Botulinum Toxin and Its Clinical Use

Justinus Kerner, a German physician and poet, provided the first accurate and complete description of the clinical symptoms of food-borne botulism. He described 230 patients in the 1820s who suffered all the muscular and autonomic symptoms including gastrointestinal disturbances, dry eyes, dry skin, and weakness associated with the ingestion of contaminated meats. Kerner termed this condition “sausage poison” and “fatty poison”. He went on to perform animal experiments and experiments on himself. He administered botulinum toxin extracted from contaminated sausages to birds, cats, rabbits, frogs, flies, locusts, and snails. Kerner developed hypotheses from his experiments on the pathophysiology of the toxin. In his monograph he stated: “The nerve conduction is brought by the toxin into a condition in which its influence on the chemical process of life is interrupted. The capacity of nerve conduction is interrupted by the toxin in the same way as in an electrical conductor by rust.” Later in the monograph, he conceives of the idea of using the toxin for therapeutic uses.

The term botulism was derived from the Latin term, “botulus”, which means sausage. Edward Schantz first isolated the toxin and he and Alan Scott began work on a standardized botulinum toxin preparation in the late 1960s. Scott first used botulinum toxin type A in monkey experiments in 1973 and he first used botulinum toxin type A in humans to treat strabismus in 1980. Botulinum toxin type A was approved by the Food and Drug Administration (FDA) in 1989 for the treatment of strabismus, blepharospasm, and hemifacial spasm in patients more than 12 years of age. Botulinum toxin type B received FDA approval for treatment of cervical dystonia in 2000, and botulinum toxin type A was approved by the FDA to treat severe primary axillary hyperhydrosis and moderate-to-severe glabellar frown lines in 2002.

In addition to the approved uses in the United States, there are other published uses of botulinum toxin, which include painful or potentially painful conditions such as: achalasia; anismus (painful); bladder detrusor hyperactivity; essential tremor; myofascial pain syndrome (painful); focal dystonias (sometimes painful); muscle spasm (often painful); piriformis syndrome (painful); spasmodic dysphonia; spasticity (sometimes painful); whiplash (painful); chronic focal painful neuropathies; migraines and other headache disorders; temporomandibular joint pain disorders; gastrointestinal dysmotility disorders; chronic low back pain.

Aside from publications, noteworthy medical organizations have commented on the effectiveness and safety of botulinum toxin. The National Institutes of Health (NIH) Consensus Development Conference published a statement in 1990 that summarized the indications and contraindications of botulinum toxin usage for the treatment of a variety of conditions. The NIH conference endorsed the use of the neurotoxin as safe and effective for the symptomatic treatment of adductor spasmodic dysphonia, blepharospasm, cervical dystonia, hemifacial spasm, jaw-closing oromandibular dystonia, and strabismus. The same year, the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology further endorsed the use of botulinum toxin for the symptomatic treatment of these conditions.

Botulinum toxin is held to be one of the deadliest poisons known to mankind, yet by harnessing this activity, it has resulted in great advances in the treatment of numerous conditions. The understanding of the mechanism of action of botulinum toxin had its beginnings in 1949 when Burgen’s group discovered that botulinum toxin blocks neuromuscular transmission. In the 1950s, researchers discovered that injecting overactive muscles with small quantities of botulinum toxin type A resulted in decreased muscle activity by blocking the release of acetylcholine (Ach) at the neuromuscular junction. The understanding of this mechanism of action led to the application of botulinum toxin in most clinical settings. Since then, significant advances have occurred in the understanding of the mechanisms of action of botulinum toxin other than muscle paralysis—and this is leading to additional applications.

