González-Díaz Sandra Nora, García-Campa Mariano, Noyola-Pérez Andrés, Guzmán-Avilán Rosa-Ivett, de Lira-Quezada Cindy Elizabeth, Álvarez-Villalobos Neri, Rodríguez-Gutiérrez René, Macouzet-Sánchez Carlos
Universidad Autónoma de Nuevo León, Centro Regional de Alergia e Inmunología Clínica, Hospital Universitario "Dr. José Eleuterio González", Francisco I. Madero Avenue, Mitras Centro, ZC 64460, Monterrey, Mexico.
Plataforma Universidad Autónoma de Nuevo León, INVEST UANL-KER Unit Mayo Clinic, School of Medicine and University Hospital "Dr José E González", Monterrey 64460, Mexico.
World Allergy Organ J. 2023 Apr 30;16(4):100769. doi: 10.1016/j.waojou.2023.100769. eCollection 2023 Apr.
Randomized Clinical Trials (RCTs) are important tools to establish the effects of a given intervention. Investigators should focus on outcomes that patients perceive: patient-important outcomes (PIOs), clinical endpoints that patients value directly and reflect how they feel, function, or survive. However, it is easier to consider surrogated outcomes to reduce costs and achieve better-looking results. The problem with these outcomes is that they indirectly measure PIOs, which might not correlate linearly or translate reliably into a positive PIO.
We systematically searched MEDLINE for atopic disease RCTs rated among the top 10 allergic diseases and general internal medicine journals from the last 10 years. Two independent reviewers worked in duplicate and independently to collect data from all eligible articles. We gathered information regarding the type of study, title, author information, journal, intervention type, atopic disease, and primary and secondary outcomes. We assessed the outcomes investigators used in RCTs of atopic diseases and asthma.
This quantitative analysis included n = 135 randomized clinical trials. The most studied atopic disease during the period selected was asthma (n = 69), followed by allergic rhinitis (n = 51). When divided by atopic disease, primary outcomes in RCTs valuing allergic rhinitis had the most significant proportion of PIOs (76.7), asthma surrogated outcomes (38), and asthma/allergic rhinitis laboratory outcomes (42.9). PIOs in allergic rhinitis trials had the most significant proportion of PIOs favoring the intervention (81.4), asthma had the greatest proportion of surrogated outcomes (33.3), and asthma/allergic rhinitis laboratory outcomes (40). When divided by atopic disease, trials studying atopic dermatitis and urticaria had the same proportion of PIOs (64.7) as their secondary outcomes. Asthma had the highest (37.5) surrogate outcomes. Journals of general/internal medicine had a greater proportion of PIOs, and a post hoc analysis showed a significant difference in the proportion and secondary outcomes that favored the intervention between PIOs and laboratory outcomes.
Approximately 7.5 out of 10 primary outcomes in RCTs published in general/internal medicine are PIOs compared to 5 out of 10 primary outcomes in atopic disease journals. Investigators should focus on selecting patient-important outcomes in their clinical trials to establish clinical guidelines with better-quality recommendations that impact patients' life and values.
International Prospective Register of Systematic Reviews (PROSPERO, NIHR) ID: CRD42021259256.
随机临床试验(RCT)是确定特定干预措施效果的重要工具。研究人员应关注患者所感知的结局:患者重要结局(PIO),即患者直接重视的临床终点,反映他们的感受、功能或生存状况。然而,考虑替代结局以降低成本并获得更可观的结果会更容易。这些结局的问题在于它们间接衡量PIO,而PIO可能与替代结局不存在线性关联,也无法可靠地转化为积极的PIO。
我们系统检索了MEDLINE中过去10年在十大过敏性疾病和普通内科期刊中排名靠前的特应性疾病RCT。两名独立的评审员重复并独立工作,从所有符合条件的文章中收集数据。我们收集了有关研究类型、标题、作者信息、期刊、干预类型、特应性疾病以及主要和次要结局的信息。我们评估了研究人员在特应性疾病和哮喘RCT中使用的结局。
这项定量分析纳入了n = 135项随机临床试验。在所选定的时期内,研究最多的特应性疾病是哮喘(n = 69),其次是过敏性鼻炎(n = 51)。按特应性疾病划分,评估过敏性鼻炎的RCT中的主要结局中,PIO的比例最高(76.7%),哮喘替代结局的比例为38%,哮喘/过敏性鼻炎实验室结局的比例为42.9%。过敏性鼻炎试验中的PIO中,支持干预措施的PIO比例最高(81.4%),哮喘替代结局的比例最大(33.3%),哮喘/过敏性鼻炎实验室结局的比例为40%。按特应性疾病划分,研究特应性皮炎和荨麻疹的试验中,PIO与其次要结局的比例相同(64.7%)。哮喘的替代结局比例最高(37.5%)。普通内科/内科期刊中PIO的比例更高,事后分析显示,PIO与实验室结局之间在支持干预措施的比例和次要结局方面存在显著差异。
普通内科/内科期刊发表的RCT中,约十分之七点五的主要结局是PIO,而特应性疾病期刊中这一比例为十分之五。研究人员在临床试验中应注重选择患者重要结局,以制定具有更高质量建议、能影响患者生活和价值观的临床指南。
国际前瞻性系统评价注册库(PROSPERO,NIHR)标识符:CRD42021259256