Management of Benzodiazepine Poisoning

Key points in Critical Care Medicine

                       “Adapted from Oxford Textbook of Critical Care”

Management of Benzodiazepine Poisoning

  • Benzodiazepines are the drugs most frequently involved in acute self-poisoning.
  • Benzodiazepine overdose usually has a good prognosis. Most patients do well with careful observation and prevention of complications. Supportive care including oxygen, intubation, respiratory support, and fluid administration may be required in some cases.
  • Care should be taken with elderly patients, or those with chronic obstructive pulmonary disease or liver disease. Fast- acting agents and ingestion of other central nervous system depressants, including alcohol, may present an additional risk.
  • Early administration of activated charcoal in fully conscious patients who are able to protect their airway is only needed if there are co-ingestants.
  • Flumazenil may help confirm the diagnosis, improve alertness, and prevent the need for respiratory support in some patients, especially after accidental poisoning in children. Contraindications include patients on long-term treatment and/or dependent on benzodiazepines, or those who have simultaneously ingested proconvulsant or prodysrhythmic substances, or at risk of increase intracranial pressure.

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Epidemiology and pathophysiology of Traumatic Brain Injury

Key points in Critical Care Medicine

                       “Adapted from Oxford Textbook of Critical Care”

Epidemiology and pathophysiology of Traumatic Brain Injury

  • Traumatic brain injury (TBI) is a devastating injury that causes a huge burden of disease around the world; approximately 1.6 million people suffer a TBI in the USA each year.
  • TBI is a bimodal disease that affects young adults (15-34), the elderly (>75), and males more than females.
  • Mechanism of injury, age, gender, and initial severity of injury are the most significant predictors of mortality.
  • Harm from TBI arises from direct damage to the brain at the time of the initial injury (primary injury), which places the brain at risk of further harm secondary injury.
  • Secondary injury may occur due to intracranial hypertension, hypotension, hypoxia, reduced cerebral perfusion, and inflammation.

Assessment of Traumatic Brain Injury

  • Early assessment is based on a careful history, clinical assessment, and neurological imaging-usually a CT scan of the brain.
  • An immediate CT scan of brain should be obtained in any adult patient at risk of harbouring intracranial pathology.
  • In adult patients who have a Glasgow Coma Scale score below 15 and indications for a brain CT scan, the scan should include the cervical spine by scanning from the base of skull to T4.
  • Establishing a reliable prognosis early after injury is notoriously difficult, but recent predictive models are readily accessible to clinicians via a web-based calculator to aid early clinical decision making and to allow better informed discussions with patient’s families.

Management of Traumatic Brain Injury

  • Admission to a centre offering specialist neurological critical care and management of extracranial injuries improves outcome.
  • Initial management priorities address the ‘ABCs’-airway with cervical spine control, breathing, and circulation. Neurological assessment using the Glasgow Coma Score and pupillary reaction should be repeated regularly to detect deterioration.
  • Intracranial haematomas causing mass effect should be surgically evacuated without delay.
  • Specific TBI management focuses on avoiding secondary cerebral insults by avoiding hypotension and hypoxia, controlling ICP, and maintaining cerebral perfusion pressure.

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Extracorporeal liver support devices in the ICU.

Key points in Critical Care Medicine

Extracorporeal liver support devices in the ICU.

 “Adapted from Oxford Textbook of Critical Care”

  • There is an unmet need for a liver support system because of the increasing shortage of organs for transplantation and the complications associated with the procedure.
  • In theory, acute liver failure and acute decompensation of chronic liver disease secondary to a precipitating event are potentially reversible. In this context, an extracorporeal liver support can temporarily substitute liver functionality to allow natural recovery through regeneration of hepatocytes and elimination of the precipitating event.
  • Goals of liver support system are to provide all functions of the liver, including synthetic and metabolic functions, and to remove as well as reduce the production of pro-inflammatory mediators to attenuate the inflammatory process.
  • Currently existing devices are either purely mechanical and/or cell-based. Detoxification is provided by both systems, but biological activities are limited only to the cell- based systems. Albumin dialysis is the major component of mechanical devices because albumin is irreversibly destroyed in liver failure.
  • Cell-based or bio-artificial systems are essentially ‘mini-livers’, but their success is limited by the lack of a continuous and abundant supply of high-quality hepatocytes.

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Pathophysiology, causes, and management of acute hepatic failure

Key points in Critical Care Medicine

Pathophysiology, causes, and management of acute hepatic failure

“Adapted from Oxford Textbook of Critical Care”

  • Acute liver failure (ALF) is a rare, life-threatening clinical syndrome occurring in a person with no prior history of liver disease.
  • Acute liver failure (ALF) occurs in patients with acute hepatic necrosis resulting in hepatic encephalopathy, jaundice, and coagulopathy.
  • Acute liver failure is a multisystem disorder.
  • Viral hepatitis is the most common cause of ALF worldwide, with drug-induced liver failure the most common in the developed world.
  • ALF is a multi-system disorder resulting in encephalopathy, coagulopathy, systemic inflammatory response syndrome, and multi-organ failure.
  • Patients can be prothrombotic or have balanced coagulation disorders.
  • Several classifications exist incorporating time to encephalopathy from the onset of jaundice. O’Grady’s classification is the most widely used.
  • The management is initially supportive. Intravenous N-acetylcysteine is recommended for all patients.
  • Elective intubation is recommended for all patients who develop Grade III hepatic encephalopathy.
  • Liver transplantation is an appropriate and viable treatment for ALF. Early and safe transfer to a transplant centre for transplant assessment is advised.

Classification      Time of onset jaundice to encephalopathy

Hyper acute            0-1 weeks

Acute                     1-4 weeks

Subacute                4-26 weeks

Causes

  • Paracetamol, ischemia, recreational drugs, toxins (amanita)
  • Hepatitis B,A, and E
  • Non-paracetamol drug-induced liver injury, seronegative
  • Hepatitis.

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