misoprostol has been researched along with Syndrome* in 7 studies
1 trial(s) available for misoprostol and Syndrome
Article | Year |
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A randomized comparison of oral misoprostol versus Foley catheter and oxytocin for induction of labor at term.
We sought to compare the efficacy and safety of oral misoprostol administered to patients with the efficacy and safety in a control group treated with a Foley catheter and oxytocin for induction of labor.. Two hundred patients requiring induction of labor at term with a Bishop score of =5 were randomized to receive oral misoprostol or a cervical Foley catheter plus oxytocin. Patients in the misoprostol group received 50 microg at 4-hour intervals for a maximum of 6 doses or until an adequate contraction pattern developed. Those in the control group had a Foley catheter inserted in the cervix, whereas oxytocin was administered intravenously by a standard incremental infusion protocol to a maximum dose of 36 mU/min.. In multiparous patients the percentage delivered of their neonates within 24 hours and the median induction-to-delivery times were similar in the 2 groups. In nulliparous patients, however, delivery within 24 hours was significantly less likely in the misoprostol group (53.4% vs 82. 5%; P <.001), and the median induction-to-delivery time was longer (23.3 hours vs 17.2 hours; P <.01). There were no differences in the incidence of meconium, chorioamnionitis, low Apgar scores, or cesarean delivery. The incidence of hyperstimulation was higher in the oxytocin-Foley group (4.1% vs 13.1%; P =.02).. Oral misoprostol is as effective as oxytocin-Foley catheter for inducing labor in multiparous women. Misoprostol appears less efficacious in nulliparous patients. Topics: Administration, Oral; Adult; Catheterization; Cervical Ripening; Female; Gestational Age; Humans; Infant, Newborn; Labor, Induced; Misoprostol; Obstetric Labor Complications; Oxytocics; Oxytocin; Parity; Pregnancy; Syndrome; Time Factors; Uterine Contraction | 1999 |
6 other study(ies) available for misoprostol and Syndrome
Article | Year |
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Fetal methotrexate syndrome following an unsuccessful medication abortion - a rare syndrome posed to become more common.
Topics: Abortion, Induced; Female; Fetus; Humans; Methotrexate; Misoprostol; Pregnancy; Syndrome | 2023 |
Factors that modify penicillamine-induced autoimmunity in Brown Norway rats: failure of the Th1/Th2 paradigm.
Idiosyncratic drug reactions appear to be immune-mediated. Immune responses are driven by helper T cells (Th); Th1 responses promote cell-mediated immunity, whereas Th2 responses drive antibody-mediated reactions. Th1 cytokines inhibit Th2 responses and Th2 cytokines inhibit Th1 responses; therefore, it may be possible to prevent idiosyncratic drug reactions by changing the Th1/Th2 cytokine balance. We tested this hypothesis in an animal model in which penicillamine causes an autoimmune syndrome in Brown Norway rats. This syndrome has the hallmarks of a Th2-mediated response and we tried to inhibit it with a polymer of inosine and cytosine (poly I:C), a Th1 cytokine-inducer. However, we found that a single dose of poly I:C, given at the onset of penicillamine treatment, significantly increased both the incidence (100 vs. 60%) and accelerated the onset (30+/-4 vs. 39+/-5 days) of penicillamine-induced autoimmunity when compared with controls. To rule out other effects of poly I:C that might overshadow the induction of Th1 cytokines, we directly tested the effects of the prototypic Th1 cytokine, interferon-gamma. Although not as dramatic, interferon-gamma-pretreatment also appeared to make the syndrome worse. Conversely, when we used misoprostol, a prostaglandin-E analog that inhibits Th1 cytokines, it completely protected the animals. Just one dose of misoprostol prior to initiation of penicillamine treatment was sufficient to provide this protection. The syndrome was also completely inhibited by aminoguanidine, an inhibitor of iNOS. These results, although dramatic, suggest that the effects of these agents were not mediated by their effects on Th1/Th2 balance, but rather by some other mechanism. Topics: Animals; Autoimmune Diseases; Autoimmunity; Drug Eruptions; Immunoglobulin E; Interferon Inducers; Interferon-gamma; Interleukin-4; Misoprostol; Models, Animal; Nitrites; Penicillamine; Poly I-C; Rats; Rats, Inbred BN; Rats, Inbred Lew; Syndrome; Th1 Cells; Th2 Cells | 2001 |
Association of misoprostol, Moebius syndrome and congenital central alveolar hypoventilation. Case report.
We report a case showing the association of Moebius syndrome, the use of misoprostol during pregnancy and the development of central congenital alveolar hypoventilation. Pathophysiological aspects of these three diseases are discussed and also the unfavorable prognosis of this association. Topics: Abnormalities, Multiple; Abortifacient Agents, Nonsteroidal; Humans; Infant; Male; Misoprostol; Respiration, Artificial; Sleep Apnea Syndromes; Syndrome | 1999 |
Vascular disruptive syndromes after exposure to misoprostol or chorionic villus sampling.
Topics: Abnormalities, Multiple; Chorionic Villi Sampling; Female; Fetus; Humans; Infant, Newborn; Misoprostol; Pregnancy; Syndrome | 1999 |
Möbius syndrome after misoprostol: a possible teratogenic mechanism.
Topics: Abnormalities, Drug-Induced; Animals; Cranial Nerves; Female; Humans; Limb Deformities, Congenital; Misoprostol; Paralysis; Rats; Syndrome; Uterine Contraction | 1995 |
Limb deficiency with or without Möbius sequence in seven Brazilian children associated with misoprostol use in the first trimester of pregnancy.
Misoprostol, a synthetic analog of prostaglandin, has been widely used in Brazil as an abortifacient. Abortion is illegal in Brazil. An uncertain number of these abortion attempts are unsuccessful and the pregnancy continues. We report on 7 patients whose mothers attempted to abort using this drug in the first trimester of gestation without success. The 7 patients presented with limb defects and in 4 of them a diagnosis of Möbius sequence was made. Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Abortion, Criminal; Brazil; Cranial Nerve Diseases; Ectromelia; Facial Paralysis; Female; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infant, Newborn; Male; Misoprostol; Pregnancy; Syndrome | 1993 |