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1.
Int J Gynaecol Obstet ; 80(2): 123-7, 2003 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-12566184

RESUMEN

OBJECTIVES: To investigate the prevalence and timing of cervical cerclage placement in multiple gestations. METHODS: Our perinatal database was queried for all multiple gestations delivered at Evanston Hospital from 12/95 through 12/00. This list was then cross-matched with billing and medical records for 'incompetent cervix' and 'cerclage.' The medical records of all deliveries /=14 weeks over a 5-year period. The number of patients that underwent cerclage placement was 29 or 3.6%. The mean gestational age at cerclage placement was 18.6+/-4.5 weeks (range 11-24.6). Twelve were elective or prophylactic while 17 were 'urgent' or 'emergent.' The mean gestational age for the 17 emergent cerclages was 21.4+/-2.2 weeks (range 16.6-24.6). When compared with those patients who did not undergo cerclage placement, there was no difference in maternal demographics including age, parity, or previous full-term delivery. There was a significant difference in the gestational age at delivery for the cerclage vs. no cerclage group; 29.3+/-5.6 vs. 34.4+/-4.6 weeks, respectively, and in the frequency of losses at

Asunto(s)
Cerclaje Cervical/estadística & datos numéricos , Embarazo Múltiple , Incompetencia del Cuello del Útero/epidemiología , Adulto , Femenino , Edad Gestacional , Humanos , Illinois/epidemiología , Embarazo , Embarazo Múltiple/estadística & datos numéricos , Prevalencia , Estudios Retrospectivos
2.
Prenat Diagn ; 21(10): 860-3, 2001 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11746130

RESUMEN

Maternal uniparental disomy (UPD) 20 was found in a 35-month-old girl, the product of a pregnancy complicated by a prenatal diagnosis of mosaic trisomy 20. Phenotypic abnormalities included pre- and postnatal growth failure, microcephaly, minor dysmorphic features and psychomotor developmental delay. Chromosomal analysis on cord blood revealed only a normal 46,XX karyotype. Microsatellite analysis of 27 chromosome 20 loci confirmed maternal UPD for all 11 informative markers. Maternal heterodisomy was detected in two and maternal isodisomy in three loci. In the remaining six loci, a non-informative maternal UPD pattern was displayed, as mother and proband are homozygous for the same allele. To our knowledge this is the first reported case of maternal disomy 20 with normal karyotype ascertained by a mosaic trisomy 20 pregnancy.


Asunto(s)
Cromosomas Humanos Par 20 , Mosaicismo , Madres , Trisomía , Disomía Uniparental , Adulto , Amniocentesis , Preescolar , Anomalías Congénitas/genética , Femenino , Edad Gestacional , Trastornos del Crecimiento/genética , Humanos , Edad Materna , Microcefalia/genética , Repeticiones de Microsatélite , Embarazo , Embarazo de Alto Riesgo , Trastornos Psicomotores/genética
3.
J Soc Gynecol Investig ; 7(5): 297-300, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11035282

RESUMEN

OBJECTIVE: To characterize the active phase of labor in triplet pregnancies and compare it with gestational age-matched twins and singletons. METHODS: Active phase rates were calculated beginning at 5 cm of dilation for women with triplet gestations longer than 24 weeks who labored and reached the second stage. Twin and singleton cohorts that also completed the first stage of labor were matched for gestational age at delivery (+/-1 week), parity, and epidural use. Intrapartum variables included oxytocin use (induction or augmentation, duration of infusion, and maximum dosage), cervical dilation at membrane rupture, and active phase dilation rate. RESULTS: Thirty-two triplet pregnancies met inclusion criteria between January 1994 and September 1998 and were each compared with twin and singleton cases in a 1:2 ratio. Triplet and twin active phase rates, while similar (1.8 versus 1.7 cm/hour, respectively), were significantly lower than the mean singleton dilation rate (2.3 cm/hour, P =.02). No other intrapartum variables differed between the three groups. Despite controlling for gestational age at delivery, mean birth weights were significantly higher in singletons and correspondingly lower in twins and triplets (2,493 versus 2,112 and 1,968 g, respectively; P =.001). An analysis of active phase dilation rates as a function of the cumulative birth weight per pregnancy demonstrated an inverse correlation, with slower progress in active labor associated with increasing total fetal weight (R = -.24; P =.002). CONCLUSIONS: Triplet and twin active phase dilation proceeds at a slower rate than that observed in singleton pregnancies. The rate of active phase dilation is inversely correlated to total fetal weight.


