Efficacy of N-acetyl Cysteine in Severe COVID-19 Patients: A Randomized Controlled Phase III Clinical Trial

IF 1 Q4 PHARMACOLOGY & PHARMACY
A. Rahimi, H. Samimagham, Ladan Hajiabdolrrasouli, M. Hassani Azad, Ali Salimi Asl, Fatemeh Khajavi Mayvan, E. Boushehri, M. Arabi, Sepideh Pazhoohesh, Mitra Kazemi Jahromi
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Abstract

Background: Today, various drugs have been investigated as the primary or complementary treatment for coronavirus disease 2019 (COVID-19). N-acetylcysteine (NAC) has been used as a mucolytic in pulmonary diseases. This drug apparently contributes to the retrieval of the intracellular antioxidant system. Objectives: This study aimed to determine the efficacy of NAC in severe COVID-19 patients admitted to the intensive care unit (ICU). Methods: This single-blinded randomized controlled phase III clinical trial included 40 patients with confirmed COVID-19 (based on polymerase chain reaction) admitted to the Shahid Mohammadi Hospital’s ICU, Bandar Abbas, Iran, in 2020. All cases had severe COVID-19. They were allocated randomly to two equal groups. Patients in the control group received standard drug therapy based on the treatment protocol of the national COVID-19 committee, while those in the NAC group received a single dose of intravenous NAC (300 mg/kg) upon admission to the ICU in addition to standard drug treatment. Clinical status and laboratory tests were done on admission to the ICU and then 14 days later or at discharge without knowing the patient grouping. Results: The two groups were comparable regarding age, gender, and other baseline laboratory and clinical parameters. At the final evaluation, respiratory rate (21.25 ± 4.67 vs. 27.37 ± 6.99 /min) and D-dimer (186.37 ± 410.23 vs. 1339.04 ± 2183.87 ng/mL) were significantly lower in the NAC group (P = 0.004 and P = 0.030, respectively). Also, a lower percentage of patients in the NAC group had lactate dehydrogenase (LDH) ≤ 245 U/L (0% vs. 25%, P = 0.047). Although the length of ward and ICU stay was shorter in the NAC group than in controls, the difference was statistically insignificant (P = 0.598 and P = 0.629, respectively). Mortality, on the other hand, was 75% in the control group and 50% in the NAC group, with no statistically significant difference (P = 0.102). Concerning the change in the study parameters, only the decrease in diastolic blood pressure (DBP) was significantly higher with NAC (P = 0.042). The intubation and mechanical ventilation rates were higher, while oxygen with mask and nasal oxygen rates were lower with NAC, but the difference was statistically insignificant. Conclusions: Based on the current research, NAC is related to a significant decrease in RR, D-dimer, and DBP in severe COVID-19. Also, LDH was significantly lower in the NAC group than in the controls. More research with larger sample sizes is needed to validate the current study results.
n -乙酰半胱氨酸治疗重症COVID-19患者的疗效:一项随机对照III期临床试验
背景:目前,已经研究了各种药物作为2019冠状病毒病(COVID-19)的主要或补充治疗。n -乙酰半胱氨酸(NAC)已被用作肺部疾病的黏液溶解剂。这种药物显然有助于细胞内抗氧化系统的恢复。目的:本研究旨在确定NAC在重症监护病房(ICU)重症COVID-19患者中的疗效。方法:该单盲随机对照III期临床试验纳入了2020年在伊朗阿巴斯港Shahid Mohammadi医院ICU收治的40例确诊COVID-19患者(基于聚合酶链反应)。所有病例均为重症COVID-19。他们被随机分为两组。对照组患者按照国家新冠肺炎防治委员会治疗方案进行标准药物治疗,NAC组患者在标准药物治疗的基础上,于入住ICU时给予单剂量NAC (300 mg/kg)静脉注射。在不知道患者分组的情况下,于入院时和14天后或出院时分别进行临床状况和实验室检查。结果:两组在年龄、性别和其他基线实验室和临床参数方面具有可比性。最终评估时,NAC组呼吸频率(21.25±4.67 vs. 27.37±6.99 /min)和d -二聚体(186.37±410.23 vs. 1339.04±2183.87 ng/mL)均显著降低(P = 0.004和P = 0.030)。NAC组乳酸脱氢酶(LDH)≤245 U/L的患者比例较低(0% vs. 25%, P = 0.047)。NAC组病区时间和ICU住院时间虽短于对照组,但差异无统计学意义(P = 0.598、P = 0.629)。NAC组死亡率为50%,对照组为75%,差异无统计学意义(P = 0.102)。在研究参数的变化方面,NAC组只有舒张压(DBP)下降明显高于NAC组(P = 0.042)。NAC组插管和机械通气率较高,面罩供氧率和鼻供氧率较低,但差异无统计学意义。结论:根据目前的研究,NAC与重症COVID-19患者RR、d -二聚体和DBP的显著降低有关。NAC组的LDH也明显低于对照组。需要更多样本量更大的研究来验证目前的研究结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.40
自引率
0.00%
发文量
26
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