Phu Vu Dinh, Nadjm Behzad, Duy Nguyen Hoang Anh, Co Dao Xuan, Mai Nguyen Thi Hoang, Trinh Dao Tuyet, Campbell James, Khiem Dong Phu, Quang Tran Ngoc, Loan Huynh Thi, Binh Ha Son, Dinh Quynh-Dao, Thuy Duong Bich, Lan Huong Nguyen Phu, Ha Nguyen Hong, Bonell Ana, Larsson Mattias, Hoan Hoang Minh, Tuan Đang Quoc, Hanberger Hakan, Minh Hoang Nguyen Van, Yen Lam Minh, Van Hao Nguyen, Binh Nguyen Gia, Chau Nguyen Van Vinh, Van Kinh Nguyen, Thwaites Guy E, Wertheim Heiman F, van Doorn H Rogier, Thwaites C Louise
National Hospital for Tropical Diseases, Hanoi, Vietnam.
Oxford University Clinical Research Unit, Hanoi, Vietnam.
J Intensive Care. 2017 Dec 19;5:69. doi: 10.1186/s40560-017-0266-4. eCollection 2017.
Ventilator-associated respiratory infection (VARI) is a significant problem in resource-restricted intensive care units (ICUs), but differences in casemix and etiology means VARI in resource-restricted ICUs may be different from that found in resource-rich units. Data from these settings are vital to plan preventative interventions and assess their cost-effectiveness, but few are available.
We conducted a prospective observational study in four Vietnamese ICUs to assess the incidence and impact of VARI. Patients ≥ 16 years old and expected to be mechanically ventilated > 48 h were enrolled in the study and followed daily for 28 days following ICU admission.
Four hundred fifty eligible patients were enrolled over 24 months, and after exclusions, 374 patients' data were analyzed. A total of 92/374 cases of VARI (21.7/1000 ventilator days) were diagnosed; 37 (9.9%) of these met ventilator-associated pneumonia (VAP) criteria (8.7/1000 ventilator days). Patients with any VARI, VAP, or VARI without VAP experienced increased hospital and ICU stay, ICU cost, and antibiotic use ( < 0.01 for all). This was also true for all VARI ( < 0.01 for all) with/without tetanus. There was no increased risk of in-hospital death in patients with VARI compared to those without (VAP HR 1.58, 95% CI 0.75-3.33, = 0.23; VARI without VAP HR 0.40, 95% CI 0.14-1.17, = 0.09). In patients with positive endotracheal aspirate cultures, most VARI was caused by Gram-negative organisms; the most frequent were (32/73, 43.8%) (26/73, 35.6%), and (24/73, 32.9%). 40/68 (58.8%) patients with positive cultures for these had carbapenem-resistant isolates. Patients with carbapenem-resistant VARI had significantly greater ICU costs than patients with carbapenem-susceptible isolates (6053 USD (IQR 3806-7824) vs 3131 USD (IQR 2108-7551), = 0.04) and after correction for adequacy of initial antibiotics and APACHE II score, showed a trend towards increased risk of in-hospital death (HR 2.82, 95% CI 0.75-6.75, = 0.15).
VARI in a resource-restricted setting has limited impact on mortality, but shows significant association with increased patient costs, length of stay, and antibiotic use, particularly when caused by carbapenem-resistant bacteria. Evidence-based interventions to reduce VARI in these settings are urgently needed.
呼吸机相关性呼吸道感染(VARI)是资源有限的重症监护病房(ICU)中的一个重大问题,但病例组合和病因的差异意味着资源有限的ICU中的VARI可能与资源丰富的ICU中的情况不同。来自这些环境的数据对于规划预防干预措施和评估其成本效益至关重要,但可用数据很少。
我们在越南的四个ICU中进行了一项前瞻性观察研究,以评估VARI的发生率和影响。年龄≥16岁且预计机械通气时间>48小时的患者被纳入研究,并在ICU入院后每天随访28天。
在24个月内共纳入450例符合条件的患者,排除后,对374例患者的数据进行了分析。共诊断出92/374例VARI(每1000个呼吸机日21.7例);其中37例(9.9%)符合呼吸机相关性肺炎(VAP)标准(每1000个呼吸机日8.7例)。患有任何VARI、VAP或无VAP的VARI的患者住院和ICU住院时间、ICU费用和抗生素使用均增加(所有P<0.01)。对于所有有/无破伤风的VARI(所有P<0.01)也是如此。与没有VARI的患者相比,患有VARI的患者院内死亡风险没有增加(VAP风险比1.58,95%置信区间0.75-3.33,P=0.23;无VAP的VARI风险比0.40,95%置信区间0.14-1.17,P=0.09)。在气管内吸出物培养阳性的患者中,大多数VARI由革兰氏阴性菌引起;最常见的是(32/73,43.8%)(26/73,35.6%)和(24/73,32.9%)。这些培养阳性的患者中有40/68(58.8%)分离出对碳青霉烯耐药的菌株。与碳青霉烯敏感菌株的患者相比,碳青霉烯耐药VARI的患者ICU费用显著更高(6053美元(四分位间距3806-7824)对3131美元(四分位间距2108-7551),P=0.04),在对初始抗生素的充分性和急性生理学与慢性健康状况评分系统II评分进行校正后,显示院内死亡风险有增加的趋势(风险比2.82,95%置信区间0.75-6.75,P=0.15)。
资源有限环境中的VARI对死亡率的影响有限,但与患者费用增加、住院时间延长和抗生素使用显著相关,尤其是由碳青霉烯耐药细菌引起时。迫切需要基于证据的干预措施来减少这些环境中的VARI。