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1.
Turk J Med Sci ; 51(4): 1775-1780, 2021 08 30.
Artículo en Inglés | MEDLINE | ID: mdl-33581708

RESUMEN

Background/aim: Although cutting edge procedures such as cell-free fetal DNA isolation from maternal blood are now available, invasive prenatal tests are still being used extensively for prenatal diagnosis. The study aims to evaluate the demographic data, indications, and cytogenetic results of 9297 results of patients who underwent prenatal invasive testing for genetic analysis that were referred for the last 20 years in a University Medical Genetics Center. Materials and methods: The records of 8363 amniocenteses, 626 chorionic villus, and 308 cordocenteses samples were retrospectively evaluated and analyzed regarding referral reasons, indications and their cytogenetic results. The total numbers and the percentages of each group were recorded; Chi-square and logistic regression analyses were performed to give the statistical likelihood of different events. Results: The number of referrals decreased significantly after 2009. Risk of having trisomy 21 as well as trisomy 13 and 18 significantly increased in parallel with advanced maternal age. When the 21­25 age group was compared to the older age groups in terms of having a trisomy 21 pregnancy, the risk doubled in the 36­40, 5 times higher in 41­45 and 10-fold in 46­50 age groups. No significant linear correlation between maternal serum screening test results and trisomy 21 was found, however the difference between the pregnancies whom cut-off value above and below 1/250 in maternal serum screening test were significant. Conclusion: These data have provided useful information on the frequency of referrals to the reference genetics department, and the feasibility of genetic services. By reviewing the indications and their corresponding results, we can offer invaluable insights that will be useful in genetic counseling and also in the development of more effective genetic strategies.


Asunto(s)
Aberraciones Cromosómicas , Síndrome de Down , Asesoramiento Genético/métodos , Diagnóstico Prenatal/estadística & datos numéricos , Adulto , Aneuploidia , Femenino , Genética Médica , Humanos , Persona de Mediana Edad , Embarazo , Estudios Retrospectivos , Turquía/epidemiología , Universidades
2.
Fetal Diagn Ther ; 36(2): 166-72, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24192343

RESUMEN

OBJECTIVE: To evaluate the association between the brain-sparing situation and perinatal outcomes in fetuses with early-onset fetal growth restriction (EO-FGR) with absent or reverse end-diastolic flow in the umbilical artery (UA A/REDF). METHODS: We evaluated fetuses with EO-FGR who had patterns of UA A/REDF without abnormal venous Doppler indices. Participants were divided into two groups according to measurements of mid-cerebral artery pulsatility index (MCA PI) just before delivery. Group 1 (n = 45) included those with a brain-sparing effect (BSE) (a MCA PI <5th percentile for the gestational age) and group 2 (n = 14) included those with a disappearing BSE, defined as an MCA PI increase towards normal values after the BSE detected at the initial evaluation. Short-term perinatal outcomes were analyzed. RESULTS: Compared to group 1, group 2 had a significantly low birth weight (p = 0.018) and high rates of extended neonatal intensive care unit hospitalization (p = 0.049 respectively). CONCLUSION: On the basis of longitudinal measurements of MCA PI, increases after the reduction <5th percentile might be related to poor perinatal outcomes in fetuses with EO-FGR who had UA A/REDF without abnormal venous flow patterns.


Asunto(s)
Encéfalo/irrigación sanguínea , Retardo del Crecimiento Fetal/diagnóstico por imagen , Feto/irrigación sanguínea , Arteria Cerebral Media/diagnóstico por imagen , Arterias Umbilicales/diagnóstico por imagen , Adulto , Femenino , Edad Gestacional , Humanos , Recién Nacido , Masculino , Embarazo , Resultado del Embarazo , Ultrasonografía Prenatal , Adulto Joven
3.
Acta Obstet Gynecol Scand ; 92(6): 656-61, 2013 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-23324102

