烧伤病房难愈性创面病原菌分布及耐药性分析

目的 分析烧伤病房难愈性创面病原菌分布及耐药性,为临床合理选用抗生素提供依据.方法 对2006年1月至2012年6月间中国人民解放军第八五医院烧伤病房收治的难愈性创面患者创面分离出的病原菌,采用K-B纸片扩散法进行药物敏感试验,分析病原菌耐药性.结果 分离出病原菌154株,革兰阳性菌62株,占40.26％;革兰阴性菌92株,占59.74％.常见病原菌为金黄色葡萄球菌、铜绿假单胞菌和鲍曼不动杆菌.烧伤难愈性创面中金黄色葡萄球菌最多见,压迫性溃疡创面中常见铜绿假单胞菌和鲍曼不动杆菌,其他难愈性创面中铜绿假单胞菌最常见.创面革兰阳性菌对利奈唑烷和呋喃妥因的耐药率较低,革兰阴性菌对头孢哌酮/舒巴坦、阿米卡星、亚胺培南、氨曲南和头孢西丁的耐药率较低,无万古霉素耐药菌.常见病原菌中金黄色葡萄球菌和鲍曼不动杆菌的耐药率较高,铜绿假单胞菌的耐药率较低.结论 不同病因的难愈性创面病原菌分布不同,引起难愈性创面的病原菌主要为多重耐药金黄色葡萄球菌和鲍曼不动杆菌.     

重症监护病房鲍曼不动杆菌和铜绿假单胞菌的分布及耐药性监测

目的探讨医院重症监护病房(ICU)鲍曼不动杆菌及铜绿假单胞菌临床分离株的分布及耐药性特点。方法回顾性调查2006年7月至2010年6月ICU患者中分离出的鲍曼不动杆菌和铜绿假单胞菌的临床感染情况,对111株鲍曼不动杆菌和73株铜绿假单胞菌的药敏结果进行统计分析,所有数据采用WHONET 5.5软件进行分析。结果鲍曼不动杆菌及铜绿假单胞菌在呼吸道标本中检出率最高(76.1%),其次是CVP导管尖端(8.7%),鲍曼不动杆菌对临床常用抗菌药物耐药率85%的有8种,对亚胺培南的耐药率也达70.3%,耐药率最低的仅有头孢哌酮/舒巴坦(17.1%);铜绿假单胞菌对替卡西林、亚胺培南有较高的耐药率,分别为45.2%、41.1%,对其他抗菌药物耐药率均25%。结论下呼吸道是ICU患者鲍曼不动杆菌和铜绿假单胞菌感染的主要部位;ICU患者感染以鲍曼不动杆菌和铜绿假单胞菌为主,鲍曼不动杆菌较铜绿假单胞菌耐药及多重耐药性严重。     

院内感染新生儿肺炎病原菌分布特点及干预对策

目的了解院内感染新生儿肺炎病原菌分布的特点,并分析原因和探讨干预对策。方法回顾性分析义乌市中心医院新生儿监护病房（NICU）2012年6月至2013年6月发生的60例院内感染新生儿肺炎患儿的痰液标本细菌培养及药敏资料,了解病原菌分布的特点,分析引起院内感染新生儿肺炎的原因,并采取相应的干预对策。结果60例患儿样本共培养出病原菌72株,其中革兰阳性菌20株,占27．8％,主要是金黄色葡萄球菌、草绿色链球菌与表皮葡萄球菌,革兰阴性菌52株,占72．2％,主要是肺炎克雷伯菌、大肠埃希菌和鲍曼不动杆菌。金黄色葡萄球菌中6株为耐甲氧西林金葡菌（MRSA）,占50％,肺炎克雷伯菌中13株为多重耐药菌,占56．5％,大肠埃希菌中6株为多重耐药菌,占46．2％,鲍曼不动杆菌中4株为多重耐药菌,占66．7％,铜绿假单胞菌中2株为多重耐药菌,占50％,嗜麦芽类单胞菌与阴沟肠杆菌均为多重耐药菌。结论院内感染新生儿肺炎病原菌分布以革兰阴性菌为主,多重耐药菌比例较高,通过有效的干预措施,可以降低院内感染新生儿肺炎的发病率。     

