- Open Access
Crystalloid fluid therapy
Critical Care volume 20, Article number: 59 (2016)
This article is one of ten reviews selected from the Annual Update in Intensive Care and Emergency medicine 2016. Other selected articles can be found online at http://www.biomedcentral.com/collections/annualupdate2016. Further information about the Annual Update in Intensive Care and Emergency Medicine is available from http://www.springer.com/series/8901.
“She filled his ancient veins with rich elixir. As he received it … his wasted form renewed, appeared in all the vigor of bright youth, no longer lean and sallow, for new blood coursed in his well‐filled veins” (Publius Ovidius Naso, Metamorphoses Book VII – The Story of Medea and Jason, 8 AD).
Our desire to find solutions that rejuvenate and resuscitate is captured in the story of Medea revitalizing Jason’s elderly father by filling his veins with a specially prepared elixir. Although no such elixir exists, intravenous fluids are an integral component of the multimodal resuscitation strategy used in medicine. Intravenous fluids were first administered over 180 years ago and despite their widespread use there remains uncertainty about their relative safety and efficacy.
Worldwide, there is variation in the prescribing of resuscitative intravenous fluids and the preferred choice of fluid appears to be based on local customs, marketing, fluid costs and availability . The majority of intravenous fluids were introduced into clinical practice during an era where they did not undergo the same scrutiny as other drugs. Hence, there is a paucity of research in this area and only recently has there been an increase in academic interest in the comparative effectiveness of different intravenous fluids.
Here, we review the composition of different crystalloid fluids, potential pathophysiological responses following crystalloid fluid infusion, evidence from animal studies, observational studies, and interventional studies comparing crystalloid fluids, and suggest future directions for research on the comparative effectiveness of various crystalloid fluids.
The composition of 0.9 % saline was first mentioned by Jakob Hamburger in the 1890s. It is unknown how 0.9 % saline became known as ‘normal saline’; however, use of term ‘normal’ may have contributed to the widespread acceptance of 0.9 % saline into clinical practice. Despite being referred to as ‘normal’, 0.9 % saline is not physiologically ‘normal’. First, 0.9 % saline has a higher chloride concentration than plasma. Second, 0.9 % saline has a different strong ion difference (SID) to plasma. According to the Stewart physiochemical approach to describing acid‐base balance, fluid pH is in part determined by the SID, which is the sum of the strong cation concentrations in the solution (e.g., sodium, potassium, magnesium), minus the sum of the strong anion concentrations in the solution (e.g., chloride and lactate). The SID of the extracellular fluid is approximately 40 mEq/l, whereas the SID of 0.9 % saline is zero. Following an infusion of 0.9 % saline there is a net decrease in the plasma SID resulting in a metabolic acidosis.
0.9 % saline is often thought of as a relatively hypertonic solution because the sum of its osmotically active components gives a theoretical in vitro osmolality of 308 mosmol/kg H2O (154 mmol/l sodium plus 154 mmol/l chloride). However, 0.9 % saline is more accurately referred to as an isotonic solution as its constituents – sodium and chloride – are only partially active, with an osmotic coefficient of 0.926. The calculated in vivo osmolality (tonicity) of saline is 285 mosmol/kgH2O, which is the same as plasma osmolality (tonicity).
Sydney Ringer’s in vitro experiments in the 1880s on the influence of crystalloid fluid composition on cardiac contractility led to the recognition of a potential benefit of the addition of other inorganic constituents to sodium chloride solutions. Alexis Hartmann further modified Ringer’s solution through the addition of sodium lactate to act as a buffering agent in an effort to combat acidosis in dehydrated pediatric patients.
