Laryngopharyngeal Reflux Study Group of Young-Otolaryngologists of the International Federations of Oto-rhino-laryngological Societies (YO-IFOS), Paris, France.
Laboratory of Anatomy and Cell Biology, Faculty of Medicine, UMONS Research Institute for Health Sciences and Technology, University of Mons (UMons), Mons, Belgium.
Clin Otolaryngol. 2021 May;46(3):602-613. doi: 10.1111/coa.13722. Epub 2021 Feb 10.
To assess the evolution of symptoms and findings of laryngopharyngeal reflux (LPR) patients according to the type of reflux (acid, non-acid, mixed and gastro-oesophageal (GERD)).
Prospective uncontrolled multicentre study.
One hundred and six patients with LPR have been recruited from 3 European Hospitals. According to the reflux characteristics at the impedance-pH monitoring (acid, non-acid, mixed, GERD), patients received a personalised treatment based on the association of diet, pantoprazole, alginate or magaldrate for 3 months. Reflux Symptom Score (RSS) was assessed at baseline, 6 and 12 weeks post-treatment. Reflux Sign Assessment (RSA) has been used to rate laryngeal and extra-laryngeal findings at baseline and 12 weeks post-treatment. Overall success rate and the evolution of symptoms and findings were evaluated according to the LPR types.
One hundred and two LPR patients (42 acid, 33 non-acid, 27 mixed, including 49 with LPR and GERD) completed the study. RSS and RSA total scores significantly improved from baseline to post-treatment time in acid, mixed and non-acid groups. The presence of GERD in addition to LPR did not impact the clinical improvement. The 3-month success rates of treatment ranged from 62% to 64%, and there were no significant differences between groups. The success rate of patients with non-acid LPR was similar to those of patients with mixed and acid LPR.
MII-pH is useful to specify the type of LPR and the related most adequate therapeutic regimen. Non-acid or mixed LPR similarly respond to treatment than acid LPR but require a treatment based on alginate or magaldrate covering the non-acid proximal reflux events.
根据反流类型(酸、非酸、混合和胃食管(GERD))评估喉咽反流(LPR)患者的症状和发现演变。
前瞻性非对照多中心研究。
从 3 家欧洲医院招募了 106 例 LPR 患者。根据阻抗-pH 监测的反流特征(酸、非酸、混合、GERD),患者接受了基于饮食、泮托拉唑、藻酸盐或镁铝碳酸盐联合治疗的个体化治疗,为期 3 个月。在治疗前、治疗后 6 周和 12 周评估反流症状评分(RSS)。在治疗前和治疗后 12 周使用反流症状评估(RSA)来评估喉部和喉部外发现。根据 LPR 类型评估总体成功率和症状及发现的演变。
102 例 LPR 患者(42 例酸反流、33 例非酸反流、27 例混合反流,包括 49 例 LPR 和 GERD)完成了研究。在酸、混合和非酸组中,RSS 和 RSA 总分从基线到治疗后时间显著改善。LPR 合并 GERD 的存在并未影响临床改善。3 个月治疗成功率为 62%至 64%,各组之间无显著差异。非酸 LPR 患者的成功率与混合和酸 LPR 患者相似。
MII-pH 可用于明确 LPR 的类型和相关的最佳治疗方案。非酸或混合 LPR 对治疗的反应与酸 LPR 相似,但需要基于藻酸盐或镁铝碳酸盐的治疗,覆盖非酸近端反流事件。