铜绿假单胞菌体外抑菌活性研究

目的 观察铜绿假单胞菌抗菌物质对鲍曼不动杆菌等细菌的体外抑菌效果.方法 用交叉条带实验方法检测了铜绿假单胞菌对鲍曼不动杆菌、耐甲氧西林表皮葡萄球菌和粪肠球菌的体外抑制活性.结果 铜绿假单胞菌对鲍曼不动杆菌、耐甲氧西林表皮葡萄球菌和粪肠球菌体外抑菌活性良好,10株铜绿假单胞菌中,有8株对鲍曼不动杆菌的抑制率均达到了100％.另外有8株对耐甲氧西林表皮葡萄球菌的抑菌率均为100％;有6株对粪肠球菌的抑菌率为100％.结论 铜绿假单胞菌对上述3种致病菌具有较强的抗菌活性,具有开发前景.     

老年气管插管患者下呼吸道感染细菌分布及 耐药性分析

目的研究老年气管插管患者下呼吸道感染的病原菌分布及耐药情况,为临床插管前预防性经验用药提供参考。方法回顾性分析2014-2016年上海市虹口区江湾医院老年气管插管患者的病原菌分布及耐药性情况。结果 560例标本中共检出177株致病菌,其中革兰阴性杆菌121株(68.36%),以肺炎克雷伯菌、铜绿假单胞菌为主;除鲍曼不动杆菌/溶血不动杆菌外,其他革兰阴性杆菌对亚胺培南、美罗培南敏感性均较高。革兰阳性球菌检出52株(29.38%),以金黄色葡萄球菌为主(其中MRSA 37株),对万古霉素敏感性较高。另外分离到真菌4株。结论气管插管患者下呼吸道感染致病菌以肺炎克雷伯菌、铜绿假单胞菌、金黄色葡萄球菌为主。在临床应用中,应根据本地区、本医院的病原菌分布状况和细菌耐药情况,给予适当药物,预防感染。     

重症监护病房革兰阴性杆菌耐药性分析

目的了解深圳市人民医院重症监护病房(ICU)革兰阴性杆菌的分布及其耐药性,指导临床合理用药。方法收集来自重症监护病房各类标本分离的革兰阴性杆菌540株,用VITEK AMS-60或VITEK-Ⅱ全自动微生物分析仪进行菌种鉴定,用K-B法进行药敏试验。结果ICU检出的革兰阴性杆菌以鲍曼不动杆菌、大肠埃希菌、铜绿假单胞菌和肺炎克雷伯菌为主,ESBLs阳性的大肠埃希菌和肺炎克雷伯菌比例为61.6%和51.8%,各类细菌对常用抗菌药物表现为严重耐药和多重耐药。结论该院ICU检出的革兰阴性杆菌以鲍曼不动杆菌、大肠埃希菌、铜绿假单胞菌和肺炎克雷伯菌为主,且呈现多重耐药性。     

908株烧伤患者病原菌分布特征及耐药性分析

目的：了解本院2011 年-2013 年烧伤患者分离病原菌的分布特征及耐药性,为合理使用抗生素提供依据。方法：对患者创面 分泌物、痰液、血液中的细菌进行分离鉴定和药敏试验,药敏数据分析用WHONET5.6 软件。结果：共分离908 株病原菌,其中最 常见的病原菌依次为：鲍曼不动杆菌、铜绿假单胞菌、肺炎克雷伯菌、表皮葡萄球菌、金黄色葡萄球菌、大肠埃希菌。在革兰阴性杆 菌中,鲍曼不动杆菌对碳青霉烯类耐药率较高,铜绿假单胞菌对氨基糖苷类、喹诺酮类的耐药率较低。在肠杆菌科细菌中,未发现 耐碳青霉烯类大肠埃希菌和肺炎克雷伯菌株。在葡萄球菌中,未发现耐万古霉素、利奈唑胺菌株。结论：我院烧伤患者分离的病原 菌以非发酵菌为主,医院应重视对其病原菌耐药性监测,指导临床合理使用抗生素。     