Asunto(s)
Trabajo de Parto/fisiología , Trillizos , Gemelos , Peso al Nacer , Femenino , Edad Gestacional , Humanos , Embarazo , Análisis de Regresión , Factores de Tiempo
4.
J Reprod Med ; 44(10): 842-8, 1999 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-10554743

RESUMEN

OBJECTIVE: To determine whether an "optional" vaginal delivery rate and novel delivery score would provide informative profiles of intrapartum care. STUDY DESIGN: Prospective survey of all parturients delivering between January and December 1996. Deliveries were categorized as standard-vaginal (V-S), optional-vaginal (V-O), standard-cesarean (C-S) or potentially avoidable-cesarean (C-PA) using specific perinatal criteria derived from the literature. A weighted equation was developed and applied, generating physician delivery scores, giving "extra credit" for V-O and a "debit" for C-PA: delivery score = [(% V-O x 2) + (% V-S) - (% C-PA] x 100. RESULTS: V-O rates and delivery scores ranged from 0% to 25% and from 52 to 113, respectively (medians of 9.8% and 92.9). Among the obstetricians (n = 38), a significant inverse correlation was noted between the total C-S rates and V-O rates (r = -.54, P < .005). The maternal-fetal medicine physicians (n = 6) had high total C-S rates (22-36%) but also had high V-O rates (17.1-23.5%) and high delivery scores (82.1-101.5). CONCLUSION: The optional vaginal delivery rate and delivery score are more-informative indicators of intrapartum management acumen than is cesarean section rate alone. We suggest incorporating these descriptors into departmental quality assurance programs.


Asunto(s)
Pautas de la Práctica en Medicina/estadística & datos numéricos , Parto Vaginal Después de Cesárea/estadística & datos numéricos , Adulto , Toma de Decisiones , Femenino , Humanos , Servicios de Salud Materna , Modelos Teóricos , Embarazo , Estudios Prospectivos
5.
Obstet Gynecol ; 94(6): 925-8, 1999 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-10576177

RESUMEN

OBJECTIVE: To determine the frequency of atypical aneuploidy resulting from prenatal testing and assess the implications of these diagnoses on prenatal decision making. METHODS: We reviewed all amniotic fluid and chorionic villus samples obtained between January 1994 and September 1997 and grouped the abnormal cases into typical or atypical subcategories. This distinction was based upon whether the diagnosis provided a straightforward range of prognoses or an ambiguous clinical implication. Results were stratified by sample source to determine whether atypical aneuploidy was more commonly seen in cultures of chorionic villi or amniocytes. We also evaluated the influence of ultrasound findings on prenatal decision making in atypical aneuploid cases. RESULTS: Of 2960 samples, 134 were abnormal (4.4%), with 27 of 134 abnormalities (20%) representing atypical aneuploidies. The percentages of chorionic villus and amniocentesis cases complicated by atypical aneuploidy (22% and 78%, respectively) were consistent with the distribution of procedures in the entire study. Ultrasound abnormalities did not invariably prompt a decision to terminate pregnancy (only two terminations of six fetuses with congenital malformation), whereas atypical karyotypes led to termination even in the presence of normal-appearing fetal anatomy (five terminations of 21 without malformations; P = .63). CONCLUSION: The frequency of atypical aneuploidy resulting from prenatal diagnosis was approximately 1.0%, and these cases represented 20% of all abnormal karyotypes observed. The ambiguity conferred by atypical aneuploidy can influence a family's decision making, even in the presence of normal ultrasound findings.


