CHAPTER 192 Joint and Soft Tissue Aspiration and Injection (Arthrocentesis)
The clinician should not withhold the benefits of injection therapy because of incomplete familiarity with the precise anatomy involved. Knowledge of soft tissue and bony landmarks provides a reliable method for identification of needle insertion sites. The emerging role of musculoskeletal ultrasound in office-based practice additionally offers new opportunities to improve diagnostic and therapeutic techniques. The reader may want to refer to Chapter 191, Ganglion Treatment, for related information.
Indications
Diagnostic
Therapeutic
Indications for Corticosteroid Injections
Box 192-1 lists the conditions that are improved with local corticosteroid therapy. Localized pain that persists more than a few weeks after a trial of NSAIDs warrants an injection with steroids. Injections should be considered primarily when the potential toxicity or intolerance to NSAIDs outweighs the risk of local corticosteroids. Tramèr and colleagues noted in their meta-analysis that individuals chronically (≥2 months) using NSAIDs had a 1 : 1220 chance of dying from a gastrointestinal complication. In contrast, death occurring after intra-articular injections comes predominantly from septic arthritis, which occurs in anywhere from 1 : 3000 to 1 : 50,000 cases—with a mortality rate of about 15%. Morbidity risks associated with prolonged NSAID use are even greater.
Indications for Hyaluronic Acid Supplementation
Contraindications
Equipment
Required equipment includes the following:
NOTE: There are two reasons to use single-dose vials. First, no allergic reaction to lidocaine (an amide) has ever been reported. Although rare, reactions do occur to the preservative (parabens) that is used in multidose vials. Local anesthetics with an ester base (e.g., procaine [Novocain]) can cause allergic reactions. So, using a single-dose vial of lidocaine makes it highly unlikely that there will be a reaction. Second, many steroids will precipitate when mixed with the parabens preservatives. This leads to uneven distribution in the syringe as well as the injection of small crystals into the site, and these crystals themselves could cause an inflammatory process (Fig. 192-1). Theoretically, a homogeneous solution would be more efficacious, although no studies have looked at the issue and many feel it is a moot point and of little concern. Certain manufacturers, however, do not recommend injecting precipitated steroids.
Corticosteroid | Relative Anti-inflammatory Potency | Approximate Equivalent Dose (mg) |
---|---|---|
Short-acting Preparations | ||
Cortisone | 0.8 | 25 |
Hydrocortisone | 1 | 20 |
Intermediate-acting Preparations | ||
Prednisone | 3.5 | 5 |
Prednisolone tebutate (Hydeltra-TBA) | 4 | 5 |
Triamcinolone (Aristocort, Aristospan, Kenalog) | 5 | 4 |
Methylprednisolone acetate (Depo-Medrol) | 5 | 4 |
Long-acting Preparations | ||
Dexamethasone (Decadron-LA) | 25 | 0.6 |
Betamethasone (Celestone Soluspan) | 25 | 0.6 |
Adapted from Leversee JH: Aspiration of joints and soft tissue injections. Prim Care 13:572, 1986.
A reasonable rule of thumb is that the greater the water solubility of the corticosteroid, the more rapid the onset of action, and the shorter the duration of effect. Thus, steroids with a lower degree of water solubility would in general be more effective in a chronic disease process, such as OA, whereas an acute inflammatory process might be more responsive to a shorter-acting preparation (Table 192-3).
Steroid | Solubility (% wt/vol) |
---|---|
Triamcinolone hexacetonide | 0.0002 |
Triamcinolone acetate | 0.004 |
Prednisolone tebutate | 0.001 |
Methylprednisolone acetate | 0.001 |
Hydrocortisone acetate | 0.002 |
NOTE: It is best to pick out one or two preparations and learn them well. It is not necessary to be familiar with all the drugs listed. There is no consensus in the literature as to the “best” drug or the optimal dosages. Table 192-2 offers our recommendations for appropriate dosing.
Preprocedure Patient Preparation
Inform the patient of the risks, benefits, and possible complications of injection therapy. This information is especially important if steroids are used. Rarely is there ever a complication from the use of lidocaine alone. However, with steroids, and especially with repeated injections, there are some adverse consequences (see the “Complications” section and) Table 192-4. Inform the patient that there is always a possibility for infection with the injection, although this is extremely rare. Bleeding into a joint can occur, but this generally does not happen unless the patient has a coagulopathy. The injection may actually cause more pain during the first 24 to 36 hours. This reaction is called steroid flare. If the pain lasts for more than 72 hours, evaluate the patient for the possibility of a septic joint. Warn the patient of a possible failure to obtain relief, and that a second or even a third injection may be needed. Whether or not steroids have significant adverse effects on the cartilage and bone itself when steroids are injected into the joint space, and the degree of this reaction, is controversial. However, the effects would appear to be minimal, especially when used appropriately. Allergic reactions are very rare. Tendon ruptures should be avoidable if the injection is placed peritendinously instead of within the tendon itself. However, rupture is always a possibility. As a final precaution, warn the patient that a steroid placed too close to the surface of the skin occasionally causes atrophy (Fig. 192-2). This reaction may leave the patient with depigmentation and a slight indentation in the skin.