Unlike 0.9 % saline, the available buffered crystalloid solutions contain physiological or near physiological amounts of chloride. One of the key differences between 0.9 % saline and buffered/balanced crystalloids is the presence of additional anions, such as lactate, acetate, malate and gluconate, which act as physiological buffers to generate bicarbonate. Further, buffered fluids, such as Hartmann’s solution and Ringer’s lactate, have near physiologically effective in vivo SIDs of 27 and 29 mEq/l, respectively. In contrast, Plasma‐Lyte 148® has an effective SID in vivo of 50 mEq/l. Despite the fact that buffered crystalloid fluids are designed to better mimic the composition of human plasma, no perfectly balanced or physiologically ‘normal’ crystalloid fluid is currently available (see Table 1).
Historically, sodium acetate was used during hemodialysis as an alternative to bicarbonate because of the incompatibility of bicarbonate with solutions containing calcium and magnesium salts. Early evidence suggested that sodium acetate solution was effective in restoring blood pH and plasma bicarbonate in patients suffering from metabolic acidosis ; however, a more recent study suggested that acetate was associated with hemodynamic instability, vasodilatation and negative inotropic affects in patients undergoing high volume renal replacement therapy (RRT) . Concern about the potential for myocardial depression with acetate is supported by studies suggesting that acetate decreases myocardial contractilityand blood pressure in dogs  and impaired contractile function in anisolated perfused rat heart model . Even the small quantity of acetate present in various dialysis fluids (usually 35 mmol/l) can result in plasma acetate concentrations of 10 to 40 times the physiological level (50 to 100 μmol/l) . Use of acetated solutions as acircuit prime for cardiac patients undergoing cardiopulmonary bypass (CPB) also results in short‐livedsupra‐physiological concentrations of acetate; however, it is not clear if these have any adverse clinical effects .
Despite these potential concerns, there are several theoretical advantages of using acetated solutions compared tolactate‐containing crystalloids. Acetate is metabolized widely throughout the body, is not reliant entirely on hepaticmetabolism and is metabolized more rapidly than lactate . A canine study showed that acetate metabolism was well‐preserved in profound shock while lactate metabolism was significantly impaired . Acetate metabolism does not result in changes in glucose or insulin concentrations, whereas exogenously administered lactate can be converted to glucose via gluconeogenesis resulting in hyperglycemia . Acetate turnover shows no age‐related differences , and acetate may protect against malnutrition by replacing fat as anoxidative fuel without affecting glucose oxidation, or causing hyperglycemia .
Little is known about the clinical effects of gluconate. Gluconate is largely excreted unchanged in the urine (80 %). In a recent Phase II evaluation of an acetate/gluconate‐based buffered solution (Plasma‐Lyte 148®) versus abicarbonate buffered crystalloid fluid for CPB circuit priming, Plasma‐Lyte 148® was associated with an immediate increase in unmeasured anions of > 10 mEq/l (presumably acetate and/or gluconate), with residual elevations still present just prior to CPB cessation . The clinical significance of elevated gluconate and/or acetate levels remains unclear in this setting.
Hartmann’s solution or Ringer’s lactate are hypotonic solutions with a calculated in vivo osmolality (tonicity) of approximately 254 mOsmol/kgH2O. Perioperative administration of hypotonic fluids can represent a significant free water load that may not be easily excreted in the presence of the high anti‐diuretic hormone concentrations commonly associated with physiological stress. Failure to excrete water in a timely fashion may result in postoperative positive fluid balance, edema, and weight gain. Hypotonic fluids are also contraindicated in patients with or at risk of cerebral edema.
In addition to differences in buffering agents, buffered solutions also vary in the presence and concentration of ancillary cations (sodium, potassium, calcium, magnesium), which means they are not biologically equivalent. Hartmann’s solution contains 2 mmol/l of calcium and is contraindicated with blood or blood‐related products due to concerns about precipitation and the possibility of coagulation and clot formation. A recent warning has been issued about mixing calcium‐containing solutions, including Hartmann’s solution or Ringer’s lactate, with ceftriaxone causing the formation of the insoluble ceftriaxone calcium salt .
