Editorial Type: Veterinary Practice Guidelines
 | 
Online Publication Date: 01 May 2013

2013 AAHA/AAFP Fluid Therapy Guidelines for Dogs and Cats*

BA, RVT, VTS (ECC),
DVM, DABVP,
DVM, DACVECC,
CVT, VTS (ECC),
DVM, DACVAA,
DVM, DAVBP (Feline), and
DVM, PhD, DACVAA
Article Category: Case Report
Page Range: 149 – 159
DOI: 10.5326/JAAHA-MS-5868
Save
Download PDF

Fluid therapy is important for many medical conditions in veterinary patients. The assessment of patient history, chief complaint, physical exam findings, and indicated additional testing will determine the need for fluid therapy. Fluid selection is dictated by the patient’s needs, including volume, rate, fluid composition required, and location the fluid is needed (e.g., interstitial versus intravascular). Therapy must be individualized, tailored to each patient, and constantly re-evaluated and reformulated according to changes in status. Needs may vary according to the existence of either acute or chronic conditions, patient pathology (e.g., acid-base, oncotic, electrolyte abnormalities), and comorbid conditions. All patients should be assessed for three types of fluid disturbances: changes in volume, changes in content, and/or changes in distribution. The goals of these guidelines are to assist the clinician in prioritizing goals, selecting appropriate fluids and rates of administration, and assessing patient response to therapy. These guidelines provide recommendations for fluid administration for anesthetized patients and patients with fluid disturbances.

Introduction

These guidelines will provide practical recommendations for fluid choice, rate, and route of administration. They are organized by general considerations, followed by specific guidelines for perianesthetic fluid therapy and for treatment of patients with alterations in body fluid volume, changes in body fluid content, and abnormal distribution of fluid within the body. Please note that these guidelines are neither standards of care nor American Animal Hospital Association (AAHA) accreditation standards and should not be considered minimum guidelines. Instead these guidelines are recommendations from an AAHA/American Association of Feline Practitioners (AAFP) panel of experts.

Therapy must be individualized and tailored to each patient and constantly re-evaluated and reformulated according to changes in status. Fluid selection is dictated by the patient’s needs, including volume, rate, and fluid composition required, as well as location the fluid is needed (interstitial versus intravascular). Factors to consider include the following:

  • Acute versus chronic conditions

  • Patient pathology (e.g., acid-base balance, oncotic pressure, electrolyte abnormalities)

  • Comorbid conditions

A variety of conditions can be effectively managed using three types of fluids: a balanced isotonic electrolyte (e.g., a crystalloid such as lactated Ringer’s solution [LRS]); a hypotonic solution (e.g., a crystalloid such as 5% dextrose in water [D5W]); and a synthetic colloid (e.g., a hydroxyethyl starch such as hetastarch or tetrastarch).

General Principles and Patient Assessment

The assessment of patient history, chief complaint, and physical exam findings will determine the need for additional testing and fluid therapy. Assess for the following three types of fluid disturbances:

  1. Changes in volume (e.g., dehydration, blood loss)

  2. Changes in content (e.g., hyperkalemia)

  3. Changes in distribution (e.g., pleural effusion)

The initial assessment includes evaluation of hydration, tissue perfusion, and fluid volume/loss. Items of particular importance in evaluating the need for fluids are described in Table 1. Next, develop a treatment plan by first determining the appropriate route of fluid administration. Guidelines for route of administration are shown in Table 2.

TABLE 1 Evaluation and Monitoring Parameters that May Be Used for Patients Receiving Fluid Therapy
TABLE 1

BP, blood pressure.

TABLE 2 Determining the Route of Fluid Administration
TABLE 2

D5W, 5% dextrose in water.

Consider the temperature of the fluids. Body temperature (warmed) fluids are useful for large volume resuscitation but provide limited usefulness at low IV infusion rates. It is not possible to provide sufficient heat via IV fluids at limited infusion rates to either meet or exceed heat losses elsewhere.1

Fluids for Maintenance and Replacement

Whether administered either during anesthesia or to a sick patient, fluid therapy often begins with the maintenance rate, which is the amount of fluid estimated to maintain normal patient fluid balance (Table 3). Urine production constitutes the majority of fluid loss in healthy patients.2,3 Maintenance fluid therapy is indicated for patients that are not eating or drinking, but do not have volume depletion, hypotension, or ongoing losses.

TABLE 3 Recommended Maintenance Fluid Rates (mL/kg/hr)49
TABLE 3

Replacement fluids (e.g., LRS) are intended to replace lost body fluids and electrolytes. Isotonic polyionic replacement crystalloids such as LRS may be used as either replacement or as maintenance fluids. Using replacement solutions for short-term maintenance fluid therapy typically does not alter electrolyte balance; however, electrolyte imbalances can occur in patients with renal disease or in those receiving long-term administration of replacement solutions for maintenance.

Administering replacement solutions such as LRS for maintenance predisposes the patient to hypernatremia and hypokalemia because these solutions contain more sodium (Na) and less potassium (K) than the patient normally loses. Well-hydrated patients with normal renal function are typically able to excrete excess Na and thus do not develop hypernatremia. Hypokalemia may develop in patients that receive replacement solutions for maintenance fluid therapy if they are either anorexic or have vomiting or diarrhea because the kidneys do not conserve K very well.4

If using a replacement crystalloid solution for maintenance therapy, monitor serum electrolytes periodically (e.g., q 24 hr). Maintenance crystalloid solutions are commercially available. Alternatively, fluid made up of equal volumes of replacement solution and D5W supplemented with K (i.e., potassium chloride [KCl], 13–20 mmol/L, which is equivalent to 13–20 mEq/L) would be ideal for replacing normal ongoing losses because of the lower Na and higher K concentration. Another option for a maintenance fluid solution is to use 0.45% sodium chloride with 13–20 mmol/L KCl added.5 Additional resources regarding fluid therapy and types of fluids are available on the AAHA and AAFP websites.

