The effect of dexmedetomidine versus midazolam on resting energy expenditure in critically ill patients: Randomized controlled study / Ayman Amin Abougabal ; Supervised Mohamed Abdulatif Mohamed , Ahmed Mohamed Mukhtar , Ahmed Mohamed Hasanin
Material type: TextLanguage: English Publication details: Cairo : Ayman Amin Abougabal , 2017Description: 52 P. : charts , facsimiles ; 25cmOther title:- دراسة اكلينيكية للمقارنة بين تأثير كل من عقاري الديكسميديتوميدين و الميدازولام علي معدل استهلاك الطاقة في مرضي الحالات الحرجة [Added title page title]
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Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.01.Ph.D.2017.Ay.E (Browse shelf(Opens below)) | Not for loan | 01010110074777000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.01.Ph.D.2017.Ay.E (Browse shelf(Opens below)) | 74777.CD | Not for loan | 01020110074777000 |
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Thesis (Ph.D.) - Cairo University -Faculty of Medicine - Department of Anesthesia
This study was designed to compare the effect of dexmedetomidine on REE in relation to the midazolam in critically ill patients using indirect calorimetry. Thirty critically ill, mechanically ventilated patients received the study drug within 24 hours after intubation. Group I patients had DEX (0.075 æg/kg/mL) and group II patients had midazolam (0.5 mg/mL). Both drugs were prepared in 0.9% sodium chloride in 50-mL syringe indistinguishable from one another. Both the agents were titrated to maintain the RASS in a range of {u2212}3 to {u2212}1. DEX infusion was started at 0.15 æg/kg/hr (2 mL/hr) and was adjusted by 0.15 æg/kg/hr increments to a maximum of 0.75 æg/kg/hr, while midazolam was started at 1 mg/hr (2 mL/hr) and was adjusted by 1 mg/hr to a maximum of 5 mg/hr. The metabolic parameters (REE, VO2), the biochemical markers (Plasma interleukin-1Ý, plasma tumor necrosis factor alpha, Plasma catecholamine), the hemodynamic data, and Richmond Agitation-Sedation Score, were reported at predetermined time assessment points. Also patient characteristics, total dose of infused drug, and the time to extubation were reported
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