Intravenous Therapy, Fluid Delivery Systems for Resuscitation, and Cell Salvage Devices






  • Chapter Outline



  • Fluid Delivery Systems for Resuscitation 218



  • Infusion Devices 218




    • Background 218



    • IV Catheters 220



    • Rapid Infusion Catheters 220



    • Intraosseous Needles 222



    • IV Tubing Sets 224



    • Air Embolism 226




  • Filtration of Blood Products 228




    • Overview 228



    • Administering Blood Products Through the Filter Set 228




  • Fluid Warmers 229




    • Background: Intraoperative Hypothermia 229



    • Overview of Fluid Warming Systems 230



    • Simple Fluid Warmers 230



    • Resuscitation Fluid Warmers 231




  • Cell Salvage Systems 231



  • Overview 231



  • Contraindications to Cell Salvage 233



  • Equipment for Cell Salvage 233




Fluid Delivery Systems for Resuscitation


Infusion Devices


Background


Determinants of Fluid Flow Rate


Numerous factors determine the flow rate of IV fluids, including characteristics of the fluid itself, characteristics of the IV circuit that are extrinsic to the patient, and patient-driven determinants of the driving pressure for fluid flow ( Figure 16–1 ).




Figure 16–1


Determinants of fluid flow rate in an IV circuit. Text highlights factors that affect the delivery rate of each infusate.


Characteristics of the infusate that affect flow rate include its viscosity and temperature, its potential to form air locks or overwhelm closed air filters (with air derived either from the fluid source or from spontaneous bubble formation as a cold solution spontaneously warms within the IV circuit), or its potential to occlude the administration set with particulate matter (such as clot, emulsifiers, or precipitates resulting from incompatible infusates) ( Table 16–1 ).



Table 16–1

Combinations Known to Occlude IV Administration Sets



















Mechanism of Occlusion Examples
Clot formation Calcium-containing solutions (lactated Ringer’s, Hetastarch) with blood products
Precipitate formation Thiopental with vecuronium/pancuronium; heparin, amiodarone, and numerous antibiotics with a variety of anesthesia drugs
Bicarbonate with calcium/many local anesthetics
Clogged filter Any of the above; air; emulsifiers such as those in propofol, intralipid

To reduce the risk of precipitate formation within the IV tubing, flush the IV tubing thoroughly after bolus doses and verify drug compatibility, particularly when using amiodarone, protamine, or unfamiliar drugs, particularly antibiotics.


Features of the IV circuit that affect fluid flow include the inner diameter of the IV catheter, tubing, injection ports and Luer- locks, the length of each circuit component (particularly the narrowest components), the distensibility of the tubing and its propensity to kink, whether the fluid delivery system is pressurized, and the vertical distance between the fluid source and the target vein. When multiple fluid sources funnel into the same IV catheter, the carrier flow rate, the relative pressurization of each fluid source, and the competency of any one-way valves at the convergence of two fluid streams can also profoundly affect the forward flow rate for each infusate. Lastly, fluid flow rate also reflects patient-specific factors such as the back-pressure in the cannulated vein (intrinsic or extrinsic [i.e., from a noninvasive blood pressure cuff]) and the pressure gradient between the vein containing the IV cannula and the right atrium.


Determinants of Drug Delivery


Drug delivery through an IV administration set is a function of the concentration of the stock solution of drug given as an infusion through a piggyback into a carrier infusion, and the flow rates of both infusions ( Figure 16–2 ). Another important factor is the size of the dead space volume (V) that lies between the convergence of the carrier and drug infusions and the tip of the IV cannula. To avoid fluctuations in drug delivery, the carrier flow rate within IV tubing should be kept constant and the dead space of the infusion system should be minimized. Avoid using concentrated solutions of potent drugs to minimize the risk of complications if carrier flow changes abruptly.




Figure 16–2


Determinants of drug delivery in a system with a carrier infusion. The mass of drug within the dead space volume ( V ) of IV tubing that lies beyond the convergence of the carrier and the drug infusion (see shaded area ) equals t × c d × Q d , where the time constant (t) = V/(Q d + Q c ), Q d is the infusion rate of the stock solution of the drug, and Q c is the carrier flow rate. The concentration of drug exiting the IV catheter, c(t), varies with time after any of the variables change. If the flow rate suddenly increases (as often happens when a previously unrecognized empty bag of carrier is replaced), this mass of drug is given as a rapid bolus to the patient, which can be clinically significant.

(Image from Lovich MA, Kinnealley ME, Sims NM, et al. The delivery of drugs to patients by continuous intravenous infusion: modeling predicts potential dose fluctuations depending on flow rates and infusion system dead volume. Anesth Analg 2006;102:1147-1153.)


