Observation on the effectiveness and safety of sodium bicarbonate Ringer's solution in the early resuscitation of traumatic hemorrhagic shock: a clinical single-center prospective randomized controlled trial

被引:7
|
作者
Zhang, Jizhe [1 ,2 ,3 ]
Han, Dong [4 ]
Zhang, Kun [1 ,2 ,3 ]
Guan, Weiqiang [1 ,2 ,3 ]
Li, Li [1 ,2 ,3 ]
Gu, Zhengtao [1 ,2 ,3 ]
机构
[1] Southern Med Univ, Dept Treatment Ctr Traumat Injuries, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[2] Acad Orthopaed, Guangdong Prov Key Lab Bone & Joint Degenerat Dis, Guangzhou, Guangdong, Peoples R China
[3] Orthopaed Hosp Guangdong Prov, Guangzhou, Guangdong, Peoples R China
[4] Southern Med Univ, Dept Qual Control & Evaluat, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
关键词
Traumatic hemorrhagic shock; Fluid resuscitation; Sodium bicarbonate Ringer's solution; Lactate clearance; BALANCED CRYSTALLOIDS; SALINE; DEATHS; INJURY; FLUIDS; EPIDEMIOLOGY; ASSOCIATION; MORTALITY; OUTCOMES; PATIENT;
D O I
10.1186/s13063-022-06752-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background Traumatic hemorrhagic shock (THS) is the main cause of death in trauma patients with high mortality. Rapid control of the source of bleeding and early resuscitation are crucial to clinical treatment. Guidelines recommend isotonic crystal resuscitation when blood products are not immediately available. However, the selection of isotonic crystals has been controversial. Sodium bicarbonate Ringer solutions (BRS), containing sodium bicarbonate, electrolyte levels, and osmotic pressures closer to plasma, are ideal. Therefore, in this study, we will focus on the effects of BRS on the first 6 h of resuscitation, complications, and 7-day survival in patients with THS. Methods /design. This single-center, prospective, randomized controlled trial will focus on the efficacy and safety of BRS in early THS resuscitation. A total of 400 adults THS patients will be enrolled in this study. In addition to providing standard care, enrolled patients will be randomized in a 1:1 ratio to receive resuscitation with BRS (test group) or sodium lactate Ringer's solution (control group) until successful resuscitation from THS. Lactate clearance at different time points (0.5, 1, 1.5, 3, and 6 h) and shock duration after drug administration will be compared between the two groups as primary end points. Secondary end points will compare coagulation function, temperature, acidosis, inflammatory mediator levels, recurrence of shock, complications, medication use, and 7-day mortality between the two groups. Patients will be followed up until discharge or 7 days after discharge. Discussion At present, there are still great differences in the selection of resuscitation fluids, and there is a lack of systematic and detailed studies to compare and observe the effects of various resuscitation fluids on the effectiveness and safety of early resuscitation in THS patients. This trial will provide important clinical data for resuscitation fluid selection and exploration of safe dose of BRS in THS patients. Trial registration. Chinese Clinical Trial Registry (ChiCTR), ChiCTR2100045044. Registered on 4 April 2021.
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页数:12
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