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Therapeutic Methods and Therapies TCIM
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1.
Int J Obstet Anesth ; 19(2): 161-6, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20171080

ABSTRACT

BACKGROUND: Adequate analgesia following caesarean section decreases morbidity, hastens ambulation, improves patient outcome and facilitates care of the newborn. Intrathecal magnesium, an NMDA antagonist, has been shown to prolong analgesia without significant side effects in healthy parturients. We therefore studied the effect of adding intrathecal magnesium sulphate to bupivacaine-fentanyl spinal anaesthesia in patients with mild preeclampsia undergoing caesarean section. METHODS: Sixty women with mild preeclampsia undergoing caesarean section were included in a prospective, double blind, placebo-controlled trial. Patients were randomly assigned to receive spinal anaesthesia with 2 mL 0.5% hyperbaric bupivacaine and 25 microg fentanyl with either 0.1 mL of 0.9% sodium chloride (control group) or 0.1 mL of 50% magnesium sulphate (50 mg) (magnesium group). Onset, duration and recovery of sensory and motor block, time to maximum sensory block, duration of spinal anaesthesia and postoperative analgesia requirements were studied. RESULTS: The onset of both sensory and motor block was slower in the magnesium group. The duration of spinal anaesthesia (229.3 vs. 187.7 min) and motor block (200 vs. 175.3 min) were significantly longer in the magnesium group. Diclofenac requirement for 24 h following surgery was significantly lower in the magnesium group (147.5 vs.182.5 mg, P=0.02). Haemodynamic parameters and side effect profile were similar in the two groups. CONCLUSIONS: In parturients with mild preeclampsia undergoing caesarean delivery, the addition of magnesium sulphate 50 mg to the intrathecal combination of bupivacaine and fentanyl prolongs the duration of analgesia and reduces postoperative analgesic requirements without additional side effects.


Subject(s)
Anesthetics/administration & dosage , Cesarean Section/methods , Magnesium Sulfate/administration & dosage , Pre-Eclampsia/drug therapy , Pregnancy Complications/drug therapy , Adult , Bupivacaine/administration & dosage , Double-Blind Method , Female , Humans , Pregnancy , Prospective Studies , Treatment Outcome
2.
Trans R Soc Trop Med Hyg ; 100(12): 1164-7, 2006 Dec.
Article in English | MEDLINE | ID: mdl-16750546

ABSTRACT

A polyherbal vaginal pessary (Praneem) has been formulated that has antimicrobial properties against genital pathogens in addition to spermicidal action. Thus, it has dual potential as a barrier method for contraception and for providing protection against some sexually transmitted infections. The present study reports the findings of a multicentre trial that was conducted to evaluate the safety of this product. Trials were carried out in 23 women in three centres in India: the Postgraduate Institute of Medical Education and Research, Chandigarh; Safdarjang Hospital, New Delhi; and Kamla Nehru Memorial Hospital, Allahabad. Thorough clinical and pelvic examinations were carried out as well as cervical cytology, blood biochemistry and haematology before and after use of the polyherbal pessary intravaginally once daily for 7 consecutive days. No toxicity was observed on clinical examination or by laboratory investigations. Daily intravaginal use of this pessary for 7 days had no adverse effects on cervical cytology or on metabolic and organ functions.


Subject(s)
Anti-Infective Agents/adverse effects , Phytotherapy/adverse effects , Plant Extracts/administration & dosage , Quinine/administration & dosage , Sexually Transmitted Diseases/prevention & control , Spermatocidal Agents/adverse effects , Administration, Intravaginal , Adult , Anti-Infective Agents/administration & dosage , Drug Combinations , Female , Humans , Pessaries , Spermatocidal Agents/administration & dosage , Vaginal Smears
3.
Indian J Med Res ; 113: 135-41, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11558322

ABSTRACT

BACKGROUND & OBJECTIVES: Though a number of barrier methods and potent spermicides are available, most of these have nonoxynol-9 (N-9) as the active ingredient which is observed to cause inflammation and genital ulceration on repeated use. The present study was undertaken to develop a safe spermicide with conjoint microbicidal properties. METHODS: A polyherbal pessary was formulated with purified ingredients from neem (Azadirachta indica) leaves, Sapindus mukerossi (pericarp of fruit) and Mentha citrata oil. Spermicidal action on human sperm was tested by Sander-Cramer slide test in vitro and by post coital tests in vivo. Contraceptive action was tested in rabbits. RESULTS: The combination of the three herbal ingredients resulted in the potentiation of the spermicidal action by 8-folds. The post coital tests confirmed the spermicidal properties of the Praneem polyherbal pessary (PPP) in women with high cervical mucous score around mid estrus. It also prevented in most women the migration of sperm into the cervical mucous. In 15 rabbits studied pregnancy was prevented by the intravaginal administration of PPP, whereas 13 of the 15 animals in the control group became pregnant. INTERPRETATION & CONCLUSION: The Praneem polyherbal pessary has potent spermicidal action on human sperm in vitro and in vivo. When applied in the vagina before mating, it prevented rabbits from becoming pregnant.


Subject(s)
Phytotherapy , Plant Extracts/analysis , Quinine/analysis , Spermatocidal Agents/analysis , Female , Humans , Male , Plant Extracts/pharmacology , Quinine/pharmacology , Spermatocidal Agents/pharmacology
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