Experimental and mathematical models demonstrate that it takes 1 to 3 time constants for the drug concentration volume (V) throughout the dead space to reach a new steady state after a change in carrier or drug flow rate. The time required for a new drug infusion to reach the patient at the desired concentration also varies significantly, depending on the dead space volume of the side port that must be primed.


Characterizing Fluid Flow Within the IV Circuit


The impact of length and inner diameter on fluid flow rates (through both catheters and IV cannulas) has long been appreciated. Historically, fluid flow through IV catheters and tubing was considered laminar (and therefore has been described by the Poiseuille formula) ( Figure 16–3 , A ). However, the Poiseuille formula does not fully describe pressure loss for fluid flow through IV cannulas and IV tubing. Laminar flow through an IV catheter is prevented by the short length and abrupt decrements in tubing diameter (i.e., where the IV administration set meets the catheter), which create eddies.




Figure 16–3


Formulae describing fluid flow through tubing. A, The Poiseuille formula describes the laminar flow rate of a Newtonian fluid (whose viscosity depends only on temperature and pressure) through a straight cylinder with a circular cross-section. When the Reynolds number of the fluid is less than 2000-2300, laminar flow is predicted. B, Experimentally derived data show that flow through IV catheters has both laminar and turbulent characteristics, and the pressure-flow relationship in plastic tubing and cannulas is nonlinear (see graph on left ). The coefficient of flow (R L ) and coefficient of the square of flow (R T ) are (respectively) the intercept and slope of the resistance flow plot (see graph on right ). The relationship between length and each of the parameters of flow is linear. Therefore the quadratic equation P = R L Q + R T Q 2 describes the pressure-flow relationship for plastic intravenous tubing and cannulas. C, Experimentally derived data show that the pressure-flow relationships for both tubing-catheter systems and isolated catheters are nonlinear; both systems are described by the equation shown in B .

(Figures in B taken from Philip BK, Philip JH. Characterization of flow in intravenous infusion systems. IEEE Trans Biomed Eng 1983;30:702-707. Figures in C taken from Philip BK, Philip JH. Characterization of flow in intravenous catheters. IEEE Trans Biomed Eng 1986;33:529-331.)


In reality, flow through IV tubing and catheters has both laminar and turbulent characteristics. Accordingly, the prevailing model for flow through IV catheters and infusion systems incorporates both types of flow by using a quadratic equation ( Figure 16–3 , B ) to describe the relationship between radius and flow, rather than Poiseuille’s quadratic relationship. For IV catheters, the laminar component of pressure loss (which has a linear pressure-flow relationship) is consistent with what the Poiseuille formula would predict, while the turbulent component reflects pressure loss due to flow disturbances at the inlet, and where the catheter changes shape. For IV tubing, there is an additional component of turbulent-flow pressure loss that is proportional to tubing length. Recent research indicates that while radius is the most powerful determinant of flow rate through an IV catheter, the effect of changing radius on flow rates through 14- to 20-gauge IV catheters is less than commonly believed.


Regulations from the International Organization for Standardization require the disclosure of maximal IV flow rates through all catheters. These quoted rates describe the flow through a perfectly straight cannula into an open receptacle, from an IV fluid source located 100 cm above the receptacle. While these idealized conditions approximate neither conditions in the operating room nor the maximum flow rates obtained clinically, the quoted rates are helpful for making comparisons among various IV catheters.


IV Catheters


Overview


IV cannulation devices consist of a tapered catheter threaded over a hollow-bore needle. Most are latex-free, radio-opaque, and nonpyrogenic. While no venipuncture system can eliminate the risk of unintended needlesticks, self-retracting safety systems eliminate the risk of needlesticks after a needle is withdrawn from its catheter.


Because of its comparatively shorter length (and lower resistance), a large-bore, well-functioning peripheral IV is considered superior to a central venous catheter for large volume fluid resuscitation. For example, as highlighted in Table 16–2 , manufacturer-quoted maximum flow rates are significantly lower for central venous catheters, as compared with peripheral IV catheters with the same inner diameter. This difference is fivefold when comparing the flow through a 16-gauge peripheral IV (approximately 330 mL/min) to that through the 16-gauge proximal port of a triple lumen central line (63 mL/min) ( Table 16–2 ).



