Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_6012_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
29.08.2026
Размер:
93 Мб
Скачать
Chapter 12 Patient History and Physical Examination: Cervical, Thoracic, and Lumbar 193
that can help narrow the dierential diagnosis, and dene further issues that may need to be addressed through addi­tional testing. Although a thorough discussion is beyond the scope of this chapter, appropriate portions of a general medical examination need to be included in the assessment of a spinal patient depending on the nature of the presenting issues. Neurologic and orthopaedic examinations of varying degree and complexity are also necessary. is chapter follows a more focused approach to the examination of the spine with a dis­cussion of basic neurologic assessment and relevant provoca­tive maneuvers appropriate to a patient’s presenting problem.
Observation
e physical examination starts with observation, which begins when the physician rst sees the patient. Movement patterns, preferred postures, inconsistencies, and gait abnor­malities should be noted by the clinician and sta members throughout the patient’s visit. is observation needs to be done casually during oce or facility interactions and during
the medical history, then in a more formal manner during the examination. Formal observation should include an examina­tion from the feet to the head. Trunk and appendicular align­ment should be noted, paying particular attention to hip and knee alignment. e spine should be assessed for alterations
from normal alignment or resting curvature, including scolio­sis, kyphosis, alterations in lumbar or cervical lordosis, a lumbar shi, and head and neck alignment with the trunk.
Symmetry of shoulder height and scapular positioning should also be noted.
Gait assessment can be done aer initial observation,
looking specically for gait patterns suggestive of neurologic
decits, such as a steppage gait associated with footdrop or a wide-based gait suggestive of proprioceptive, cerebellar, or myelopathic pathology. Gait can be tested further by tandem gait testing (heel-to-toe walking). Balance can be assessed by simple observation and performing a single-leg stance with various postural challenges (e.g., crouching on one leg). If a patient has an antalgic gait (i.e., shortened stance phase of the gait cycle), consideration should be given to a musculoskeletal problem involving the hips, knees, or foot and ankle. Gener­ally, patients with a lumbar radiculopathy do not exhibit an antalgic gait pattern.
Spine range of motion (ROM) should be assessed for all relevant spine segments. ere is debate as to what constitutes “normal” range of spine motion and the signicance of any perceived restriction of motion. In the lumbar spine, ROM has been variably reported by using inclinometry, measuring the distance from the ngertips to the oor, assessing segmental
motion, measuring dynamic motion, measuring motion with the pelvis restrained, radiographic measurement, and using variations of the Schober test (measuring the change in dis­tance between a mark over the S1 spinous process and one made 10 cm above this in standing that occurs between stand­ing and exion).
e value of ROM measurements is questionable, however, because some data do indicate that there is no consistent rela­tionship between ROM and physical or functional impairment
82–85
in subjects with chronic low back pain.83 ROM generally seems to decline with age, further complicating attempts at establish­ing normative data.82 Gross lumbar motions generally include motion from the hips and lower extremities, and any lateral
exion or rotation involves coupled motion at multiple levels, making it dicult to assess these reliably. It is important to
examine hip motion, however, because painful and restricted hip motion, particularly in exion with internal rotation, that
mimics the patient’s usual pain would generally implicate the hip as a source of pain.
Despite these substantial limitations, it is still important to assess active spine motion in exion, extension, rotation, and lateral exion. Along with absolute degrees of movement, the examiner can assess symmetry of motion, preferred move­ment patterns, pain or symptom reproduction associated with motion, the relative contributions of associated body segments to motion (e.g., hips), motor control, and inconsistencies between movement noted on formal examination and that seen during casual observation or while the patient is other­wise distracted. Generally, patient motion should be assessed actively within the patient’s range of comfort. ere is little or
no role for passive ROM because this adds little to the clinical assessment and may place the patient at risk for further
38
injury.
For cervical and thoracic complaints, it is also important to assess shoulder and scapular motion. Shoulder ROM can be assessed actively by exion and abduction along with
passive motion of the glenohumeral joint. Scapular position at rest and with various arm positions can reveal abnormal movement patterns and may indicate problems with scapulo­thoracic function, other shoulder joint complex disorders, or neurologic injury aecting the parascapular musculature (e.g.,
a long thoracic or spinal accessory nerve injury). Scapulotho­racic dysfunction of various kinds may also be a source of pain in patients with thoracic complaints.86 Reproduction of a patient’s shoulder region pain by passive shoulder motion, particularly if it is restricted, would generally implicate the shoulder rather than the neck as the source of pain. Patients with a cervical radiculopathy obtain relief with ipsilateral shoulder abduction (the shoulder abduction relief maneuver); patients with intrinsic shoulder pathology oen have repro-
duction of pain with shoulder abduction.
Observation should also include looking for atrophy, edema, vasomotor changes, skin lesions, limb or joint defor­mity, contracture, and other signs that may have an impact on a patient’s care.
Palpation
e relevant areas of the patient’s spine and related structures should be palpated with the patient standing or, when appro­priate, in side-lying or prone position. Palpation may aid in the localization of the patient’s symptoms, the identication of an
injured structure, or the identication of associated so tissue or bony abnormalities. It should be noted whether tenderness is elicited in the midline or to either side of the midline, potentially dierentiating between spinal pain and pain from an adjacent so tissue source.38 Localized tenderness should
SECTION
II
194 DIAGNOSIS
be distinguished from diuse tenderness, the latter being less consistent with a focal injury.
