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Assessing variability in neonatal blood pressure, notably in hypotension
Germaine Cornelissen, Franz Halberg, Elena Vasilievna Syutkina, Galina Victorovna Yatsyk, Anatoly Victorovich Masalov, Othild Schwartzkopff, Dana Johnson
Jazyk angličtina Země Česko
NLK
Free Medical Journals
od 2003 do 2013
Freely Accessible Science Journals
od 2003 do 2013
ROAD: Directory of Open Access Scholarly Resources
od 2002
- MeSH
- biomedicínský výzkum MeSH
- cerebrovaskulární poruchy diagnóza etiologie MeSH
- chronobiologie (obor) metody MeSH
- cirkadiánní rytmus MeSH
- dítě MeSH
- experimenty na lidech MeSH
- financování organizované MeSH
- hypotenze diagnóza etiologie komplikace MeSH
- kojenec MeSH
- krevní tlak fyziologie MeSH
- lidé MeSH
- měření krevního tlaku metody využití MeSH
- mozková hypoxie a ischemie diagnóza etiologie komplikace MeSH
- nervový systém patofyziologie patologie růst a vývoj MeSH
- růst a vývoj fyziologie MeSH
- statistika jako téma MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
New reports corroborate our prior finding that hypotension in infancy is associated with impaired neurodevelopment later in childhood. We had also found that neurological deficit is further associated with a more pronounced circadian variation in transcutaneous pO2 (tcpO2). New evidence in adulthood prompts the recommendation to automatically monitor vital signs for continued surveillance, relying on the methods of chronobiology for data analysis as-one-goes. This applies notably early in extra-uterine life when infants may be particularly sensitive to ischemic cerebral injury secondary to systemic hypotension. Monitoring at this sensitive lifetime stage has also provided a glimpse of unseen effects of the cosmos on the patterns of blood pressure variability, detected by chronomics.
Citace poskytuje Crossref.org
Lit.: 16
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- $a New reports corroborate our prior finding that hypotension in infancy is associated with impaired neurodevelopment later in childhood. We had also found that neurological deficit is further associated with a more pronounced circadian variation in transcutaneous pO2 (tcpO2). New evidence in adulthood prompts the recommendation to automatically monitor vital signs for continued surveillance, relying on the methods of chronobiology for data analysis as-one-goes. This applies notably early in extra-uterine life when infants may be particularly sensitive to ischemic cerebral injury secondary to systemic hypotension. Monitoring at this sensitive lifetime stage has also provided a glimpse of unseen effects of the cosmos on the patterns of blood pressure variability, detected by chronomics.
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