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黄色ブドウ球菌菌血症に対するPET-CTの死亡率に対する影響

2023-10-07 | 微生物:細菌・真菌
Clinical infectious diseases,2023 

要点
・7施設でブドウ球菌菌血症に対するPET/CTの影響を解析(観察研究)
・476名中178名でPET/CT使用、多変量解析では0.50(0.34-0.74)の効果
・一方でImmortal time biasで調整の結果、1.00(0.68-1.48)で有意差なし

要約
・2大学・5病院で連続的に18歳以上の1セットブドウ球菌菌血症陽性患者をリクルート(2017-2019), 全医療施設でPET/CT利用可(必須ではない), 観察研究
・プライマリアウトカム:90日間全死亡、セカンダリーアウトカム:90日間感染死亡

・476名が対象、178名(37.4%)でPET/CT(90日死亡31% )
・PET/CT使用に伴う単変量解析は0.59(0.41-0.86)。多変量解析で0.50(0.34-0.74)
→不死時間バイアス(Immortal time bias)で調整の結果、1.00(0.68-1.48)で有意差なし

Background: Several studies have suggested that in patients with Staphylococcus aureus bacteremia (SAB) [18F] fluorodeoxyglucose positron emission tomography/computed tomography ([18F]FDG-PET/CT) improves outcome. However, these studies often ignored possible immortal time bias.
Methods: Prospective multicenter cohort study in 2 university and 5 non-university hospitals, including all patients with SAB. [18F]FDG-PET/CT was performed on clinical indication as part of usual care. Primary outcome was 90-day all-cause mortality. Effect of [18F]FDG-PET/CT was modeled with a Cox proportional hazards model using [18F]FDG-PET/CT as a time-varying variable and corrected for confounders for mortality (age, Charlson score, positive follow-up cultures, septic shock, and endocarditis). Secondary outcome was 90-day infection-related mortality (assessed by adjudication committee) using the same analysis. In a subgroup-analysis, we determined the effect of [18F]FDG-PET/CT in patients with high risk of metastatic infection.
Results: Of 476 patients, 178 (37%) underwent [18F]FDG-PET/CT. Day-90 all-cause mortality was 31% (147 patients), and infection-related mortality was 17% (83 patients). The confounder adjusted hazard ratio (aHR) for all-cause mortality was 0.50 (95% confidence interval [CI]: .34-.74) in patients that underwent [18F]FDG-PET/CT. Adjustment for immortal time bias changed the aHR to 1.00 (95% CI .68-1.48). Likewise, after correction for immortal time bias, [18F]FDG-PET/CT had no effect on infection-related mortality (cause specific aHR 1.30 [95% CI .77-2.21]), on all-cause mortality in patients with high-risk SAB (aHR 1.07 (95% CI .63-1.83) or on infection-related mortality in high-risk SAB (aHR for 1.24 [95% CI .67-2.28]).
Conclusions: After adjustment for immortal time bias [18F]FDG-PET/CT was not associated with day-90 all-cause or infection-related mortality in patients with SAB.
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