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1.
J Pediatr Hematol Oncol ; 44(8): e1046-e1049, 2022 11 01.
Artículo en Inglés | MEDLINE | ID: mdl-35380549

RESUMEN

Management of hemolytic disease of the fetus and newborn relies on monitoring of maternal antibody titers, fetal ultrasound, and fetal middle cerebral artery peak systolic velocity studies and is generally treated by intrauterine transfusion (IUT). Few studies have explored fetal and neonate physiological responses to IUT. Our objective was to examine fetal erythropoietic response and to examine neonatal erythropoietic effects after treatment. Thirty-six patients treated from 2005 to 2015 were identified retroactively. The time course of treatment, including gestational age and number of IUT, and timing of delivery were reviewed. Fetal reticulocyte count and neonatal hemoglobin and reticulocyte counts were analyzed for each IUT. For each gestational week, reticulocyte count decreased by ∼8.6% (95% confidence interval [CI]: 5.3-12.0). In the neonatal period, there was significant correlation between hemoglobin at birth and number of transfusions (Spearman correlation 0.473, 95% CI: 0.113-0.715, P =0.01) as well as reticulocyte count at birth and number of transfusions (Spearman correlation: 0.393, 95% CI: 0.058-0.642, P =0.02). IUT appears to have a direct and measurable effect on fetal reticulocyte production which persists in neonates.


Asunto(s)
Anemia Hemolítica Autoinmune , Eritroblastosis Fetal , Enfermedades del Recién Nacido , Isoinmunización Rh , Recién Nacido , Embarazo , Femenino , Humanos , Transfusión de Sangre Intrauterina/efectos adversos , Recuento de Reticulocitos , Feto , Hemoglobinas , Eritrocitos , Anemia Hemolítica Autoinmune/etiología , Sangre Fetal , Estudios Retrospectivos , Isoinmunización Rh/terapia
2.
Obstet Gynecol ; 136(6): 1204-1210, 2020 12.
Artículo en Inglés | MEDLINE | ID: mdl-33156200

RESUMEN

OBJECTIVE: To evaluate differences between fasting and nonfasting bile acid levels in asymptomatic and symptomatic pregnant women. METHODS: This is a report of two prospective cohort studies describing bile acid levels in the fasting and nonfasting state in pregnancy. The first cohort included asymptomatic women with singleton pregnancies. Women with a diagnosis of cholestasis, symptoms of cholestasis, or intolerance to components of a standardized meal were excluded. Bile acid levels were measured during the second and third trimesters after fasting and again 2 hours after a standardized meal. The second cohort included symptomatic women with singleton pregnancies in whom fasting and nonfasting bile acid levels were measured at the time of symptom evaluation. A cutoff of 10 micromoles/L was used for diagnosis. RESULTS: A total of 27 women were included in the asymptomatic cohort. Median [interquartile range] fasting bile acid levels were significantly lower than nonfasting levels in both the second trimester (4.65 micromoles/L [1.02-29.57] vs 13.62 micromoles/L [2.03-40.26]; P<.001) and third trimester (8.31 micromoles/L [1.14-51.26] vs 17.35 micromoles/L [1.77-62.93]; P<.001). Bile acid levels exceeded 10 micromoles/L in 21% of the fasting samples and in 58% of the nonfasting samples in the third trimester. A total of 26 women were included in the symptomatic cohort. Median [interquartile range] fasting bile acid levels were significantly lower than nonfasting values (11.5 micromoles/L [7-56] vs 13.5 micromoles/L [9-142]; P<.001). Six patients in the symptomatic cohort (23%) had nonfasting bile acid levels greater than 10 micromoles/L that dropped below 10 micromoles/L when fasting. CONCLUSION: Fasting bile acid levels are significantly lower when compared with nonfasting values in both asymptomatic and symptomatic pregnant women. In asymptomatic women, nonfasting bile acid levels often exceeded 10 micromoles/L whereas fasting values did not. In symptomatic women, fasting bile acid levels resulted in 23% fewer diagnoses of cholestasis when compared with nonfasting values. These findings suggest that fasting evaluation of bile acid levels or a higher threshold for diagnosis of cholestasis should be considered.


