Réanimation Chirurgicale Polyvalente, Service d'Anesthésie-Réanimation, Hôpital Laennec, CHU Nantes, Boulevard Jacques-Monod, Saint-Herblain, 44093, Nantes Cedex 1, France,
Intensive Care Med. 2013 Nov;39(11):1953-62. doi: 10.1007/s00134-013-3086-6. Epub 2013 Sep 6.
To assess whether invasive and non-invasive blood pressure (BP) monitoring allows the identification of patients who have responded to a fluid challenge, i.e., who have increased their cardiac output (CO).
Patients with signs of circulatory failure were prospectively included. Before and after a fluid challenge, CO and the mean of four intra-arterial and oscillometric brachial cuff BP measurements were collected. Fluid responsiveness was defined by an increase in CO ≥10 or ≥15% in case of regular rhythm or arrhythmia, respectively.
In 130 patients, the correlation between a fluid-induced increase in pulse pressure (Δ500mlPP) and fluid-induced increase in CO was weak and was similar for invasive and non-invasive measurements of BP: r² = 0.31 and r² = 0.29, respectively (both p < 0.001). For the identification of responders, invasive Δ500mlPP was associated with an area under the receiver-operating curve (AUC) of 0.82 (0.74-0.88), similar (p = 0.80) to that of non-invasive Δ500mlPP [AUC of 0.81 (0.73-0.87)]. Outside large gray zones of inconclusive values (5-23% for invasive Δ500mlPP and 4-35% for non-invasive Δ500mlPP, involving 35 and 48% of patients, respectively), the detection of responsiveness or unresponsiveness to fluid was reliable. Cardiac arrhythmia did not impair the performance of invasive or non-invasive Δ500mlPP. Other BP-derived indices did not outperform Δ500mlPP.
As evidenced by large gray zones, BP-derived indices poorly reflected fluid responsiveness. However, in our deeply sedated population, a high increase in invasive pulse pressure (>23%) or even in non-invasive pulse pressure (>35%) reliably detected a response to fluid. In the absence of a marked increase in pulse pressure (<4-5%), a response to fluid was unlikely.
评估有创和无创血压(BP)监测是否能够识别对液体挑战有反应的患者,即增加心输出量(CO)的患者。
前瞻性纳入有循环衰竭迹象的患者。在进行液体挑战前后,收集 CO 和四个动脉内和袖带式肱动脉 BP 测量的平均值。液体反应性定义为 CO 增加≥10%或在有规律节律或心律失常的情况下增加≥15%。
在 130 例患者中,脉压(Δ500mlPP)与 CO 之间的液体诱导增加之间的相关性较弱,并且与有创和无创 BP 测量相似:r²=0.31 和 r²=0.29,均为 p<0.001。对于识别应答者,有创 Δ500mlPP 与接受者操作特征曲线(AUC)的面积相关,AUC 为 0.82(0.74-0.88),与无创 Δ500mlPP 相似(p=0.80)[AUC 为 0.81(0.73-0.87)]。在无明确值的大灰色区域(有创 Δ500mlPP 为 5-23%,无创 Δ500mlPP 为 4-35%,分别涉及 35%和 48%的患者)之外,对液体的反应性或无反应性的检测是可靠的。心脏心律失常不会影响有创或无创 Δ500mlPP 的性能。其他 BP 衍生指数没有优于 Δ500mlPP。
大灰色区域表明,BP 衍生指数不能很好地反映液体反应性。然而,在我们深度镇静的人群中,有创脉冲压力的大幅增加(>23%)甚至无创脉冲压力的大幅增加(>35%)可靠地检测到对液体的反应。在脉冲压力没有明显增加(<4-5%)的情况下,液体反应的可能性不大。