Although some authors have argued that hyperchloremia secondary to 0.9 % saline is a benign and self‐limiting phenomenon, there is some evidence that hyperchloremia is independently associated with adverse clinical outcomes . The biological plausibility that 0.9 % saline may affect renal function is supported by a cross‐over study of 12 volunteers that reported significantly higher serum chloride levels, reduced renal artery blood velocity and reduced renal cortical tissue perfusion in subjects who received 2 l of 0.9 % saline over 1 h compared to those that had received Plasma‐Lyte 148® . This study also found that although 0.9 % saline and Plasma‐Lyte 148® expanded the intravascular volume to the same degree, 0.9 % saline expanded the extracellular fluid volume significantly more than did Plasma‐Lyte 148® meaning that 0.9 % saline may be more likely to result in fluid overload and interstitial edema.
Experimental research has identified possible hematological and gastrointestinal pathways that may be impaired with the use of 0.9 % saline. Ex vivo testing of diluted whole blood reported that dilution with Ringer’s lactate resulted in less impairment in thrombin generation and platelet activation when compared to 0.9 % saline . A swine study reported that metabolic acidosis significantly impaired gastropyloric motility by reducing pyloric contraction amplitude, which results in delayed gastric emptying or gastroparesis .
Animal studies comparing 0.9 % saline to buffered crystalloid fluids
Recently, Zhou et al. reported decreased rates of acute kidney injury (AKI) and improved survival in rats receiving Plasma‐Lyte® compared to 0.9 % saline in an animal model of sepsis . In this experiment, 60 rats were randomized to receive 0.9 % saline or Plasma‐Lyte® for 4 h (10 ml/kg for the first hour and 5 ml/kg over the next 3 h) after 18 h of cecal ligation and puncture. Rats that received 0.9 % saline had higher rates of AKI (100 % vs. 76 %, p < 0.05) and significantly worse AKI severity based on the Risk, Injury, Failure, Loss of kidney function, End‐stage kidney disease (RIFLE) criteria creatinine definitions (RIFLE‐I or F: 83 % vs. 28 %, p < 0.001). Histopathological and biomarkers (urine cystatin C and urine neutrophil gelatinase‐associated lipocalin) of AKI were also significantly worse in rats that received 0.9 % saline compared to rats that received Plasma‐Lyte®.
The largest animal study comparing 0.9 % saline versus buffered fluid was a swine model of hemorrhagic shock that randomized 116 pigs to crystalloid fluid replacement at different percentages of replacement (0.9 % saline at 14 % replacement of blood loss; 0.9 % saline at 100 % replacement of blood loss; 0.9 % saline at 300 % replacement of blood loss; Ringer’s lactate at 300 % replacement of blood loss; Plasma‐Lyte A® at 300 % replacement of blood loss; Plasma‐Lyte R® at 300 % replacement of blood loss) . In a comparison of the different 300 % treatment groups, a significant difference was found in survival at 24 h in pigs that received Ringer’s lactate (67 %) compared to Plasma‐Lyte A® (30 %). No difference was found in survival rates in 0.9 % saline (50 %) or Plasma‐Lyte R® (40 %) groups.
Observational studies comparing 0.9 % saline to buffered crystalloid fluids
The majority of evidence demonstrating potential adverse clinical effects with the use of 0.9 % saline compared to buffered crystalloids originated from recent observational studies in critically unwell and surgical patients [20–22]. In a single center, open‐label, sequential 6‐month study of 1533 critically ill patients, the change from standard chloride‐liberal fluids (0.9 % saline, 4 % succinylate gelatin or 4 % albumin) to chloride‐restrictive fluids (Hartmann’s solution, Plasma‐Lyte 148® and 20 % albumin) was associated with a significant decrease in the risk of developing RIFLE‐defined AKI (odds ratio [OR] 0.52, 95 % CI 0.37–0.75, p < 0.01) and requirements for RRT while in the intensive care unit (ICU) (OR 0.52, 95 % CI, 0.33–0.81, p = 0.004) . No difference between groups was found in hospital mortality and hospital or ICU length of stay. A recently published extended analysis over the 12 months before and after the strategy change, which included 2994 patients, reported persistently lower rates of AKI according to the Kidney Disease: Improving Global Outcomes (KDIGO) creatinine definitions and decreased requirements of RRT . Because multiple changes in fluids occurred simultaneously in this observational study it is not possible to determine what component of the fluid change strategy (if any) was responsible for the observed changes.
