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1.
Digestive and Liver Disease ; 55:S34, 2023.
Article in English | EMBASE | ID: covidwho-2240346

ABSTRACT

Background: From January 2022 the Omicron SARS-CoV-2 variant became the dominant circulating variant worldwide, showing increased transmissibility and the ability to evade immunity. Booster vaccinations improved the protective effects of neutralizing antibodies and might have lowered the risk of hospitalization and mortality, as recently observed. Aim: to evaluate the prevalence and outcome of Omicron-related infection in a cohort of liver transplant (LT) recipients. Material and Methods: From January to September 2022, we enrolled in a longitudinal study all LT recipients who became SARS-CoV-2 infected (95% vaccinated;88% receiving a 1st booster dose and 25% a 2nd booster). All patients were included in a protocol of testing anti-spike (a-S) and anti-nucleocapsid (a-N) antibodies titres before/after each dose (Elecsys Anti-SARS-CoV-2, Roche Diagnostic). Diagnostic criteria for SARS-CoV-2 infection were 1) presence of a positive nasopharyngeal swab (NFS) by PCR or antigenic assays or 2) presence of a-N seroconversion (if previously a-N negative). Reinfection was defined by a new NFS positivity or an increased value of a-N titre. Results: Overall, 201 LT-recipients have been infected by SARS-CoV-2 (62% males, median age=61yr, 50% viral-etiology, 35% with HCC, all received a CNI-based regimen, plus MMF=63%). Most of infections were diagnosed by NFS (72%);mild flu-like symptoms were observed in 59% of our LT recipients;72% of them remained untreated, while 28% received antivirals (11%) or monoclonal antibodies (17%). Fifteen LT recipients were hospitalized, 6 of them for interstitial pneumonia and 2 (both with previous lung diseases) died for COVID-19. Conclusions: A mild or asymptomatic infection occurred frequently in our LT recipients with a less severe outcome than the past waves. A possible explanation could be the high prevalence of vaccinated patients in our cohort. Interestingly, the overall prevalence of SARS Cov2 infection might be underestimated without a careful monitoring of SARS-CoV-2 serology against nucleocapsid.

2.
Turkish Journal of Biochemistry ; 47(5):680-685, 2022.
Article in English | EMBASE | ID: covidwho-2228671

ABSTRACT

Objectives: For a definitive diagnosis of COVID-19, respiratory tract samples are evaluated by polymerase chain reaction (PCR). In our study, PCR using a tear sample was used to diagnose COVID-19, and it was questioned whether it was a screening method. Unlike the general practice, Schirmer strips were used instead of a swab for tear sample collection in this study. In addition, the diagnostic values of serum procalcitonin (PCT), C-reactive protein (CRP), and Neutrophil (NEU) count in predicting COVID-19 disease from tears were also questioned. Method(s): A total of 94 patients who were positive for COVID-19 by PCR test were included in this study. Tear samples were obtained from patients with Schirmer strips, commonly used in eye examination, and studied with the PCR technique. CRP, PCT value, and NEU count were also compared between the positive and negative groups of the PCR. The obtained data were analyzed using the R Studio software, and the results were considered statistically significant for p<0.05. Result(s): Of these patients, 61 (64.9%) tear PCR was negative, and 33 (35.1%) tear PCR was positive. The mean age was 61.72 +/- 17.62 years. The patients were divided into two groups: tear PCR positive and negative. There was no significant age difference between these groups. As a result of ROC Analysis;When serum PCT, CRP, and NEU % values were examined in predicting COVID-19 disease from tears, it was seen that CRP (p=0.027) and especially PCT (p=0.003) values of patients with PCR-positive were significantly higher. Conclusion(s): PCR study on tears collected with Schirmer strips is a different and non-invasive method, but it was concluded that the proposed method could not be used as a screening test. In addition, significantly higher serum PCT values were found in patients with COVID-19 positivity in tears (p<0.05). Copyright © 2022 the author(s), published by De Gruyter.

3.
Turkish Journal of Biochemistry ; 47(5):672-679, 2022.
Article in English | EMBASE | ID: covidwho-2227885

ABSTRACT

Objectives: Studies have shown that fibrinolysis activity is insufficient in COVID-19 patients. Plasminogen activator inhibitor-1 (PAI-1) is an important antifibrinolytic molecule that plays a key role in the fibrinolytic system. In our study;we aimed to evaluate serum PAI-1 and other biochemical parameters of COVID-19 patients in terms of disease course and mortality. Method(s): A total of 40 COVID-19 patients were hospitalized in the service and intensive care unit (ICU) of our hospital from October to December 2020 and 20 healthy volunteers were included in our study. The patients were grouped as those who transferred to the ICU from the service and transferred to service from the ICU. The first and second values of the same patients in both the service and the ICU were analyzed by SPSS. Result(s): The PAI-1 levels of the patients in the ICU were significantly higher than the levels of the same patients in the service and the healthy control group (p<0.001). IL-6, ferritin, and D-dimer levels in the ICU of the same patients were significantly higher than the levels of service and healthy control group (p<0.001). A positive correlation was found between initial serum PAI-1 and D-dimer levels in patients hospitalized in the service (p=0.039) and initial serum ferritin and IL-6 levels in the ICU (p=0.031). Conclusion(s): In our study, we found that PAI-1 levels increased significantly with the increase in mortality in COVID-19 patients. Copyright © 2022 the author(s), published by De Gruyter.

5.
Open Forum Infectious Diseases ; 9(Supplement 2):S776, 2022.
Article in English | EMBASE | ID: covidwho-2189967
6.
Open Forum Infectious Diseases ; 9(Supplement 2):S462-S463, 2022.
Article in English | EMBASE | ID: covidwho-2189743
7.
Arthritis and Rheumatology ; 74(Supplement 9):1497-1499, 2022.
Article in English | EMBASE | ID: covidwho-2172644
9.
Arthritis and Rheumatology ; 74(Supplement 9):1588-1590, 2022.
Article in English | EMBASE | ID: covidwho-2172517
10.
Biochimica Clinica ; 46(3):S175, 2022.
Article in English | EMBASE | ID: covidwho-2169553
11.
Multiple Sclerosis Journal ; 28(3 Supplement):973-974, 2022.
Article in English | EMBASE | ID: covidwho-2138921
12.
Lab Medicine ; 52(5):E137-E146, 2021.
Article in English | EMBASE | ID: covidwho-2135433
13.
Journal of the American Society of Nephrology ; 33:310, 2022.
Article in English | EMBASE | ID: covidwho-2124498
14.
Journal of Clinical and Diagnostic Research ; 16(9):DC12-DC17, 2022.
Article in English | EMBASE | ID: covidwho-2067199
17.
American Journal of Transplantation ; 22(Supplement 3):640-641, 2022.
Article in English | EMBASE | ID: covidwho-2063541
18.
American Journal of Transplantation ; 22(Supplement 3):1060, 2022.
Article in English | EMBASE | ID: covidwho-2063522
19.
American Journal of Transplantation ; 22(Supplement 3):873, 2022.
Article in English | EMBASE | ID: covidwho-2063493
20.
American Journal of Transplantation ; 22(Supplement 3):766, 2022.
Article in English | EMBASE | ID: covidwho-2063482
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