Pengaruh Pemberian Parasetamol Intravena untuk Mengurangi Nyeri Persalinan Kala 1 Fase Aktif

Juli Sitorus, Ova Emilia, Detty Siti Nurdiati
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Abstract

Background: Labor was a physiological process, labor pain appeared from regularly uterine contraction, cervix distention and pressure to pelvic floor that stimulate free end nerves. Pain labor can influenced the mother, fetus and the progress of labor. There are various of effort to decrease pain labor by pharmacological or non pharmacological. The best therapy must be safe, effective, and minimal adverse effect to mother and fetus. Objective: To evaluate the effect of paracetamol intraveneous for pain relief in active labor versus saline water. Methods: In randomized controlled trial, with single blinded, 66 primigravid in active labor at RSUD Hj. ANNA LASMANAH Banjarnegara and RSUD Banyumas from November 2016 to January 2017. Sampels divided in two groups, paracetamol group (n=33) and normal saline group (n=33). The primary  outcome was the efficacy of paracetamol to relief pain. Intensity of the pain measure by VAS (visual analogue scale), pain measured before drug administration, after 30 minutes, at 1, 2, 3, and 4 hours in both groups. The secondary outcomes include the adverse effect to the mother and baby in both group. Results: The reduction in pain score was significantly greater in paracetamol group than normal saline after 30 minutes, 1, 2, 3, and 4 hours after adiministration of the drug (p<0.05). There was no adverse effect to mother and baby in both groups. Conclusion: Paracetamol intravenous statistically significant decreasing mean pain score than normal saline and safe in active labor. Keywords: Paracetamol, analgesia, active phase in labor
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静脉注射扑热息痛以缓解分娩时的1个活跃阶段
背景:分娩是一个生理过程,产痛表现为子宫有规律的收缩、宫颈扩张和盆底受压刺激自由端神经。阵痛可影响母体、胎儿及产程。有各种各样的努力,以减轻疼痛分娩药物或非药物。最好的治疗方法必须是安全、有效、对母亲和胎儿的不良影响最小。目的:评价对乙酰氨基酚静脉滴注与生理盐水对产程疼痛的缓解效果。方法:采用随机对照试验,采用单盲法,对66例在RSUD Hj进行主动分娩的原孕患者进行分析。ANNA LASMANAH Banjarnegara和RSUD Banyumas, 2016年11月至2017年1月。样本分为两组,扑热息痛组(n=33)和生理盐水组(n=33)。主要结局是扑热息痛缓解疼痛的效果。采用视觉模拟评分法(VAS)测量疼痛强度,分别在给药前、给药后30分钟、给药后1、2、3、4小时测量疼痛。次要结局包括两组对母婴的不良反应。结果:扑热息痛组在给药后30 min、1、2、3、4 h疼痛评分的降低程度显著高于生理盐水组(p<0.05)。两组对母婴均无不良反应。结论:与生理盐水相比,静脉注射扑热息痛可显著降低产妇平均疼痛评分,且在产程中安全。关键词:扑热息痛,镇痛,产程活跃期
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