There are seven serotypes (A, B, C1, D, E, F and G) of botulinum toxin that act by inhibiting the exocytosis of Ach from presynaptic boutons of cholinergic neurons. Botulinum toxin is synthesized as a single-chain polypeptide (~150 kDa) that is activated by proteolytic cleavage into a 100-kDa heavy chain and 50-kDa light chain linked by a disulfide bond. The heavy chain domain is involved in cellular uptake into the presynaptic terminal by binding to extracellular receptors and in the transport of the neurotoxin through the lipid bilayer. The toxin is now intracellular but is sequestered in a membranous organelle without access to its targets, which reside in the cytoplasm. It is one of the functional domains (amino) of the heavy chain of the toxin that undergoes a conformational change facilitating translocation of the light chain through the lipid bilayer into the cytoplasm. Finally, the disulfide bond between the heavy and light chain is cleaved, allowing the light chain access to the cytoplasm. The light chain is a zinc-dependent endoprotease and the targets of the protease are presynaptic proteins required for intracellular trafficking of acetylcholine vesicles into the synaptic cleft. The presynaptic proteins targeted by the protease are called SNARE proteins (soluble N -ethylmaleimide-sensitive fusion protein attachment receptor) and are critical for the exocytosis of synaptic vesicles. It is this step, the proteolytic cleavage of the SNARE proteins, that is best understood in the intoxication by botulinum neurotoxin.

The release of Ach into the synaptic cleft requires docking of the Ach-containing vesicle to the presynaptic membrane. The docking of the vesicle requires various proteins that are located in the wall of the vesicle, in the presynaptic membrane or in the cytoplasm. This family of proteins (SNAREs) includes vesicle-associated membrane protein (VAMP)/synaptobrevin, syntaxin, and SNAP-25. These proteins form a complex that allows the vesicle to fuse with the motor nerve terminus membrane and release the acetylcholine into the synaptic cleft. The site of action of botulinum toxin type A is SNAP-25 (synaptosome-associated protein with a molecular weight of 25 kDa), which is a presynaptic membrane protein. Botulinum toxin type B targets VAMP (vesicle-associated membrane protein), which is located in the wall of the vesicle. Cleavage of the proteins prevents the assembly of the fusion complex and thereby blocks the docking of the vesicle and the release of the Ach leading to relaxation of the muscle cell and a state of chemical denervation.

Of significant clinical importance is the duration of action of the toxin effect. In general terms, the clinical effects of botulinum toxin injections are delayed a day or two with the maximal effects of functional muscular weakness peaking at about 2 weeks. The therapeutic effect of botulinum toxin-induced neuromuscular blockade usually lasts 3 to 4 months and ranges 2 to 6 months following an injection. Several factors likely contribute to the duration of action of the toxin. The best understood factor and most often quoted is the synaptic remodeling; however, other factors such as the duration of protease activity in the nerve terminal, the rate of replacement of the cleaved SNARE proteins, and the activity of the cleavage products may also influence the rate of function recovery.

The development of neutralizing antibodies to botulinum toxin can be a therapeutic problem for patients and physicians. Patients who initially respond well to treatment with botulinum toxin can become nonresponders. The incidence rates of neutralizing antibody development and the exact cause in individual patients remains unknown. More frequent injections, more “booster injections,” and higher doses are possible risk factors, thus extending the time between injections, minimizing the dose, and avoiding booster injections may decrease the development of neutralizing antibodies.

Some authors have noted that the pain relief preceded muscle decontraction and exceeded the degree and duration expected as a consequence of its neuromuscular actions. These observations suggest that botulinum toxin may have antinociceptive properties independent of the muscle relaxation. These observations and the expanding body of literature examining botulinum toxin for primary headache disorders and muscle conditions including a pain component led to further investigation into botulinum toxin in pain.

A number of in vitro experiments have provided evidence that botulinum toxin inhibits neurogenic inflammation by attenuation of the release of neurotransmitters. Botulinum toxin was found to inhibit substance P release from cultured embryonic dorsal root ganglion neurons and to reduce stimulated release of calcitonin gene-related peptide from cultured trigeminal ganglia neurons.

Additional support has come from animal experiments demonstrating reduction in nociceptive behaviors in animal models of inflammatory and traumatic neuropathic pain following peripheral injections of botulinum toxin. In rats with induced trigeminal neuropathy, intradermal injection of botulinum toxin in the area of the infraorbital branch of the trigeminal nerve alleviated the mechanical allodynia and reduced the exaggerated neurotransmitter release. In another experiment by Cui and colleagues, a rat formalin model of inflammatory pain was inhibited by subcutaneous administration of botulinum toxin injection and this inhibition was associated with a reduction in neurotransmitter release from the peripheral terminals of nociceptive sensory neurons. It was Cui’s study in 2002 that provided the first evidence that botulinum toxin had an effect on nociceptive sensory nerves in vivo. In studies by Aoki, botulinum toxin inhibited several of the neurophysiologic and neurochemical effects of formalin in the rat formalin-pain model including glutamate release, Fos-LI in the dorsal horn, and evoked-activity of WDR neurons in the spinal cord.

