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1.
J Adolesc ; 93: 134-145, 2021 12.
Article in English | MEDLINE | ID: mdl-34749167

ABSTRACT

INTRODUCTION: Social networking sites such as Instagram have provided young people with unprecedented opportunities for social comparison, and such behaviour can have implications for identity development. Although initial evidence suggests that there may be developmental differences in terms of how such behaviour informs identity development during adolescence and emerging adulthood, all previous research has been conducted in highly individualistic cultural contexts (i.e., the UK and the US). METHOD: To shed further light on these possible developmental differences and to determine whether results replicate amongst young people from more collectivist cultural contexts, cross-sectional survey data were collected from 1,085 (M age = 18.87, SD = 2.57; Female = 77.8%) adolescents and emerging adults in Romania and Serbia between December 2019 and March 2020. The relationships between social comparisons of ability and opinion on Instagram and three key identity processes (i.e., commitment, in-depth exploration, and reconsideration of commitment) were then examined. RESULT: Hierarchical multiple regression analyses identified significant age differences in terms of how social comparisons of ability and opinion on Instagram associated with identity commitment and in-depth exploration. Furthermore, possible cultural differences were identified in terms of how social comparisons of opinion on Instagram associated with the identity processes. CONCLUSION: Overall, results suggest that whilst social comparisons on Instagram can elicit self-focus and prompt further exploration, developmental and cultural factors may influence how such behaviour informs identity development during adolescence and emerging adulthood.


Subject(s)
Social Comparison , Adolescent , Adult , Cross-Sectional Studies , Female , Humans
2.
Physiol Rep ; 9(17): e15012, 2021 09.
Article in English | MEDLINE | ID: mdl-34491003

ABSTRACT

OBJECTIVE: The present study investigates whether ScvO2 variations induced by passive leg raising (PLR) are able to predict fluid responsiveness (FR) in mechanically ventilated patients. DESIGN: A monocentric prospective clinical study. SETTING: An intensive care division in a tertiary hospital. PATIENTS: The inclusion criteria were elective postoperative cardiac surgery patients who were over 18 years old, deeply sedated, mechanically ventilated and needed volume expansion (VE). Fluid responders (R) were defined as patients who increased their left ventricular outflow tract velocity time integral (VTI) ≥15% after VE. INTERVENTION: In patients included in this study, continuous ScvO2  monitoring (CeVOX device, Pulsion Medical Systems) and VTI (transthoracic echocardiography) were measured simultaneously before and during a PLR test and before and after VE (with 500 ml of saline). MEASUREMENTS AND MAIN RESULTS: Thirty-three consecutive patients were included in this study. In 15 patients with a positive PLR test (increase in VTI ≥15%), ScvO2 increased during PLR by 9 ± 4%. In the 18 patients with a negative PLR test, ScvO2 did not significantly change during PLR. VE increased ScvO2 by 9 ± 6% and 2 ± 4% in responders and nonresponders, respectively. If ScvO2 increased by >4% during the PLR test, then a positive VTI response (≥15%) was diagnosed with a sensitivity of 93% (68-99%) and a specificity of 94% (63-99%) (Area under the receiver operating characteristic curve 0.92 ± 0.58, p < 0.05). Moreover, ScvO2 variations were able to distinguish responders to VE from nonresponders to VE with a sensitivity of 87% (68-99%) and a specificity of 89% (63-99%) (Area under the receiver operating characteristic curve 0.89 ± 0.07, p < 0.05). CONCLUSIONS: ScvO2 variation induced by PLR is a reliable, minimally invasive parameter for predicting FR at the postoperative cardiac surgery bedside of mechanically ventilated, critically ill patients.


