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1.
Electronic Journal of General Medicine ; 18(3):1-8, 2021.
Article in English | CINAHL | ID: covidwho-1219966

ABSTRACT

Objective: The COVID-19 is a rapidly ongoing pandemic. 368.513 cases and 10.027 fatalities have been reported in Turkey up to this day. Pregnant women and newborns constitute a special patient group in this disease. In our study, we aimed to measure the knowledge level, attitude to protective measures, perspective of education and medicolegal issues of obstetricians - gynecologists (OB-GYN) and pediatricians on pregnant and newborn health about COVID-19. Material-Methods: A cross-sectional, online-survey consisted of 22 questions. Age, academic degree, duration of the profession in the first three questions, level of knowledge about COVID-19 in the next 14 questions, attitude to protective measures, perspective of education and medicolegal issues in the last five questions were queried. Results: The questionnaire was applied to 145 physicians. 65.5% of them were pediatricians, 34.4% were OB-GYN. The level of having adequate knowledge about COVID-19 was determined as 44% and 34.7% for OB-GYN and pediatricians. No statistically significant relationship was found between the way of acquiring knowledge and academic degree in both physician groups (p>0.05). Positive attitude of OB-GYN about preventive measures during - after the pandemic were 94% - 90%, 96.8% - 92.6% for pediatricians. The positive perspective of education and medicolegal measures were determined 72% and 80 % for OB-GYN, 80% and 94.7% for pediatricians. Conclusion: Current education related to clinic approach- treatment algoritms about COVID-19 on pregnant and newborn health should be increased for OB-GYN and pediatricians, legal arrangements should be made to make them feel safe.

2.
Cellular and molecular biology (Noisy-le-Grand, France) ; 66(3):221-229, 2020.
Article | WHO COVID | ID: covidwho-601948

ABSTRACT

It can be misleading to think that the new severe acute respiratory syndrome coronavirus (SARS-CoV2) which has a very strong mutation and adaptation capabilities, uses only the angiotensin-converting enzyme II (ACE2) pathway to reach target cells. Despite all the precautions taken, the pandemic attack continues and the rapid increase in the number of deaths suggest that this virus has entered the cell through different pathways and caused damage through different mechanisms. The main reason why the ACE2 pathway comes to the fore in all scientific studies is that this receptor is located at the entry point of basic mechanisms that provide alveolo-capillary homeostasis. SARS-CoV-2 has to use nuclear factor-kappaB (NF-kB), caveloae, clathrin, lipoxin, serine protease and proteasome pathways in addition to ACE2 to enter the target cell and initiate damage. For this reason, while new drug development studies are continuing, in order to be beneficial to patients in their acute period, it is imperative that we are able to come up with drugs that activate or inhibit these pathways and are currently in clinical use. It is also critical that we adopt these new pathways to the treatment of pregnant women affected by SARS-CoV-2, based on the scientific data we use to treat the general population.

3.
Cell Mol Biol (Noisy-le-grand) ; 66(3): 221-229, 2020 Jun 05.
Article in English | MEDLINE | ID: covidwho-603065

ABSTRACT

It can be misleading to think that the new severe acute respiratory syndrome coronavirus (SARS-CoV2) which has a very strong mutation and adaptation capabilities, uses only the angiotensin-converting enzyme II (ACE2) pathway to reach target cells. Despite all the precautions taken, the pandemic attack continues and the rapid increase in the number of deaths suggest that this virus has entered the cell through different pathways and caused damage through different mechanisms. The main reason why the ACE2 pathway comes to the fore in all scientific studies is that this receptor is located at the entry point of basic mechanisms that provide alveolo-capillary homeostasis. SARS-CoV-2 has to use nuclear factor-κB (NF-kB), caveloae, clathrin, lipoxin, serine protease and proteasome pathways in addition to ACE2 to enter the target cell and initiate damage. For this reason, while new drug development studies are continuing, in order to be beneficial to patients in their acute period, it is imperative that we are able to come up with drugs that activate or inhibit these pathways and are currently in clinical use. It is also critical that we adopt these new pathways to the treatment of pregnant women affected by SARS-CoV-2, based on the scientific data we use to treat the general population.


