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1.
Am J Obstet Gynecol MFM ; 3(1): 100276, 2021 01.
Article in English | MEDLINE | ID: mdl-33451607

ABSTRACT

BACKGROUND: Data regarding maternal and fetal morbidities are limited to surgical morbidity per each additional hour in the second stage of labor. OBJECTIVE: This study aimed to quantify perinatal morbidities associated with cesarean delivery by duration of the second stage of labor. STUDY DESIGN: Our work is a retrospective cohort study of cesarean deliveries during the second stage of labor using the Consortium on Safe Labor database. All term, singleton pregnancies in cephalic presentation were included. Women with stillbirth or contraindications to vaginal delivery were excluded. Groups were divided by duration of the second stage of labor: ≤3 hours, 3-4 hours, 4-5 hours, 5-6 hours, and >6 hours. The primary outcome was a composite of maternal morbidities. The secondary outcomes were a composite of neonatal morbidities and individual maternal and neonatal morbidities. Baseline demographic and clinical characteristics were compared among groups. Univariate and multivariate analyses were performed. RESULTS: We included 6273 women in total. In addition, 3652 women (58.2%) went through the second stage for ≤3 hours, 854 (13.6%) for 3 to 4 hours, 618 (9.9%) for 4 to 5 hours, 397 (6.3%) for 5 to 6 hours, and 752 (12.0%) for >6 hours. Neither the maternal nor neonatal morbidity composite outcomes were statistically different among the groups. Extended maternal length of stay (>5 days), increased birthweight, and lower rates of general anesthesia were associated with an increased duration of the second stage of labor. Chorioamnionitis, wound complications, postpartum hemorrhage, and thrombosis did not increase over time. CONCLUSION: Women should be counseled regarding the duration of the second stage of labor, which should include a discussion of the risks associated with a cesarean delivery with a prolonged second stage of labor. However, these risks may not be as high as anticipated.


Subject(s)
Cesarean Section , Labor Stage, Second , Cesarean Section/adverse effects , Delivery, Obstetric , Female , Humans , Infant, Newborn , Pregnancy , Retrospective Studies , Time Factors
2.
Am J Obstet Gynecol MFM ; 1(4): 100042, 2019 11.
Article in English | MEDLINE | ID: mdl-33345837

ABSTRACT

Students at all stages of their medical careers rely on the internet to research programs during the application process to help them learn and make educated decisions. In fact, studies with prospective emergency medicine residents have shown that the quality of information online can even impact an applicant decision to apply. Fellowship program information on institutional websites in the fields of pediatrics, orthopedics surgery, and sports medicine have been studied each highlighting poor content and accessibility of information within the domains of program information, application process and educational curriculum. In this call to action, we aim to shed light on the content and accessibility of information on Maternal Fetal Medicine (MFM) fellowship program websites and discuss the benefits of further centralizing and standardizing program information.


Subject(s)
Orthopedics , Sports Medicine , Child , Curriculum , Fellowships and Scholarships , Humans , Orthopedics/education , Prospective Studies
3.
Obstet Gynecol ; 130(4): 870-872, 2017 10.
Article in English | MEDLINE | ID: mdl-28885403

ABSTRACT

A 26-year-old woman, gravida 1 para 1, experiences a severe perineal laceration that extends through the rectal mucosa after a vaginal delivery. She asks you, "What can be done to optimize my recovery?"


Subject(s)
Anal Canal/injuries , Delivery, Obstetric/adverse effects , Puerperal Disorders/therapy , Adult , Anti-Bacterial Agents/administration & dosage , Female , Humans , Pain Measurement , Postnatal Care , Pregnancy
4.
Obstet Gynecol ; 129(2): 377-379, 2017 02.
Article in English | MEDLINE | ID: mdl-28079783

ABSTRACT

This month we focus on current research in global women's health in obstetrics and gynecology. Drs. Autry and Petersen discuss six recent publications, which are concluded with a "bottom line" that is the take-home message. The complete reference for each can be found in on this page, along with direct links to the abstracts.