In the cervical spine, palpation should include the occipital region; the anterior neck; the clavicular, supraclavicular, and scapular regions; and the areas of the associated cervicotho­racic musculature.38 In the thoracic region, palpation should also extend across the posterior ribs to identify focal bony tenderness that may suggest rib pathology rather than spine pathology. Pain with palpation or percussion of the costover­tebral angle may suggest renal pathology.87 Spondylolisthesis can frequently be appreciated by a palpable step-o of the spinous processes in the lumbar spine. In the lumbar region, palpation should include not only the lumbar spine but also the iliac crests, sacrum, sacroiliac joints, ischial tuberosities, proximal hamstring, and greater trochanteric areas, as indi­cated, to assess for the possibility of contributing problems from these regions. Trochanteric pain may mimic pain from a spine etiology.
Clinicians need to recognize that the ability to accurately identify a spinal level by palpation is quite limited. Multiple studies have conrmed high rates of inaccuracy with manual palpation, which raises concerns for the manual identication of structural problems and for the precise placement of medical instruments for spinal interventions.
88,89
Neurologic Examination
As with the general medical examination, the neurologic examination may cover a wide range of factors, depending on the particular presenting problem. e most common neuro­logic manifestations of spine pathology generally involve the spinal nerve roots or the spinal cord, resulting in radicular or myelopathic ndings on examination. e symptoms result­ing from spine pathology may frequently overlap, however, with symptoms of various peripheral nerve processes, central nervous system disease, or anterior horn cell disease. An examiner needs to be aware of the clinical presentations and neurologic ndings associated with these disorders. A full discussion of all relevant examination techniques and neuro­logic pathology is beyond the scope of this chapter, but can be found in general neurology texts. is section focuses on ndings more directly related to spine pathology.
A thorough understanding of dermatomal patterns is essential for all clinicians examining spine patients. As a refer­ence, the key sensory points identied by the American Spinal Injury Association90 can be helpful in assessing or screening patients with spine pathology (see Fig. 12.5). So-touch and pin-prick sensation can be assessed well in most patients; the examiner should distinguish between a dermatomal distribu­tion suggesting nerve root pathology, a stocking or stocking­and-glove distribution suggesting peripheral polyneuropathy, multiple nerve distribution suggesting alternative peripheral nerve pathology, or a nonorganic distribution. Proprioception, vibration, position sense, and temperature sensation may also be tested, particularly when there is concern for a spinal cord or central nervous system process or a peripheral neuropathy.
Motor examination consists of several parts, including strength, tone, coordination, muscle bulk, and involuntary
movements.87 Strength is the modality most generally assessed by clinicians, but all portions of the motor examination may be important in some patients with spine disorders. Involun­tary movements may be noted in patients with cervical dysto­nia or in various neurologic diseases that may aect function, such as Parkinson disease. e presence or absence of focal muscle atrophy should be noted in all patients. e mere pres­ence of focal atrophy implies neurologic injury or disease, and the distribution of atrophic muscles can be helpful in dening
the type of pathology present. Fasciculations associated with atrophic muscles imply the presence of lower motor neuron injury. Muscle tone can be aected by many neurologic pro­cesses. Reduced tone suggests lower motor neuron involve­ment, whereas increased tone or spasticity is seen with upper motor neuron disease. Coordination may be disrupted by numerous pathways, generally involving the cerebellum or its pathways, but weakness, proprioceptive loss, and cognitive disturbance may also aect motor performance on tests of coordination. Clinical methods to assess coordination include rapid alternating hand and foot movements and nger-to­nose testing.
87
Strength testing is generally done isometrically, but some­times weakness can be better appreciated through dynamic or repetitive movements that address endurance (e.g., multiple single-leg toe raises to assess plantar exor strength). It is
essential to be aware of key muscle groups by myotome and the peripheral nerve origin of those muscles. Important muscle groups and motions associated with cervical and lumbar myotomes are as follows:
C5—elbow exors, shoulder abductors and external rotators C6—elbow exors, wrist extensors and pronators, shoulder
external rotators C7—elbow extensors, wrist pronators C8—extension of index nger, nger abduction and exion,
abduction of thumb
T1—nger abduction L2—hip exion
L3—hip exion, hip adduction, knee extension L4—knee extension, ankle dorsiexion L5—ankle dorsiexion, great toe extension, ankle eversion,
hip abduction and internal rotation S1—ankle plantar exion, toe exion
Strength is generally graded on a scale of 0 to 5 as follows:
87
5—active movement against full resistance (normal strength) 4—active movement against gravity and some resistance 3—active movement against gravity 2—active movement with gravity eliminated 1—trace movement or barely detectable contraction 0—no muscular contraction identied
Active movement is generally meant to imply joint motion through the full available ROM. For some muscle groups, patients can oen have signicant loss of strength that is not detectable by providing manual resistance with the examiner’s arms; thus, other test maneuvers may be necessary to identify more subtle weakness. Examples of such maneuvers would be having the patient do a partial squat or arise from sitting
Chapter 12 Patient History and Physical Examination: Cervical, Thoracic, and Lumbar 195
without using the upper extremities to assess for weakness in the knee extensors. e Beevor sign (in which the umbilicus moves craniad during contraction of the abdominal muscles with supine neck exion) indicates weakness of the lower
abdominal muscles.
