• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

普萘洛尔治疗婴幼儿血管瘤患者后生活质量提高。

Quality of life improving after propranolol treatment in patients with Infantile Hemangiomas.

机构信息

Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties, University of Palermo, Palermo, Italy.

出版信息

Ital J Pediatr. 2022 Aug 4;48(1):140. doi: 10.1186/s13052-022-01334-2.

DOI:10.1186/s13052-022-01334-2
PMID:35927685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9351120/
Abstract

Infantile hemangiomas may affect the quality of life (QoL) of patients and their family members, as anxiety and worry may commonly occur in parents, also linked to the social adversion they experience. We underline the beneficial impact of oral propranolol therapy on QoL of patients with infantile hemangiomas (IH) and of their relatives. A specific questionnaire measuring QoL was administered to parents of IH patients at beginning and end of a treatment with oral propranolol. Different aspects were investigated: site of the lesion, age of patients at starting therapy, length of treatment, occurrence of adverse effects and persistence/recurrence of the vascular anomaly. In all cases the questionnaire revealed a significant improvement of QoL, which was independent from all analyzed factors. It showed that oral propranolol administration in these patients combines optimal clinical results with relevant improvement of QoL, especially in cases of early management. The improvement of QoL seems unrelated to site of lesion, timing and duration of therapy, occurrence of drug-related adverse effects and persistence/recurrence of disease.

摘要

婴儿血管瘤可能会影响患者及其家庭成员的生活质量 (QoL),因为父母通常会感到焦虑和担忧,这也与他们所经历的社会歧视有关。我们强调了口服普萘洛尔治疗对婴儿血管瘤 (IH) 患者及其亲属生活质量的有益影响。在开始口服普萘洛尔治疗前后,我们向 IH 患者的父母发放了一份专门测量生活质量的问卷。调查了以下几个方面:病变部位、开始治疗时患者的年龄、治疗时间、不良反应的发生以及血管畸形的持续/复发。在所有情况下,问卷均显示 QoL 显著改善,且与所有分析因素无关。这表明,在这些患者中使用口服普萘洛尔治疗可同时获得最佳的临床疗效和生活质量的显著改善,特别是在早期治疗的情况下。生活质量的改善似乎与病变部位、治疗的时机和持续时间、药物相关不良反应的发生以及疾病的持续/复发无关。

