Ortner C M, Combrinck B, Allie S, Story D, Landau R, Cain K, Dyer R A
Department of Anesthesiology and Pain Medicine, University of Washington, 1959 NE Pacific Street, Suite BB1415, Box 356540, Seattle, WA 98195-6540, USA
Department of Anaesthesia, University of Cape Town and New Groote Schuur Hospital, Cape Town, South Africa.
Br J Anaesth. 2015 Aug;115(2):275-84. doi: 10.1093/bja/aev221.
The influence of common disturbances seen in preeclampsia, such as changes in strong ions and weak acids (particularly albumin) on acid-base status, has not been fully elucidated. The aims of this study were to provide a comprehensive acid-base analysis in severe preeclampsia and to identify potential new biological predictors of disease severity.
Fifty women with severe preeclampsia, 25 healthy non-pregnant- and 46 healthy pregnant controls (26-40 weeks' gestation), were enrolled in this prospective case-control study. Acid-base analysis was performed by applying the physicochemical approach of Stewart and Gilfix.
Mean [sd] base excess was similar in preeclamptic- and healthy pregnant women (-3.3 [2.3], and -2.8 [1.5] mEq/L respectively). In preeclampsia, there were greater offsetting contributions to the base excess, in the form of hyperchloraemia (BE(Cl) -2 [2.3] vs -0.4 [2.3] mEq/L, P<0.001) and hypoalbuminaemia (BE(Alb) 3.6 [1] vs 2.1 [0.8] mEq/L, P<0.001). In preeclampsia, hypoalbuminaemic metabolic alkalosis was associated with a non-reassuring/abnormal fetal heart tracing (P<0.001). Quantitative analysis in healthy pregnancy revealed respiratory and hypoalbuminaemic alkalosis that was metabolically offset by acidosis, secondary to unmeasured anions and dilution.
While the overall base excess in severe preeclampsia is similar to that in healthy pregnancy, preeclampsia is associated with a greater imbalance offsetting hypoalbuminaemic alkalosis and hyperchloraemic acidosis. Rather than the absolute value of base excess, the magnitude of these opposing contributors may be a better indicator of the severity of this disease. Hypoalbuminaemic alkalosis may also be a predictor of fetal compromise.
clinicaltrials.gov: NCT 02164370.
先兆子痫中常见的干扰因素,如强离子和弱酸(尤其是白蛋白)的变化对酸碱平衡状态的影响尚未完全阐明。本研究的目的是对重度先兆子痫进行全面的酸碱分析,并确定疾病严重程度的潜在新生物学预测指标。
本前瞻性病例对照研究纳入了50例重度先兆子痫患者、25例健康非孕女性和46例健康孕妇(妊娠26 - 40周)。采用Stewart和Gilfix的物理化学方法进行酸碱分析。
先兆子痫患者和健康孕妇的平均[标准差]碱剩余相似(分别为-3.3 [2.3]和-2.8 [1.5] mEq/L)。在先兆子痫中,以高氯血症(碱剩余(Cl) -2 [2.3] vs -0.4 [2.3] mEq/L,P<0.001)和低白蛋白血症(碱剩余(Alb) 3.6 [1] vs 2.1 [0.8] mEq/L,P<0.001)形式对碱剩余的抵消作用更大。在先兆子痫中,低白蛋白血症性代谢性碱中毒与胎儿心率异常/异常(P<0.001)相关。对健康妊娠的定量分析显示存在呼吸性和低白蛋白血症性碱中毒,继发于未测定阴离子和稀释的酸中毒对其进行代谢性抵消。
虽然重度先兆子痫的总体碱剩余与健康妊娠相似,但先兆子痫与更大的失衡有关,抵消了低白蛋白血症性碱中毒和高氯血症性酸中毒。这些相反因素的大小而非碱剩余的绝对值可能是该疾病严重程度的更好指标。低白蛋白血症性碱中毒也可能是胎儿窘迫的预测指标。
clinicaltrials.gov:NCT 02164370。