Fluids and Anesthesia

One of the most common uses of fluid therapy is for patient support during the perianesthetic period. Decisions regarding whether to provide fluids during anesthesia and the type and volume used depend on many factors, including the patient’s signalment, physical condition, and the length and type of the procedure. Advantages of providing perianesthetic fluid therapy for healthy animals include the following:

  • Correction of normal ongoing fluid losses, support of cardiovascular function, and ability to maintain whole body fluid volume during long anesthetic periods

  • Countering of potential negative physiologic effects associated with the anesthetic agents (e.g., hypotension, vasodilation)

  • Continuous flow of fluids through an IV catheter prevents clot formation in the catheter and allows the veterinary team to quickly identify problems with the catheter prior to needing it in an emergency

When fluids are provided, continual monitoring of the assessment parameters is essential (Table 1). The primary risk of providing excessive IV fluids in healthy patients is the potential for vascular overload. Current recommendations are to deliver < 10 mL/kg/hr to avoid adverse effects associated with hypervolemia, particularly in cats (due to their smaller blood volume), and all patients anticipated to be under general anesthesia for long periods of time (Table 4).68 In the absence of evidence-based anesthesia fluid rates for animals, the authors suggest initially starting at 3 mL/kg/hr in cats and 5 mL/kg/hr in dogs. Preoperative volume loading of normovolemic patients is not recommended.

TABLE 4 Recommendations for Anesthetic Fluid Rates
TABLE 4

The paradigm of “crystalloid fluids at 10 mL/kg/hr, with higher volumes for anesthesia-induced hypotension” is not evidence-based and should be reassessed. Those high fluid rates may actually lead to worsened outcomes, including increased body weight and lung water; decreased pulmonary function; coagulation deficits; reduced gut motility; reduced tissue oxygenation; increased infection rate; increased body weight; and positive fluid balance, with decreases in packed cell volume, total protein concentration, and body temperature.9,10 Note that infusion of 10–30 mL/kg/hr LRS to isoflurane-anesthetized dogs did not change either urine production or O2 delivery to tissues.11 A fluid-consuming “third space” has never been reliably shown, and, in humans, blood volume was unchanged after overnight fasting.12

Preanesthetic Fluids and Preparing the Sick Patient

Correct fluid and electrolyte abnormalities in the sick patient as much as possible before anesthesia by balancing the need for preanesthetic fluid correction with the condition requiring surgery. For example, patients with uremia benefit from preanesthetic fluid administration.13 Further, develop a plan for how fluids will be used in an anesthesia-related emergency based on individual comoribund conditions, such as hypertrophic cardiomyopathy and oliguric/polyuric renal disease.

Monitoring and Responding to Hypotension During Anesthesia

Blood pressure (BP) is the parameter often used to estimate tissue perfusion, although its accuracy as an indicator of blood flow is not certain.11,14,15 Hypotension under anesthesia is a frequent occurrence, even in healthy anesthetized veterinary patients. Assess excessive anesthetic depth first because it is a common cause of hypotension.7,16 Exercise caution when using fluid therapy as the sole method to correct anesthesia-related hypotension as high rates of fluids can exacerbate complications rather than prevent them.10,11

If relative hypovolemia due to peripheral vasodilation is contributing to hypotension in the anesthetized patient, proceed as described in the following list:

  • Decrease anesthetic depth and/or inhalant concentration.

  • Provide an IV bolus of an isotonic crystalloid such as LRS (3–10 mL/kg). Repeat once if needed.

  • If response is inadequate, consider IV administration of a colloid such as hetastarch. Slowly administer 5–10 mL/kg for dogs and 1–5 mL/kg for cats, titrating to effect to minimize the risk of vascular overload (measure BP every 3–5 min).9 Colloids are more likely to increase BP than crystalloids.15

  • If response to crystalloid and/or colloid boluses is inadequate and patient is not hypovolemic, techniques other than fluid therapy may be needed (e.g., vasopressors or, balanced anesthetic techniques).9

  • Caution: Do not use hypotonic solutions to correct hypovolemia or as a fluid bolus because this can lead to hyponatremia and water intoxication.

Postanesthetic Fluid Therapy

Postanesthetic fluid administration varies based on intra-anesthetic complications and comorbid conditions. Patients that may benefit from fluid therapy after anesthesia include geriatric patients and patients with either renal disease or ongoing fluid losses from gastrointestinal disease. Details regarding anesthesia management may be found in the AAHA Anesthesia Guidelines for Dogs and Cats.17

Fluid Therapy in the Sick Patient

First, determine the initial rate and volume based on whether the patient needs whole body rehydration or vascular space volume expansion. Next, determine the fluid type based on replacement and maintenance needs as described in the following sections. Fluid therapy for disease falls into one or more of the following three categories: the need to treat changes in volume, content, and/or distribution.

