Anna Maria Spanaki
University of Crete
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Featured researches published by Anna Maria Spanaki.
Pediatric Critical Care Medicine | 2017
Theonymfi Tavladaki; Anna Maria Spanaki; Helen Dimitriou; Efmorfia Kondili; Christianna Choulaki; Dimitris Georgopoulos; George Briassoulis
Objectives: To examine whether the septic profiles of heat shock protein 72, heat shock protein 90&agr;, resistin, adiponectin, oxygen consumption, CO2 production, energy expenditure, and metabolic pattern, along with illness severity, nutritional, and inflammatory indices, differ between adult and pediatric patients compared with systemic inflammatory response syndrome and healthy controls. To evaluate whether these biomolecules may discriminate sepsis from systemic inflammatory response syndrome in adult and pediatric patients. Design: Prospective cohort study. Setting: University ICU and PICU. Patients: Seventy-eight adults (sepsis/23; systemic inflammatory response syndrome/23; healthy controls/33), 67 children (sepsis/18; systemic inflammatory response syndrome/23; controls/27), mechanically ventilated. Interventions: None. Measurements and Main Results: Flow cytometry determined mean fluorescence intensity for monocyte or neutrophil heat shock protein expression. Resistin, adiponectin, and extracellular heat shock proteins were measured using enzyme-linked immunosorbent assay; energy expenditure by E-COVX (GE Healthcare). Genomic DNA was extracted with PureLink Genomic DNA kit (Invitrogen, Carlsbad, CA) to detect heat shock protein 72 single nucleotide polymorphisms. Similarly, in adult and pediatric patients, Acute Physiology and Chronic Evaluation-II/Acute Physiology and Pediatric Risk of Mortality-III, Simplified Acute Physiology Score-III, C-reactive protein, lactate, and resistin were higher and myocardial contractility, monocyte heat shock protein 72, oxygen consumption, CO2 production, energy expenditure, metabolic pattern, glucose, and albumin lower in sepsis compared with systemic inflammatory response syndrome or controls (p < 0.05). For discriminating sepsis from systemic inflammatory response syndrome, resistin, extracellular heat shock protein 90&agr;, and lactate achieved a receiver operating characteristic curve greater than 0.80 in children and greater than 0.75 in adults (p < 0.05). In both, adults and children, genotype heat shock protein 72 analysis did not disclose any diagnosis or mortality group differences regarding either rs6457452 or rs1061581 haplotypes. Conclusions: Sepsis presents with similar profiles in adult and pediatric patients, characterized by enhanced inflammatory hormonal response and by repressed innate immunity, metabolism, and myocardial contractility. These features early distinguish sepsis from systemic inflammatory response syndrome across all age groups.
Journal of Parenteral and Enteral Nutrition | 2018
Anna Maria Spanaki; Theonymfi Tavladaki; Helen Dimitriou; Andrey V. Kozlov; J. Catharina Duvigneau; Eftychia Meleti; Adelheid Weidinger; Evangelos Papakonstantinou; George Briassoulis
BACKGROUND Experimental data indicate that sepsis influences the mitochondrial function and metabolism. We aim to investigate longitudinal bioenergetic, metabolic, hormonal, amino-acid, and innate immunity changes in children with sepsis. METHODS Sixty-eight children (sepsis, 18; systemic inflammatory response syndrome [SIRS], 23; healthy controls, 27) were enrolled. Plasma amino acids were determined by high-performance liquid chromatography (HPLC); flow-cytometry expressed as mean fluorescence intensity (MFI) of heat shock protein (HSP) levels from monocytes (m) and neutrophils (n); resistin, adiponectin, and extracellular (e) HSPs evaluated by ELISA; ATP levels in white blood cells by luciferase luminescent assay; lipid peroxidation products (TBARS) by colorimetric test; nitrite and nitrate levels by chemiluminescent assay; biliverdin reductase (BVR) activity by enzymatic assay; and energy-expenditure (EE) by E-COVX. RESULTS Resistin, eHSP72, eHSP90α, and nitrate were longitudinally higher in sepsis compared with SIRS (p<0.05); mHSP72, nHSP72, VO2 , VCO2 , EE, and metabolic pattern were repressed in sepsis compared with SIRS (p<0.05). Septic patients had lower ATP and TBARS compared with controls on day 1, lower ATP compared with SIRS on day 3 (p<0.05), but higher levels of BVR activity. Sepsis exhibited higher phenylalanine levels on day 1, serine on day 3; lower glutamine concentrations on days 3 and 5 (p<0.05). Resistin, inversely related to ATP, was independently associated with sepsis, along with mHSP72 and eHSP90α (p<0.05); TBARS and VO2 were independently associated with organ failure (p<0.05)). Septic nonsurvivors had malnutrition, persistently repressed metabolism, mHSP72, and induced resistin and adiponectin (p<0.05). CONCLUSIONS A pattern of early longitudinal induction of metabolic-hormones and eHSP72/HSP90α, repression of bioenergetics and innate immunity, hypo-metabolism, and amino-acid kinetics changes discriminate sepsis from SIRS; malnutrition, hypo-metabolism, and persistently increased resistin and adiponectin are associated with poor outcome.
Archives of Disease in Childhood | 2008
George Briassoulis; M-D Fitrolaki; E. Mihailidou; Anna Maria Spanaki
A 7-year-old boy presented with neck (fig 1A), chest and abdominal contusions following a frontal impact motor-vehicle accident. He had severe dyspnoea with cyanosis, recessions, hoarseness, deep stridor and haemoptysis. Diffuse crepitus and oedema with neck asymmetry were also noted. On impact, the patient was restrained by a three-point belt system, …
Journal of Emergency Medicine | 2014
George Sakellaris; Evangelos Blevrakis; Ioannis Petrakis; Anastasia Dimopoulou; Olga Dede; Nikolaos Partalis; Athanasios Alegakis; Chrysa Seremeti; Anna Maria Spanaki; George Briassoulis
Cases Journal | 2009
Nikolaos Katzilakis; Michalis Michalakis; John Vlachakis; John Arbiros; Efrosyni Vassilaki; John Germanakis; Emmanuel Velivassakis; Nikolaos Rikos; Anna Maria Spanaki; George Briassoulis
Pediatric Critical Care Medicine | 2014
Theonymfi Tavladaki; Anna Maria Spanaki; Helen Dimitriou; A. Kozlov; C. Duvigneau; M. Venihaki; D.M. Fitrolaki; E. Kondili; D. Georgopoulos; George Briassoulis
Pediatric Critical Care Medicine | 2014
D.M. Fitrolaki; Helen Dimitriou; M. Venihaki; M. Katrinaki; Anna Maria Spanaki; Theonymfi Tavladaki; George Briassoulis
Pediatric Critical Care Medicine | 2014
Anna Maria Spanaki; Theonymfi Tavladaki; Helen Dimitriou; M. Venihaki; D.M. Fitrolaki; E. Kondili; D. Georgopoulos; George Briassoulis
Toxicology Letters | 2007
Maria Toutoudaki; Manolis Tzatzarakis; George Briassoulis; Anna Maria Spanaki; Stamatis Belivanis; Aristidis M. Tsatsakis