The efficacy of botulinum toxin in neuropathic pain initially was suggested in small anecdotal case studies and small open-label trials. An open study of botulinum toxin in 13 volunteers with trigeminal neuralgia found a reduction in visual analog scale scores and surface area of pain. Tsai and coworkers conducted an open label, prospective pilot study using botulinum toxin injected intracarpally in five patients with primary carpal tunnel syndrome. Their data suggested a long-acting antinociceptive effect of botulinum toxin.

More recently, two well designed clinical trials evaluated the efficacy of botulinum toxin for chronic neuropathic pain and diabetic neuropathic pain. Ranoux and colleagues published a randomized, double-blind, placebo-controlled, parallel group study providing evidence in support of the efficacy of botulinum toxin for the pain associated with focal neuropathies such as postherpetic neuralgia and posttraumatic or postoperative neuropathy. The study included 29 patients with focal painful neuropathies and mechanical allodynia, and treatment consisted of a one-time intradermal administration of botulinum toxin into the painful area. Outcome measures included average spontaneous pain intensity, quantified testing of thermal and mechanical perception of pain, allodynia to brush and decreased pain threshold to cold; the measures were evaluated at baseline, 4, 12, and 24 weeks. The results indicated that botulinum toxin treatment, relative to placebo, was associated with persistent effects on spontaneous pain intensity from 2 weeks after the injection to 14 weeks. A recent study by Yuan and associates report the results of a double-blind, placebo-controlled, crossover trial of intradermal botulinum toxin for diabetic neuropathic pain in 18 patients. The authors found a significant reduction in visual analog scale of pain at 1, 4, 8, and 12 weeks after botulinum toxin injection when compared to the placebo group. Specifically, within the botulinum toxin group, 44.4% of the participants experienced a reduction of the visual analog scale greater than or equal to 3 within 3 months after the injection, in contrast to the placebo group that reported no similar response. In addition, the authors evaluated sleep quality using the Chinese version of the Pittsburgh Sleep Quality Index and found a difference in the improvement in sleep quality between the botulinum toxin treatment group and the placebo group. The difference between the groups reached significance ( P < .05) only 4 weeks after the initial injection, but did not support sleep improvement with botulinum toxin at week 12, which was the endpoint of the study design.

Both reports (Yuan and colleagues and Ranoux and associates ) are small studies but each support a trend of reduced pain perception beginning at 1 week postinjection and extending to 12 weeks in the Yuan and colleagues’ study and 14 weeks in the Ranoux and associates’ study. Both studies report essentially no adverse events and this is supported by the general botulinum toxin literature. Although this suggests a promising approach to the treatment of neuropathy, additional larger, well designed, multicenter clinical trials with longer periods of follow-up are necessary.

Cervical Dystonia

Cervical dystonia (CD), also known as spasmodic torticollis and torsion dystonia, is a common form of focal dystonia manifesting as involuntary contraction and twisting of the neck muscles. These features lead to abnormal postures and movements of the head. The deviation of the head can be multidirectional and is described as torticollis (the most common form of CD with patient’s head turned to one side); laterocollis (lateral flexion of the neck), anterocollis (flexion of the neck) and retrocollis (extension of the neck). It is possible that one can have a combination of these forms. The prevalence of CD was reported to be 8.9/1,000,000 and it is recently estimated by the Dystonia Medical Research Foundation that 250,000 people suffer from CD in the United States. It is believed that 66% to 75% of the patients with CD are disabled from the pain associated with CD. CD is mostly idiopathic and about 12% of those affected have a family history. Idiopathic CD is the most common form of adult-onset focal dystonia slowly developed over several years in patients 30 to 50 years old. Cervical dystonia can be caused by any injury or inflammation of the cervical muscles or cranial nerves from various disease processes, including head, neck, and shoulder trauma or from taking dopaminergic block agents. There is evidence indicating that CD arises from basal ganglia circuit abnormalities leading to dopaminergic dysfunction, which in turn causes disinhibited thalamocortical output and dystonic postures.

