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10.1055/s-0034-1387930 http://scihub22266oqcxt.onion/10.1055/s-0034-1387930 C4369158!4369158 !25241107     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25241107 &cmd=llinks): Failed to open stream: HTTP request failed! 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Effect of magnesium sulfate administration for neuroprotection on latency in women with preterm premature rupture of membranes |pdf=|usr=}}{{25241107 }} gab.com Text Effect of magnesium sulfate administration for neuroprotection on latency in women with preterm premature rupture of membranes JO: Am J Perinatol http://www.kidney.de/pget.php?&tw=1&pmid=25241107 #FOAvip OBJECTIVE: This study aims to evaluate whether magnesium sulfate administration for neuroprotection prolongs latency in women with preterm premature rupture of membranes (PPROM) between 24 and 31(6/7) weeks' gestation. STUDY DESIGN: This is a secondary analysis of a randomized controlled trial of magnesium sulfate for prevention of cerebral palsy. Gravid women with a singleton pregnancy between 24 and 31(6/7) weeks' gestation with PPROM without evidence of labor were randomized to receive magnesium sulfate, administered intravenously as a 6-g bolus followed by a constant infusion of 2 g per hour up to 12 hours, or placebo. Maternal outcomes for this analysis were delivery in less than 48 hours and in less than 7 days from randomization. Neonatal outcomes included a composite of respiratory distress syndrome, interventricular hemorrhage grades 3 or 4, periventricular leukomalacia, sepsis, necrotizing enterocolitis, retinopathy of prematurity, or death. RESULTS: A total of 1,259 women were included. The rate of delivery < 48 hours was not different in the magnesium sulfate and the placebo groups (22.2 and 20.7%, p = 0.51). Delivery < 7 days was similar between groups (55.4 and 51.4%, p = 0.16). Median latency was also similar between groups (median [interquartile range], 6.0 days [range, 2.4-13.8 days] and 6.6 days [range, 2.4-15.1 days], p = 0.29). Composite neonatal outcomes did not differ between groups. CONCLUSION: Magnesium sulfate administration given for neuroprotection in women with a singleton gestation with PPROM and without labor before 32 weeks does not impact latency. Twit Text FOAVip Effect of magnesium sulfate administration for neuroprotection on latency in women with preterm premature rupture of membranes ????Am J Perinatol http://www.kidney.de/pget.php?&tw=1&pmid=25241107 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25241107 #FOAvip English Wikipedia <ref>{{Cite pmid|25241107 }}</ref> Effect of magnesium sulfate administration for neuroprotection on latency in women with preterm premature rupture of membranes #MMPMID25241107 Horton AL ; Lai Y ; Rouse DJ ; Spong CY ; Leveno KJ ; Varner MW ; Mercer BM ; Iams JD ; Wapner RJ ; Sorokin Y ; Thorp JM ; Ramin SM ; Malone FD ; O'Sullivan MJ ; Hankins GD ; Caritis SN Am J Perinatol 2015[Mar]; 32 (4 ): 387-92 PMID25241107 show ga OBJECTIVE: This study aims to evaluate whether magnesium sulfate administration for neuroprotection prolongs latency in women with preterm premature rupture of membranes (PPROM) between 24 and 31(6/7) weeks' gestation. STUDY DESIGN: This is a secondary analysis of a randomized controlled trial of magnesium sulfate for prevention of cerebral palsy. Gravid women with a singleton pregnancy between 24 and 31(6/7) weeks' gestation with PPROM without evidence of labor were randomized to receive magnesium sulfate, administered intravenously as a 6-g bolus followed by a constant infusion of 2 g per hour up to 12 hours, or placebo. Maternal outcomes for this analysis were delivery in less than 48 hours and in less than 7 days from randomization. Neonatal outcomes included a composite of respiratory distress syndrome, interventricular hemorrhage grades 3 or 4, periventricular leukomalacia, sepsis, necrotizing enterocolitis, retinopathy of prematurity, or death. RESULTS: A total of 1,259 women were included. The rate of delivery < 48 hours was not different in the magnesium sulfate and the placebo groups (22.2 and 20.7%, p = 0.51). Delivery < 7 days was similar between groups (55.4 and 51.4%, p = 0.16). Median latency was also similar between groups (median [interquartile range], 6.0 days [range, 2.4-13.8 days] and 6.6 days [range, 2.4-15.1 days], p = 0.29). Composite neonatal outcomes did not differ between groups. CONCLUSION: Magnesium sulfate administration given for neuroprotection in women with a singleton gestation with PPROM and without labor before 32 weeks does not impact latency. |Adult [MESH] |Cerebral Palsy/prevention & control [MESH] |Delivery, Obstetric [MESH] |Female [MESH] |Fetal Membranes, Premature Rupture/*drug therapy [MESH] |Gestational Age [MESH] |Humans [MESH] |Infant, Newborn [MESH] |Infant, Premature [MESH] |Infant, Premature, Diseases/prevention & control [MESH] |Magnesium Sulfate/*therapeutic use [MESH] |Neuroprotective Agents/*therapeutic use [MESH] |Obstetric Labor, Premature/prevention & control [MESH] |Pregnancy [MESH] |Tocolytic Agents/*therapeutic use [MESH] |Treatment Outcome [MESH]Effect of magnesium sulfate administration for neuroprotection on late(epmc).pdf DeepDyve Pubget Overpricing