王新 蘇新曼 郭昕卉 張維福 郭強(qiáng)
[摘要]目的了解有無(wú)心臟基礎(chǔ)疾病的感染性心內(nèi)膜炎患者致病菌感染譜和耐藥性的變化,為臨床經(jīng)驗(yàn)性使用抗菌藥物提供依據(jù)。方法選擇2018年1月至2020年12月在山東第一醫(yī)科大學(xué)第二附屬醫(yī)院和濟(jì)南市第五人民醫(yī)院住院的感染性心內(nèi)膜炎患者171例為研究對(duì)象,按有無(wú)心臟基礎(chǔ)性疾病,分成 A 組(無(wú)心臟基礎(chǔ)性疾?。┖?B 組(有心臟基礎(chǔ)性疾病),分別進(jìn)行靜脈血培養(yǎng),分離菌株,分析病原菌分布;分析主要革蘭陽(yáng)性菌和革蘭陰性菌耐藥性,比較兩組的差異性。結(jié)果 A 組83例患者中檢出病原菌103株,其中革蘭陽(yáng)性菌主要為草綠色鏈球菌、金黃色葡萄球菌,革蘭陰性菌主要為大腸埃希菌、鮑氏不動(dòng)桿菌;革蘭陽(yáng)性菌占比高于革蘭陰性菌株、真菌,革蘭陰性菌株高于真菌,差異有統(tǒng)計(jì)學(xué)意義( P <0.05)。B 組88例患者中檢出病原菌99株,其中革蘭陽(yáng)性菌主要為草綠色鏈球菌、金黃色葡萄球菌,革蘭陰性主要為大腸埃希菌、鮑氏不動(dòng)桿菌,革蘭陽(yáng)性菌占比高于革蘭陰性菌株、真菌,革蘭陰性菌株高于真菌,差異有統(tǒng)計(jì)學(xué)意義(P <0.05)。兩組患者主要致病菌是草綠色鏈球菌和金黃色葡萄球,A 組革蘭陰性菌和真菌顯著高于 B 組,革蘭陽(yáng)性菌顯著低于 B 組,差異有統(tǒng)計(jì)學(xué)意義( P <0.05)。藥敏結(jié)果顯示兩組草綠色鏈球菌對(duì)青霉素耐藥率均較高,對(duì)左氧氟沙星、利福平耐藥率均較低,對(duì)莫西沙星、萬(wàn)古霉素、利奈唑胺均不耐藥;兩組金黃色葡萄球菌對(duì)青霉素、氨芐西林耐藥率均較高,對(duì)左氧氟沙星、萬(wàn)古霉素耐藥率差別較大,差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)利奈唑胺均不耐藥;兩組大腸埃希菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮耐藥率均較高,對(duì)慶大霉素、阿米卡星耐藥率差別較大,差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)左氧氟沙星、環(huán)丙沙星、美羅培南、亞胺培南均不耐藥;鮑氏不動(dòng)桿菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮、哌拉西林耐藥率均較高,對(duì)環(huán)丙沙星、阿米卡星耐藥率均較低,對(duì)左氧氟沙星、美羅培南差異較大,差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)亞胺培南均不耐藥。結(jié)論了解有無(wú)心臟基礎(chǔ)性疾病,初步判斷感染性心內(nèi)膜炎患者致病菌感染譜分布、掌握細(xì)菌耐藥的最新動(dòng)態(tài)變遷,指導(dǎo)臨床合理應(yīng)用抗菌藥物。
[關(guān)鍵詞]感染性心內(nèi)膜炎;病原菌;抗菌藥物;耐藥性
[中圖分類號(hào)] R542.41? [文獻(xiàn)標(biāo)識(shí)碼] A?? [文章編號(hào)]2095-0616(2021)23-0209-06
Clinical? study? on? bacterial? culture? and? antimicrobial? drug selection in patients with infective endocarditis
WANG? Xin1????? SU? Xinman2????? GUO? Xinhui3????? ZHANG? Weifu1????? GUO? Qiang4
1.Department of Public Health, the Second Affiliated Hospital of Shandong First Medical University, Shandong, Tai'an 271000, China;2. Intensive Care Unit, the Second People's Hospital of Juancheng County in Shandong Province, Shandong, Juancheng 274600, China;3.Department of Cardiology, the Fifth People's Hospital ofJi'nan City, Shandong, Ji'nan 250022, China;4.Department of Infectious Diseases, the Second Affiliated Hospital of Shandong First Medical University, Shandong, Tai'an 271000, China
[Abstract] Objective To understand the changes in the infection spectrum and drug resistance of pathogenic bacteria in patients with infective endocarditis with or without underlying cardiac disease, so as to provide a basis for the empirical clinical use of antimicrobial drugs. Methods A total of 171 patients with infective endocarditis hospitalized in the Second Affiliated Hospital of Shandong First Medical University and the Fifth People's Hospital of Ji'nan City in Shandong Province from January 2018 to December 2020 were divided into group A (without underlying cardiac disease) and group B (with underlying cardiac disease) according to the presence or absence of underlying cardiac disease. The venous blood of the two groups of patients was collected and cultured, followed by isolatingstrains and analyzing the distribution of pathogenic bacteria. The drug resistance of major Gram-positive and