The two largest studies that have assessed the effects of buffered versus unbuffered crystalloid fluid were retrospective observational studies with patient data collected from centralized health‐economic databases [21, 22]. The most recent study was conducted in non‐surgical, adult patients with the International Classification of Disease, Ninth Edition Clinical Modification (ICD‐9‐CM) codes for sepsis who were receiving vasopressors in the ICU by day two, and had received three consecutive days of antibiotics and had had a blood culture . In total 53,448 patients were identified from 360 hospitals over five years. Of this cohort, only 3365 patients (6.4 %) had received some “balanced fluids” during their first two hospital days. This sample was compared with a propensity‐matched group of 3365 patients who had “not received balanced fluids” (received either 0.9 % saline or 5 % dextrose). Patients who had received balanced fluids had a significantly lower in‐hospital mortality (19.6 % vs. 22.8 %; relative risk [RR] 0.86, 95 % CI 0.78–0.94, p = 0.001) compared to the group that had not received balanced fluids. No difference was found between groups in acute renal failure (defined by ICD‐9‐CM codes), need for dialysis and hospital or ICU length of stay. The vast majority of patients in the balanced group had received a mixture of intravenous fluids and it was reported that less than 1 % of patients in the balanced fluid group had exclusively received balanced fluids. On further analysis, patients were stratified by the proportion of balanced to unbalanced fluid they had received. The relative risk of in‐hospital mortality was progressively lower among patients who received a greater proportion of balanced fluid.
A similar retrospective study was conducted in adult patients who had undergone non‐traumatic, open, general surgical abdominal operations who had exclusively received either 0.9 % saline or a balanced fluid (defined as a calcium‐free buffered fluid: Plasma‐Lyte 148® or Plasma‐Lyte A®) on the day of surgery . In total 271,189 patients from approximately 600 hospitals had received fluids on the day of surgery. Of these patients, 30,994 received 0.9 % saline and 926 received balanced fluid. Propensity matching was used to mitigate for baseline group imbalances, which included a significantly higher proportion of minorities, less commercial insurance, greater proportion of patients from non‐teaching hospitals, greater proportion of admissions via the emergency department and significantly higher rates of co‐morbidities (based on ICD‐9‐CM codes), such as renal failure, diabetes and congestive heart failure in patients that had exclusively received 0.9 % saline. On matched analysis, patients who exclusively received balanced fluid had a decreased risk of major complications (OR 0.79, 95 % CI 0.66–0.97, p < 0.05) including need for blood transfusion (1.8 % vs. 11.5 %, p < 0.001) and need for dialysis (1.0 % vs. 4.8 %, p < 0.001). However, those in the balanced fluid group had higher rates of minor gastrointestinal complications (OR 1.45; 95 % CI 1.17–1.79, p < 0.05) and longer hospital lengths of stay (6.4 vs. 5.9 days, p < 0.001).
Overall, existing data from observational studies suggest that the use of high chloride, unbuffered crystalloid fluid may be associated with major complications following surgery and increased mortality in critically ill patients with sepsis. However, due to the retrospective nature of these studies and potential for unmeasured confounding, it is not possible to establish whether using buffered crystalloid fluid instead of 0.9 % saline is beneficial or harmful on the basis of observational studies.