Patients with CD can have a wide spectrum of symptoms involving the head, neck, upper extremity, and other body parts with sustained painful muscle contraction, pulling, and/or stiffness. The severity of the pain is usually relative to the intensity of the dystonia and muscle spasms. Jahanshahi and colleagues reported progression of dystonic symptoms to extranuchal, but still cervical, innervated sites such as hand, arm, and oromandibular region in one third of the 72 patients with adult-onset cervical dystonia. Patients with CD may develop neck pain from the muscle contraction and muscle strain from correcting the abnormal posture. The chronic abnormal posture may also lead to degenerative changes in the cervical spine leading to facet pain, radiculopathy, or spinal stenosis. Headaches associated with CD are common. Acute posttraumatic CD is different and the symptoms include immediate local pain after trauma, followed by a significant limitation in cervical range of motion, and abnormal posture of the head and shoulder. Trapezius hypertrophy may occur as well. Those changes often result in abnormal muscle contraction and pain. The abnormal posture and pain in patients with CD are part of their functional limitation and interfere with the patients’ activities of daily living. Rondot and coworkers found that 99% of the 220 patients they studies had various functional difficulties. Dysphasia and subclinical swallowing motility disturbances were reported in those patients. Permanent disability from the decreased cervical range of motion, involuntary movements, and intractable pain may occur. The diagnosis of CD is clinical and inspection is usually enough. However, a though physical examination should be conducted to rule out “pseudodystonia” due to structural abnormalities and secondary dystonia.

Myofascial Pain Syndrome

Myofascial pain syndrome (MPS) is a painful disorder that is characterized by the presence of the palpable taut band of muscle fibers and myofascial trigger points (MTrP). The International Association for the Study of Pain defines the trigger point as a discrete tender point palpable in the taut muscle band. A myofascial pain syndrome caused by MTrPs characteristically results from either an acute episode of muscle overload or a chronic and/or repetitive muscle overload. In addition, there are autonomic phenomena (piloerection, localized sweating, or even regional temperature changes in the skin because of altered blood flow), concomitant disorders, psychosocial factors, and psychiatric presentations including depression and anxiety. There are different opinions about what MPS represents. Some scholars think that it should cover all the regional pain caused by any soft tissue pathology. Thus, MPS may be considered as a primary local or original pain syndrome or a secondary syndrome caused by other disorders.

Research studies indicate that the clinical characteristics of an MTrP can be explained by hypercontracted muscle fibers located at and produced by a region of muscle with multiple dysfunctional motor end plates (neuromuscular junctions). The dysfunction is a markedly excessive continuous release of the normal synaptic transmitter, Ach. The noise-like potentials and spikes that are strongly associated with MTrPs were first interpreted as coming from muscle spindles. However, electromyographic studies clearly identify these noise-like and spike potentials as motor endplate potentials of skeletal muscle fibers. Electromyographers generally recognize these end-plate potentials as normal. However, physiologists have distinguished these potentials from normal miniature end-plate potentials and have shown that they represent a pathologic increase in spontaneous release of Ach. The end-plate noise component can result from mechanical strain of the neuromuscular junction caused by stresses applied to the nerve terminal or produced by muscle overload. The end-plate noise component of end-plate potentials appears to be present before the needle examination and is commonly caused by stressful activity of the muscle, especially in latent MTrPs that cause no clinical pain complaint. The end-plate spikes, however, are often induced by the presence of the needle and are more likely to appear in more active MTrPs.

Histologically, MTrPs show large, darkly stained, round myofibers in cross section in canine, equine and in human studies. Longitudinal sections of myofibers several hundred microns in length of canine muscle show hypercontracted fibers (also called “contraction knots”). The integrated hypothesis for the pathophysiology of MTrPs attributes these contraction knots to the observed depolarization of the post-junctional membrane that continuously releases calcium from the sarcoplasmic reticulum. This hypothesis identifies contraction knots as limiting circulation because the strong contraction of the sarcomeres is sustained within the hypercontracted fiber, whereas local energy consumption is increased. The resulting energy crisis should exhibit severe local hypoxia, demonstrated in the MTrPs. Increased tension of involved muscle fibers accounts for the palpable taut band consistently associated with an MTrP. The energy crisis and local hypoxia that was observed to extend for several millimeters could account for the release of substances that sensitize local nociceptors, causing the local and referred pain characteristic of MTrPs. An interesting study examined rabbit muscle after a marker (iron deposit) was placed at precisely the location where an active trigger point was identified by twitch response, taut band, and spontaneous electrical activity. Small C nerve fibers (most likely nerves that carry pain information) were found in the immediate vicinity. Taken together, these data support the idea that MTrPs are related to abnormal motor end-plate activity and subsequent hypercontraction of the associated myofibers.

