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1.
J Perinatol ; 33(10): 754-8, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-23702620

RESUMEN

OBJECTIVE: To determine if serum screen analytes identify preeclamptic patients at risk for small-for-gestational age newborns, maternal laboratory abnormalities and preterm delivery (<37 weeks gestation). STUDY DESIGN: Using a retrospective cohort of 102 preeclamptic patients, associations between serum screen analytes and newborn birth-weight percentile, gestational age (GA) at delivery and maternal pre-delivery laboratory abnormalities were evaluated using correlation coefficients and local polynomial regression. RESULT: Inhibin-A and maternal serum alpha fetoprotein were inversely correlated with newborn birth-weight percentile (-0.27, P=0.006; -0.35, P=0.00004) and delivery GA (r=-0.42, P<0.0001; r=-0.26, P=0.008) and positively correlated with pre-delivery aspartate aminotransferase (r=0.22, P=0.03; r=0.21, P=0.04) and lactate dehydrogenase (r=0.33, P=0.0007; r=0.29, P=0.004). A positive correlation was noted between both second-trimester beta human chorionic gonadotropin and estriol and maternal pre-delivery creatinine (0.28, P=0.004; 0.4, P<0.0001, respectively). Hundred percent of patients with ≥ 2 abnormal analytes delivered before 37 weeks gestation. CONCLUSION: Preeclamptic patients with abnormal serum screen analytes are more likely to have small-for-gestational age newborns, deliver preterm and have pre-delivery laboratory abnormalities.


Asunto(s)
Pruebas de Detección del Suero Materno , Preeclampsia/sangre , Proteínas Gestacionales/sangre , Adulto , Peso al Nacer , Gonadotropina Coriónica Humana de Subunidad beta/sangre , Estriol/sangre , Femenino , Edad Gestacional , Síndrome HELLP/sangre , Humanos , Recién Nacido , Recién Nacido Pequeño para la Edad Gestacional/sangre , Inhibinas/sangre , Preeclampsia/clasificación , Preeclampsia/diagnóstico , Embarazo , Segundo Trimestre del Embarazo , Proteína Plasmática A Asociada al Embarazo/análisis , Nacimiento Prematuro/sangre , Estudios Retrospectivos , alfa-Fetoproteínas/análisis
2.
Hum Reprod ; 28(1): 160-71, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23117129

RESUMEN

STUDY QUESTION: What is the current literature on the safety and efficacy of selective serotonin reuptake inhibitor (SSRI) use in infertile women? SUMMARY ANSWER: There is little evidence that infertile women benefit from taking an SSRI, therefore they should be counseled appropriately about the risks and be advised to consider alternate safer treatments to treat depressive symptoms. WHAT IS KNOWN ALREADY: SSRI use is associated with possible reduced infertility treatment efficacy as well as higher rates of pregnancy loss, preterm birth, pregnancy complications, neonatal issues and long-term neurobehavioral abnormalities in offspring. STUDY DESIGN, SIZE, DURATION: Review of existing literature. PARTICIPANTS/MATERIALS, SETTING, METHODS: We conducted a review of all published studies that evaluate females with depressive symptoms who are taking antidepressant medications and who are experiencing infertility. MAIN RESULTS AND THE ROLE OF CHANCE: Antidepressant use during pregnancy is associated with increased risks of miscarriage, birth defects, preterm birth, newborn behavioral syndrome, persistent pulmonary hypertension of the newborn and possible longer term neurobehavioral effects. There is no evidence of improved pregnancy outcomes with antidepressant use. There is some evidence that psychotherapy, including cognitive-behavioral therapy as well as physical exercise, is associated with significant decreases in depressive symptoms in the general population; research indicates that some forms of counseling are effective in treating depressive symptoms in infertile women. LIMITATIONS, REASONS FOR CAUTION: Our findings are limited by the availability of published studies in the field, which are often retrospective and of small size. WIDER IMPLICATIONS OF THE FINDINGS: Practitioners who care for infertility patients should have a thorough understanding of the published literature so that they can adequately counsel their patients. STUDY FUNDING/COMPETING INTEREST(S): None.


