EviMed Research Group, LLC, P.O. Box 303, Goshen, MA, 01032, USA.
OptiStatim, LLC, Longmeadow, MA, USA.
BMC Infect Dis. 2022 Oct 5;22(1):775. doi: 10.1186/s12879-022-07755-y.
Inappropriate empiric antimicrobial treatment (IET) contributes to worsened outcomes. While IET's differential impact across types of nosocomial pneumonia (NP: non-ventilated [nvHABP], ventilated [vHABP] hospital-acquired and ventilator-associated [VABP] bacterial pneumonia) is established, its potential interaction with the bacterial etiology is less clear.
We conducted a multicenter retrospective cohort study in the Premier Healthcare Database using an administrative algorithm to identify NP. We paired respective pathogens with empiric treatments. Antimicrobial coverage was appropriate if a drug administered within 2 days of infection onset covered the recovered organism(s). All other treatment was IET.
Among 17,819 patients with NP, 26.5% had nvHABP, 25.6% vHABP, and 47.9% VABP. Gram-negative (GN) organisms accounted for > 50% of all infections. GN pathogens were ~ 2 × as likely (7.4% vHABP to 10.7% nvHABP) to engender IET than Gram-positive (GP, 2.9% vHABP to 4.9% nvHABP) pathogens. Although rare (5.6% nvHABP to 8.3% VABP), GN + GP infections had the highest rates of IET (6.7% vHABP to 12.9% nvHABP). Carbapenem-resistant GNs were highly likely to receive IET (33.8% nvHABP to 40.2% VABP). Hospital mortality trended higher in the IET group, reaching statistical significance in GN + GP vHABP (47.8% IET vs. 29.3% non-IET, p = 0.016). 30-day readmission was more common with IET (16.0%) than non-IET (12.6%, p = 0.024) in GN VABP. Generally post-infection onset hospital length of stay and costs were higher with IET than non-IET.
IET is ~ 2 × more common in GN than GP infections. Although the magnitude of its impact varies by NP type, IET contributes to worsened clinical and economic outcomes.
不适当的经验性抗菌治疗(IET)会导致预后恶化。虽然已经确定了医院获得性肺炎(NP:非机械通气[nvHABP]、机械通气[vHABP]医院获得性和呼吸机相关性[VABP]细菌性肺炎)中 IET 的差异影响,但它与细菌病因学的潜在相互作用尚不清楚。
我们使用行政算法在 Premier Healthcare Database 中进行了一项多中心回顾性队列研究,以确定 NP。我们将相应的病原体与经验性治疗配对。如果在感染发作后 2 天内给予的药物覆盖了已恢复的病原体,则抗菌覆盖是适当的。所有其他治疗均为 IET。
在 17819 例 NP 患者中,26.5%为 nvHABP,25.6%为 vHABP,47.9%为 VABP。革兰氏阴性(GN)病原体占所有感染的比例超过 50%。GN 病原体导致 IET 的可能性是革兰氏阳性(GP)病原体的 2 倍(vHABP 中的 7.4%比 nvHABP 中的 10.7%;vHABP 中的 2.9%比 nvHABP 中的 4.9%)。虽然罕见(nvHABP 中的 5.6%比 VABP 中的 8.3%),但 GN+GP 感染的 IET 发生率最高(vHABP 中的 6.7%比 nvHABP 中的 12.9%;nvHABP 中的 12.9%)。耐碳青霉烯的 GN 极有可能接受 IET(nvHABP 中的 33.8%比 VABP 中的 40.2%)。IET 组的医院死亡率呈上升趋势,在 GN+GP vHABP 中达到统计学意义(IET 组的 47.8%比非 IET 组的 29.3%,p=0.016)。在 GN VABP 中,IET 组的 30 天再入院率(16.0%)高于非 IET 组(12.6%,p=0.024)。与非 IET 组相比,IET 组在感染后住院时间和费用均较高。
与 GP 感染相比,GN 感染中 IET 更为常见。尽管其影响的程度因 NP 类型而异,但 IET 会导致临床和经济结果恶化。