Division of Paediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Department of Dermatology, Oslo University Hospital, Oslo, Norway; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Lancet. 2020 Mar 21;395(10228):951-961. doi: 10.1016/S0140-6736(19)32983-6. Epub 2020 Feb 19.
Skin emollients applied during early infancy could prevent atopic dermatitis, and early complementary food introduction might reduce food allergy in high-risk infants. The study aimed to determine if either regular skin emollients applied from 2 weeks of age, or early complementary feeding introduced between 12 and 16 weeks of age, reduced development of atopic dermatitis by age 12 months in the general infant population.
This population-based 2×2 factorial, randomised clinical trial was done at Oslo University Hospital and Østfold Hospital Trust, Oslo, Norway; and Karolinska University Hospital, Stockholm, Sweden. Infants of women recruited antenatally at the routine ultrasound pregnancy screening at 18 weeks were cluster-randomised at birth from 2015 to 2017 to the following groups: (1) controls with no specific advice on skin care while advised to follow national guidelines on infant nutrition (no intervention group); (2) skin emollients (bath additives and facial cream; skin intervention group); (3) early complementary feeding of peanut, cow's milk, wheat, and egg (food intervention group); or (4) combined skin and food interventions (combined intervention group). Participants were randomly assigned (1:1:1:1) using computer- generated cluster randomisation based on 92 geographical living area blocks as well as eight 3-month time blocks. Carers were instructed to apply the interventions on at least 4 days per week. Atopic dermatitis by age 12 months was the primary outcome, based on clinical investigations at 3, 6 and 12 months by investigators masked to group allocation. Atopic dermatitis was assessed after completing the 12-month investigations and diagnosed if either of the UK Working Party and Hanifin and Rajka (12 months only) diagnostic criteria were fulfilled. The primary efficacy analyses was done by intention-to-treat analysis on all randomly assigned participants. Food allergy results will be reported once all investigations at age 3 years are completed in 2020. This was a study performed within ORAACLE (the Oslo Research Group of Asthma and Allergy in Childhood; the Lung and Environment). The study is registered at clinicaltrials.gov, NCT02449850.
2697 women were recruited between Dec 9, 2014, and Oct 31, 2016, from whom 2397 newborn infants were enrolled from April 14, 2015, to April 11, 2017. Atopic dermatitis was observed in 48 (8%) of 596 infants in the no intervention group, 64 (11%) of 575 in the skin intervention group, 58 (9%) of 642 in the food intervention group, and 31 (5%) of 583 in the combined intervention group. Neither skin emollients nor early complementary feeding reduced development of atopic dermatitis, with a risk difference of 3·1% (95% CI -0·3 to 6·5) for skin intervention and 1·0% (-2·1 to 4·1) for food intervention, in favour of control. No safety concerns with the interventions were identified. Reported skin symptoms and signs (including itching, oedema, exanthema, dry skin, and urticaria) were no more frequent in the skin, food, and combined intervention groups than in the no intervention group.
Neither early skin emollients nor early complementary feeding reduced development of atopic dermatitis by age 12 months. Our study does not support the use of these interventions to prevent atopic dermatitis by 12 months of age in infants.
The study was funded by several public and private funding bodies: The Regional Health Board South East, The Norwegian Research Council, Health and Rehabilitation Norway, The Foundation for Healthcare and Allergy Research in Sweden-Vårdalstiftelsen, Swedish Asthma and Allergy Association's Research Foundation, Swedish Research Council-the Initiative for Clinical Therapy Research, The Swedish Heart-Lung Foundation, SFO-V at the Karolinska Institute, Freemason Child House Foundation in Stockholm, Swedish Research Council for Health, Working Life and Welfare-FORTE, Oslo University Hospital, the University of Oslo, and Østfold Hospital Trust.
在婴儿早期使用皮肤保湿剂可以预防特应性皮炎,而早期补充食物可能会降低高危婴儿的食物过敏风险。本研究旨在确定在一般婴儿人群中,从 2 周龄开始常规使用皮肤保湿剂,或在 12 至 16 周龄之间引入早期补充食物,是否可以在 12 个月龄时减少特应性皮炎的发生。
这是一项基于人群的 2×2 析因随机临床试验,在挪威奥斯陆大学医院和奥斯特福德医院信托基金以及瑞典斯德哥尔摩卡罗林斯卡大学医院进行。在 18 周的常规超声妊娠筛查时招募的孕妇,在分娩时根据以下分组进行了聚类随机分组:(1)无皮肤护理具体建议但被建议遵循婴儿营养国家指南的对照组(无干预组);(2)皮肤保湿剂(沐浴添加剂和面部霜;皮肤干预组);(3)早期补充花生、牛奶、小麦和鸡蛋(食物干预组);或(4)皮肤和食物联合干预(联合干预组)。参与者随机分配(1:1:1:1),使用基于 92 个地理居住区域块和 8 个 3 个月时间块的计算机生成的聚类随机化。护理人员被指示每周至少使用干预措施 4 天。根据调查人员在 3、6 和 12 个月时进行的临床调查,以 12 个月时出现特应性皮炎为主要结局,在完成 12 个月的调查后诊断,如果符合英国工作组和 Hanifin 和 Rajka(仅 12 个月)诊断标准中的任何一个标准。主要疗效分析是对所有随机分配的参与者进行意向治疗分析。一旦所有 3 岁时的调查在 2020 年完成,食物过敏的结果将报告。这是在奥拉斯卡(儿童哮喘和过敏研究的奥斯陆研究组;肺与环境)内进行的一项研究。该研究在 clinicaltrials.gov 上注册,NCT02449850。
2014 年 12 月 9 日至 2016 年 10 月 31 日期间,有 2697 名妇女被招募,其中 2397 名新生儿于 2015 年 4 月 14 日至 2017 年 4 月 11 日入组。无干预组中 596 名婴儿中有 48 名(8%)出现特应性皮炎,皮肤干预组 575 名中有 64 名(11%),食物干预组 642 名中有 58 名(9%),联合干预组 583 名中有 31 名(5%)。皮肤保湿剂和早期补充食物都没有减少特应性皮炎的发生,皮肤干预的风险差异为 3.1%(95%CI-0.3 至 6.5),食物干预的风险差异为 1.0%(-2.1 至 4.1),均有利于对照组。干预措施没有发现安全问题。皮肤、食物和联合干预组的皮肤症状和体征(包括瘙痒、水肿、出疹、皮肤干燥和荨麻疹)比无干预组更频繁。
早期使用皮肤保湿剂或早期补充食物都不能在 12 个月龄时减少特应性皮炎的发生。我们的研究不支持在婴儿 12 个月龄时使用这些干预措施来预防特应性皮炎。
该研究由多个公共和私人资助机构提供资金:南东地区卫生局、挪威研究理事会、挪威卫生与康复局、瑞典过敏症与哮喘研究基金会-瓦尔达尔基金会、瑞典哮喘和过敏协会研究基金会、瑞典研究理事会临床治疗研究倡议、瑞典心脏与肺基金会、卡罗林斯卡研究所的 SFO-V、斯德哥尔摩的共济会儿童基金会、瑞典研究理事会健康、工作生活和福利-FORTE、奥斯陆大学医院、奥斯陆大学和奥斯特福德医院信托基金。