Department of Obstetrics and Gynecology, Hackensack Meridian Health, Hackensack, New Jersey.
Division of Maternal-Fetal Medicine and Surgery, Department of Obstetrics and Gynecology, Hackensack Meridian Health, Hackensack, New Jersey.
Am J Perinatol. 2018 Jun;35(7):655-659. doi: 10.1055/s-0037-1613675. Epub 2017 Dec 5.
This article compares hemorrhage recognition and transfusion using accurate, contemporaneous blood loss measurement versus visual estimation during cesarean deliveries.
A retrospective cohort study using visually estimated blood loss (traditional, = 2,025) versus estimates using a mobile application that photographs sponges and canisters and calculates their hemoglobin content (device, = 756).
Blood loss > 1,000 mL was recognized in 1.9% of traditional visual estimation patients, while measured blood loss of > 1,000 mL occurred in 8.2% of device patients ( < 0.0001). In both groups, this was accompanied by a greater decrease in transfusion-adjusted hemoglobin levels than occurred in patients without hemorrhage ( < 0.0001). Despite similar transfusion rates (1.6% in both groups), fewer red cell units were given to transfused patients in the device group (1.83 ± 0.58 versus 2.56 ± 1.68 units; = 0.038). None of the patients in the device group received plasma or cryoprecipitate. Seven patients in the traditional group received these products ( = 0.088). Device use was associated with shorter hospital stays (4.0 ± 2.3 versus 4.4 ± 2.9 days; = 0.0006).
The device identified hemorrhages more frequently than visual estimation. Device-detected hemorrhages appeared clinically relevant. Blood product transfusion was reduced possibly due to earlier recognition and treatment, although further studies are needed to verify the conclusion.
本文比较了在剖宫产术中使用准确的、即时的出血量测量与视觉估计来识别和输血。
回顾性队列研究,使用视觉估计失血量(传统方法,n=2025)与使用可以拍摄海绵和容器并计算其血红蛋白含量的移动应用程序(设备组,n=756)估计的失血量。
传统视觉估计患者中,出血量>1000ml 的比例为 1.9%,而设备组患者中出血量>1000ml 的比例为 8.2%(<0.0001)。在这两组中,与无出血患者相比,输血调整后的血红蛋白水平下降幅度更大(<0.0001)。尽管输血率相似(两组均为 1.6%),但设备组输血患者的红细胞单位数较少(1.83±0.58 比 2.56±1.68 单位;=0.038)。设备组无一例患者输注血浆或冷沉淀。传统组有 7 例患者接受了这些产品(=0.088)。设备的使用与较短的住院时间相关(4.0±2.3 比 4.4±2.9 天;=0.0006)。
与视觉估计相比,设备更频繁地识别出出血。设备检测到的出血似乎具有临床相关性。由于更早的识别和治疗,输血减少可能是由于更早的识别和治疗,尽管还需要进一步的研究来验证这一结论。