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    Antimicrobial resistance pattern in ventilator-associated pneumonia in an intensive care unit of Babol, northern Iran

    2018-06-20 07:17:42MahmoudSadeghiHaddadZavarehHadiAhmadiJouybariMostafaJavanianMehranShokriMasomehBayaniMohammadRezaHasanjaniRoushanArefehBabazadehSoheilEbrahimpourParvizAmriMaleh
    Journal of Acute Disease 2018年2期
    關(guān)鍵詞:山石波段器材

    Mahmoud Sadeghi-Haddad-Zavareh, Hadi Ahmadi Jouybari, Mostafa Javanian, Mehran Shokri, Masomeh Bayani, Mohammad Reza Hasanjani Roushan, Arefeh Babazadeh, Soheil Ebrahimpour, Parviz Amri Maleh

    1Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, I.R. Iran

    2Department of Anesthesiology, School of Medicine, Babol University of Medical Sciences, Babol, I.R. Iran

    1. Introduction

    Ventilator-associated pneumonia (VAP) is one of the most common infectious complications and the leading cause of death in intensive care units (ICUs)[1,2]. VAP based on time event is divided into two types: early VAP that occurs within 4 d and late VAP which happens after the 5thday of hospitalization[3]. Risk factors of VAP include oropharyngeal colonization, trauma, surgery,imunosuppression, old age, urgent intubation, prolonged admission in ICU, sedative drugs steroids usage and previous hospitalization.Prevalent etiological agents in generating VAP in several studies consist ofStaphylococcus aureus (S. aureus),Pseudomonas. aeruginosa(P. aeruginosa),Acinetobacter baumannii (A. baumannii)[4,5].Generally, etiological agents of VAP are different based on hospital or geographical position and their antibiotic resistance rates is also different among various areas[6]. The results of the different studies show that resistance rates of bacteria are increasing[7]. Increasing resistance to antibiotics raises the mortality rate, admission duration and expenses, in patients who suffer VAP in ICU. The mortality rate in VAP was reported 20%– 76% in different studies[8,9].

    In various studies ofP. aeruginosaandA. baumanniiin VAP the mortality of was 65% and 87% and for MRSA to was 84%[10].

    In some study, using antibiotics of choice for treating VAP based on antibiotic resistance pattern in the same hospitals could decrease usage of inappropriate antibiotics and increase treatment success[11]. Considering that a study based on Bronchoscopy sampling method and bronchoalveolar lavage (BAL) and quantitative culture performance and investigating microorganisms resistance with microdilution method and determining minimal inhibitory concentration (MIC) of antibiotic, has not been carried out so far in ICU of Ayatollah Rouhani Hospital of Babol (northern Iran), this study was done with the purpose of determining microorganisms involved in creating pneumonia from ventilation and their antibiotic resistance evaluation noticing method above.

    2. Materials and methods

    This cross sectional study was conducted on 50 patients suffering ventilator associated pneumonia in ICU of Ayatollah Rouhani Hospital of Babol during the 2014–2015.

    In this study with daily visit of hospitalized patients in Ayatollah Rouhani ICU, considering clinical criteria based on Clinical Pulmonary Infection Score (CPIS), patients who at least acquired six points based on CPIS and from the clinical signs, diagnosis of pnenumonia was possible for them, were under sampling method BAL and bronchoscopy[12]. The samples were cultured in blood agar and MacConkey agar, and culture media after 24–48 h incubation at(35±2) °C were evaluated. Samples were cultured under quantitative method and if growth of more than 104CFU/mL bacteria were detected presumped as VAP etiological agents, in next step for determining sensitivity of microorganisms, Broth microdilution method was used. Ninety six part microplate which was applied in this method, has 12 columns that hole of the 11thcolumn as negative control and the 12thcolumn as positive control were used. In hole of the first group and the first hole of negative control, 200 mL of brain heart infusion (BHI) culture area of broth were poured and then in the rest of holes, 100 mL of BIH broth area were added. In the next step, antibiotic were added to the entire first column hole and the first hole of negative column and then based on standard method, suitable dilution of antibiotic in holes were prepared and after that diluted bacteria suspension to 0.1 and 5 mL of bacteria was added to holes except the negative control hole. Eventually,the final volume of all holes was 100 mL. The negative control was without bacteria and positive control was without antibiotic. Then micro plate were incubated in the temperature of 37 ℃ for 24 h.After 24 h micro plate were investigated under the light of the lamp and the last hole which turbidity wasn’t seen in it, was considered as MIC and by comparison with the table CLSI 20/3, resistance,semi-sensitivity or sensitivity of the bacteria relative to antibiotic was reported[13]. In this study, the investigated antibiotics for grampositive bacteria included nafcillin, cloxacillin, co-trimoxazole,cefazolin, vancomycin and the investigated antibiotics for gramnegative bacteria included ciprofloxacin, ceftazidime, piperacillin/tazobactam, gentamycin, amikacin, cefepime, clavulanate/ticarcillin,meropenem and imipenem.