MTrPs are identified on physical examination by palpating a localized tender spot in a nodular portion of a taut band of muscle fibers. Pressure (usually with the examiner’s fingertip) over a trigger point elicits pain at that area and may also elicit pain at a distance from the point under the fingertip. This is known as referred pain. Another important feature of the trigger point is that the elicited pain mirrors the patient’s experience. Insertion of a needle, snapping palpation, or even a brisk tap with the fingertip directly over the MTrP may elicit a brief muscle contraction detectable by the examiner. This brisk contraction of muscle fibers of the taut band is termed a local twitch response . There is a burst of electrical activity within the muscle band that has the twitch response (end-plate noise), and such activity is not observed in the other muscle bands. This type of end-plate noise is found more prevalently in myofascial trigger points than in sites that are outside the MTrP but still within the end-plate zone. Animal studies and a human study have shown that this response is propagated as a spinal reflex. This response is a valuable indicator that the needle being injected into an MTrP has effectively reached at least one necessary target in the MTrP. Demonstration of a local twitch is additional confirmation of the diagnosis. In addition, passive stretch range of motion of the muscle is limited by pain, and both maximum contraction in the shortened position and maximum voluntary contraction are likely to be inhibited or to be associated with pain.

If abnormal end-plate activity is responsible for MTrPs, then a powerful rationale exists for the use of neuromuscular blocking agents, such as botulinum toxin, in the treatment of myofascial pain syndrome. Injection of muscles with botulinum toxin can be appropriate therapy for myofascial pain caused by MTrP but is unlikely to be so for treatment of myofascial pain of unspecified origin, when that term is used in the general sense. Myofascial pain with muscle tenderness versus specific MTrPs responsible for the clinical pain is an ambiguous diagnosis. The tender spots may be due to fibromyalgia, bursitis, or one of many other diagnoses that do not justify injection with this product.

At present, no routine laboratory test or routine imaging test is available to confirm the presence of MTrPs. Usually two objective tests can be used to confirm the presence of MTrPs. One requires electrodiagnostic technique and the other uses ultrasound imaging. Both animal and human research studies have shown that MTrPs are characterized by electrically active loci that exhibit end-plate noise and often spikes.

Piriformis Syndrome

Piriformis syndrome (PS) is a myofascial pain disorder that manifests with a spectrum of symptoms, including buttock pain, referred pain to the ipsilateral lower extremity, and/or low back pain, caused by piriformis muscle inflammation, spasms, contracture, anatomic anomalies, or irritation to the sciatic nerve. The piriformis is from the Latin words pirum (pear) and forma (shape). It is a flat muscle originating from the anterior lateral surface of sacrum (second to fourth vertebrae); exiting through the greater sciatic foramen; and inserting onto the superomedial greater trochanter. It neighbors with five hip rotator muscles: the superior and inferior gemelli, the obturator externus and internus, and the quadratus femoris. During lower extremity weight bearing or ambulation, the piriformis muscle contracts to prevent rapid internal rotation of the hip. It externally rotates the hip when the hip and knee are extended, whereas it abducts the hip when it is flexed to 90 degrees. The sciatic nerve, posterior femoral cutaneous nerve, gluteal nerves, and the gluteal vessels pass below the piriformis muscle. However, there are anatomic variations of the sciatic nerve to the piriformis muscle: superior to, divided by, or piercing through the piriformis muscle.

There were numerous studies in the past in attempting to find out the cause of low back pain and sciatica. Yeoman dissected 100 cadavers to find the relationship of the sacroiliitis and sciatica. In 1934, Freiberg and Vinke assumed that the sacroiliac joint (SIJ) lesion caused inflammation in the piriformis muscle, its fascia, and the lumbosacral plexus leading to the irritation of sciatic nerve. Beaton and Anson related the anomalies of the piriformis muscle to sciatica. The term PS was first used by Robinson in 1947 when he described this syndrome with six cardinal features to describe this syndrome. The six key features are (1) a history of trauma or fall to the buttock; (2) gluteal or SIJ pain with radiation to the lower extremity; (3) gluteal atrophy; (4) a palpable sausage-shaped mass; (5) positive Lasègue’s sign (pain on voluntary flexion, adduction, and internal rotation of the hip); and (6) exacerbation of pain with bending or lifting.

