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1.
J Pers Med ; 13(6)2023 May 29.
Article in English | MEDLINE | ID: mdl-37373899

ABSTRACT

We investigated the antibody kinetics after vaccination against COVID-19 in healthcare workers of a Greek tertiary hospital. Eight hundred and three subjects were included, of whom 758 (94.4%) received the BNT162b2 vaccine (Pfizer-BioNTech), eight (1%) mRNA-1273 (Moderna), 14 (1.7%) ChAdOx1 (Oxford-AstraZeneca) and 23 (2.9%) Ad26.COV2.S (Janssen). Before the second dose, at 2, 6 and 9 months after the second dose and at 2 and 6 months after the third dose, anti-spike IgG were quantified by the chemiluminescence microparticle immunoassay method. One hundred subjects were infected before vaccination (group A), 335 were infected after receiving at least one vaccine dose (group B), while 368 had never been infected (group C). Group A presented a greater number of hospitalizations and reinfections compared to group B (p < 0.05). By multivariate analysis, younger age was associated with an increased risk of reinfection (odds ratio: 0.956, p = 0.004). All subjects showed the highest antibody titers at 2 months after the second and third dose. Group A showed higher antibody titers pre-second dose, which remained elevated 6 months post-second dose compared to groups B and C (p < 0.05). Pre-vaccine infection leads to rapid development of high antibody titer and a slower decline. Vaccination is associated with fewer hospitalizations and fewer reinfections.

2.
Curr Top Med Chem ; 23(22): 2158-2171, 2023.
Article in English | MEDLINE | ID: mdl-37138428

ABSTRACT

Oxidative stress plays a central role in atherogenesis, implicated in endothelial dysfunction, coronary plaque formation, and destabilization. Therefore, identifying oxidative stress in the vascular wall by reliable biomarkers could aid in early diagnosis and better coronary artery disease (CAD) prognostication. Because of the short half-life of reactive oxygen species, the current approach is to measure stable products generated by the oxidation of macromolecules in plasma or urine. Most popular oxidative stress biomarkers are oxidized low-density lipoprotein, myeloperoxidase and lipid peroxidation biomarkers, such as malondialdehyde and F2-isoprostanes. Oxidative protein modification biomarkers and oxidized phospholipids have also been studied and discussed in the present review. Most of these biomarkers are associated with the presence and extent of CAD, are elevated in patients with acute coronary syndromes, and may predict outcomes independent of traditional CAD risk factors. However, further standardization of measurement methods and assessment in large randomized clinical trials are required to integrate these biomarkers into clinical practice. In addition, evidence that these biomarkers detect oxidative stress in the vascular wall lacks and more specific biomarkers should be developed to identify vascular oxidative stress. Consequently, several oxidative stress biomarkers have been developed, most of which can be associated with the presence and extent of CAD and event prognosis. However, they still have significant limitations that hinder their integration into clinical practice.


Subject(s)
Coronary Artery Disease , Humans , Coronary Artery Disease/diagnosis , Coronary Artery Disease/etiology , Biomarkers , Oxidative Stress , Oxidation-Reduction , Lipid Peroxidation
4.
Am J Infect Control ; 38(8): 631-5, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20471716

ABSTRACT

BACKGROUND: Nosocomial infections are a frequent and continuously increasing problem worldwide, have a rapidly increasing multidrug resistance to antibiotics, and are associated with significant morbidity and mortality. OBJECTIVE: Our objectives were to evaluate Acinetobacter baumannii infection incidence in our surgical intensive care unit (SICU), the clinical features and outcome of these patients, and, particularly, to investigate predictors of A baumannii infection-related mortality. METHODS: Ours was a prospective study of all patients with ICU-acquired A baumannii infection from January 1, 2006, to December 31, 2007. RESULTS: Among 680 patients, 60 (8.8%) sustained A baumannii infection. Mean age was 68.4 ± 6.2 years, Acute Physiology and Chronic Health Evaluation (APACHE) II score on SICU admission 20.6 ± 8.1 and Sequential Organ Failure Assessment (SOFA) score on infection day 9.5 ± 4.2 (women: 50%). Multidrug resistance, morbidity, and mortality were 45%, 65%, and 46.6% (n = 28), respectively. In multivariate analysis, age (P = .03; odds ratio [OR], 1.13; 95% confidence interval [CI]: 1.018-1.259), acute renal failure (P = .001; OR, 17.9; 95% CI: 6.628-75.565), and thrombocytopenia (P = .03; OR, 26.4; 95% CI: 1.234-56.926) complicating the infection and subsequent Enterococcus faecium bacteremia (P = .01; OR, 3.5; 95% CI: 1.84-6.95) were mortality predictors. CONCLUSION: A baumannii infections are frequent and associated with high drug multiresistance, morbidity, and mortality. Age, renal failure, thrombocytopenia, and subsequent E faecium bacteremia were predictors of A baumannii infection-associated mortality.


