Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtrer
1.
Article de Anglais | IMSEAR | ID: sea-183292

RÉSUMÉ

Background: To compares the effectiveness and acceptability of sublingual versus vaginal route of misoprostol for cervical priming prior to vacuum aspiration. Material and methods: In this prospective clinical study, a total of 70 women with period of gestation between 6 and 12 weeks selected randomly for day surgery abortion were sequentially allocated into two groups of 36 and 34. All selected women received 400 mg of misoprostol 3 hours prior to vacuum aspiration either by sublingual or by vaginal route in the hospital. Results: For all periods of gestation, sublingual misoprostol significantly improved cervical dilatation. Duration of the procedure and amount of blood loss were comparable in both the groups. Patient acceptability was higher in the sublingual group. Conclusion: Cervical priming with sublingual misoprostol is effective and convenient route with high patient acceptability rate.

2.
Article de Anglais | IMSEAR | ID: sea-182392

RÉSUMÉ

Objective: To compare the effect of sublingual versus vaginal misoprostol on preoperative cervical priming in first trimester abortion. Material and methods: One hundred women seeking first trimester abortion were randomized into either sublingual or vaginal groups of 50 each. They were given 400 μg misoprostol via sublingual or vaginal route for cervical priming three hours before the procedure. The outcome measures assessed were cervical dilatation before surgery, duration of procedure, intraoperative blood loss and preoperative side effects. Results: Subjects in the sublingual group achieved significantly higher mean cervical dilatation compared to vaginal group (8.34 ± 0.62 mm vs 7.60 ± 0.67 mm, p = 0.0001). The mean duration of procedure for sublingual group was significantly lower compared to the vaginal group (2.62 ± 0.64 minutes vs 3.17 ± 0.71 minutes, p = 0.0001). The mean intraoperative blood loss was found to be more in sublingual group as compared to vaginal group (34.90 ± 10.90 ml vs 32.90 ± 7.42 ml), but the difference was not significant (p = 0.286). The sublingual group experienced more preoperative side effects such as pain, bleeding, nausea and shivering as compared to vaginal group. Conclusion: Sublingual misoprostol is more effective and convenient route than vaginal misoprostol for preoperative cervical priming in first trimester abortion.

3.
Indian J Med Sci ; 2010 Aug; 64(8) 356-362
Article de Anglais | IMSEAR | ID: sea-145553

RÉSUMÉ

Background: Misoprostol is effective for cervical priming before manual vacuum aspiration (MVA). Aim of study was to determine whether sublingual misoprostol with a shorter interval of 2 hours before MVA would be as effective as its standard vaginal administration. Study Design: This randomized control trial included 82 women randomly assigned to receive 400 mcg of misoprostol, either sublingually or vaginally. MVA was performed 2 hours and 3 hours after in sublingual and vaginal group, respectively. Results: Cervical dilatation of 8 mm was achieved within 2 hours in sublingual group. Mean time taken for procedure (14.4 ± 5.3: sublingual group and 16.2 ± 5.7: vaginal group), and blood loss was comparable (12.2 ± 9.7 ml in sublingual group and 13.7 ± 8.5 ml in vaginal group). Conclusion: 2 hour of cervical priming with 400 mcg of sublingual misoprostol before MVA was as good as 3 hours with vaginal administration of the same dose.


Sujet(s)
Avortement provoqué/méthodes , Administration par voie vaginale , Administration par voie sublinguale , Adulte , Perte sanguine peropératoire , Maturation du col utérin/effets des médicaments et des substances chimiques , Col de l'utérus/effets des médicaments et des substances chimiques , Voies d'administration de substances chimiques et des médicaments , Femelle , Humains , Misoprostol/administration et posologie , Misoprostol/usage thérapeutique , Soins préopératoires/méthodes , Curetage aspiratif/méthodes
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE