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1.
Obstet Gynecol ; 130(5): 994-1000, 2017 11.
Artículo en Inglés | MEDLINE | ID: mdl-29016512

RESUMEN

OBJECTIVE: To examine whether labor compared with planned cesarean delivery is associated with increased maternal and neonatal morbidity. METHODS: We conducted a retrospective cohort study of all women with body mass indexes (BMIs) at delivery of 50 or greater delivering a live fetus at 34 weeks of gestation of greater between January 1, 2008, and December 31, 2015. Pregnancies with multiple gestations and major fetal anomalies were excluded. The primary outcome was a composite of maternal and neonatal morbidity and was estimated to be 50% in superobese women based on institutional data. A sample size of 338 women determined the study period and was selected to show a 30% difference in the incidence of the primary outcome between the two groups. Multivariate logistic regression adjusted for potential confounders. RESULTS: There were 344 women with BMIs of 50 or greater who met eligibility criteria, of whom 201 (58%) labored and 143 (42%) underwent planned cesarean delivery. Women who labored were younger, more likely to be nulliparous, and less likely to have pre-existing diabetes. Among women who labored, 45% underwent a cesarean delivery, most commonly for labor arrest (61%) or nonreassuring fetal status (28%). Composite maternal and neonatal morbidity was reduced among women who labored even after adjusting for age, parity, pre-existing diabetes, and prior cesarean delivery (adjusted odds ratio 0.42, 95% CI 0.24-0.75). In the subgroup of women (n=234) who underwent a cesarean delivery, whether planned (n=143) or after labor (n=91), there were no differences in maternal and neonatal morbidity except that severe maternal morbidity was increased in women (n=12) who labored (8.8% compared with 2.1%, relative risk 4.2, 95% CI 1.14-15.4). CONCLUSION: Despite high rates of cesarean delivery in women with superobesity, labor is associated with lower composite maternal and neonatal morbidity. Severe maternal morbidity may be higher in women who require a cesarean delivery after labor.


Asunto(s)
Cesárea/estadística & datos numéricos , Enfermedades del Recién Nacido/epidemiología , Obesidad Mórbida/complicaciones , Complicaciones del Trabajo de Parto/epidemiología , Esfuerzo de Parto , Adulto , Cesárea/efectos adversos , Femenino , Humanos , Recién Nacido , Enfermedades del Recién Nacido/etiología , Morbilidad , Complicaciones del Trabajo de Parto/etiología , Oportunidad Relativa , Paridad , Embarazo , Resultado del Embarazo , Estudios Retrospectivos
2.
Adv Skin Wound Care ; 18(9): 491-500; quiz 501-2, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16365547

RESUMEN

PURPOSE: To provide the physician and registered professional nurse with an understanding of angiogenesis and an overview of therapeutic angiogenesis modalities used to manage wounds and other tissue repair situations. TARGET AUDIENCE: This continuing education activity is intended for physicians and nurses with an interest in learning more about angiogenesis and therapeutic angiogenesis modalities to manage wounds and other tissue repair situations. OBJECTIVES: After reading the article and taking the test, the participant should be able to:


Asunto(s)
Inductores de la Angiogénesis/uso terapéutico , Neovascularización Fisiológica , Cicatrización de Heridas , Inductores de la Angiogénesis/farmacología , Plaquetas/fisiología , Factores de Crecimiento de Fibroblastos/uso terapéutico , Técnicas de Transferencia de Gen , Humanos , Neovascularización Fisiológica/efectos de los fármacos , Neovascularización Fisiológica/fisiología , Regeneración Nerviosa , Factor de Crecimiento Derivado de Plaquetas/uso terapéutico , Factores de Riesgo , Cuidados de la Piel/métodos , Células Madre/fisiología , Ingeniería de Tejidos , Resultado del Tratamiento , Factor A de Crecimiento Endotelial Vascular/uso terapéutico , Cicatrización de Heridas/efectos de los fármacos , Cicatrización de Heridas/fisiología
3.
J Drugs Dermatol ; 4(6): 708-17, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16302556

RESUMEN

Imiquimod (imidazoquinoline 5%) is a topical immune response modifier agent that inhibits angiogenesis, the growth of new blood vessels. In addition to its stimulation of cell-mediated immunity, imiquimod's antiangiogenic activity contributes to its clinical efficacy by interfering with pathological neovascularization that promotes disease progression. The antiangiogenic mechanisms of imiquimod are due to its: 1) induction of cytokines that themselves inhibit angiogenesis (interferons, IL-10, IL-12); 2) local up-regulation of endogenous angiogenesis inhibitors (TIMP, TSP-1); 3) local down-regulation of pro-angiogenic factors (bFGF, MMP-9); and 4) promotion of endothelial cell apoptosis. This report discusses these mechanisms and the rationale for imiquimod's use as an antiangiogenic agent. Key principles of antiangiogenic therapy are presented to describe how imiquimod may be applied in a well-tolerated fashion to treat a broad range of angiogenesis-dependent dermatological conditions, including actinic keratosis (AK), basal cell carcinoma (BCC), squamous cell carcinoma (SCC), lentigo maligna, hemangiomas, Kaposi's sarcoma, pyogenic granuloma, and external genital warts.


Asunto(s)
Adyuvantes Inmunológicos , Aminoquinolinas/farmacología , Aminoquinolinas/uso terapéutico , Inhibidores de la Angiogénesis/farmacología , Inhibidores de la Angiogénesis/uso terapéutico , Adyuvantes Inmunológicos/farmacología , Adyuvantes Inmunológicos/uso terapéutico , Aminoquinolinas/inmunología , Inhibidores de la Angiogénesis/inmunología , Apoptosis/efectos de los fármacos , Citocinas/efectos de los fármacos , Regulación hacia Abajo/efectos de los fármacos , Células Endoteliales/efectos de los fármacos , Factor 2 de Crecimiento de Fibroblastos/efectos de los fármacos , Factor 2 de Crecimiento de Fibroblastos/metabolismo , Humanos , Imiquimod , Metaloproteinasa 9 de la Matriz/efectos de los fármacos , Metaloproteinasa 9 de la Matriz/metabolismo , Trombospondina 1/efectos de los fármacos , Trombospondina 1/metabolismo , Inhibidores Tisulares de Metaloproteinasas/efectos de los fármacos , Inhibidores Tisulares de Metaloproteinasas/metabolismo , Regulación hacia Arriba/efectos de los fármacos
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