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Assessing circadian rhythms during prolonged midazolam infusion in the pediatric intensive care unit (PICU) children
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نویسنده
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bienert a. ,bartkowska-śniatkowska a. ,wiczling p. ,rosada-kurasińska j. ,grzeoekowiak m. ,zaba c. ,tezyk a. ,sokołowska a. ,kaliszan r. ,grzeoekowiak e.
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منبع
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pharmacological reports - 2013 - دوره : 65 - شماره : 1 - صفحه:107 -121
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چکیده
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Background: this study evaluates possible circadian rhythms during prolonged midazolam infusion in 27 pediatric intensive care unit (picu) children under mechanical ventilation. methods: blood samples for midazolam and 1-oh-midazolam assay were collected throughout the infusion at different times of the day. the blood pressure,heart rate and body temperature were recorded every hour for the rhythms analysis. population nonlinear mixed-effect modeling with nonmem was used for data analysis. results: a two-compartment model for midazolam pharmacokinetics and a one-compartment model for midazolam metabolite adequately described the data. the 24 h profiles of all monitored physiological parameters were greatly disturbed/abolished in comparison with the well-known 24 h rhythmic patterns in healthy subjects. there was no significant circadian rhythm detected with respect to midazolam pharmacokinetics,its active metabolite pharmacokinetics and all monitored parameters. conclusions: we concluded that the light-dark cycle did not influence midazolam pharmacokinetics in intensive care units children. also,endogenous rhythms in critically ill and sedated children are severely disturbed and desynchronized. our results confirmed that it is necessary to adjust the dose of midazolam to the patient's body weight. the low value of midazolam clearances observed in our study was probably caused by mechanical ventilation,which was shown to decrease the cardiac output. copyright © 2013 by institute of pharmacology polish academy of sciences.
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کلیدواژه
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Children; Circadian rhythms; Critically ill; Mechanical ventilation; Midazolam; Pharmacokinetics
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آدرس
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department of clinical pharmacy and biopharmacy,karol marcinkowski university of medical sciences,mari magdaleny 14,pl 61-861 poznań, Poland, department of pediatric anesthesiology and intensive therapy and pain,poznan university of medical sciences,szpitalna 27/33,pl 60-572 poznań, Poland, department of biopharmaceutics and pharmacodynamics,medical university of gdańsk,halera 107,pl 80-401,gdańsk, Poland, department of pediatric anesthesiology and intensive therapy and pain,poznan university of medical sciences,szpitalna 27/33,pl 60-572 poznań, Poland, department of pediatric anesthesiology and intensive therapy and pain,poznan university of medical sciences,szpitalna 27/33,pl 60-572 poznań, Poland, department of forensic medicine,karol marcinkowski university of medical sciences,świȩcickiego 6,pl 60-781 poznań, Poland, department of forensic medicine,karol marcinkowski university of medical sciences,świȩcickiego 6,pl 60-781 poznań, Poland, department of clinical pharmacy and biopharmacy,karol marcinkowski university of medical sciences,mari magdaleny 14,pl 61-861 poznań, Poland, department of biopharmaceutics and pharmacodynamics,medical university of gdańsk,halera 107,pl 80-401,gdańsk, Poland, department of clinical pharmacy and biopharmacy,karol marcinkowski university of medical sciences,mari magdaleny 14,pl 61-861 poznań, Poland
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Authors
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