RESUMEN

OBJECTIVE: To identify the role of longitudinal measurements of fetal aortic isthmus blood flow using Doppler ultrasonography in the prediction of perinatal morbidity and mortality. SETTING: Obstetrics department of a university hospital. POPULATION AND DESIGN: This prospective study includes women with fetal growth restriction and abnormal umbilical artery Doppler results, seen between November 2009 and January 2011. METHODS: 31 women were divided into two groups according to the aortic isthmus blood flow pattern just before birth: anterograde (n = 12) or retrograde (n = 19). MAIN OUTCOME MEASURE: Longitudinal measurements of fetal aortic isthmus in relation to perinatal outcome. RESULTS: Total morbidity and mortality rates were significantly higher in the retrograde flow group. There was no statistically significant difference for respiratory distress syndrome, intraventricular hemorrhage, bronchopulmonary dysplasia or necrotizing enterocolitis, but the neonatal sepsis rate was significantly higher in the retrograde flow group. An abnormal aortic isthmus flow pattern was detected approximately 15-20 days after umbilical artery and middle cerebral artery Doppler flow abnormalities and 3-7 days before deterioration in ductus venosus blood flow. CONCLUSION: We suggest that aortic isthmus Doppler measurements are useful for identifying fetal growth restriction before deterioration in ductus venosus blood flow and fetal acidosis.


Asunto(s)
Aorta Torácica/diagnóstico por imagen , Retardo del Crecimiento Fetal/diagnóstico por imagen , Desprendimiento Prematuro de la Placenta/epidemiología , Aorta Torácica/embriología , Puntaje de Apgar , Velocidad del Flujo Sanguíneo/fisiología , Displasia Broncopulmonar/epidemiología , Enterocolitis Necrotizante/epidemiología , Femenino , Muerte Fetal/epidemiología , Humanos , Recién Nacido , Hemorragias Intracraneales/epidemiología , Arteria Cerebral Media/diagnóstico por imagen , Embarazo , Estudios Prospectivos , Síndrome de Dificultad Respiratoria del Recién Nacido/epidemiología , Sepsis/epidemiología , Ultrasonografía Doppler , Arterias Umbilicales/diagnóstico por imagen , Venas Umbilicales/diagnóstico por imagen
4.
Gynecol Endocrinol ; 29(9): 867-72, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23875965

RESUMEN

We aimed to compare the effects of different types of hormone treatment (HT) on endothelial function by means of brachial artery ultrasonographic examination in postmenopausal women. Sixty-two healthy postmenopausal women were included in this study. Subjects were assigned to one of the five groups receiving 6 months of treatment [estrogen (conjugated estrogen), estrogen (conjugated estrogen) plus progesterone (medroxyprogesterone acetate; MPA), raloxifene, tibolone or control]. Endothelial function was assessed by measurement of flow-mediated dilatation (FMD) and nitrate-dependent dilatation in the brachial artery. At the end of 6 months, FMD values were found to be significantly increased in women with HT use than the control group (p = 0.001). In subgroups, FMD increased significantly in the estrogen [12 ± 7 versus 25 ± 8, p = 0.001] and raloxifene groups [7 ± 5 versus 11 ± 3, p < 0.01] compared to tibolone and estrogen plus progesterone groups. In conclusion, endothelial function is impaired in postmenopausal women. Both estrogen and raloxifene regimens may improve endothelial functions in healthy postmenopausal women. The direct protective effects of these HT on the healthy endothelium may be more remarkable than the favorable effects on lipid profile.


Asunto(s)
Arteria Braquial/efectos de los fármacos , Endotelio Vascular/efectos de los fármacos , Terapia de Reemplazo de Estrógeno/métodos , Estrógenos Conjugados (USP)/farmacología , Acetato de Medroxiprogesterona/farmacología , Posmenopausia , Clorhidrato de Raloxifeno/farmacología , Adulto , Arteria Braquial/diagnóstico por imagen , Arteria Braquial/fisiología , Combinación de Medicamentos , Endotelio Vascular/diagnóstico por imagen , Endotelio Vascular/fisiología , Terapia de Reemplazo de Estrógeno/efectos adversos , Femenino , Salud , Humanos , Persona de Mediana Edad , Norpregnenos/farmacología , Posmenopausia/efectos de los fármacos , Posmenopausia/fisiología , Ultrasonografía , Vasodilatación/efectos de los fármacos
5.
J Clin Ultrasound ; 41 Suppl 1: 38-41, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23686518

RESUMEN

We present a case of infantile myofibromatosis of the lung detected at 32 weeks' gestation. The fetus was monitored with weekly ultrasound examinations measuring the mass size and amniotic fluid index. On day 2 after delivery, due to respiratory distress, an exploratory thoracotomy was undertaken and the mass was resected.


