CHAPTER 16 Discography
In 1948, Lindblom1 originally reported discography as a method to identify herniated discs in the lumbar spine by injecting contrast medium into the disc and following the outline of contrast medium into the spinal canal. It was noted as only a secondary consideration of the test that reproduction of the patient’s usual sciatica sometimes occurred during the disc injection. It was observed later that back pain was sometimes reproduced during the injection, as opposed to sciatica. Eventually some clinicians began using the test to evaluate discs as the source of axial pain in patients without radicular symptoms.
Since the early use of discography, it has been unclear whether reproduction of pain with injection indicated that the injected disc is the true primary source of clinical back pain, or whether the injection had simulated the usual pain in an artificial manner. Over time, attempts have been made to determine the specificity of the test and to refine the technique to reduce the risk of false-positive or false-negative results. Still this test remains highly controversial. Even the staunchest proponents of the procedure state that “discography is a test that is easily abused.”2 Basic diagnostic test assessment has found fundamental problems with test reliability (i.e., does the test give the same result on repeated testing?) and validity (i.e., does the test prove what it purports to prove?). Also, it has not been shown that using the test improves the outcomes in patients receiving the test compared with patients not receiving the test. More recently, the long-term safety of disc puncture and injection has also been questioned. This chapter discusses the rationale and technique of provocative discography when used in patients with primary axial pain syndromes.
Clinical Context
Back and neck pain are very common, and in most cases determining the “cause” of a specific episode of back or neck pain is unimportant because these symptoms frequently resolve in a short time or do not seriously interfere with function.1 Provocative discography may be described as representing a tertiary diagnostic evaluation, which should be considered only in a select group of patients.
Discography Technique
Criteria for Positive Test
In an effort to improve the specificity of discography in diagnosing so-called discogenic pain, some investigators have used additional criteria beyond pain reproduction on injection. The criteria for establishing a positive discogram are controversial. The primary criteria for a “positive” disc injection are pain of “significant” intensity on disc injections (usually defined as ≥6 out of 10 pain scale) and a reported similarity of that pain to the patient’s usual, clinical discomfort (concordant pain). These basic criteria were proposed in the experimental work by Walsh and colleagues in 1990,29 which proposed “significant pain” be defined as 3 out of 5 (or 6 out of 10) on an arbitrary pain thermometer. “Bad pain” was defined as 3 out of 5 pain, and “moderate pain” was described as 2 out of 5 pain. The authors did not stringently define concordance of pain reproduction. Some investigators have proposed additional and sometimes idiosyncratic criteria for positive injections (Table 16–1).
Test Criteria for Positive Result | Positive Test Threshold | Comments |
---|---|---|
Pain response (intensity) | ≥6/10 or 3/5 | Subjective and arbitrary scale. No data on reliability. Data on validity in small groups of asymptomatic subjects without psychosocial comorbidity are good (specificity >90%). Data in several studies of subjects with increased psychosocial or chronic pain comorbidity indicate validity in these subgroups is poor (specificity 20%-60%) |
“Bad” pain or worse on pain thermometer | ||
≥7/10 | ||
Qualitative pain assessment (concordant pain) | “Concordant pain” usually including “similar” but not exact pain | Subjective response. Data on reliability are unknown. Data on validity in small study of experimental nondiscogenic low back pain indicate validity is questionable |
“Exact” pain only | ||