The PS remains a controversial diagnosis as to whether it is a distinct clinical diagnosis of the tender piriformis muscle with the pathology of muscle spasms or hypertrophy, or the compression of the sciatic nerve by the piriformis muscle causing neuropathic pain; and is complicated with the pain from five neighboring short external rotators. However, the authors think that the two entities could be the manifestation of the same diagnosis with different stage or severity of the disorder. The incidence of PS ranges from 0.33% to 6% and accounts for 6% to 8% of the yearly cases of low back pain and sciatica in the United States. Patients with PS are typically 30 to 40 years old, female (three to six times more than their male counterparts) with a recent history of trauma to the buttocks or pelvis (usually from a fall), exacerbated activity intensity, or changes of low back, pelvis and lower extremity biomechanics due to lower extremity injuries, leg length discrepancy (≤0.5 inch), hip joint replacement, gait disturbances, even pregnancy. It is also seen more in long distance truck drivers, cyclists, tennis players, ballet dancers, and the like. The typical symptoms of PS include buttock pain with or without radiation to the ipsilateral lower extremity, to or below the knee. These symptoms may be exacerbated with ipsilateral hip adduction, internal rotation or prolonged sitting (sitting intolerance), intercourse or bowel movement. Severe cases of PS may lead to gluteal atrophy, motor weakness of the S1 innervated muscles, foot drop, and sensory deficits. The diagnosis of PS was once thought to be a diagnosis of exclusion and because of the aforementioned symptoms, PS is very often misdiagnosed as sacroiliitis or lumbosacral radiculopathy. Therefore, careful evaluation to rule out the other causes is essential for the correct diagnosis and effective treatment. Patients with PS often have tenderness at the buttock region overlying the greater sciatic notch or the piriformis muscle or a taut muscle band (with or without trigger point) to palpation, with or without radiation to the ipsilateral lower radiation reproducing the patients’ symptoms. Several provocative maneuvers have been used to aid the diagnosis of PS, including the FADIR test (hip F lexion, AD duction and I nternal R otation, also known as FAIR, which is also a therapeutic position), the Pace test, the Freiberg test, and the Beatty test. Because the piriformis muscle is so deep, palpation of the muscle and the trigger point can be properly performed only by rectal or vaginal examination. Imaging studies, such as computed tomography (CT), ultrasound, or magnetic resonance imaging (MRI) are employed to rule out other potential sources of compression at or near the sciatic notch, such as intrapelvic abscess, occult tumor, or hematoma or in the lumbosacral spine. One helpful diagnostic aid is EMG. In the case of lumbosacral radiculopathy, the EMG examination may reveal abnormal spontaneous electrical activity in the lumbar paraspinal muscles, whereas in piriformis syndrome, no such abnormal electrical activity should be seen. Because the site of nerve compression is distal to the nerve root, other investigators have reported that H-wave studies are delayed when comparing the patient’s extended painful leg to the same leg in a position of adduction, internal rotation, and flexion. Conduction may be delayed when the muscle is at its thickest in the shortened position.

The injury to the piriformis muscle may lead to the inflammation and muscle spasms, and the irritation of the sciatic nerve. Histamine, serotonin, prostaglandin, and bradykinin from the inflammation may irritate the sciatic nerve resulting in a cycle of pain, spasms, inflammation, and irritation. The characteristic signs and symptoms are sometimes caused by pain referred from piriformis MTrPs and sometimes are caused by compression of the sciatic nerve between the bony rim of the sciatic foramen and a hypertrophied piriformis muscle. Pace and Nagle suggested that focal irritation of the piriformis muscle leads to myofascial pain syndrome that can be treated with trigger point injection. The nodular MTrP and its taut band can provide the increased muscle bulk and tension. Pain in these patients may come from the nerve entrapment and the referred pain from the piriformis MTrPs. An additional source of pain in these patients is the tendency for compression of motor nerves to activate MTrPs in the muscles supplied by that nerve. Although some clinicians think that this diagnosis is controversial, numerous peer-reviewed articles clearly define clinical, anatomic, and electrophysiologic evidence for this distinct condition causing low back and leg pain. The attachment of the muscle at the greater trochanter is prone to be equally involved and tender and is readily available for palpation. It is very useful to identify the central TrP tenderness in the region of the mid-belly as well as the attachment tenderness at both ends. This strengthens the MTrP diagnosis considerably. Contraction of muscles with MTrPs appears to be most painful when the muscle is voluntarily contracted in the shortened position. If the enthesopathy is sensitive enough, the muscle hurts when forcefully loaded in any position but particularly in the shortened position.