Gram-negative bacteria in both groups was analyzed, and the differences between the two groups were compared. Results In group A, 103 pathogenic strains were detected in 83 patients, among which Gram-positive bacteria were mainly Streptococcus viridans and Staphylococcus aureus, and Gram-negative bacteria were mainly Escherichia coli and Acinetobacter baumannii. The proportion of Gram-positive strains was higher than that of Gram-negative strains and fungi, and the proportion of Gram-negative strains was higher than that of fungi, with statistically significant differences (P <0.05). A total of 99 pathogenic strains were detected in 88 patients in group B, among which Gram- positive bacteria were mainly Streptococcus viridans and Staphylococcus aureus, Gram-negative bacteria were mainly Escherichia coli and Acinetobacter baumannii. The proportion of Gram-positive strains was higher than that of Gram- negative strains and fungi, and the proportion of Gram-negative strains was higher than that of fungi, with statistically significant differences (P <0.05). The main pathogenic bacteria in both groups were Streptococcus viridans and Staphylococcus aureus, and the numbers of Gram-negative bacteria and fungi in group A were significantly higher than those in group B, while the number of the Gram-positive bacteria in group A was significantly lower than that in group B, with statistically significant differences (P <0.05). The drug sensitivity results showed that Streptococcus viridans in both groups had high resistance rate to penicillin, low resistance rate to levofloxacin and rifampicin, and no resistance to moxifloxacin, vancomycin and linezolid. The Staphylococcus aureus in both groups had high resistance rate to penicillin and ampicillin, and had a great difference in resistance rate to levofloxacin and vancomycin, but without statistically significant difference between the two groups (P >0.05). Meanwhile, the Staphylococcus aureus in both groups had no resistance to linezolid. The Escherichia coli in both groups had high resistance rate to cefazolin, ceftriaxone and cefoperazone, and had a great difference in resistance rate to gentamicin and amikacin, but without statistically significant difference between the two groups (P >0.05). Meanwhile, the Escherichia coli in both groups had no resistance to levofloxacin, ciprofloxacin, meropenem and imipenem. The Acinetobacter baumannii in both groups had high resistance rate to cefazolin, ceftriaxone, cefoperazone and piperacillin, low resistance rate to ciprofloxacin and amikacin, and had a great difference in resistance rate to levofloxacin and meropenem, but without statistically significant difference between the two groups (P >0.05). Meanwhile, the Acinetobacter baumannii had no resistance to imipenem. Conclusion It is necessary to understand the presence of underlying cardiac diseases and preliminarily determine the distribution of the infection spectrum of pathogenic bacteria in patients with infective endocarditis, as well as grasp the latest dynamic changes in bacterial resistance, so as to guide the rational application of antimicrobial drugs in clinic.