Asunto(s)
Ácidos y Sales Biliares/sangre , Colestasis Intrahepática/sangre , Ayuno , Complicaciones del Embarazo/sangre , Adulto , Colestasis Intrahepática/diagnóstico , Femenino , Humanos , Embarazo , Complicaciones del Embarazo/diagnóstico , Segundo Trimestre del Embarazo , Tercer Trimestre del Embarazo , Estudios Prospectivos , Adulto Joven
3.
J Womens Health (Larchmt) ; 27(5): 646-650, 2018 05.
Artículo en Inglés | MEDLINE | ID: mdl-29185840

RESUMEN

BACKGROUND: Single-dose levonorgestrel has been legally available over the counter in the United States without age restriction since 2013. The objective of this study was to discover if there are barriers to access and to determine if such barriers vary based on the gender of the person making the purchase. MATERIALS AND METHODS: A male and female caller contacted 146 Richmond, Virginia pharmacies listed on the Plan B One Step® website. Ultimately, these callers interviewed 90 pharmacies via phone and used a rehearsed standardized script to ask eight questions regarding emergency contraception (EC) in relation to availability, age restrictions, parental consent, counseling requirements, and a male's ability to purchase the product. The statistical data were analyzed using Fisher's exact test. RESULTS: Pharmacy employees provided incorrect information to both men and women regarding age restrictions for purchasing Plan B One Step 51% of the time. However, only seven of the pharmacy employees counseled that males were unable to purchase the medication. Both callers received correct information regarding parental consent and in-store counseling at the time of purchase. Pharmacy technicians provided the majority of information, and the male caller was more likely to be transferred to another person when requesting the medication (9 vs. 0 transfers for the male and female callers, respectively). CONCLUSION: Given the inconsistent data provided to the public regarding the purchase of EC, clinicians are obligated to convey accurate up-to-date information to patients about emergency contraceptive products as part of their counseling and should not assume that consumers receive accurate information when inquiring about over-the-counter EC.


Asunto(s)
Anticoncepción Postcoital , Anticonceptivos Sintéticos Orales/provisión & distribución , Anticonceptivos Poscoito/provisión & distribución , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Levonorgestrel/provisión & distribución , Medicamentos sin Prescripción/provisión & distribución , Farmacias , Adulto , Anticoncepción Postcoital/estadística & datos numéricos , Femenino , Encuestas de Atención de la Salud , Humanos , Masculino , Virginia , Adulto Joven
4.
Am J Obstet Gynecol ; 212(4): 494.e1-6, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25460835

RESUMEN

OBJECTIVE: The objective of the study was to examine the clinical impact of specific fetal monitoring-related practices during induced labor. STUDY DESIGN: This was a prospective, nonrandomized study. RESULTS: We studied 14,398 women undergoing oxytocin induction of labor. A decrease in the infusion rate of oxytocin in the face of specified category II fetal heart rate tracings was associated with a significantly reduced rate of neonatal intensive care unit admission (3.8% vs 5.2%, P = .01) and Apgar score less than 7 at 1 and 5 minutes (4.9% vs 6.4%, P = .01, 0.6% vs 1.1%, P = .04). Compliance with an in-use checklist was associated with both a reduction in the rate of neonatal intensive care unit admission (2.9 vs 4.4, P = .00) and a reduction in the cesarean delivery rate (15.8% vs 18.8%, P = .00). CONCLUSION: Electronic fetal heart rate monitoring improves neonatal outcomes when unambiguous definitions of abnormal fetal heart rate and tachysystole are coupled with specific interventions. Utilization of a checklist for oxytocin monitoring is associated with improved neonatal outcomes and a reduction in the cesarean delivery rate.


Asunto(s)
Cesárea/estadística & datos numéricos , Monitoreo Fetal/métodos , Frecuencia Cardíaca Fetal/efectos de los fármacos , Trabajo de Parto Inducido/efectos adversos , Oxitócicos/efectos adversos , Oxitocina/efectos adversos , Adulto , Puntaje de Apgar , Lista de Verificación , Femenino , Humanos , Recién Nacido , Infusiones Intravenosas , Unidades de Cuidado Intensivo Neonatal/estadística & datos numéricos , Trabajo de Parto Inducido/métodos , Evaluación de Resultado en la Atención de Salud , Oxitócicos/administración & dosificación , Oxitocina/administración & dosificación , Admisión del Paciente/estadística & datos numéricos , Embarazo , Estudios Prospectivos
5.
Lifetime Data Anal ; 13(4): 545-63, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17828621

RESUMEN

Breslow and Holubkov (J Roy Stat Soc B 59:447-461 1997a) developed semiparametric maximum likelihood estimation for two-phase studies with a case-control first phase under a logistic regression model and noted that, apart for the overall intercept term, it was the same as the semiparametric estimator for two-phase studies with a prospective first phase developed in Scott and Wild (Biometrica 84:57-71 1997). In this paper we extend the Breslow-Holubkov result to general binary regression models and show that it has a very simple relationship with its prospective first-phase counterpart. We also explore why the design of the first phase only affects the intercept of a logistic model, simplify the calculation of standard errors, establish the semiparametric efficiency of the Breslow-Holubkov estimator and derive its asymptotic distribution in the general case.


Asunto(s)
Funciones de Verosimilitud , Modelos Logísticos , Estudios de Casos y Controles , Humanos
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