首页> 外文期刊>American journal of dentistry >Clinical and microbiological efficacy of systemic roxithromycin as an adjunct to non-surgical periodontal therapy in treatment of chronic periodontitis. A randomized, double-blinded, placebo-controlled clinical trial
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Clinical and microbiological efficacy of systemic roxithromycin as an adjunct to non-surgical periodontal therapy in treatment of chronic periodontitis. A randomized, double-blinded, placebo-controlled clinical trial

机译:系统性罗红霉素作为非手术性牙周治疗的辅助治疗慢性牙周炎的临床和微生物功效。一项随机,双盲,安慰剂对照的临床试验

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Purpose: The objective of this randomized clinical trial was to evaluate the clinical and microbiological effects of systemic administration of roxithromycin (RXM) as an adjunct to non-surgical periodontal therapy (NSPT) in the treatment of individuals with moderate to severe chronic periodontitis (CP). Methods: 70 individuals (38 males and 32 females, aged 25 to 60 years) with moderate to severe CP were randomly allocated into two groups. 35 individuals were allocated to full mouth SRP+RXM while 35 individuals were allocated to SRP+ Placebo group. The clinical parameters evaluated were probing depth (PD), clinical attachment level (CAL), gingival index (GI), plaque index (PI) and % bleeding on probing sites (%B0P) at baseline (B/L), 1-, 3- and 6-month intervals while microbiologic parameters included percentage of sites positive for periodontopathic bacteria A. actinomycetemcomitans, P. gingivalis and T. forsythia at B/L, 3 and 6 months using polymerase chain reaction. Results: Both groups showed improved clinical and microbiologic parameters over 6 months. RXM group showed a statistically significant reduction in mean PD and CAL gain as compared to the placebo group (P< 0.0001). There was reduction in percentage of sites positive for periodontopathic bacteria over the duration of the study in both groups and a statistically significant reduction in the number of sites positive for A. actinomycetemcomitans in RXM group (P< 0.001).
机译:目的:这项随机临床试验的目的是评估罗非霉素(RXM)全身性给药作为非手术性牙周治疗(NSPT)的辅助治疗中重度慢性牙周炎(CP)患者的临床和微生物学作用)。方法:将70例中度至重度CP患者(38例男性和32例女性,年龄25至60岁)随机分为两组。 35个人被分配到全口SRP + RXM,而35个人被分配到SRP +安慰剂组。评估的临床参数为基线(B / L)处的探查深度(PD),临床依从水平(CAL),牙龈指数(GI),菌斑指数(PI)和探查部位出血百分比(%B0P),1-, 3个月和6个月的间隔,而微生物学参数包括使用聚合酶链反应在B / L,3个月和6个月时对牙周病菌A.放线菌,牙龈卟啉单胞菌和连翘的阳性位点的百分比。结果:两组均在6个月内显示出改善的临床和微生物学指标。与安慰剂组相比,RXM组显示出平均PD和CAL增益有统计学意义的下降(P <0.0001)。在整个研究过程中,两组牙周病菌阳性位点的百分比均降低,而RXM组中放线菌的阳性位点数在统计学上显着降低(P <0.001)。

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