儿童重症监护病房呼吸机相关性肺炎病原菌分布及耐药性分析

目的探讨儿童重症监护病房(PICU)机械通气患儿呼吸机相关性肺炎(VAP)的病原菌群,并对细菌耐药性进行分析,为抗生素的使用提供依据。方法对2012年6月至2015年5月我院PICU中发生的34例VAP患儿的下呼吸道分泌物细菌培养结果进行回顾性分析。结果共计检出病原菌40株,其中革兰阴性菌34株(85.0%),革兰阳性菌4株(10.0%),真菌2株(5.0%)。前四位致病菌依次为:鲍曼不动杆菌(25.0%)、肺炎克雷伯菌(20.0%)、铜绿假单胞菌(15.0%)、大肠埃希菌(12.5%),均对儿科常用抗生素耐药性严重。鲍曼不动杆菌对头孢哌酮/舒巴坦耐药率较低,肺炎克雷伯菌、大肠埃希菌对亚胺培南、哌拉西林/他唑巴坦的耐药率较低,铜绿假单胞菌则对喹诺酮类耐药率较低。结论应加强机械通气儿童患者呼吸道管理及病原学监测,合理应用抗生素。     

鲍曼不动杆菌和铜绿假单胞菌在低碱性氨基酸培养基中对抗菌药物的敏感性

为了探讨鲍曼不动杆菌和铜绿假单胞菌在低碱性氨基酸培养基中对抗菌药物的敏感性,本研究利用常规培养基和低碱性氨基酸培养基,采用琼脂稀释法检测140株鲍曼不动杆菌和60株铜绿假单胞菌对亚胺培南、帕尼培南和罗美培南的最低抑菌浓度,利用K-B纸片扩散法进行药敏实验并计算敏感率。结果显示,在低碱性培养基中,铜绿假单胞菌和鲍曼不动杆菌对三种药物的最低抑菌浓度(MIC)值显著降低,铜绿假单胞菌在低碱性氨基酸培养基中对帕尼培南的敏感率显著上升,而鲍曼不动杆菌对三种药物的敏感性均显著上升。研究表明,在低碱性氨基酸培养基中,鲍曼不动杆菌和铜绿假单胞菌对帕尼培南、亚胺培南和美罗培南的敏感性有所增强,在临床检验中需考虑由培养基导致的敏感性差异。     

无多重耐药危险医院获得性肺炎病原菌分布特点与耐药性分析

目的分析温州医科大学附属义乌医院无多重耐药危险医院获得性肺炎（HAP）病原菌分布特点及耐药性。方法人选无多药耐药危险因素的医院获得性肺炎（HAP）患者352例,按照发病时间分为早发HAP组与晚发HAP组,采集合格痰标本,进行细菌分离、鉴定和药敏试验,并分析比较患者病原菌分布特点及耐药性。结果人选的352例患者共分离m393株病原菌,HAP最常见的病原菌排名前五位的分别是为肺炎克雷伯杆菌、大肠埃希菌、铜绿假单胞菌、金黄色葡萄球菌及鲍曼不动杆菌,早发HAP排名前五位的分别是肺炎克雷伯杆菌、大肠埃希菌、金黄色葡萄球菌、肺炎链球菌和铜绿假单胞菌,晚发HAP排名前五位的分别是肺炎克雷伯杆菌、大肠埃希菌、铜绿假单胞菌、鲍曼不动杆菌和金黄色葡萄球菌,两组患者革兰阳性菌与革兰阴性菌所占比例差异无统计学意义（P〉0．05）,78株革兰阳性菌对常用抗生素的耐药率早发与晚发HAP差异无统计学意义（P〉0．05）,296株革兰阴性菌对常用抗生素的耐药率,早发HAP与晚发HAP除了对哌拉西林和阿莫西林克拉维酸钾的耐药率差异有统计学意义（P〈0．05）,其余的差异有统计学意义（P〉0．05）,但是晚发HAP中检出耐甲氧西林金葡菌（MRSA）、产ESBLs肺炎克雷伯杆菌及耐碳青霉烯鲍曼不动杆菌（CR—AB）比例增高。结论无多重耐药危险因素的医院获得性肺炎（HAP）患者,早发与晚发HAP感染病原菌差别不大,虽晚发HAP的耐药率相对较高,但对大部分抗菌素敏感,所以适当使用抗菌素,对于减轻选择抗菌药物的压力、减少耐药菌株的产生和二重感染有重要意义。     

Changes in lactate dehydrogenase activity in chicken tissues in hyperthyreosis in ontogenesis

The lactate dehydrogenase activity in reactions of lactate oxidation and synthesis was studied in subfractions of the chicken brain, heart and liver at the embryonal, early postembryonal and adult stages of development after thyroxine administration. It has been shown that during embryogenesis thyroxine predominantly enhanced the rate of lactate oxidation in the mitochondrial tissues. A marked increase in the lactate synthesis was found in cytoplasm of the adult chicken tissues. Specificity of enzyme activity alterations was detected in the chicken brain during ontogenesis after thyroxine administration.     