Subject(s)
Critical Illness/therapy , Fluid Therapy/methods , Leg/physiology , Oxygen Saturation/physiology , Patient Positioning/methods , Range of Motion, Articular/physiology , Aged , Cardiac Output/physiology , Echocardiography/methods , Electrocardiography/methods , Female , Humans , Male , Middle Aged , Oximetry/methods , Predictive Value of Tests , Prospective Studies , Respiration, Artificial/methods , Tidal Volume/physiology , Treatment Outcome
3.
Microb Pathog ; 120: 23-31, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29684542

ABSTRACT

The microbiologically contaminated vegetables represent a risk for consumers, especially vegetables without thermal processing. It is known that human pathogen bacteria, such as Listeria monocytogenes, could exist on fresh vegetables. The fresh vegetables could become Listeria-contaminated if they come in touch with contaminated soil, manure, irrigation water. The aim of this work was to investigate the presence of Listeria spp. and L. monocytogenes in different kind of vegetables grown in field and greenhouse condition as well as surface and endophytic colonization plant roots of different vegetables species by L. monocytogenes in laboratory conditions. The detection of Listeria spp. and L. monocytogenes in vegetable samples was done using ISO and PCR methods. The investigation of colonization vegetable roots and detection Listeria-cells inside plant root tissue was done using Fluorescence in situ hybridization (FISH) method in combination with confocal laser scanning microscopy (CLSM). The results showed that 25.58% vegetable samples were positive for Listeria spp. and only one sample (carrot) was positive for L. monocytogenes out of 43 samples in total collected from field and greenhouse. The strain L. monocytogenes EGD-E surface and endophytic colonized carrot root in highest degree while strain L. monocytogenes SV4B was the most represented at leafy vegetable plants, such at lettuce (1.68 × 106 cells/mm3 absolutely dry root) and spinach (1.39 × 106 cells/mm3 absolutely dry root) root surface. The cells of L. monocytogenes SV4B were visible as single cells in interior tissue of plant roots (celery and sweet corn roots) as well as in the interior of the plant root cell at sweet corn root. The cells of L. monocytogenes EGD-E bind to the surface of the plant root and they were less commonly found out on root hair. In the inner layers of the root, those bacterial cells were inhabited intercellular spaces mainly as single cells very close to the larval vessels of root. Our results suggest that L. monocytogenes is very good endophytic colonizer of vegetable plant roots.


Subject(s)
Food Contamination/analysis , Food Microbiology , Listeria monocytogenes/isolation & purification , Vegetables/microbiology , Agricultural Irrigation , Bacterial Typing Techniques , Colony Count, Microbial , DNA, Bacterial/analysis , Humans , In Situ Hybridization, Fluorescence , Listeria/classification , Listeria/genetics , Listeria/growth & development , Listeria/isolation & purification , Listeria monocytogenes/genetics , Listeria monocytogenes/growth & development , Oligonucleotide Probes , Plant Leaves/microbiology , Plant Roots/microbiology , Polymerase Chain Reaction , Serbia
4.
Microb Pathog ; 115: 199-207, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29248516

ABSTRACT

Contamination of vegetables and fruits is the result of presence of human pathogen bacteria which can contaminate products in any part of production chain. There is an evidence of presence of: Salmonella spp. on the fresh vegetables and Salmonellosis is connected with tomato, sprouts, cantaloupe etc. The goal of this research is transmission of pathogen bacteria from irrigation water to plants and studying/monitoring the ability of the Salmonella spp. to colonize the surface and interior (endophytic colonization) of root at different vegetable species. Transmission of three Salmonella spp. strains from irrigation water to plants, as well as colonization of plants by these bacteria was investigated by using Fluorescence In Situ Hybridization (FISH) in combination with confocal laser scanning microscopy (CLSM). All tested Salmonella spp. strains showed ability to more or less colonize the surface and interior niches of the root, stem and leaf of the investigated plant species. These bacteria also were found in plant cells cytoplasm, although the mechanism of their entrance has not been clarified yet.


Subject(s)
Food Contamination/analysis , Fruit/microbiology , Plant Leaves/microbiology , Plant Roots/microbiology , Plants/microbiology , Salmonella typhimurium/isolation & purification , Vegetables/microbiology , Colony Count, Microbial , Humans , In Situ Hybridization, Fluorescence , Salmonella Infections/microbiology
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