26
Reex testing can further aid in the localization of neuro­logic injury and help distinguish upper motor neuron from lower motor neuron disease. In lower motor neuron injuries, deep tendon reexes of aected regions are generally reduced,
whereas they are brisk in upper motor neuron injuries. e Babinski response to appropriate plantar stimulation, Homan
sign in the hand, and clonus all can indicate the presence of upper motor neuron injury. As with other physical examina­tion ndings, the sensitivity and specicity of these ndings are
limited for any particular condition. In a study assessing the prevalence of physical examination ndings in cervical myelop­athy treated surgically, it was noted that 21% of the patients had no myelopathic ndings on examination. Of the ndings just mentioned, the Homan sign was the most sensitive (59%), whereas the Babinski response had very low sensitivity (13%) but was highly specic.91 Various other reexes—including
abdominal, cremasteric, and palmomental—can also be used as part of the neurologic examination when appropriate.
Although a neurologic injury oen manifests as either an
upper or a lower motor neuron lesion, it can also manifest with a mixed pattern of upper and lower motor neuron fea­tures, as can be seen with amyotrophic lateral sclerosis. e
segmental distribution of commonly tested deep tendon reexes is as follows87:
Biceps reex—C5, C6 Brachioradialis reex—C5, C6 Triceps reex—C6, C7 Patellar tendon reex—L2, L3, L4 Medial hamstring reex—L5, S1 Ankle jerk reex (Achilles tendon)—S1
For the most part, the sensitivity and specicity of isolated tests for sensation, strength, and reexes are relatively limited in the assessment of spine conditions, particularly when any one single test is considered.
22,85,92
ere may be more utility
in combining a variety of ndings across multiple modalities,
especially when the ndings are consistently reproducible. e degree of consistency between examination ndings, history, imaging results, and self-reported levels of pain and disability for aected patients should always be considered when clinical decisions on care are made.
Special Tests and Provocative Maneuvers
In addition to the standard examination techniques described earlier, various provocative maneuvers and other tests have been used to aid in the diagnosis of patients with spine condi­tions. e sensitivity and specicity of many of these tests are either unclear or suboptimal, but a working knowledge of their applicability is useful in the diagnosis and management of patients with spine conditions.
e Lhermitte sign, although more technically a symptom, is the presence of an electric shock–type sensation radiating
into the limbs with cervical exion. Although rst described in a patient with multiple sclerosis, this sign is associated with various spinal cord lesions.
26,38
If elicited with neck exion,
this sign should raise concern for the presence of a cervical cord lesion. If elicited with trunk exion, this may indicate a thoracic cord lesion.
26
e Spurling maneuver is a test for cervical nerve root compression or irritation. A positive test is elicited by extend­ing, rotating, and laterally bending the head to one side with reproduction of radicular pain into the aected ipsilateral
extremity.
26,38
One study comparing the Spurling maneuver with the results of electrodiagnostic testing found that the maneuver had poor sensitivity (30%) but good specicity
(93%) in the diagnosis of electrodiagnostically conrmed cervical radiculopathy.
93
e Valsalva maneuver is performed by having a patient hold his or her breath and bear down. A reproduction of the patient’s radicular symptoms or spinal pain with this maneuver is believed to indicate a space-occupying lesion, such as a disc herniation, in the spinal canal.
26,38
Dural tension signs are frequently used to assess lumbar spine pathology. Many dierent maneuvers have been described. A supine straight-leg raise is performed by elevating the leg with knee extended and assessing for the reproduction of pain into the leg. e test is considered positive if pain occurs between 30 degrees and 70 degrees of elevation because no true change in tension on the nerve roots is believed to occur outside of this range.
3,85
Variations on this test include the Lasègue sign or Bragard sign, which involves raising the leg to the point of symptom reproduction and then lowering the leg slightly and dorsiexing the foot passively; a positive test
results in reproduction of the patient’s radiating leg pain.
3,94
Other variants include internally rotating the leg to increase “dural tension,” raising the leg with knee exed and then slowly extending the knee to the point of reproduction of leg pain (also sometimes referred to as the Lasègue sign), and either relieving pain by exing the already extended knee at the point of symptom reproduction or eliciting pain by press­ing on the popliteal fossa of the elevated leg with the knee partially exed (both varyingly called the bow string sign).
3,85,92,94
Additional tests include the crossed straight-leg raise, in which symptoms are reproduced in the symptomatic leg by performing a supine straight-leg raise on the contralateral leg, and the femoral nerve stretch test or reverse straight-leg raise, in which the patient is prone and the knee is passively exed, with a positive test reproducing pain into the anterior thigh. A positive straight-leg raise test and its variations indicates tension on the lower lumbar roots and upper sacral root (L4, L5, and S1 nerve roots). A positive femoral nerve stretch test is the equivalent tension sign for the upper lumbar (L2–L4) nerve roots.
3,85,92
Numerous studies have looked at the sensitivity and specicity of some of these maneuvers. As might be surmised
by the varying descriptions and terminology, there are some
diculties with consistency in the literature. Overall, the ipsilateral straight-leg raise test has a good sensitivity of 72% to 97% but a poorer specicity of 11% to 66%.92 e
crossed straight-leg raise test is less sensitive (23–42%) but
SECTION
II
196 DIAGNOSIS
more specic (85–100%) than the ipsilateral straight-leg
85,92
raise.