Interventional studies comparing 0.9 % saline to buffered crystalloid fluids
Until 2015, all interventional studies comparing 0.9 % saline to buffered crystalloid had a small sample size (n < 100) and focused primarily on short term physiological or biochemical outcomes (see Table 2). A systematic review and meta‐analysis published in 2014 identified 28 prospective, randomized controlled trials with at least 20 adult participants that had compared the effects of different crystalloid fluids . Twenty‐three studies that explored acid‐base balance reported that 0.9 % saline was associated with decreased serum pH, elevated serum chloride levels and decreased bicarbonate levels. In 11 studies that explored renal function, based on urine volume or serum creatinine, no significant difference was found between fluids. In three surgical studies (n = 156) that reported volumes of red blood cells transfused, patients who had received Ringer’s lactate required significantly less volume of red blood cells than those who had received 0.9 % saline (RR 0.42, 95 % CI 0.11–0.73). No differences were found between Ringer’s lactate and 0.9 % saline in requirements for transfusion or operative blood loss, except in an exploratory sub‐group analysis of “high‐risk” patients that showed increased blood loss with the use of 0.9 % saline in patients that were at increased risk of bleeding.
Based on the published evidence prior to 2014, the National Institute for Health and Care Excellence (NICE) guidelines on intravenous fluid therapy in adults in hospital currently recommend the use of crystalloids that contain sodium in the range 130–154 mmol/l for fluid resuscitation . However, the guidelines state that the available evidence at the time of writing was limited and of “poor” quality. Research todate has been in heterogeneous populations and has been underpowered to allow for differences to be detected inclinically significant outcome measures. The NICE committee specifically identified that research comparing balanced solutions to 0.9 % saline for fluid resuscitation was a high priority.
The SPLIT program
The 0.9 % saline vs. Plasma‐Lyte 148® for intravenous fluid therapy research program is an investigator‐initiated, bi‐national collaborative research program investigating the comparative effectiveness of 0.9 % saline versus a buffered crystalloid as intravenous fluid therapy. Specific details on the study design, methods of analyzing and reporting of the research program have been published previously . At the time of writing, four of the six planned studies in critically unwell and elective surgical patients have been completed.
The largest study was the 0.9 % Saline versus Plasma‐Lyte 148® for Intensive care fluid Therapy (SPLIT) trial. The SPLIT trial was a multicenter, blinded, cluster randomized, double crossover study that compared Plasma‐Lyte 148® with 0.9 % saline as the routine ICU intravenous fluid . All ICU patients needing crystalloid fluid therapy were eligible to be included. Patients who were on dialysis, expected to require RRT within six hours and patients admitted to the ICU solely for organ donation or for palliative care were excluded. In total, 2262 patients in four New Zealand tertiary ICUs over a 28‐week period were enrolled and analyzed, with 1152 patients assigned to receive Plasma‐Lyte 148® and 1110 assigned to receive 0.9 % saline. The two groups of patients had similar admission diagnoses and baseline characteristics. There were no differences between patients who received Plasma‐Lyte 148® compared to 0.9 % saline in rates of AKI (9.6 % vs. 9.2 % [difference 0.4 %, 95 % CI −2.1 %–2.9 %; RR 1.04, 95 % CI 0.80–1.36, p = 0.77]) or requirements for RRT (3.3 % vs. 3.4 % [difference 0.1 %, 95 % CI −1.5 %–1.4 %; RR 0.96, 95 % CI 0.62–1.50, p = 0.91]). There were also no significant differences in need for mechanical ventilation, readmission to the ICU, ICU length of stay or in hospital mortality.
Two single‐centered, pilot, nested cohort studies were also conducted in patients enrolled in the SPLIT trial. The first of these studies evaluated 251 adults who had undergone cardiac surgery: 131 were allocated to Plasma‐Lyte 148® and 120 were allocated to 0.9 % saline. No difference was found between groups in postoperative chest drain output or in the proportion of patients developing a major postoperative complication (death, myocardial infarction, new focal neurological deficit or renal failure requiring dialysis). However, fewer patients in the 0.9 % saline group required blood products (packed red blood cells, fresh frozen plasma, platelets or cryoprecipitate) compared to patients in the Plasma‐Lyte 148® group (18.3 % vs. 30.5 %, p = 0.03). The second nested cohort study compared gastrointestinal feeding intolerance in 69 patients (35 assigned to receive Plasma‐Lyte 148® and 34 to receive 0.9 % saline) expected to require mechanical ventilation for greater than 48 h and receiving enteral nutrition exclusively by a nasogastric tube. Despite no difference between groups in the proportion of patients with gastrointestinal feeding intolerance (defined as high gastric residual volume, diarrhea or vomiting while receiving nasogastric feeding in the ICU), a significantly lower proportion of patients in the Plasma‐Lyte 148® group developed high gastric residual volumes (11.4 % vs. 32.4 %, p = 0.04).
