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Auswahl der wissenschaftlichen Literatur zum Thema „Hypoxie foetale – diagnostic“
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Zeitschriftenartikel zum Thema "Hypoxie foetale – diagnostic"
G N, Manjunath. „Importance of Doppler study of Umbilical Artery and FoetalMiddle Cerebral Artery in PIH and IUGR“. Annals of International Medical and Dental Research 8, Nr. 1 (15.01.2022): 287–95. http://dx.doi.org/10.53339/aimdr.2022.8.1.37.
Der volle Inhalt der QuelleLavanya B, Rashmi Ullagaddi, Pavani M und K. Srinivas Rao. „Evaluation of serum lactate dehydrogenase as early diagnostic biomarker in pregnancy with preeclampsia and eclampsia“. Indian Journal of Obstetrics and Gynecology Research 9, Nr. 1 (15.02.2022): 83–87. http://dx.doi.org/10.18231/j.ijogr.2022.016.
Der volle Inhalt der QuelleMurugan, R., C. Hastie, N. Narayanan und S. Wong. „622 Potential Application of Electrocardiographs (ECG) to Diagnose Breech Presentations of Fetuses“. British Journal of Surgery 108, Supplement_2 (01.05.2021). http://dx.doi.org/10.1093/bjs/znab134.210.
Der volle Inhalt der QuelleMonika Kochhar, Seema Acharya und Ragini Singh. „To Evaluate Diagnostic Efficacy of Nucleated Red Blood Cells (NRBCs) in Neonatal Sepsis“. Journal of Evolution of Medical and Dental Sciences, 21.04.2022, 557–62. http://dx.doi.org/10.14260/jemds/2022/112.
Der volle Inhalt der QuelleDissertationen zum Thema "Hypoxie foetale – diagnostic"
Chevalier, Geoffroy. „Analyse de la variabilité de la fréquence cardiaque en cas de syndrome de réponse inflammatoire fœtale aigu isolé ou associé à une hypoxie : Étude expérimentale chez le foetus de brebis“. Electronic Thesis or Diss., Université de Lille (2022-....), 2024. http://www.theses.fr/2024ULILS060.
Der volle Inhalt der QuelleIntroduction: Fetal infection during labor, accompanied by fetal inflammatory response syndrome (FIRS), is linked to neurodevelopmental impairments, cerebral palsy, neonatal sepsis, and even mortality. Existing diagnostic methods for FIRS remain insufficient. Acidosis associated with FIRS during labor presents a significant risk to the fetus. This study hypothesizes that analysing fetal heart rate variability (HRV) could serve as a tool for detecting FIRS. Therefore, the first study aim was to explore whether fetal HRV change during FIRS and the second aim was to explore how HRV changes during acute FIRS-associated hypoxia, compared to isolated hypoxia. Material and methods: In near-term fetal sheep with chronic instrumentation, lipopolysaccharide (LPS) was administered intravenously to simulate FIRS, while a control group received an injection of saline solution. Hemodynamic parameters, blood gas levels, interleukin-6 (IL-6), and 14 heart rate variability (HRV) indices were recorded during a stability period and for six hours after injection. For these different parameters, hourly comparisons were made between the LPS and control groups. For the second aim, two other groups were compared: one with isolated hypoxia, the other with hypoxia and FIRS. Worsening hypoxia was induced by repeated umbilical cord occlusions in three one-hour phases: mild, moderate, and severe. Hemodynamic, gasometric, and HRV parameters were compared between the groups. Results: For the first aim, a total of 15 lambs were instrumented. In the LPS-treated group (n = 8), IL-6 levels significantly increased following LPS administration (p < 0.001), validating the FIRS model. Additionally, fetal heart rate showed a significant increase after H5 (p < 0.01). Significant differences between LPS and control groups were observed between H2 and H4 for five HRV measures (Standard Deviation of Normal to Normal (SDNN), Standard Deviation 2 (SD2), Detrended Fluctuation Analysis (DFA) alpha 1 and 2 and Long-Term Variability (LTV)). The hypoxia and FIRS group had a higher mortality rate (n = 4/9) compared with isolated hypoxia group (n = 0/9). Gasometric state was altered earlier in the hypoxia and FIRS group after mild occlusions (pH = 7.22 [7.12–7.24] vs 7.28 [7.23–7.34], p = 0.01; lactate = 10.3 mmol/L [9.4–11.0] vs 6.0 mmol/L [4.1–8.2], p <0.001). After mild occlusions, the hypoxia and FIRS group had higher values for six HRV parameters compared with the hypoxia group (SDNN, Root Mean Square of Successive Differences (RMSSD), Short Term Variability (STV), LTV, Low Frequencies (LF) and High frequencies (HF). After moderate occlusions, only SDNN and RMSSD remained significantly higher. Conclusion: During acute FIRS, associated or not with hypoxia, HRV is significantly changed. These changes appear to be mediated by an increase of global variability and a loss of signal complexity. HRV indices may therefore be valuable for early detection in these two situations
Serrière, Sophie. „Recherche de biomarqueurs précoces par SRM 1 H haute résolution dans l'hypoxie ischémie cérébrale néonatale et dans l'inflammation materno-foetale“. Tours, 2005. http://www.theses.fr/2005TOUR3308.
Der volle Inhalt der QuelleA metabonomic approach using high resolution resonance magnetic spectroscopy was investigated on newborn (piglet model of cerebral hypoxia ischemia) and maternal (rat model of maternofetal inflammation induced by E Coli lipopolysaccharid injections) biological fluids. The aim of this study was to evidence an early biomarker of these two pathologies. Neither in the urine and nor in the cerebrospinal fluid of hypoxic ischemic animals, specifi biomarkers of the pathology were evidenced. Metabonomic studies combined with multivaried analysis on the maternal blood plasma and on the amniotic fluid of inflammation-induced animals at day eighteen and nineteen of gestation had evidenced some specific biomarkers. In addition, inflammation impact was demonstrated on pregnancy outcome, on the mean number of newborn per litter and on the newborn growth during the fourteen's days of life