In vitro comparison of cerumenolytic efficacy: 2.5 % sodium bicarbonate versus 0.5 % sodium docusate based on cerumen weight gain

IF 1.7 4区 医学 Q2 OTORHINOLARYNGOLOGY American Journal of Otolaryngology Pub Date : 2025-03-01 Epub Date: 2025-01-13 DOI:10.1016/j.amjoto.2024.104592
Cheerasook Chongkolwatana , Paiboon Sureepong , Kunkanya Chansomboon , Navarat Kasemsuk , Chatchawan Srisawat
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Abstract

Objective

This study aimed to compare the cerumenolytic efficacy of 2.5 % sodium bicarbonate prepared in-house with that of commercially available 0.5 % sodium docusate, utilizing cerumen weight gain and disintegration degree as metrics.

Methods

Cerumen samples were collected from patients at an otorhinolaryngology outpatient clinic at a tertiary care hospital. This study evaluated the differences in cerumen weight and degree of disintegration in vitro before and after treatment with cerumenolytic agents at 15 and 30 min and at 1, 2, 4, 6, and 24 h. The agents tested were 2.5 % sodium bicarbonate and 0.5 % sodium docusate. Each experiment was conducted at least five times. We hypothesized that greater weight gain and higher disintegration scores indicate better cerumenolytic efficacy.

Results

Both cerumenolytic agents caused significant increases in wet and dry cerumen weights at all time points (P < 0.001). After 24 h, the cerumen weight increased approximately sevenfold from the initial weight. Notably, the weight increased by 50 % of the 24-hour value within the first hour. A comparison of the average weight gain between the 2.5 % sodium bicarbonate and 0.5 % sodium docusate groups revealed no significant differences at any time point (P = 0.406). Similarly, disintegration scores obtained via the 96-well plate method were not significantly different (P = 0.749).

Conclusions

In terms of cerumen weight gain and degree of disintegration, the cerumenolytic efficacy of 2.5 % sodium bicarbonate is not inferior to that of 0.5 % sodium docusate. A 1-hour application of a cerumenolytic agent is effective for cerumen removal in outpatient settings.
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体外溶脑膜效果比较:2.5%碳酸氢钠与0.5%醋酸钠基于脑膜增重。
目的:以耵聍增重和崩解程度为指标,比较国产2.5%碳酸氢钠与市售0.5%醋酸钠的溶耵聍效果。方法:采集某三级医院耳鼻喉科门诊患者的耵聍标本。本研究评估了溶耵聍剂在15和30分钟以及1、2、4、6和24小时治疗前后的体外耵聍重量和崩解程度的差异。测试的药物是2.5%碳酸氢钠和0.5%醋酸钠。每个实验至少进行5次。我们假设体重增加和解体评分越高表明溶脑膜效果越好。结果:两种溶耵聍剂在各时间点均引起干、湿耵聍重量的显著增加(P)。结论:在耵聍重量增加和崩解程度方面,2.5%碳酸氢钠的溶耵聍效果不逊于0.5%乙酸钠。在门诊使用溶脑膜剂1小时可有效去除脑膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Journal of Otolaryngology
American Journal of Otolaryngology 医学-耳鼻喉科学
CiteScore
4.40
自引率
4.00%
发文量
378
审稿时长
41 days
期刊介绍: Be fully informed about developments in otology, neurotology, audiology, rhinology, allergy, laryngology, speech science, bronchoesophagology, facial plastic surgery, and head and neck surgery. Featured sections include original contributions, grand rounds, current reviews, case reports and socioeconomics.
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