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马来酸噻吗洛尔滴眼液联合超脉冲CO2点阵激光治疗婴幼儿皮肤血管瘤的疗效分析
作者:张均秀1 2  齐帅3  高磊4 
单位:1. 保定市儿童医院 皮肤科, 河北 保定 071000;
2. 保定市儿童呼吸消化疾病临床研究重点实验室, 河北 保定 071000;
3. 石家庄市栾城人民医院 普外科, 河北 石家庄 051430;
4. 保定市第一医院 皮肤科, 河北 保定 071000
关键词:血管瘤 马来酸噻吗洛尔滴眼液 CO2点阵激光 疗效 婴幼儿 
分类号:R751.05;R732.2
出版年·卷·期(页码):2019·47·第七期(835-838)
摘要:

目的:探讨马来酸噻吗洛尔滴眼液联合超脉冲CO2点阵激光治疗婴幼儿皮肤血管瘤的临床疗效。方法:将100例皮肤血管瘤患儿随机分为对照组和观察组,各50例。对照组采用马来酸噻吗洛尔滴眼液局部外用治疗,观察组采用马来酸噻吗洛尔滴眼液联合CO2点阵激光治疗,比较两组临床疗效、平均治疗时间及不良反应发生情况。结果:观察组治愈22例,显效17例,总有效率为78%,平均治愈时间(1.92±0.95)个月。对照组治愈11例,显效18例,总有效率为58%,平均治愈时间(2.76±1.43)个月。观察组患儿总有效率明显高于对照组,差异有统计学意义(P<0.05);观察组患儿平均治愈时间短于对照组,但差异无统计学意义(P>0.05)。结论:马来酸噻吗洛尔滴眼液联合超脉冲CO2点阵激光可有效提高婴幼儿皮肤血管瘤的治疗效果,相对缩短治疗时间,且无明显不良反应,值得在临床上应用与推广。

Objective:To investigate the curative effect of timolol maleate eye drops combined with CO2 ultrapulse fractional laser in treatment of children with hemangioma. Methods:One hundred children with hemangioma were randomly divided into the control and the observation group with 50 cases in each group. The control group received timolol maleate eye drops local application, while the observation group received timolol maleate eye drops combined with CO2 ultrapulse fractional laser. The curative effect, average curing time and incidence condition of adverse reaction of the two groups were compared. Results:Among the 50 children in observation group, 22 were cured, 17 were developed, and the total effective rate was 78%, the average curing time was (1.92±0.95) months. And among the 50 children in control group, 11 were cured, 18 were developed, and the total effective rate was 58%, the average curing time was (2.76±1.43) months. The total effective rate of the children in the observation group were significantly higher than that of the control group(P<0.05).The average curing time was shorter than that of the control group,but there was no significant difference (P>0.05).Conclusion:Timolol maleate eye drops combined with CO2 ultrapulse fractional laser is effective in improving the therapeutic effect of children with hemangioma, relatively shortening the treatment time, and there is no obvious adverse reaction.It is worthy of clinical application and promotion.

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