盐酸利托君联合硫酸镁治疗胎膜早破患者的显著效果

Fulin Tian, Jun Zhang, Jun Liu
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The treatment effects, levels of inflammatory factors, negative emotions, as well as maternal and child outcomes, along with any adverse reactions during the medication, were compared between the two groups. The effective\n rate of treatment in the observation group was 78.95%, and that in the experimental group was 97.37%. The effective rate in the experimental group was significantly higher than that in the observation group (P < 0.05). The levels of α and IFN-y were significantly lower\n than those of the observation group (all, P < 0.05); the SAS scores and SDS scores of the experimental group after treatment were significantly lower than those of the observation group (all, P < 0.05). The observation group showed significantly lower uterine contraction\n inhibition time and postpartum hemorrhage compared to the observation group, along with significantly higher gestational age extension time (all, P <0.05). In terms of neonatal outcomes, the birth weight, Apgar. 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引用次数: 0

摘要

为探究硫酸镁联合盐酸利托君对胎膜早破(PROM)患者母婴结局的影响,选取我院2021年7月-2022年7月收治的76例胎膜早破(PROM)患者作为研究对象,根据患者的治疗方法分为观察组和实验组。观察组 38 例患者接受硫酸镁单药治疗,实验组在观察组患者治疗的基础上加用盐酸利托君。对两组患者的治疗效果、炎症因子水平、负面情绪、母婴结局以及用药期间的不良反应进行了比较。观察组的治疗有效率为 78.95%,实验组为 97.37%。实验组的有效率明显高于观察组(P < 0.05)。实验组的α和IFN-y水平明显低于观察组(均P<0.05);实验组治疗后的SAS评分和SDS评分明显低于观察组(均P<0.05)。观察组的子宫收缩抑制时间和产后出血量明显低于观察组,胎龄延长时间明显高于观察组(均为 P 0.05)。硫酸镁联合盐酸利托君治疗PROM患者效果显著。联合方案的应用能有效减轻患者的炎症反应,调节患者的不良情绪,改善患者的母婴预后。此外,联合方案不会增加患者出现不良反应的风险,体现了其在临床用药中的理想安全性。
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Significant Effect of Ritodrine Hydrochloride Combined with Magnesium Sulfate for Treatment of Patients with Premature Rupture of Membranes
To investigate the effect of magnesium sulfate combined with ritodrine hydrochloride on maternal and infant outcomes in patients with premature rupture of membranes (PROM), a total of 76 PROM patients admitted to our hospital from July 2021 to July 2022 were selected as the research objects, and they were divided into observation group and experimental group according to the treatment methods of the patients. The observation group consisted of 38 patients who received magnesium sulfate monotherapy, whereas the experimental group received ritodrine hydrochloride in addition to the treatment received by the patients in the observation group. The treatment effects, levels of inflammatory factors, negative emotions, as well as maternal and child outcomes, along with any adverse reactions during the medication, were compared between the two groups. The effective rate of treatment in the observation group was 78.95%, and that in the experimental group was 97.37%. The effective rate in the experimental group was significantly higher than that in the observation group (P < 0.05). The levels of α and IFN-y were significantly lower than those of the observation group (all, P < 0.05); the SAS scores and SDS scores of the experimental group after treatment were significantly lower than those of the observation group (all, P < 0.05). The observation group showed significantly lower uterine contraction inhibition time and postpartum hemorrhage compared to the observation group, along with significantly higher gestational age extension time (all, P <0.05). In terms of neonatal outcomes, the birth weight, Apgar. The scores were significantly higher than those of the observation group, and the incidence of complications was significantly lower than that of the observation group (all, P < 0.05). The incidence of adverse reactions in the observation group was 21.05%, compared to 23.68% in the experimental group. There was no significant difference in the incidence of adverse reactions between the two groups of patients (P > 0.05). Magnesium sulfate combined with ritodrine hydrochloride has a significant effect in the treatment of patients with PROM. The application of the combined program can effectively reduce the inflammatory response of patients, regulate the negative emotions of patients, and improve the maternal and infant outcomes of patients. Moreover, the combined program does not increase the risk of adverse reactions in patients, demonstrating its ideal safety in clinical medication.
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