Asunto(s)
Aneuploidia , Diagnóstico Prenatal , Adulto , Amniocentesis , Muestra de la Vellosidad Coriónica , Toma de Decisiones , Femenino , Asesoramiento Genético , Humanos , Cariotipificación , Edad Materna , Embarazo , Ultrasonografía Prenatal
6.
Am J Obstet Gynecol ; 179(4): 942-5, 1998 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-9790375

RESUMEN

OBJECTIVE: This study aimed to compare neonatal outcomes in a cohort of triplet gestations undergoing a trial of labor with those of a similar cohort delivered by elective cesarean delivery. STUDY DESIGN: Thirty-three women with triplet gestations who underwent a trial of labor were compared with a matched cohort of 33 women with triplet gestations who were delivered of their infants by elective cesarean delivery. Neonatal outcomes assessed included respiratory distress syndrome, retinopathy of prematurity, necrotizing enterocolitis, intraventricular hemorrhage, Apgar scores, and birth trauma. RESULTS: Twenty-nine of 33 women (87.9%) who underwent a trial of labor had a successful vaginal delivery of all 3 neonates. One patient was delivered of her first triplet vaginally but then required a cesarean delivery for abruptio placentae; 3 other patients were delivered of their infants by cesarean section for active-phase arrest of labor. There were no differences in neonatal outcomes between the 2 groups, although triplet neonates delivered by elective cesarean section demonstrated a trend toward a greater incidence of respiratory distress syndrome (P = .09). CONCLUSION: Our experience suggests that offering vaginal delivery is an acceptable management plan for triplet gestations.


Asunto(s)
Resultado del Embarazo , Esfuerzo de Parto , Trillizos , Adulto , Puntaje de Apgar , Traumatismos del Nacimiento/epidemiología , Hemorragia Cerebral/epidemiología , Cesárea , Estudios de Cohortes , Enterocolitis Necrotizante/epidemiología , Femenino , Sangre Fetal , Edad Gestacional , Humanos , Concentración de Iones de Hidrógeno , Recién Nacido , Masculino , Embarazo , Síndrome de Dificultad Respiratoria del Recién Nacido/epidemiología , Retinopatía de la Prematuridad/epidemiología
7.
J Reprod Med ; 43(3): 191-5, 1998 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-9564643

RESUMEN

OBJECTIVE: To evaluate the impact of operator caseload on the sampling efficiency for early and standard, midtrimester amniocentesis. STUDY DESIGN: Prospective ascertainment of genetic amniocenteses performed during 36 months, grouped into early (13-14 weeks' gestation) and standard procedures (15-20 weeks' gestation). Details of each amniocentesis were recorded immediately after sampling, and pregnancy outcomes were retrieved via questionnaires completed by the delivering physician. Sampling efficiency was evaluated separately in the early and standard cohorts in relation to operator caseload. RESULTS: In total, 193 and 707 patients underwent early and standard amniocentesis, respectively. Forty of 46 physician-operators performed < 50 total procedures during the study interval (group A). When compared to operators performing > or = 50 cases (group B, n = 6), a higher rate of single-pass success was noted among group B physicians for both early and standard procedures (A vs. B, early: 40/45 vs. 145/148, P = .018; standard: 243/295 vs. 384/412, P < .0001). Logistic regression confirmed an independent effect of physician caseload on sampling efficiency and a significant interaction between physician caseload and simultaneous ultrasound guidance in predicting single-attempt success. CONCLUSION: Operator caseload directly influenced sampling efficiency for both early and standard, midtrimester amniocentesis.


Asunto(s)
Amniocentesis/normas , Médicos/normas , Carga de Trabajo , Adulto , Femenino , Humanos , Embarazo , Resultado del Embarazo , Primer Trimestre del Embarazo , Segundo Trimestre del Embarazo , Estudios Prospectivos , Reproducibilidad de los Resultados , Ultrasonografía Prenatal
8.
Fertil Steril ; 67(1): 30-3, 1997 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-8986679