[Key words] Infective endocarditis; Pathogenic bacteria; Antibacterial drugs; Drug resistance
感染性心內(nèi)膜炎(infective endocarditis, IE)是病原微生物感染心臟瓣膜或心室壁內(nèi)膜造成的炎癥,常有瓣膜贅生物形成[1],該病發(fā)病率及致死率均較高,且預(yù)后不理想[2-3]。臨床調(diào)查顯示,感染性心內(nèi)膜炎的住院死亡率約為7%,醫(yī)院感染性心內(nèi)膜炎患者的預(yù)后更差,病死率高達(dá)17.9%[4-5]。感染性心內(nèi)膜炎的臨床癥狀較多,同時(shí)也可能伴隨自身免疫疾病,這對(duì)該病的診斷干擾較大[6]。該病病灶較為隱蔽,病原菌血培養(yǎng)陽(yáng)性率較低,給臨床帶來(lái)較大困難。盡管有越來(lái)越廣譜的抗菌藥物,但死亡率仍達(dá)10%~50%[7]。確定 IE 致病菌分布及耐藥性的變化、選取敏感抗菌藥物治療對(duì)該病的預(yù)后至關(guān)重要。國(guó)內(nèi)外文獻(xiàn)資料顯示[8-10],IE 的病原菌發(fā)生了較大的變化,且存在地域差異。本研究旨在了解有無(wú)心臟基礎(chǔ)疾病的 IE 患者致病菌感染譜和耐藥性的差別,及時(shí)掌握病原菌耐藥的最新動(dòng)態(tài),指導(dǎo)臨床合理應(yīng)用抗菌藥物,現(xiàn)報(bào)道如下。
1資料與方法
1.1一般資料
171例 IE(診斷標(biāo)準(zhǔn)符合改良 Duke[11])患者來(lái)源于2018年1月至2020年12月期間山東第一醫(yī)科大學(xué)第二附屬醫(yī)院和濟(jì)南市第五人民醫(yī)院住院病例,男93例,女78例,年齡35~81歲,平均(52.7±6.3)歲。按有無(wú)心臟基礎(chǔ)性疾病,分成 A、B 兩組,A 組無(wú)心臟基礎(chǔ)性疾病83例,男45例,女38例,年齡35~79歲,平均(51.4±5.3)歲, B 組有心臟基礎(chǔ)性疾病88例,男48例,女40例,年齡36~81歲,平均(52.6±7.4)歲,其中先天性心臟病12例,風(fēng)濕性心臟瓣膜病25例,瓣膜置換術(shù)后17例,瓣膜修補(bǔ)術(shù)后34例。本研究已獲得山東第一醫(yī)科大學(xué)第二附屬醫(yī)院醫(yī)學(xué)倫理委員會(huì)批準(zhǔn),所有患者均對(duì)研究?jī)?nèi)容知情同意并簽署知情同意書。
納入標(biāo)準(zhǔn):①所有選取的病例診斷均符合改良 Duke[11]標(biāo)準(zhǔn),臨床資料完整;②血培養(yǎng)結(jié)果陽(yáng)性;③年齡18~90歲。
排除標(biāo)準(zhǔn):①不符合改良 Duke[11]診斷標(biāo)準(zhǔn),臨床資料不完整者;②合并嚴(yán)重腦、肝、腎、肺等其他嚴(yán)重疾病者;③血液標(biāo)本污染者;④存在嚴(yán)重免疫抑制者;⑤入院前開始抗感染治療者;⑥依從性差或拒絕合作者。
1.2標(biāo)本采集和菌株鑒定
在應(yīng)用抗菌藥物之前,所有患者均采集20 ml 靜脈血液標(biāo)本,需氧瓶、厭氧瓶分別注入10 ml。血培養(yǎng)瓶在2 h 內(nèi)放入梅里埃 BACT/ALERT 3D 培養(yǎng)系統(tǒng)進(jìn)行培養(yǎng)7 d,陽(yáng)性標(biāo)本用 Phoenix.100全自動(dòng)微生物鑒定儀進(jìn)行菌株鑒定。
1.3藥敏試驗(yàn)
依據(jù)美國(guó)臨床實(shí)驗(yàn)室標(biāo)準(zhǔn)化(clinical and laboratory standards institute,CLSI)標(biāo)準(zhǔn)[12-14]及《全國(guó)臨床檢驗(yàn)操作規(guī)程(第4版)》[15]敏感度判定依據(jù),分離菌株和質(zhì)控菌株的藥敏試驗(yàn)應(yīng)用 AMS 配套藥敏進(jìn)行。質(zhì)控菌株同時(shí)進(jìn)行 K-B 法藥敏試驗(yàn)。質(zhì)控菌(國(guó)家藥品生物制品鑒定所提供)為金黃色葡萄球菌(ATCC25923)、大腸埃希菌(ATCC25922)、肺炎鏈球菌(ATCC49619)、腸球菌(ATCC29212)和銅綠假單胞菌(ATCC27853)。