Typically, the goal is to restore normal fluid and electrolyte status as soon as possible (within 24 hr) considering the limitations of comoribund conditions. Once those issues are addressed, the rate, composition, and volume of fluid therapy can be based on ongoing losses and maintenance needs. Replace the deficit as well as normal and abnormal ongoing losses simultaneously (e.g., continued vomiting/diarrhea as described below in the “Changes in Fluid Volume” section). Accurate dosing is essential, particularly in small patients, to prevent volume overload.

Monitor Response to Fluid Therapy

Individual patients’ fluid therapy needs change often. Monitor for a resolution of the signs that indicated the patient was in need of fluids (Table 1). Monitor for under-administration (e.g., persistent increased heart rate, poor pulse quality, hypotension, urine output), and overadministration (e.g., increased respiratory rate and effort, peripheral and/or pulmonary edema, weight gain, pulmonary crackles [a late indicator]) as described in Table 1. Patients with a high risk of fluid overload include those with heart disease, renal disease, and patients receiving fluids via gravity flow.16

Cats require very close monitoring. Their smaller blood volume, lower metabolic rate, and higher incidence of occult cardiac disease make them less tolerant of high fluid rates.7,18

Changes in Fluid Volume

The physical exam will help determine if the patient has whole body fluid loss (e.g., dehydration in patients with renal disease), vascular space fluid loss (e.g., hypovolemia due to blood loss), or hypervolemia (e.g., heart disease, iatrogenic fluid overload). Acute renal failure patients, if oliguric/anuric, may be hypervolemic, and if the patient is polyuric they may become hypovolemic. Reassessment of response to fluid therapy will help refine the determination of which fluid compartment (intravascular or extravascular) has the deficit or excess.

Dehydration

Estimating the percent dehydration gives the clinician a guide in initial fluid volume needs; however, it must be considered an estimation only and can be grossly inaccurate due to comorbid conditions such as age and nutritional status (Table 5).

TABLE 5 Dehydration Assessment
TABLE 5

Not all animals will exhibit all signs.

Fluid deficit calculation

General principles for fluid therapy to correct dehydration include the following:

  • Add the deficit and ongoing losses to maintenance volumes. Replace ongoing losses within 2–3 hr of the loss, but replace deficit volumes over a longer time period. The typical goal is to restore euhydration within 24 hr (pending limitations of comorbid conditions such as heart disease).

  • Frequency of monitoring will depend on the rate at which fluid resuscitation is being administered (usually q 15–60 min). Assess for euhydration, and avoid fluid overload through monitoring for improvement.

  • Maintenance solutions low in Na should not be used to replace extracellular deficits (to correct dehydration) because that may lead to hyponatremia and hyperkalemia when those solutions are administered in large volumes.

Hypovolemia

Hypovolemia refers to a decreased volume of fluid in the vascular system with or without whole body fluid depletion. Dehydration is the depletion of whole body fluid. Hypovolemia and dehydration are not mutually exclusive nor are they always linked. Hypotension may exist separately or along with hypovolemia and dehydration (Figure 1). Hypotension is discussed under “Fluids and Anesthesia.”

FIGURE 1. Patients may be hypovolemic, dehydrated, hypotensive, or a combination of all three.FIGURE 1. Patients may be hypovolemic, dehydrated, hypotensive, or a combination of all three.FIGURE 1. Patients may be hypovolemic, dehydrated, hypotensive, or a combination of all three.
FIGURE 1 Patients may be hypovolemic, dehydrated, hypotensive, or a combination of all three.

Citation: Journal of the American Animal Hospital Association 49, 3; 10.5326/JAAHA-MS-5868

Common causes of hypovolemia include severe dehydration, rapid fluid loss (gastrointestinal losses, blood, polyuria), and vasodilation. Hypovolemic patients have signs of decreased tissue perfusion, such as abnormal mentation, mucous membrane color, capillary refill time, pulse quality, pulse rate, and/or cold extremity temperature.

Hypovolemia due to decreased oncotic pressure is suspected in patients that have a total protein < 35 g/L (3.5 g/dL) or albumin < 15 g/L (1.5 g/dL).19 Patients in shock may have hypovolemia, decreased BP, and increased lactate (> 2 mmol/L).2022 Note that cats in hypovolemic shock may not be tachycardic.

Treating hypovolemia

When intravascular volume expansion without whole blood is needed, use crystalloids, colloids, or both. IV isotonic crystalloid fluids are the initial fluid of choice. If electrolytes such as K are needed in the emergent situation, administer through a second IV catheter. High K administration rates may lead to cardiac arrest; therefore, do not exceed 0.5 mmol/kg/hr.2325

How to administer crystalloids

  • Standard crystalloid shock doses are essentially one complete blood volume.26

  • Shock rates are 80–90 mL/kg IV in dogs and 50–55 mL/kg IV in cats.

  • Begin by rapidly administering 25% of the calculated shock dose. Reassess the patient for the need to continue at each 25% dose increment.

  • Monitor signs as described in the patient assessment portion of this document. In general, if 50% of the calculated shock volume of isotonic crystalloid has not caused sufficient improvement, consider either switching to or adding a colloid.

  • Once shock is stabilized, replace initial calculated volume deficits over 6–8 hr depending on comorbidities such as renal function and cardiac disease.

When to administer colloids

  • When it is difficult to administer sufficient volumes of fluids rapidly enough to resuscitate a patient and/or when achieving the greatest cardiovascular benefit with the least volume of infused fluids is desirable (e.g., large patient, emergency surgery, large fluid loss).