Role for dopamine in malonate-induced damage in vivo in striatum and in vitro in mesencephalic cultures

Defects in mitochondrial energy metabolism have been implicated in the pathology of several neurodegenerative disorders. In addition, the reactive metabolites generated from the metabolism and oxidation of the neurotransmitter dopamine (DA) are thought to contribute to the damage to neurons of the basal ganglia. We have previously demonstrated that infusions of the metabolic inhibitor malonate into the striata of mice or rats produce degeneration of DA nerve terminals. In the present studies, we demonstrate that an intrastriatal infusion of malonate induces a substantial increase in DA efflux in awake, behaving mice as measured by in vivo microdialysis. Furthermore, pretreatment of mice with tetrabenazine (TBZ) or the TBZ analogue Ro 4-1284 (Ro-4), compounds that reversibly inhibit the vesicular storage of DA, attenuates the malonate-induced DA efflux as well as the damage to DA nerve terminals. Consistent with these findings, the damage to both DA and GABA neurons in mesencephalic cultures by malonate exposure was attenuated by pretreatment with TBZ or Ro-4. Treatment with these compounds did not affect the formation of free radicals or the inhibition of oxidative phosphorylation resulting from malonate exposure alone. Our data suggest that DA plays an important role in the neurotoxicity produced by malonate. These findings provide direct evidence that inhibition of succinate dehydrogenase causes an increase in extracellular DA levels and indicate that bioenergetic defects may contribute to the pathogenesis of chronic neurodegenerative diseases through a mechanism involving DA.     

Scurvy in capybaras bred in captivity in Argentine

In order to determine if the absence of vitamin C in the diet of capybaras (Hydrochoerus hydrochaeris) causes scurvy, a group of seven young individuals were fed food pellets without ascorbic acid, while another group of eight individuals received the same food with 1 g of ascorbic acid per animal per day. Animals in the first group developed signs of scurvy-like gingivitis, breaking of the incisors and death of one animal. Clinical signs appeared between 25 and 104 days from the beginning of the trial in all individuals. Growth rates of individuals deprived of vitamin C was considerably less than those observed in the control group. Deficiency of ascorbic acid had a severe effect on reproduction of another population of captive capybaras. We found that the decrease in ascorbic acid content in the diet affected pregnancy, especially during the first stages. The results obtained suggest that it is necessary to supply a suitable quantity of vitamin C in the diet of this species in captivity.     

SSTR5 ablation in islet results in alterations in glucose homeostasis in mice

Somatostatin (SST) peptide is a potent inhibitor of insulin secretion and its effect is mediated via somatostatin receptor 5 (SSTR5) in the endocrine pancreas. To investigate the consequences of gene ablation of SSTR5 in the mouse pancreas, we have generated a mouse model in which the SSTR5 gene was specifically knocked down in the pancreatic beta cells (betaSSTR5Kd) using the Cre-lox system. Immunohistochemistry analysis showed that SSTR5 gene expression was absent in beta cells at three months of age. At the time of gene ablation, betaSSTR5Kd mice demonstrated glucose intolerance with lack of insulin response and significantly reduced serum insulin levels. Insulin tolerance test demonstrated a significant increase of insulin clearance in vivo at the same age. In vitro studies demonstrated an absence of response to SST-28 stimulation in the betaSSTR5Kd mouse islet, which was associated with a significantly reduced SST expression level in betaSSTR5Kd mice pancreata. In addition, betaSSTR5Kd mice had significantly reduced serum glucose levels and increased serum insulin levels at 12 months of age. Glucose tolerance test at an older age also indicated a persistently higher insulin level in betaSSTR5Kd mice. Further studies of betaSSTR5Kd mice had revealed elevated serum C-peptide levels at both 3 and 12 months of age, suggesting that these mice are capable of producing and releasing insulin to the periphery. These results support the hypothesis that SSTR5 plays a pivotal role in the regulation of insulin secretion in the mouse pancreas.