González Pedraza Avilés A, Ortiz Zaragoza M C
Centro de Salud Dr. José Castro Villagrana, Facultad de Medicina, UNAM, México.
Aten Primaria. 2000 May 15;25(8):542-5. doi: 10.1016/s0212-6567(00)78564-7.
To assess the frequency of association between Streptococcus pyogenes and beta-lactamase-producing-bacteria in the pharyngotonsillitis and the evaluate the in vitro susceptibility.
Prospective, descriptive, transverse study.
The present study was carried out in the Health Center Dr. José Castro Villagrana, in Tlalpan, México, D.F., from Juanary, 1996 to February 1999.
In three hundred and ninety four patients with pharyngotonsillitis diagnosis we isolated the same number of Streptococcus pyogenes, and possible beta-lactamase-producing-bacteria.
In 180 patients (45.7%) we isolated at least one possible beta-lactamase-producing-bacteria. Of these, in 138 patients (35%) were confirmed the enzyme presence. In total, we isolated 218 possible beta-lactamase-producing bacteria, and 152 (69.7%) were beta-lactamase positive. We found no significant change in the in vitro susceptibility of group A Streptococcus to penicillin, but erythromycin resistance is relatively common, approximately 10% in this study.
Streptococcus pyogenes was uniformly susceptible to all penicillins and cephalosporins in vitro. Erythromycin treatment should not be promoted as first-line therapy because the consequent increase of bacterial resistance could create difficulty in treating penicillin-allergic patients. Because of the poor activity of trimetoprimsulfametoxazol, this drug no longer can be considered the drug of choice for the management of group A Streptococcal infections.
评估化脓性链球菌与产β-内酰胺酶细菌在咽扁桃体炎中的关联频率,并评估其体外敏感性。
前瞻性、描述性横断面研究。
本研究于1996年1月至1999年2月在墨西哥城特拉尔潘的何塞·卡斯特罗·比利亚格拉纳医生健康中心进行。
在394例诊断为咽扁桃体炎的患者中,我们分离出相同数量的化脓性链球菌和可能产β-内酰胺酶的细菌。
在180例患者(45.7%)中,我们分离出至少一种可能产β-内酰胺酶的细菌。其中,138例患者(35%)证实存在该酶。我们总共分离出218株可能产β-内酰胺酶的细菌,152株(69.7%)β-内酰胺酶呈阳性。我们发现A组链球菌对青霉素的体外敏感性没有显著变化,但红霉素耐药相对常见,在本研究中约为10%。
化脓性链球菌在体外对所有青霉素和头孢菌素均敏感。不应将红霉素治疗作为一线治疗方法推广,因为随之而来的细菌耐药性增加可能会给青霉素过敏患者的治疗带来困难。由于复方新诺明活性较差,该药不再被视为治疗A组链球菌感染的首选药物。