  • In patients with large volume losses where crystalloids are not effectively improving or maintaining blood volume restoration.

  • When increased tissue perfusion and O2 delivery is needed.27

  • If edema develops prior to adequate blood volume restoration.

  • When decreased oncotic pressure is suspected or when the total protein is < 35 g/L (or albumin is < 15 g/L).

  • When there is a need for longer duration of effect. Preparations vary, and some colloids are longer lasting than crystalloids (up to 24 hr).28 Use of colloids can prolong the effects of hypertonic saline administration. The typical hydroxyethyl starch dose for the dog is up to 20 mL/kg/24 hr (divide into 5 mL/kg boluses and reassess). For the cat, the dose range is 10–20 mL/kg/24 hr (typically, 10 mL/kg in 2.5–3 mL/kg boluses).2931 Titrate the amount of colloid infused to effect.

Simultaneously administering crystalloids and colloids

  • Use this technique when it is necessary to both increase intravascular volume (via colloids) and replenish interstitial deficits (via crystalloids).

  • Administer colloids at 5–10 mL/kg in the dog and 1–5 mL/kg in the cat. Administer the crystalloids at 40–45 mL/kg in the dog and 25–27 mL/kg in the cat, which is equivalent to approximately half the shock dose. Titrate to effect and continually reassess clinical parameters to adjust rate and type of fluid administered (crystalloid and/or colloid).

Using hypertonic saline

  • To achieve the greatest cardiovascular benefit with the least volume of infused fluids (typically reserved for large patients or very large volume losses).

  • To achieve translocation of fluids from the interstium to the intravascular space (e.g., for initial management of hemorrhage).

  • In animals with hemorrhagic hypovolemic shock as a fast-acting, low-volume resuscitation. Shock doses of hypertonic saline are 4–5 mL/kg for the dog and 2–4 mL/kg for the cat. Direct effects of hypertonic saline last 30–60 min in the vascular space before osmotic forces equilibrate between the intra- and extravascular space. Once the patient is stabilized, continue with crystalloid therapy to replenish the interstitial fluid loss.

  • In conjunction with synthetic colloids to potentiate the effects of the hypertonic saline.28,29

  • Do not use hypertonic saline in cases of either hypernatremia or severe dehydration.

Treating hypovolemia due to blood loss

The decision of when to use blood products instead of balanced electrolyte solutions is based on the severity of estimated blood loss. Use of blood products is addressed elsewhere.32,33 If blood products are not deemed necessary, note that patients with low vascular volume (due to either vasodilation or hemorrhage) will benefit more from the use of colloids than crystalloids. Following 15 mL/kg of hemorrhage, even 75 mL/kg of crystalloid will not return blood volume to prehemorrhage levels because crystalloids are highly redistributed. Large volumes may be needed to achieve blood volume restoration goals, and large volumes may be detrimental to patients with normal whole body fluid volume but decreased vascular volume resulting from acute blood loss.34

Hypervolemia

Hypervolemia can be due to heart failure, renal failure, and/or iatrogenic fluid overload. Hypertension is not an indicator of hypervolemia. Treatment is directed at correcting underlying disease (e.g., chronic renal disease, heart disease), decreasing or stopping fluid administration, and (possibly) use of diuretics. Consider using hypotonic 0.45% sodium chloride as maintenance fluid therapy in patients susceptible to volume overload (such as those with heart disease) due to the decreased Na load.

Hyperthermia

Increased body temperature can rapidly lead to dehydration. Treatment includes administering IV replacement fluids while monitoring for overhydration. Subcutaneous fluids are not adequate to treat hyperthermia.

Changes in Fluid Content

Patients with body fluid content changes include those with electrolyte disturbances, blood glucose alterations, anemia, and polycythemia. Patient assessment will dictate patient fluid content needs. It is acceptable, and often desirable, to initiate fluid therapy with an isotonic balanced crystalloid solution while awaiting the electrolyte status of the patient. Tailor definitive fluid therapy as the results of diagnostic tests become available.

Hyperkalemia

Suspect hyperkalemia in cases of obvious urinary obstruction, uroabdomen, acute kidney injury, diabetic ketoacidosis (DKA), or changes on an electrocardiogram. If life-threatening hyperkalemia is either suspected or present (K > 6 mmol/L), begin fluid therapy immediately along with medical therapy for hyperkalemia.35

There are several benefits associated with administering K-containing balanced electrolyte solutions pending laboratory test results. Volume expansion associated with the fluid administration results in hemodilution and lowering of serum K concentration. The relief of any urinary obstruction results in kaliuresis that offsets the effect of the administered K. The relative alkalinizing effect of the balanced solution promotes the exchange of K with hydrogen ions as the pH increases toward normal.

Most K-containing balanced electrolyte solutions contain lower K concentrations than those typically seen in cats with urethral obstruction, so the use of such solutions does not affect blood K in those cats.36 LRS contains 4 mmol/L, which is typically much lower than the serum K levels in cats with urethral obstruction.

Hypokalemia

Charts are available in many texts to aid in K supplementation of fluids and determination of administration rate.37 It is essential to mix added KCl thoroughly in the IV bag as inadvertent K overdoses can occur and are often fatal. Do not exceed an IV administration rate of 0.5 mmol/kg/hr of K.38 If hypophosphatemia exists along with hypokalemia (e.g., DKA), use potassium phosphate instead of KCl.