Annular disruption | Dye must show fissure to or through outer anulus | Tested only in clinical studies without follow-up to confirm outcome or other “gold standard.” Radiologic reliability best with computed tomography scan after disc injection compared with x-ray alone. Validity of additional criteria as confirming true-positive test unknown; positive injection in discs without annular disruption more common in psychologically disturbed subjects |
Control disc injections | “Negative” injection (minimal or discordant pain) required adjacent to proposed “positive” disc | Injections in morphologically normal discs seem to be reliably negative even in subjects with serious psychological distress and no back pain. Reliability in other disc morphology unknown. Validity of this additional criterion as confirming true-positive test unknown |
“Normal” injection (i.e., no pain) | ||
Some authors insist that adjacent “control disc” must also have grade 3 annular fissure, which is “relatively painless” at equal or higher pressures than “positive disc” | ||
Demonstration of pain behavior | Facial expressions of pain must be observed to confirm verbal pain report | Reliability and validity of this criterion as confirming true-positive test unknown |
Pressure-controlled injection | Disc injections should be classified into low (<15 psi or <20 psi) or high (>50 psi) pressures at time of significant pain response; responses at pressures in between are indeterminate | Small outcomes series suggest low pressure sensitive discs are better treated with interbody fusion techniques. Reliability and validity unknown |
Volume-controlled injections | “Excessive volume” or speed to injection invalidated injection | Unvalidated concept based on anecdotal evidence. Primary data unavailable to analyze |
Maximum one or two positive disc injections | More than one or two positive disc injections invalidates study (all are indeterminate) | Assumption is made that generalized hyperalgesic effect may lead to multiple positive discs around single pain generator |
Quantify pain tolerance by response to buffered anesthetic injection | Subjects with poor pain tolerance may not be “ideal” candidates for discography; this feature needs to be detected | It is unclear that pain tolerance to intradermal anesthetic injection is valid test to determine “pain tolerance” in patients with long-standing axial pain |
Needles should be inserted from asymptomatic or least symptomatic side | Theoretically this may decrease confusion between injection and insertion pain | Some data suggest this is not an important technique. No “gold standard” confirmation was applied |
Any positive disc injection must be repeated with similar outcomes before accepting result as “positive” | Intraprocedure reliability test | No data available on whether this improved or decreased test accuracy |
Pain Generator Concept and Provocative Discography
When only degenerative changes are found, it is controversial whether or not a discrete local pain generator as the cause of serious back pain illness can be commonly identified. Some clinicians believe that serious axial pain and disability can be so multifactorial (mechanical, psychological, social, and neurophysiologic contributors) that it is unreasonable to expect specific diagnostic studies to confirm an anatomic “diagnosis” for axial pain illness in every patient.3–5 Even if a pain generator is suspected, it is unclear how this can be reliably confirmed to be the cause of the patient’s perceived pain, impairment, and disability in the face of complex social, emotional, and neurophysiologic confounders.
Other clinicians believe that identifying a pain generator is central to spine evaluations, is an expectation of patients, and determines the choice of treatments by focusing on the anatomic structure deemed responsible for the pain. In this model, social issues such as disability, litigation, psychological distress, and pain intolerance are believed to be secondary issues to the structural pathology.1,6–12 These clinicians generally believe that although the history and physical examination may be helpful in suggesting serious underlying pathology such as infection and tumor, these methods are not helpful in determining the true pain generator among many degenerative structures.
