基于真实世界数据的冠脉旁路移植术后肺炎疾病负担研究:临床结局与成本分析
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R181.3+2

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河南省医学科技攻关计划联合共建项目(LHGJ20210315)


Disease burden of pneumonia after coronary artery bypass grafting based on real-world data: clinical outcomes and cost analysis
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    摘要:

    目的 探索接受冠脉旁路移植术(CABG)患者术后肺炎(POP)的疾病负担及其影响因素,为防控提供依据。方法 回顾性收集2020年1月1日—2024年11月30日接受CABG且符合研究标准的5 566例患者的临床资料,分析重症POP和术后90 d内死亡的独立危险因素,并比较各亚组组间医疗成本相关指标的差异。结果 5 566例CABG患者中,627例发生POP,发病率为11.3%,其中重症POP占1.4%(76例)。POP患者在术后90 d内死亡风险高于非POP患者(HR=4.16,95%CI:2.39~7.26)。单因素和多因素Cox回归分析显示,手术时长、输注红细胞、多重耐药菌(MDRO)感染和细菌混合感染与重症POP的发生相关;细菌混合感染和全机械通气时长是POP患者术后90 d内死亡的独立危险因素。POP患者术后中位住院日数、ICU中位住院日数和中位住院费用均高于非POP患者,增幅分别为25.0%(15.0 d VS 12.0 d)、100%(8.0 d VS 4.0 d)和26.1%(183 911.6元VS 145 851.6元)。在POP患者中,重症POP、细菌混合感染及MDRO感染患者的住院时长与费用均进一步增加:与普通POP组相比,重症POP组上述三项指标分别增加63.3%、83.3%和57.9%;较非混合感染者,混合感染者的增幅分别为40.0%、46.7%和57.7%;与敏感菌感染者和病原学阴性者相比,MDRO感染者术后住院日数均增加14.3%,ICU住院日数分别增加66.7%、150.0%,住院费用则分别增加11.7%、21.5%;上述差异均具有统计学意义(均P<0.001)。结论 手术时长、输注红细胞、MDRO感染及细菌混合感染是CABG术后重症POP的独立危险因素,细菌混合感染还将进一步增加术后90 d内死亡风险。POP显著加重医疗资源消耗,其影响程度因病情严重程度和感染特征呈现异质性。

    Abstract:

    Objective To explore the disease burden and impacting factors of postoperative pneumonia (POP) in patients undergoing coronary artery bypass grafting (CABG), provide basis for the prevention and control of POP. Methods Clinical data of 5 566 patients who underwent CABG from January 1, 2020 to November 30, 2024 and met the study criteria were retrospectively collected. Independent risk factors for severe POP and postoperative 90-day mortality were analyzed, and differences in medical cost-related indicators among subgroups were compared. Results Among 5 566 CABG patients, 627 had POP,with an incidence of 11.3%, out of which 1.4% (n=76) were severe POP. Risk of postoperative 90-day mortality in POP patients was higher than non-POP patients (HR=4.16, 95%CI: 2.39-7.26). Univariate and multivariate Cox regression analysis showed that duration of surgery, red blood cell transfusion, multidrug-resistant organism (MDRO) infection, and mixed bacterial infection were associated with the occurrence of severe POP; Mixed bacterial infection and duration of controlled mechanical ventilation were independent risk factors for postoperative 90-day mortality. The median length of hospital stay, median length of intensive care unit (ICU) stay, and median hospitalization cost for POP patients were all higher than non-POP patients, with the increases of 25.0% (15.0 days vs 12.0 days), 100% (8.0 days vs 4.0 days), and 26.1% (183 911.6 Yuan vs 145 851.6 Yuan), respectively. Among POP patients, those with severe POP, mixed bacterial infection and MDRO infection further increased the length of hospital stay and cost: compared with the common POP group, the above three indicators in severe POP group increased by 63.3%, 83.3%, and 57.9%, respectively; Compared with non-mixed infection, the above three indicators in patients with mixed infection increase by 40.0%, 46.7%, and 57.7%, respectively; Compared with patients with sensitive bacterial infection and pathogen-negative, length of postoperative hospital stay in MDRO-infected patients both increased by 14.3%, length of ICU stay increased by 66.7% and 150.0% respectively, hospitalization cost increased by 11.7% and 21.5%, respectively; The above differences were all statistically significant (all P<0.001). Conclusion Duration of surgery, red blood cell transfusion, MDRO infection, and mixed bacterial infection are independent risk factors for severe POP after CABG, and mixed bacterial infection can further increase the risk of postoperative 90-day mortality. POP can significantly increase the consumption of medical resources, and its impacting extent exhibits heterogeneity depending on the severity of disease condition and characteristics of infection.

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湛玉晓,张俭,杨阳,等.基于真实世界数据的冠脉旁路移植术后肺炎疾病负担研究:临床结局与成本分析[J]. 中国感染控制杂志,2026,25(2):213-221. DOI:10.12138/j. issn.1671-9638.20267397.
ZHAN Yuxiao, ZHANG Jian, YANG Yang, et al. Disease burden of pneumonia after coronary artery bypass grafting based on real-world data: clinical outcomes and cost analysis[J]. Chin J Infect Control, 2026,25(2):213-221. DOI:10.12138/j. issn.1671-9638.20267397.

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  • 收稿日期:2025-09-17
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  • 在线发布日期: 2026-03-04
  • 出版日期: 2026-02-28