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1.
J Gynecol Obstet Biol Reprod (Paris) ; 35(3): 288-92, 2006 May.
Artículo en Francés | MEDLINE | ID: mdl-16645565

RESUMEN

The migration into the bladder of an intrauterine contraceptive device (IUCD) by uterine perforation is a rare complication. We report two cases of IUCD which migrated into the bladder and subsequently became calcified. The two patients having had their IUCD respectively for 3 and 13 years. Revealing signs were related to bladder irritation for the first patient and hematuria for the second. The diagnosis was suggested on the plain abdominal X-ray and on ultrasound and was confirmed by cystoscopy. Ballistic lithotripsy of the bladder stone with endoscopic extraction of the IUCD was then performed. Performing a transvaginal sonographic examination of the pelvic organs, especially of the uterine anatomy is interesting before insertion of an intrauterine contraceptive device (IUCD), and repeat transvaginal sonographic examinations immediately after the insertion and 4-12 weeks later are advisable. This approach would permit early detection of any complications related to insertion of the IUCD.


Asunto(s)
Migración de Cuerpo Extraño/diagnóstico por imagen , Dispositivos Intrauterinos/efectos adversos , Cálculos de la Vejiga Urinaria/etiología , Perforación Uterina/etiología , Adulto , Femenino , Migración de Cuerpo Extraño/cirugía , Humanos , Ultrasonografía , Cálculos de la Vejiga Urinaria/diagnóstico por imagen , Cálculos de la Vejiga Urinaria/cirugía , Perforación Uterina/diagnóstico por imagen , Perforación Uterina/cirugía
2.
Afr. j. urol. (Online) ; 12(3): 161-164, 2006.
Artículo en Francés | AIM (África) | ID: biblio-1258037
3.
J Gynecol Obstet Biol Reprod (Paris) ; 34(5): 454-62, 2005 Sep.
Artículo en Francés | MEDLINE | ID: mdl-16142136

RESUMEN

OBJECTIVE: Our purpose was to determine the optimal management of pregnancies beyond 41 week's gestation with a cervix unfavorable for induction. MATERIAL AND METHOD: All uncomplicated pregnancies that reached 41 weeks'gestation with a Bishop score of< or =4, were randomly assigned to one of two groups RESULTS: The duration of labor was shorter in the group "prépidil" compared with the control group (P=0.002). Identification of an unfavorable cervix at 41 weeks was unlikely to change by 42 weeks and cervical ripening was required in 40% cases. There was no significant difference in caesarean section rates. Rates of admission into the neonatal unit and fetal outcomes were similar in the two groups. CONCLUSION: Cervical ripening with prostaglandin gel at 41 week's gestation for uncomplicated singleton pregnancies is safe and should be advocated.


Asunto(s)
Cuello del Útero/fisiología , Embarazo Prolongado , Maduración Cervical/efectos de los fármacos , Dinoprostona/administración & dosificación , Femenino , Macrosomía Fetal/epidemiología , Humanos , Mortalidad Infantil , Recién Nacido , Tiempo de Internación , Embarazo , Resultado del Embarazo
4.
J Gynecol Obstet Biol Reprod (Paris) ; 34(3 Pt 1): 257-61, 2005 May.
Artículo en Francés | MEDLINE | ID: mdl-16012386

RESUMEN

OBJECTIVES: To assess the clinical efficacy of mifepristone 100 mg followed two days later by misoprostol 400 microg orally in women undergoing medical termination of pregnancy up to 56 days gestational age. MATERIALS AND METHODS: Retrospective study over 8.5 months of 762 cases early medical abortion. 100 mg mifepristone was used on day 1 after clinic visit and vaginal ultrasonography. Misoprostol 400 microg was administered orally on day 3. Following administration of prostaglandin, women were observed in the ward for 4 hours. A control visit on day 15 was systematic. Success was defined as a complete uterine evacuation without the need for surgical intervention. RESULTS: Medical terminations accounted for 42% of all abortions. 16% of women were pregnant for < 42 days, 76% for 43 to 49 days and 8% for 50 to 56 days. Termination occurred within 4 hours after administration of misoprostol in 80.2% of the women. Only one woman aborted within 48 hours of mifepristone administration only. The success rate in this study was 94.4% and the failure rate increased with the gestational age. Pain was the predominant side effect. Six cases of bleeding required a surgical intervention. No patient required transfusion. 96% of patients attended a control visit on day 15. The acceptability rate of the method has been 94%. CONCLUSION: Mifepristone 100 mg followed two days later by misoprostol 400 microg orally is safe and effective for early termination of pregnancy.


Asunto(s)
Abortivos Esteroideos/administración & dosificación , Aborto Inducido/métodos , Mifepristona/administración & dosificación , Abortivos no Esteroideos/administración & dosificación , Abortivos no Esteroideos/efectos adversos , Abortivos Esteroideos/efectos adversos , Adulto , Femenino , Humanos , Mifepristona/efectos adversos , Misoprostol/administración & dosificación , Misoprostol/efectos adversos , Paridad , Embarazo , Estudios Retrospectivos , Resultado del Tratamiento
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