170 research outputs found
Competing risk models of stillbirth inform populations but not individuals.
This is the final version of the article. It first appeared from Wiley via http://dx.doi.org/10.1111/1471-0528.1394
The relationship between human placental morphometry and ultrasonic measurements of utero-placental blood flow and fetal growth.
INTRODUCTION: Ultrasonic fetal biometry and arterial Doppler flow velocimetry are widely used to assess the risk of pregnancy complications. There is an extensive literature on the relationship between pregnancy outcomes and the size and shape of the placenta. However, ultrasonic fetal biometry and arterial Doppler flow velocimetry have not previously been studied in relation to postnatal placental morphometry in detail. METHODS: We conducted a prospective cohort study of nulliparous women in The Rosie Hospital, Cambridge (UK). We studied a group of 2120 women who had complete data on uterine and umbilical Doppler velocimetry and fetal biometry at 20, 28 and 36 weeks' gestational age, digital images of the placenta available, and delivered a liveborn infant at term. Associations were expressed as the difference in the standard deviation (SD) score of the gestational age adjusted ultrasound measurement (z-score) comparing the lowest and highest decile of the given placental morphometric measurement. RESULTS: The lowest decile of placental surface area was associated with 0.87 SD higher uterine artery Doppler mean pulsatility index (PI) at 20 weeks (95% CI: 0.68 to 1.07, P < 0.001). The lowest decile of placental weight was associated with 0.73 SD higher umbilical artery Doppler PI at 36 weeks (95% CI: 0.54 to 0.93, P < 0.001). The lowest decile of both placental weight and placental area were associated with reduced growth velocity of the fetal abdominal circumference between 20 and 36 weeks (both P < 0.001). CONCLUSION: Placental area and weight are associated with uterine and umbilical blood flow, respectively, and both are associated with fetal growth rate.This study was funded by the NIHR Cambridge Comprehensive Biomedical Research Centre (grant number A019057) and Stillbirth and Neonatal Death Society (SANDS). GE donated two ultrasound machines for use in the project.This is the author accepted manuscript. The final version is available from Elsevier via http://dx.doi.org/10.1016/j.placenta.2015.12.00
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Blinded ultrasonic fetal biometry at 36 weeks and the risk of emergency caesarean delivery: A prospective cohort study of 3,047 low risk nulliparous women
OBJECTIVES: We studied the risk of emergency caesarean delivery (CD) using blinded ultrasonographic estimated fetal weight (EFW) at 36 weeks of gestational age (wkGA): (1) to compare the association for customised and non-customised EFW, (2) to determine whether adding ultrasonic EFW improved prediction based on maternal characteristics alone, and (3) to determine whether women at high predicted risk of emergency CD had higher risks of maternal and perinatal morbidity than other women. METHODS: We studied 3,047 low risk women (no pre-existing medical conditions or acquired complications of pregnancy) from the Pregnancy Outcome Prediction study (Cambridge UK) who had ultrasonic EFW at ~36 weeks gestational age, where women and clinicians were blinded to the result. RESULTS: Blinded EFW was strongly associated with the risk of emergency CD (coefficient for a 1 standard deviation increase in EFW = 0.39 [95% CI 0.30 to 0.48], odds ratio [OR] = 1.48 [95% CI 1.35 to 1.62]). The coefficient for customised EFW was similar (0.42 [95% CI 0.33 to 0.51], OR = 1.53 [95% CI 1.39 to 1.67]), hence, for simplicity, non-customised EFW was subsequently employed. Maternal characteristics (age, height, body mass index, and weight gain between 12 and 36 weeks) when combined in a multivariate logistic regression model were moderately predictive for emergency CD (AUROCC = 0.68). Adding blinded EFW to the model increased the AUROCC to 0.71 and this model was more predictive (P < 0.0001). When using this model and defining screen positive as a predicted risk of emergency CD ≥40%, 189 (6.2%) women screened positive and the proportion delivered by caesarean was 48%. Compared with screen negative women, they had elevated risks (relative risk [95% CI]) of severe postpartum hemorrhage (2.49 [1.83 to 3.38]), any adverse neonatal outcome (1.86 [1.22 to 2.82]), and severe adverse neonatal outcome (4.03 [1.35 to 12.03]). The risks of these events were also higher compared to women who had a term CD for breech presentation. The model was similarly predictive of the risk of emergency CD and perinatal morbidity when evaluated using routinely collected data from 55,337 births in Scotland between 2003 and 2008. CONCLUSIONS: Ultrasonic EFW at 36 weeks, combined with maternal characteristics, identifies women who are at increased risk of subsequent emergency CD. These women were at increased risk of maternal and perinatal morbidity compared with women at low risk of emergency CD and with women having CD for breech presentation at term
