Department of Surgery, Baqiyatallah University of Medical Sciences, Tehran, Iran; Trauma Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Trauma Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Chin J Traumatol. 2023 Mar;26(2):116-120. doi: 10.1016/j.cjtee.2022.10.002. Epub 2022 Oct 13.
Patients with multiple traumas are at high risk of developing respiratory complications, including pneumonia and acute respiratory distress syndrome. Many pulmonary complications are associated with systemic inflammation and pulmonary neutrophilic infiltration. Leukotriene-receptor antagonists are anti-inflammatory and anti-oxidant drugs subsiding airway inflammation. The present study investigates the effectiveness of montelukast in reducing pulmonary complications among trauma patients.
This randomized, double-blind, placebo-control trial was conducted in patients with multiple blunt traumas and evidence of lung contusion detected via CT scan. We excluded patients if they met at least one of the following conditions: < 16 years old, history of cardiopulmonary diseases or positive history of montelukast-induced hypersensitivity reactions. Patients were allocated to the treatment (10 mg of montelukast) or placebo group using permuted block randomization method. The primary measured outcome was the volume of pulmonary contusion at the end of the trial. The secondary outcomes were intensive care unit and hospital length of stay, ventilation days, multi-organ failure, and the in-hospital mortality rate.
In total, 65 eligible patients (treatment = 31, placebo = 34) were included for the final analysis. The treatment group had more pulmonary contusion volume (mean (SD), mm) at the right (68726.97 (93656.54) vs. 59730.27 (76551.74)) and the left side (67501.71 (91514.04) vs. 46502.21 (80604.21)), higher initial C-reactive peptide level (12.16 (10.58) vs. 10.85 (17.87)) compared to the placebo group, but the differences were not statistically significant (p > 0.05). At the end of the study, the mean (SD) of pulmonary contusion volume (mm) (right side = 116748.74 (361705.12), left side = 64522.03 (117266.17)) of the treatment group were comparable to that of the placebo group (right side = 40051.26 (64081.56), left side = 25929.12 (47417.13), p = 0.228 and 0.082, respectively). Moreover, both groups have statistically similar hospital (mean (SD), days) (10.87 (9.83) vs. 13.05 (10.12)) and intensive care unit length of stays (mean (SD), days) (7.16 (8.15) vs. 7.82 (7.48)). Of note, the frequency of the in-hospital complications (treatment vs. control group) including acute respiratory distress syndrome (12.9% vs. 8.8%, p = 0.71), pneumonia (19.4% vs. 17.6%, p = 0.85), multi-organ failure (12.9% vs. 17.6%, p = 0.58) and the mortality rate (22.6% vs. 14.7%, p = 0.41) were comparable between the groups.
Administrating montelukast has no preventive or therapeutic effects on lung contusion or its complications.
多发创伤患者存在发生呼吸系统并发症(包括肺炎和急性呼吸窘迫综合征)的高风险。许多肺部并发症与全身炎症和肺部中性粒细胞浸润有关。白三烯受体拮抗剂是具有抗炎和抗氧化作用的药物,可缓解气道炎症。本研究旨在调查孟鲁司特在降低创伤患者肺部并发症方面的有效性。
这是一项随机、双盲、安慰剂对照试验,纳入了经 CT 扫描证实存在肺挫伤的多发性钝性创伤患者。如果患者符合以下至少一项条件,则将其排除在外:<16 岁、心肺疾病病史或对孟鲁司特诱导的过敏反应史。采用区组随机化方法将患者分配至治疗(10mg 孟鲁司特)或安慰剂组。主要观察结局为试验结束时的肺挫伤体积。次要结局包括重症监护病房和住院时间、通气天数、多器官衰竭以及住院死亡率。
共有 65 名符合条件的患者(治疗组=31 名,安慰剂组=34 名)纳入最终分析。治疗组右侧(68726.97(93656.54)比 59730.27(76551.74))和左侧(67501.71(91514.04)比 46502.21(80604.21))的肺挫伤体积更大,初始 C 反应蛋白水平(12.16(10.58)比 10.85(17.87))更高,但差异无统计学意义(p>0.05)。研究结束时,治疗组右侧(116748.74(361705.12),左侧 64522.03(117266.17))和左侧(40051.26(64081.56),25929.12(47417.13))的肺挫伤体积平均值(SD)与安慰剂组相似(p=0.228 和 0.082)。此外,两组的住院(平均(SD),天)(10.87(9.83)比 13.05(10.12))和重症监护病房住院时间(平均(SD),天)(7.16(8.15)比 7.82(7.48))均无统计学差异。值得注意的是,两组的院内并发症(治疗组与对照组)发生率相似,包括急性呼吸窘迫综合征(12.9%比 8.8%,p=0.71)、肺炎(19.4%比 17.6%,p=0.85)、多器官衰竭(12.9%比 17.6%,p=0.58)和死亡率(22.6%比 14.7%,p=0.41)。
孟鲁司特对肺挫伤或其并发症无预防或治疗作用。