1.4統(tǒng)計(jì)學(xué)方法
采用 SPSS 22.0統(tǒng)計(jì)學(xué)軟件進(jìn)行數(shù)據(jù)處理,計(jì)量資料用(x ±s)表示,組間比較采用 t 檢驗(yàn),計(jì)數(shù)資料用[n (%)]表示,組間比較采用χ2檢驗(yàn),P <0.05為差異有統(tǒng)計(jì)學(xué)意義。
2結(jié)果
2.1兩組患者性別、年齡比較
兩組患者性別、年齡比較,差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05)。見(jiàn)表1。
2.2兩組的病原菌分布
2.2.1 A 組的病原菌分布 A 組檢出病原菌103株,其中革蘭陽(yáng)性菌59株、革蘭陰性菌34株、真菌10株,革蘭陽(yáng)性菌主要為草綠色鏈球菌、金黃色葡萄球菌,革蘭陰性菌主要為大腸埃希菌、鮑氏不動(dòng)桿菌;革蘭陽(yáng)性菌占比遠(yuǎn)高于革蘭陰性菌株、真菌,革蘭陰性菌株高于真菌,差異有統(tǒng)計(jì)學(xué)意義( P <0.05)。見(jiàn)表1。
2.2.2 B 組的病原菌分布 B 組檢出病原菌99株,其中革蘭陽(yáng)性菌79株、革蘭陰性菌19株、真菌1株,革蘭陽(yáng)性菌主要為草綠色鏈球菌、金黃色葡萄球菌,革蘭陰性菌主要為大腸埃希菌、鮑氏不動(dòng)桿菌;革蘭陽(yáng)性菌占比高于革蘭陰性菌株、真菌,革蘭陰性菌株高于真菌,差異均有統(tǒng)計(jì)學(xué)意義( P <0.05)。見(jiàn)表1。
2.2.3兩組致病菌比較 A 組病原菌檢出率(117.05%)高于 B 組(112.50%),但是兩組比較差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05);兩組患者主要致病菌是草綠色鏈球菌和金黃色葡萄球,A 組革蘭陰性菌和真菌顯著高于 B 組,革蘭陽(yáng)性菌顯著低于 B 組,差異有統(tǒng)計(jì)學(xué)意義( P <0.05)。見(jiàn)表1。
2.3兩組主要病原菌耐藥性比較
2.3.1兩組患者主要革蘭陽(yáng)性菌耐藥性比較兩組草綠色鏈球菌對(duì)青霉素耐藥率均較高,對(duì)左氧氟沙星、利福平耐藥率均較低,對(duì)莫西沙星、萬(wàn)古霉素、利奈唑胺均不耐藥;兩組金黃色葡萄球菌對(duì)青霉素、氨芐西林耐藥率均較高,對(duì)左氧氟沙星、萬(wàn)古霉素耐藥率差異較大,兩組差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)利奈唑胺均不耐藥。見(jiàn)表2。
2.3.2兩組患者主要革蘭陰性菌耐藥性比較兩組大腸埃希菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮耐藥率均較高,對(duì)慶大霉素、阿米卡星耐藥率差異較大,兩組差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)左氧氟沙星、環(huán)丙沙星、美羅培南、亞胺培南均不耐藥;鮑氏不動(dòng)桿菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮、哌拉西林耐藥率均較高,對(duì)環(huán)丙沙星、阿米卡星耐藥率均較低,對(duì)左氧氟沙星、美羅培南差異較大,兩組差異無(wú)統(tǒng)計(jì)學(xué)意義( P >0.05),對(duì)亞胺培南均不耐藥。見(jiàn)表3。
3討論
IE 指由病原微生物直接感染心內(nèi)膜或心臟瓣膜而產(chǎn)生的炎癥。研究發(fā)現(xiàn)[16],IE 病原菌中革蘭陽(yáng)性菌株至少占45.0%,革蘭陰性菌株及真菌菌株比例多低于5.0%。近年來(lái)隨著人口老齡化,退行性心瓣膜、風(fēng)濕性心臟病等基礎(chǔ)性心臟疾病發(fā)病率增多,導(dǎo)致 IE 患者越來(lái)越多;除此以外,隨著現(xiàn)代醫(yī)學(xué)技術(shù)的發(fā)展與進(jìn)步,植入性器械、人工心瓣膜置換術(shù)、血液透析等增多,這也使得 IE 發(fā)病率逐漸上升,其發(fā)病率約為(3~10)/10萬(wàn)[17]。因此,該病引起醫(yī)學(xué)領(lǐng)域高度重視[18]。