RESUMEN

OBJECTIVE: To compare pregnancy outcome in twin gestations resulting from multifetal reduction to "primary" twin pregnancies derived from either spontaneous conception or infertility therapy. DESIGN: Case-control study. SETTING: University-affiliated tertiary center. PATIENT(S): Multifetal pregnancies (quadruplets or more) reduced to twins (group A) compared with twin gestations conceived either spontaneously (group B) or through infertility therapy (group C). INTERVENTION(S): Multifetal reduction for group A; perinatal care for groups A, B, and C. MAIN OUTCOME MEASURE(S): Comparison of perinatal complications between groups including antepartum bleeding, premature membrane rupture, and preterm labor. Neonatal outcomes compared including gestational age at delivery, birth weight, incidence of fetal growth restriction, and twin discordancy. RESULT(S): A higher incidence of idiopathic preterm labor was noted in group A cases (14/18) compared with either of the control groups (B: 26/54, or C: 24/54). As a consequence, group A had the lowest gestational age at delivery (32.6 +/- 3.9 weeks) compared with groups B (33.6 +/- 4.4 weeks) and C (36.0 +/- 3.4 weeks). Corresponding birth weights of both first- and second-born twins were significantly lower in group A compared with group C, whereas the birth weight comparison between groups A and B showed a nonsignificant difference. The proportion of pregnancies in which one or both twins weighted less than the 10th percentile was greatest in group A pregnancies (A: 5/18 versus C: 5/54). Discordant birth weight among twin pairs was proportionately greater for group A cases at both the 20% and 30% discordance levels. CONCLUSION(S): Twin gestations resulting from multifetal reduction are at increased risk for preterm birth, fetal growth restriction, and discordancy when compared with fertility therapy-derived, nonreduced twins.


Asunto(s)
Retardo del Crecimiento Fetal/etiología , Trabajo de Parto Prematuro/etiología , Reducción de Embarazo Multifetal/efectos adversos , Gemelos , Adulto , Peso al Nacer , Estudios de Casos y Controles , Femenino , Humanos , Recién Nacido , Embarazo
9.
Clin Perinatol ; 23(3): 465-72, 1996 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-8884120

RESUMEN

Despite advances in neonatal medicine, the mortality rate for congenital diaphragmatic hernia remains high. The results of work in animal models suggest that this anomaly may be amenable to in utero surgical correction. In this article, the natural history of congenital diaphragmatic hernia in humans is reviewed, and the development of antenatal management strategies is traced. The ethical issues surrounding the management of fetuses with diaphragmatic hernias are also discussed. The ground-breaking nature of the development of strategies for management of congenital diaphragmatic hernia underscores the importance of establishing scientific and ethical guidelines for future endeavors with in utero therapy.


Asunto(s)
Ética Médica , Enfermedades Fetales/cirugía , Hernias Diafragmáticas Congénitas , Animales , Modelos Animales de Enfermedad , Femenino , Humanos , Embarazo , Mujeres Embarazadas , Diagnóstico Prenatal , Pronóstico , Medición de Riesgo , Ovinos , Experimentación Humana Terapéutica
10.
Am J Obstet Gynecol ; 173(4): 1254-8, 1995 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-7485332

RESUMEN

OBJECTIVE: The objective of this study was to determine the significance of isolated hyperechoic fetal bowel. STUDY DESIGN: Forty-five cases with prospective, ultrasonographic diagnosis of isolated hyperechoic fetal bowel were reviewed. Fetal variables, including aneuploidy, deoxyribonucleic acid studies for cystic fibrosis, congenital infection, growth retardation, and intrauterine death were reported. RESULTS: Thirty-four of the 45 cases (76%) resulted in live-born infants without detected abnormalities. However, hyperechoic bowel was associated with cystic fibrosis in two cases (4%), congenital infection in two cases (4%), and fetal alcohol syndrome in one case. Termination of pregnancy was elected in three cases and intrauterine fetal death occurred in three cases (7%). Growth retardation was observed in five of 39 (13%) live-born infants. CONCLUSION: Isolated hyperechoic fetal bowel is associated with significant pathologic disorders. Women whose fetuses are diagnosed as having isolated hyperechoic bowel should be offered additional prenatal diagnostic options, including maternal serologic studies for congenital infection, fetal karyotype, and deoxyribonucleic acid testing for cystic fibrosis. In addition, continuing ultrasonographic evaluation of fetal growth and antenatal biophysical assessment should be considered.


Asunto(s)
Enfermedades Fetales/diagnóstico por imagen , Intestinos/diagnóstico por imagen , Ultrasonografía Prenatal , Fibrosis Quística/diagnóstico por imagen , Femenino , Trastornos del Espectro Alcohólico Fetal/diagnóstico por imagen , Muerte Fetal/diagnóstico por imagen , Retardo del Crecimiento Fetal/diagnóstico por imagen , Humanos , Infecciones/diagnóstico por imagen , Intestinos/embriología , Embarazo , Segundo Trimestre del Embarazo , Tercer Trimestre del Embarazo , Estudios Prospectivos
11.
J Reprod Med ; 40(6): 477-8, 1995 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-7544411

