To determine the efficacy and safety of acetic acid gel in comparison to silver sulfadiazine cream in patients suffering from second-degree burns

Chandrashekar Chalwade, M. Pawar, Abhijeet D. Sawant
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引用次数: 0

Abstract

Acetic acid solution is effective in healing of chronic wounds by its ability to eradicate biofilms. One percent silver sulfadiazine (SSD) cream is the commonly used topical antimicrobial agent in burn wound care. In our study, we compared the efficacy and safety of 1% acetic acid gel with 1% SSD in partial-thickness burn wound with <20% total body surface area. Context: Bacterial colonization of burn wounds results in delayed wound healing. SSD is commonly used as a topical antibiotic in the second degree and third-degree burn wounds. The acetic acid solution is found to be clinically effective against the eradication of mature or chronic biofilm.[6] We have used 1% acetic acid gel as an anti-microbial dressing for acute burn wounds and compared it with 1% SSD. Aims: To evaluate the efficacy and safety of acetic acid gel with SSD cream in patients with second-degree burn wounds involving up to 20% of total body surface area. Outcome parameters evaluated were Wound healing (BWAT score and status as on Day 21), Pain (VAS score), Healing quality (VSS score at 1 and 3 months) and adverse effects if any. Settings and Design: The study was conducted in the burn department affiliated with a tertiary care centre. It is a prospective randomized, investigator-initiated open-label case-control study. Inclusion criteria 1. Males and females between the ages of 18 and 65 years 2. Second-degree burn involving total body surface area up to 20% at 48 h of burn injury. Exclusion criteria1.Patients with pre-existing comorbidities. Uncontrolled diabetes Mellitus. Renal insufficiency.2. Patients with known keloid tendency3.Patients with electrical burn4.Patients with inhalation burn. Patients were included in the study in accordance with mentioned inclusion and exclusion criteria. Informed consent was obtained from all patients. All procedures contributing to this work comply with the ethical standards of the relevant national and institutional guidelines on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. The study group received 1% Acetic acid gel while the control group received 1% SSD cream for antimicrobial dressings. Simple randomization was followed for the allocation of patients. Outcome parameters were assessed, compiled, and were statistically analyzed. Subjects and Methods: Eighty cases were included in the study, forty in each group. Each group patient underwent dressing with respective allotted topical antimicrobial agent, and outcome parameters were compared. In both groups, Bates-Jensen Wound Assessment Tool (BWAT), Visual Analog Scale (VAS), and Vancouver Scar Scale (VSS) scores were documented. Parameters compared were wound healing, patient acceptability, any adverse events, and quality of the healed scar. Statistical Analysis Used: The data was compiled and analyzed statistically for Outcome parameters will be analyzed for distribution, central tendency, and variability by calculating Mean, SD and p-value using Microsoft excel software (2007). Results: At 21 days, the acetic acid group showed complete reepithelialization in 45% of the cases and complete granulation in 7.5% of the cases, whereas the SSD group showed complete reepithelialization in 32.5% of the cases. The remaining cases in both groups healed after 21 days. BWAT scores were reduced in both groups. Mean VAS and mean VSS scores were comparable in both groups. No adverse event was noted in any group due to respective agent. Conclusions: In our study, we found that 1% acetic acid gel was comparable to 1% SSD in terms of efficacy and is safe to use in partial-thickness burn wounds <20% total body surface area (TBSA) with good clinical outcomes.
醋酸凝胶与磺胺嘧啶银乳膏治疗二度烧伤的疗效和安全性比较
醋酸溶液通过其清除生物膜的能力在慢性伤口愈合中是有效的。百分之一磺胺嘧啶银乳膏是烧伤创面护理中常用的局部抗菌剂。在我们的研究中,我们比较了1%醋酸凝胶和1% SSD在体表面积<20%的部分厚度烧伤创面中的疗效和安全性。背景:烧伤创面的细菌定植导致伤口愈合延迟。SSD常被用作二度和三度烧伤创面的局部抗生素。临床发现醋酸溶液对成熟或慢性生物膜的根除有效我们采用1%醋酸凝胶作为急性烧伤创面的抗菌敷料,并与1%醋酸凝胶进行比较。目的:评价醋酸凝胶联合SSD霜治疗占体表面积达20%的二度烧伤创面的疗效和安全性。评估的结果参数包括伤口愈合(BWAT评分和第21天的状态)、疼痛(VAS评分)、愈合质量(1个月和3个月的VSS评分)和不良反应(如果有的话)。环境和设计:本研究在一家三级护理中心的烧伤科进行。这是一项前瞻性随机、研究者发起的开放标签病例对照研究。纳入标准年龄在18至65岁之间的男性和女性烧伤后48小时二级烧伤,烧伤面积占全身表面积的20%。排除criteria1。既往存在合并症的患者。未控制的糖尿病。肾insufficiency.2。已知有瘢痕疙瘩倾向的患者。4.电烧伤患者。吸入性烧伤患者。患者按照上述纳入和排除标准纳入研究。获得了所有患者的知情同意。所有有助于这项工作的程序都符合相关国家和机构人体实验准则的道德标准,以及1975年《赫尔辛基宣言》(2008年修订)。研究组给予1%醋酸凝胶,对照组给予1% SSD抗菌敷料乳膏。患者的分配遵循简单随机化。评估、汇编结局参数并进行统计分析。对象与方法:80例病例纳入研究,每组40例。各组患者分别使用各自分配的局部抗菌药物进行包扎,并比较结果参数。两组均记录了贝茨-詹森伤口评估工具(BWAT)、视觉模拟量表(VAS)和温哥华疤痕量表(VSS)评分。比较的参数是伤口愈合、患者可接受性、任何不良事件和愈合疤痕的质量。使用统计分析:对数据进行整理和统计分析,使用Microsoft excel软件(2007)计算Mean、SD和p值,分析结果参数的分布、集中趋势和变异性。结果:在第21天,乙酸组有45%的病例完全上皮化,7.5%的病例完全肉芽化,而SSD组有32.5%的病例完全上皮化。两组其余病例均于21 d后痊愈。两组BWAT评分均降低。两组平均VAS和平均VSS评分具有可比性。在任何一组中均未发现由于各自的药物而引起的不良事件。结论:在我们的研究中,我们发现1%醋酸凝胶与1% SSD的疗效相当,可以安全用于<20%体表面积(TBSA)的部分厚度烧伤创面,临床效果良好。
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