Asunto(s)
Neoplasias Pulmonares/diagnóstico por imagen , Miofibromatosis/congénito , Ultrasonografía Prenatal , Adulto , Femenino , Humanos , Recién Nacido , Neoplasias Pulmonares/cirugía , Miofibromatosis/diagnóstico por imagen , Miofibromatosis/cirugía , Embarazo , Toracotomía , Ultrasonografía Doppler en Color
6.
Ginekol Pol ; 84(1): 65-7, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23488313

RESUMEN

Neural tube defects are congenital defects of the central nervous system caused by lack of neural tube closure. First trimester screening for aneuploidy has become widespread in the recent years. Fetal intracranial translucency (IT) can be easily observed in normal fetuses in the mid-sagittal plane. The absence of IT should be an important factor taken into consideration in the early diagnosis of open spinal defects. 3D ultrasonography is especially useful in cases of spinal anomalies where the visualization of the fetal structure is insufficient due to fetal position. We present a combination of intracranial translucency and 3D sonography used in the first trimester diagnosis of a neural tube defect case.


Asunto(s)
Tronco Encefálico/diagnóstico por imagen , Tronco Encefálico/embriología , Feto/anomalías , Feto/ultraestructura , Defectos del Tubo Neural/diagnóstico por imagen , Adulto , Femenino , Humanos , Medida de Translucencia Nucal , Embarazo , Primer Trimestre del Embarazo , Ultrasonografía Prenatal
7.
Arch Gynecol Obstet ; 285(3): 635-9, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21837429

RESUMEN

OBJECTIVE: The aim of this study was to investigate the effects of HbA1c levels and umbilical cord thickness upon birth weight, particularly in pregestational and gestational diabetic patients. METHOD: Pregnant women were included in the study and were divided into two groups. The first group consisted of patients who were diagnosed with pregestational or gestational diabetes mellitus. The control group consisted of pregnant women who were not diagnosed with pregestational or gestational diabetes mellitus. Ultrasound examination was performed twice. Examinations were performed at 27-28 weeks and 36-37 weeks of gestation, respectively. During ultrasound examinations, fetal anthropometric parameters, biparietal diameter, abdominal circumference, femur length and estimated fetal weight (which was calculated automatically according to Hadlock's formula) were measured. Additionally, the sonographic cross-sectional areas of the umbilical cord, the umbilical arteries and the umbilical vein were measured in a free loop of the umbilical cord, using the software of the ultrasound machine. The cross-sectional area of Wharton's jelly was computed by subtracting the cross-sectional area of the vessels from that of the umbilical cord. HbA1c levels were measured for diabetic patients. RESULTS: At 27-28 gestational weeks, umbilical cord area and Wharton's jelly values were found to be statistically different in macrosomic fetuses compared with non-macrosomic fetuses for both groups (for cord area, P = 0.012; for Wharton's jelly, P = 0.001). Additionally, umbilical cord diameter vein and artery values were not statistically different between the two groups when macrosomic fetuses were compared with non-macrosomic fetuses. At 36-37 gestational weeks, when the relationship between umbilical cord components and birth weight was examined, there was a statistically significant difference when comparing macrosomic fetuses with non-macrosomic fetuses. There was a statistically significant correlation between umbilical cord area, umbilical cord diameter and fetal weight estimation at 36-37 gestational weeks. HbA1c values and fetal macrosomia did not show a statistically significant relationship (P = 0.701). CONCLUSION: A significant relationship between umbilical cord components and birth weight was not specific for the diabetic group. There was a significant relationship between birth weight and umbilical cord components for the control group as well. If the estimated fetal weight is combined with umbilical cord components, macrosomic fetuses can be predicted with more accuracy.


