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1.
Eur Rev Med Pharmacol Sci ; 27(17): 8301-8313, 2023 09.
Article in English | MEDLINE | ID: mdl-37750658

ABSTRACT

OBJECTIVE: In this study, demographic, clinical, and laboratory data of patients aged 65 and over who are followed on mechanical ventilators due to COVID-19 in intensive care clinics will be useful in terms of strategies to be developed in the fight against COVID-19 and other infectious agents. PATIENTS AND METHODS: Our study included 299 patients aged 65 years and older, who were not chronically ill, and who were followed up on mechanical ventilators due to COVID-19 in intensive care clinics in the period between 2020 and 2022. Our study was designed as a retrospective cross-sectional study. The demographic characteristics of the patients included in the study, their complaints during hospitalization, the time between the beginning of the complaint and the admission to the hospital, the vital signs at the time of admission to the hospital, the lung computed tomography findings during hospitalization, and the treatments given were examined. RESULTS: 55.9% of all patients were males, and the mean age was 75.45±7.47 years. While there was no significant difference in terms of mean age between the groups of patients with/without a higher risk of mortality, there was a significant difference in gender (p=0.025). There was a statistically significant difference between the COVID-19 intensive care (p=0.001) and renal failure (p=0.014) and mortality groups. The mean nutric score, Procalcitonin (PCT), Lactate Dehydrogenase (LDH), Blood Urea Nitrogen (BUN), Phosphorus, and lactate values, which are important parameters, were statistically higher in the group with a higher risk of mortality (p<0.001). In addition, there was a statistically significant difference in terms of sepsis, neuromuscular blocker (Nmb), vasopressor, and intubation between the groups of patients with/without a higher risk of mortality (p<0.001). In the group with high mortality, 34.2% (n=55) had plasmapheresis treatment, and 14.2% had hemodiafiltration treatment (p<0.001). According to the results of the multivariate logistic regression model in determining the factors associated with a higher risk of mortality, those who were males (p=0.001), those with kidney failure (p<0.001), those with organ failure (p=0.006), increased in alanine aminotransferase (ALT) values (p=0.019), those with sedation (p=0.001) and those with vasopressors (p<0.001) were found to have an increased risk of mortality. CONCLUSIONS: We think that our study is valuable in terms of determining the most appropriate treatment strategies by following the patients in terms of parameters that are significant in the findings during their follow-up period in the Intensive Care Unit.


Subject(s)
COVID-19 , Male , Humans , Aged , Aged, 80 and over , Female , COVID-19/therapy , Cross-Sectional Studies , Retrospective Studies , Intensive Care Units , Chronic Disease , Lactic Acid
2.
Nano Lett ; 18(9): 6002-6008, 2018 09 12.
Article in English | MEDLINE | ID: mdl-30142981

ABSTRACT

Optical nanoantennas mediate near and far optical fields. Operating a directional nanoantenna in transmitting mode is challenging because the antenna needs to be driven by a nanosized optical frequency generator, which must work at the antenna's resonance frequency and be precisely attached to the antenna's feed with correct polarization. Quantum emitters have been used as optical nanogenerators, but their precise positioning relative to the nanoantenna is technically challenging, setting up a barrier to the practical implementation. One unique source to drive nanoantenna is the photoluminescence from the material of the nanoantenna because the high operational frequency of the antenna reaches the regime for the electronic transitions in matter. Here, we exploit plasmon-modulated photoluminescence (PMPL) as an effective optical source to drive directional nanoantennas. We experimentally realize two technically challenging theoretical proposals, namely, an optical nanospectrometer based on Yagi-Uda nanoantennas and tunable broadband directional emission from log-periodic nanoantennas. Using photoluminescence from the nanoantenna as an optical source promotes practical implementation of transmitting optical nanoantennas.

3.
Genet Couns ; 22(1): 35-40, 2011.
Article in English | MEDLINE | ID: mdl-21614986

ABSTRACT

We report a female infant with partial trisomy 8p (8p11.2-->pter) and deletion of 13q (13q32-->qter). She was born with mild hypotonia, intrauterine growth retardation, microcephaly, micrognathia, large low set ears, pectus excavatum, anteriorly placed anus, and bilateral clinodactyly. Echocardiography showed left ventricular hypertrophy, bicuspid aortic valve, dilatation of the aorta and pulmonary artery, and prolapse of atrio-venticular valve leaflets. Cytogenetic investigation of her sister and her father showed that the altered region resulted from a balanced translocation between the part of the long arm of chromosome 13 and short arm of chromosome 8. In partial trisomy 8p, the clinical picture of the patients comprises hypotonia, structural brain abnormalities, facial anomalies including a large mouth with a thin upper lip, a high arched palate, a broad nasal bridge, an abnormal maxilla or mandible, malformed, low set ears, and orthopedic anomalies. Although patients with proximal deletions of 13q that do not extend into band q32 have mild to moderate mental and growth delays with variable minor anomalies, patients with more distal deletions including at least part of band q32 usually have major malformations such as retinoblastoma, mental-motor growth retardation, malformation of brain and heart, anal atresia, and anomalies of the face and limbs. To our knowledge partial trisomy 8p and partial monosomy of 13q have not been reported previously in the same person.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Deletion , Chromosomes, Human, Pair 13/genetics , Heart Defects, Congenital/genetics , Abnormalities, Multiple/diagnosis , Chromosomes, Human, Pair 8/genetics , Craniofacial Abnormalities/diagnosis , Craniofacial Abnormalities/genetics , Echocardiography , Female , Genetic Carrier Screening , Heart Defects, Congenital/diagnosis , Humans , Infant, Newborn , Intellectual Disability/diagnosis , Intellectual Disability/genetics , Karyotyping , Translocation, Genetic/genetics , Trisomy/diagnosis , Trisomy/genetics
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