期刊论文详细信息
BMC Pregnancy and Childbirth
Fetal growth restriction and the risk of perinatal mortality–case studies from the multicentre PORTO study
Fergal D Malone5  Elizabeth C Tully5  Patrick Dicker1  Gerard Burke8  John J Morrison9  Alyson Hunter2  Fionnuala M McAuliffe3  Mairead M Kennelly4  Michael P Geary6  Sean Daly7  Keelin O’Donoghue1,10  Julia Unterscheider5 
[1] Epidemiology & Public Health, Royal College of Surgeons in Ireland, Dublin, Ireland;Obstetrics & Gynaecology, Royal Jubilee Maternity Hospital, Belfast, Ireland;Obstetrics & Gynaecology, UCD School of Medicine and Medical Science, National Maternity Hospital, Dublin, Ireland;UCD Centre for Human Reproduction, Coombe Women and Infants University Hospital, Dublin, Ireland;Obstetrics & Gynaecology, Royal College of Surgeons in Ireland, Dublin, Ireland;Obstetrics & Gynaecology, Rotunda Hospital, Dublin, Ireland;Obstetrics & Gynaecology, Coombe Women and Infants University Hospital, Dublin, Ireland;Obstetrics & Gynaecology, Graduate Entry Medical School, University of Limerick, Limerick, Ireland;Obstetrics & Gynaecology, National University of Ireland, Galway, Ireland;Obstetrics & Gynaecology, University College Cork, Cork University Maternity Hospital, Cork, Ireland
关键词: PORTO Study;    Intrauterine growth restriction;    Neonatal death;    Antepartum stillbirth;    Perinatal mortality;   
Others  :  1128522
DOI  :  10.1186/1471-2393-14-63
 received in 2013-11-11, accepted in 2014-02-07,  发布年份 2014
PDF
【 摘 要 】

Background

Intrauterine growth restriction (IUGR) is the single largest contributing factor to perinatal mortality in non-anomalous fetuses. Advances in antenatal and neonatal critical care have resulted in a reduction in neonatal deaths over the past decades, while stillbirth rates have remained unchanged. Antenatal detection rates of fetal growth failure are low, and these pregnancies carry a high risk of perinatal death.

Methods

The Prospective Observational Trial to Optimize Paediatric Health in IUGR (PORTO) Study recruited 1,200 ultrasound-dated singleton IUGR pregnancies, defined as EFW <10th centile, between 24+0 and 36+6 weeks gestation. All recruited fetuses underwent serial sonographic assessment of fetal weight and multi-vessel Doppler studies until birth. Perinatal outcomes were recorded for all pregnancies. Case records of the perinatal deaths from this prospectively recruited IUGR cohort were reviewed, their pregnancy details and outcome were analysed descriptively and compared to the entire cohort.

Results

Of 1,116 non-anomalous singleton infants with EFW <10th centile, 6 resulted in perinatal deaths including 3 stillbirths and 3 early neonatal deaths. Perinatal deaths occurred between 24+6 and 35+0 weeks gestation corresponding to birthweights ranging from 460 to 2260 grams. Perinatal deaths occurred more commonly in pregnancies with severe growth restriction (EFW <3rd centile) and associated abnormal Doppler findings resulting in earlier gestational ages at delivery and lower birthweights. All of the described pregnancies were complicated by either significant maternal comorbidities, e.g. hypertension, systemic lupus erythematosus (SLE) or diabetes, or poor obstetric histories, e.g. prior perinatal death, mid-trimester or recurrent pregnancy loss. Five of the 6 mortalities occurred in women of non-Irish ethnic backgrounds. All perinatal deaths showed abnormalities on placental histopathological evaluation.

Conclusions

The PNMR in this cohort of prenatally identified IUGR cases was 5.4/1,000 and compares favourably to the overall national rate of 4.1/1,000 births, which can be attributed to increased surveillance and timely delivery. Despite antenatal recognition of IUGR and associated maternal risk factors, not all perinatal deaths can be prevented.

【 授权许可】

   
2014 Unterscheider et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150224020802965.pdf 1189KB PDF download
Figure 2. 54KB Image download
Figure 1. 43KB Image download
【 图 表 】

Figure 1.

Figure 2.

