Page 540 - ACCCN's Critical Care Nursing
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Gastrointestinal, Liver and Nutritional Alterations 517

             which is secreted by the hepatocytes. Bile drains from the   areas  of  surviving  cells  to  restore  the  lost  tissue  whilst
             hepatocytes into bile ducts and then into the common   maintaining  homeostasis  during  hepatic  regenera-
             hepatic duct, before passing into the gall bladder via the   tion. 234,239,240   However,  with  chronic  injury,  fibrosis  or
             common bile duct.                                    scarring  occurs,  resulting  in  the  loss  of  the  functional
                                                                  architecture  and  cell  mass  and  ultimately  in  cirrhosis.
             The arrangement of the circulation to the liver with its
             rich vascular architecture enables it to perform the vital   Cirrhosis results in destruction of the normal liver vascu-
             functions of carbohydrate, fat and protein metabolism;   lature, increased resistance to blood flow, and back pres-
             production  of  bile  to  aid  in  digestion;  the  production,   sure into the portal circulation. Dilation of the venous
             conjugation and elimination of bilirubin; immunologi-  system leading into the liver results in the formation of
                                                                        241
             cal  and  inflammatory  responses;  glycogen  storage;  and   varices.
             detoxification of toxins and drugs. 1                Liver cell injury may occur to such a degree that a critical
                                                                  amount of hepatic necrosis results in the failure of the
             As  the  kidneys  are  responsible  for  clearance  of  water-  liver to maintain metabolic, synthetic and clearance func-
             soluble  toxins  from  the  body,  the  liver  clears  protein   tions leading to death. Liver cell injury may also occur
             (largely albumin)-bound toxins and excretes them into   more slowly, giving rise to chronic liver injury. 236
             the gastrointestinal tract for elimination, or reabsorption
             in water-soluble form for subsequent renal excretion.  EPIDEMIOLOGY OF VIRAL HEPATITIS

             MECHANISMS OF LIVER CELL INJURY                      In  developed  countries  such  as  Australia  and  New
                                                                  Zealand, viral infection, primarily from hepatitis B and
             Liver  cell  injury  and  death  can  occur  either  as  a  direct   hepatitis C viruses, is the major cause of liver cell injury
             result of injury to the cell, resulting in cell necrosis, or as   leading to liver failure. 242,243  Although viral hepatitis can
             a result of ‘cellular stress’ and the triggering of apoptotic   result in acute liver failure, it more often results in chronic
             pathways,  leading  to  ‘programmed  cell  death’. 233   Major   disease  that  may  lead  to  cirrhosis  and  hepatocellular
             factors  for  the  triggering  of  the  apoptotic  pathway  are   carcinoma. 243  While the prevalence of hepatitis B in Aus-
             hypoxia with resulting ischaemia and reperfusion; reac-  tralia and New Zealand is generally low, infection rates
             tive  oxygen  metabolites  resulting  from  alcohol  or  drug   among social subgroups, such as the socially disadvan-
             ingestion; accumulation of bile acids resulting from cho-  taged,  migrants  from  Asian  countries,  injecting  drug
             lestasis;  and  inflammatory  cytokines  such  as  tumour   users,  homosexual  males,  and  those  with  a  history  of
             necrosis factor alpha (TNF-α). 233  The apoptotic pathway   incarceration, are high. 244,245  Hepatitis C is blood-borne,
             results in the deconstruction of the cellular structure from   with  intravenous  drug  use  the  cause  of  about  80%  of
             the inside out, while necrosis results in cell rupture and   hepatitis C infections. Blood screening has greatly reduced
             release of cellular contents. Although these processes may   the incidence of hepatitis C infections. 246  In Australia in
             overlap, it is thought that the apoptotic pathway is a way   2009,  approximately  217,000  people  were  living  with
             of preventing the inflammatory response that is triggered   chronic hepatitis C infection, with 46,000 in the moder-
             with  cell  necrosis.  The  activation  of  the  inflammatory   ate  to  severe  liver  disease  category. 247   However,  about
             response results in secondary liver cell injury and contrib-  25% of people with exposure to hepatitis C virus have
             utes  to  the  multiple  organ  dysfunction  seen  in  liver   cleared  the  virus  and  are  not  chronically  infected.  It  is
             failure. 233,234                                     estimated that the number of people with hepatitis C will
             The degree and time course of liver cell damage from viral   increase  in  Australia  and  New  Zealand  due  to  lack  of
                                                                                           247-249
             hepatitis depends on the immune response. Immune rec-  access  to  antiviral  therapy.    Vertical  transmission
             ognition and destruction of infected cells may result in   (transmission from the mother to the child during the
             either  clearance  of  the  virus  or  ongoing  inflammation,   perinatal period) at birth is a major cause of such infec-
                                                                                 243
             cell  death  and  fibrosis  if  the  virus  is  not  cleared.  This   tions in children.
             process may progress over 20–40 years to cirrhosis and
             hepatocellular  carcinoma. 235   Chronic  excessive  alcohol   Practice tip
             intake may also result in a slower chronic course of liver
             injury that eventually results in cirrhosis, liver failure or   Use appropriate infection control practices and personal pro-
             hepatocellular carcinoma. 236                          tective equipment for patients at high risk of hepatitis B virus
                                                                    (HBV) and hepatitis C (HCV) infections.
             Liver cells may also be injured by the toxic effects of drugs
             or their metabolites, as in paracetamol overdose, or by
             drugs  at  therapeutic  doses  (e.g.  non-steroidal  anti-  LIVER DYSFUNCTION/FAILURE
             inflammatory  drugs,  phenytoin,  antimalarial  agents).   Liver dysfunction can be acute or chronic. Chronic liver
             Other poisoning from the ingestion of mushrooms (e.g.   disease  is  usually  associated  with  cirrhosis  and  can
             Amanita phalloides), and from recreational drug use (e.g.   develop from viral (hepatitis B and C), drug (alcohol),
             ecstasy and amphetamines), may result in liver cell death   metabolic  (Wilson’s  disease),  or  autoimmune  (primary
             and liver failure. 237  Diseases of the biliary system such as   biliary cirrhosis) conditions. Acute liver failure (ALF) is
             primary biliary cirrhosis and primary sclerosing cholan-  an uncommon condition associated with rapid liver dys-
             gitis also result in liver dysfunction and failure. 238
                                                                  function leading to jaundice, hepatic encephalopathy and
                                                                              250
             The  liver  has  a  remarkable  regenerative  capacity.  After   coagulopathy.   The  term  ‘fulminant  hepatic  failure’  is
             injury and necrosis, liver cells rapidly regenerate around   often used synonymously; however, it has been proposed
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