Tests proposed for assessing the sacroiliac joint include the Gillet, Patrick, and Gaenslen tests. Although the sacroiliac joint can be a source of pain, the diagnosis of “sacroiliac joint dysfunction” is debated as a true pathologic entity. Dreyfuss and colleagues28 studied numerous supposedly diagnostic tests for this condition, including the Gillet, Patrick, and Gaenslen tests, and compared the responses on these test maneuvers with the results of uoroscopically guided sacro-
iliac joint blocks. ey found that no historical feature, none of the diagnostic tests performed, and no combination of these tests showed any signicant and reliable diagnostic value.
Nonorganic Signs
Chronic pain behavior is oen believed to display common physical examination ndings suggesting symptom magni­cation and psychological distress, possibly an expression of suering.
95,96
Waddell and colleagues95 dened and studied a group of ve ndings on physical examination, commonly known as Waddell signs. ese ndings consist of a supercial or nonanatomic distribution of tenderness; a nonanatomic motor or sensory impairment (regional disturbance); exces­sive verbalization of pain or gesturing (overreaction); produc­tion of pain complaints by tests that simulate only a specic movement, such as low back pain that occurs with axial loading on the crown of the head (simulation); and inconsis­tent reports of pain when the same movement is performed in dierent positions, such as a straight-leg raise in a seated versus supine position (distraction).
95
e presence of three or more of these signs indicates a nonorganic component to an individual’s pain complaints. e presence of Waddell signs does not mean, however, that there is no signicant organic pathology present or that the patient is malingering; objective clinical signs may be present as well. Although some studies have found these maneuvers to be reproducible, an evidence-based review by Fishbain and colleagues97 noted that these ndings do not correlate with psychological distress or secondary gain, and they do not discriminate nonorganic from organic problems. ey are associated with poorer treatment outcomes and higher pain levels. Although these maneuvers may be useful, the clinician should be wary of placing too much emphasis on any one part of the physical examination.
Additional Orthopaedic Assessment
Depending on the area of the spine involved, it is frequently important to cover additional areas of the orthopaedic examination. As was previously mentioned, examination of the shoulder complex is oen necessary in evaluating the cervical and thoracic spine. Following the concept of the kinetic chain, it is also oen helpful to assess multiple other joint structures and movement patterns from the feet up through the trunk to the neck, depending on the individual patient’s situation.98 For the lumbar spine, examination of the hip is also generally important, although examination of more
distal lower extremity structures and more cranial regions of the spine and upper extremities may be necessary as well. Because other conditions—such as carpal tunnel syndrome, ulnar neuropathy, brachial plexopathy, peroneal neuropathy, and femoral nerve injury (among others)—can masquerade as radiculopathies, examination for these entities is also oen
indicated. As noted previously, an appropriate history can help greatly in dening the scope of examination necessary
to evaluate a particular patient.
ere is a large body of literature on manual orthopae-
dic examination.
99,100
ese techniques generally are poorly validated and of uncertain correlation to some of the more “objective” ndings noted earlier. A systematic review of the literature on the reliability of palpatory examination maneu­vers found that most procedures have moderate or strong evi­dence for low reliability.
101
e authors noted that “a consistent nding from work in this eld is the generally low reliability of palpation-based assessment.”
101
ese techniques may be helpful in certain treatment paradigms, however, and they may be more useful when symptom response with repeated movements is considered.
101
Another systematic review assessed the literature on chiropractic tests of the lumbar spine and found insucient evidence on the reliability and validity
of these tests to support their clinical role.
102
Risk Stratication
Distinct from the idea of the evaluation of an individual patient is the concept of risk stratication within a population. Within
the clinical array of patients with spinal disorders, there are clearly those who will require more extensive care and/or be at risk for particularly poor outcomes. ere is increasing inter­est in applying screening mechanisms across a population to help identify those patients with a poor prognosis for recovery or in need of more intensive or multidisciplinary care. is type of assessment may be incorporated into a patient’s initial evaluation. An example of such a screening approach is the STarT Back tool. on prognostic factors for those with spinal pain, the STarT Back questionnaire consists of nine questions addressing the bothersomeness of pain, the presence of leg pain or concur­rent neck symptoms, and the presence of fear avoidance or other generally detrimental belief systems regarding pain. e intent is to separate patients with more limited symptom complexes and better coping skills who will likely do well with standard treatments from those who may require more advanced or complex interventions in order to improve outcomes. In the primary study of the STarT Back tool, the researchers developed and implemented a psychologically driven physical therapy program for the more at-risk popula­tion, nding improvements in outcomes for those treated based on risk stratication from those managed without any such tool. ey also found that primary care providers did a relatively poor job of appropriately identifying the physical therapy needs of patients without using the questionnaire. e broader applicability of this tool is currently under study, but this type of work highlights the potential benets of strati­fying patients for treatment. is may become an important
103
Consistent with the data noted earlier
104
103
Chapter 12 Patient History and Physical Examination: Cervical, Thoracic, and Lumbar 197
component of the medical history for patients with spinal disorders.