Subject(s)
Betacoronavirus/metabolism , Caveolin 1/metabolism , Coronavirus Infections/metabolism , Lipoxins/metabolism , NF-kappa B/metabolism , Pneumonia, Viral/metabolism , Pregnancy Complications, Infectious/metabolism , Proteasome Endopeptidase Complex/metabolism , Angiotensin II Type 1 Receptor Blockers/therapeutic use , Angiotensin-Converting Enzyme 2 , Anticholesteremic Agents/therapeutic use , Binding Sites , COVID-19 , Coronavirus Infections/drug therapy , Coronavirus Infections/transmission , Coronavirus Infections/virology , Drug Discovery/methods , Drug Repositioning/methods , Female , Humans , Infectious Disease Transmission, Vertical/prevention & control , NF-kappa B/antagonists & inhibitors , Off-Label Use , Pandemics , Peptidyl-Dipeptidase A/metabolism , Pneumonia, Viral/drug therapy , Pneumonia, Viral/transmission , Pneumonia, Viral/virology , Pregnancy , Pregnancy Complications, Infectious/virology , Proteasome Inhibitors/therapeutic use , SARS-CoV-2 , Serine Endopeptidases/metabolism , Serine Proteinase Inhibitors/therapeutic use , Virus Internalization
4.
Placenta ; 97: 1-5, 2020 08.
Article in English | MEDLINE | ID: covidwho-437293

ABSTRACT

Although many pregnant women have been infected by coronavirus, the presence of intrauterine vertical transmission has not been conclusively reported yet. What prevents this highly contagious virus from reaching the fetus? Is it only the presence of a strong placental barrier, or is it the natural absence of the some receptor that the viruses use for transmission? We, therefore, need to comprehensively understand the mechanism of action of the mammalian epithelial barriers located in two different organs with functional similarity. The barriers selected as potential targets by SARS-CoV-2 are the alveolo-capillary barrier (ACB), and the syncytio-capillary barrier (SCB). Caveolae are omega-shaped structures located on the cell membrane. They consist of caveolin-1 protein (Cav-1) and are involved in the internalisation of some viruses. By activating leukocytes and nuclear factor-κB, Cav-1 initiates inflammatory reactions. The presence of more than one Cav-1 binding sites on coronavirus is an important finding supporting the possible relationship between SARS-CoV-2-mediated lung injury. While the ACB cells express Cav-1 there is no caveolin expression in syncytiotrophoblasts. In this short review, we will try to explain our hypothesis that the lack of caveolin expression in the SCB is one of the most important physiological mechanisms that prevents vertical transmission of SARS-CoV-2. Since the physiological Cav-1 deficiency appears to prevent acute cell damage treatment algorithms could potentially be developed to block this pathway in the non-pregnant population affected by SARS-CoV-2.


Subject(s)
Betacoronavirus/physiology , Coronavirus Infections/prevention & control , Coronavirus Infections/transmission , Fetal Diseases/prevention & control , Infectious Disease Transmission, Vertical/prevention & control , Maternal-Fetal Exchange/immunology , Pandemics/prevention & control , Pneumonia, Viral/prevention & control , Pneumonia, Viral/transmission , Betacoronavirus/immunology , COVID-19 , Caveolin 1/physiology , Coronavirus Infections/immunology , Epithelium/physiology , Epithelium/virology , Female , Fetal Diseases/immunology , Fetal Diseases/virology , Giant Cells/physiology , Giant Cells/virology , Humans , Immunity, Innate/physiology , Pneumonia, Viral/immunology , Pregnancy , Risk Factors , SARS-CoV-2 , Virus Internalization
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