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1.
Obstet Gynecol Int ; 2022: 7342061, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36274656

RESUMEN

Objectives: The study aims to report on the feasibility and associated adverse events of HPV-Vaccination (HPVV) in a private clinic setting in Lebanon and, when available, the results of subsequent cervical cancer screening. Methods: Opportunistic HPV vaccination is offered at the Women's Health Center of the AUBMC. We retrospectively reviewed the patients' demographic data, the incidence of adverse events, and their cytological screening. Results: A cohort of healthy women (n = 1013) aged 26.2 years (12-54 years) were opportunistically vaccinated with one of two HPV vaccines; 845 (83.4%) received the quadrivalent vaccine (Q4V), and 151 (14.1%) received the bivalent vaccine (B2V). The majority (75.8%) received three doses while 16% received two doses. Out of these women, 26.3% (267) became sexually active postvaccination (NS2), whereas 17% (174) were sexually active prior to vaccination (SA) and the rest 57% (572) reported no sexual activity (NS1). Among the SA group, 26% (46/147) presented with abnormal cytology at time of vaccination. As for the NS2 women, 5% (14/267) had subsequently abnormal screening within 37 (12-103) months following vaccination. Conclusions: In this observational study, we report the successful introduction of HPVV with negligible adverse events. The incidence of abnormal cervical cytology was low among our patients.

2.
J Matern Fetal Neonatal Med ; 35(18): 3453-3459, 2022 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-32954875

RESUMEN

OBJECTIVES: To evaluate the practice patterns among Lebanese obstetricians regarding obstetric care of twins and to compare selected practice patterns between general obstetricians and maternal fetal medicine physicians. METHODS: Questionnaires distributed during the annual meeting of the Lebanese Society of Obstetrics and Gynecology. RESULTS: Questionnaires were returned by 69.2% of the 296 physicians approached. Ten percent had fellowship training in Maternal Fetal Medicine (MFM). Thirty-nine percent perform cervical length measurement at 20-24 weeks of gestation and 34% recommend vaginal progesterone in case of a short cervix. When comparing selected practice patterns between MFM & general obstetricians, MFM specialists were less likely to perform cervical cerclage in the first trimester (5.9% versus 49%, p = .001), more likely to offer prenatal screening for aneuploidy (66.6% vs 46.4%, p = .03), less likely to use vaginal progesterone in the second trimester in the case of a short cervix (42.1% vs 61.8%, p = .04), less likely to perform serial ultrasound exam in the third trimester to assess fetal growth (50% vs 78%, p = .005) and more likely to deliver monoamniotic twins at 32-34 weeks of gestation (55% vs 37%, p = .05). CONCLUSION: Because of the different background of the Lebanese physicians, MFM specialists are more likely to follow obstetric care guidelines in twin gestation.


Asunto(s)
Ginecología , Obstetricia , Medición de Longitud Cervical , Femenino , Humanos , Embarazo , Embarazo Gemelar , Progesterona , Derivación y Consulta
3.
J Perinat Med ; 44(5): 533-42, 2016 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-27092644

RESUMEN

Magnetic resonance imaging (MRI) has been increasingly adopted in obstetrics practice in the past three decades. MRI aids prenatal ultrasound and improves diagnostic accuracy for selected maternal and fetal conditions. However, it should be considered only when high-quality ultrasound cannot provide certain information that affects the counseling, prenatal intervention, pregnancy course, and delivery plan. Major indications of fetal MRI include, but are not restricted to, morbidly adherent placenta, selected cases of fetal brain anomalies, thoracic lesions (especially in severe congenital diaphragmatic hernia), and soft tissue tumors at head and neck regions of the fetus. For fetal anatomy assessment, a 1.5-Tesla machine with a fast T2-weighted single-shot technique is recommended for image requisition of common fetal abnormalities. Individual judgment needs to be applied when considering usage of a 3-Tesla machine. Gadolinium MRI contrast is not recommended during pregnancy. MRI should be avoided in the first half of pregnancy due to small fetal structures and motion artifacts. Assessment of fetal cerebral cortex can be achieved with MRI in the third trimester. MRI is a viable research tool for noninvasive interrogation of the fetus and the placenta.


