Department of Critical Care Medicine, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China.
Center of Severe Acute Pancreatitis (CSAP), Department of Critical Care Medicine, Jinling Hospital, Medical School of Nanjing University, Nanjing, China.
Clin Transl Gastroenterol. 2024 Jul 1;15(7):e00726. doi: 10.14309/ctg.0000000000000726.
Fine-needle aspiration (FNA) is no longer recommended for diagnosing infected pancreatic necrosis (IPN) due to a high false-negative rate. Metagenomic next-generation sequencing (mNGS) is a valuable tool for identifying potential pathogens. We hypothesized that adding mNGS to the standard FNA procedure may increase diagnostic accuracy.
This is a prospective, single-arm feasibility study enrolling patients with acute necrotizing pancreatitis complicated by suspected IPN. Computed tomography-guided FNA was performed immediately after enrollment, and the drainage samples were subjected to culture and mNGS assays simultaneously. Confirmatory IPN within the following week of the index FNA procedure was the reference standard. The diagnostic performance of FNA-mNGS and the impact of mNGS results on treatment were evaluated. Historical controls were used for comparison of clinical outcomes.
There was no significant difference between mNGS and culture in the positive rate (75% vs 70%, P = 0.723). The accuracy of FNA-mNGS was 80.0%, with a sensitivity of 82.35%, specificity of 66.67%, positive predictive value of 93.3%, and negative predictive value of 40.0%. The results of the mNGS led to treatment change in 16 of 20 patients (80%), including implementing percutaneous catheter drainage (n = 7), expanding antibiotic coverage (n = 2), percutaneous catheter drainage and expanding coverage (n = 4), narrowing antibiotic coverage (n = 1), and discontinuation of antibiotics (n = 2). The FNA-mNGS approach was not associated with improved clinical outcomes compared with the historical control group.
The addition of mNGS to standard FNA has comparable diagnostic accuracy with culture-based FNA and may not be associated with improved clinical outcomes.
由于假阴性率高,细针抽吸(FNA)不再推荐用于诊断感染性胰腺坏死(IPN)。宏基因组下一代测序(mNGS)是鉴定潜在病原体的有价值工具。我们假设将 mNGS 添加到标准 FNA 程序中可能会提高诊断准确性。
这是一项前瞻性、单臂可行性研究,纳入了患有急性坏死性胰腺炎并伴有疑似 IPN 的患者。在入组后立即进行计算机断层扫描引导的 FNA,同时对引流样本进行培养和 mNGS 检测。在索引 FNA 程序后的一周内确认 IPN 是参考标准。评估了 FNA-mNGS 的诊断性能以及 mNGS 结果对治疗的影响。使用历史对照来比较临床结果。
mNGS 和培养在阳性率方面没有显著差异(75%对 70%,P = 0.723)。FNA-mNGS 的准确性为 80.0%,灵敏度为 82.35%,特异性为 66.67%,阳性预测值为 93.3%,阴性预测值为 40.0%。mNGS 的结果导致 20 名患者中的 16 名(80%)发生治疗改变,包括实施经皮导管引流(n = 7)、扩大抗生素覆盖范围(n = 2)、经皮导管引流和扩大覆盖范围(n = 4)、缩小抗生素覆盖范围(n = 1)和停止使用抗生素(n = 2)。与历史对照组相比,FNA-mNGS 方法并未改善临床结局。
将 mNGS 添加到标准 FNA 中与基于培养的 FNA 具有相当的诊断准确性,并且可能不会改善临床结局。