Subject(s)
Acinetobacter Infections/mortality , Acinetobacter baumannii , Cross Infection/mortality , Intensive Care Units/statistics & numerical data , Acinetobacter Infections/epidemiology , Aged , Aging , Anti-Bacterial Agents/therapeutic use , Bacteremia/epidemiology , Cross Infection/epidemiology , Drug Resistance, Multiple, Bacterial , Enterococcus faecium , Gram-Positive Bacterial Infections/epidemiology , Greece/epidemiology , Humans , Prospective Studies , Risk Factors , Treatment Outcome
5.
J Med Microbiol ; 59(Pt 7): 862-865, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20395379

ABSTRACT

Fungal peritonitis is a rare, potentially lethal, complication of continuous ambulatory peritoneal dialysis (CAPD). We report what we believe to be the first confirmed Neosartorya hiratsukae CAPD-related peritonitis case in Europe. The patient died, despite early removal of the peritoneal catheter and antifungal therapy. This report highlights the impact of emerging fungal pathogens and the importance of early diagnosis on the outcome in CAPD-related fungal peritonitis.


Subject(s)
Mycoses/microbiology , Neosartorya/isolation & purification , Peritonitis/microbiology , Anti-Bacterial Agents/therapeutic use , Antifungal Agents/therapeutic use , Ascitic Fluid/microbiology , Enterococcus faecalis/isolation & purification , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/microbiology , Humans , Male , Middle Aged , Molecular Sequence Data , Neosartorya/classification , Neosartorya/genetics
6.
J Infect ; 56(6): 432-6, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18501431

ABSTRACT

OBJECTIVE: To compare the safety and efficacy of ampicillin/sulbactam (Amp/Sulb) and colistin (COL) in the treatment of multidrug resistant Acinetobacter baumannii ventilator-associated pneumonia (VAP). METHODS: A prospective cohort study in adult critically ill patients with VAP. Patients were randomly assigned to receive Amp/Sulb (9 g every 8h) or COL (3 MIU every 8h) intravenously. Dosage was adjusted according to creatinine clearance. RESULTS: A total of 28 patients were enrolled (15 COL, 13 Amp/Sulb). Resolution of symptoms and signs occurred in 60% (9/15) of the COL group and 61.5% (9/13) of the Amp/Sulb group, improvement in 13.3% (2/15) vs. 15.3% (1/13) and failure in 26.6% (4/15) vs. 23% (3/13), respectively. The difference was not statistically significant. Bacteriologic success was achieved in 66.6% (10/15) vs. 61.5% (8/13) in the COL and Amp/Sulb groups, respectively (p<0.2). Mortality rates (14 days and 28 days) were 15.3% and 30% for the Amp/Sulb and 20% and 33% for the COL group, respectively. Adverse events were 39.6% (including 33% nephrotoxicity) for the COL group and 30.7% (15.3% nephrotoxicity) for the Amp/Sulb group (p=NS). CONCLUSION: Colistin and high-dose ampicillin/sulbactam were comparably safe and effective treatments for critically ill patients with MDR A. baumannii VAP.


Subject(s)
Acinetobacter Infections/drug therapy , Acinetobacter baumannii/drug effects , Anti-Bacterial Agents/therapeutic use , Pneumonia, Bacterial/drug therapy , Pneumonia, Ventilator-Associated/drug therapy , Acinetobacter Infections/microbiology , Aged , Ampicillin/pharmacology , Ampicillin/therapeutic use , Anti-Bacterial Agents/pharmacology , Colistin/pharmacology , Colistin/therapeutic use , Drug Resistance, Multiple, Bacterial , Female , Humans , Male , Middle Aged , Pneumonia, Bacterial/microbiology , Sulbactam/pharmacology , Sulbactam/therapeutic use
7.
Scand J Infect Dis ; 39(1): 38-43, 2007.
Article in English | MEDLINE | ID: mdl-17366011

