中华皮肤科杂志 ›› 2025, Vol. 58 ›› Issue (10): 952-956.doi: 10.35541/cjd.20250003

• 论著·儿童皮肤病 • 上一篇    下一篇

口服普萘洛尔治疗增殖期婴儿血管瘤的时机选择

章开智    邱桐    周江元    龚雪    张梓欣    兰钰茹    吉毅   

  1. 四川大学华西医院小儿外科,成都  610041
  • 收稿日期:2025-01-02 修回日期:2025-08-07 发布日期:2025-09-30
  • 通讯作者: 吉毅 E-mail:jijiyuanyuan@163.com
  • 基金资助:
    国家自然科学基金(82473553、82273556);四川省杰出青年基金(2025NSFJQ0070)

Investigation of the timing of oral propranolol treatment for proliferative infantile hemangioma

Zhang Kaizhi, Qiu Tong, Zhou Jiangyuan, Gong Xue, Zhang Zixin, Lan Yuru, Ji Yi   

  1. Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu 610041, China
  • Received:2025-01-02 Revised:2025-08-07 Published:2025-09-30
  • Contact: Ji Yi E-mail:jijiyuanyuan@163.com
  • Supported by:
    National Natural Science Foundation of China (82473553, 82273556); Excellent Youth Foundation of Sichuan Province of China (2025NSFJQ0070)

摘要: 【摘要】 目的 探讨口服普萘洛尔治疗增殖期婴儿血管瘤(IH)的时机。方法 本研究为双向队列研究。分析2015年6月至2019年5月在四川大学华西医院小儿外科接受口服普萘洛尔治疗的增殖期IH患儿的一般情况和IH相关临床信息。主要结局指标为口服普萘洛尔持续治疗6 ~ 12个月期间IH瘤体的消退满意率;次要结局指标为口服普萘洛尔治疗IH达到消退满意的时间、不良反应发生率、IH伴发溃疡的发生率以及复发率。采用多因素logistic回归模型分析影响普萘洛尔治疗IH后达到瘤体消退满意的因素,使用受试者工作特征(ROC)曲线明确普萘洛尔治疗IH的最佳年龄。结果 共纳入122例IH患儿,男32例(26.2%)、女90例(73.8%),年龄[M(Q1,Q3)]为8.6(6.3,12.3)周;IH位于头面部56例(45.9%);局限性IH 57例(46.7%),节段性IH 53例(43.4%);混合型IH 86例(70.5%);17例(13.9%)IH患儿发生溃疡。治疗6个月后IH治疗失败8例(6.6%),普萘洛尔停药6个月内有12例(9.8%)复发。口服普萘洛尔治疗6个月内,56例(45.9%)发生轻中度不良反应,未见药物相关性死亡。多因素logistic回归分析显示,开始接受普萘洛尔治疗的年龄是IH达到消退满意的独立影响因素(OR = 0.879,95% CI: 0.808 ~ 0.957)。ROC曲线分析显示,口服普萘洛尔治疗IH的年龄截断值为9.9周,灵敏度为75.7%,特异度为61.5%。年龄 ≤ 9.9周组(73例)瘤体消退满意率(72.6%,53/73)明显高于年龄 > 9.9周组(49例,34.7%,17/49),差异有统计学意义(χ2 = 17.23,P < 0.001);年龄 ≤ 9.9周组治疗后达到瘤体消退满意的时间[M(Q1,Q3),46.0(38.5,48.0)周]明显短于年龄 > 9.9周组[57.0(40.0,73.5)周],差异有统计学意义(Z = -2.01,P = 0.045)。结论 需要系统治疗的IH患儿中,在10周龄内口服普萘洛尔治疗可提高瘤体消退满意率。

关键词: 血管瘤, 婴儿血管瘤, 普萘洛尔, 治疗时机, 影响因素, 年龄

Abstract: 【Abstract】 Objective To investigate the optimal timing of oral propranolol treatment for proliferative infantile hemangiomas (IH). Methods A bidirectional cohort study was conducted. Infants with proliferative IH receiving oral propranolol treatment were collected from the Department of Pediatric Surgery, West China Hospital, Sichuan University between June 2015 and May 2019, and their general information and IH-related clinical data were analyzed. The primary outcome was the satisfactory regression rate of IH during 6–12 months of continuous oral propranolol treatment; secondary outcomes included the time to achieve satisfactory regression, incidence of adverse reactions, incidence of IH ulceration, and IH recurrence rate. Multivariate logistic regression was performed to identify factors influencing the satisfactory regression of IH after propranolol treatment, and a receiver operating characteristic (ROC) curve was employed to determine the optimal age for initiating propranolol therapy. Results A total of 122 IH infants were enrolled in the study, including 32 males (26.2%) and 90 females (73.8%), with ages (M[Q1, Q3]) of 8.6 [6.3, 12.3] weeks. IH was located on the head and face in 56 cases (45.9%). There were 57 cases (46.7%) of localized IH, 53 (43.4%) of segmental IH, and 86 (70.5%) of mixed-type IH. Ulceration occurred in 17 cases (13.9%). After 6 months of propranolol treatment, 8 patients (6.6%) experienced treatment failure, and 12 (9.8%) experienced relapse within 6 months after discontinuation of propranolol. During 6 months of oral propranolol treatment, 56 infants (45.9%) experienced mild to moderate adverse reactions, with no drug-related deaths observed. Multivariate logistic regression analysis revealed that the age at initiation of propranolol treatment was an independent factor influencing satisfactory regression of IH (OR = 0.879, 95% CI: 0.808–0.957). ROC curve analysis revealed that the optimal age for starting propranolol therapy was 9.9 weeks, with a sensitivity of 75.7% and a specificity of 61.5%. Infants aged ≤ 9.9 weeks (73 cases) had a significantly higher satisfactory regression rate (72.6% [53/73]) compared with those aged > 9.9 weeks (49 cases, 34.7% [17/49]; χ2 = 17.23, P < 0.001); the time to achieve satisfactory regression of IH was significantly shorter in the infants aged ≤ 9.9 weeks (M[Q1, Q3]: 46.0 [38.5, 48.0] weeks) than in those aged > 9.9 weeks (57.0 [40.0, 73.5] weeks; Z = -2.01, P = 0.045). Conclusion For IH infants requiring systemic therapy, initiation of oral propranolol before the age of 10 weeks appeared to improve the satisfactory regression rate of IH.

Key words: Hemangioma, Infantile hemangioma, Propranolol, Treatment timing, Influencing factor, Age

引用本文

章开智 邱桐 周江元 龚雪 张梓欣 兰钰茹 吉毅. 口服普萘洛尔治疗增殖期婴儿血管瘤的时机选择[J]. 中华皮肤科杂志, 2025,58(10):952-956. doi:10.35541/cjd.20250003

Zhang Kaizhi, Qiu Tong, Zhou Jiangyuan, Gong Xue, Zhang Zixin, Lan Yuru, Ji Yi. Investigation of the timing of oral propranolol treatment for proliferative infantile hemangioma[J]. Chinese Journal of Dermatology, 2025, 58(10): 952-956.doi:10.35541/cjd.20250003