Al-Dhubaibi Mohammed Saleh, Bahaj Saleh Salem, Noman Aref, Alkasser Waleed Yahya, AbdElneam Ahmed Ibrahim, Mohammed Ghada Farouk, Nawaz Hassan, Allana Zeeshan, Ali Sarosh Sher
Departments of Dermatologym College of Medicine, Shaqra University, Dawadmi, Saudi Arabia.
Department of Microbiology and Immunology, Faculty of Medicine and Health Sciences, Sana'a University, Sana'a, Yemen.
BMC Infect Dis. 2024 Dec 28;24(1):1476. doi: 10.1186/s12879-024-10349-5.
Mucocutaneous leishmaniasis (MCL) is a severe form of leishmaniasis causing chronic and destructive lesions. Accurate diagnosis is crucial for effective treatment. Traditional methods, such as the Montenegro skin test is delayed hypersensitivity test. Polymerase chain reaction (PCR) has emerged as a superior diagnostic tool for detecting Leishmania DNA, offering higher sensitivity and specificity.
This meta-analysis adhered to PRISMA guidelines and included studies focusing exclusively on the diagnostic accuracy of PCR for MCL. A comprehensive literature search was conducted across multiple databases. Inclusion criteria mandated studies with relevant diagnostic accuracy metrics, while those mixing other forms of leishmaniasis or lacking a control group were excluded. Quality was assessed using the STARD checklist, and ensuring a low risk of bias assessed through QUADAS-2 tool.
Eight studies were included, showing PCR sensitivity ranging from 50% to 97.1% and consistently high specificity, often reaching 100%. The studies demonstrated a low risk of bias and applicability concerns, supporting the robustness of the findings. Heterogeneity was substantial, necessitating a random-effects model for pooled estimates.
This analysis confirms PCR's high specificity for MCL diagnosis, despite variable sensitivity. Compared to previous meta-analyses, this study's focus on MCL exclusively provides a more targeted evaluation. Future research should aim to standardize PCR protocols and explore non-invasive sampling techniques to enhance diagnostic accuracy and patient comfort, ultimately improving clinical outcomes for MCL patients.
皮肤黏膜利什曼病(MCL)是利什曼病的一种严重形式,可导致慢性破坏性病变。准确诊断对于有效治疗至关重要。传统方法,如 Montenegro 皮肤试验是一种迟发型超敏反应试验。聚合酶链反应(PCR)已成为检测利什曼原虫 DNA 的一种更优诊断工具,具有更高的敏感性和特异性。
本荟萃分析遵循 PRISMA 指南,纳入仅关注 PCR 对 MCL 诊断准确性的研究。在多个数据库中进行了全面的文献检索。纳入标准要求研究具有相关诊断准确性指标,而那些混合了其他形式利什曼病或缺乏对照组的研究被排除。使用 STARD 清单评估质量,并通过 QUADAS - 2 工具确保低偏倚风险。
纳入了八项研究,显示 PCR 的敏感性范围为 50%至 97.1%,特异性始终很高,通常达到 100%。这些研究显示出低偏倚风险和适用性问题,支持了研究结果的稳健性。异质性很大,需要采用随机效应模型进行汇总估计。
本分析证实了 PCR 对 MCL 诊断具有高特异性,尽管敏感性存在差异。与之前的荟萃分析相比,本研究仅关注 MCL 提供了更具针对性的评估。未来的研究应旨在标准化 PCR 方案,并探索非侵入性采样技术,以提高诊断准确性和患者舒适度,最终改善 MCL 患者的临床结局。