Asunto(s)
Diabetes Gestacional/diagnóstico por imagen , Macrosomía Fetal/diagnóstico por imagen , Hemoglobina Glucada/metabolismo , Ultrasonografía Prenatal , Cordón Umbilical/patología , Adulto , Peso al Nacer , Diabetes Gestacional/epidemiología , Femenino , Macrosomía Fetal/epidemiología , Hemoglobina Glucada/análisis , Humanos , Incidencia , Embarazo , Arterias Umbilicales/diagnóstico por imagen , Cordón Umbilical/diagnóstico por imagen , Venas Umbilicales/diagnóstico por imagen , Gelatina de Wharton/anatomía & histología , Gelatina de Wharton/diagnóstico por imagen
8.
J Clin Ultrasound ; 40(4): 231-3, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-22508320

RESUMEN

Placental chorioangioma is an angioma arising from chorionic tissue. Fetal thanatophoric dysplasia is a lethal skeletal dysplasia due to mutation of fibroblast growth factor receptor 3 gene. These two conditions are rare and their coexistence in a given fetus is even rarer. We present a case of a fetus with thanatophoric dysplasia having high-output cardiac failure due to a large placental chorioangioma.


Asunto(s)
Insuficiencia Cardíaca/diagnóstico por imagen , Hemangioma/patología , Enfermedades Placentarias/patología , Complicaciones Neoplásicas del Embarazo/patología , Displasia Tanatofórica/diagnóstico por imagen , Ultrasonografía Prenatal , Adulto , Femenino , Insuficiencia Cardíaca/etiología , Hemangioma/complicaciones , Humanos , Embarazo , Displasia Tanatofórica/complicaciones , Adulto Joven
9.
Turk J Pediatr ; 54(3): 230-3, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23094531

RESUMEN

The rubella vaccine is contraindicated in pregnancy. Between July and August 2009, the Turkish Republic Ministry of Health implemented a vaccine program to eradicate rubella in women in the reproductive period. In this program, many pregnant women were also vaccinated inadvertently. In this study, 62 pregnant women applied to our clinic who were vaccinated either during pregnancy or within one month before the last menstrual period. Seventeen of them were followed until the end of the pregnancy by fetal echocardiography and detailed ultrasonography. Rubella immunoglobulin (Ig) M and IgG antibodies were studied in the cord blood obtained at birth. All fetuses were examined by a pediatrician, an ophthalmologist and a pediatric cardiologist. A hearing test was also performed on all neonates. No signs of congenital rubella syndrome could be found.


Asunto(s)
Programas de Inmunización/organización & administración , Complicaciones Infecciosas del Embarazo/prevención & control , Síndrome de Rubéola Congénita/epidemiología , Síndrome de Rubéola Congénita/prevención & control , Vacuna contra la Rubéola/inmunología , Adolescente , Adulto , Ecocardiografía , Femenino , Pruebas Auditivas , Humanos , Recién Nacido , Masculino , Atención Preconceptiva , Embarazo , Complicaciones Infecciosas del Embarazo/epidemiología , Complicaciones Infecciosas del Embarazo/inmunología , Resultado del Embarazo , Prevalencia , Vacuna contra la Rubéola/efectos adversos , Turquía/epidemiología , Ultrasonografía Prenatal
10.
J Turk Ger Gynecol Assoc ; 22(4): 343-345, 2021 12 06.
Artículo en Inglés | MEDLINE | ID: mdl-32706232

RESUMEN

Endosalpingiosis is, like endometriosis, the presence of cystic masses outside of the salpinx which contains fallopian tube epithelium. Endosalpingiosis can be seen on the surface of ovaries, tubal serosa, uterine serosa, myometrium, and also in the bladder. The main clinical features of endosalpingiosis are pelvic pain, adnexal mass which mimics cancer, and urinary symptoms. Herein, we present a surgical video of endosalpingiosis in a woman with endometriosis and a dermoid cyst.

