University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Deputy Drugs Controller, Specialized Healthcare and Medical Education Department, Punjab, Lahore, Pakistan.
Syst Rev. 2023 Jun 2;12(1):92. doi: 10.1186/s13643-023-02261-x.
Intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections play a key role in treating a range of macular diseases. The effectiveness of these therapies is dependent on patients' adherence (the extent to which a patient takes their medicines as per agreed recommendations from the healthcare provider) and persistence (continuation of the treatment for the prescribed duration) to their prescribed treatment regimens. The aim of this systematic review was to demonstrate the need for further investigation into the prevalence of, and factors contributing to, patient-led non-adherence and non-persistence, thus facilitating improved clinical outcomes.
Systematic searches were conducted in Google Scholar, Web of Science, PubMed, MEDLINE, and the Cochrane Library. Studies in English conducted before February 2023 that reported the level of, and/or barriers to, non-adherence or non-persistence to intravitreal anti-VEGF ocular disease therapy were included. Duplicate papers, literature reviews, expert opinion articles, case studies, and case series were excluded following screening by two independent authors.
Data from a total of 409,215 patients across 52 studies were analysed. Treatment regimens included pro re nata, monthly and treat-and-extend protocols; study durations ranged from 4 months to 8 years. Of the 52 studies, 22 included a breakdown of reasons for patient non-adherence/non-persistence. Patient-led non-adherence varied between 17.5 and 35.0% depending on the definition used. Overall pooled prevalence of patient-led treatment non-persistence was 30.0% (P = 0.000). Reasons for non-adherence/non-persistence included dissatisfaction with treatment results (29.9%), financial burden (19%), older age/comorbidities (15.5%), difficulty booking appointments (8.5%), travel distance/social isolation (7.9%), lack of time (5.8%), satisfaction with the perceived improvement in their condition (4.4%), fear of injection (4.0%), loss of motivation (4.0%), apathy towards eyesight (2.5%), dissatisfaction with facilities 2.3%, and discomfort/pain (0.3%). Three studies found non-adherence rates between 51.6 and 68.8% during the COVID-19 pandemic, in part due to fear of exposure to COVID-19 and difficulties travelling during lockdown.
Results suggest high levels of patient-led non-adherence/non-persistence to anti-VEGF therapy, mostly due to dissatisfaction with treatment results, a combination of comorbidities, loss of motivation and the burden of travel. This study provides key information on prevalence and factors contributing to non-adherence/non-persistence in anti-VEGF treatment for macular diseases, aiding identification of at-risk individuals to improve real-world visual outcomes. Improvements in the literature can be achieved by establishing uniform definitions and standard timescales for what constitutes non-adherence/non-persistence.
PROSPERO CRD42020216205.
玻璃体内抗血管内皮生长因子(抗 VEGF)注射在治疗多种黄斑疾病方面发挥着关键作用。这些治疗方法的有效性取决于患者的依从性(患者按照医疗保健提供者的建议服药的程度)和持久性(按照规定的疗程继续治疗)。本系统评价的目的是证明需要进一步研究患者导致的不依从和不持续治疗的普遍性和促成因素,从而促进改善临床结果。
在 Google Scholar、Web of Science、PubMed、MEDLINE 和 Cochrane Library 中进行了系统搜索。纳入了在 2023 年 2 月之前以英文发表的报告抗 VEGF 眼内疾病治疗中不依从或不持续治疗的水平和/或障碍的研究。经过两位独立作者筛选,排除了重复论文、文献综述、专家意见文章、病例报告和病例系列。
对来自 52 项研究的总共 409,215 名患者的数据进行了分析。治疗方案包括按需治疗、每月治疗和治疗和延长方案;研究持续时间从 4 个月到 8 年不等。在 52 项研究中,有 22 项研究分析了患者不依从/不持续治疗的原因。根据使用的定义,患者导致的不依从率在 17.5%至 35.0%之间变化。总体上,患者主导的治疗不持续的累积患病率为 30.0%(P=0.000)。不依从/不持续治疗的原因包括对治疗结果不满意(29.9%)、经济负担(19%)、年龄较大/合并症(15.5%)、预约困难(8.5%)、旅行距离/社会隔离(7.9%)、缺乏时间(5.8%)、对病情改善的满意度(4.4%)、对注射的恐惧(4.0%)、缺乏动力(4.0%)、对视力的冷漠(2.5%)、对设施的不满(2.3%)和不适/疼痛(0.3%)。有三项研究发现,在 COVID-19 大流行期间,不依从率在 51.6%至 68.8%之间,部分原因是担心接触 COVID-19 和在封锁期间旅行困难。
结果表明,抗 VEGF 治疗的患者不依从/不持续率较高,主要原因是对治疗结果不满意、多种合并症、缺乏动力和旅行负担。本研究提供了关于黄斑疾病抗 VEGF 治疗中不依从/不持续的流行程度和促成因素的关键信息,有助于识别有风险的个体,以改善现实世界的视觉结果。通过建立不依从/不持续的统一定义和标准时间范围,可以改进文献。
PROSPERO CRD42020216205。