Treatment of Piriformis Syndrome with Botulinum Toxin

In most cases, the conservative treatments, such as physical therapy with piriformis muscle stretching, NSAIDs, muscle relaxants, ultrasound, vapo-coolant spray coupled with soft tissue stretching, are effective in reducing the inflammation, spasms, and pain. It is also reported that repeated piriformis muscle injections with clonidine and bupivacaine provide long-lasting pain relief in patients with PS. For patients who failed to improve with conservative treatments, local injections of anesthetics and/or corticosteroids may be considered and has been shown to be effective. However, some patients may gain short-term benefits from local MTrP injections but remain refractory to other treatment for long-term pain control. This subset of patients has demonstrated clear benefit from botulinum toxin treatment, especially if the piriformis muscle shows EMG evidence of involuntary muscle contraction.

Porta conducted a comparative trial of botulinum toxin type A and methylprednisolone in group of 40 subjects included 23 patients with piriformis syndrome. Subjects were randomized to receive methylprednisolone or botulinum toxin type A (100 units). The 23 patients received injections in the piriformis muscle. At 60 days, the botulinum toxin group demonstrated statistically significant pain reductions as determined by their visual analog pain scale scores ( P <0.0001). In addition, a trend was noted at 30 days post-injection with the botulinum toxin group having lower pain scores but this did not reach statistical significance. The exact benefit derived from the piriformis muscle injection is uncertain because the data was not subanalyzed by the muscle injected.

Childers and colleagues conducted one of the earliest studies to examine the effectiveness of intramuscular botulinum toxin injections as a treatment for piriformis muscle syndrome. The authors examined a convenient sample of three consecutive patients. All patients presented with findings consistent with a diagnosis of piriformis syndrome and all had failed a trial of conservative management including NSAIDs, stretching, ultrasound, and piriformis trigger point injections. H-reflexes and segmental nerve conduction studies in all patients confirmed conduction block along the sciatic nerve above the gluteal fold, consistent with the diagnosis. The involved piriformis muscle in each patient was injected under fluoroscopic guidance with 100 units of botulinum toxin type A reconstituted in 5 mL of preservative-free saline. Pain reduction was assessed through pretreatment to post-treatment differences on a patient self-reporting instrument that recorded visual analog pain scale scores of pain intensity, psychological distress from pain, spasm frequency, and interference with daily activities. Results of this open label case series demonstrated that the average pain scores decreased from 6.1 to 3.4 and were 3.6 two weeks later. Twelve weeks later, two out of three patients had returned to their previous pain levels, whereas one patient sustained longer lasting benefit. The same author was the first to report a randomized, double-blind, placebo-controlled crossover trial of the effectiveness of botulinum toxin type A injections for refractory piriformis syndrome. Ten women initially enrolled and nine women completed the study. The subjects were randomized to receive either 100 units of botulinum toxin injection or saline under the guidance of fluoroscopy or EMG. The primary outcome measure of interest was differences between the pre-injection and post-injection visual analog pain scale scores (VAS). After injection with the vehicle, decreases were detected, but only in one of the four categories (distress), in contrast to the botulinum toxin group in which decreases were observed under all VAS categories.

In 2002, Fishman and colleagues evaluated the efficacy of botulinum toxin type A used in conjunction with physical therapy for piriformis syndrome in 67 subjects. The results in this double-blind, placebo-controlled trial were measured on the visual analog scale. The patients injected with botulinum toxin experienced more relief from pain than the subjects receiving placebo ( P = .001) and more relief than patients receiving lidocaine with steroid ( P < .05).