Table 16–2

Characteristics of Commonly Used IV Catheters









































































Gauge Inner Diameter (mm) Length Manufacturer-Quoted Flow (mL/min)



  • 14 Jelco



  • Introcan




  • 2.25 mm



  • 2.2 mm

50 mm


  • 315



  • 345




  • 16 Jelco



  • Introcan




  • 1.85 mm



  • 1.7 mm

50 mm 210



  • 18 Jelco



  • Introcan




  • 1.35 mm



  • 1.3 mm

45 mm 100



  • 20 Jelco



  • Introcan




  • 1.15 mm



  • 1.1 mm

32 mm


  • 63



  • 60




  • 22 Jelco



  • Introcan

0.9 mm 25 mm


  • 33



  • 35




  • 24 Jelco



  • Introcan

0.7 mm


  • 16 mm



  • 19 mm




  • 24



  • 22

7F Triple-lumen arrow central catheter for use only with 8.5 or 9F percutaneous sheath introducer (PSI)
16 (proximal) 140 mm 76
18 (medial) 35
18 (distal) 36
7F Triple-lumen arrow central catheter for use only with MAC two-lumen central venous access device
16 (proximal) 63
18 (medial) 26
18 (distal) 25

Overview of key parameters for commonly used peripheral IV catheters (Jelco Smiths Medical, St Paul, Minn; Introcan B. Braun Medical, Bethlehem, Pa), including inner diameter, catheter length, and manufacturer-quoted flow rates (derived using ISO standards). For comparison, the maximal flow rates through representative central venous catheters (Arrow International Corp, Reading, Pa.) are also shown.


Other Features of IV Cannulation Systems


Other important design features include the conformation of the orifice on the needle tip and the distance between this orifice and the catheter tip (see Figure 16–5). A flash of blood appears (whose location may vary, see Figure 16–4 ) when the tip of the needle orifice enters the vessel lumen; the needle must then be advanced further to project the catheter tip into the vessel lumen before the catheter can be threaded. Because unfamiliarity with these product-specific spatial relationships can predispose one to transect or tear a vein during attempted cannulation, it is useful to become facile with a variety of IV cannulation systems.




Figure 16–4


Examples of self-retracting and “unprotected” IV cannulation devices. A, Unprotected cannulation sets ( top to bottom) : 14-, 16-, 18-, 20-, 22-gauge sets (Jelco, Smiths Medical, St. Paul, Minn.). B, Safety cannulation systems: Top : 22-gauge catheter set ready for use (needle retracts when white button is pressed), carets point to sites where the flash of blood is visible during cannulation; middle : 14-gauge catheter set ready for use; bottom : 14-gauge catheter fully deployed with needle manually retracted.

(Insyte Autoguard 22-gauge, Becton Dickinson Infusion Therapy Systems, Sandy, Utah; PROTECTIV Jelco 14-gauge, Smiths Medical, St. Paul, Minn.)


Other product-specific features also affect the cannulation process ( Figure 16–5 ). These include the needle penetration force required (which can range from 50 to 150 g) during cannulation (which is largely determined by the needle bevel), the type of hub used to advance the catheter, and the degree to which the catheter tapers (which affects catheter penetration force, a force that typically exceeds needle penetration force by onefold to twofold). Material memory can cause severe kinks to persist, even after extrinsic forces are removed.




Figure 16–5


Product features affecting the cannulation process. Several factors determine how far a needle must be advanced after obtaining flashback before attempting to advance the catheter. These include (A) the inner diameter of the vessel (bracket), the angle of the needle relative to the vessel (), and (B) the distance between the proximal tip of the needle opening and the distal tip of the catheter (as indicated by the distance d1, as well as the distance between the proximal opening of the needle and the distal tip of the catheter, as indicated by the distance d2) . Because the bevel of the needle (1>2) is sharper and the needle diameter is narrower, less force would be required to use the cannulation set in (C) as compared to the set in B .


Rapid Infusion Catheters


Rationale


The rapid infusion catheter is designed to replace an in situ 20-gauge (or larger) peripheral IV catheter, to facilitate large volume rapid infusions ( Figure 16–6 ). RIC lines allow for more rapid infusion rates as compared to central and conventional peripheral catheters, owing to their larger diameter and shorter length. Relative to central lines, RIC lines can be easier or faster to place (and even have a role in pediatrics), although central access can be easier to obtain and more reliable when peripheral veins are small or friable. Because of the dire consequences of intra-arterial infusion of air, pharmacologic agents or fluids (especially under pressure), it is critical to confirm that the RIC is intravenous before using it.




Figure 16–6


RIC equipment. A, This 8.5F × 2.5” (6.4 cm) radiopaque, latex-free rapid infusion catheter (RIC, Arrow International Corp, Reading, Pa.) is characteristic of those available in North America. A 7F × 2” (5.08 cm) is also available. The kit also includes a dilator, a 13.125” (33 cm) spring-wire guide and a #11 scalpel. B, Relative sizes of (from left to right) an 8.5F RIC, various peripheral IV catheters (14g, 16g, 18g) and the dilator supplied for use with the 8.5F RIC catheter.


Technique


To place a RIC, the guidewire is advanced through an in situ IV catheter (with limited force, to avoid damaging the vein), and the preexisting IV catheter is removed. Next, the skin opening is enlarged, by advancing the scalpel away from the guidewire, carefully to avoid cutting the guidewire or creating a skin bridge. The dilator is then threaded over the guidewire, grasped close to the skin incision, and advanced through the skin and subcutaneous tissues into the vein with a slight twisting motion. Finally, the dilator is removed, and the infusion catheter is inserted, connected to IV tubing, and sutured into place.