Summary

e history and physical examination of a spine patient is a complex undertaking. e nature of the patient’s presenting complaints and relevant aspects of the history have a strong bearing on the nature and extent of assessment required. Clinicians caring for patients with spine disorders need to be aware of all of the issues that may aect the presentation of a patient and how these issues can aect the delivery of care. As noted previously, it is of paramount importance to realize that the person presenting with the spine problem is the primary concern, and the spine problem is only secondary. Only by speaking with and directly examining a patient can clinicians truly understand the nature of the problem that they are being asked to address.

KEY POINTS

1. A thorough and appropriate history and physical examination are essential in the assessment of patients with spine disorders to identify the physical manifestations of a spine disorder and the root causes of the patient’s distress, suering, and disability.
2.
It is crucial to identify red ags and yellow ags in a patient’s
clinical presentation. Red ags are factors suggestive of the presence of an urgent or emergent medical issue (e.g., infection, tumor, fracture, cauda equina injury, progressive neurologic loss). Yellow ags are factors associated with poor outcomes and persisting pain and disability.
3.
The medical history can be used to narrow down the dierential
diagnosis and direct further diagnostic eorts through physical examination and other tools.
4.
The value of isolated ndings on physical examination is limited,
although physical examination ndings become much more signicant in the context of correlating history and imaging.
5.
Despite the importance of a thorough medical history, clinicians
need to realize that psychosocial factors are a more important predictor of outcome in patients with spinal pain than biomedical factors.

KEY REFERENCES

1. Bogduk N. The anatomy and pathophysiology of neck pain. Phys Med Rehabil Clin N Am. 2003;14:455-472. This is a concise overview of some important issues in assessing patients with neck pain.
2.
Henschke N, Maher CG, Ostelo RWJG, et al. Red ags to screen
for malignancy in patients with low-back pain. Cochrane
Database Syst Rev. 2013;(2):CD008686. An overview of the existing evidence on the use of red ags.
3.
Linton SJ. A review of psychosocial risk factors in back and neck
pain. Spine. 2000;25:1148-1156.
This is a useful and well-executed review of the role of psychosocial risk factors in the development of chronic spinal pain.
4.
http://www.healthmeasures.net/explore-measurement-systems/
promis.
This is the website for the Patient-Reported Outcomes Measurement Instrumentation System, a publically available set of outcome tools for a variety of health conditions, including pain, developed by the National Institutes of Health.
5. Solomon J, Nadler SF, Press J. Physical examination of the lumbar spine. In: Malanga G, Nadler SF, eds. Musculoskeletal Physical Examination: An Evidence-Based Approach. Philadelphia: Hanley & Belfus; 2006:189-226.
This is one of many useful chapters in a well-prepared text assessing the literature on musculoskeletal physical examination.
6.
Hill JC, Whitehurst DGT, Lewis M, et al. Comparison of Stratied
Primary Care Management for Low Back Pain with Current Best Practice (STarT Back): a randomised controlled trial. Lancet. 2011;378:1560-1571.
Article on the STarT Back screening tool to assist in the treatment stratication of patients with low back pain.

REFERENCES

1. Bogduk N. e anatomy and pathophysiology of neck pain. Phys Med Rehabil Clin N Am. 2003;14:455-472.
2. Bogduk N. Clinical Anatomy of the Lumbar Spine and Sacrum. 3rd ed. New York: Churchill-Livingstone; 1997.
3. Borenstein DG, Wiesel SW. Low Back Pain: Medical Diagnosis and Comprehensive Management. Philadelphia: WB Saunders;
1989.
4. Liss H, Liss D, Pavell J. History and past medical history. In: Cole AJ, Herring SA, eds. e Low Back Pain Handbook. 2nd ed. Philadelphia: Hanley & Belfus; 2003:49-67.
5. Weinstein SM, Herring SA, Standaert CJ. Low back pain. In: Delisa JA, Gans BM, Walsh NE, eds. Physical Medicine and Rehabilitation: Principles and Practice. 4th ed. Philadelphia: Lippincott-Williams & Wilkins; 2005:653-678.
6. Dwyer A, Aprill C, Bogduk N. Cervical zygapophyseal joint pain patterns I: a study in normal volunteers. Spine. 1990;15:453-457.
7. Aprill C, Dwyer A, Bogdul N. Cervical zygapophyseal joint pain patterns II: a clinical evaluation. Spine. 1990;15:458-461.
8. Lord SM, Barnsley L, Wallis BJ, et al. Chronic cervical zygapophyseal joint pain aer whiplash: a placebo-controlled
prevalence study. Spine. 1996;21:1737-1745.
9. Dreyfuss P, Tibiletti C, Dreyer S. oracic zygapophyseal
joint pain patterns: a study in normal volunteers. Spine. 1994;19:807-811.
10. Schwarzer AC, Aprill CN, Derby R, et al. Clinical features of patients with pain stemming from the lumbar zygapophysial joints: is the lumbar facet syndrome a clinical entity? Spine. 1994;19:1132-1137.
11. Marks R. Distribution of pain provoked from lumbar facet joints and related structures during diagnostic spinal
inltration. Pain. 1989;39:37-40.
12. Cloward RB. Cervical discography: a contribution to the etiology and mechanism of neck, shoulder and arm pain. Ann Surg. 1959;150:1052-1064.
13. Grubb SA, Kelly CK. Cervical discography: clinical implications from 12 years of experience. Spine. 2000;25:1382-1389.
