Division of Neonatology, Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Acta Paediatr. 2023 Sep;112(9):1884-1891. doi: 10.1111/apa.16856. Epub 2023 May 29.
(i) To compare perfusion index (PI) and plethysmography variability index (PVI) between neonates with proven or probable sepsis versus no-sepsis, (ii) to examine an association of PI and PVI with in-hospital mortality.
We enrolled neonates with clinically presumed sepsis. Culture-proven or probable sepsis were categorised as 'cases' and no-sepsis as 'controls'. PI and PVI were recorded hourly for 120 h and averaged in 20-time epochs (0-6 h to 115-120 h).
We analysed 148 neonates with sepsis (proven sepsis = 77, probable sepsis = 71) and 126 with no-sepsis. Neonates with proven/probable sepsis and no-sepsis had comparable PI and PVI values. Among 148 neonates with sepsis, 43 (29%) died. Non-survivors had significantly lower PI values than survivors (mean difference 0.21 [95% CI 0.14-0.29], p-value <0.001). PI had a significant but modest discriminative ability to identify non-survivors. However, PI did not independently predict mortality.
Neonates with proven/probable sepsis and no-sepsis had comparable PI and PVI values in the first 120 h of sepsis. PI but not PVI values were significantly lower in non-survivors than survivors. PI did not independently predict in-hospital mortality. Due to modest discriminative ability, PI should be interpreted along with other vital signs to take clinical decisions.
(i)比较已确诊或可能患有败血症的新生儿与无败血症新生儿之间的灌注指数(PI)和容积描记变异指数(PVI),(ii)检验 PI 和 PVI 与院内死亡率之间的关联。
我们纳入了有临床疑似败血症的新生儿。经培养证实的败血症或可能败血症被归类为“病例”,无败血症归类为“对照”。记录每小时的 PI 和 PVI,共 120 小时,并在 20 个时间区间(0-6 小时至 115-120 小时)进行平均。
我们分析了 148 例患有败血症的新生儿(确诊败血症 77 例,可能败血症 71 例)和 126 例无败血症新生儿。有确诊/可能败血症和无败血症的新生儿具有相似的 PI 和 PVI 值。在 148 例败血症新生儿中,43 例(29%)死亡。非幸存者的 PI 值明显低于幸存者(平均差异 0.21 [95%CI 0.14-0.29],p 值<0.001)。PI 具有识别非幸存者的显著但适度的判别能力。然而,PI 并不能独立预测死亡率。
在败血症的前 120 小时内,患有已确诊/可能败血症和无败血症的新生儿具有相似的 PI 和 PVI 值。非幸存者的 PI 值明显低于幸存者,而 PVI 值则无差异。PI 不能独立预测院内死亡率。由于判别能力有限,PI 应与其他生命体征一起解读,以便做出临床决策。