11.
Balkan Med J ; 35(2): 163-166, 2018 03 15.
Artículo en Inglés | MEDLINE | ID: mdl-29219113

RESUMEN

BACKGROUND: Down syndrome, which is the most common human chromosomal anomaly that can affect people of any race and age, can be diagnosed prenatally in most cases. Prenatal diagnosis via culture method is time-consuming; thus, genetic analysis has thus been introduced and is continually being developed for rapid prenatal diagnosis. For this reason, the effective use of microRNA profiling for the rapid analysis of prenatal amniotic fluid samples for the diagnosis of Down syndrome was investigated. AIMS: To evaluate the expression levels of 14 microRNAs encoded by chromosome 21 in amniotic fluid samples and their utility for prenatal diagnosis of Down syndrome. STUDY DESIGN: Case-control study. METHODS: We performed invasive prenatal testing for 56 pregnant women; 23 carried fetuses with Down syndrome, and 33 carried fetuses with a normal karyotype. Advanced maternal age and increased risk for Down syndrome in the screening tests were indications for invasive prenatal testing. The age of gestation in the study and control groups ranged between 17 and 18 weeks. The expression levels of microRNA were measured by real-time polymerase chain reaction. RESULTS: The expression levels of microRNA-125b-2, microRNA-155, and microRNA-3156 were significantly higher in the study group than in the control group. CONCLUSION: The presence of significantly dysregulated microRNAs may be associated with either the phenotype or the result of abnormal development. Further large-scale comparative studies conducted in a variety of conditions may bring novel insights in the field of abnormal prenatal conditions.


Asunto(s)
Líquido Amniótico/metabolismo , Síndrome de Down/diagnóstico , MicroARNs/análisis , Adulto , Estudios de Casos y Controles , Síndrome de Down/genética , Femenino , Humanos , Embarazo , Diagnóstico Prenatal
12.
Obstet Gynecol Int ; 2017: 7171520, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28149307

RESUMEN

Objective. Controlling excessive bleeding in cesarean sections which may cause a life-threatening event even under well-prepared conditions. We used a novel atraumatic tourniquet technique to temporary arrest blood flow through the uterine and ovarian vessels and compare with other techniques. Toothless vascular clamps were used as clamp. Methods. Tourniquet technique performed postpartum hemorrhage (PPH) cases (19 out of 37) were compared with 18 other cases with PPH. Results. The difference between preoperative and postoperative hemoglobin values was significantly lower in the study group as well as the number of blood products needed during and after surgery. Conclusions. This technique not only prevented massive bleeding from the uterus but also allowed physicians time to consider the necessity of further interventions.

13.
Biomed Res Int ; 2016: 5312674, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27110565

RESUMEN

BACKGROUND: Currently, the data available on the utility of miRNAs in noninvasive prenatal testing is insufficient in the literature. We evaluated the expression levels of 14 miRNAs located on chromosome 21 in maternal plasma and their utility in noninvasive prenatal testing of Down Syndrome. METHOD: A total of 56 patients underwent invasive prenatal testing; 23 cases were carrying Down Syndrome affected fetuses, and 33 control cases carrying unaffected, normal karyotype fetuses were included for comparison. Indications for invasive prenatal testing were advanced maternal age, increased risk of Down Syndrome in screening tests, and abnormal finding in the sonographic examination. In both the study and control groups, all the pregnant women were at 17th and 18th week of gestation. miRNA expression levels were measured using real-time RT-PCR. RESULTS: Significantly increased maternal plasma levels of miR-3156 and miR-99a were found in the women carrying a fetus with Down Syndrome. CONCLUSION: Our results provide a basis for multicenter studies with larger sample groups and microRNA profiles, particularly with the microRNAs which were found to be variably expressed in our study. Through this clinical research, the utility of microRNAs in noninvasive prenatal testing can be better explored in future studies.


Asunto(s)
Síndrome de Down/diagnóstico , Síndrome de Down/genética , MicroARNs/biosíntesis , Diagnóstico Prenatal , Adulto , Cromosomas Humanos Par 21/genética , Síndrome de Down/patología , Femenino , Feto , Edad Gestacional , Humanos , Cariotipo , Edad Materna , MicroARNs/genética , Embarazo , Ultrasonografía Prenatal
14.
Eur J Obstet Gynecol Reprod Biol ; 121(2): 159-63, 2005 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-16054956