14. Campbell JN. Nerve lesions and the generation of pain. Muscle Nerve. 2001;24:1261-1273.
15. Carragee EJ, Alamin TF. Discography: a review. Spine J. 2001;1:364-372.
16. Hogan Q. Back pain: beguiling physiology (and politics). Reg Anesth. 1997;22:395-399.
17. Sinclair JD. Chronic noncancer pain basics for the primary care physician. Primary Care Rep. 2002;8:63-73.
18. Sheather-Reid RB, Cohen ML. Psychophysiological evidence for a neuropathic component of chronic neck pain. Pain. 1998;75:341-347.
SECTION
II
198 DIAGNOSIS
19. Agency for Health Care Policy and Research. Acute Low Back Problems in Adults: Assessment and Treatment. Washington,
DC: US Department of Health and Human Services; 1994.
20. Akuthota V, Willick SE, Harden RN. e adult spine: a practical approach to low back pain. In: Rucker KS, Cole AJ, Weinstein SM, eds. Low Back Pain: A Symptom-Based Approach to Diagnosis and Treatment. Boston: Butterworth-Heinemann; 2001:15-41.
21. Carragee EJ, Hannibal M. Diagnostic evaluation of low back pain. Orthop Clin North Am. 2004;35:7-16.
22. Deyo RA, Rainville J, Kent DL. What can the history and physical examination tell us about low back pain? JAMA. 1992;268:760-765.
23. Henschke N, Maher CG, Ostelo RWJG, et al. Red ags
to screen for malignancy in patients with low-back pain. Cochrane Database Syst Rev. 2013;(2):CD008686.
24. Downie A, Williams CM, Henschke N, et al. Red ags to screen for malignancy and fracture in patients with low back pain: systematic review. BMJ. 2013;347:f7095.
25. Enthoven WTM, Geuze J, Scheele J, et al. Prevalence and “red ags” regarding specied causes of back pain in older adults
presenting in general practice. Phys er. 2016;96:305-312.
26. Bland JH. Disorders of the Cervical Spine: Diagnosis and Medical Management. 2nd ed. Philadelphia: WB Saunders;
1994.
27. Mazanec D. Pseudospine pain: conditions that mimic spine pain. In: Cole AJ, Herring SA, eds. e Low Back Pain Handbook. 2nd ed. Philadelphia: Hanley & Belfus; 2003:117-131.
28. Dreyfuss P, Michaelsen M, Pauza K, et al. e value of medical history and physical examination in diagnosing sacroiliac joint pain. Spine. 1996;21:2594-2602.
29. Konstantinou K, Hider SL, Jordan JL, et al. e impact of low back-related leg pain on outcomes as compared with low back pain alone. A systematic review of the literature. Clin J Pain. 2013;29:644-654.
30. Micheli LJ, Wood R. Back pain in young athletes: signicant dierences from adults in causes and patterns. Arch Pediatr Adolesc Med. 1995;149:15-18.
31. Roche MA, Rowe GG. e incidence of separate neural arch and coincident bone variations: a survey of 4,200 skeletons. Anat Rec. 1951;109:233-252.
32. Standaert CJ, Herring SA. Spondylolysis: a critical review. Br J Sports Med. 2000;34:415-422.
33. Burton AK, Clarke RD, McClune TD, et al. e natural history of low back pain in adolescents. Spine. 1996;21:2323-2328.
34. Kovacs FM, Gestoso M, Gil del Real MT, et al. Risk factors for non-specic low back pain in schoolchildren and their parents: a population based study. Pain. 2003;103:259-268.
35. Andersen SJ. Adolescent lumbar spine disorders. In: Rucker KS, Cole AJ, Weinstein SM, eds. Low Back Pain: A Symptom-based Approach to Diagnosis and Treatment. Boston: Butterworth-Heinemann; 2001:3-14.
36. Hosalkar H, Dormans J. Back pain in children requires extensive workup. Biomechanics. 2003;10:51-58.
37. Malanga GA, Nadler SF, Ageson T. Epidemiology. In: Cole AJ, Herring SA, eds. e Low Back Pain Handbook. 2nd ed. Philadelphia: Hanley & Belfus; 2003:1-7.
38. Borenstein DG, Wiesel SW, Boden SD. Neck Pain: Medical Diagnosis and Comprehensive Management. Philadelphia: WB Saunders; 1996.
39. Bovim G, Schrader H, Sand T. Neck pain in the general population. Spine. 1994;19:1307-1309.
40. Makela M, Heliovaara M, Sievers K, et al. Prevalence, determinants, and consequences of chronic neck pain in Finland. Am J Epidemiol. 1991;134:1356-1367.
41. Volinn E. e epidemiology of low back pain in the rest of the world: a review of surveys in low- and middle-income countries. Spine. 1997;22:1747-1754.
42. Belanger TA, Rowe DE. Diuse idiopathic skeletal
hyperostosis: musculoskeletal manifestations. J Am Acad Orthop Surg. 2001;9:258-267.
43. Paassilta P, Lohiniva J, Goring HH, et al. Identication of a novel common genetic risk factor for lumbar disk disease. JAMA. 2001;285:1843-1849.
