上海市某三甲综合医院38例碳青霉烯耐药黏质沙雷菌感染病例耐药性

Drug resistance in 38 cases of carbapenem-resistant Serratia marcescens infection in a gradelevel A general hospital in Shanghai

  • 摘要:
    目的 了解上海市某综合医院碳青霉烯耐药黏质沙雷菌(CRSM)感染特征及耐药情况,为临床抗感染治疗和预防耐药菌的产生提供理论依据。
    方法 回顾性收集2022年6月—2024年6月上海市某三甲综合医院临床送检标本中检出CRSM的病例的临床资料,分析其临床分布、医院感染因素、预后及耐药情况。
    结果 2022年6月—2024年6月共检出CRSM 38例,CRSM菌株数占SM菌株数的25.00%(38/152)。38株CRSM样本均来源于痰液。CRSM分布于9个临床科室,CRSM菌株数占SM菌株数的比例由高至低排名前3位的科室分别为重症监护病房(ICU)(78.79%,26/33)、胃肠外科(57.14%,4/7)和甲状腺疝外科(50.00%,1/2)。38例CRSM感染患者中有8例医院感染患者,医院感染率为21.05%。38例CRSM感染患者检出CRSM后30 d内死亡率为23.68%(9/38)。多因素logistic回归分析结果显示,序贯器官衰竭评估(SOFA)评分6.5分(OR=15.33,P<0.001)、感染性休克(OR=4.85,P=0.032)和患肿瘤性疾病(OR=0.12,P=0.018)是CRSM感染患者检出CRSM后30 d内死亡的相关因素。药敏试验结果显示,38例CRSM对甲氧苄啶/磺胺甲噁、替加环素、头孢他啶/阿维巴坦敏感率为100.00%(38/38),对β⁃内酰胺类抗菌药物有较高的耐药性,仅对三代头孢中的头孢他啶耐药率较低18.42%(7/38);对喹诺酮类药物左氧氟沙星和环丙沙星有较高的耐药率,分别为89.47%(35/38)和94.74%(36/38);对四环素类药物多西环素和米诺环素有较高的敏感率,分别为97.37%(37/38)和76.32%(29/38);对氨基糖苷类药物中的庆大霉素敏感性较高,为94.74%(36/38),对妥布霉素有较高的耐药率,为86.84%(34/38)。38株CRSM的丝氨酸碳青霉烯酶阳性率为100.00%(38/38),金属酶均为阴性。
    结论 2022年6月—2024年6月上海市某三甲综合医院CRSM检出率较高,ICU尤为突出,CRSM对第一、第二代头孢菌素,喹诺酮类、多肽类抗菌药物耐药率高,应及时追踪耐药菌流行动态,以指导临床合理应用抗菌药物。

     

    Abstract:
    Objective To understand the infection characteristics and drug resistance of carbapenem-resistant Serratia marcescens (CRSM) in a general hospital in Shanghai, and to provide a theoretical basis for clinical anti-infective treatment and prevention of drug-resistant bacteria.
    Methods Clinical data on cases with CRSM infections detected in clinical specimens at a gradeⅢ level A general hospital in Shanghai from June 2022 to June 2024 were retrospectively collected, and their clinical distributions, factors of hospital-acquired infections, prognosis, and drug-resistant situation were analyzed simultaneously.
    Results A total of 38 cases with CRSM were detected from June 2022 to June 2024, and the number of CRSM strains accounted for 25.00% (38/152) of the number of SM strains. The 38 CRSM infection samples were all derived from sputum. CRSM were distributed in 9 clinical departments, and the top 3 departments having the highest percentages of CRSM among SM strains, were intensive care unit (ICU) (78.79%, 26/33), gastrointestinal surgery department (57.14%, 4/7), and thyroid hernia surgery department (50.00%, 1/2). Among the 38 patients with CRSM infections, 8 cases were identified as hospital-acquired infection, resulting in a hospital-acquired infection rate of 21.05. The mortality rate of the 38 cases of CRSM infected patients within 30 days after detection of CRSM was 23.68% (9/38). The results of multivariate logistic regression analysis showed that sequential organ failure assessment (SOFA) score 6.5 points (OR=15.33, P<0.001), septic shock (OR=4.85, P=0.032), and suffering from neoplastic diseases (OR=0.12, P=0.018) were the related factors for death within 30 days after the detection of CRSM in patients with CRSM infection. The results of drug sensitivity test showed that the 38 cases of CRSM exhibited 100.00% (38/38) sensitivity to trimethoprim/sulfamethoxazole, tigecycline, or ceftazidime/avibactam; demonstrated high resistance to β-lactams except for ceftazidime (18.42%, 7/38), the latter of which was one of the third-generation of cephalosporins; showed elevated resistance to fluoroquinolones levofloxacin (89.47%, 35/38), ciprofloxacin (94.74%, 36/38); maintained good tetracycline sensitivity doxycycline (97.37%, 37/38), minocycline (76.32%, 29/38); and displayed high susceptibility to the aminoglycoside gentamicin (94.74%, 36/38) and elevated resistance to tobramycin (86.84%, 34/38). The detection rate of serine carbapenemase in the 38 strains of CRSM was 100.00%, while all strains tested negative for metallo-β-lactamases.
    Conclusion From June 2022 to June 2024, the detection rate of CRSM in a gradeⅢ level A general hospital in Shanghai was relatively high, especially in the ICU. CRSM has a high resistance rate to commonly used antibacterial drugs such as the first and second-generation cephalosporins, quinolones, and polypeptide antibacterial drugs. Therefore the dynamics of drug-resistant bacteria should be tracked in a timely manner to guide the rational clinical application of antibacterial drugs.

     

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