIDS; INTENSIVE ENTERAL NUTRITION; SEVERE ALCOHOLIC HEPATITIS; ACUTE KIDNEY INJURY; CRITICAL-CARE; PARENTERAL-NUTRITION; NITROGEN-BALANCE; ENERGY; METABOLISM; SUPPORT;
D O I
10.1177/0884533616687501
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Diseases leading to critical illness induce proteolysis resulting in muscle wasting and negative nitrogen balance. Muscle wasting has been associated with poor intensive care unit (ICU)-related outcomes, including an increased risk for mortality. Acute kidney injury (AKI) represents a common organ dysfunction associated with ICU-related disorders, such as sepsis, trauma, and respiratory failure. AKI and renal replacement therapy lead to amino acid loss. Decompensated liver cirrhosis (DLC) and acute liver failure (ALF) represent more severe forms of liver dysfunction leading to ICU admission. DLC and ALF are associated with proteolysis and amino acid loss. AKI, DLC, and ALF uniquely contribute to negative nitrogen balance. The purpose of this review is to outline proteolysis associated with critical illness; define specific protein abnormalities in AKI, DLC, and ALF; define protein requirements in AKI, DLC, and ALF; and discuss barriers associated with optimal protein supplementation in these disorders.
引用
收藏
页码:101S / 111S
页数:11
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