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2.
Asia Oceania J Obstet Gynaecol ; 19(2): 121-6, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8379859

ABSTRACT

A prospective evaluation of 140 forceps deliveries with the Hay's flexion rotation obstetric forceps was undertaken over a 5-year period. The Hay's forceps was used for a variety of indications and included outlet forceps application in 35.7%, low or midforceps application in 29.3% with forceps rotation in 16.4%, 19.3% of applications for an aftercoming head and 19.3% applications at caesarean section. Outlet forceps deliveries had maternal and neonatal outcomes comparable with the Wrigley's short obstetric forceps. Midforceps applications were compared to the Simpson's long forceps, with maternal morbidity at 21% being significantly less, blade marks being the only neonatal morbidity and the Apgar scores being significantly higher with the Hay's forceps. Every forceps application at caesarean section resulted in an easy delivery. Thus the Hay's forceps with innovations such as parallelism and flexion potential could revalidate the role of the forceps in contemporary obstetrics.


Subject(s)
Extraction, Obstetrical/instrumentation , Obstetrical Forceps , Cesarean Section/instrumentation , Extraction, Obstetrical/adverse effects , Female , Humans , Obstetrical Forceps/adverse effects , Pregnancy , Pregnancy Outcome , Prospective Studies
3.
J Postgrad Med ; 38(2): 58-9, 1992.
Article in English | MEDLINE | ID: mdl-1432827

ABSTRACT

The study evaluates breast stimulation and oxytocin infusion as methods for cervical ripening in patients where an obstetric indication for induction of labour exists. Forty patients with a Bishop score of 5 or 6 were randomly selected for either breast stimulation or oxytocin infusion. In a similar group of 20 cases, no method was employed. The Bishop score improved in 41.2% of cases where breast stimulation was used as compared to 75% where an oxytocin infusion was given. Three foetal deaths in the breast stimulation group brought the study to a stop after 17 cases. Cervical ripening with an oxytocin infusion drip appears to be a better method since infusion dosage can be precisely controlled making the technique more predictable and reliable. Though breast stimulation is effective in ripening the cervix, it may be used only in cases of intrauterine foetal death as it may otherwise adversely affect foetal outcome.


Subject(s)
Breast/physiology , Cervix Uteri/physiology , Labor, Induced/standards , Oxytocin/therapeutic use , Physical Stimulation , Cervix Uteri/drug effects , Female , Fetal Death/etiology , Humans , Infusions, Intravenous , Labor, Induced/methods , Oxytocin/administration & dosage , Pregnancy , Pregnancy Outcome
4.
J Postgrad Med ; 36(3): 136-9, 1990 Jul.
Article in English | MEDLINE | ID: mdl-2102912

ABSTRACT

Two hundred consecutive cases up to 19 years of age admitted for confinement at The Nowrosjee Wadia Maternity Hospital, Bombay, were studied. Out of these 200 girls, 6 were unmarried, 51 were anaemic, 20 had toxaemia of pregnancy. Six girls (43%) in the age group 15-17 years delivered prematurely as compared to only 26 girls (14%) in the age group of 17-19 years. This difference is statistically significant. Also, only, 4 girls (29%) in the age group of 15-17 years had full term normal delivery as compared to 113 girls (61%) in the age group of 17-19 years signifying that the outcome of pregnancy becomes worst in girls below the age of 17 years. Ten babies (71%) of mothers in the age group of 15-17 years were LBW as compared to 75 babies (44%) of mothers in the age group of 17-19 years signifying that the incidence of LBW babies is inversely proportional to maternal age. Teenage pregnant girls needed more attention for prevention and treatment of preeclampsia eclampsia, anaemia, prematurity and LBW.


Subject(s)
Pregnancy in Adolescence , Adolescent , Birth Weight , Female , Humans , Pregnancy , Pregnancy Complications , Pregnancy Outcome
6.
Curr Med Res Opin ; 6(9): 614-8, 1980.
Article in English | MEDLINE | ID: mdl-6996931

ABSTRACT

A double-blind, placebo-controlled trial was carried out in 299 patients suffering from post-episiotomy pain to compare the analgesic effectiveness and tolerance of single doses of 500 mg dipyrone and 500 mg paracetamol. Assessments of pain relief over a 6-hour period showed that dipyrone produced significantly better results than placebo within half an hour of intake and maintained this superiority throughout the 6 hours. It also afforded consistently better pain relief than paracetamol and was significantly more effective at the 6-hour assessment. Side-effects were few and mild.


Subject(s)
Acetaminophen/therapeutic use , Aminopyrine/analogs & derivatives , Dipyrone/therapeutic use , Pain, Postoperative/drug therapy , Adult , Clinical Trials as Topic , Double-Blind Method , Episiotomy , Female , Humans , Placebos
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