Carbonell Raquel, Moreno Gerard, Martín-Loeches Ignacio, Gomez-Bertomeu Frederic, Sarvisé Carolina, Gómez Josep, Bodí María, Díaz Emili, Papiol Elisabeth, Trefler Sandra, Nieto Mercedes, Estella Angel, Jiménez Herrera María, Vidal Cortés Pablo, Guardiola Juan José, Solé-Violán Jordi, Rodríguez Alejandro
Critical Care Department, Hospital Universitari Joan XXIII, 43005 Tarragona, Spain.
Department of Anaesthesia and Critical Care, St James's University Hospital, Trinity Centre for Health Sciences, Multidisciplinary Intensive Care Research Organization (MICRO), Dublin 8, Ireland.
Antibiotics (Basel). 2021 Mar 26;10(4):350. doi: 10.3390/antibiotics10040350.
: Procalcitonin (PCT) and C-Reactive protein (CRP) are well-established sepsis biomarkers. The association of baseline PCT levels and mortality in pneumonia remains unclear, and we still do not know whether biomarkers levels could be related to the causative microorganism (GPC, GNB). The objective of this study is to address these issues. : a retrospective observational cohort study was conducted in 184 Spanish ICUs (2009-2018). : 1608 patients with severe influenza pneumonia with PCT and CRP available levels on admission were included, 1186 with primary viral pneumonia (PVP) and 422 with bacterial Co-infection (BC). Those with BC presented higher PCT levels (4.25 [0.6-19.5] 0.6 [0.2-2.3]ng/mL) and CRP (36.7 [20.23-118] 28.05 [13.3-109]mg/dL) as compared to PVP ( < 0.001). Deceased patients had higher PCT (ng/mL) when compared with survivors, in PVP (0.82 [0.3-2.8]) 0.53 [0.19-2.1], = 0.001) and BC (6.9 [0.93-28.5] 3.8 [0.5-17.37], = 0.039). However, no significant association with mortality was observed in the multivariate analysis. The PCT levels (ng/mL) were significantly higher in polymicrobial infection (8.4) and GPC (6.9) when compared with GNB (1.2) and (1.7). The AUC-ROC of PCT for GPC was 0.67 and 0.32 for GNB. The AUROC of CRP was 0.56 for GPC and 0.39 for GNB. : a single PCT/CRP value at ICU admission was not associated with mortality in severe influenza pneumonia. None of the biomarkers have enough discriminatory power to be used for predicting the causative microorganism of the co-infection.
降钙素原(PCT)和C反应蛋白(CRP)是公认的脓毒症生物标志物。肺炎患者基线PCT水平与死亡率之间的关联尚不清楚,而且我们仍然不知道生物标志物水平是否与致病微生物(革兰氏阳性菌、革兰氏阴性菌)有关。本研究的目的是解决这些问题。:对184家西班牙重症监护病房(2009 - 2018年)进行了一项回顾性观察队列研究。:纳入了1608例入院时可获得PCT和CRP水平的重症流感肺炎患者,其中1186例为原发性病毒性肺炎(PVP),422例为细菌合并感染(BC)。与PVP患者相比,BC患者的PCT水平更高(4.25[0.6 - 19.5]对比0.6[0.2 - 2.3]ng/mL),CRP水平也更高(36.7[20.23 - 118]对比28.05[13.3 - 109]mg/dL)(P<0.001)。与幸存者相比,PVP组(0.82[0.3 - 2.8]对比0.53[0.19 - 2.1],P = 0.001)和BC组(6.9[0.93 - 28.5]对比3.8[0.5 - 17.37],P = 0.039)中死亡患者的PCT(ng/mL)更高。然而,多变量分析未观察到与死亡率的显著关联。与革兰氏阴性菌(1.2)和……(1.7)相比,多重微生物感染(8.4)和革兰氏阳性菌(6.9)患者的PCT水平(ng/mL)显著更高。PCT对革兰氏阳性菌的曲线下面积(AUC-ROC)为0.67,对革兰氏阴性菌为0.32。CRP对革兰氏阳性菌的AUROC为0.56,对革兰氏阴性菌为0.39。:重症流感肺炎患者在重症监护病房入院时的单个PCT/CRP值与死亡率无关。没有一种生物标志物具有足够的鉴别能力来用于预测合并感染的致病微生物。 (注:原文中“(1.7)”前面的“and”后面内容缺失,翻译时保留了原文格式)