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ppt.pptx

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ppt• protein binding, drug distribution and clearance may be altered.
• Because of the alteration in these variables, wide intraindividual variation of pharmacokinetic parameters occurs depending upon the time since thermal injury and fluid resuscitation.
• Interindividual variations may be correlated with the percentage of the body surface area that is burnt,

ppt• protein binding, drug distribution and clearance may be altered.
• Because of the alteration in these variables, wide intraindividual variation of pharmacokinetic parameters occurs depending upon the time since thermal injury and fluid resuscitation.
• Interindividual variations may be correlated with the percentage of the body surface area that is burnt,

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ppt.pptx

  1. 1. BURNS: The pharmacokinetics and pharmacodynamics of drugs are significantly altered in the burn patient, and the burn patient population shows wide inter- and intraindividual variation in drug handling.
  2. 2. • Burn injury evolves in two phases. • The first phase corresponds to the burn shock, which occurs during the first 48 hours after thermal injury.
  3. 3. In this phase, hypovolaemia, oedema, hypoalbuminaemia and a low glomerular filtration rate are observed, which result in a slower rate of drug distribution and lower renal clearance.
  4. 4. • The second phase (beyond 48 hours after injury) is a hyperdynamic state with high blood flow in the kidneys and liver, an increased α1-acid-glycoprotein level and loss of the drug with exudate leakage. As a result, protein binding, drug distribution and clearance may be altered.
  5. 5. • protein binding, drug distribution and clearance may be altered. • Because of the alteration in these variables, wide intraindividual variation of pharmacokinetic parameters occurs depending upon the time since thermal injury and fluid resuscitation. • Interindividual variations may be correlated with the percentage of the body surface area that is burnt,

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