Hypernatremia

Hypernatremia may be common, yet mild and clinically silent. Causes of hypernatremia include loss of free water (e.g., through water deprivation), and/or iatrogenically (through the long-term use [> 24 hr] of replacement crystalloids). Another cause of hypernatremia is salt toxicity (through oral ingestion of high salt content materials).

Provide for ongoing losses and (in hypotensive patients) volume deficits with a replacement fluid having a Na concentration close to that of the patient’s serum (e.g., 0.9% saline). Once volume needs have been met, replace the free water deficit with a hypotonic solution (e.g., D5W). Additionally, for anorexic patients, provide maintenance fluid needs with an isotonic balanced electrolyte solution. The cause and duration of clinical hypernatremia will dictate the rate at which Na levels can be reduced without causing cerebral edema. Do not exceed changes in Na levels of 1 mmol/hr in acute cases or 0.5mmol/hr in chronic cases because of the risk of cerebral edema. Although the complexities of managing Na disorders often benefits from the involvement of a specialist/criticalist, this is not always feasible. The amount of free water (in the form of D5W) to infuse over the calculated timeframe (to decrease the Na concentration by the above guidelines) can be calculated as follows:

Hyponatremia

Hyponatremia is most commonly seen in DKA and with water intoxication. Changes in serum Na levels must occur slowly, as with hypernatremia. Monitor electrolyte levels frequently, and use a fluid with Na content similar to the measured plasma Na to keep the rate of change at an appropriate level.

In patients with water intoxication, restrict water and/or use diuretics with caution. Patients with DKA may have pseudohyponatremia associated with osmotic shifts of water following glucose into the intravascular space. In pseudohyponatremia, a relationship exists between serum glucose and serum Na levels: the higher the glucose, the lower the Na. Specifically, for every 100 mg/dL increase in serum glucose over 120 mg/dL, the serum Na will decrease by 1.6 mmol/L.39

Hypoproteinemia/hypoalbuminemia

Colloid osmotic pressure is related to plasma albumin and protein levels and governs whether fluid remains in the vascular space. Fluid loss into the pulmonary, pleural, abdominal, intestinal, or interstitial spaces is uncommon until serum albumin is < 15 g/L or total protein is < 35 g/L.19,40 Evidence of fluid loss from the vascular space is used in conjunction with either serum albumin or total solid values in determining when to initiate colloid therapy.

Guidelines for fluid therapy when treating hypoalbuminemia include the following:

  • Nutritional support is critical to treatment of hypoalbuminemia.

  • Plasma administration is often not effective for treatment of hypoalbuminemia due to the relatively low albumin levels for the volume infused. Human serum albumin is costly and can cause serious hypersensitivity reactions.41 Canine albumin is not readily available in most private practice settings but may be the most efficient means of supplementation when available.42

  • Synthetic colloids (e.g., hydroxyethyl starch) are beneficial because they can increase oncotic pressure in patients with symptomatic hypoalbuminemia to maintain fluid in the intravascular space; however, synthetic colloids will not appreciably change total solids as measured by refractometry. Therefore, patient assessment determines response.43 Use up to 20 mL/kg/day of hetastarch for dogs and 10–20 mL/kg/day for cats.2931

Hyperglycemia

Fluid therapy in hyperglycemic patients is aimed at correcting dehydration and electrolyte abnormalities. Monitor the patient to guide the rate of correction. As with hyperkalemia, the choice of initial replacement fluid is not as important as correcting the patient’s hydration status. See the AAHA Diabetes Management Guidelines for details on managing hyperglycemia.44

Hypoglycemia

Initial therapy for hypoglycemia is based on severity of clinical signs more than on laboratory findings. Treatment options include oral glucose solutions, IV dextrose-containing fluids, or food (if not contraindicated). To prepare a dilute dextrose solution of 2.5–5% dextrose, add concentrated stock dextrose solution (usually 50% or 500 mg/mL) to an isotonic balanced electrolyte solution (e.g., add 100 mL of 50% dextrose to 900 mL of fluid to make a solution containing 5% dextrose).

Anemia and Polycythemia

Blood products may be needed to treat anemia. The decision to transfuse the anemic patient is not based on either the packed cell volume or hematocrit alone, but on multiple factors as described in the “General Principles and Physical Assessment” section of this document. Use of blood products is not addressed in this document. Blood loss and hemorrhage are discussed above in volume changes.

Treatment of symptomatic polycythemia involves reducing the number of red blood cells through phlebotomy and replacing the volume removed with balanced electrolyte solutions to reduce viscosity and improve blood flow and O2 delivery.

Multiple Content Changes

Many patients present with multiple serum chemistry abnormalities, making appropriate fluid choice problematic. The vast majority of patients will benefit from early empirical fluid therapy while awaiting lab results, knowing that more specific treatment will be tailored to individual needs as diagnostic information becomes available.

Changes in Fluid Distribution

Fluid distribution abnormalities include edema (pulmonary, peripheral, interstitial) and effusions (pleural, abdominal, through the skin of burn patients). Two main causes of edema/effusion are loss of intravascular oncotic pressure and loss of vascular integrity. Consider concurrent dehydration and whole patient volume deficits when treating patients with abnormal fluid distribution.

Suggested specific approaches to fluid therapy include the following:

  • Pulmonary edema/volume overload: stop fluid administration, consider diuretics, address cardiovascular disease if present, and provide mechanical ventilation with positive end-expiratory pressure (if indicated).

