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dc.creatorAggelina A., Pantazopoulos I., Giokas G., Chalkias A., Mavrovounis G., Papalois A., Douvanas A., Xanthos T., Iacovidou N.en
dc.date.accessioned2023-01-31T07:30:28Z
dc.date.available2023-01-31T07:30:28Z
dc.date.issued2021
dc.identifier10.1016/j.ajem.2021.04.009
dc.identifier.issn07356757
dc.identifier.urihttp://hdl.handle.net/11615/70301
dc.description.abstractBackground: Guidelines for neonatal resuscitation recommend a 3:1 compression to ventilation ratio. However, this recommendation is based on expert opinion and consensus rather than strong scientific evidence. Our primary aim was to assess whether continuous chest compressions with asynchronous ventilations would increase return of spontaneous circulation (ROSC) rate and survival compared to the 3:1 chest compression to ventilation ratio. Methods: This was a prospective, randomized, laboratory study. Twenty male Landrace-Large White pigs, aged 1–4 days with an average weight 1.650 ± 228.3 g were asphyxiated and left untreated until heart rate was less than 60 bpm or mean arterial pressure was below 15 mmHg. Animals were then randomly assigned to receive either continuous chest compressions with asynchronous ventilations (n = 10), or standard (3:1) chest compression to ventilation ratio (n = 10). Heart rate and arterial pressure were assessed every 30 s during cardiopulmonary resuscitation (CPR) until ROSC or asystole. All animals with ROSC were monitored for 4 h. Results: Coronary perfusion pressure (CPP) at 30 s of CPR was significantly higher in the experimental group (45.7 ± 16.9 vs. 21.8 ± 6 mmHg, p < 0.001) and remained significantly elevated throughout the experiment. End-tidal carbon dioxide (ETCO2) was also significantly higher in the experimental group throughout the experiment (23.4 ± 5.6 vs. 14.7 ± 5.9 mmHg, p < 0.001). ROSC was observed in six (60%) animals treated with 3:1 compression to ventilation ratio and nine (90%) animals treated with continuous chest compressions and asynchronous ventilation (p = 0.30). Time to ROSC was significantly lower in the experimental group (30 (30−30) vs. 60 (60–60) sec, p = 0.021). Of note, 7 (77.8%) animals in the experimental group and 1 (16.7%) animal in the control group achieved ROSC after 30 s (0.02). At 4 h, 2 (20%) animals survived in the control group compared to 7 (70%) animals in the experimental group (p = 0.022). Conclusion: Continuous chest compressions with asynchronous ventilations significantly improved CPP, ETCO2, time to ROSC, ROSC at 30 s and survival in a porcine model of neonatal resuscitation. © 2021 Elsevier Inc.en
dc.language.isoenen
dc.sourceAmerican Journal of Emergency Medicineen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85103764189&doi=10.1016%2fj.ajem.2021.04.009&partnerID=40&md5=31252a517dcdf2661ae5fa8a01182caa
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectarterial pressureen
dc.subjectArticleen
dc.subjectasphyxiaen
dc.subjectcontinuous chest compressionen
dc.subjectcontrolled studyen
dc.subjectcoronary artery blood flowen
dc.subjectend tidal carbon dioxide tensionen
dc.subjectheart arresten
dc.subjectheart rateen
dc.subjectLandrace pigen
dc.subjectlung ventilationen
dc.subjectmaleen
dc.subjectnewbornen
dc.subjectnewborn careen
dc.subjectnonhumanen
dc.subjectpigen
dc.subjectporcine modelen
dc.subjectpriority journalen
dc.subjectprospective studyen
dc.subjectresuscitationen
dc.subjectreturn of spontaneous circulationen
dc.subjectsurvivalen
dc.subjectanimalen
dc.subjectasphyxiaen
dc.subjectdouble blind procedureen
dc.subjectheart arresten
dc.subjectproceduresen
dc.subjectrandomizationen
dc.subjectresuscitationen
dc.subjecttreatment outcomeen
dc.subjectAnimalsen
dc.subjectAnimals, Newbornen
dc.subjectAsphyxiaen
dc.subjectCardiopulmonary Resuscitationen
dc.subjectDouble-Blind Methoden
dc.subjectHeart Arresten
dc.subjectMaleen
dc.subjectProspective Studiesen
dc.subjectRandom Allocationen
dc.subjectSus scrofaen
dc.subjectTreatment Outcomeen
dc.subjectW.B. Saundersen
dc.titleContinuous chest compressions with asynchronous ventilation improve survival in a neonatal swine model of asphyxial cardiac arresten
dc.typejournalArticleen


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