Department of Otolaryngology-Head and Neck Surgery, Monash Health, Melbourne, Australia.
Department of Surgery, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Australia.
Otolaryngol Head Neck Surg. 2021 Feb;164(2):375-380. doi: 10.1177/0194599820951183. Epub 2020 Sep 8.
Laryngopharyngeal reflux (LPR) is defined as the retropulsion of gastric contents into the larynx, oropharynx, and/or nasopharynx. The 24-hour combined hypopharyngeal-esophageal multichannel intraluminal impedance with dual pH probe (24h-HEMII-pH) is currently the gold standard in LPR diagnosis; however, it is invasive, user dependent, and not always tolerated. This study assesses the diagnostic utility of salivary pepsin (Peptest) at different thresholds and during symptomatic periods as compared with the 24h-HEMII-pH probe in diagnosing LPR.
Prospective cohort study.
Private laryngology clinic in Melbourne, Australia.
Thirty-five patients with a clinical history and endoscopic findings of LPR were recruited and simultaneously evaluated for LPR via 24h-HEMII-pH probe and salivary pepsin analysis at 5 key time points over the same 24-hour period.
Salivary pepsin was 76.9% sensitive and had a positive predictive value (PPV) of 87.0% at a threshold of 16 ng/mL when compared with the 24h-HEMII-pH probe. If the pathologic pepsin threshold was raised to 75 ng/mL, salivary pepsin had a sensitivity of 57.7%, a specificity of 75.0%, and a PPV of 93.8%. Symptomatic testing conferred a superior specificity at 16 ng/mL (66.7%) and 75 ng/mL (100.0%) and a superior PPV at 16 ng/mL (92.3%) and 75 ng/mL (100.0%).
Salivary pepsin detection is a simpler, more cost-effective, and less traumatic universal first-line alternative to 24h-HEMII-pH probe in diagnosing LPR. Superior specificities conferring greater diagnostic value may be achieved with higher thresholds and symptomatic testing. If clinical suspicion remains high following negative salivary pepsin analysis, a 24h-HEMII-pH study could provide further diagnostic information.
胃内容物反流至喉、咽和/或鼻后即为咽-喉反流(LPR)。24 小时联合食管多通道腔内阻抗-pH 监测(24h-HEMII-pH)是目前诊断 LPR 的金标准;然而,它具有侵袭性、依赖使用者且并非总被耐受。本研究旨在评估不同阈值和症状期唾液胃蛋白酶(Peptest)检测诊断 LPR 的诊断效能,并与 24h-HEMII-pH 探针进行比较。
前瞻性队列研究。
澳大利亚墨尔本私人喉科诊所。
35 例有 LPR 临床病史和内镜检查结果的患者,在同一 24 小时内的 5 个关键时间点同时通过 24h-HEMII-pH 探针和唾液胃蛋白酶分析评估 LPR。
当以 16ng/ml 为阈值时,唾液胃蛋白酶的敏感性为 76.9%,阳性预测值(PPV)为 87.0%,与 24h-HEMII-pH 探针相比。如果将病理性胃蛋白酶阈值提高至 75ng/ml,唾液胃蛋白酶的敏感性为 57.7%,特异性为 75.0%,PPV 为 93.8%。症状检测在 16ng/ml(66.7%)和 75ng/ml(100.0%)时特异性较高,在 16ng/ml(92.3%)和 75ng/ml(100.0%)时 PPV 较高。
与 24h-HEMII-pH 探针相比,唾液胃蛋白酶检测是一种更简单、更经济、创伤更小的 LPR 诊断一线替代方法。采用较高阈值和症状检测可能会获得更高的特异性,从而提高诊断价值。如果唾液胃蛋白酶检测阴性,而临床仍高度怀疑 LPR,24h-HEMII-pH 研究可能会提供进一步的诊断信息。