RESUMEN

The incidence of antepartum Rh isoimmunization has been limited by third-trimester Rh immune globulin (RhIg) administration. Prophylactic failures are uncommon but can occur if sensitization takes place prior to the 28th week of gestation. We report a case of midtrimester Rh sensitization in an anticardiolipin antibody-positive primipara coincident with the discovery of an elevated maternal serum alpha-fetoprotein value, oligohydramnios and fetal growth retardation. This case suggests that fetal-maternal hemorrhage and subsequent sensitization may be facilitated by anticardiolipin antibody-induced placental damage. Prophylactic midtrimester RhIg administration might avoid sensitization in similar cases.


Asunto(s)
Anticuerpos Anticardiolipina/sangre , Síndrome Antifosfolípido/sangre , Complicaciones del Embarazo/sangre , Isoinmunización Rh/etiología , alfa-Fetoproteínas/metabolismo , Adulto , Síndrome Antifosfolípido/complicaciones , Femenino , Muerte Fetal , Retardo del Crecimiento Fetal/etiología , Humanos , Oligohidramnios/etiología , Enfermedades Placentarias/complicaciones , Embarazo , Segundo Trimestre del Embarazo , Isoinmunización Rh/sangre
12.
Obstet Gynecol ; 85(4): 570-2, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7898835

RESUMEN

OBJECTIVE: To evaluate the perinatal outcome in fetuses with single umbilical artery detected on targeted prenatal ultrasound without other anomalies. METHODS: During a 3.5-year period, an isolated single umbilical artery was suspected on prenatal ultrasound examination in 57 fetuses evaluated at two referral centers. Targeted imaging to rule out concurrent fetal anomalies was normal in all cases. Pregnancy and perinatal outcome data were retrieved by review of the medical records or from conversations with referring physicians. Complete follow-up was available in 50 cases. RESULTS: A two-vessel umbilical cord was confirmed at birth in 50 neonates. The mean gestational age at delivery was 38.6 +/- 2.8 weeks; the mean birth weight was 3202.8 +/- 835.8 g. Seventeen patients (34%) underwent genetic amniocentesis, and all fetuses had a normal karyotype. The only neonate ascertained to have a congenital anomaly after birth was diagnosed with total anomalous pulmonary venous return. This neonate underwent a corrective surgical procedure and is thriving with no apparent problems at 3.5 years of age. There were no perinatal deaths. CONCLUSION: In the absence of additional sonographically detectable anomalies, an isolated single umbilical artery does not seem to affect clinical outcome and therefore should not alter routine obstetric management.


Asunto(s)
Resultado del Embarazo , Ultrasonografía Prenatal , Arterias Umbilicales/anomalías , Arterias Umbilicales/diagnóstico por imagen , Adulto , Amniocentesis , Peso al Nacer , Femenino , Estudios de Seguimiento , Humanos , Recién Nacido , Masculino , Valor Predictivo de las Pruebas , Embarazo
13.
Prenat Diagn ; 14(6): 421-7, 1994 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-7937577

RESUMEN

We wished to identify the types and frequencies of malformations among continuing pregnancies exposed to chorionic villus sampling (CVS) and to determine whether selected procedure-related variables differ between the normal and anomalous cohorts. CVS was performed in 1048 patients between May 1988 and January 1992. Prospective assessment of perinatal outcome was ascertained by (1) physician-patient phone contact within 1 week of sampling, (2) ultrasound evaluation of the fetal anatomy at mid-gestation, (3) a detailed post-partum questionnaire completed by the referring obstetrician, and (4) a telephone interview with each patient after the expected date of confinement. Twenty-seven major malformations were documented among 938 pregnancies (live born, n = 934; electively terminated, n = 4), and included cardiac malformations (5), hypospadias (5), craniosynostosis (2), pyloric stenosis (2), inguinal hernia (2), polydactyly (2), syndactyly, distal extremely hemimelia, anencephaly, hydrocephalus, cleft lip and palate, omphalocele, diaphragmatic hernia, thanatophoric dysplasia, and unilateral cataract. Normal and anomalous cohorts were similar with respect to sampling method (transabdominal/transcervical ratio), mean gestational age at CVS, single-pass success rate, and mean total sample weight. No relationship between any procedure-related variable and the risk of malformation was observed.