【 参考文献 】
  • [1]Unterscheider J, Daly S, Geary MP, McAuliffe FM, Kennelly MM, Morrison JJ, O’Donoghue K, Hunter A, Burke G, Dicker P, Tully E, Malone FD: Optimizing the definition of intrauterine growth restriction–results of the multicenter prospective PORTO study. AJOG 2013, 208(4):290.e1-6.
  • [2]Baschat AA, Cosmi E, Bilardo CM, et al.: Predictors of neonatal outcome in early onset placental dysfunction. Obstet Gynecol 2007, 109:253-261.
  • [3]Lawn JE, Blencowe H, Pattinson R, Cousens S, Kumar R, Ibiebele I, Gardosi J, Day L, Stanton C: Stillbirths: where? When? Why? How to make the data count? Lancet 2011, 377(9775):1448-1463.
  • [4]Cousens S, Blencowe H, Stanton C, Chou D, Ahmed S, Steinhardt L, Creanga AA, Tunçalp O, Balsara ZP, Gupta S, Say L, Lawn JE: National, regional and worldwide estimates of stillbirth rates in 2009 with trends since 1995: a systematic analysis. Lancet 2011, 377(9774):1319-1330.
  • [5]Gardosi J, Madurasinghe V, Williams M, Malik A, Francis A: Maternal and fetal risk factors for stillbirth: population based study. BMJ 2013, 346:f108.
  • [6]National Perinatal Reporting System (NPRS): Health Research and Information Division, the Economic and Social Research Institute. Ireland: Perinatal Statistics Report; 2010.
  • [7]Manning E, Corcoran P, Meaney S, Greene RA, on behalf of the Perinatal Mortality Group: Perinatal Mortality in Ireland Annual Report 2011. National Perinatal Epidemiology Centre: Cork; 2013.
  • [8]McCowan LM, Roberts CT, Dekker GA, et al.: Risk factors for small-for gestational-age infants by customised birthweight centiles: data from an international prospective cohort study. BJOG 2010, 117(13):1599-1607.
  • [9]Chauhan SP, Beydoun H, Chang E, et al.: Prenatal detection of fetal growth restriction in newborns classified as small for gestational age: correlates and risk of neonatal morbidity. Am J Perinatol 2013. Apr 16. [Epub ahead of print]
  • [10]Unterscheider J, Daly S, Geary MP, McAuliffe FM, Kennelly MM, Morrison JJ, O’Donoghue K, Hunter A, Burke G, Dicker P, Tully E, Malone FD: Predictable progressive doppler deterioration in IUGR–does it really exist? AJOG 2013. doi:10.1016/j.ajog.2013.08.039
  • [11]Hadlock FP, Harrist RB, Sharman RS, Deter RL, Park SK: Estimation of fetal weight with the use of head, body, and femur measurements–a prospective study. Am J Obstet Gynecol 1985, 151(3):333-337.
  • [12]Redline RW: Placental pathology: a systematic approach with clinical correlations. Placenta 2008, 29(Suppl A):S86-S91.
  • [13]de Graaf JP, Steegers EA, Bonsel GJ: Inequalities in perinatal and maternal health. Curr Opin Obstet Gynecol 2013 Apr, 25(2):98-108.
  • [14]Friars AE, Luikenaar RA, Sullivan AE, Lee RM, Porter TF, Branch DW, Silver RM: Poor obstetric outcome in subsequent pregnancies in women with prior fetal death. Obstet Gynecol 2004, 104(3):521-526.
  • [15]Royal College of Obstetricians and Gynaecologists (RCOG): Green-top guideline No 31: The investigation and management of the small-forgestational-age fetus. 2nd edition. London: RCOG Press; 2013.
  • [16]Barker ED, McAuliffe FM, Alderdice F, Unterscheider J, Daly S, Geary MP, Kennelly MM, O’Donoghue K, Hunter A, Morrison JJ, Burke G, Dicker P, Tully E, Malone FD: The role of growth trajectories in classifying fetal growth restriction. Obstet Gynecol 2013, 122(2, PART1):248-254.
  • [17]Institute of Obstetricians and Gynaecologists, Royal College of Physicians of Ireland and Health Service Executive: Clinical Practice Guideline No 29: Fetal Growth Restriction - Recognition, Diagnosis and Management. Dublin: RCPI; 2014. In press. http://www.hse.ie webcite
  文献评价指标  
  下载次数:41次 浏览次数:3次