Yoon and colleagues conducted a prospective, single site, open label trial to evaluate the efficacy of botulinum toxin type A (150 units) in patients with piriformis syndrome resistant to conventional therapy. Twenty patients had botulinum toxin injected using CT guidance and nine patients served as active controls receiving an injection of dexamethasone (5 mg) and 1% lidocaine. Pain intensity scores, using a numeric rating system, were significantly lower at 4, 8, and 12 weeks after treatment than at baseline ( P < .0001).

Fishman and coworkers performed the first dose finding study for botulinum toxin type B in a cohort of eight consecutive patients receiving injections with 5000, 7500, 10,000 or 12,500 units. Visual analog pain scale scores were assessed at 0, 2, 4, 8, and 12 weeks. The subjects receiving the 12,500 units of botulinum toxin type B had the greatest clinical improvement at 3 weeks postinjection but then regressed over the following 5 weeks. Lang conducted a single center, open label study to evaluate the clinical safety and efficacy of botulinum toxin type B in patients with piriformis syndrome in 2004. Twenty patients were enrolled in the study and the injections were performed under electromyographic guidance with 5000 units of botulinum toxin type B. The study did not have controls and the single examiner was not blinded. Significant reductions in mean visual analog scale scores for buttock and hip pain were noted at 4, 12, and 16 weeks and low back pain at weeks 2, 12, and 16.

When injecting myofascial trigger points in the piriformis muscle, it is difficult to localize accurately in such a deep muscle and the trigger points are located in the end-plate zone in the mid-belly region of the muscle. In this case, use of EMG guidance to inject the neurotoxin specifically where end-plate potentials are observed will ensure optimal placement of the product. Because all or part of the sciatic nerve may occasionally traverse this part of the muscle, this use of EMG guidance is of additional importance.

The local anesthetic, corticosteroid, and botulinum toxin injections in the aforementioned reports were all performed under some sort of guidance, including EMG, ultrasound, fluoroscopy, and CT. Additional studies also demonstrated the convenience, accuracy, and efficacy in the injection of piriformis muscle. Therefore, the authors strongly recommend that the piriformis injection therapy should be conducted under the guidance of one of the proven methods to ensure the safety, accuracy, and efficacy.

Although there are associated disadvantages such as radiation exposure, contrast reaction, and increased cost, guided piriformis injections are widely used to ensure accurate placement of the medications and to avoid nerve injury around the piriformis muscle. After cadaver study, Benzon and colleagues used the lower border of the SIJ as their reference for the steroid injection to the piriformis muscle and near the sciatic nerve for better symptom relief. They inserted the needle 2 cm lateral and 1 cm caudal to the SIJ—guided with a fluoroscopy while patients were prone. The insulated needle was advance until a motor response was elicited in the foot with a nerve stimulator. The needle was then withdrawn until the elicited motor response disappeared and the steroid was injected near the sciatic nerve. The needle was then further pulled back to the piriformis muscle belly, confirmed with contrast ( Fig. 14-1 ), and followed with steroid injection to the muscle. Similar technique was reported by Betts and confirmed with a cadaver study. In a 10-year study of the diagnosis, treatment, and outcome of the PS, Fishman and colleagues inserted the needle at a point one third the distance from the greater trochanter to the area of maximum tenderness in the buttock at the depth of approximately 3 to 5 cm. Electromyographic localization of the piriformis muscle was conducted only when the location or depth of the needle placement was uncertain. We use a fluoroscopically guided technique published by one of the authors (MKC). The patient is placed in the prone position, the skin over the largest bulk of the buttocks is prepped and draped in a sterile fashion. The greater trochanter of the femur, the body of the sacrum, and the sciatic notch are identified using fluoroscopy. The skin is marked at the midway on a line that crosses the middle of the sciatic notch between the sacrum and the greater trochanter of the hip. A dual-purpose injection/electromyographic needle is inserted in an angle slightly lateral to medial until the ileum is encountered. It is then withdrawn slightly, and the injection site is visualized by fluoroscopy. To further verify the needle placement within the piriformis muscle, an electromyographic electrode is connected to the hub of the needle and a ground and reference electrode is secured to the lateral upper thigh. The patient is instructed to externally rotate the thigh to activate the piriformis muscle until brisk motor unit action potentials are observed.

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