Asunto(s)
Muestra de la Vellosidad Coriónica/efectos adversos , Anomalías Congénitas/etiología , Anomalías Congénitas/diagnóstico por imagen , Anomalías Congénitas/epidemiología , Femenino , Edad Gestacional , Humanos , Embarazo , Encuestas y Cuestionarios , Ultrasonografía Prenatal
14.
Obstet Gynecol ; 83(5 Pt 1): 657-60, 1994 May.
Artículo en Inglés | MEDLINE | ID: mdl-8164920

RESUMEN

OBJECTIVE: To evaluate the comparative safety of transcervical and transabdominal chorionic villus sampling (CVS). METHODS: From May 1988 to January 1992, CVS was performed by two operators at 9-12 weeks' gestation in 1048 singleton pregnancies. The sampling method for each patient, transabdominal or transcervical, was chosen primarily based upon placental location; the transabdominal route was used for anterior or fundal location and the transcervical route for posterior placentation. Perinatal outcome was assessed by post-procedure patient telephone contact, mid-gestation ultrasound evaluation, postpartum questionnaire completed by the referring obstetrician, and telephone interview with each patient after delivery. RESULTS: Complete follow-up was available in 1012 cases (97%). Excluding 39 elective abortions, 35 of 973 euploid pregnancies aborted spontaneously. The difference in fetal loss rate between transcervical and transabdominal CVS approached statistical significance (5.2 versus 2.9%; P = .058). Bleeding before CVS (P = .006) and multiple placental aspirations (P = .022) were associated with fetal loss for the entire study group. An interaction between uterine position and sampling method was also indicated; an increased loss rate was associated with transcervical CVS in the presence of uterine retroversion (P = .0017). CONCLUSION: Despite choosing the preferred CVS method for each patient, an increased loss rate may be associated with transcervical sampling in the presence of uterine retroversion.


Asunto(s)
Aborto Espontáneo/etiología , Muestra de la Vellosidad Coriónica/métodos , Trabajo de Parto Prematuro/etiología , Abdomen , Aborto Espontáneo/epidemiología , Adulto , Cuello del Útero , Muestra de la Vellosidad Coriónica/efectos adversos , Estudios de Cohortes , Intervalos de Confianza , Femenino , Estudios de Seguimiento , Humanos , Modelos Logísticos , Trabajo de Parto Prematuro/epidemiología , Oportunidad Relativa , Embarazo , Factores de Riesgo
15.
Am J Obstet Gynecol ; 169(6): 1411-7, 1993 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-8267038

RESUMEN

OBJECTIVE: We compared the use of aspirin alone with combined therapy (prednisone plus aspirin) in antiphospholipid antibody-positive obstetric patients with prior adverse pregnancy outcome. STUDY DESIGN: Thirty-nine patients meeting specific laboratory and clinical inclusion criteria were randomized to receive either combined therapy (prednisone plus low-dose aspirin, n = 17) or aspirin alone (n = 22). The daily aspirin dose was 81 mg; prednisone was begun at 20 mg/day and increased or decreased on the basis of observed changes in serial antibody levels. Perinatal outcomes were compared between groups. Evaluation of treatment-related maternal complications and serial antibody titers was also accomplished. RESULTS: Thirty-four randomized subjects were evaluable (prednisone plus low-dose aspirin, n = 12 vs aspirin only, n = 22); no perinatal losses were observed in the study cohort. Preterm delivery was experienced by significantly more patients receiving prednisone plus low-dose aspirin than aspirin only (8/12 vs 3/22, respectively; p = 0.003), and prednisone exposure appeared to be an independent risk factor for preterm birth. CONCLUSIONS: The use of prednisone therapy in conjunction with low-dose aspirin does not appear to improve outcome and may provoke obstetric complications in antiphospholipid antibody-positive patients.