RESUMEN

OBJECTIVE: The aim of this study was to determine the value of detecting insulin-like growth factor binding protein-1 (IGFBP-1) in the cervical-vaginal secretion in the prediction of delivery in women with clinically uncorfirmed preterm premature rupture of membranes (PPROM). MATERIAL AND METHODS: A total of 87 women, gestational age between 20 and 36 weeks were enrolled into this prospective study. Based on the clinical diagnosis, patients were grouped as clinically evident PPROM (n = 25), clinically suspected PPROM (n = 42) and women with intact fetal membranes (n = 20). Detection of IGFBP-1 in the cervical-vaginal secretions was done using a one-step immunochromatographic dipstick test in all women. The outcome measures were gestational age at delivery, neonatal birth weight and duration of the interval between the test and delivery between women with positive and negative test results. RESULTS: The test was positive in all 25 women (100% sensitivity) with clinically evident PPROM and all delivered prematurely, and negative in 19 out of the 20 (95% specificity) women with intact fetal membranes. Among 36 women with clinically suspected PPROM, 13 (36%) tested positive and 23 (63%) tested negative for IGFBP-1. In this group, the mean gestational age and birth weight at the time of delivery were significantly lower in patients with positive test (31.38+/-2.6 weeks versus 38.61+/-0.99 weeks and 1761+/-527g versus 3500+/-355g, P < 0.05 for both). Eleven (85%) of the 13 women with positive test, delivered within 2 weeks after the performance of the test whereas all the women with negative test results delivered after 2 weeks (P = 0.001). The test had 100, 92, 84 and 100% sensitivity, specificity, positive predictive value and negative predictive value, respectively, for the outcome measure of test-delivery interval. CONCLUSION: The screening test for IGFBP-1 in the cervical-vaginal secretions is a useful adjunct in the prediction of delivery in women with clinically unconfirmed PPROM.


Asunto(s)
Secreciones Corporales/química , Cuello del Útero/metabolismo , Rotura Prematura de Membranas Fetales/diagnóstico , Proteínas de Unión a Factor de Crecimiento Similar a la Insulina/análisis , Proteínas Gestacionales/análisis , Adulto , Cromatografía , Parto Obstétrico , Femenino , Humanos , Proteína 1 de Unión a Factor de Crecimiento Similar a la Insulina , Valor Predictivo de las Pruebas , Embarazo , Estudios Prospectivos , Tiras Reactivas , Vagina/metabolismo
15.
Eur J Obstet Gynecol Reprod Biol ; 121(1): 18-23, 2005 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-15989982

RESUMEN

BACKGROUND: Combined spinal-epidural block (CSEB) has aroused increasing interest, as it combines the reliability of a spinal block and the flexibility of an epidural block (EB). We have conducted a comparative investigation of the maternal and fetal effects of CSEB and of EB administered for Cesarean section. METHODS: Eighty pregnant women at term were randomized into two groups. Women in the CSEB group (N = 40) were each given 1.5-1.8 mL 0.5% hyperbaric bupivacaine intrathecally, followed by 10 mL 0.25% bupivacaine and 50 microg fentanyl through the epidural catheter 10 min later. Women in the EB group (N = 40) received 14-16 mL 0.5% bupivacaine and 100 microg fentanyl. The quality and side effects of surgical anesthesia and the hemodynamic parameters, Apgar scores, and postoperative duration of pain were compared between the two groups. RESULTS: The time for the block to reach the T-4 level differed significantly between the two groups (8.02 +/- 3.4 versus 18.34 +/- 4.6; P < 0.01). More women in the CSEB group achieved complete motor blockade (Bromage score 3), and it was reached earlier than in the EB group (P < 0.05). Muscle relaxation and motor block were better in the CSEB group than in the EB group (P < 0.01). Apgar scores were 7 or more in almost all newborns in both groups. There were no significant differences between the groups in the incidences of adverse effects such as hypotension or nausea and vomiting, but the patients in the EB group experienced more shivering (P < 0.001). The time to postoperative pain was significantly shorter in the CSEB group. CONCLUSION: We decided that CSEB, and more specifically spinal anesthesia with supporting epidural anesthesia, has greater efficacy and fewer side effects than EB when administered for Cesarean section.


