Saline vs. Lactated Ringers for Emergency Department IV Fluid Resuscitation

Phase 4

Completed

Conditions: Emergencies
Fluid Loss
Symptom Complex, Triple

Interventions: Drug: Normal Saline 0.9% Infusion Solution Bag
Drug: Lactated Ringer Solution

Registration Number: NCT03133767

Lead Sponsor: Nicholas M Mohr

Brief Summary: Administration of intravascular (IV) fluid is the most common emergency department (ED) procedure. IV fluids are integral to increasing effective blood volume and ensuring organ perfusion in patients with volume depletion and dehydration. There are many options of IV fluids providers can use when treating ED patients. Surveys show physicians do not cite an evidence-based reason for selecting the crystalloid IV fluid used; the decision was likely to be influenced by type and location of practice. A gap exists in the current literature, as there is no evidence for the optimal IV fluid choice for the ED patient requiring IV fluid before discharge.

Normal saline (NS) is commonly used as an IV fluid replacement in ED patients. However, NS has been associated with increased risk of acidosis and acute kidney injury. This study will use a novel approach of a patient-centered outcome in a non-critically ill population to ascertain the optimal IV fluid for patient quality of recovery. The results of this study will inform provider's IV fluid decisions between NS and LR. More importantly, the results of this study will have the power to improve patient's quality of recovery following IV fluid administration and subsequent ED discharge.

ED patients will be recruited, and participants will be randomized to receive one of two IV solutions (Lactated ringer's or normal saline). Participants will answer a survey before and after the intervention to assess their quality of recovery. The post-survey will be administered by phone after ED discharge. Participants will also be contacted by text message one week following their ED visit to gather information on their healthcare utilization.

Detailed Description: This is a single-center randomized, single-blinded, controlled clinical trial testing superiority of LR compared to NS in patients receiving IV fluid before discharge.

The study site is the University of Iowa Emergency Department (annual patient volume is 60,000 patients/year).

The study population will include adult ED patients presenting with chief complaints associated with volume depletion. Figure 1 outlines the enrollment flowchart for the study with inclusion and exclusion criteria. Research assistants (RAs) are available in the ED from 9am - 10pm every day, and an automated paging system will alert the team when patients qualify, as the study team has done previously. All participants will receive 2 liters of blinded IV fluid as part of the study. The intervention group will receive lactated ringer's, and the control group will receive normal saline (0.9% sodium chloride). Nursing staff will establish the peripheral IV access, and subjects will be blinded to group.

The primary outcome, Quality of Recovery-40, will be analyzed using a t-test (if parametric) or Mann Whitney U Test (non-parametric) in an intention-to-treat (ITT) analysis. Normality will be assessed with a Kolmogorov-Smirnov (K-S) and visualization of data. Due to the nature of time-critical emergency department research, an additional analysis will be done by treatment received and compared to the primary ITT analysis as a sensitivity analysis. Secondary outcomes will be reported as a relative risk with 95%CI in an ITT analysis. A safety analysis of secondary outcomes will be performed by treatment received (see page 37). Baseline characteristics will be reported with summary statistics as appropriate (mean, SD, median, IQR) and differences in characteristics will be conducted using a t-test and chi-square test, as appropriate. The following variables will also be assessed: actual fluid administered(mL), pre-intervention QoR-40 score, and time from intervention to primary outcome. If differences in these characteristics exist between the control and intervention groups, multivariate linear regression and multivariate logistic regression (primary and secondary outcomes, respectively) will be used.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 157

Inclusion Criteria

Emergency department patient
Chief complaint of nausea, vomiting or emesis, diarrhea, abdominal pain, dehydration, heat stroke or exhaustion
ED provider approves administration of two liters of fluid
ED provider states patient is likely to be discharged
Patient has followed up with PCP in the last two years
Patient has access to phone for next two days following ED discharge

Exclusion Criteria

Prisoners
Children
Women known to be pregnant
Jaundice
Current chemotherapy

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Normal saline solution	Normal Saline 0.9% Infusion Solution Bag	Participants in this arm will receive two liters of IV 0.9% sodium chloride solution during their emergency department stay
Lactated ringers solution	Lactated Ringer Solution	Participants in this arm will receive two liters of IV Lactated Ringer's solution during their emergency department stay

Primary Outcome Measures

Name	Time	Method
Quality of Recovery-40 Score at 24 Hours	24 hours after ED visit	The Quality of Recovery-40 (QoR-40) is a validated instrument that quantifies patient's self-assessment of functional recovery, symptoms, and physical comfort. The QoR-40 scores range from 40 to 200 with a 200 representing a better recovery outcome. The survey consists of 40 questions scored from one to five with a Likert scale, and the total score is the sum of each question.

Secondary Outcome Measures

Name	Time	Method
Quality of Recovery-40 Score After Administration	Immediately after fluid administration	The Quality of Recovery-40 (QoR-40) is a validated instrument that quantifies patient's self-assessment of functional recovery, symptoms, and physical comfort. The QoR-40 scores range from 40 to 200 with a 200 representing a better recovery outcome. The survey consists of 40 questions scored from one to five with a Likert scale, and the total score is the sum of each question.
Number of Participants That Filled an ED Prescription	7 days after study enrollment	Seven days after study enrollment, participants were asked by text message, "Have you filled any prescriptions from the emergency department?"
Number of Participants That Returned to the ED Within 7 Days for the Same Complaint	7 days	Seven days after study enrollment, participants were asked by text message, "Have you returned to the emergency department for the same problem?"
Participants That Sought Care From Another Healthcare Provider for the Same Complaint	7 days	Seven days after study enrollment, participants were asked by text message, "Have you seen another medical provider for the same complaint?".

Trial Locations

Locations (1): University of Iowa Hospitals and Clinics
🇺🇸
Iowa City, Iowa, United States
University of Iowa Hospitals and Clinics
🇺🇸Iowa City, Iowa, United States