Asunto(s)
Síndrome Antifosfolípido/tratamiento farmacológico , Aspirina/uso terapéutico , Prednisona/uso terapéutico , Complicaciones del Embarazo/tratamiento farmacológico , Adulto , Anticuerpos Anticardiolipina/sangre , Síndrome Antifosfolípido/sangre , Quimioterapia Combinada , Femenino , Humanos , Trabajo de Parto Prematuro/inducido químicamente , Prednisona/efectos adversos , Embarazo , Complicaciones del Embarazo/sangre , Resultado del Embarazo , Estudios Prospectivos
16.
Am J Obstet Gynecol ; 168(6 Pt 1): 1724-9; discussion 1729-31, 1993 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-8317514

RESUMEN

OBJECTIVE: Our objective was to identify those obstetric and neonatal factors associated with survival in infants delivered at 24 weeks' gestation. STUDY DESIGN: The obstetric and pediatric data bases from the two hospitals in our perinatal center were examined to ascertain all infants delivered between 1987 and 1989 whose gestational age was 24 weeks to 24 weeks 6 days. This time interval was chosen to coincide with the introduction of prophylactic exogenous surfactant. Data were abstracted from the maternal antepartum and intrapartum records and the neonatal records, with specific attention to objective risk factors related to survival. RESULTS: Forty-five pregnant patients were identified and delivered of 52 infants. Seventeen newborn infants survived (33%). Univariate comparisons between survivors and nonsurvivors revealed more aggressive intrapartum care in the former cohort as represented by the frequencies of internal fetal heart rate monitoring (p = 0.005), maternal oxygen therpay (p = 0.003), and maternal position change to remediate decelerations (p = 0.001). Planned exclusion of cesarean delivery was more common in those pregnancies that ended in fetal or neonatal death (29/35 vs 7/17; p = 0.006). Although a greater proportion of infants delivered by cesarean section survived (6/11 vs 11/41), this difference was not significant (p = 0.17). With the use of logistic regression, the best predictor of survival was gestational age at delivery. Neonatal care was more aggressive among survivors, as measured by the relative frequencies of resuscitation and surfactant administration. Respiratory distress syndrome was either absent (n = 6) or mild (n = 6) in a majority of the survivors, and respiratory insufficiency was the major cause of neonatal death. CONCLUSION: Perinatal outcome at 24 weeks' gestation appears most dependent on gestational age at delivery. The intensity of intrapartum care and neonatal support, as well as clinical biases regarding survivability, may also influence outcome.


Asunto(s)
Recien Nacido Prematuro , Resultado del Embarazo , Peso al Nacer , Parto Obstétrico , Femenino , Edad Gestacional , Humanos , Recién Nacido , Cuidado Intensivo Neonatal , Embarazo
17.
Int J Gynaecol Obstet ; 41(1): 23-6, 1993 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8098290

RESUMEN

OBJECTIVE: The purpose of this study was to determine those factors influencing contemporary antenatal steroid use in pregnancies delivered prior to 33 weeks of gestation. METHOD: We analyzed the clinical circumstances of 86 consecutive patients who delivered prior to 33 weeks of gestation and compared to 20 women who received dexamethasone prior to delivery with the remaining 66 untreated cases. RESULT: Known risk factors for preterm delivery (e.g. prior preterm birth, n = 17; prior admission and tocolysis during the index pregnancy, n = 15) did not discriminate between treated and untreated subsets. Premature membrane rupture (3/20 vs. 34/66; P < 0.01) and documented preterm labor (1/20 vs. 23/66 P < 0.01) were more common in the untreated cohort and a shorter mean interval from admission to delivery was also observed (2.8 vs 11.2 days). However, a full course of steroids would have been possible in 22/66 untreated women, since delivery was delayed for at least 36 h in these patients. CONCLUSION: These observations reflect the fact that many preterm births cannot be anticipated, even among hospitalized patients. We would therefore suggest that universal steroid treatment be considered for all women with documented preterm labor prior to 33 weeks of gestation. Initiation of steroid therapy at the referral center, (prior to maternal transport) should also be considered. Since both premature membrane rupture and early gestational age (24-28 weeks') confounded many of these cases, steroid use in patients with these circumstances should be reevaluated.


Asunto(s)
Dexametasona/uso terapéutico , Enfermedades del Prematuro/prevención & control , Trabajo de Parto Prematuro , Síndrome de Dificultad Respiratoria del Recién Nacido/prevención & control , Estudios de Cohortes , Femenino , Rotura Prematura de Membranas Fetales , Humanos , Recién Nacido , Recien Nacido Prematuro , Embarazo , Factores de Riesgo
18.
Obstet Gynecol ; 80(3 Pt 2): 497-9, 1992 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-1495720

RESUMEN

Middle cerebral artery infarction explains some cases of congenital hemiparesis with or without neonatal stroke. The etiology of the stroke is often obscure. We describe two infants with imaging evidence of middle cerebral artery infarction whose mothers had elevated anticardiolipin antibody levels after delivery. We speculate that these antibodies may have been responsible for intrauterine thromboembolic stroke.


