8 research outputs found

    Fatores de risco maternos associados Ă  acidose fetal Maternal risk factors associated with fetal acidosis

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    OBJETIVOS: avaliar os fatores de risco maternos associados à acidose fetal. MÉTODOS: estudo tipo caso-controle composto por 188 recém-nascidos, sendo que 47 compuseram o grupo casos (pH de artéria umbilical <7,0) e 141 os de controles (pH de artéria umbilical <7,1 <7,3) nascidos imediatamente após cada caso. Consideraram-se fatores de inclusão: recém-nascidos de gestações únicas e sem malformação congênita. Analisaram-se variáveis maternas e fetais. Foram realizadas a Odds Ratio bruta e ajustada, teste t de Student, teste do qui-quadrado e análise multivariada através da regressão logística nãocondicional pelo método Enter. Assumiu-se como nível de significância estatística um p<0,05. RESULTADOS: no grupo de casos foi observado maior percentual de cesarianas, de recém-nascidos pré-termo, que apresentaram quase cinco vezes mais necessidade de cuidados intensivos e vinte cinco vezes mais chance de Apgar no 5º minuto <7. Não foram observadas associação entre os grupos e a apresentação fetal, idade materna, história de abortos anteriores, escolaridade materna e frequência ao pré-natal. Após a análise multivariada persistiram como fator de risco complicações relacionadas com a placenta e cordão. Os recémnascidos cujos partos associaram-se a complicações da placenta ou do cordão umbilical apresentaram três vezes mais chance de acidemia fetal. CONCLUSÕES: os recém-nascidos acidóticos estiveram relacionados à maior percentual de cesarianas, de prematuridade, necessidade de cuidados de tratamento intensivo e índice de Apgar <7 no 5º minuto. Após a análise multivariada, persistiram como fator de risco para acidemia fetal as complicações relacionadas ao descolamento prematuro de placenta e cordão umbilical.<br>OBJECTIVES: to assess maternal risk factors associated with fetal acidosis. METHODS: a case-control type study was conducted of 188 neonates, of whom 47 comprised the case group (umbilical arterial pH <7.0) and 141 the control (umbilical arterial pH E7.1 <7.3). The study included only single-gestation neonates without congenital malformations. Both maternal and fetal variables were taken into consideration. Statistical analysis involved the calculation of the raw and adjusted Odds Ratio, Student's t-test, the chi-squared test and multivariate analysis using Enter-method non-conditional logistic regression. The level of statistical significance was set at p<0.05. RESULTS: in the case group higher percentages of caesarian sections and pre-term births were observed, involving almost five times as much intensive care and twenty-five times more likelihood of Apgar in the 5th minute <7. No association was observed between the groups and fetal presentation, mother's age, history of miscarriage, years of schooling of mother or attendance at prenatal sessions. After multivariate analysis, the only risk factors that remained significant were complications relating to the placenta or the umbilical cord. Deliveries involving complications relating to the placenta or the umbilical cord were three times more likely to involve fetal acidemia. CONCLUSIONS: acidemia among neonates was associated with a higher percentage of caesarians, premature births, a need for intensive care and treatment and an Apgar index of <7 in the 5th minute. After multivariate analysis, complications relating to premature displacement of the placenta and the umbilical cord were the only remaining risk factors associated with fetal acidemia

    Effects of delayed versus immediate umbilical cord clamping in reducing death or major disability at 2 years corrected age among very preterm infants (APTS): a multicentre, randomised clinical trial

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    Background: Very preterm infants are at increased risk of adverse outcomes in early childhood. We assessed whether delayed clamping of the umbilical cord reduces mortality or major disability at 2 years in the APTS Childhood Follow Up Study. Methods: In this long-term follow-up analysis of the multicentre, randomised APTS trial in 25 centres in seven countries, infants (&lt;30 weeks gestation) were randomly assigned before birth (1:1) to have clinicians aim to delay clamping for 60 s or more or clamp within 10 s of birth, both without cord milking. The primary outcome was death or major disability (cerebral palsy, severe visual loss, deafness requiring a hearing aid or cochlear implants, major language or speech problems, or cognitive delay) at 2 years corrected age, analysed in the intention-to-treat population. This trial is registered with the Australian and New Zealand Clinical Trials Registry (ACTRN12610000633088). Findings: Between Oct 21, 2009, and Jan 6, 2017, consent was obtained for follow-up for 1531 infants, of whom 767 were randomly assigned to delayed clamping and 764 to immediate clamping. 384 (25%) of 1531 infants were multiple births, 862 (56%) infants were male, and 505 (33%) were born before 27 weeks gestation. 564 (74%) of 767 infants assigned to delayed clamping and 726 (96%) of 764 infants assigned to immediate clamping received treatment that fully adhered to the protocol. Death or major disability was determined in 1419 (93%) infants and occurred in 204 (29%) of 709 infants who were assigned to delayed clamping versus 240 (34%) of 710 assigned to immediate clamping, (relative risk [RR]) 0·83, 95% CI 0·72–0·95; p=0·010). 60 (8%) of 725 infants in the delayed clamping group and 81 (11%) of 720 infants in the immediate clamping group died by 2 years of age (RR 0·70, 95% CI 0·52–0·95); among those who survived, major disability at 2 years occurred in 23% (144/627) versus 26% (159/603) of infants, respectively (RR 0·88, 0·74–1·04). Interpretation: Clamping the umbilical cord at least 60 s after birth reduced the risk of death or major disability at 2 years by 17%, reflecting a 30% reduction in relative mortality with no difference in major disability. Funding: Australian National Health and Medical Research Council
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