3%高渗生理盐水雾化治疗中度毛细支气管炎住院婴儿的疗效

Mp Joshi, BS Majagaiya, Huan-Ji Cheng, Jia-ning Yin, M. Chaudhary
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Objective: Our main aim of this study is to determine the improvement of patient’s condition by comparing the length of hospital stay and improvement in clinical severity score (CS score) in infants with moderate bronchiolitis nebulized with 3% hypertonic saline or 0.9% saline. Methods: 124 patients were arranged randomly to nebulize either 3% hypertonic saline with salbutamol plus budesonide (Group 1) or 0.9% saline with salbutamol plus budesonide (Group 2) three times per day until conditions were stable enough for discharge (with a CS score below 3). We recorded the SC scores of each patient before and after the first nebulization every day. Outcomes, considered mainly as ①differences in the length of hospital stay from admission to time taken to reach CS score < 3; ②the change in CS score after the first nebulization every day. A P value <0.05 was considered statistically significant. Results: 124 patients of them completed the study. Their mean age was 6.92±0.24 months (range, 3 to 12 months). The cases were diagnosed as moderate bronchiolitis with CS scores varying from 6 to 9. The mean length of hospital stay from admission to time taken to reach CS score <3 was 4.83 ±0.077 days for the whole subjects investigated, and it differed significantly between the two groups: 4.27±0.90 days in Group 1 and 5.39±0.610 days in Group 2. On the first day of treatment, the mean CS scores at baseline were 7.34±0.1 and 7.39±0.99 for Group 1 and Group 2, respectively. After the first nebulization, the CS scores decreased to 5.94±0.89 (SD-0.698) and 6.50±0.094 (SD 0.741) of Group 1 and Group 2, respectively. The P value in both groups were less than 0.001, indicating statistically differences between CS scores before and after nebulization by both groups of solutions in the treatment of moderate bronchiolitis. However, the differences of the mean values and standard deviation (SD) results after nebulization in the two groups suggested a better treatment outcome of 3% hypertonic saline with salbutamol plus budesonide than 0.9% normal saline. There were no significant differences between the respiratory rate, heart rate, saturation and add-on therapy in the two groups. No adverse events noted in both groups. Conclusion: The curative effect of 3% hypertonic saline group was significant better in comparison with the 0.9% normal saline group in terms of the improvement of CS score and length of hospital stay. 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引用次数: 0

摘要

毛细支气管炎是婴儿最常见的下呼吸道传染病,表现为咳嗽和/或喘息,最常见于冬季。用吸入皮质类固醇和支气管扩张剂如沙丁胺醇或异丙托溴铵雾化治疗毛细支气管炎被认为是有效的方法。通常,0.9%生理盐水与上述药物一起使用。然而,有研究表明,与生理盐水相比,3%的高渗盐水可能是更好的选择。目的:本研究的主要目的是通过比较3%高渗生理盐水和0.9%生理盐水雾化治疗的中度毛细支气管炎婴儿的住院时间和临床严重程度评分(CS评分)的改善来确定患者病情的改善。方法:随机选择124例患者,分别雾化3%高渗生理盐水加沙丁胺醇加布地奈德(1组)或0.9%生理盐水加沙丁胺醇加布地奈德(2组),每天3次,直至病情稳定出院(CS评分低于3分)。记录患者每天第一次雾化前后的SC评分。结果主要考虑:①从入院到达到CS评分< 3所需时间的住院时间差异;②每天第一次雾化后CS评分的变化。P值<0.05为差异有统计学意义。结果:124例患者完成研究。平均年龄6.92±0.24个月(3 ~ 12个月)。这些病例被诊断为中度细支气管炎,CS评分从6到9不等。从入院到达到CS评分<3的平均住院时间为4.83±0.077天,两组比较差异有统计学意义:1组为4.27±0.90天,2组为5.39±0.610天。治疗第1天,组1和组2的基线平均CS评分分别为7.34±0.1和7.39±0.99。第一次雾化后,组1和组2的CS评分分别降至5.94±0.89 (SD-0.698)和6.50±0.094 (SD 0.741)。两组P值均小于0.001,说明两组溶液雾化治疗中度毛细支气管炎前后CS评分差异有统计学意义。然而,两组雾化后的平均值和标准差(SD)结果的差异表明,3%高渗盐水联合沙丁胺醇加布地奈德治疗效果优于0.9%生理盐水。两组患者呼吸频率、心率、饱和度及附加治疗差异无统计学意义。两组均未发现不良事件。结论:3%高渗盐水组在CS评分和住院时间的改善方面明显优于0.9%生理盐水组。结论:3%高渗盐水治疗中度毛细支气管炎是安全有效的。
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Outcome of treatment with nebulized 3% hypertonic saline solution in infants hospitalized with moderate bronchiolitis
Bronchiolitis is the most common lower respiratory infectious disease in infants presenting with cough and/or wheeze and occurs most frequently in the winter months. Treatment of bronchiolitis by means of nebulization with inhaled corticosteroids and bronchodilator such as salbutamol or ipratropium bromide considered an effective method. Usually, 0.9% normal saline used together with the medications mentioned above. However, there are studies showing that 3% hypertonic saline might be a better choice compared with the normal saline. Objective: Our main aim of this study is to determine the improvement of patient’s condition by comparing the length of hospital stay and improvement in clinical severity score (CS score) in infants with moderate bronchiolitis nebulized with 3% hypertonic saline or 0.9% saline. Methods: 124 patients were arranged randomly to nebulize either 3% hypertonic saline with salbutamol plus budesonide (Group 1) or 0.9% saline with salbutamol plus budesonide (Group 2) three times per day until conditions were stable enough for discharge (with a CS score below 3). We recorded the SC scores of each patient before and after the first nebulization every day. Outcomes, considered mainly as ①differences in the length of hospital stay from admission to time taken to reach CS score < 3; ②the change in CS score after the first nebulization every day. A P value <0.05 was considered statistically significant. Results: 124 patients of them completed the study. Their mean age was 6.92±0.24 months (range, 3 to 12 months). The cases were diagnosed as moderate bronchiolitis with CS scores varying from 6 to 9. The mean length of hospital stay from admission to time taken to reach CS score <3 was 4.83 ±0.077 days for the whole subjects investigated, and it differed significantly between the two groups: 4.27±0.90 days in Group 1 and 5.39±0.610 days in Group 2. On the first day of treatment, the mean CS scores at baseline were 7.34±0.1 and 7.39±0.99 for Group 1 and Group 2, respectively. After the first nebulization, the CS scores decreased to 5.94±0.89 (SD-0.698) and 6.50±0.094 (SD 0.741) of Group 1 and Group 2, respectively. The P value in both groups were less than 0.001, indicating statistically differences between CS scores before and after nebulization by both groups of solutions in the treatment of moderate bronchiolitis. However, the differences of the mean values and standard deviation (SD) results after nebulization in the two groups suggested a better treatment outcome of 3% hypertonic saline with salbutamol plus budesonide than 0.9% normal saline. There were no significant differences between the respiratory rate, heart rate, saturation and add-on therapy in the two groups. No adverse events noted in both groups. Conclusion: The curative effect of 3% hypertonic saline group was significant better in comparison with the 0.9% normal saline group in terms of the improvement of CS score and length of hospital stay. In conclusion, 3% hypertonic saline is safe and effective in infants with moderate bronchiolitis.
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