Finally, a prospective single center blinded study investigated the safety and efficacy of using 0.9 % saline or Plasma‐Lyte® 148 as fluid therapy in adult patients undergoing major surgery. Trial fluid was used intraoperatively and postoperatively for three consecutive days. Inclusion criterion included patients undergoing surgery of at least two hours duration and requiring at least one overnight stay. Patients with end‐stage renal disease and those undergoing liver or renal transplantation were excluded. The primary outcome measure was the proportion of patients with either acute kidney injury or failure based on creatinine levels in accordance with RIFLE‐criteria during the index hospital admission. Intraoperatively, there was 100 % compliance with the trial protocol. A total of 746 patients received Plasma‐Lyte 148® and 634 patients received 0.9 % saline. Patients in both groups had similar baseline characteristics with respect to age, sex, body mass index, American Society of Anesthesiologists (ASA) status, types and number of comorbidities, duration and types of surgery. The median amount of trial fluid received was greater in the Plasma‐Lyte 148® group: 2000 ml (interquartile range [IQR] 1000, 2000) vs. 1925 ml (1000, 2000) in the 0.9 % saline group (p = 0.007). Patients receiving 0.9 % saline developed a transient hyperchloremic metabolic acidosis on postoperative Day 1 compared to patients receiving Plasma‐Lyte 148®. Postoperatively, there were no differences in the incidence of AKI between the groups: 52 (10.9 %) patients in the Plasma‐Lyte 148® group developed postoperative AKI compared to 59 (9.3 %) patients in the 0.9 % saline group (p = 0.41, 95 % CI 0.6–1.2). Patients who developed AKI were older, had larger volumes of fluid both intraoperatively and on postoperative Day 1, and had greater fluid balances intraoperatively and on postoperative Day 1. There were no differences in the development of postoperative complications between the groups. Median lengths of stay were similar between treatment groups: Plasma‐Lyte 148® 5.0 days (2.77–8.98) vs. 0.9 % saline 5.0 days (2.81–9.04).
Intravenous fluid therapy is a ubiquitous intervention in critically ill patients. While pre‐clinical and observational data raise the possibility that the choice of crystalloid fluid therapy may affect patient‐centered outcomes, there are currently no convincing data from interventional studies demonstrating that this is the case. Recent data suggest that 0.9 % saline and Plasma‐Lyte® 148 result in similar rates of renal complications when used for fluid therapy in patients undergoing major surgery and in ICU patients. Further large randomized controlled trials are needed to assess the comparative effectiveness of 0.9 % saline and balanced/buffered crystalloids in high‐risk populations and to measure clinical outcomes such as mortality. Moreover, given the widespread use of a range of balanced/buffered crystalloids in current clinical practice, high quality studies comparing the various buffered crystalloids available are also needed.
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Publication of this article was funded by the Medical Research Institute of New Zealand.
Laurence Weinberg has received research funding from Baxter Healthcare. Paul Young report receiving honoraria (<USD$5000) from Baxter Healthcare Pty Ltd for consulting activities. No other disclosures are reported.
SR, LW, and PY, have contributed in the literature review and drafting of the manuscript. All authors read and approved the final manuscript.
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Reddy, S., Weinberg, L. & Young, P. Crystalloid fluid therapy. Crit Care 20, 59 (2016). https://doi.org/10.1186/s13054-016-1217-5
- Renal Replacement Therapy
- Acute Kidney Injury
- Intensive Care Unit Length
- Crystalloid Fluid
- Hypotonic Fluid