Diagnostic Injections and Modulation of Pain Perception in Axial Pain Syndromes
Many common factors are known to have potential dampening or amplifying effects on the perception of back and neck pain. These factors must be considered when evaluating the validity of diagnoses determined by diagnostic injections.13–18
Adjacent Tissue Injury
Injury to adjacent tissues may increase the perception of pain in surrounding structures by a local hyperalgesic effect. This is a well-known phenomenon that occurs with any tissue damage; it may amplify pain perception by increasing local inflammatory processes with secondary neurologic sensitization in areas not directly injured, such as the area surrounding a burn or a fracture that is sensitive but without any thermal or mechanical injury. This is an important phenomenon in patients with low back pain with serious disease at one or more levels, which may sensitize the adjacent segments to provocative testing (e.g., a spine that has undergone multiple operations).13,19
Local Anesthetic
Local anesthetic injections may decrease the perception of pain at a local site. This is the specific, active effect used in diagnostic blocks. This decrease in pain perception can also be a source of confounding effects if the exact placement of the agent is not well controlled. In addition to this direct local effect, a nonspecific placebo effect and a neurophysiologic modulation effect may occur. A relevant example is the effect of local anesthetic blockade on the perception of painful stimulus along the neuraxis proximal to the injection. A local anesthetic injection in the lower extremity may be perceived as relieving sciatica owing to disc herniation.20 This is not a placebo effect (i.e., the phenomenon is seen only with an active anesthetic agent) but rather an effect on neuromodulation. This effect is important in diagnostic anesthetic blockade as a source of false-positive and false-negative findings.21
Tissue Injury and Nociception in Adjacent or Same Sclerotome
Tissue injury having the same or adjacent sclerotomal afferents as lower spinal elements may increase pain sensitivity at any given site. This effect is thought to be due to physiologic and anatomic changes at the level of the dorsal root ganglion or spinal cord ascending tracts. In animal models, single afferent neurons from a dorsal root ganglion may innervate three adjacent discs and a wide range of adjacent structures. This effect is important in considering the specificity of discography at sites of similar embryonic derivation to a known pathologic structure (e.g., nonunion, spondylolisthesis, painful iliac crest bone graft site). The confounding effect of this phenomenon in discography has been experimentally and empirically shown (see later).13,22
Chronic Pain Syndromes
Chronic pain syndromes may complicate the evaluation of low back pain syndromes. Chronic pain from regional sites near the lumbar spine (chronic pelvic pain, irritable bowel syndrome, failed hip arthroplasty) or distant to the lumbar spine (chronic neck pain, chronic headache, temporomandibular joint syndrome) may increase pain sensitivity at lower spinal elements. This effect may be regional or global and may be related to neurophysiologic changes at multiple levels along the neuraxis. Preexisting chronic pain syndromes are also associated with depression, narcotic use, and habituation, which have independent pain perception effects. This effect has been shown to have an impact on the intensity of pain intensity from discography in experimental subjects.13,22
Narcotic Analgesia
Narcotic medications act at multiple levels to decrease pain sensitivity thresholds, intensity, and affective response. Administration of a narcotic medication may act as a common confounder of diagnostic techniques of any type requiring accurate feedback of pain perception from a patient.13,23,24
Depression, Anxiety, and Somatic Distress
Clinical depression, anxiety disorders, and increased somatic awareness may be seen as predisposing factors to chronic low back pain syndromes or reactions to the pain and disability of chronic low back pain illness or both. In either event, psychological distress usually decreases the pain threshold perception and increases perceived pain intensity and affective response.5,23,25 These effects are likely due to central neurochemical changes and systemic effects and have been shown to affect pain responses in discographic evaluation.
Summary
When considering the diagnostic certainty of a possible pain generator in chronic axial pain illness, it is necessary to view the aforementioned confounding factors for contribution to the illness behavior observed (Table 16–2). An injured soldier with facial trauma, after narcotic administration and in the heat of combat, may mask the perception of a significant low back pain injury, which otherwise could be clearly symptomatic. In this case, a bona fide local pain generator results in little pain perception. Conversely, a very minor nociceptive input (common backache) from a disc can be amplified in the case of a patient with multiple chronic pain syndromes, narcotic habituation, depression, and compensation issues (social disincentives). In this case, a common mild backache pain generator is amplified to become a catastrophic illness.
Modulator of Diagnostic Injection Effect | Type of Effect on Pain Perception at Site of Injection | Diagnostic Effect |
---|---|---|
Adjacent tissue injury | Increased regional pain perception | Decreased specificity in provocative injection |
Local anesthetic | Decreased pain perception at depot site and sometimes in sclerotomal or referral pattern | Decreased specificity in provocative injection |
Tissue injury in adjacent or same sclerotome | Increased regional pain perception | Decreased specificity in provocative injection |
Chronic pain syndrome | Increased generalized pain perception | Decreased specificity in provocative injection |
Narcotic analgesia | Decreased generalized pain perception and affective response |