Quinolones cross maternal barriers into amniotic fluid and breast milk

1990 ◽  
Vol &NA; (720) ◽  
pp. 17
Author(s):  
&NA;
Keyword(s):  
2007 ◽  
Vol 34 (2) ◽  
pp. 191-204 ◽  
Author(s):  
Carol L. Wagner ◽  
Sarah N. Taylor ◽  
Donna Johnson

2021 ◽  
Vol 10 (22) ◽  
pp. 5253
Author(s):  
Cosmin Citu ◽  
Radu Neamtu ◽  
Virgiliu-Bogdan Sorop ◽  
Delia Ioana Horhat ◽  
Florin Gorun ◽  
...  

We designed and implemented a prospective study to analyze the maternal and neonatal outcomes associated with COVID-19 and determine the likelihood of viral transmission to the fetus and newborn by collecting samples from amniotic fluid, placenta, umbilical cord blood, and breast milk. The study followed a prospective observational design, starting in July 2020 and lasting for one year. A total of 889 pregnant women were routinely tested for SARS-CoV-2 infection in an outpatient setting at our clinic, using nasal swabs for PCR testing. A total of 76 women were diagnosed with COVID-19. The positive patients who accepted study enrollment were systematically analyzed by collecting weekly nasal, urine, fecal, and serum samples, including amniotic fluid, placenta, umbilical cord, and breast milk at hospital admission and postpartum. Mothers with COVID-19 were at a significantly higher risk of developing gestational hypertension and giving birth prematurely by c-section than the general pregnant population. Moreover, their mortality rates were substantially higher. Their newborns did not have negative outcomes, except for prematurity, and an insignificant number of newborns were infected with SARS-CoV-2 (5.4%). No amniotic fluid samples were positive for SARS-CoV-2, and only 1.01% of PCR tests from breast milk were confirmed positive. Based on these results, we support the idea that SARS-CoV-2 positive pregnant women do not expose their infants to an additional risk of infection via breastfeeding, close contact, or in-utero. Consequently, we do not support maternal–newborn separation at delivery since they do not seem to be at an increased risk of SARS-CoV-2 infection.


2021 ◽  
Vol 1 (2) ◽  
Author(s):  
Alen J Salerian

This paper advances a previous hypothesis “Human body may produces bacteria”, and proposes that some infections may be endogenous. It has been demonstrated that the Christensenellaceae, a family in the phylum Firmicutes, is heritable suggesting that human genetic material and gut bacterial material are related and human cells may generate some gut microbes It has also been shown that the fetus is exposed to bacteria prior to birth -without any evidence that they are contaminants or acquired from the environment -suggesting a possible endogenous origin of bacteria in breast milk, meconium, placenta , umbilical cord blood and amniotic fluid. Malassezia yeasts are not contagious, not culturable from the environment, cannot colonize human skin by inoculation without occlusion and neonate skin is free of Malassezia but is colonized in the first month of life suggesting that they may be endogenous. Human stem cells seem to be the most likely candidates to produce microbes: This is because they differentiate to epithelial cells and cancer cells and contain the essentials to transform to microorganisms. Future experimental studies are necessary to validate this hypothesis which may offer a new paradigm to combat opportunistic infections of possible endogenous origin.


2020 ◽  
Vol 36 (9) ◽  
pp. 999-1007
Author(s):  
Rachel Filler ◽  
Bo Li ◽  
Sinobol Chusilp ◽  
Agostino Pierro

2002 ◽  
Vol 37 (1) ◽  
pp. 1-6 ◽  
Author(s):  
M.P. Michalsky ◽  
M. Lara-Marquez ◽  
L. Chun ◽  
G.E. Besner

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