5.
Obstet Gynecol ; 129(1): 197-199, 2017 01.
Article in English | MEDLINE | ID: mdl-27926656

ABSTRACT

This month we focus on current research in global women's health in obstetrics and gynecology. Drs. Autry and Petersen discuss six recent publications, which are concluded with a "bottom line" that is the take-home message. The complete reference for each can be found in Box 1 on this page, along with direct links to the abstracts.

6.
Obstet Gynecol ; 127(6): 1064-1066, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27159750

ABSTRACT

BACKGROUND: Double aneuploidies account for 0.21-2.8% of spontaneous abortions resulting from chromosomal abnormalities. Rarely, cell-free DNA testing detects multiple aneuploidies; however, to discern among maternal, placental, and fetal origin, further evaluation is required. CASE: A 49-year-old woman, gravida 5 para 0, underwent cell-free DNA testing at 11 4/7 weeks of gestation, which revealed a fetus that was high risk for trisomies 18 and 21. On ultrasonography at 14 weeks of gestation, she was diagnosed with a missed abortion and underwent surgical management. Fetal and placental tissues were sent for analysis and were positive for trisomies 18 and 21, confirming the results of cell-free DNA testing. CONCLUSION: Our case highlights the ability of cell-free DNA testing to recognize a double aneuploidy confirmed by fetal tissue analysis.


Subject(s)
Aneuploidy , DNA/blood , Prenatal Diagnosis , Chromosomes, Human, Pair 18/genetics , Chromosomes, Human, Pair 21/genetics , Diagnosis, Differential , Female , Humans , Middle Aged , Pregnancy , Pregnancy Trimester, First
7.
Obstet Gynecol ; 122(2 Pt 2): 498-500, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23884274

ABSTRACT

BACKGROUND: Twin reversed arterial perfusion sequence is a rare complication of monochorionic twin gestations for which therapy involves the disruption of vascular anastomoses between the pump twin and acardiac twin and death of the acardius. CASE: A 37-year-old woman, gravida 11 para 2, with a monochorionic twin pregnancy complicated by twin reversed arterial perfusion sequence who underwent umbilical cord occlusion at 24 weeks of gestation was admitted in preterm labor at 33 weeks of gestation. Maternal disseminated intravascular coagulation (DIC) was diagnosed and her labor was induced. She received multiple blood products to correct her coagulopathy and had an uncomplicated vaginal delivery of the viable pump twin. CONCLUSION: Maternal DIC may complicate fetal death after umbilical cord occlusion.


Subject(s)
Diseases in Twins/surgery , Disseminated Intravascular Coagulation/etiology , Fetofetal Transfusion/surgery , Laser Therapy/adverse effects , Pregnancy, Twin , Adult , Female , Humans , Pregnancy , Umbilical Cord/surgery
8.
Case Rep Genet ; 2013: 159143, 2013.
Article in English | MEDLINE | ID: mdl-23533844

ABSTRACT

Bardet-Biedl syndrome (BBS) is an autosomal recessive ciliopathic human genetic disorder with variable expression that is difficult to diagnose in pregnancy without known risk factors. Homozygosity testing has been shown to be a useful tool in identifying BBS mutations and candidate genes in affected individuals. We present the first case of prenatal diagnosis of BBS in consecutive pregnancies aided by homozygosity testing via SNP microarray analysis. This case demonstrates a novel approach to the evaluation of recurrent echogenic kidneys in consanguineous couple with no significant family history.

9.
Fetal Diagn Ther ; 33(2): 116-21, 2013.
Article in English | MEDLINE | ID: mdl-23343577

ABSTRACT

OBJECTIVE: In utero hematopoietic stem cell transplantation (IUHSCT) is a promising therapy for a variety of congenital disorders. Our objective was to determine the optimal time in gestation for IUHSCT in a canine model. METHODS: IUHSCT was performed in day 31-50 (term 63) fetal canines with CD34+ cells isolated from paternal bone marrow at doses of 0.09-3.4 × 109 CD34+ cells/kg and T cells (CD3+/CD5+) from paternal blood at 0.11-1.1 × 109 cells/kg. Engraftment was assayed using PCR-based chimerism analysis (SRY gene detection for female recipients, and unique microsatellite loci for both sexes). RESULTS: Microchimerism and chimerism were present in multiple recipients across most gestational ages at transplant. Maximal engraftment was obtained in hematopoietic tissues in transplants performed at 42 days. At extremes of recipient gestational age, minimal to no engraftment was seen. CONCLUSION: Fetal age at the time of IUHSCT plays an important role in achieving engraftment in our canine model.


