复方丹参注射液和50%硫酸镁溶液湿敷在新生儿输液外渗中的效果对比

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Abstract Objective To observe the clinical effects of compound Danshen Injection and 50%Magnesium Sulfate Solution wet deposition in treating neonatal transfusion extravasation.Methods 131 neonatal were accepted intravenous infusion from March 2015 to March 2016 of our hospital were selected.All neonatal had the symptoms of transfusion extravasation.Neonatal were randomly divided into control group(65 cases)and observation group(66 cases).Neonatal in control group were used 50%Magnesium Sulfate Solution wet deposition,and neonatal in observation group were used compound Danshen Injection.Swelling time,effective time,treatment effects and adverse effects in two groups were compared.Results The beginning swelling time,totally swelling time and effective time in observation group were respectively(2.78±0.57),(9.12±1.13),(5.73±0.63)h,and the control group was respectively(5.61±1.49),(16.32±1.43),(10.54±1.05)h in control group,those time of the observation group was shorter than the control group,and the differences were significant(P＜0.01).The effective time in observation group was 98.48%,which was 73.85%in control group,and the difference was significant(P＜0.01).The incidence rate of adverse effects in observation group was 0,which was 12.3%in control group,and the difference was significant(P＜0.05).Conclusion Using compound Danshen Injection wet deposition for neonatal with transfusion extravasation in clinical,which has the advantages of rapid onset,good effects and high safety, and it is worth to popularize.

Key words： Transfusion extravasation Neonatal Compound Danshen Injection 50%Magnesium Sulfate Solution Wet deposition

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	Articles by authors
	YUAN Yu-huan
	LIU Er-ying
	MAI Hui-qiong
	LUO Huan-ping

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YUAN Yu-huan,LIU Er-ying,MAI Hui-qiong, et al. Effects comparison of compound Danshen Injection and 50%Magnesium Sulfate Solution wet deposition in treating neonatal transfusion extravasation[J]. 中国当代医药, 2017, 24(7): 176-179.

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http://dangdaiyiyao.com/EN/ OR http://dangdaiyiyao.com/EN/Y2017/V24/I7/176

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