Asunto(s)
Enfermedades Fetales/diagnóstico por imagen , Imagen por Resonancia Magnética/métodos , Diagnóstico Prenatal/métodos , Ultrasonografía Prenatal/métodos , Sistema Nervioso Central/anomalías , Sistema Nervioso Central/diagnóstico por imagen , Contraindicaciones , Medios de Contraste , Femenino , Gadolinio , Hernias Diafragmáticas Congénitas/diagnóstico por imagen , Humanos , Neuroimagen/métodos , Enfermedades Placentarias/diagnóstico por imagen , Embarazo , Seguridad
4.
J Matern Fetal Neonatal Med ; 29(14): 2293-6, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26372104

RESUMEN

OBJECTIVE: The association between echogenic intracardiac focus (EIF) and trisomy 21 is well established, with a recognized ethnic variation. Our study aimed to determine the prevalence of EIF in a Middle Eastern population and to examine its association with trisomy 21 and other adverse pregnancy outcomes. METHODS: Retrospective case-control study of second-trimester obstetric sonograms (16-28 weeks) performed at a tertiary care center over a 5-year period. Cases with EIF were retrieved, and a matched control group with no EIF was identified. The incidence of trisomy 21 and other adverse pregnancy outcomes was compared. RESULTS: A total of 9270 obstetric sonograms were examined, with an EIF prevalence of 2.5% (95% CI: 2.2-2.8%). Of patients with available outcome data, EIF was not associated with trisomy 21 (0/163 versus 1/163; p value = 1.00). Additionally, EIF was not associated with trisomy 18, trisomy 13, small for gestational age, preterm birth, fetal demise, cesarean delivery, operative vaginal delivery, or admission to the neonatal intensive care unit. CONCLUSION: In a contemporary Middle Eastern population, EIF is a rare occurrence. As an isolated finding, it is not associated with aneuploidy or other adverse pregnancy outcomes. EIF appears to be incidental with no impact on clinical practice.


Asunto(s)
Calcinosis/diagnóstico por imagen , Corazón Fetal/diagnóstico por imagen , Ultrasonografía Prenatal , Adulto , Estudios de Casos y Controles , Síndrome de Down/diagnóstico , Femenino , Humanos , Líbano , Embarazo , Segundo Trimestre del Embarazo , Estudios Retrospectivos
5.
J Perinat Med ; 44(2): 131-7, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26506099

RESUMEN

Mid trimester fetal anatomy scan is a fundamental part of routine antenatal care. Some U/S soft markers or controversial U/S signs are seen during the scan and create some confusion regarding their relation to fetal chromosomal abnormalities. Example of these signs: echogenic focus in the heart, echogenic bowel, renal pyelectasis, ventriculomegaly, polydactely, club foot, choroid plexus cyst, single umbilical artery. We are presenting an evidence based approach from the literature for management of these controversial U/S signs.


Asunto(s)
Ultrasonografía Prenatal , Encefalopatías/congénito , Encefalopatías/diagnóstico por imagen , Cardiomegalia/congénito , Cardiomegalia/diagnóstico por imagen , Plexo Coroideo/diagnóstico por imagen , Pie Equinovaro/diagnóstico por imagen , Anomalías Congénitas/diagnóstico por imagen , Quistes/congénito , Quistes/diagnóstico por imagen , Ecocardiografía , Intestino Ecogénico/diagnóstico por imagen , Medicina Basada en la Evidencia , Femenino , Humanos , Recién Nacido , Masculino , Polidactilia/diagnóstico por imagen , Embarazo , Segundo Trimestre del Embarazo , Pielectasia/diagnóstico por imagen , Arteria Umbilical Única/diagnóstico por imagen
6.
J Perinat Med ; 44(2): 119-23, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26389632