Subject(s)
Fetal Development , Graft Survival , Graft vs Host Disease/prevention & control , Hematopoietic Stem Cell Transplantation/methods , Animals , Antigens, CD34/metabolism , Bone Marrow Transplantation/adverse effects , Bone Marrow Transplantation/immunology , Chimera , Dogs , Female , Genes, sry , Gestational Age , Graft vs Host Disease/embryology , Graft vs Host Disease/immunology , Graft vs Host Disease/metabolism , Hematopoietic Stem Cell Transplantation/adverse effects , Male , Microsatellite Repeats , Peripheral Blood Stem Cell Transplantation/adverse effects , Pregnancy , T-Lymphocytes/immunology , T-Lymphocytes/metabolism , T-Lymphocytes/transplantation
10.
Case Rep Obstet Gynecol ; 2012: 783408, 2012.
Article in English | MEDLINE | ID: mdl-23097728

ABSTRACT

Maternal mirror syndrome is a rare consequence of fetal hydrops. By convention, delivery is recommended in pregnancies complicated by mirror syndrome due to grave fetal prognosis. We describe a case of a dichorionic, diamniotic twin gestation complicated by hydrops fetalis of twin B. The patient declined selective feticide. Two weeks later, intrauterine fetal demise of fetus B was diagnosed and complete resolution of mirror syndrome followed. Unaddressed, mirror syndrome can lead to significant maternal and fetal complications. This case illustrates resolution of mirror syndrome following spontaneous intrauterine demise of the hydropic fetus.

11.
Fetal Diagn Ther ; 22(3): 175-9, 2007.
Article in English | MEDLINE | ID: mdl-17228153

ABSTRACT

AIM: Microchimerism following canine in utero hematopoietic stem cell transplantation (IUHSCT) development of T-cell dosing regimens. OBJECTIVE: To investigate the use of anti-T-cell antibodies for cell dosing of the donor graft in a canine model of IUHSCT. STUDY DESIGN: Canine IUHSCT was performed by ultrasound-guided intraperitoneal injection in days 35-38 of fetal canines with CD34(+) cells at doses of 4.5 x 10(8) to 1.3 x 10(9) cells/kg and T cells (CD3(+) CD5(+)) at doses of 8 x 10(6) to 8.8 x 10(8) cells/kg. Postnatal studies included tissue histology and polymerase chain reaction-based chimerism analysis. RESULTS: Term survival was 86-100%. Microchimerism (0-2%) was detected in five of eight recipients in multiple tissues. Histopathology revealed no evidence of graft-versus-host disease (GVHD). CONCLUSION: Canine IUHSCT is a useful model to investigate the role of donor T cells in engraftment and GVHD. IUHSCT at early gestational ages with high doses of donor T cells in the graft yields microchimerism in multiple tissues without GVHD.


Subject(s)
Fetal Therapies/methods , Fetal Tissue Transplantation/methods , Hematopoietic Stem Cell Transplantation/methods , Animals , Animals, Newborn , Antilymphocyte Serum/administration & dosage , Base Sequence , DNA Primers/genetics , Dogs , Female , Fetal Tissue Transplantation/immunology , Graft Survival/immunology , Male , Models, Animal , Pregnancy , T-Lymphocytes/immunology , Tissue Donors , Transplantation Chimera/genetics , Transplantation Chimera/immunology
12.
Obstet Gynecol ; 108(3 Pt 1): 656-66, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16946228

