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Effect of pentoxifylline on sepsis and protein C level in preterm neonates / Shahenda Abdelaziz Khairy Mohamed ; Supervised Dahlia Bayoumi Elsebaie , Yasmeen Amr Mansi , Angie Mohamed Samir Tosson

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Shahenda Abdelaziz Khairy Mohamed , 2019Description: 134 P. : charts , facsimiles ; 25cmOther title:
  • تاثير عقار البنتوكسيفيللين على عدوى الدم و مستويات بروتين سى فى الاطفال المبتسرين [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics Summary: Background: Neonatal sepsis is almost invariably associated with pathological activation of the coagulation system, which in turn leads to microcirculatory derangement and multiple organ dysfunction syndrome (MODS). The key role in the pathogenesis of sepsis has been attributed to pro-inflammatory cytokines which trigger the development of disseminated intravascular coagulation (DIC). Pentoxifylline (PTX), a methylxanthine derivative, has the potential to modify inflammatory response via decreasing the inflammatory cytokines like tumor necrosis factor alpha, (TNF-Ü) and interleukin (IL-6). It is also used in peripheral vascular disease, and was found to enhance protein C system when given to septic adults. This work aim was to evaluate the potential effect of pentoxifylline on protein C in septic preterm neonates, and its effect on their clinical outcome, morbidity and mortality. Subjects and methods: This double blind randomized controlled trial included 80 preterm with clinical or culture proven late onset sepsis (LOS), with gestational ages <36 weeks and ages ranging from 3 to 28 days of life, Randomized into 2 groups the PTX group received pentoxifylline 5mg/kg/hr/6hrs for 6 successive days, while the control group received normal saline as a placebo, Protein C levels were measured before and after the intervention, and the short term morbidities and mortality was documented
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.28.Ph.D.2019.Sh.E (Browse shelf(Opens below)) Not for loan 01010110079868000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.28.Ph.D.2019.Sh.E (Browse shelf(Opens below)) 79868.CD Not for loan 01020110079868000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pediatrics

Background: Neonatal sepsis is almost invariably associated with pathological activation of the coagulation system, which in turn leads to microcirculatory derangement and multiple organ dysfunction syndrome (MODS). The key role in the pathogenesis of sepsis has been attributed to pro-inflammatory cytokines which trigger the development of disseminated intravascular coagulation (DIC). Pentoxifylline (PTX), a methylxanthine derivative, has the potential to modify inflammatory response via decreasing the inflammatory cytokines like tumor necrosis factor alpha, (TNF-Ü) and interleukin (IL-6). It is also used in peripheral vascular disease, and was found to enhance protein C system when given to septic adults. This work aim was to evaluate the potential effect of pentoxifylline on protein C in septic preterm neonates, and its effect on their clinical outcome, morbidity and mortality. Subjects and methods: This double blind randomized controlled trial included 80 preterm with clinical or culture proven late onset sepsis (LOS), with gestational ages <36 weeks and ages ranging from 3 to 28 days of life, Randomized into 2 groups the PTX group received pentoxifylline 5mg/kg/hr/6hrs for 6 successive days, while the control group received normal saline as a placebo, Protein C levels were measured before and after the intervention, and the short term morbidities and mortality was documented

Issued also as CD

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