肌肉内注射与肠内青霉素预防风湿性心脏病进展的比较:一项非劣效性随机试验研究方案(GOALIE 试验)。

Intramuscular versus enteral penicillin prophylaxis to prevent progression of rheumatic heart disease: Study protocol for a noninferiority randomized trial (the GOALIE trial).

机构信息

Division of Adult Cardiology, Department of Adult Cardiology, Uganda Heart Institute, Kampala, Uganda.

Division of Paediatric Cardiology, Department of Paediatric Cardiology, Uganda Heart Institute, Kampala, Uganda.

出版信息

Am Heart J. 2024 Sep;275:74-85. doi: 10.1016/j.ahj.2024.05.012. Epub 2024 May 24.

Abstract

BACKGROUND

Rheumatic Heart Disease (RHD) persists as a major cardiovascular driver of mortality and morbidity among young people in low-and middle-income countries. Secondary antibiotic prophylaxis (SAP) with penicillin remains the cornerstone of RHD control, however, suboptimal treatment adherence undermines most secondary prevention programs. Many of the barriers to optimal SAP adherence are specific to the intramuscular form of penicillin and may potentially be overcome by use of oral penicillin. This noninferiority trial is comparing the efficacy of intramuscular to oral penicillin SAP to prevent progression of mild RHD at 2 years.

METHODS/DESIGN: The Intramuscular vs Enteral Penicillin Prophylaxis to Prevent Progression of Rheumatic Heart Disease (GOALIE) trial is randomizing Ugandan children aged 5 to 17 years identified by echocardiographic screening with mild RHD (Stage A or B as defined by 2023 World Heart Federation criteria) to Benzathine Benzyl Penicillin G (BPG arm, every-28-day intramuscular penicillin) or Phenoxymethyl Penicillin (Pen V arm, twice daily oral penicillin) for a period of 2 years. A blinded echocardiography adjudication panel of 3 RHD experts and 2 cardiologists is determining the echocardiographic stage of RHD at enrollment and will do the same at study completion by consensus review. Treatment adherence and study retention are supported through peer support groups and case management strategies. The primary outcome is the proportion of children in the Pen V arm who progress to more advanced RHD compared to those in the BPG arm. Secondary outcomes are patient-reported outcomes (treatment acceptance, satisfaction, and health related quality of life), costs, and cost-effectiveness of oral compared to intramuscular penicillin prophylaxis for RHD. A total sample size of 1,004 participants will provide 90% power to demonstrate noninferiority using a margin of 4% with allowance for 7% loss to follow-up. Participant enrollment commenced in October 2023 and final participant follow-up is expected in December 2026. The graphical abstract (Fig. 1) summarizes the flow of echocardiographic screening, participant enrollment and follow-up.

DISCUSSION

The GOALIE trial is critical in global efforts to refine a pragmatic approach to secondary prevention for RHD control. GOALIE insists that the inferiority of oral penicillin be proven contemporarily and against the most important near-term clinical outcome of progression of RHD severity. This work also considers other factors that could influence the adoption of oral prophylaxis and change the calculus for acceptable efficacy including patient-reported outcomes and costs.

TRIAL REGISTRATION

ClinicalTrials.gov: NCT05693545.

摘要

背景

风湿性心脏病(RHD)仍然是中低收入国家年轻人死亡和发病的主要心血管驱动因素。使用青霉素进行二级抗生素预防(SAP)仍然是 RHD 控制的基石,然而,治疗依从性不佳破坏了大多数二级预防计划。许多影响 SAP 最佳依从性的障碍是青霉素肌内注射特有的,可能可以通过口服青霉素来克服。这项非劣效性试验正在比较肌内注射青霉素和口服青霉素 SAP 在预防 2 年内轻度 RHD 进展方面的疗效。

方法/设计:肌肉内 vs 肠内青霉素预防风湿性心脏病进展(GOALIE)试验正在随机分配乌干达年龄在 5 至 17 岁之间的儿童,这些儿童通过超声心动图筛查确定为轻度 RHD(根据 2023 年世界心脏联合会标准定义为 A 期或 B 期),分为苄星青霉素 G(BPG 组,每 28 天肌内注射青霉素)或苯氧甲基青霉素(Pen V 组,每日两次口服青霉素)组,为期 2 年。一个由 3 名 RHD 专家和 2 名心脏病专家组成的盲法超声心动图裁决小组正在确定入组时 RHD 的超声心动图阶段,并通过共识审查在研究结束时同样进行。通过同伴支持小组和病例管理策略来支持治疗依从性和研究保留。主要结局是与 BPG 组相比,Pen V 组中进展为更严重 RHD 的儿童比例。次要结局是患者报告的结局(治疗接受度、满意度和与健康相关的生活质量)、成本以及口服青霉素与肌内青霉素预防 RHD 的成本效益。总共 1004 名参与者的样本量将提供 90%的效力,使用 4%的边缘来证明非劣效性,允许 7%的失访率。参与者招募于 2023 年 10 月开始,预计最后一次参与者随访于 2026 年 12 月完成。图形摘要(图 1)总结了超声心动图筛查、参与者入组和随访的流程。

讨论

GOALIE 试验对于全球努力完善 RHD 控制的二级预防实用方法至关重要。GOALIE 坚持认为,必须证明口服青霉素的劣势,并针对 RHD 严重程度进展这一最重要的近期临床结局来证明其劣势。这项工作还考虑了可能影响口服预防措施采用并改变可接受疗效的其他因素,包括患者报告的结局和成本。

试验注册

ClinicalTrials.gov:NCT05693545。

相似文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索