Journal Article10.1080/14767058.2018.1479390
Placenta in intrauterine fetal demise (IUFD): a comprehensive study from a tertiary care hospital.
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TL;DR: Lesions of MVM were the most common cause of IUFD and served as a direct contributor to fetal demise and were identified in 51 cases and major, minor, unlikely contribution in 21, 11 and nine cases.
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Abstract: Background: Intrauterine fetal demise (IUFD) is an unpredictable and challenging obstetric complication. Its etiology is multifactorial with more than 60% attributed to the placental cause. The present study was done with a primary objective of understanding the placental lesions underlying IUFD. Methods: In this retrospective observational study, IUFD cases (>22 weeks) between January 2012 and September 2015 were collected from pathology database. The clinical details with ultrasound findings were collected from mother's charts. The lesions were classified into (A) maternal vascular malperfusion (MVM) including retroplacental hematomas, (B) fetal vascular malperfusion (FVM), (C) inflammatory lesions, and (D) idiopathic. The contributor to fetal death was classified as direct, major, minor, unlikely, or unknown. Placental findings of fetal hypoxia were recorded. Results: The study included 100 cases of IUFD. The mean maternal age was 26 years (18-36 years). Primipara were 46. There were 65 early preterm (PT) ( 37 weeks) IUFD. The mean gestation age was 30 weeks. The ratio of male:female fetuses was 1:1.7. Relevant obstetric complications included preeclampsia (n = 39), intrauterine growth restriction (IUGR) (n = 7), pre-gestational diabetes (n = 7), bad obstetric history (n = 6), oligohydramnios (n = 5). The mean placental weight was 256 g. Maternal vascular malperfusion had the highest incidence (30%), followed by combined maternal and FVM (10%). Exclusive inflammatory lesions and FVM were seen in 12 and 6%, respectively. No cause was identified in 18%. Direct contributor to IUFD was identified in 51 cases and major, minor, unlikely contribution in 21, 11 and nine cases, respectively. In nine cases, it was unknown. Lesions indicating fetal hypoxia were noted in 35 cases. In both early and late PT, MVM featured more commonly (23 and 5%). In term placentas, the most common cause was idiopathic. Conclusions: Lesions of MVM were the most common cause of IUFD and served as a direct contributor to fetal demise.
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Citations
Disorders of placental villous maturation in fetal death.
Sunil Jaiman,Roberto Romero,Percy Pacora,Percy Pacora,Eun Jung Jung,Eun Jung Jung,Gaurav Bhatti,Gaurav Bhatti,Lami Yeo,Lami Yeo,Yeon Mee Kim,Yeon Mee Kim,Bomi Kim,Bomi Kim,Chong Jai Kim,Chong Jai Kim,Jung Sun Kim,Jung Sun Kim,Faisal Qureshi,Faisal Qureshi,Suzanne M. Jacques,Suzanne M. Jacques,Offer Erez,Offer Erez,Offer Erez,Nardhy Gomez-Lopez,Nardhy Gomez-Lopez,Chaur-Dong Hsu,Chaur-Dong Hsu +28 more
TL;DR: It is demonstrated that placentas of women with fetal death were 44 times more likely to present disorders of villous maturation compared to placenta of those with normal pregnancy, which suggests that the burden of placental disorders of Villa-Bouchutian maturation lesions is substantial.
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Interventions, outcomes and outcome measurement instruments in stillbirth care research: A systematic review to inform the development of a core outcome set
Danya Bakhbakhi,Dimitrios Siassakos,Anna Davies,Abi Merriel,Katie Barnard,Emma Stead,C. Shakespeare,James Duffy,Lisa Hinton,Karolina McDowell,Anna Lyons,Abigail Fraser,Christy Burden +12 more
TL;DR: A core outcome set could address inconsistent outcome reporting and improve evidence for stillbirth care research as mentioned in this paper , which have been identified as an important research priority in the field of obstetrics.
5
Interdependence of placenta and fetal cardiac development.
Rachel L. Leon,Lynn Bitar,V. Rajagopalan,Catherine Y. Spong +3 more
TL;DR: Evidence from animal studies suggests a plausible cause and effect connection between placental abnormalities and fetal CHD, and this relationship may eventually lead to preventative strategies for some forms of CHD by targeting placental influences on fetal heart development.
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Evaluation of Intrauterine Fetal Death at Tertiary Care Centre: A Descriptive Cross-Sectional Study
TL;DR: In this article , a descriptive cross-sectional study was conducted in a tertiary care center from 1st November 2020 to 31st October 2021, where Demographic data were collected using predesigned proforma in pregnant women with intrauterine fetal demise identified before, during labor and delivery.
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Placental Pathology and Its Importance in Preterm Infants.
Duygu Tugrul Ersak,Hakkı Şerbetçi̇,Bergen Laleli Koç,Özgür Kara,Gülsüm Kadıoğlu Şimşek,Fuat Emre Canpolat,Özlem Moraloğlu Tekin,Dilek Sahin +7 more
TL;DR: In this paper , the authors evaluated what placental pathologies were associated with adverse preterm births and found that inflammatory responses other than histological chorioamnionitis (HCA), and placentas with combined maternal vascular malperfusion (MVM) and HCA were correlated with infant outcomes.
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References
•Book
Pathology of the human placenta
Kurt Benirschke,Peter Kaufmann +1 more
- 01 Jan 1967
TL;DR: Early development of the human placenta and histopathologic approach to villous alterations are studied.
2.1K
•Book
The Pathology of the Human Placenta
Kurt Benirschke,Shirley G. Driscoll +1 more
- 01 Jan 1974
TL;DR: A methodical gross examination should be undertaken in all births and the results incorporated in the patient’s record.
1.6K
Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement
T. Yee Khong,Eoghan E. Mooney,Ilana Ariel,Nathalie C.M. Balmus,Theonia K. Boyd,Marie Anne Brundler,Hayley Derricott,Margaret J. Evans,Ona Faye-Petersen,John Gillan,Alexander E. P. Heazell,Debra S. Heller,Suzanne M. Jacques,Sarah Keating,Peter Kelehan,Ann Maes,Eileen McKay,Terry K. Morgan,Peter G. J. Nikkels,W. Tony Parks,Raymond W. Redline,Irene Scheimberg,Mirthe H. Schoots,Neil J. Sebire,Albert Timmer,Gitta Turowski,J. Patrick van der Voorn,Ineke Van Lijnschoten,Sanne J. Gordijn +28 more
TL;DR: The group agreed on sets of uniform sampling criteria, placental gross descriptors, pathologic terminologies, and diagnostic criteria for placental lesions, which will assist in international comparability of clinicopathologic and scientific studies and assist in refining the significance of lesions associated with adverse pregnancy and later health outcomes.
Placental pathology: a systematic approach with clinical correlations.
TL;DR: A simple conceptual framework is outlined separating placental patterns of injury and maladaptation into three categories of lesions affecting the maternal and fetal vasculature (maldevelopment, obstruction, and disruption) and two categories of inflammatory lesions (infectious and idiopathic).
393
•Book
Manual of Pathology of the Human Placenta
Rebecca N. Baergen,Kurt Benirschke +1 more
- 06 Jan 2011
TL;DR: Evaluation of the First Trimester Products of Conception, and Macroscopic Evaluation of the Second and Third Trimester Placenta.
196