ABSTRACT

The increased incidence of multidrug-resistant (MDR) Acinetobacter baumannii ventilator-associated pneumonia in critically ill patients poses a severe therapeutic problem. The aim of this study was to evaluate the efficacy and safety of 2 high-dose treatment regimens of ampicillin-sulbactam (A/S) for MDR Acinetobacter baumannii VAP. We undertook a randomized, prospective trial of critically ill patents with (MDR) Acinetobacter baumannii VAP. Patients were randomly assigned to 1 of 2 treatment regimens of A/S (at a rate 2:1 every 8 h): 1) group A, 18/9 g daily dose (n = 14); and 2) group B, 24/12 g daily dose (n = 13). The duration of therapy was 8+/-2 d for both groups. A total of 27 patients were enrolled in the study. Clinical improvement was seen in 66.7% of the study population in 9/14 (64.3%) of group A patients and 9/13 (69.2%) of group B patients, respectively. Bacteriological success was achieved in 77.8% of the study population (12/14, 85.7% of group A) and in 9/13 (69.2%) of group B patients. The 14-d mortality rate was 25.9% and the all cause 30-d mortality was 48.1%. Both mortality rates did not differ significantly between the 2 groups. No major adverse reactions were recorded. We concluded that clinical and bacteriological results of the study support the use of high-dose regimen of ampicillin-sulbactam for MDR Acinetobacter baumannii VAP.


Subject(s)
Acinetobacter Infections/drug therapy , Acinetobacter baumannii/drug effects , Anti-Bacterial Agents/administration & dosage , Drug Resistance, Multiple, Bacterial/drug effects , Pneumonia, Ventilator-Associated/drug therapy , Aged , Ampicillin/administration & dosage , Bronchoalveolar Lavage Fluid/microbiology , Cross Infection , Disk Diffusion Antimicrobial Tests , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Humans , Intensive Care Units , Male , Middle Aged , Pneumonia, Ventilator-Associated/microbiology , Sulbactam/administration & dosage , Treatment Outcome
8.
Liver Int ; 25(1): 57-61, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15698399

ABSTRACT

AIM: To evaluate the characteristics and possible recent changes of the microbial causes of spontaneous bacterial peritonitis (SBP) in cirrhotic patients. METHODS: We retrospectively evaluated 42 cirrhotic patients with positive ascitic fluid culture and without evidence of secondary peritonitis who were admitted consecutively to our Department between 1998 and 2002. RESULTS: Twenty (48%) of 42 patients with positive ascitic fluid culture were diagnosed during 1998-1999 (period A) and the remaining 22 (52%) patients during 2000-2002 (period B). Gram-negative bacteria were the cause of SBP in 15 (75%) of the 20 patients during period A and in only nine (41%) of the 22 patients during period B (P=0.026). SBP patients with Gram-positive bacteria compared with those with Gram-negative bacteria were less frequently in Child class C (P=0.058) and had significantly higher ascitic fluid protein (P=0.014) and albumin concentrations (P=0.009) and lower ascitic fluid neutrophil count (P=0.008). Resistance to quinolones was detected significantly more frequently in the isolated Gram-positive than Gram-negative bacteria (P<0.001). CONCLUSION: Culture-positive SBP in cirrhotic patients are caused more frequently by Gram-positive bacteria during the recent years, which are, in their vast majority, resistant to quinolones.


Subject(s)
Gram-Positive Bacteria/isolation & purification , Gram-Positive Bacterial Infections/complications , Liver Cirrhosis/complications , Peritonitis/microbiology , Aged , Anti-Infective Agents/pharmacology , Anti-Infective Agents/therapeutic use , Ascites/etiology , Ascites/microbiology , Drug Resistance, Bacterial , Female , Gram-Negative Bacterial Infections/complications , Gram-Negative Bacterial Infections/drug therapy , Gram-Negative Bacterial Infections/pathology , Gram-Positive Bacteria/drug effects , Gram-Positive Bacteria/physiology , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/pathology , Humans , Liver Cirrhosis/pathology , Male , Middle Aged , Peritonitis/pathology , Quinolones/pharmacology , Quinolones/therapeutic use
9.
Scand J Infect Dis ; 34(9): 687-9, 2002.
Article in English | MEDLINE | ID: mdl-12374363

ABSTRACT

Bacteremia due to Plesiomonas shigelloides was associated with rapidly fulminant septicemia, disseminated intravascular coagulation and massive adrenal hemorrhage in a splenectomized patient suffering from thalassemia intermedia who was treated with hydroxyurea. P. shigelloides was isolated in blood cultures; despite a vigorous combination of antibiotics the patient died after 24 h in the ICU. Lethal sepsis due to P. shigelloides has not previously been reported in Greece.


Subject(s)
Gram-Negative Bacterial Infections/complications , Plesiomonas/isolation & purification , Thalassemia/complications , Adult , Anti-Bacterial Agents/therapeutic use , Disseminated Intravascular Coagulation/complications , Fatal Outcome , Female , Gram-Negative Bacterial Infections/drug therapy , Gram-Negative Bacterial Infections/physiopathology , Greece , Humans , Plesiomonas/pathogenicity , Sepsis/complications , Splenectomy
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