ABSTRACT

OBJECTIVE: Electronic fetal heart rate monitoring (EFM) is the most widely used method of intrapartum surveillance, and our objective is to review its ability to prevent perinatal brain injury and death. DATA SOURCES: Studies that quantified intrapartum EFM and its relation to specific neurologic outcomes (seizures, periventricular leukomalacia, cerebral palsy, death) were eligible for inclusion. MEDLINE was searched from 1966 to 2006 for studies that examined the relationship between intrapartum EFM and perinatal brain injury using these MeSH and text words: "cardiotocography," "electronic fetal monitoring," "intrapartum fetal heart rate monitoring," "intrapartum fetal monitoring," and "fetal heart rate monitoring." METHODS OF STUDY SELECTION: This search strategy identified 1,628 articles, and 41 were selected for further review. Articles were excluded for the following reasons: in case reports, letters, commentaries, and review articles, intrapartum EFM was not quantified, or specific perinatal neurologic morbidity was not measured. Three observational studies and a 2001 meta-analysis of 13 randomized controlled trials were selected for determination of the effect of intrapartum EFM on perinatal brain injury. TABULATION, INTEGRATION, AND RESULTS: Electronic fetal monitoring was introduced into widespread clinical practice in the late 1960s based on retrospective studies comparing its use to historical controls where auscultation was performed in a nonstandardized manner. Case-control studies have shown correlation of EFM abnormalities with umbilical artery base excess, but EFM was not able to identify cerebral white matter injury or cerebral palsy. Of 13 randomized controlled trials, one showed a significant decrease in perinatal mortality with EFM compared with auscultation. Meta-analysis of the randomized controlled trials comparing EFM with auscultation have found an increased incidence of cesarean delivery and decreased neonatal seizures but no effect on the incidence of cerebral palsy or perinatal death. CONCLUSION: Although intrapartum EFM abnormalities correlate with umbilical cord base excess and its use is associated with decreased neonatal seizures, it has no effect on perinatal mortality or pediatric neurologic morbidity.


Subject(s)
Birth Injuries/prevention & control , Brain Injuries/prevention & control , Cardiotocography/methods , Heart Rate, Fetal , Perinatal Care/methods , Pregnancy Outcome , Delivery, Obstetric/methods , Female , Fetal Distress/diagnosis , Fetal Hypoxia/diagnosis , Heart Rate, Fetal/physiology , Humans , Perinatal Care/standards , Pregnancy
13.
Obstet Gynecol ; 105(3): 458-65, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15738008

ABSTRACT

OBJECTIVE: Although preterm delivery occurs in only 10% of all births, these infants are at high risk for cerebral white matter injury and constitute a third of all cerebral palsy cases. Our objective was to estimate if electronic monitoring can identify preterm fetuses diagnosed with brain injury during the neonatal period. METHODS: In this case-control study, 150 consecutive neonates with ultrasonography-diagnosed cerebral white matter injury were matched by gestational age within 7 days to 150 controls with normal head ultrasonograms. Tracings were retrieved for 125 cases (83%) and 121 controls (81%) and reviewed by 3 perinatologists blinded to outcome. Vaginal (64 cases, 72 controls) and cesarean deliveries (61 cases, 49 controls) were analyzed separately. RESULTS: There was no difference in baseline heart rate, tachycardia, bradycardia, short-term variability, accelerations, reactivity, number or types of decelerations, or bradycardic episodes between cases and controls in either the vaginal or cesarean delivery groups. For the 6 neonates with metabolic acidosis severe enough to increase the risk for long-term neurologic morbidity, there was a significant increase in baseline amplitude range less than 5 beats per minute; however, its positive predictive value in predicting severe metabolic acidosis was only 7.7%. Increasing late decelerations were associated with decreasing umbilical arterial pH and base excess, but were not significantly different in the acidosis and control groups (1.0 +/- 1.8, 0.55 +/- 1.23 late decelerations per hour, P = .39). CONCLUSION: Although decreased short-term variability and increased late decelerations are associated with decreasing umbilical arterial pH and base excess, electronic fetal monitoring is unable to identify preterm neonates with cerebral white matter injury.


Subject(s)
Fetal Monitoring , Heart Rate, Fetal , Infant, Premature, Diseases/diagnosis , Leukomalacia, Periventricular/diagnosis , Acidosis/diagnosis , Adult , Case-Control Studies , Cesarean Section , Female , Humans , Infant, Newborn , Leukomalacia, Periventricular/diagnostic imaging , Predictive Value of Tests , Pregnancy , Risk Factors , Ultrasonography, Prenatal
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