RESUMEN

Today we are living in a globalized world in which information on what is happening in one part of the world is easily communicated to other parts of the world. This happens thanks to advancement in science and technology. One area where technology has made the greatest impact is heath care provision. Ultrasound technology is now playing a critical role in health care provision particularly in Obstetrics and Gynaecology. This has significantly assisted in provision of quality health care to pregnant women and their unborn infants and in reducing maternal and neonatal morbidity and mortality in the developed world. Africa the continent with greatest health care challenges and with the highest maternal and neonatal mortalities is yet to fully utilize this important technology. The need for this technology is great as the conditions requiring its application abound. The effective application of Ultrasound however faces serious challenges in Africa. To successfully entrench Ultrasound in quality Obstetrics and Gynaecology care various approaches must be adopted to overcome the challenges. The aim of this paper is to identify the benefits and the challenges inimical to the application Ultrasound in Obstetrics and Gynecology in Africa. It also examines what needs to be done to achieve better application of Ultrasound in Obstetrics and Gynecology.


Asunto(s)
Ultrasonografía Prenatal/estadística & datos numéricos , África , Países en Desarrollo , Femenino , Ginecología/tendencias , Humanos , Recién Nacido , Obstetricia/tendencias , Perinatología/tendencias , Embarazo , Calidad de la Atención de Salud/tendencias , Ultrasonografía Prenatal/tendencias
7.
J Perinat Med ; 44(2): 125-9, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26376219

RESUMEN

Gray-scale image data are processed in 3D ultrasound by repeated scans of multiple planes within a few seconds to achieve one surface rendering image and three perpendicular plane images. The 4D image is achieved by repeating 3D images in short intervals, i.e. 3D and 4D ultrasound are based on simple B-mode images. During 3D/4D acquisition, a fetus in utero is exposed by ultrasound beam for only a few seconds, and it is as short as real-time B-mode scanning. Therefore, simple 3D imaging is as safe as a simple B-mode scan. The 4D ultrasound is also as safe as a simple B-mode scan, but the ultrasound exposure should be shorter than 30 min. The thermal index (TI) and mechanical index (MI) should both be lower than 1.0, and the ultrasound study is regulated by the Doppler ultrasound if it is combined with simple 3D or 4D ultrasound. Recently, some articles have reported the functional changes of animal fetal brain neuronal cells and liver cell apoptosis with Doppler ultrasound. We discuss cell apoptosis by ultrasound in this report. Diagnostic ultrasound safety is achieved by controlling the output pulse and continuous ultrasound waves using thermal and mechanical indices, which should be <1.0 in abdominal and transvaginal scan, pulsed Doppler, as well as 3D and 4D ultrasound. The lowest spatial peak temporal average (SPTA) intensity of the ultrasound to suppress cultured cell growth is 240 mW/cm2, below which no ultrasound effect has been reported. An ultrasound user must be trained to recognize the ultrasound bioeffects; thermal and mechanical indices, and how to reduce these when they are higher than 1.0 on the monitor display; and guide the proper use of the ultrasound under the ALARA principle, because the user is responsible for ensuring ultrasound safety.


Asunto(s)
Imagenología Tridimensional/métodos , Ultrasonografía Prenatal/métodos , Animales , Femenino , Feto/diagnóstico por imagen , Humanos , Imagenología Tridimensional/efectos adversos , Recién Nacido , Embarazo , Seguridad , Ultrasonografía Prenatal/efectos adversos
8.
J Perinat Med ; 44(7): 737-743, 2016 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-26124046

RESUMEN

Fetal surgery involves a large number of heterogeneous interventions that vary from simple and settled procedures to very sophisticated or still-in-development approaches. The overarching goal of fetal interventions is clear: to improve the health of children by intervening before birth to correct or treat prenatally diagnosed abnormalities. This article provides an overview of fetal interventions, ethical approaches in fetal surgery, and benefits obtained from antenatal surgeries.