  • Pleural/abdominal effusions: stop fluid administration, administer diuretics if indicated, address cause(s) of effusion, perform either abdomino- or thoracocentesis if respiration is compromised.

Equipment and Staffing

Staffing considerations and a description of useful equipment for delivery of fluid therapy are described below.

Staff

To optimize the success of fluid therapy, it is critical to provide staff training on assessment of patient fluid status, catheter placement and maintenance, use of equipment related to fluid administration, benefits and risks of fluid therapy, and drug/fluid incompatibility. A variety of veterinary conferences and online resources from universities and commercial vendors provide such continuing education.45

IV fluid administration is ideally monitored continually by trained technical staff. Without adequate monitoring, severe consequences can occur and patient care is compromised; however, there are many practices that are either unable to provide 24 hr care or are geographically unable to refer to a 24 hr facility. If it is not possible to monitor around the clock and unmonitored fluid administration is deemed necessary, take the following steps to make the process as safe as possible:

  • Consider giving higher rate of fluids while staff members are present, and administer subcutaneous fluids overnight.

  • Use fluid pumps whenever possible, and check them regularly for proper function and calibration.

  • Use a smaller volume of fluid in the bag to reduce chance of overloading (note that even 250 mL could fatally volume-overload a small patient. Know the maximum volume for safe infusion over a given time [based on rates described in this document], and match the unattended volume to that value).

  • Consider using an Elizabethan collar to prevent patient removal of the catheter.

  • Luer lock connections prevent inadvertent disconnection.

General Guidelines for IV Fluid Administration

  • Use a new IV line and bag for each patient, regardless of route of administration.46

  • Ensure lines are primed to avoid air embolism.47

  • Fluid pumps and gravity flow systems require frequent monitoring. Check patients with gravity flow systems more frequently because catheter positioning can affect rate.

  • If using gravity flow, select appropriate size/volume bag for patient size, particularly in small patients, to minimize risk of inadvertent overload if the entire bag volume is delivered to the patient.

  • Use a buretrol if frequent fluid composition changes are anticipated to reduce changing entire bag.

  • Consider using T-ports to easily medicate a patient receiving IV fluids and Y-ports in animals receiving more than one compatible infusion.

  • Consider using a syringe pump to either infuse small amounts of fluids or to provide a constant rate infusion. For small volume infusions, place the end of the extension set associated with the small volume delivered close to the patient’s IV catheter so that the infusion will reach the patient in a timely manner.

  • Consider a pressure bag for the delivery of boluses during resuscitation.

Catheter Maintenance and Monitoring

  • Clip the hair and perform a sterile preparation.

  • Maintain strict aseptic placement and maintenance protocols to permit the extended use of the catheter.

  • Place the largest catheter that can be safely and comfortably used. Very small catheters (24 gauge) dramatically reduce flow.

  • Flush the catheter q 4 hr unless continuous fluid administration is being performed. Research suggests that normal saline is as effective as heparin solutions for this purpose.48

  • If a nonsterile catheter is placed in an emergency setting, prepare a clean catheter site and insert a new catheter after resolution of the emergency.

  • Unwrap the catheter and evaluate the site daily. Aspirate and flush to check for patency. Replace if the catheter dressing becomes damp, loosened, or soiled. Inspect for signs of phlebitis, thrombosis, perivascular fluid administration, infection, or constriction of blood flow due to excessively tight bandaging.

  • To minimize the risk of nosocomial infection, the Centers for Disease Control recommend that fluid administration lines be replaced no more than q 4 days.46

Conclusion

Fluid therapy is important for many medical conditions in veterinary patients. It is dictated by many factors and is highly patient variable. Fluid selection for a given patient may change during therapy, depending on patient needs. The goal of these guidelines is to assist the clinician in prioritizing goals, selecting appropriate fluids and rates of administration, and assessing patient response to therapy.

The reader must recognize the highly individual patient variables and dynamic nature of fluid therapy. Because fluid therapy can be highly individualized in complex cases, having a relationship with a referral facility for consultation can be helpful.

Ongoing research is challenging current dogma regarding fluid administration rates, particularly rates for administration during anesthesia (Table 6). There are few evidence-based recommendations, and limited research has been performed related to fluid administration in veterinary patients. The reader is encouraged to be alert to future data as it becomes available and incorporate that information in practice protocols.

TABLE 6 Relearning What You Thought You Knew*
TABLE 6

See text for details.

LRS, lactated Ringer’s solution.