相似文献

1
Quality of life improving after propranolol treatment in patients with Infantile Hemangiomas.普萘洛尔治疗婴幼儿血管瘤患者后生活质量提高。
Ital J Pediatr. 2022 Aug 4;48(1):140. doi: 10.1186/s13052-022-01334-2.
2
Parental experiences with propranolol versus oral corticosteroids for complicated infantile hemangioma, a retrospective questionnaire study.普萘洛尔与口服皮质类固醇治疗复杂婴儿血管瘤的家长体验:一项回顾性问卷调查研究
Eur J Dermatol. 2013 Nov-Dec;23(6):857-63. doi: 10.1684/ejd.2013.2176.
3
Worsening ulceration of infantile hemangioma after initiation or escalation of propranolol.普萘洛尔起始或升级治疗后婴儿血管瘤溃疡加重。
Pediatr Dermatol. 2022 Mar;39(2):255-259. doi: 10.1111/pde.14933. Epub 2022 Feb 17.
4
Treatment of problematic infantile hemangiomas with propranolol: a series of 40 cases and review of the literature.普萘洛尔治疗婴幼儿血管瘤40例分析并文献复习
Postepy Hig Med Dosw (Online). 2014 Sep 12;68:1138-44. doi: 10.5604/17322693.1120990.
5
Propranolol therapy of infantile hemangiomas: efficacy, adverse effects, and recurrence.普萘洛尔治疗婴幼儿血管瘤:疗效、不良反应及复发情况。
Pediatr Surg Int. 2013 Jun;29(6):575-81. doi: 10.1007/s00383-013-3283-y. Epub 2013 Mar 22.
6
Propranolol treatment in life-threatening airway hemangiomas: a case series and review of literature.普萘洛尔治疗危及生命的气道血管瘤:病例系列及文献综述
Int J Pediatr Otorhinolaryngol. 2013 Nov;77(11):1791-800. doi: 10.1016/j.ijporl.2013.08.011. Epub 2013 Aug 22.
7
Propranolol for the treatment of infantile hemangiomas: a nine-year monocentric experience from a tertiary hospital.普萘洛尔治疗婴儿血管瘤:来自一家三级医院的九年单中心经验。
Eur J Dermatol. 2023 Jun 1;33(3):265-269. doi: 10.1684/ejd.2023.4484.
8
Oral Nadolol for Children with Infantile Hemangiomas and Sleep Disturbances with Oral Propranolol.口服纳多洛尔治疗患有婴儿血管瘤且伴有口服普萘洛尔所致睡眠障碍的儿童。
Pediatr Dermatol. 2015 Nov-Dec;32(6):853-7. doi: 10.1111/pde.12686. Epub 2015 Oct 8.
9
Atenolol as an alternative to propranolol for the management of sleep disturbances in the treatment of infantile hemangiomas.阿替洛尔可作为普萘洛尔的替代药物,用于治疗婴儿血管瘤时改善睡眠障碍。
Pediatr Dermatol. 2019 Jul;36(4):556-557. doi: 10.1111/pde.13839. Epub 2019 Apr 15.
10
Efficacy and safety of propranolol cream in infantile hemangioma: A prospective pilot study.普萘洛尔乳膏治疗婴儿血管瘤的疗效和安全性:一项前瞻性初步研究。
J Pharmacol Sci. 2022 Jun;149(2):60-65. doi: 10.1016/j.jphs.2022.03.004. Epub 2022 Mar 26.

引用本文的文献

1
Clinical Insights into Risk Factors for Infantile Hemangioma and Propranolol Treatment Outcomes.婴儿血管瘤危险因素及普萘洛尔治疗效果的临床见解
Diagnostics (Basel). 2025 Jul 16;15(14):1792. doi: 10.3390/diagnostics15141792.
2
Concurrent mutations in RNU4ATAC, PLEC, and CD96 in a child with severe short stature and skeletal dysplasia: a case report.一名患有严重身材矮小和骨骼发育不良儿童的RNU4ATAC、PLEC和CD96基因并发突变:病例报告
Ital J Pediatr. 2025 Jul 15;51(1):226. doi: 10.1186/s13052-025-02054-z.
3
PHACE syndrome: looking backward and forward.