血培養(yǎng)技術(shù)是 IE 主要診斷依據(jù)[19],對(duì)陽(yáng)性標(biāo)本菌種分離鑒定及藥敏試驗(yàn)后,能有效指導(dǎo)其臨床用藥,進(jìn)而促進(jìn)病原菌的清除,使病情得到良好控制及改善。本研究中,A 組83例患者中檢出病原菌103株,革蘭陽(yáng)性菌、革蘭陽(yáng)性菌、真菌占比分別為57.28%、33.01%、9.71%,與吳梓芳等[6]對(duì)80例(無(wú)基礎(chǔ)心臟疾病的54例、有基礎(chǔ)心臟疾病的26例)IE 患者通過(guò)血培養(yǎng)檢出病原菌139株,其中革蘭陽(yáng)性菌105株占75.54%,革蘭陰性菌34株占24.46%相近;而 B 組88例患者中檢出病原菌99株,革蘭陽(yáng)性菌、革蘭陰性菌、真菌占比分別為79.80%、19.19%、1.01%,與程軍等[20]對(duì)802例(有基礎(chǔ)心臟疾病)IE 患者通過(guò)血培養(yǎng)檢出病原菌156株,其中革蘭陽(yáng)性菌146株占93.59%,革蘭陰性菌8株占5.13%基本一致。兩組患者主要致病菌是草綠色鏈球菌和金黃色葡萄球,與近年來(lái)國(guó)內(nèi)外研究結(jié)論一致[6,10]。兩組真菌占比與國(guó)際報(bào)道結(jié)論比較接近[21]。
由于抗菌藥物的廣泛使用,病原菌對(duì)抗菌藥物的耐藥性增強(qiáng)。本研究發(fā)現(xiàn),兩組患者主要革蘭陽(yáng)性菌中草綠色鏈球菌對(duì)青霉素耐藥率均較高,對(duì)左氧氟沙星、利福平耐藥率均較低,對(duì)莫西沙星、萬(wàn)古霉素、利奈唑胺均不耐藥;金黃色葡萄球菌對(duì)青霉素、氨芐西林耐藥率均較高,對(duì)左氧氟沙星、萬(wàn)古霉素耐藥率差別較大,對(duì)利奈唑胺均不耐藥。兩組患者主要革蘭陰性菌中大腸埃希菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮耐藥率均較高,對(duì)慶大霉素、阿米卡星耐藥率差別較大,對(duì)左氧氟沙星、環(huán)丙沙星、美羅培南、亞胺培南均不耐藥;鮑氏不動(dòng)桿菌對(duì)頭孢唑林、頭孢曲松、頭孢哌酮、哌拉西林耐藥率均較高,對(duì)環(huán)丙沙星、阿米卡星耐藥率均較低,對(duì)左氧氟沙星、美羅培南差別較大,對(duì)亞胺培南均不耐藥。因此,建議在藥敏試驗(yàn)未明確之前,在治療革蘭陽(yáng)性菌引起的 IE 可將左氧氟沙星、利福平、莫西沙星、萬(wàn)古霉素、利奈唑胺作一線用藥,而青霉素、氨芐西林、頭孢唑林等已不適合該類 IE 臨床治療;在治療革蘭陰性菌引起的 IE 可將環(huán)丙沙星、左氧氟沙星、阿米卡星、美羅培南、亞胺培南作一線用藥,而頭孢唑林、頭孢曲松、頭孢哌酮已不適合該類 IE 臨床治療。
IE 患者根據(jù)有無(wú)基礎(chǔ)心臟疾病分別研究分析,引發(fā) IE 的致病菌占比不同,但致病菌仍以革蘭陽(yáng)性菌為主,其中草綠色鏈球菌和金黃色葡萄球分居第一、二位。耐藥性分析提示,病原菌對(duì)常用抗菌藥物普遍存在不同程度的耐藥,臨床應(yīng)結(jié)合當(dāng)?shù)夭≡瓕W(xué)資料先期經(jīng)驗(yàn)性選擇抗菌藥物,并根據(jù)藥敏實(shí)驗(yàn)結(jié)果及時(shí)調(diào)整用藥方案。若按照藥敏結(jié)果,合理應(yīng)用抗菌藥物,仍不能達(dá)到效果預(yù)期,應(yīng)當(dāng)考慮合并兩種或者兩種以上的致病微生物的可能,尤其是合并真菌感染的可能,值得注意。
本研究存在局限性,樣本量較小,未進(jìn)行多中心、大樣本研究,有無(wú)基礎(chǔ)心臟疾病對(duì)該病病原菌譜的變化有待進(jìn)一步探討。
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(收稿日期:2021-04-19)