Complication | Estimated Prevalence |
---|---|
Postinjection flare | 2%–5% |
Steroid arthropathy | 0.8% |
Tendon rupture | <1% |
Facial flushing | <1% |
Skin atrophy, depigmentation | <1% |
Iatrogenic infectious arthritis | 0.01% |
Transient paresis of injected extremity | Rare |
Hypersensitivity reaction | Rare |
Asymptomatic pericapsular calcification | 43% |
Acceleration of cartilage attrition | Unknown |
From Gray RG, Gottlieb NL: Intra-articular corticosteroids: An updated assessment. Clin Orthop Relat Res 177:253, 1983.
Technique
Before injection therapy, consider the differential diagnosis. If a tumor or fracture is possible, radiographs should be obtained. Many times, especially with trigger-point injection (see Chapter 197, Trigger-Point Injection), x-rays are unnecessary. Other diagnoses may also be fairly straightforward and not require a prior radiographic examination either. If the diagnosis is in question or if the patient is at risk for bone metastases (e.g., a history of breast or prostate cancer), the condition should be clarified before injection therapy.
The recommended dosages of medications (Table 192-5) and the specific techniques for various injection sites (Figs. 192-3 to 192-25) are included in this chapter.
Figure 192-3 Injecting finger and toe joints. A, Appropriate technique for injecting a finger joint. Tendons run over the dorsum of the finger, whereas nerves and vessels run laterally. Open the joint slightly by flexing it and then inject between the ligaments and the vascular structures as noted. The needle enters at a 45-degree angle to the joint. Any of the finger (B) and toe (C) joints may be aspirated or injected in the lateral or medial aspect. Slightly flex the joint to open the joint space. Direct the needle to enter just medial or lateral to the extensor tendon, avoiding too lateral or medial an approach where the nerve and vascular structures run. Use a 25-gauge, 1-inch needle with 0.5 to 1.0 mL 1% lidocaine and 4 to 10 mg of methylprednisolone acetate or equivalent (see Tables 192-2 and 192-5).
Figure 192-4 Trigger finger. A, The anatomy of a finger showing the annular pulleys, which maintain the flexor close to the bony structures. When the tendon becomes inflamed and enlarges, it catches on the pulleys, causing a snapping with extension or a “trigger finger.” B, Identify the flexor tendon involved. Insert the needle at the distal palmar crease. Attempt to position it peritendinously. When the needle is in position, the syringe will move with flexion of the finger. Use a 25-gauge, 1-inch needle with 0.25 to 0.5 mL 1% lidocaine and 4 to 10 mg of methylprednisolone acetate or equivalent (see Tables 192-2 and 192-5).
Figure 192-5 Wrist joint. A, Injection of the wrist joint. The hand is held in slight flexion, and the needle is inserted just distal to the radius in the “snuff box.” B, Flex the joint 20 degrees to open the joint spaces. The dorsal approach is generally used. Position the needle perpendicular to the skin surface. Enter at a site distal to the radial head and lateral to the extensor pollicis longus tendon (just ulnar to the anatomic “snuff box”). If the needle can be easily inserted to 1 or 2 cm, it is correctly positioned in the joint space. The intercarpal joints have interconnecting synovial spaces, and the contents of one correctly placed injection will disperse into the entire joint complex. Use an 18- to 20-gauge, 1- to -inch needle with 0.5 to 1.0 mL 1% lidocaine and 4 to 10 mg of methylprednisolone acetate or equivalent (see Tables 192-2 and 192-5).
Figure 192-6 A ganglion is a manifestation of joint inflammation. A, Frontal view. B, Side view. C, Example of an unusual ganglion cyst on the thenar eminence. D, Aspiration of the cyst. Hold the needle in position with the hemostat and remove the syringe. Attach the steroid-containing syringe and inject the contents. (Some have used fibrin sealants, hypertonic saline, and other irritants for attempts to “scar down” the cyst.) E, The contents are often thick, and there may only be minimal return of a gel-like material. F, Use an 18- to 20-gauge, 1- to -inch needle with 0.5 to 1.0 mL 1% lidocaine and 4 to 10 mg of methylprednisolone acetate or equivalent (see Tables 192-2 and 192-5).
(A–E, Courtesy of The Medical Procedures Center, PC, John L. Pfenninger, MD.)
Figure 192-7 De Quervain’s disease. Maximally abduct the thumb to accentuate and identify the tendon. Insert the needle parallel to (but not into) the tendon. Inject at the areas of greatest tenderness. Postinjection splinting may still be necessary. Use a 25-gauge, -inch needle with 3 to 4 mL 1% lidocaine and 10 to 20 mg of methylprednisolone acetate or equivalent (see Tables 192-2 and 192-5).