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.

Jizhe Zhang, Dong Han, Kun Zhang, Weiqiang Guan, Li Li, Zhengtao Gu

Journal: Trials 2022;23(1):825

PMID: 36175936

Abstract

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.

© 2022. The Author(s).

Address: Department of Treatment Center For Traumatic Injuries, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China.; Guangdong Provincial Key Laboratory of Bone and Joint Degenerative Diseases, Academy of Orthopaedics, Guangdong Province, Guangzhou, China.; Orthopaedics Hospital of Guangdong Province, Guangzhou, Guangdong, China.; Department of Quality Control and Evaluation, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China.; Department of Treatment Center For Traumatic Injuries, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China. [email protected].; Guangdong Provincial Key Laboratory of Bone and Joint Degenerative Diseases, Academy of Orthopaedics, Guangdong Province, Guangzhou, China. [email protected].; Orthopaedics Hospital of Guangdong Province, Guangzhou, Guangdong, China. [email protected].; Department of Treatment Center For Traumatic Injuries, The Third Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong, China. [email protected].; Guangdong Provincial Key Laboratory of Bone and Joint Degenerative Diseases, Academy of Orthopaedics, Guangdong Province, Guangzhou, China. [email protected].; Orthopaedics Hospital of Guangdong Province, Guangzhou, Guangdong, China. [email protected].
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