44. Canoso JJ. Rheumatology in Primary Care. Philadelphia: WB Saunders; 1997.
45. Gaunt AM. Caring for patients who have acute and subacute low back pain. CME Bull. 2008;7:1-7.
46. Linton SJ. A review of psychosocial risk factors in back and neck pain. Spine. 2000;25:1148-1156.
47. Valat JP, Goupille P, Vedere V. Low back pain: risk factors for chronicity. Rev Rheum [Engl Ed]. 1997;64:189-194.
48. van der Giezen AM, Bouter LM, Nijhuis FJN. Prediction of return-to-work of low back pain patients sicklisted 3-4 months. Pain. 2000;87:285-294.
49. Fransen M, Woodward M, Norton R, et al. Risk factors associated with the transition from acute to chronic occupational back pain. Spine. 2002;27:92-98.
50. Radanov BP, Sturzenegger M. e eect of accident mechanisms and initial ndings on the long-term outcome of whiplash injury. J Musculoskelet Pain. 1996;4:47-59.
51. McIntosh G, Frank J, Hogg-Johnson S, et al. Prognostic factors for time receiving workers’ compensation benets in a cohort of patients with low back pain. Spine. 2000;25:147-157.
52. Walton DM, Macdermid JC, Giorgianni AA, et al. Risk factors for persistent problems following acute whiplash injury: update of a systematic review and meta-analysis. J Orthop Sports Phys er. 2013;43:31-43.
53. Krause N, Ragland DR, Greiner BA, et al. Physical workload and ergonomic factors associated with prevalence of back and neck pain in urban transit operators. Spine. 1997;22:2117-2126.
54. McGill CM. Industrial back problems: a control program. J Occup Med. 1968;10:174-178.
55. Waddell G. Epidemiology: a new clinical model for the treatment of low back pain. In: Weinstein JN, Wiesel SW, eds.
e Lumbar Spine: e International Society for the Study of the Lumbar Spine. Philadelphia: Saunders; 1990:38-56.
56. Pincus T, Burton AK, Vogel S, et al. A systematic review of psychosocial factors as predictors of chronicity/ disability in prospective cohorts of low back pain. Spine. 2002;27:E109-E120.
57. Gatchel RJ, Polatin PB, Mayer TG. e dominant role of psychosocial risk factors in the development of chronic low back pain disability. Spine. 1995;20:2702-2709.
58. Wallis BJ, Lord SM, Bogduk N. Resolution of psychological distress of whiplash patients following treatment by radiofrequency neurotomy: a randomized, double-blind, placebo-controlled trial. Pain. 1997;73:15-22.
59. Carroll LJ, Cassidy JD, Cote P. Depression as a risk factor for onset of an episode of troublesome neck and low back pain. Pain. 2004;107:134-139.
Chapter 12 Patient History and Physical Examination: Cervical, Thoracic, and Lumbar 199
60. Chaichana KL, Mukherjee D, Adogwa O, et al. Correlation of preoperative depression and somatic perception scales with postoperative disability and quality of life aer lumbar discectomy. J Neurosurg Spine. 2011;14:261-267.
61. Daubs MD, Norvell DC, McGuire R, et al. Fusion versus nonoperative care for chronic low back pain. Do psychological factors aect outcomes? Spine. 2011;36:S96-S109.
62. DeBerard MS, Masters KS, Colledge AL, et al. Outcomes of posterolateral lumbar fusion in Utah patients receiving workers’ compensation: a retrospective cohort study. Spine. 2001;26:738-747.
63. Junge A, Dvorak J, Ahrens S. Predictors of bad and good outcomes of lumbar disc surgery: a prospective clinical study with recommendations for screening to avoid bad outcomes. Spine. 1995;20:460-468.
64. Loupasis GA, Stamos K, Katonis PG, et al. Seven to 20-year outcome of lumbar discectomy. Spine. 1999;24:2313-2317.
65. Pappas CTE, Harrington T, Sonntag VK. Outcome analysis in 654 surgically treated lumbar disc herniations. Neurosurgery. 1992;30:862-866.
66. Keller RB, Atlas SJ, Soule DN, et al. Relationship between rates and outcomes of operative treatment for lumbar disc herniation and spinal stenosis. J Bone Joint Surg Am. 1999;81:752-762.
67. Fishbain DA, Goldberg M, Meagher BR, et al. Male and female chronic pain patients categorized by DSM-III psychiatric diagnostic criteria. Pain. 1986;26:181-197.
68. Ormel J, VonKor M, Ustun TB, et al. Common mental disorders and disability across cultures: results from the WHO Collaborative Study on Psychological Problems in General Health Care. JAMA. 1994;272:1741-1748.
69. Hagg O, Fritzell P, Hedlund R, et al. Pain-drawing does not predict the outcome of fusion surgery for chronic low-back pain: a report from the Swedish Lumbar Spine Study. Eur Spine J. 2003;12:2-11.
70. Ohnmeiss DD. Repeatability of pain drawings in a low back pain population. Spine. 2000;25:980-988.
71. Dahl B, Gehrchen PM, Kiaer T, et al. Nonorganic pain drawings are associated with low psychological scores on the preoperative SF-36 questionnaire in patients with chronic low back pain. Eur Spine J. 2001;10:211-214.
72. Carnes D, Ashbey D, Underwood M. A systematic review of pain drawing literature: should pain drawings be used for psychologic screening? Clin J Pain. 2006;22:449-457.