Asunto(s)
Síndrome Antifosfolípido/complicaciones , Autoanticuerpos/inmunología , Cardiolipinas/inmunología , Infarto Cerebral/inmunología , Enfermedades Fetales/inmunología , Hemiplejía/congénito , Adulto , Infarto Cerebral/congénito , Femenino , Hemiplejía/inmunología , Humanos , Recién Nacido , Embarazo
19.
Am J Obstet Gynecol ; 166(6 Pt 1): 1780-4; discussion 1784-7, 1992 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-1615987

RESUMEN

OBJECTIVE: Because of the widespread use of antiphospholipid antibody testing in the evaluation of patients with recurrent pregnancy loss, we evaluated the consistency of results among laboratories testing for anticardiolipin antibody and the lupus anticoagulant. STUDY DESIGN: A questionnaire regarding methods used and samples of blood from 20 patients were sent to five university-based and five commercial facilities for antiphospholipid antibody testing. RESULTS: The responses of the participating laboratories to the questionnaires revealed significant differences in methods, standardization, and units of reporting. For anticardiolipin antibody, the number of specimens found to be positive for any isotype (immunoglobulin G, M, or A) varied considerably among laboratories, with a range of 5 to 13. All laboratories were in agreement (i.e., at least one isotype was present or all were absent) for only 5 of 20 specimens (25%). In contrast, lupus anticoagulant results were more reproducible, although one facility reported results markedly discordant from the other four laboratories. CONCLUSION: These observations suggest that significant interlaboratory variation exists in antiphospholipid antibody, and particularly anticardiolipin antibody, testing and might lead to unnecessary therapeutic interventions.


Asunto(s)
Anticuerpos/análisis , Técnicas de Laboratorio Clínico , Fosfolípidos/inmunología , Cardiolipinas/inmunología , Técnicas de Laboratorio Clínico/métodos , Humanos , Isotipos de Inmunoglobulinas/análisis , Inhibidor de Coagulación del Lupus/análisis , Reproducibilidad de los Resultados , Encuestas y Cuestionarios
20.
Prenat Diagn ; 12(3): 183-8, 1992 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-1589420

RESUMEN

Multiple placental passes during chorionic villus sampling (CVS) increase the risk of fetal loss; however, specific factors that predispose to repeat aspiration have not been delineated. To identify anatomic and technical variables associated with multiple-pass procedures, a detailed review of 205 videotaped CVS procedures (single pass = 163; multiple pass = 42) was performed, blinded to pregnancy outcome. The route of sampling did not influence the need for multiple aspiration attempts (transabdominal--30/135; transcervical--12/70), nor was placental location alone discriminatory. However, the combination of a posterior placenta and uterine retroversion was observed more frequently in the multiple-pass cohort (8/42 vs. 9/163; p less than 0.05). In transabdominal cases, suboptimal needle placement (e.g., perpendicular to the placental long axis) was more common in the initial aspiration of a multiple-pass procedure (21/30 vs. 38/105; p less than 0.01), while limited penetration of the catheter tip (e.g., just inside the placental edge) characterized a majority of multiple-pass cases in the transcervical subset (7/12 vs. 3/58; p less than 0.0001). A case-control cohort was constructed to evaluate the impact of these technical variables on sampling efficacy, independent of the influence of uterine position and placental site. In that analysis, suboptimal location and/or orientation of the sampling device remained characteristic of multiple-pass cases. We conclude that further reduction in the frequency of multiple-pass procedures might be achieved by consistent placement of the device tip in the central placental mass. Unlike amniocentesis, where any point of amnion entry will suffice, this technical nuance should be emphasized with CVS to maximize the single-pass success rate.


Asunto(s)
Muestra de la Vellosidad Coriónica/métodos , Estudios de Casos y Controles , Femenino , Humanos , Placenta/anatomía & histología , Embarazo , Primer Trimestre del Embarazo , Estudios Retrospectivos , Útero/anatomía & histología , Grabación de Cinta de Video
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