...
首页> 外文期刊>Regulatory Mechanisms in Biosystems >Мон?торинг умовно-патогенних ? патогенних м?кроорган?зм?в у л?карняних в?дд?леннях х?рург?чного проф?лю м. Дн?продзержинськ
【24h】

Мон?торинг умовно-патогенних ? патогенних м?кроорган?зм?в у л?карняних в?дд?леннях х?рург?чного проф?лю м. Дн?продзержинськ

机译:监测机会性病原体? Dniprodzerzhynsk外科概况的医院科室中病原微生物的检测

获取原文

摘要

The paper presents monitoring results of the spread of opportunistic and pathogenic microorganisms in patients of surgical departments of the Dniprodzerzhynsk city hospital No 7. 1464 strains of bacteria isolated from biological material of the patients from January to December 2012 were studied. Relevant standard methods of research and data interpretation in accordance with the regulatory guidelines were used. The microorganisms’ sensitivity to antibiotics was determined by the disk diffusion method. Assessment of the resistance of isolated microorganisms to antibiotics was made with the software Whonet 5.1. At the first stage of investigation sampling biological material and inoculation in the culture medium were made. The discharges of wounds, throat, nose, ears, vagina and urethra, and also urine from patients of surgical departments were sampled for bacteriological analysis. The main substratum was 5% blood agar. There may additionally be used the selective growth media (yolk-salt agar, Endo, and Saburo). At the second stage we identify microorganisms with bacterioscopic, bacteriological and biochemical methods. Identifying microorganisms of the genus Staphylococcus was made by the reaction of lecithinase presence, plasma-coagulation reaction and the mannitol oxidation reaction. For the identification of bacteria of the family Streptococcaceae the growth pattern in 0.5% sugar medium was used. It was differentiated from bacteria of the genus Enterococcus by plating onto egg yolk agar base?and milk with 0.1% methylene blue. Identification of bacteria of the Enterobacteriaceae family was made by studying their colonies on dense differential diagnostic media. Suspicious colonies were transferred on a combined medium for primary identification (Olkenitsky's medium). Then the biochemical signs of enterobacteria were studied in the minimum number of tests. The third phase of the study included the determination of the sensitivity of microorganisms to antibiotics. To do that, we use the disc diffusion method. The?antibiogram?tests of isolated bacterial strains used Mueller-Hinton agar. According to the data obtained we assign of microorganisms to certain category of sensitivity: sensitive, moderately resistant or resistant. Monitoring of prevalent microorganisms showed that 61% (893 of 1464) isolates were gram-positive bacteria, 696 strains of them are staphylococci. 477 of these are identified as S. aureus, representing 68.5% of all Staphylococcus. We found coagulase negative staphylococci in 192 patients, and the strains of S.?haemolyticus are dominated. Strains of the family Streptococcaceae isolated from 197 patients. Among them the E. faecalis accounted for 66% of the total number of Streptococcus. Gram negative bacteria were presented by the families Enterobacteriaceae and Pseudomonaceae. Enterobacteriaceae accounted for 90.7% (518 of 571). E.?coli plays the leading role and accounted for 42% of all Enterobacteriaceae. The strains of P. aeruginosa were identified in 53 patients. S.?haemolyticus has played an important role as a pathogen as well as S. aureus. Its resistance to antibiotics is much higher than that of S.?aureus. Although S. haemolyticus is opportunistic coagulase negative, it can be isolated from patients not only with chronic, but with acute infection. Thus nowadays the strains of S. haemolyticus gained high pathogenic and virulent properties.
机译:本文介绍了Dniprodzerzhynsk市第7医院外科部门患者机会性和致病性微生物传播的监测结果,研究了从2012年1月至2012年12月从患者生物材料中分离的1464株细菌。使用了符合监管准则的相关标准研究和数据解释方法。通过圆盘扩散法确定微生物对抗生素的敏感性。使用Whonet 5.1软件评估了分离的微生物对抗生素的抗性。在调查的第一阶段,对生物材料进行采样并在培养基中进行接种。对来自外科部门患者的伤口,咽喉,鼻子,耳朵,阴道和尿道的分泌物以及尿液进行采样,以进行细菌学分析。主要基质是5%血琼脂。可以另外使用选择性生长培养基(卵黄琼脂,Endo和Saburo)。在第二阶段,我们通过细菌学,细菌学和生化方法鉴定微生物。通过卵磷脂酶的存在,血浆凝结反应和甘露醇氧化反应来鉴定葡萄球菌属的微生物。为了鉴定链球菌科的细菌,使用在0.5%糖培养基中的生长模式。通过将其涂在蛋黄琼脂基础液和含0.1%亚甲蓝的牛奶中,可将其与肠球菌属细菌区分开。肠杆菌科细菌的鉴定是通过在致密的鉴别诊断培养基上研究其菌落来进行的。将可疑菌落转移至混合培养基上以进行初步鉴定(Olkenitsky培养基)。然后在最少的测试中研究肠杆菌的生化迹象。研究的第三阶段包括确定微生物对抗生素的敏感性。为此,我们使用光盘扩散方法。分离的细菌菌株的抗菌素测试使用Mueller-Hinton琼脂。根据获得的数据,我们将微生物归为某种敏感性类别:敏感,中等抗性或抗性。对流行微生物的监测表明,有61%(1464的893)分离株是革兰氏阳性菌,其中696株是葡萄球菌。其中有477例被鉴定为金黄色葡萄球菌,占所有葡萄球菌的68.5%。我们在192例患者中发现了凝固酶阴性葡萄球菌,并且溶血链球菌菌株占主导地位。从197名患者中分离出链球菌科的菌株。其中粪肠球菌占链球菌总数的66%。肠杆菌科和假单胞菌科呈现革兰氏阴性细菌。肠杆菌科占90.7%(571为518)。大肠杆菌起着主导作用,占所有肠杆菌科的42%。在53例患者中鉴定出铜绿假单胞菌的菌株。溶血链球菌与金黄色葡萄球菌一样,都起着病原体的重要作用。它对抗生素的抵抗力比金黄色葡萄球菌高得多。尽管溶血链球菌是机会性凝固酶阴性,但它不仅可以从慢性感染患者中分离,而且可以从急性感染患者中分离出来。因此,如今溶血链球菌菌株具有高致病性和强毒性。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号