University College of Medicine and Dentistry, University of Lahore, Lahore, Pakistan.
Karachi Medical and Dental College, Karachi, Pakistan.
Curr Med Res Opin. 2024 Jan;40(1):141-149. doi: 10.1080/03007995.2023.2287608. Epub 2024 Jan 3.
Due to limited research on the effectiveness and safety of intravenous (IV) fluids administered during labor, there are no guidelines available. Thus, this meta-analysis aims to evaluate efficacy of IV Ringer's lactate during labor as compared to usual care.
Six databases were searched for the randomized controlled trials (RCTs) comparing the effects of IV Ringer's lactate at 125 mL/h or 250 mL/hr during labor in nulliparous women at term as compared to usual care, and the search results were imported to Covidence for screening of the articles. All the concerned outcomes were pooled as risk ratios (RR) or mean difference (MD) with 95% CI in the meta-analysis models using RevMan 5.4.
Pooled data from 7 RCTs with 967 nulliparous women showed that the active stage of labor duration (MD -32.16 with 95% CI [40.43 to -23.90], < 0.00001), need of oxytocin augmentation (RR 0.72 with 95% CI [0.54 to 0.96], = 0.03) and incidence of prolonged labor (RR 0.57 with 95% CI [0.34 to 0.95], = 0.03) was significantly lower with IV Ringer's lactate. However, the total duration of labor ( = 0.23), duration of second stage of labor ( = 0.31) and cesarean section rate ( = 0.070) did not differ between the two groups. The test for subgroup analysis based on infusion rate was significant ( = 0.01) for the active stage of labor.
IV Ringer's lactate reduced the duration of active labor, the need for oxytocin augmentation and the prolonged labor incidence. However, it did not differ in effect on immediate neonatal health but was found to have more potential for reducing maternal vomiting as compared to usual care with unrestricted oral intake. Further research is needed to explore its effects in the larger and more diverse populations and with different IV fluids for evidence-based guidelines.
由于静脉输液(IV)在分娩期间的有效性和安全性的研究有限,因此尚无可用的指南。因此,本荟萃分析旨在评估与常规护理相比,分娩期间输注林格氏乳酸盐的效果。
在六个数据库中搜索了比较在足月初产妇中以 125mL/h 或 250mL/hr 输注林格氏乳酸盐与常规护理相比的效果的随机对照试验(RCT),并将搜索结果导入 Covidence 进行文章筛选。使用 RevMan 5.4 中的荟萃分析模型,将所有相关结局作为风险比(RR)或均数差(MD),并使用 95%CI 进行汇总。
来自 7 项 RCT 的汇总数据涉及 967 名初产妇,结果显示活跃期产程时间(MD -32.16,95%CI [40.43 至 -23.90],<0.00001)、催产素需求增加(RR 0.72,95%CI [0.54 至 0.96],=0.03)和产程延长发生率(RR 0.57,95%CI [0.34 至 0.95],=0.03)显著降低。然而,两组的总产程时间(=0.23)、第二产程时间(=0.31)和剖宫产率(=0.070)没有差异。基于输注速度的亚组分析检验具有统计学意义(=0.01)。
IV 林格氏乳酸盐缩短了活跃期产程时间、催产素需求增加和产程延长的发生率。然而,它对即刻新生儿健康没有差异,但与常规护理相比,它减少了产妇呕吐的可能性,同时常规护理对产妇的口头摄入量没有限制。需要进一步研究以探索其在更大、更多样化的人群中的效果以及使用不同的 IV 液体的效果,以制定基于证据的指南。