Asunto(s)
Anestesia Epidural/métodos , Anestesia Raquidea/métodos , Bupivacaína/administración & dosificación , Cesárea , Adolescente , Adulto , Anestesia Epidural/efectos adversos , Anestesia Obstétrica/métodos , Distribución de Chi-Cuadrado , Terapia Combinada , Femenino , Edad Gestacional , Humanos , Dimensión del Dolor , Embarazo , Resultado del Embarazo , Probabilidad , Medición de Riesgo , Estadísticas no Paramétricas , Resultado del Tratamiento
16.
Turk J Pediatr ; 57(1): 26-33, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26613217

RESUMEN

Mannose-binding lectin (MBL) is a component of the innate immune system and acts as a complement activator through the lectin pathway. Genetic variations of MBL and low MBL levels cause several infection problems, which may also be related to pregnancy problems. We aimed to investigate the role of MBL gene codon 54 polymorphism and serum MBL levels in pregnancy problems and premature delivery. In this prospective study, MBL gene codon 54 polymorphism and serum MBL levels were studied in 45 mothers who delivered earlier than 35 gestational weeks. The frequency of MBL gene codon 54 variant allele B was much higher (homozygous 4.4% and heterozygous 33.3%) in the study group mothers than the previously reported frequency in the healthy Turkish population (homozygous 2-6%, heterozygous 12-20%). MBL variant allele B frequency was closely related to low MBL levels (<0.1 µg/ml), vaginitis and increased IL-6 levels. The median MBL levels were lower than the critical level of 0.1 µg/ ml in study mothers who had recurrent miscarriage, infertility, preeclampsia, gestational diabetes mellitus, preterm premature rupture of membranes with duration of longer than 72 hours, tocolysis, histological chorioamnionitis, urinary tract infection and vaginitis. MBL gene codon 54 variant allele B is related to low serum MBL levels, increased IL-6 levels, genitourinary infections and may cause pregnancy-related problems such as infertility, recurrent miscarriage and preterm delivery.


Asunto(s)
Lectina de Unión a Manosa/genética , Complicaciones del Embarazo/genética , Adulto , Alelos , Codón , Femenino , Genotipo , Humanos , Interleucina-6/sangre , Lectina de Unión a Manosa/sangre , Polimorfismo Genético , Embarazo , Complicaciones del Embarazo/sangre , Resultado del Embarazo , Estudios Prospectivos , Turquía , Adulto Joven
17.
J Reprod Med ; 49(5): 368-72, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15214710

RESUMEN

OBJECTIVE: To determine the value of cervical phosphorylated insulinlike growth factor binding protein-1 (IGFBP-1) in the prediction of preterm labor. STUDY DESIGN: In this prospective study, 77 pregnant women, gestational age 24-36 weeks, were enrolled in the study. Twenty women with completely healthy pregnancies formed the control group. Fifty-seven women with signs and symptoms of preterm labor formed the study group. Phosphorylated IGFBP-1 in cervical secretions was assessed in all patients by using a qualitative, immunochromatographic, 1-step dipstick test. Cervical length was measured by transvaginal sonography. RESULTS: The IGFBP-1 test was negative in all patients in the control group (n = 20), and all of them delivered after 37 weeks, while the test was positive in 15 of 45 (33.3%) patients in the study group. The correlation between cervical length and gestational age at the time of delivery in patients with a positive phosphorylated IGFBP-1 test (n = 15) was significant (r = .553, P = .03). The sensitivity, specificity, positive predictive value and negative predictive value for the phosphorylated IGFBP-1 test were 78%, 87%, 73% and 90%, respectively. CONCLUSION: Use of a 1-step dipstick test for detecting phosphorylated IGFBP-1 in cervical secretions is of value in the prediction of preterm labor. The high negative predictive value of the test may be useful in avoiding unnecessary medical interventions.


