Khooharo Tahseen Shabbir, Hassan Sayed Umer, Shaikh Abdul Hafeez
Dow University of Health Sciences, Karachi, Pakistan.
J Pak Med Assoc. 2021 Feb;71(2(B)):585-589. doi: 10.47391/JPMA.09-1107.
To compare the efficacy of metronidazole and amoxicillin as preoperative single dose treatment with conventional therapy in prevention of dry socket.
A double blind randomized controlled trial was conducted at the oral and maxillofacial surgery OPD at DUHS, Karachi. Patients attending and requiring surgical extraction of madibular 3rd molar during October 2018 till April 2019 were randomly divided into 3 groups. Ethical approval was taken from Institutional Review Board of DUHS, Karachi. Informed consent was also taken from patients. First group was given single preoperative oral dose of 400mg metronidazole one hour before extraction, second group was treated with single oral dose of 500mg amoxicillin an hour before tooth extraction, and both of the groups were given painkillers postoperatively. Third group was given 500mg of Amoxicillin BD, 400mg of metronidazole and painkillers postoperatively. Every group had a follow-up on fifth postoperative day.
Dry socket was reported among patients 19(8.4 %), among them 4 were males and 15 were females. Chi-square test was used to calculate the p-value (0.066). Results of the present trial were statistically insignificant. Incidence of dry socket in amoxicillin group was 3 (5.5%), in metronidazole was 4 (7.5) and in conventional therapy group was 12(16%).
Present trial was not effective in preventing the occurrence of dry socket by means of single preoperative oral dose of metronidazole and amoxicillin compared to conventional therapy. However, clinically percentage of occurrence of dry socket was higher in conventional group compared to amoxicillin and metronidazole group.
比较甲硝唑和阿莫西林术前单剂量治疗与传统疗法在预防干槽症方面的疗效。
在卡拉奇DUHS口腔颌面外科门诊进行了一项双盲随机对照试验。2018年10月至2019年4月期间前来就诊且需要拔除下颌第三磨牙的患者被随机分为3组。获得了卡拉奇DUHS机构审查委员会的伦理批准。同时也取得了患者的知情同意。第一组在拔牙前1小时口服400mg甲硝唑单剂量,第二组在拔牙前1小时口服500mg阿莫西林单剂量,两组术后均给予止痛药。第三组术后给予500mg阿莫西林每日两次、400mg甲硝唑和止痛药。每组在术后第5天进行随访。
报告有19名(8.4%)患者发生干槽症,其中男性4名,女性15名。采用卡方检验计算p值(0.066)。本试验结果无统计学意义。阿莫西林组干槽症发生率为3例(5.5%),甲硝唑组为4例(7.5%),传统治疗组为12例(16%)。
与传统疗法相比,本试验采用术前口服单剂量甲硝唑和阿莫西林预防干槽症的发生无效。然而,临床上传统治疗组干槽症的发生率高于阿莫西林组和甲硝唑组。