Effect of Body Mass Index on pregnancy outcomes in nulliparous women delivering singleton babies
Peer reviewedPublisher PD
Bias modelling in evidence synthesis
Policy decisions often require synthesis of evidence from multiple sources, and the source studies typically vary in rigour and in relevance to the target question. We present simple methods of allowing for differences in rigour (or lack of internal bias) and relevance (or lack of external bias) in evidence synthesis. The methods are developed in the context of reanalysing a UK National Institute for Clinical Excellence technology appraisal in antenatal care, which includes eight comparative studies. Many were historically controlled, only one was a randomized trial and doses, populations and outcomes varied between studies and differed from the target UK setting. Using elicited opinion, we construct prior distributions to represent the biases in each study and perform a bias‐adjusted meta‐analysis. Adjustment had the effect of shifting the combined estimate away from the null by approximately 10%, and the variance of the combined estimate was almost tripled. Our generic bias modelling approach allows decisions to be based on all available evidence, with less rigorous or less relevant studies downweighted by using computationally simple methods
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Universal versus selective ultrasonography to screen for large for gestational age infants and associated morbidity
Objective
To compare the diagnostic effectiveness of selective versus universal ultrasonography as a screening test for large for gestational age (LGA) infants, and to determine whether previously described ultrasonic markers of excessive fetal growth could identify which suspected LGA fetuses were at increased risk of neonatal morbidity.
Methods
We analysed data from a prospective cohort study of nulliparous women, the Pregnancy Outcome Prediction study. All women had clinically indicated scans as per routine care. Additionally, all women had blinded ultrasonic estimated fetal weight (EFW) performed at around 36 weeks of gestational age (wkGA). Screen positive for LGA was defined as an EFW >90th percentile ≥34wkGA.
Results
The current analysis included 3,866 eligible women. Of these, 177 (5%) infants had a birth weight >90th percentile. 1,354 (35%) women had a clinically indicated ultrasonography ≥34wkGA. The sensitivity of selective ultrasonography was 27% and the sensitivity of universal ultrasonography was 38%. The specificity of both approaches was high (99% and 97%, respectively). Using universal ultrasonography, neonatal outcome differed (P for interaction) by abdominal circumference growth velocity (ACGV) for both any neonatal morbidity (P = 0.08) and severe adverse neonatal outcome (P = 0.03). LGA fetuses with increased ACGV had a relative risk (95% CI, P) of any neonatal morbidity of 2.0 (1.1-3.6, P = 0.04) and severe adverse neonatal outcome of 6.5 (2.0-21.1, P = 0.01), whereas LGA fetuses with normal ACGV were not at increased risk.
Conclusion
Screening using universal ultrasonographic fetal biometry increases the detection of LGA infants and combined with ACGV identifies infants at increased risk of adverse neonatal outcome.The work was supported by the National Institute for Health Research (NIHR) Cambridge Comprehensive Biomedical Research Centre (Women's Health theme), and a project grant from the Stillbirth and neonatal death society (Sands). The study was also supported GE Healthcare (donation of two Voluson i ultrasound systems for this study), and by the NIHR Cambridge Clinical Research Facility, where all research visits took place
Elevated risk of stillbirth in males: systematic review and meta-analysis of more than 30 million births
Background
Stillbirth rates have changed little over the last decade, and a high proportion of cases are unexplained. This meta-analysis examined whether there are inequalities in stillbirth risks according to sex.
Methods
A systematic review of the literature was conducted, and data were obtained on more than 30 million birth outcomes reported in observational studies. The pooled relative risk of stillbirth was estimated using random-effects models.
