The patients who infected with Carbapenem resistant Klebsiella pneumoniae were high mortality rate. Appropriate antibiotics therapy adjusted by Pharmacokinetic/Pharmacodynamic plays an important role in determining outcomes in Critically ill patients. Consequently, standard antibiotics dose may not be adequate to achieve pharmacokinetic/pharmacodynamic target in Critically ill patients. The purpose of this study is to compare the clinical outcomes between the critically ill patients who received antibiotics dose adjusted by pharmacokinetic/pharmacodynamic using Monte Carlo simulation and historical critically ill patients who received antibiotics from standard practice.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
76
Dose-adjustment by pharmacokinetic and pharmacodynamic using Monte Carlo simulation
Phramongkutklao Hospital
Ratchathewi, Bangkok, Thailand
RECRUITINGMortality
Alive or death
Time frame: 14 day
Mortality
Alive or death
Time frame: 30 days
Microbiological cure rate
Evaluated culture of bloodstream
Time frame: 14 days
Hospital length of stay
Time interval (day) from hospital admission (after enrolled) to hospital discharge or death from any cause
Time frame: With in 30 days
ICU length of stay
Time interval (day) from ICU admission (after enrolled) to ICU discharge or death from any cause
Time frame: With in 30 days
Clinical cure rate
Evaluated sign and symptoms of infection or culture no growth
Time frame: Through treatment completion or with in 30 days
Duration of vasopressor or Inotropic agents
Time interval (day) from time of vasopressor or Inotropic agents initiation to time to vasopressor or Inotropic agents discontinuation
Time frame: With in 30 days
Duration of ventilator
Time interval (day) of ventilator
Time frame: Assessed with in 30 days
Ventilator free day
Day alive and free of ventilator
Time frame: 30 days
Vasopressor or Inotropic drug free day
Day alive and free of vasopressor or inotropic drug
Time frame: 30 days
Procalcitonin
Evaluated serum procalcitonin
Time frame: 14 days
Adverse event
Evaluated side effect (eg. seizure, liver impairment, renal impairment)
Time frame: Day 0, 5, 7 and finish course of Antibiotics or discharge
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