阿米卡星聯(lián)合抗假單胞菌β-內(nèi)酰胺類抗菌藥物經(jīng)驗性治療醫(yī)院獲得性肺炎的系統(tǒng)評價
[Abstract]:Objective:
The effectiveness and safety of the initial empirical treatment of hospital acquired pneumonia (Hospital acquired pneumonia, HAP) with Amikacin combined with anti Pseudomonas p- lactam antibiotics was evaluated by the Cochrane system evaluation method.
Method:
According to the standard of Cochrane Collaboration, the computer completely retrieves CENTRAL (Cochrane library clinical controlled trial center database, seventh period 2012), MEDLINE (1950 ~ 2012.11), EMBASE (1980 ~ 2012.11), Chinese biomedical literature database (CBM, 1970 to 2012.11), Chinese Journal Network full text database (CNKI, 1970 to 2012.11), VP number According to the library (VIP, 1970 ~ 2012.11), conference data and Internet data, retrieval of non limited languages, the clinical randomized controlled trial (Randomized controlled trials, RCT) for the empirical treatment of HAP for beta lactam antibiotics against Pseudomonas aeruginosa (Randomized trials, RCT) was collected and the risk of bias was evaluated by two independent evaluators. Cross check the relevant data, such as disagreement can be discussed or third into arbitration with relevant professional knowledge. Treatment efficiency, failure rate, bacteriological clearance rate, Pseudomonas aeruginosa clearance rate, double infection rate, mortality and adverse reaction rate are the outcome indicators of Amikacin combined with anti Pseudomonas p- The efficacy and safety of empirical treatment of HAP with lactam antibiotics were evaluated. RevMan 5.2 software was used to analyze the data.
Result:
Finally, a total of 6 RCT and 703 HAP patients were included in the study. The quality of.2 research was higher and the quality of the 4 studies was lower.
1. Amikacin combined with ceftazidime VS meropenem: the clinical treatment failure rate of Amikacin combined with ceftazidime was higher than meropenem, with a statistically significant difference of [RR=1.73,95%CI (1.01,2.98)]; in clinical treatment, bacteriological clearance rate, Pseudomonas aeruginosa clearance rate, double infection rate, mortality, and bad condition There were no statistical differences between the two groups (the results were RR=0.82,95%CI (0.67,1.01); RR=0.82,95%CI (0.67,1.01); RR=0.87,95%CI (0.58,1.31); RR=1.12,95%CI (0.66,1.92); RR=0.58,95%CI (0.14,2.35); RR=1.21,95%CI (0.69,2.14)).
2. Amikacin combined with Pseudomonas sp. B- lactam drugs VS quinolone antibiotics combined with Pseudomonas beta lactam: Amikacin combined with Pseudomonas beta lactam for the empirical treatment of HAP, the bacterial clearance rate is superior to quinolone antibiotics combined with Pseudomonas beta lactam drugs, Statistical significance [RR=1.34,95%CI (1.07,1.67)]; there were no statistical differences in the two groups of Pseudomonas aeruginosa clearance rate, double infection rate and mortality rate (RR=1.13,95%CI (0.74,1.73), RR=1.05,95%CI (0.24,4.59), RR=0.88,95%CI (0.55,1.43)).
3. Amikacin combined cefepime VS cefepime single use: the clinical efficacy of HAP combined with cefepime in combination with cefepime, the bacterial clearance rate is better than cefepime alone, with statistical differences (RR=1.25,95%CI (1.09,1.45) and RR=l.32,95%CI (1.09,1.59), respectively, and the failure rate is lower than cefepime alone. [RR=0.38,95%CI (0.20,0.72)); there were no statistical differences in the two groups of Pseudomonas aeruginosa clearance rate, double infection rate and mortality rate (RR=1.29,95%CI (0.9,1.72); RR=3.16,95%CI (0.36,27.78); RR=1.85,95%CI (0.37,9.18)).
Conclusion:
The systematic evaluation showed the effectiveness and safety of Amikacin combined with p- lactam drug for the treatment of HAP. The evidence supported by the drug was low in quality and weak recommendation. The number of studies included is small, the sample size is small, and most of the research methodology is not high, and more high quality and large-scale RCT is needed. When the evidence is applied, the evidence is applied. Be careful.
【學(xué)位授予單位】:湖南師范大學(xué)
【學(xué)位級別】:碩士
【學(xué)位授予年份】:2013
【分類號】:R96;R563.1
【參考文獻(xiàn)】
相關(guān)期刊論文 前10條
1 肖瑤;;細(xì)菌耐藥機(jī)制研究進(jìn)展[J];北京醫(yī)學(xué);2011年03期
2 聶大平;董楓;石宏宴;;左氧氟沙星、環(huán)丙沙星單用和聯(lián)合其他抗菌藥物對銅綠假單胞菌防突變濃度的研究[J];中國感染控制雜志;2007年06期
3 張櫻,陳亞崗,楊青;不動桿菌感染及耐藥機(jī)制的研究進(jìn)展[J];國外醫(yī)學(xué).流行病學(xué)傳染病學(xué)分冊;2005年02期
4 鄭衛(wèi);氨基糖苷類抗生素研究的新進(jìn)展[J];國外醫(yī)藥(抗生素分冊);2005年03期
5 李政;;醫(yī)院獲得性肺炎的主要致病菌及耐藥現(xiàn)狀[J];華夏醫(yī)學(xué);2012年03期
6 陳勁龍;謝長江;馬洪明;;廣州地區(qū)老年患者醫(yī)院獲得性肺炎致病菌288株及耐藥情況分析[J];廣東醫(yī)學(xué);2012年07期
7 李耘;呂媛;鄭波;;衛(wèi)生部全國細(xì)菌耐藥監(jiān)測網(wǎng)2011年度非發(fā)酵革蘭陰性桿菌耐藥監(jiān)測[J];中國臨床藥理學(xué)雜志;2012年12期
8 呂媛;王珊;;衛(wèi)生部全國細(xì)菌耐藥監(jiān)測網(wǎng)2011年度腸桿菌科細(xì)菌耐藥監(jiān)測[J];中國臨床藥理學(xué)雜志;2012年12期
9 黃蓓潔;羅艷蓉;;產(chǎn)超廣譜β內(nèi)酰胺酶細(xì)菌感染抗菌治療概況[J];中國感染與化療雜志;2009年06期
10 由然;孫立穎;;耐阿米卡星銅綠假單胞菌氨基糖苷類耐藥基因及其基因型研究[J];檢驗醫(yī)學(xué);2010年05期
,本文編號:2156089
本文鏈接:http://sikaile.net/yixuelunwen/huxijib/2156089.html