Puech Bérénice, Canivet Clémence, Teysseyre Laura, Miltgen Guillaume, Aujoulat Thomas, Caron Margot, Combe Chloé, Jabot Julien, Martinet Olivier, Allyn Jerome, Ferdynus Cyril, Allou Nicolas
Réanimation Polyvalente, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.
Service de Microbiologie, Hôpital Universitaire Félix Guyon, Allée des Topazes, 97400, Saint Denis, France.
Ann Intensive Care. 2021 Nov 26;11(1):160. doi: 10.1186/s13613-021-00950-1.
Ventilator-associated pneumonia (VAP) caused by Stenotrophomonas maltophilia is poorly described in the literature. However, it has been shown to be associated with increased morbidity and mortality. Probabilistic antibiotic therapy against S. maltophilia is often ineffective as this pathogen is resistant to many antibiotics. There is no consensus at present on the best therapeutic strategy to adopt (class of antibiotics, antibiotic combination, dosage, treatment duration). The aim of this study was to evaluate the effect of antibiotic therapy strategy on the prognosis of patients with VAP caused by S. maltophilia.
This retrospective study evaluated all consecutive patients who developed VAP caused by S. maltophilia between 2010 and 2018 while hospitalized in the intensive care unit (ICU) of a French university hospital in Reunion Island, in the Indian Ocean region. A total of 130 patients with a median Simplified Acute Physiology Score II of 58 [43-73] had VAP caused by S. maltophilia after a median duration of mechanical ventilation of 12 [5-18] days. Ventilator-associated pneumonia was polymicrobial in 44.6% of cases, and ICU mortality was 50.0%. After multivariate Cox regression analysis, the factors associated with increased ICU mortality were older age (hazard ratio (HR): 1.03; 95% CI 1.01-1.04, p = 0.001) and high Sequential Organ Failure Assessment score on the day of VAP onset (HR: 1.08; 95% CI 1.03-1.14, p = 0.002). Appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU mortality (HR: 0.42; 95% CI 0.24-0.74, p = 0.003) and decreased hospital mortality (HR: 0.47; 95% CI 0.28-0.79, p = 0.04). Time to start of appropriate antibiotic therapy, combination therapy, and duration of appropriate antibiotic therapy had no effect on ICU mortality (p > 0.5).
In our study, appropriate antibiotic therapy, and in particular trimethoprim-sulfamethoxazole, was associated with decreased ICU and hospital mortality in patients with VAP caused by S. maltophilia.
嗜麦芽窄食单胞菌引起的呼吸机相关性肺炎(VAP)在文献中的描述较少。然而,已证明其与发病率和死亡率增加有关。针对嗜麦芽窄食单胞菌的概率性抗生素治疗通常无效,因为该病原体对许多抗生素耐药。目前对于采用何种最佳治疗策略(抗生素类别、抗生素联合使用、剂量、治疗持续时间)尚无共识。本研究的目的是评估抗生素治疗策略对嗜麦芽窄食单胞菌引起的VAP患者预后的影响。
这项回顾性研究评估了2010年至2018年间在印度洋地区留尼汪岛一家法国大学医院的重症监护病房(ICU)住院期间发生嗜麦芽窄食单胞菌引起的VAP的所有连续患者。共有130例患者,简化急性生理学评分II中位数为58[43 - 73],在机械通气中位数持续时间12[5 - 18]天后发生嗜麦芽窄食单胞菌引起的VAP。44.6%的病例中呼吸机相关性肺炎为多微生物感染,ICU死亡率为50.0%。多变量Cox回归分析后,与ICU死亡率增加相关的因素是年龄较大(风险比(HR):1.03;95%置信区间1.01 - 1.04,p = 0.001)和VAP发病当天较高的序贯器官衰竭评估评分(HR:1.08;95%置信区间1.03 - 1.14,p = 0.002)。适当的抗生素治疗,尤其是复方新诺明,与ICU死亡率降低(HR:0.42;95%置信区间0.24 - 0.74,p = 0.003)和医院死亡率降低(HR:0.47;95%置信区间0.28 - 0.79,p = 0.04)相关。开始适当抗生素治疗的时间、联合治疗以及适当抗生素治疗的持续时间对ICU死亡率无影响(p > 0.5)。
在我们的研究中,适当的抗生素治疗,尤其是复方新诺明,与嗜麦芽窄食单胞菌引起的VAP患者的ICU和医院死亡率降低相关。