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Pharmacokinetics of Tocolytic Agents

Clinical Pharmacokinetics, 2004
Tocolytic agents are drugs designed to inhibit contractions of myometrial smooth muscle cells. Such an effect has been demonstrated in vitro or in vivo for several pharmacological agents, including beta-adrenergic agonists, calcium channel antagonists, oxytocin antagonists, NSAIDs and magnesium sulfate. However, the aim of tocolysis is not only to stop
Vassilis, Tsatsaris   +2 more
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Magnesium sulfate as a tocolytic agent

Seminars in Perinatology, 2001
Although magnesium sulfate is widely used as a tocolytic agent in the hope of preventing spontaneous preterm birth, there is a paucity of data from large well-designed randomized clinical studies demonstrating the efficacy of magnesium sulfate therapy. Given the potential for untoward side effects and the inherent risks of magnesium sulfate therapy, a ...
P S, Ramsey, D J, Rouse
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Leptin – A tocolytic agent for the future?

Medical Hypotheses, 2010
Leptin - a protein hormone is synthesised in the adipose tissue in humans. Its level therefore should be directly proportional to the amount of adipose tissue in the body. When biopsies of human myometrium from obese women were exposed to leptin, it showed a cumulative inhibitory effect on spontaneous as well as induced contractions.
Rekha, Wuntakal, Tony, Hollingworth
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New tocolytic agents

European Clinics in Obstetrics and Gynaecology, 2005
Prematurity has not decreased significantly over the past 20 years, whereas early prematurity has increased. New tocolytic agents have been developed that are increasingly successful at preventing preterm delivery, and that have improved maternal tolerance.
Georges Abitayeh   +3 more
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Evidence for Magnesium Sulfate as a Tocolytic Agent

Obstetrical & Gynecological Survey, 1997
The objective of our study is to quantitatively examine the available evidence regarding the efficacy and side effects of magnesium sulfate for acute tocolysis (from randomized trials) compared with placebo and beta-agonist agents. Randomized trials comparing magnesium sulfate with placebo or beta-agonists for tocolysis were identified with a MEDLINE ...
G A, Macones   +4 more
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Pharmacology of Tocolytic Agents

Clinics in Obstetrics and Gynaecology, 1984
Various drugs have been used to inhibit preterm labour. Selective beta-receptor agonists are the drugs of choice and have been extensively studied for more than ten years. Several controlled studies have demonstrated a significant prolongation of the pregnancy after treatment with beta-receptor agonists and some have demonstrated improved fetal outcome.
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Magnesium sulfate as a tocolytic agent

American Journal of Obstetrics and Gynecology, 1983
Magnesium sulfate (MgSO4) has been successfully used to inhibit premature labor. A retrospective review was performed on the use of MgSO4 as a tocolytic agent at Memorial Hospital, Long Beach, California, during a 4-year period (1978-1982). Three hundred fifty-five patients with diagnoses of premature labor were treated with MgSO4 after transport from ...
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Thermic Effects of Tocolytic Agents

Obstetric Anesthesia Digest, 1987
The effect of the tocolytic agents terbutaline and magnesium sulfate on patients' temperatures was examined. Fifty-two women admitted for preterm labor were randomized to a treatment protocol for one of the two agents. Oral temperatures were measured initially and every two hours during treatment. There was no significant difference between the initial
M T, Parsons, C A, Owens, W N, Spellacy
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Complications Associated with the Administration of Tocolytic Agents

Journal SOGC, 1998
Abstract Because maternal antenatal steroid administration has been shown to improve neonatal outcome at gestational age Jess then 34 weeks, many obstetrical practitioners choose to use tocolytic agents in an attempt to delay premature delivery and, thereby, allow enough time for steroid treatment. Unfortunately, tocolytics are not without potentially
Andrée Gruslin, Brigitte Bonin
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A Comparison of the Relative Toxicities of β-Sympathomimetic Tocolytic Agents

American Journal of Perinatology, 1985
To define the relative toxicities of ritodrine sulfate, terbutaline sulfate, hexaprenaline sulfate, and ritodrine with betamethasone mongrel dogs were treated with these agents for 19 hours. The maximum dose of ritodrine was 900 microgram/min (N = 5), terbutaline 120 micrograms/min (N = 4) and hexaprenaline 1.5 micrograms/min (N = 4). Betamethasone was
G D, Hankins, J C, Hauth
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