Ampicillin-Sulbactam for the Treatment of Aspiration Pneumonia in Patients with Opioid Overdose: A Randomized Controlled Clinical Trial

M. Tabatabaei, R. Soltani, Gholamali Dorvashy, S. Samsamshariat, Rokhsareh Meamar, A. Sabzghabaee
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Abstract

Background: Aspiration pneumonia is among overdose complications, requiring timely appropriate treatment. The present study aimed to evaluate the effects of ampicillin-sulbactam, compared to our usual regimen ceftriaxone + clindamycin on aspiration pneumonia in opioid-poisoned patients. Methods: In a randomized-controlled clinical trial, opioid-poisoned patients with aspiration pneumonia were randomly divided into the experimental and control groups to receive ampicillin-sulbactam 3 g Intravenously (IV) every 6 hours (experimental group) and ceftriaxone 1 g IV every 12 hours + clindamycin 600 mg IV every 8 hours (control group) followed by co-amoxiclav 625 mg orally every 8 hours and cefixime 400 mg once daily + clindamycin 600 mg orally every 8 hours in experimental and control groups, respectively, to complete a 7-day course of therapy. White blood cell count and temperature (axillary) at baseline and the third day of the intervention and the treatment outcome on the third day of the intervention, defined as either complete response, partial response, or failure, were evaluated and recorded for all patients. Results: Except for the number of cases of leukocytosis on the third day of the intervention, i.e., lower in the control group (5 patients, 26.30%) than the experimental group (13 patients, 68.40%) (P=0.020), no significant difference was observed between the study groups regarding other outcome variables. Clinical response was similar between the study groups; so that, 10.50% and 63.20% of patients in the experimental group and 21.10% and 47.4% of patients in the control group presented complete and partial responses, respectively (P=0.550). Conclusion: The obtained data suggested that ampicillin-sulbactam is an effective antibiotic for the treatment of aspiration pneumonia in patients with opioid overdose, in which case, it has the same efficacy as the two-drug regimen of ceftriaxone + clindamycin.
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氨苄西林-舒巴坦治疗阿片类药物过量患者吸入性肺炎:一项随机对照临床试验
背景:吸入性肺炎是服药过量的并发症之一,需要及时适当的治疗。本研究旨在评估氨苄青霉素-舒巴坦与我们常用的头孢曲松+克林霉素方案对阿片类药物中毒患者吸入性肺炎的疗效。方法:在随机对照临床试验中,阿片类药物中毒的吸入性肺炎患者随机分为实验组和对照组,分别给予氨苄青霉素-舒巴坦3g,每6小时静脉注射(IV)(实验组)和头孢曲松1g,每12小时静脉注射+克林霉素600mg,每8小时静脉注射对照组),然后给予复方阿莫西林625mg,每8 h口服,头孢克肟400mg,每日1次+克林霉素600实验组和对照组分别每8小时口服一次mg,以完成7天的疗程。评估并记录所有患者在基线和干预第三天的白细胞计数和温度(腋窝),以及干预第三天后的治疗结果,定义为完全缓解、部分缓解或失败。结果:除了干预第三天白细胞增多的病例数,即对照组(5例,26.30%)低于实验组(13例,68.40%)(P=0.020)外,研究组之间在其他结果变量方面没有观察到显著差异。研究组之间的临床反应相似;因此,实验组10.50%和63.20%的患者和对照组21.10%和47.4%的患者分别出现完全和部分缓解(P=0.550),与头孢曲松+克林霉素两种给药方案疗效相同。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
50
审稿时长
12 weeks
期刊最新文献
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