REFERENCES

  • 1.
    English MJ , PapenbergR, FariasE et al.. Heat loss in an animal experimental model. J Trauma1991;31(
    1
    ):368.
  • 2.
    Anderson RR . Water balance in the dog and cat. J Small Anim Pract1982;23:588.
  • 3.
    Wellman ML , DiBartolaSP, KohnCW. Applied physiology of body fluids in dogs and cats. In: DiBartolaSP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:15.
  • 4.
    Macintire DK , DrobatzKJ, HaskinsSC et al., eds. Manual of small animal emergency and critical care medicine.
    1st ed
    .
    Philadelphia (PA)
    :
    Lippincott Williams & Wilkins
    ; 2004:67.
  • 5.
    Macintire DK , DrobatzKJ, HaskinsSC et al., eds. Manual of small animal emergency and critical care medicine.
    2nd ed
    .
    Philadelphia (PA)
    :
    Wiley Blackwell
    ; 2012:69.
  • 6.
    Brodbelt DC , PfeifferDU, YoungLE et al.. Risk factors for anaesthetic-related death in cats: results from the confidential enquiry into perioperative small animal fatalities (CEPSAF). Br J Anaesth2007;99(
    5
    ):61723.
  • 7.
    Pascoe PJ . Periopeative management of fluid therapy. In: DiBartolaSP, ed. Fluid, elecrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:41620.
  • 8.
    Tang J , WuG, PengL. Pharmacokinetics of propofol in patients undergoing total hip replacement: effect of acute hypervolemic hemodilution. Anaesthesist2011;60(
    9
    ):83540.
  • 9.
    Chappell D , JacobM, Hofmann-KieferK et al.. A rational approach to perioperative fluid management. Anesthesiology2008;109(
    4
    ):72340.
  • 10.
    Branstrup B . Fluid therapy for the surgical patient. Best Pract Res Clin Anaesthesiol.2006;20(
    2
    ):26583.
  • 11.
    Muir WW III , KijtawornratA, UeyamaY et al.. Effects of intravenous administration of lactated Ringer’s solution on hematologic, serum biochemical, rheological, hemodynamic, and renal measurements in healthy isoflurane-anesthetized dogs. J Am Vet Med Assoc2011;239(
    5
    ):6307.
  • 12.
    Jacob M , ChappellD, ConzenP et al.. Blood volume is normal after pre-operative overnight fasting. Acta Anaesthesiol Scand2008;52(
    4
    ):5229.
  • 13.
    Conger JD . Interventions in clinical acute renal failure: what are the data?Am J Kidney Dis1995;26(
    4
    ):56576.
  • 14.
    Grandy JL , DunlopCI, HodgsonDS et al.. Evaluation of the Doppler ultrasonic method of measuring systolic arterial blood pressure in cats. Am J Vet Res1992;53(
    7
    ):11669.
  • 15.
    Aarnes TK , BednarskiRM, LercheP et al.. Effect of intravenous administration of lactated Ringer’s solution or hetastarch for the treatment of isoflurane-induced hypotension in dogs. Am J Vet Res2009;70(
    11
    ):134553.
  • 16.
    Monk TG , SainiV, WeldonBC et al.. Anesthetic management and one-year mortality after noncardiac surgery. Anesth Analg2005;100(
    1
    ):410.
  • 17.
    Bednarski R , GrimmK, HarveyR et al.. AAHA anesthesia guidelines for dogs and cats. J Am Anim Hosp Assoc2011;47(
    6
    ):37785.
  • 18.
    Paige CF , AbbottJA, ElvingerF et al.. Prevalence of cardiomyopathy in apparently healthy cats. J Am Vet Med Assoc2009;234(
    11
    ):1398403.
  • 19.
    de Brito Galvao JF , CenterSA. Fluid, electrolyte, and acid-base disturbances in liver disease. In: DiBartolaSP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:462.
  • 20.
    Pang DS , BoysenS. Lactate in veterinary critical care: pathophysiology and management. J Am Anim Hosp Assoc2007;43(
    5
    ):2709.
  • 21.
    Fall PJ , SzerlipHM. Lactic acidosis: from sour milk to septic shock. J Intensive Care Med2005;20(
    5
    ):25571.
  • 22.
    Lagutchik MS , OgilvieGK, HackettTB et al.. Increased lactate concentrations in ill and injured dogs. J Vet Emerg Crit Care1998;8(
    2
    ):11727.
  • 23.
    Graefe U , MilutinovichJ, FolletteWC et al.. Less dialysis-induced morbidity and vascular instability with bicarbonate in dialysate. Ann Intern Med1978;88(
    3
    ):3326.
  • 24.
    Iseki K , OnoyamaK, MaedaT et al.. Comparison of hemodynamics induced by conventional acetate hemodialysis, bicarbonate hemodialysis and ultrafiltration. Clin Nephrol1980;14(
    6
    ):2948.
  • 25.
    Saragoca MA , BessaAM, MulinariRA et al.. Sodium acetate, an arterial vasodilator: haemodynamic characterisation in normal dogs. Proc Eur Dial Transplant Assoc Eur Ren Assoc1985;21:2214.
  • 26.
    Hopper K , SilversteinD, BatemanS. Shock syndromes. In: DiBartolaSP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:564.
  • 27.
    Hiltebrand LB , KimbergerO, ArnbergerM et al.. Crystalloids versus colloids for goal-directed fluid therapy in major surgery. Crit Care2009;13(
    2
    ):R40.
  • 28.
    Falk JL , RackowEC, WeilMH. Colloid and crystalloid fluid resuscitation. Acute Care1983–84;10(
    2
    ):5994.
  • 29.
    Hughes D , BoagA. Fluid therapy with macromolecular plasma volume expanders. In: DiBartolaSP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:64764.
  • 30.
    Lunn K , JohnsonA, JamesK. Fluid therapy. In: LittleS, ed. The cat: clinical medicine and management.
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:5289.
  • 31.
    Concannon KT , HaskinsSC, FeldmanBF. Hemostatic defects associated with two infusion rates of dextran 70 in dogs. Am J Vet Res1992;53(