    All of the applied antibiotics in this recent study were produced and made by German company Merk and information yield from.All data were analyzed by SPSS software 16.

    3. Results

    Of the 50 patients who suffer VAP in our study, 33 (66%) are male and 17 (34%) were female. The mean age of the patients was 67.43 year old. Among the patients 52% previously admitted in hospital and 60% had a history of antibiotic use in past 3 months(Table 1).the most common cause of admission of patients was neurologic disease (36%) and then respiratory disease. 12% of patients admitted with sepsis. And16%of patients was on stroid therapy. Demographic data of the patients are shown in Table 1.The most common microorganisms in our study wereA. baumannii(70%),P. aeruginosa(12%),S. aureus(8%) andKlebsiella pneumonia(K.pneumonia)(6%). Meanwhile, from these 50 investigated samples, two samples (4%) did not grow in culture media.

    3.1. Evaluation of antibiotics resistance based on microdilution method in Acinetobacterbaumannii

    Five antibiotics did not have any effect on 35 samples ofA.baumanniiin our study including that ciprofloxacin, ceftazidime,amikacin, clavulanate/ticarcillin and cefepime. Meropenem,imipenem and piperacillin/tazobactam had 97.1% resistance respectively, and gentamycine had 94.3% resistance (Table 1).

    Table 1Resistance pattern of antibiotics in A. baumannii [n, (%)].

    3.2. Evaluation of antibiotic resistance based on micro dilution method in P. aeruginosa

    In our study, the most resistance was related to ceftazidime,clavulanate/ticarcillin, cefepime, (each with 66.7% resistance) and the least resistance was related to imipenem (16.7%) and gentamycin(16.7%) (Table 2).

    Table 2Resistance pattern of antibiotics in P. aeruginosa [n, (%)].

    3.3. Evaluation of antibiotic resistance based on microdilution method in K. pneumonia

    Among the three samples ofK. pneumoniain our study, the most resistance was related to ceftazidime, cefepime and clavulanate/ticarcillin eaach with 100% of resistance. Gentamycin, meropenem,imipenem, piperacillin/tazobactam and ciprofloxacin each with 33.3% had the least resistance (Table 3).

    Table 3Resistance pattern of antibiotics in K. pneumonia[n, (%)].

    3.4. Evaluation of antibiotic resistance based on microdilution method in S. aureus

    Among the four samples ofS. aureusin our study, resistance to cloxacillin and nafcillin was 75%. 25% of cases were sensitive to cotrimoxazole and no complete resistance to vancomycin was reported(Table 4).

    Table 4Resistance pattern of antibiotics in S. aureus [n, (%)].

    4. Discussion

    Considering the extension of antibiotic resistance, early diagnosis of VAP and identification of the type of microorganisms and antibiotics resistance pattern, can modify the method of antibiotic prescription and as result decrease medication resistance. In our study the most common microorganisms of causing VAP wereA.baumannii,P. aeruginosaandS. aureusthat these results are similar to other studies[14-16].

    The resistance rate ofA. baumanniito carbapenemes like imipenem and meropenem in our study was 97.1% and in study done with Balkhyet al., in Saudi Arabia was 64.1% and in study of Salehifaret al., in Imam khomeili hospital of sari (Iran) was 100%[15,16]. In current study, the resistance rate ofP. aeruginosato carbapenem as meropenem was 33.3% and to imipenem 16.7%,while the resistance rate to carbapenem was reported 14.7% in study of Jamaatiet al, that was accomplished in Masih Daneshvari hospital of Tehran and it was reported 32.8% by Balkhyet al., in Saudi Arabia[16].

