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1.
Ultrasound Obstet Gynecol ; 49(5): 612-616, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-27222097

RESUMEN

OBJECTIVE: Preterm delivery after fetoscopic laser surgery (FLS) for twin-twin transfusion syndrome (TTTS) is a major complication. The causative factors leading to preterm delivery continue to be elusive and a better understanding of the risk factors could reduce complications. The objective of this study was to determine the etiology of preterm delivery after FLS for TTTS and its associated risk factors. METHODS: This was a secondary analysis of a prospective study of 203 patients with TTTS who underwent FLS at a single center between September 2011 and December 2014. Preoperative, operative, postoperative, delivery and neonatal data were reviewed. Preterm delivery was categorized according to etiology into three groups: spontaneous (SPT), indicated (IND) and elective (ELC). Comparisons between groups were performed by ANOVA. Kaplan-Meier survival analysis was performed to compare the procedure-to-delivery interval between groups. To identify risk factors for preterm delivery, logistic regression, with calculation of relative risks (RR), was performed, with P < 0.05 considered statistically significant. RESULTS: Mean gestational age at time of FLS was 20.6 ± 2.4 weeks and mean gestational age at delivery was 30.9 ± 4.7 weeks. Iatrogenic preterm prelabor rupture of membranes (iPPROM) occurred in 39% of cases. SPT preterm delivery occurred in 97 (48%) patients, IND preterm delivery in 65 (32%) and ELC preterm delivery in 41 (20%). In the IND group, 30 (46%) patients delivered for fetal indications, 31 (48%) for maternal indications and four (6%) for combined fetal and maternal indications. The overall chorioamnionitis rate was 6.4%; of these, nine (9%) were in the SPT group and four (6%) were in the IND group, with no case occurring in the ELC group. There was a significant difference in procedure-to-delivery interval between groups (P < 0.0001). Using variables from the ELC group as a baseline, significant risk factors for SPT preterm delivery were iPPROM (RR, 16.2 (95% CI, 4.5-57.7)), preoperative cervical length (RR, 0.96 (95% CI, 0.92-0.998)) and number of anastomoses (RR, 1.14 (95% CI, 1.02-1.27)). Significant risk factors for IND preterm delivery were iPPROM (RR, 9.6 (95% CI, 2.6-35.0)) and number of ablated anastomoses (RR, 1.13 (95% CI, 1.02-1.30)). CONCLUSION: iPPROM and an increased number of ablated placental anastomoses were associated independently with SPT and IND preterm deliveries. A shorter preoperative cervical length was associated with SPT preterm delivery. Strategies to prevent iPPROM and for management of cervical length shortening are needed urgently in these pregnancies. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.


Asunto(s)
Rotura Prematura de Membranas Fetales/epidemiología , Transfusión Feto-Fetal/cirugía , Fetoscopía/efectos adversos , Embarazo Triple , Embarazo Gemelar , Adulto , Femenino , Rotura Prematura de Membranas Fetales/etiología , Rotura Prematura de Membranas Fetales/mortalidad , Edad Gestacional , Humanos , Embarazo , Resultado del Embarazo , Estudios Prospectivos , Factores de Riesgo , Análisis de Supervivencia , Texas/epidemiología , Factores de Tiempo
2.
Prenat Diagn ; 33(1): 95-101, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23225162

RESUMEN

OBJECTIVE: To determine the sensitivity and specificity of circulating cell-free fetal DNA in determining the fetal RHD status and fetal sex. METHODS: Maternal blood was collected in each trimester of pregnancy from RhD negative nonalloimmunized women. Whole blood was centrifuged, separated into plasma and buffy coat, and frozen at -80°C. DNA analysis was conducted via allele-specific primer extensions for exons 4, 5, and 7 of the RHD gene and for a 37-base pair insertion in exon 4 (RHD pseudogene; psi) three Y-chromosome sequences (SRY, DBY, and TTY2), and an extraction control (TGIFL-like X/Y). RhD serotyping on cord blood and gender assessment of the newborns were entered into a Web-based database. RESULTS: One hundred twenty women were enrolled. The median gestational age at the first venipuncture was 12.4 (range: 10.6-13.9) weeks with 120 samples drawn; 118 samples were drawn at 17.6 (16-20.9) weeks; and 113 samples at 28.7 (27.9-33.9) weeks. Overall accuracy for RHD was 99.1%, 99.1%, and 98.1% for each trimester and was 99.1%, 99.1%, and 100% for fetal sex determination. CONCLUSIONS: Fetal RHD genotyping and sex can be very accurately determined in all three trimesters using circulating cell-free fetal DNA in the maternal circulation.


Asunto(s)
Tipificación y Pruebas Cruzadas Sanguíneas/métodos , ADN/sangre , Sangre Fetal , Sistema del Grupo Sanguíneo Rh-Hr/sangre , Análisis para Determinación del Sexo/métodos , Femenino , Genes sry/genética , Genotipo , Edad Gestacional , Humanos , Masculino , Embarazo , Sistema del Grupo Sanguíneo Rh-Hr/genética , Sensibilidad y Especificidad
3.
Hosp Prog ; 61(3): 67-70, 1980 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-10278018

RESUMEN

Hospice programs can develop multi-institutional arrangements to ensure high-quality care and to plan for orderly distribution and location of programs. Three Illinois hospitals in conjunction with the local HSA have developed a hospice network that will maintain institutional autonomy while coordinating many administrative functions.


Asunto(s)
Hospitales para Enfermos Terminales/organización & administración , Planificación Hospitalaria/organización & administración , Sistemas Multiinstitucionales/organización & administración , Agencias de los Sistemas de Salud , Hospitales con 100 a 299 Camas , Hospitales con 300 a 499 Camas , Illinois , Estados Unidos
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