To achieve maximal flow rates with the RIC, standard-gauge stopcocks and any small-diameter or unnecessary lengths of IV tubing should be removed from the IV administration set. The maximal flow rate through a RIC doubles when IV tubing with a large inner diameter is used.


Intraosseous Needles


Rationale


Sometimes intravenous access is impossible. However all patients have long bones, and the bone marrow space is connected to the circulation. In fact, the bone marrow space, or intraosseous compartment, is considered to be connected to the central circulation and is suitable for administration of fluids for resuscitation and potent vasopressors.


Intraosseous cannulation has been described using various needles, typically as a technique of last resort. Pain on insertion, pain on injection, and concerns about osteomyelitis have limited use of the technique in the past. Recently available commercial kits and changes in technique have effectively addressed most of these concerns these obstacles.


Technique


A commercially available intraosseous access kit is illustrated in Figure 16–7 . The kit contains all of the items needed to make the technique safe and relatively painless. The skin over the selected bony prominence should be disinfected with a germicidal, persistent solution, such as chlorhexidine in alcohol (shown as part of the kit in Figure 16–7 ). Local anesthesia is provided at the skin puncture site. The appropriate length of needle is chosen; typically only one diameter is available. The needle is inserted with a powered driver, shown in Figure 16–8 . Use of a powered driver to spin the needle shortens the duration of painful stimulus, reduces the insertion force required, and adds an element of control in placement. Pain from injection is alleviated by first giving a dose of local anesthetic such as lidocaine. After lidocaine administration, the needle should be flushed under pressure, with one or more 10-mL syringes of sterile normal saline to establish flow.




Figure 16–7


Intraosseous needle insertion kit. This commercially available kit has been customized so that it contains all items needed to obtain intraosseous access, including the needle and driver, a disinfectant applicator, lidocaine to blunt the pain of injection, and syringes of flush solution. Hidden behind the drugs is a graphic instruction card showing sites and insertion technique.



Figure 16–8


Intraosseous needle mounted on powered driver, ready for insertion.


Confirmation of successful insertion hinges on a constellation of “soft” findings, including a firmly seated needle, potential (but not certain) ability to aspirate blood from the needle, easy flow of fluids under pressure, and expected responses to pharmacological agents. Because the intramedullary pressure is higher than venous pressure (typically 35 to 50 mm Hg), fluids must be given under pressure to achieve high flow rates.


Intraosseous administration provides quick access to the circulation and should be considered when access is difficult. This is particularly true when difficulty obtaining intravenous access is delaying administration of resuscitation drugs. Even in elective settings, the intraosseous route may be preferable to repeated attempts at starting a peripheral IV. Common insertion sites include the distal and proximal tibia and the proximal humerus. All of these have the key feature of being palpable even in obesity, and well removed from any major nerves or blood vessels.


Contraindications include: infection at the potential insertion site, fracture of the target bone, and recent procedures involving the target bone.


IV Tubing Sets


Overview


Simple fluid administration sets typically consist of a dripper, a drip chamber, a rolling side-clamp to adjust flow, sliding clamps to occlude flow, and, typically, some kind of injection port ( Figure 16–9 , A ). Manufacturer-quoted drop size (often 15 gtt/mL for adult sets, 60 gtt/mL for pediatric sets) describes the flow rate of a standard crystalloid infusate at room temperature. The internal diameter of tubing typically ranges from approximately 0.1 to 0.3 mm. Many sets also contain an air filter (typically capable of sequestering less than 5 mL of air).




Figure 16–9


Various types of IV tubing and injection ports. A, Various drip sets. Left-to-right : pediatric burette (60 gtt/mL dripper; burette has access point for aspiration of air or injection of exogenous fluids); administration set with pressure reservoir, helpful for administration of viscous infusates (15 gtt/mL dripper); standard administration set (15 gtt/mL dripper); piggyback tubing (60 gtt/mL dripper). B, Various types of injection ports. Clockwise from top right : (1) Two-gang stopcock capped injection ports; (2) injection port compatible for use with lever-locking blunt connectors, blunt connectors and sharps (arranged from left to right above the port); (3) close-up of aforementioned injection port; (4) injection port with female Luer lock, also compatible for use with sharps; (5) set of three parallel injection ports (commonly used in TIVA) with female Luer locks, which funnels distally through narrow-bore tubing to terminate with a male Luer lock; (6) swabbable injection port built into a standard IV administration set.

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Mar 25, 2019 | Posted by in ANESTHESIA | Comments Off on Intravenous Therapy, Fluid Delivery Systems for Resuscitation, and Cell Salvage Devices

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