    The resistance rate ofS. aureusin our study to nafcillin and cloxacillin was 75% and it was reported 80%, 41.1%, 65.4% and 66.7% bysome studies[16-18]. One of the features of this study in comparison with many other studies, like the study was carried outby Aziz Japoniet al., in shiraz in 2008–2009 and Balkhyet al.,study that was done in Saudi Arabia in 2004 to 2009 was related to sampling method that in our study bronchoscopy method and BAL were applied which were often more precise than ETA method[16,19].Also, in our study one of the characteristics was using CPIS and performing quantitative culture in order to positive consideration of BAL sample with colon of more than 104cfu/mL[10,20]. The value of quantitative culture was much more than qualitative culture for diagnosing and deciding to start the treatment of VAP.

    The prevalence ofA. baumanniiin our study was 70% and it was reported by some studies 35.1%, 29% and 18% which shows that high prevalence ofA. baumanniias a producing organism of VAP at our hospital relative to the other studies and can be a serious warning in outbreaks of hospital acquired infections caused byA.baumannii[15, 17].

    The clear role ofA. baumanniitypes among gram-negative microorganisms in hospital acquired infections like bacteremia,urinary tract infection, soft tissue infections and especially VAP and also high ability of these microorganisms in generating antibiotic resistance with various mechanisms, now a days is a major problem[21,22]. Various studies about antibiotic resistance ofA. baumanniiwas carried out which often they have reported high resistance of this microorganism[23,24].

    In many countries, in case of severe infections ofA. baumannii.Use of carbapenems as a treatment choice is a rule but resistance toward them is also increasing[25-27].

    The most common microorganisms involved in wereA.baumannii,P. aeruginosaandS. aureusthat among themA.baumanniiwas much more one and antibiotic resistance on all of the investigated antibiotics was about 100%. Noticing the results, high resistance of gram negative organisms to ceftazidime, cefepime and clavulanate/ticarcillin makes their use in empirical treatment of the VAP patients not appropriate.

    坑道工程口部偽裝是工程防護(hù)重要研究方向之一,一些工程在施工過程中破壞了原有地貌,偽裝時(shí)需要輕質(zhì)仿石器材來模擬口部附近的真山石,造成口部是一些普通石塊的假象,從而形成有效欺騙。隨著園林行業(yè)的發(fā)展、仿石技術(shù)的進(jìn)步,在可見光波段模擬山石已非難事。然而軍事偵察主要波段除了可見光外還有近紅外、熱紅外、雷達(dá)等波段[1-3],而真山石的光學(xué)、熱紅外和雷達(dá)波段特征具有獨(dú)特性,園林仿石很容易被揭露。所以,能起到偽裝作用的仿石器材需要一些新技術(shù)、新材料才能達(dá)到對抗多頻譜偵察的需要。

    Conflict of interest statement

    The authors declare that there is no conflict of interest.

    [1] Rea-Neto A, Youssef NCM, Tuche F, Brunkhorst F, Ranieri VM, Reinhart K, et al. Diagnosis of ventilator-associated pneumonia: A systematic review of the literature.Crit Care2008; 12(2): R56.

    [2] Shokri M, Ghasemian R, Bayani M, Maleh VA, Kamrani M, Sadeghi-Haddad-Zavareh M, et al. Serum and alveolar procalcitonin had a weak diagnostic value for ventilator-associated pneumonia in patients with pulmonary infection score≥ 6.Rom J Intern Med2018; 56(1): 9-14.

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    [4] Resende MM, Monteiro SG, Callegari B, Figueiredo PM, Monteiro CR,Monteiro-Neto V. Epidemiology and outcomes of ventilator-associated pneumonia in northern Brazil: An analytical descriptive prospective cohort study.BMC Infect Dis2013; 13(1): 119.

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    [6] Koenig SM, Truwit JD. Ventilator-associated pneumonia: diagnosis,treatment, and prevention.Clin Microbiol Rev2006; 19(4): 637-657.

    [7] Chi SY, Kim TO, Park CW, Yu JY, Lee B, Lee HS, et al. Bacterial pathogens of ventilator associated pneumonia in a tertiary referral hospital.Tuberc Respir Dis2012; 73(1): 32-37.

    [8] Alp E, Voss A. Ventilator associated pneumonia and infection control.Ann Clin Microbiol Antimicrob2006; 5(1): 7.

    [9] Banjar A, Felemban M, Dhafar K, Gazzaz Z, Al Harthi B, Baig M, et al.Surveillance of preventive measures for ventilator associated pneumonia(VAP) and its rate in Makkah Region hospitals, Saudi Arabia.Turk J Med Sci2017; 47(1): 211-216.

