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1.
J Obstet Gynaecol Can ; 40(8): e622-e629, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-30103886
2.
J Obstet Gynaecol Can ; 40(8): e615-e621, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-30103885

RESUMEN

OBJECTIVE: To provide an update on rubella and pregnancy so that health professionals remain aware of the potentially devastating effects on the developing fetus. OUTCOMES: Rubella vaccination has been effective in virtually eliminating congenital rubella syndrome in Canada. EVIDENCE: Medline, PubMed, and Cochrane Database were searched for articles published between 1985 and 2007. VALUES: The quality of evidence was rated using the criteria described in the report of the Canadian Task Force on Preventive Health Care. SPONSOR: The Society of Obstetricians and Gynaecologists of Canada.


Asunto(s)
Complicaciones Infecciosas del Embarazo/prevención & control , Atención Prenatal/normas , Síndrome de Rubéola Congénita/prevención & control , Vacuna contra la Rubéola/uso terapéutico , Rubéola (Sarampión Alemán)/prevención & control , Canadá , Femenino , Ginecología , Humanos , Recién Nacido , Obstetricia , Embarazo , Sociedades Médicas , Vacunación
3.
J Obstet Gynaecol Can ; 33(2): 153-158, 2011 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21352635

RESUMEN

OBJECTIVE: Fetal safety has never been studied for any drug used in the treatment of hemorrhoids. Proctofoam-HC is a combination of a corticosteroid and a local anaesthetic that is proven effective for the treatment of hemorrhoids. The objective of this study was to assess prospectively the fetal safety of third trimester exposure to Proctofoam-HC. METHODS: In a multicentre study, 204 [corrected] women exposed to Proctofoam-HC in the third trimester and a similar number of control pregnant women were followed up postnatally. RESULTS: When compared to controls exposure to Proctofoam-HC was not associated with any adverse fetal effects on birth weight, gestational age, rates of prematurity, or pre- or postnatal complications. CONCLUSION: Proctofoam-HC is safe to use in the treatment of hemorrhoids in late pregnancy.


Asunto(s)
Anestésicos Locales/efectos adversos , Antiinflamatorios/efectos adversos , Desarrollo Fetal/efectos de los fármacos , Hemorroides/tratamiento farmacológico , Hidrocortisona/efectos adversos , Morfolinas/efectos adversos , Complicaciones del Embarazo/tratamiento farmacológico , Adulto , Peso al Nacer , Combinación de Medicamentos , Femenino , Humanos , Embarazo , Tercer Trimestre del Embarazo
4.
J Obstet Gynaecol Can ; 30(2): 152-158, 2008 Feb.
Artículo en Inglés, Francés | MEDLINE | ID: mdl-18254998

RESUMEN

OBJECTIVE: To provide an update on rubella and pregnancy so that health professionals remain aware of the potentially devastating effects on the developing fetus. OUTCOMES: Rubella vaccination has been effective in virtually eliminating congenital rubella syndrome in Canada. EVIDENCE: Medline, PubMed, and Cochrane Database were searched for articles published between 1985 and 2007. VALUES: The quality of evidence was rated using the criteria described in the report of the Canadian Task Force on Preventive Health Care. SPONSOR: The Society of Obstetricians and Gynaecologists of Canada.


Asunto(s)
Medicina Basada en la Evidencia , Complicaciones Infecciosas del Embarazo , Síndrome de Rubéola Congénita/prevención & control , Rubéola (Sarampión Alemán)/diagnóstico , Rubéola (Sarampión Alemán)/tratamiento farmacológico , Canadá , Femenino , Humanos , Embarazo , Vacuna contra la Rubéola
5.
J Obstet Gynaecol Can ; 27(11): 1013-8, 2005 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-16529667

RESUMEN

OBJECTIVE: To compare the efficacy of oral misoprostol with that of intra-amniotic prostaglandin F2alpha (PGF2alpha) for second trimester pregnancy termination. METHODS: One hundred seventeen women with pregnancies of between 16 and 22 weeks' gestation were randomly assigned after insertion of laminaria to receive either oral misoprostol 400 microg every 4 hours (to a maximum of four doses) or intra-amniotic PGF2alpha 40 mg. The rate of complete abortion within 24 hours was the primary outcome for power analysis. Secondary outcome measures were the rate of dilatation and curettage (D&C) for retained placenta and the rates of fever and gastrointestinal complications. RESULTS: Patient characteristics were similar in both groups. The rate of complete abortion within 24 hours was similar in the misoprostol (63%) and PGF2alpha (66%) groups. The rate of retained placenta requiring D&C was significantly greater in the PGF2alpha group (22.4% vs. 3.4%, P = 0.002). There were no differences in other maternal morbidities. Parous patients treated with oral misoprostol had a significantly greater rate of complete abortion than nulliparous patients (84% vs. 57%, P = 0.04). CONCLUSIONS: Oral misoprostol is as effective as intra-amniotic PGF2alpha for second trimester pregnancy termination when laminaria is inserted before treatment. Parous patients have a higher success rate than nulliparous patients with use of oral misoprostol. Oral misoprostol is associated with a very low rate of placental retention.


Asunto(s)
Abortivos no Esteroideos/normas , Aborto Inducido , Dinoprost/normas , Misoprostol/normas , Administración Oral , Adulto , Líquido Amniótico , Femenino , Humanos , Laminaria , Paridad , Retención de la Placenta/epidemiología , Embarazo , Segundo Trimestre del Embarazo , Factores de Tiempo , Resultado del Tratamiento
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