Asunto(s)
Feto/cirugía , Ablación por Catéter/ética , Ablación por Catéter/métodos , Femenino , Enfermedades Fetales/diagnóstico por imagen , Enfermedades Fetales/cirugía , Fetoscopía/ética , Fetoscopía/métodos , Humanos , Recién Nacido , Internacionalidad , Procedimientos Quirúrgicos Mínimamente Invasivos/ética , Procedimientos Quirúrgicos Mínimamente Invasivos/métodos , Obstetricia , Atención Perinatal , Embarazo , Sociedades Médicas , Ultrasonografía Prenatal
9.
Am J Epidemiol ; 172(12): 1424-30, 2010 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-20978088

RESUMEN

Consanguinity promotes homozygosity of recessive susceptibility gene variants and can be used to investigate a recessive component in diseases whose inheritance is uncertain. The objective of this study was to assess the association between consanguinity and preterm birth (PTB), stratified by gestational age and clinical presentation (spontaneous vs. medically indicated). Data were collected on 39,745 singleton livebirths without major birth defects, admitted to 19 hospitals in Lebanon, from September 2003 to December 2007. Deliveries before completed 33 weeks' gestation and deliveries at 33-36 weeks' gestation were compared, with respect to cousin marriage, with those after completed 36 weeks' gestation by using multinomial multiple logistic regression. Overall, infants of consanguineous parents had a statistically significant 1.6-fold net increased risk of being born at less than 33 weeks' gestation compared with infants of unrelated parents. This association was statistically significant only with spontaneous PTB. There was no increased risk of being born at 33-36 weeks' gestation associated with consanguinity for both clinical presentations of PTB. Our findings support a genetic contribution to early onset PTB and suggest that early PTB should be targeted in future genetic studies rather than the classic lumping of all births less than 37 weeks' gestation.


Asunto(s)
Consanguinidad , Nacimiento Prematuro/epidemiología , Nacimiento Prematuro/genética , Adulto , Estudios Transversales , Femenino , Edad Gestacional , Humanos , Recién Nacido , Recien Nacido Prematuro , Líbano , Persona de Mediana Edad , Embarazo , Estudios Retrospectivos , Factores de Riesgo , Factores Socioeconómicos , Adulto Joven
12.
Prenat Diagn ; 26(5): 409-14, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16532522

RESUMEN

OBJECTIVES: Quantitative Fluorescent PCR (QF-PCR) is a simpler and faster method of detecting common chromosomal abnormalities when compared to cytogenetic analysis. The aim of our study is to investigate the applicability of this methodology in a population where consanguineous marriages are common and to estimate the heterozygous frequency of the PCR markers used. METHODS: Four hundred and twenty-three DNA samples were extracted from uncultured amniocytes and amplified with 18 short tandem repeats (STR) markers specific to chromosomes 13, 18 and 21. Amplification products were analyzed using the GeneScan software. RESULTS: QF-PCR correctly identified all the numerical abnormalities related to chromosomes 13, 18 and 21. A total of 24 autosomal trisomies (5.7%) were detected. The markers D21S1432 and D21S11 were the most consistent in providing unequivocal positive results for chromosome 21 and the heterozygosity percentages of the markers used were lower than the values reported in Western populations. CONCLUSION: QF-PCR is reliable for the prenatal diagnosis of numerical anomalies of the chromosomes 13, 18 and 21 in our study population. The absence of STR heterozygosity data from Lebanon and surrounding countries makes our study very useful for the development of a reliable QF-PCR trisomy detection test.


Asunto(s)
Trastornos de los Cromosomas/diagnóstico , Consanguinidad , Pruebas Genéticas/métodos , Hibridación Fluorescente in Situ/métodos , Reacción en Cadena de la Polimerasa/métodos , Adulto , Trastornos de los Cromosomas/genética , Cromosomas Humanos Par 13 , Cromosomas Humanos Par 18 , Cromosomas Humanos Par 21 , Femenino , Tamización de Portadores Genéticos/métodos , Marcadores Genéticos , Pruebas Genéticas/normas , Humanos , Hibridación Fluorescente in Situ/normas , Reacción en Cadena de la Polimerasa/normas , Embarazo , Reproducibilidad de los Resultados , Programas Informáticos , Secuencias Repetidas en Tándem
13.
Am J Obstet Gynecol ; 189(2): 513-8, 2003 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-14520227