    [10] Chastre J, Fagon J-Y. Ventilator-associated pneumonia.Am J Respir Crit Care Med2002; 165(7): 867-903.

    [11] Porzecanski I, Bowton DL. Diagnosis and treatment of ventilatorassociated pneumonia.Chest J2006; 130(2): 597-604.

    [12] Saensom D, Merchant A, Wara-aswapati N, Ruaisungnoen W, Pitiphat W. Oral health and ventilator-associated pneumonia among critically ill patients: A prospective study.Oral Dis2016; 22(7): 709-714.

    [13] Yayan J, Ghebremedhin B, Rasche K. Antibiotic resistance ofP.aeruginosain pneumonia at a single university hospital center in germany over a 10-year period.PLos One2015; 10(10): e0139836.

    [14] Jamaati HR, Malekmohammad M, Hashemian MR, Nayebi M,Basharzad N. Ventilator-associated pneumonia: Evaluation of etiology,microbiology and resistance patterns in a tertiary respiratory center.Tanaffos2010; 9(1): 21-27.

    [15] Salehifar E, Abedi S, Mirzaei E, Kalhor S, Eslami G, Ala S, et al.Profile of microorganisms involved in nosocomial pneumonia and their antimicrobial resistance pattern in intensive care units of Imam Khomeini Hospital, Sari, 2011–2012.J Mazandaran Univ Med Sci2013.

    [16] Balkhy HH, El-Saed A, Maghraby R, Al-Dorzi HM, Khan R, Rishu AH,et al. Drug-resistant ventilator associated pneumonia in a tertiary care hospital in Saudi Arabia.Ann Thorac Med2014; 9(2): 104.

    [17] Rocha LdAd, Vilela CAP, Cezário RC, Almeida AB, Gontijo Filho P.Ventilator-associated pneumonia in an adult clinical-surgical intensive care unit of a Brazilian university hospital: incidence, risk factors,etiology, and antibiotic resistance.Braz J Infect Dis2008; 12(1): 80-85.

    [18] Magazine R, Chogtu B, Rao S, Chawla K. Bacterial isolates from the bronchoalveolar lavage fluid of patients with pneumonia not responding to initial antimicrobial therapy.Sahel Med J2013; 16(3): 102.

    [19] Japoni A, Vazin A, Davarpanah MA, Ardakani MA, Alborzi A, Japoni S,et al. Ventilator-associated pneumonia in Iranian intensive care units.J Infect Dev Countr2011; 5(4): 286-293.

    [20] Sanchez-Nieto J, Torres A, Garcia-Cordoba F, El-Ebiary M, Carrillo A, Ruiz J, et al. Impact of invasive and noninvasive quantitative culture sampling on outcome of ventilator-associated pneumonia: A pilot study.Am J Respir Crit Care Med1998; 157(2): 371-376.

    [21] Dijkshoorn L, Nemec A, Seifert H. An increasing threat in hospitals:multidrug-resistantA. baumannii.Nature Rev Microbiol2007; 5(12): 939-951.

    [22] Schmier J, Hulme-Lowe C, Klenk J, Sulham K. Economic burden and healthcare resource utilization associated with multi-drug resistantA.baumannii: A structured review of the literature.J Pharma Care Health Sys2016; 3(155): 2376-0419.1000155.

    [23] Mugnier PD, Poirel L, Naas T, Nordmann P. Worldwide dissemination of the blaOXA-23 carbapenemase gene ofA. baumannii1.Emerg Infect Dis2010; 16(1): 35.

    [24] Morovat T, Bahram F, Mohammad E, Setareh S, Mohamad Mehdi F.Distribution of different carbapenem resistant clones ofA. baumanniiin Tehran hospitals.New Microbiol2009; 32(3): 265.

    [25] Dent LL, Marshall DR, Pratap S, Hulette RB. Multidrug resistantA.baumannii: A descriptive study in a city hospital.BMC Infect Dis2010;10(1): 196.

    [26] Taherikalani M, Etemadi G, Geliani KN, Fatollahzadeh B, Soroush S, Feizabadi MM. Emergence of multi and pan-drug resistanceA.baumanniicarrying blaOXA-type-carbapenemase genes among burn patients in Tehran, Iran.Saudi Med J2008; 29(4): 623-624.

    [27] Higgins PG, Dammhayn C, Hackel M, Seifert H. Global spread of carbapenem-resistantA. baumannii.J Antimicrob Chemother2009; 65(2):233-238.

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