Asunto(s)
Antidepresivos de Segunda Generación/efectos adversos , Infertilidad Femenina/psicología , Inhibidores Selectivos de la Recaptación de Serotonina/efectos adversos , Adulto , Antidepresivos de Segunda Generación/uso terapéutico , Depresión/complicaciones , Depresión/tratamiento farmacológico , Femenino , Humanos , Recién Nacido , Enfermedades del Recién Nacido/inducido químicamente , Masculino , Embarazo , Complicaciones del Embarazo/inducido químicamente , Inhibidores Selectivos de la Recaptación de Serotonina/uso terapéutico
3.
J Perinatol ; 32(10): 757-62, 2012 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-22193928

RESUMEN

OBJECTIVE: Uric acid is known to be elevated in preeclampsia. We sought to determine if uric acid levels on admission correlate with the length of expectant management in preterm patients with preeclampsia. STUDY DESIGN: A retrospective chart review was conducted on singleton preeclamptic pregnancies delivered between 24 0/7 and 37 0/7 weeks' gestation at Tufts Medical Center between January 2005 and December 2007. Patients with a multiple gestation and those transferred or discharged before delivery were excluded. Data regarding signs and symptoms of preeclampsia, laboratory values, pregnancy complications and outcome were abstracted from the medical records. Correlation between admission uric acid level and days of expectant management was assessed. The relative risk (RR) was used to estimate the effect of uric acid levels on expectant management length >7 days. Mantel-Haenszel χ(2) values were used to construct 95% confidence intervals (CIs) around the RR. RESULT: Four hundred seventy-one charts were reviewed. Of these, 190 met inclusion criteria. In all, 55 patients (28.9%) were managed expectantly for >1 week. Admission uric acid level correlated with days of expectant management (P<0.0001). Uric acid levels at admission were categorized as ≤4.0 mg dl(-1) (low uric acid level), 4.1 to 6.0 mg dl(-1) (medium) and ≥6.1 mg dl(-1) (high). Relative to women with high uric acid levels at admission, we observed a sevenfold higher rate of extending expectant management for >1 week among women with low uric acid level (7.0; 95% CI: 3.34 to 14.68). Women with medium uric acid levels at admission also had a higher likelihood of prolonging pregnancy relative to women with high uric acid levels (RR: 2.81; 95% CI: 1.32 to 5.96) (P-value for trend <0.0001). CONCLUSION: Admission uric acid levels correlate with the length of expectant management in preterm patients with preeclampsia. Pregnancy prolongation for >1 week is significantly more likely in patients with low and medium uric acid levels at the time of admission. Uric acid levels may be helpful in assessing disease severity and counseling preeclamptic patients regarding likelihood of extended expectant management.


Asunto(s)
Preeclampsia/sangre , Ácido Úrico/sangre , Adolescente , Adulto , Parto Obstétrico , Femenino , Edad Gestacional , Humanos , Admisión del Paciente , Preeclampsia/terapia , Embarazo , Pronóstico , Estudios Retrospectivos , Análisis de Supervivencia , Adulto Joven
4.
Am J Obstet Gynecol ; 179(1): 260-1, 1998 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-9704798

RESUMEN

May-Hegglin anomaly is a rare, autosomal dominant disorder characterized by thrombocytopenia and a variable bleeding tendency. In almost all the case reports in the recent literature, platelet transfusion and cesarean section were performed to avoid maternal and neonatal bleeding. We present a case of a woman with May-Hegglin anomaly who had no history of a bleeding tendency. She had a vaginal delivery and a platelet count of 16,000/mm3; the neonate's platelet count was 35,000/mm3. There were no complications. We advocate a reappraisal of basing platelet transfusion and mode of delivery on the platelet count in patients with May-Hegglin anomaly.


Asunto(s)
Parto Obstétrico/métodos , Enfermedades Fetales/terapia , Genes Dominantes , Complicaciones Hematológicas del Embarazo/terapia , Trombocitopenia/terapia , Adulto , Tiempo de Sangría , Femenino , Enfermedades Fetales/genética , Humanos , Recuento de Plaquetas , Transfusión de Plaquetas , Embarazo , Trombocitopenia/genética , Vagina
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