本文引用的文献

1
Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene.心脏-颜面-皮肤综合征与胃肠道缺陷:19p13.3缺失(包括MAP 2 K2基因)新生儿病例报告
Ital J Pediatr. 2022 May 4;48(1):65. doi: 10.1186/s13052-022-01241-6.
2
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles.1p 号染色体间区缺失:1 例颅缝早闭、眼眶裂和腭裂新生儿的 1p31.3p22.2 微缺失,并复习相关基因组和表型特征
Ital J Pediatr. 2022 Mar 4;48(1):38. doi: 10.1186/s13052-022-01232-7.
3
PHACE综合征:回顾与展望。
Orphanet J Rare Dis. 2025 Jul 7;20(1):345. doi: 10.1186/s13023-025-03899-7.
4
Complicated Infantile Hemangiomas in the palate: case report of a newborn patient and review of the literature.腭部复杂婴幼儿血管瘤:1例新生儿患者病例报告及文献复习
Ital J Pediatr. 2025 Jun 5;51(1):171. doi: 10.1186/s13052-025-02030-7.
5
Gender-specific association of multiple risk factors with neonatal moderate or severe hypoxic ischemic encephalopathy: a cross-sectional study.多因素与新生儿中-重度缺氧缺血性脑病性别相关性的横断面研究。
Ital J Pediatr. 2024 Sep 9;50(1):169. doi: 10.1186/s13052-024-01748-0.
6
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome.肉碱棕榈酰转移酶II(CPT II)缺乏症可导致难治性心律失常、急性多器官功能衰竭和早期死亡结局。
Ital J Pediatr. 2024 Apr 14;50(1):67. doi: 10.1186/s13052-024-01632-x.
7
Report and follow-up on two new patients with congenital mesoblastic nephroma.报告并随访 2 例先天性中胚层肾瘤新病例。
Ital J Pediatr. 2023 Sep 19;49(1):124. doi: 10.1186/s13052-023-01523-7.
8
Advances for pediatricians in 2022: allergy, anesthesiology, cardiology, dermatology, endocrinology, gastroenterology, genetics, global health, infectious diseases, metabolism, neonatology, neurology, oncology, pulmonology.2022 年儿科医生的进展:过敏、麻醉学、心脏病学、皮肤病学、内分泌学、胃肠病学、遗传学、全球健康、传染病、代谢、新生儿学、神经病学、肿瘤学、肺病学。
Ital J Pediatr. 2023 Sep 8;49(1):115. doi: 10.1186/s13052-023-01522-8.
9
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception.关于部分 3q 三体综合征的新认识:一例新生儿 3q27.1-q29 重复的先证者具有产前和产后过度生长,且采用辅助生殖技术受孕。
Ital J Pediatr. 2023 Feb 9;49(1):17. doi: 10.1186/s13052-023-01421-y.
10
Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene.女性新生儿肠旋转不良,患有 Osteopathia Striata with Cranial Sclerosis,病因是 AMER1 基因的新发杂合无义突变。
Ital J Pediatr. 2022 Dec 29;48(1):206. doi: 10.1186/s13052-022-01403-6.
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up.
TP63 基因新错义突变导致新生儿 Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) 综合征:临床报告及随访。
Ital J Pediatr. 2021 Sep 28;47(1):196. doi: 10.1186/s13052-021-01152-y.
4
Smartphone use and addiction during the coronavirus disease 2019 (COVID-19) pandemic: cohort study on 184 Italian children and adolescents.智能手机在 2019 冠状病毒病(COVID-19)大流行期间的使用与成瘾:对 184 名意大利儿童和青少年的队列研究。
Ital J Pediatr. 2021 Jul 2;47(1):150. doi: 10.1186/s13052-021-01102-8.
5
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents' associations.关于在一级分娩中心工作的新生儿科医生和儿科医生在遗传疾病和畸形综合征诊断的首次沟通方面的建议:6 个意大利科学协会和 4 个家长协会发布的共识。
Ital J Pediatr. 2021 Apr 19;47(1):94. doi: 10.1186/s13052-021-01044-1.
6
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome.常染色体隐性多囊肾病:一例罕见 PKHD1 突变新生儿病例报告,其表现为快速肾增大和早期致命结局。
Ital J Pediatr. 2020 Oct 15;46(1):154. doi: 10.1186/s13052-020-00922-4.
7
NF1 microdeletion syndrome: case report of two new patients.NF1 微缺失综合征:两例新病例报告。
Ital J Pediatr. 2019 Nov 8;45(1):138. doi: 10.1186/s13052-019-0718-7.
8
Clinical Practice Guideline for the Management of Infantile Hemangiomas.婴幼儿血管瘤管理临床实践指南。
Pediatrics. 2019 Jan;143(1). doi: 10.1542/peds.2018-3475.
9
Infantile haemangioma.婴儿血管瘤。
Lancet. 2017 Jul 1;390(10089):85-94. doi: 10.1016/S0140-6736(16)00645-0. Epub 2017 Jan 13.
10
A randomized, controlled trial of oral propranolol in infantile hemangioma.口服普萘洛尔治疗婴儿血管瘤的随机对照试验。
N Engl J Med. 2015 Feb 19;372(8):735-46. doi: 10.1056/NEJMoa1404710.