RESUMEN

OBJECTIVE: The purpose of this study was to compare maternal and neonatal complications in spontaneous versus in vitro fertilization twins. STUDY DESIGN: Twin gestations that were delivered from 1995 to 2000 were reviewed. Cases consisted of 56 in vitro fertilization twins, each of which was matched to two control mothers by age and parity. They were compared regarding various maternal and neonatal complications. RESULTS: In vitro fertilization twins were more likely to have preterm labor compared with control twins, with no difference in the incidences of pregnancy-induced hypertension, gestational diabetes mellitus, placenta previa, or preterm premature rupture of membranes between the two groups. The cesarean delivery rate was significantly higher in cases of twins who were conceived by in vitro fertilization (76.8% vs 58.0%, P=.026), despite a similar rate of elective cesarean delivery and the incidence of nonvertex twin A in both groups. The preterm delivery rate was significantly higher (67.9% vs 41.1%, P=.002) and the gestational age was significantly lower (35+/-3 weeks vs 36+/-3 weeks, P=.043) in cases compared with control subjects. Both twins were, on the average, 230 g lighter in the in vitro fertilization group compared with the control group. However, intrauterine growth restriction was more frequent in the control group (36.6% vs 25%, P=.044). There was a significantly higher incidence of admission to the neonatal intensive care unit, respiratory distress syndrome, a need for mechanical ventilation, and pneumothorax in cases compared with control subjects. CONCLUSION: When compared with spontaneous twins, in vitro fertilization twins are more likely to be delivered by cesarean delivery and to have a higher incidence of preterm birth and prematurity-related respiratory complications with a longer nursery stay.


Asunto(s)
Fertilización In Vitro , Resultado del Embarazo , Embarazo Múltiple , Gemelos , Adulto , Estudios de Casos y Controles , Cesárea , Femenino , Retardo del Crecimiento Fetal/epidemiología , Edad Gestacional , Humanos , Incidencia , Recién Nacido , Recien Nacido Prematuro , Unidades de Cuidado Intensivo Neonatal/estadística & datos numéricos , Presentación en Trabajo de Parto , Tiempo de Internación , Embarazo , Trastornos Respiratorios/epidemiología
14.
Fertil Steril ; 77(1): 179-82, 2002 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11779612

RESUMEN

OBJECTIVE: To describe a previously unreported isolated congenital cervical diverticulum and its gynecologic, reproductive, and obstetrical implications. DESIGN: Case report. SETTING: A university hospital. PATIENT: A 31-year-old woman presenting with menometrorrhagia and primary infertility. Investigation revealed an isolated collecting cervical diverticulum causing prolonged postmenstrual spotting, possibly interfering with sperm capacitation and access to the uterine cavity. INTERVENTION(S): The examination included hysterosalpingography and magnetic resonance imaging. The combined hysteroscopy and laparoscopy revealed a 5 x 5 cm cervical diverticulum, around 1 cm from the external cervical os, leading to a short cervical canal connected to a normal uterine cavity. The patient achieved a pregnancy after controlled ovarian hyperstimulation and ultrasonographically guided intrauterine insemination. MAIN OTUCOME MEASURE(S): Pregnancy and obstetrical outcome. RESULT(S): Extensive evaluation revealed the patient's condition to be a previously undescribed congenital cervical anomaly. The patient's infertility was corrected by ovulation induction and sonographically guided intrauterine insemination, which resulted in a twin pregnancy. After 27 weeks of gestation, preterm labor complicated the delivery. CONCLUSION(S): The diagnosis and management of this unusual congenital cervical diverticulum present a particular challenge, as this congenital abnormality has not been previously described or reported.


Asunto(s)
Divertículo/complicaciones , Infertilidad Femenina/etiología , Enfermedades del Cuello del Útero/complicaciones , Adulto , Cuello del Útero/anomalías , Divertículo/diagnóstico , Divertículo/diagnóstico por imagen , Divertículo/cirugía , Femenino , Humanos , Histerosalpingografía , Embarazo , Enfermedades del Cuello del Útero/diagnóstico , Enfermedades del Cuello del Útero/diagnóstico por imagen , Enfermedades del Cuello del Útero/cirugía
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