Asunto(s)
Cuello del Útero/química , Proteína 1 de Unión a Factor de Crecimiento Similar a la Insulina/análisis , Trabajo de Parto Prematuro , Adulto , Femenino , Humanos , Valor Predictivo de las Pruebas , Embarazo , Resultado del Embarazo , Segundo Trimestre del Embarazo , Tercer Trimestre del Embarazo , Estudios Prospectivos , Factores de Riesgo , Sensibilidad y Especificidad
18.
Singapore Med J ; 44(5): 243-7, 2003 May.
Artículo en Inglés | MEDLINE | ID: mdl-13677360

RESUMEN

OBJECTIVE: Although the only objective finding of intrapartum fetal distress is obtained through the measurement the fetal scalp pH, this invasive procedure is not available in every institution. The careful examination of fetal heart rate tracings for abnormalities, especially of the most commonly seen one, variable decelerations gains great importance under these circumstances. The aim of the present study is to determine the prognostic significance of variable decelerations in intrapartum fetal heart rate monitoring. METHODS: A total of 96 fetal heart rate tracings were analysed to assess the prognostic significance of variable decelerations. Sixty-six percent (64/96) of cases exhibited atypia characterised with (1) slow return of the fetal heart rate to the baseline; (2) loss of variability during the decelerations; (3) loss of initial and/or secondary accelerations; (4) persistence of secondary acceleration (overshoot); and (5) continuation of the baseline fetal heart rate at a lower level; (6) biphasic deceleration. One and five-minute Apgar scores and umbilical artery pH were used to assess the final fetal condition. RESULTS: Adverse fetal outcome characterised by fetal acidosis and Apgar score lower than 7 at one and five minutes were uncommon with pure variable decelerations. Typical and atypical variable decelerations were associated with low Apgar scores (< 7) at one minute in 9.3% and 54.6% of cases (p < 0.001) and at five minutes in 6.25% and 25% of cases (p < 0.05), respectively. In addition umbilical artery pH found to be lower than 7.2 in these cases ( 18.75% - p < 0.05). There was no danger for the fetal haemodynamic conditions when typical uterus contraction/variable deceleration ratios were two or more than two. However, risk of fetal hypoxia damage was quite high when this ratio was lower than two in atypical variable 5th minute low Apgar scores and pH (81.8% and 36.6% respectively). Atypical features are helpful in the identification of distress characterised by low Apgar scores in fetuses with variable decelerations. Admission to the neonatal intensive care unit was more common in patients with atypical variable decelerations in comparison with typical variable decelerations (34.3% versus 3.1%). CONCLUSION: While typical variable decelerations are frequently harmless, atypical variations pose a significant risk of fetal hypoxia.


Asunto(s)
Monitoreo Fetal , Frecuencia Cardíaca Fetal/fisiología , Acidosis , Distribución de Chi-Cuadrado , Femenino , Humanos , Concentración de Iones de Hidrógeno , Valor Predictivo de las Pruebas , Embarazo , Resultado del Embarazo , Pronóstico , Contracción Uterina
19.
Case Rep Obstet Gynecol ; 2013: 285846, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23653875

RESUMEN

Uterine artery pseudoaneurysm is a rare but serious complication of cesarean section. If inadequately treated, it can lead to life-threatening postpartum hemorrhage. Herein, we report the case of a 28-year-old woman who developed secondary postpartum hemorrhage resulting from uterine artery pseudoaneurysm and cesarean scar dehiscence after cesarean section. Angiographic embolization is a safe and effective procedure for treating postpartum hemorrhage resulting from pseudoaneurysm in hemodynamically stable patients. However, uterine artery ligation may be the surgical procedure of choice for hemodynamically unstable patients when fertility preservation is desired.

20.
J Turk Ger Gynecol Assoc ; 14(3): 178-81, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24592100

RESUMEN

Vein of Galen aneurysm malformation (VGAM) is a rare congenital vascular anomaly. Although the cause of VGAM remains to be elucidated, the current hypothesis is persistence of the embryonic vascular supply, which leads to progressive enlargement and formation of the aneurysmal component of a typical VGAM. Here, we present a 36-year-old woman at 23 weeks' gestation (gravida 3, para 2) who was evaluated using 3D power Doppler sonography for the prenatal diagnosis of a vein of Galen aneurysm. Investigation using 3D power Doppler sonography allowed for a non-invasive yet diffuse and detailed prenatal assessment of VGAM. Thus, we suggest that prenatal sonography with 3D power Doppler may be an option in cases of VGAM.

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