    8
    ):136975.
  • 32.
    Liumbruno GM , BennardelloF, LattanzioA et al.. Recommendations for the transfusion management of patients in the peri-operative period. II. The intra-operative period. Blood Transfus2011;9(
    2
    ):189217.
  • 33.
    Silverstein D , HopperK. Small animal critical care medicine.
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2008:281.
  • 34.
    Iijima T . Complexity of blood volume control system and its implications in perioperative fluid management. J Anesth2009;23(
    4
    ):53442.
  • 35.
    Meyer RE . Renal disease. In: GreenSA, ed. Veterinary anesthesia and pain management secrets.
    Philadelphia (PA)
    :
    Hanley and Belfus
    ; 2002:190.
  • 36.
    Drobatz KJ , ColeSG. The influence of crystalloid type on acid-base and electrolyte status of cats with urethral obstruction. J Vet Emerg Crit Care2008;18(
    4
    ):35561.
  • 37.
    Muir WW , DiBartolaSP. Fluid therapy. In: KirkRW, ed. Current veterinary therapy VIII. Small animal practice.
    Philadelphia (PA)
    :
    WB Saunders
    ; 1983:38.
  • 38.
    DiBartola SP . Fluid therapy in small animal practice.
    3rd ed.
    Philadelphia (PA)
    :
    WB Saunders
    ; 2006.
  • 39.
    Katz MA . Hyperglycemia-induced hyponatremia—calculation of expected serum sodium depression. N Engl J Med1973;289(
    16
    ):8434.
  • 40.
    Hall JE . Guyton and Hall textbook of medical physiology.
    12th ed.
    Philadelphia (PA)
    :
    Saunders Elsevier
    ; 2011:298.
  • 41.
    Cohn LA , KerlME, LenoxCE et al.. Response of healthy dogs to infusions of human serum albumin. Am J Vet Res2007;68(
    6
    ):65763.
  • 42.
    Francis AH , MartinLG, HaldorsonGJ et al.. Adverse reactions suggestive of type III hypersensitivity in six healthy dogs given human albumin. J Am Vet Med Assoc2007;230(
    6
    ):8739.
  • 43.
    Bumput S , HaskinsS, KassP. Effect of synthetic colloids on refractometric readings of total solids. J Vet Emerg Crit Care1998;8(
    1
    ):216.
  • 44.
    Rucinsky R , CookA, HaleyS et al.. AAHA diabetes management guidelines. J Am Anim Hosp Assoc2010;46(
    3
    ):21524.
  • 45.
    Davis H . Fluid therapy for veterinary technicians. Available at: http://www.dcavm.org/11%20oct%20technotes2.pdf. Accessed March 14, 2013.
  • 46.
    O’Grady NP , AlexanderM, BurnsLA et al.. Guidelines for the prevention of intravascular catheter-related infections, 2011. Department of Health & Human Services, USA. Centers for Disease Control. Available at: www.cdc.gov/hicpac/pdf/guidelines/bsi-guidelines-2011.pdf. Accessed March 14, 2013.
  • 47.
    Wang AZ , ZhouM, JiangW et al.. The differences between venous air embolism and fat embolism in routine intraoperative monitoring methods, transesophageal echocardiography, and fatal volume in pigs. J Trauma2008;65(
    2
    ):41623.
  • 48.
    Bertoglio S , SolariN, MeszarosP et al.. Efficacy of normal saline versus heparinized saline solution for locking catheters of totally implantable long-term central vascular access devices in adult cancer patients. Cancer Nurs2012;35(
    4
    ):E3542.
  • 49.
    DiBartola SP , BatemanS. Introduction to fluid therapy.
    3rd ed.
    St. Louis (MO)
    :
    Saunders Elsevier
    ; 2006:32544.
  • 50.
    Rudloff E , KirbyR. Fluid therapy. Crystalloids and colloids. Vet Clin North Am Small Anim Pract1998;28(
    2
    ):297328.
  • 51.
    Cunha MG , FreitasGC, CarregaroAB et al.. Renal and cardiorespiratory effects of treatment with lactated Ringer’s solution or physiologic saline (0.9% NaCl) solution in cats with experimentally induced urethral obstruction. Am J Vet Res2010;71(
    7
    ):8406.
  • 52.
    Allen SE , HolmJL. Lactate: physiology and clinical utility. J Vet Emerg Crit Care. 2008;18(
    2
    ):12332.
  • 53.
    Gajewski M , HillelZ. Anesthesia management of patients with hypertrophic obstructive cardiomyopathy. Prog Cardiovasc Dis2012;54(
    6
    ):50311.
  • 54.
    Hansen B . Technical aspects of fluid therapy. In: DiBartolaSP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice.
    4th ed
    .
    St. Louis (MO)
    :
    Elsevier Saunders
    ; 2012:373.

Footnotes

    AAFP American Association of Feline Practitioners AAHA American Animal Hospital Association BP blood pressure D5W 5% dextrose in water DKA diabetic ketoacidosis K potassium KCl potassium chloride LRS lactated Ringer's solution
Copyright: © 2013 by American Animal Hospital Association 2013
FIGURE 1
FIGURE 1

Patients may be hypovolemic, dehydrated, hypotensive, or a combination of all three.


Contributor Notes

This document is intended as a guideline only. Evidence-based support for specific recommendations has been cited whenever possible and appropriate. Other recommendations are based on practical clinical experience and a consensus of expert opinion. Further research is needed to document some of these recommendations. Because each case is different, veterinarians must base their decisions and actions on the best available scientific evidence, in conjunction with their own expertise, knowledge, and experience. These guidelines are supported by a generous educational grant from Abbott Animal Health.

  • Download PDF