Results
The crude mean rate (stillbirths/1,000 total births) was 6.23 for males and 5.74 for females. The pooled relative risk was 1.10 (95% confidence interval (CI): 1.07-1.13). The attributable fraction in the whole population was 4.2% (95% CI: 3.70-4.63), and the attributable fraction among male fetuses was 7.8% (95% CI: 7.0-8.66). Study populations from countries with known sex-biased sex selection issues had anomalous stillbirth sex ratios and higher overall stillbirth risks than other countries, reflecting increased mortality among females.
Conclusions
Risk of stillbirth in males is elevated by about 10%. The population-attributable risk is comparable to smoking and equates to approximately 100,000 stillbirths per year globally. The pattern is consistent across countries of varying incomes. Given current difficulties in reducing stillbirth rates, work to understand the causes of excess male risk is warranted. We recommend that stillbirths are routinely recorded by sex. This will also assist in exposing prenatal sex selection as elevated or equal risks of stillbirth in females would be readily apparent and could therefore be used to trigger investigation
Conceptualizing pathways linking women's empowerment and prematurity in developing countries.
BackgroundGlobally, prematurity is the leading cause of death in children under the age of 5. Many efforts have focused on clinical approaches to improve the survival of premature babies. There is a need, however, to explore psychosocial, sociocultural, economic, and other factors as potential mechanisms to reduce the burden of prematurity. Women's empowerment may be a catalyst for moving the needle in this direction. The goal of this paper is to examine links between women's empowerment and prematurity in developing settings. We propose a conceptual model that shows pathways by which women's empowerment can affect prematurity and review and summarize the literature supporting the relationships we posit. We also suggest future directions for research on women's empowerment and prematurity.MethodsThe key words we used for empowerment in the search were "empowerment," "women's status," "autonomy," and "decision-making," and for prematurity we used "preterm," "premature," and "prematurity." We did not use date, language, and regional restrictions. The search was done in PubMed, Population Information Online (POPLINE), and Web of Science. We selected intervening factors-factors that could potentially mediate the relationship between empowerment and prematurity-based on reviews of the risk factors and interventions to address prematurity and the determinants of those factors.ResultsThere is limited evidence supporting a direct link between women's empowerment and prematurity. However, there is evidence linking several dimensions of empowerment to factors known to be associated with prematurity and outcomes for premature babies. Our review of the literature shows that women's empowerment may reduce prematurity by (1) preventing early marriage and promoting family planning, which will delay age at first pregnancy and increase interpregnancy intervals; (2) improving women's nutritional status; (3) reducing domestic violence and other stressors to improve psychological health; and (4) improving access to and receipt of recommended health services during pregnancy and delivery to help prevent prematurity and improve survival of premature babies.ConclusionsWomen's empowerment is an important distal factor that affects prematurity through several intervening factors. Improving women's empowerment will help prevent prematurity and improve survival of preterm babies. Research to empirically show the links between women's empowerment and prematurity is however needed
Risk of uterine rupture in women undergoing trial of labour with a history of both a caesarean section and a vaginal delivery
Evolutionary history of endogenous Human Herpesvirus 6 reflects human migration out of Africa
Human herpesvirus 6A and 6B (HHV-6) can integrate into the germline, and as a result, ∼70 million people harbor the genome of one of these viruses in every cell of their body. Until now, it has been largely unknown if 1) these integrations are ancient, 2) if they still occur, and 3) whether circulating virus strains differ from integrated ones. Here, we used next-generation sequencing and mining of public human genome data sets to generate the largest and most diverse collection of circulating and integrated HHV-6 genomes studied to date. In genomes of geographically dispersed, only distantly related people, we identified clades of integrated viruses that originated from a single ancestral event, confirming this with fluorescent in situ hybridization to directly observe the integration locus. In contrast to HHV-6B, circulating and integrated HHV-6A sequences form distinct clades, arguing against ongoing integration of circulating HHV-6A or “reactivation” of integrated HHV-6A. Taken together, our study provides the first comprehensive picture of the evolution of HHV-6, and reveals that integration of heritable HHV-6 has occurred since the time of, if not before, human migrations out of Africa
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