Comparison of inhaled salbutamol and intravenous furosemide in the treatment of transient tachypnea of the newborn regarding their safety and efficacy

Amira M Sabry, Mohammed Azeem, Marwa M. Ismail, Dina El Khatib, Iman Abdelaziz
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Abstract

Background Postnatal respiratory complications among term infants are common. The most commonly reported cause of neonatal respiratory distress is transient tachypnea of the newborn (TTN), with an estimated incidence of 0.5–2.8% of all newborns. Aim To evaluate and compare the efficacy and safety of inhaled salbutamol and intravenous (i.v.) furosemide in the treatment of TTN and to monitor of their possible adverse effects in neonates. Patients and methods This was a randomized controlled clinical trial on 100 neonates who were admitted immediately or shortly after birth owing to persistence of tachypnea to neonatal intensive care unit of pediatric hospitals, Cairo University, over a 1-year period. Our study included 100 neonates (25 in the salbutamol group, 25 in the furosemide group, and 50 in the control group) with TTN born between 35 and 39 weeks of gestational age. They were randomized in a blinded manner to receive one nebulized dose of salbutamol 0.15 mg/kg in 0.9% saline solution or i.v. furosemide 1 mg/kg once in addition to oxygen and i.v. fluids or received oxygen and i.v. fluids alone. Results The efficacy of inhaled salbutamol and furosemide was assessed by determining the respiratory rate, heart rate, TTN clinical score, and the level of respiratory support before receiving medication and 30 min, 1, and 4 h after drug therapy. The duration and level of respiratory support and the period of hospitalization were shorter in the salbutamol group. There was a significant decrease in the respiratory rate and TTN score in the salbutamol group 4 h after nebulized salbutamol. Conclusion Comparing the three groups after respiratory support, TTN score was significantly improved in the salbutamol group. The total duration of oxygen treatment in hours and total neonatal intensive care unit stay in days were significantly shorter in the salbutamol group than in furosemide and control groups. Regarding the safety of salbutamol, our study did not show a significant difference in adverse effects. Inhaled salbutamol treatment was effective in TTN without adverse events. Further studies at larger or repeated doses of furosemide may be needed.
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吸入沙丁胺醇与静脉速尿治疗新生儿短暂性呼吸急促的安全性和有效性比较
背景足月婴儿出生后呼吸系统并发症很常见。新生儿呼吸窘迫最常见的报告原因是新生儿短暂性呼吸急促(TTN),估计发病率为所有新生儿的0.5-2.8%。目的评价和比较吸入沙丁胺醇与静脉滴注呋塞米治疗新生儿TTN的疗效和安全性,并监测两者可能出现的不良反应。患者和方法这是一项随机对照临床试验,对100名因持续呼吸急促而在出生后立即或不久入住开罗大学儿科医院新生儿重症监护室的新生儿进行了为期1年的研究。我们的研究包括100名出生在35 - 39周孕龄的TTN新生儿(沙丁胺醇组25名,速尿组25名,对照组50名)。随机采用盲法,在0.9%生理盐水溶液中雾化沙丁胺醇0.15 mg/kg 1次或速尿1 mg/kg 1次,同时给予氧气和静脉输液或单独给予氧气和静脉输液。结果通过测定用药前及用药后30min、1h、4h呼吸频率、心率、TTN临床评分、呼吸支持水平,评价吸入沙丁胺醇和呋塞米的疗效。沙丁胺醇组呼吸支持持续时间、水平和住院时间较短。沙丁胺醇组在雾化后4 h呼吸频率和TTN评分均明显降低。结论三组呼吸支持后,沙丁胺醇组TTN评分明显提高。沙丁胺醇组总耗氧时间(h)和新生儿重症监护病房总住院时间(d)均显著短于速尿组和对照组。关于沙丁胺醇的安全性,我们的研究没有显示出不良反应的显著差异。吸入沙丁胺醇治疗TTN有效,无不良反应。可能需要更大剂量或重复使用呋塞米的进一步研究。
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