73. Gatchel RJ, ed. Compendium of Outcome Instruments for Assessment and Research of Spinal Disorders. La Grange, IL: North American Spine Society; 2001.
74. Patrick DL, Deyo RA, Atlas SJ, et al. Assessing health-related quality of life in patients with sciatica. Spine. 1995;20:1899-1908.
75. Fairbank JCT, Couper J, Davies JB, et al. e Oswestry low back pain disability questionnaire. Physiotherapy. 1980;66:271-273.
76. Millard RW. A critical review of questionnaires for assessing pain-related disability. J Occup Rehabil. 1991;1:289-302.
77. Vernon H, Mior S. e neck disability index: a study of reliability and validity. J Manipulative Physiol er. 1991;14:409-415.
78. Waddell G, Newton M, Henderson I, et al. A fear-avoidance beliefs questionnaire (FABQ) and the role of fear-avoidance beliefs in chronic back pain and disability. Pain. 1993;52:157-168.
79. Sullivan MJL, Bishop SR, Pivik J. e pain catastrophizing scale: development and validation. Psychol Assess. 1995;7:524-532.
80. Webster LR, Webster RM. Predicting aberrant behaviours in opioid treated patients: preliminary validation of the opioid risk tool. Pain Med. 2005;6:432-442.
81. Health Measures. PROMIS: Patient-Reported Outcomes Measurement Information System. Available at: http://
www.healthmeasures.net/explore-measurement-systems/ promis.
82. McGregor AH, McCarthy ID, Hughes SP. Motion characteristics of the lumbar spine in the normal population. Spine. 1995;20:2421-2428.
83. Nattrass CL, Nitschke JE, Disler PB, et al. Lumbar spine range of motion as a measure of physical and functional impairment: an investigation of validity. Clin Rehabil. 1999;13:211-218.
84. Ng JKF, Kippers V, Richardson CA, et al. Range of motion and lordosis of the lumbar spine: reliability and measurement of normative values. Spine. 2001;26:53-60.
85. Solomon J, Nadler SF, Press J. Physical examination of the lumbar spine. In: Malanga G, Nadler SF, eds. Musculoskeletal Physical Examination: An Evidence-based Approach. Philadelphia: Hanley & Belfus; 2006:189-226.
86. Burkhart SS, Morgan CD, Kibler WB. e disabled throwing shoulder: spectrum of pathology, part III: the SICK scapula, scapular dyskinesis, the kinetic chain, and rehabilitation. Arthroscopy. 2003;19:641-661.
87. Bates B. A Guide to Physical Examination and History Taking. 5th ed. Philadelphia: JB Lippincott; 1991.
88. Merz O, Wolf U, Robert M, et al. Validity of palpation techniques for the identication of the spinous process L5.
Man er. 2013;18:333-338.
89. Tanaka K, Irikoma S, Kokubo S. Identication of the lumbar interspinous spaces by palpation and veried by x-rays. Rev Bras Anestesiol. 2013;63:245-248.
90. American Spinal Injury Association. International Standards for Neurological Classication of Spinal Cord Injury [reprint]. Chicago: American Spinal Injury Association; 2008.
91. Rhee JM, Hein JA, Hamasaki T, et al. Prevalence of physical
signs in cervical myelopathy: a prospective, controlled study. Spine. 2009;34:890-895.
92. Andersson GBJ, Deyo RA. History and physical examination in patients with herniated lumbar discs. Spine. 1996;21:10S-18S.
93. Tong HC, Haig AJ, Yamakawa K. e Spurling test and
cervical radiculopathy. Spine. 2002;27:156-159.
94. Supik LF, Broom MJ. Sciatic tension signs and lumbar disc herniation. Spine. 1994;19:1066-1069.
95. Waddell G, McCulloch JA, Kummel E, et al. Nonorganic physical signs in low-back pain. Spine. 1980;5:117-125.
96. Maruta T, Goldman S, Chan CW, et al. Waddell’s nonorganic signs and Minnesota Multiphasic Personality Inventory proles in patients with chronic low back pain. Spine.
1997;22:72-75.
97. Fishbain DA, Cole B, Cutler RB, et al. A structured evidence-based review on the meaning of nonorganic physical signs: Waddell signs. Pain Med. 2003;4:141-181.
98. Kibler WB. Determining the extent of the functional decit. In: Kibler WB, Herring SA, Press JM, et al., eds. Functional Rehabilitation of Sports and Musculoskeletal Injuries. Gaithersburg, MD: Aspen; 1998:1-8.
SECTION
II
200 DIAGNOSIS
99. Basmajian JV, Nyberg R, eds. Rational Manual erapies. Baltimore: Williams & Wilkins; 1993.
100. Brieve GP. Mobilization of the Spine. 4th ed. New York: Churchill-Livingstone; 1984.
101. May S, Littlewood C, Bishop A. Reliability of procedures used in the physical examination of non-specic low back pain: a systematic review. Aust J Physiother. 2006;52:91-102.
102. Hestbaek L, Leboeuf-Yde C. Are chiropractic tests for the lumbo-pelvic spine reliable and valid? A systematic critical literature review. J Manipulative Physiol er. 2000;23:258-275.
103. Hill JC, Whitehurst DGT, Lewis M, et al. Comparison of Stratied Primary Care Management for Low Back Pain with
Current Best Practice (STarT Back): a randomised controlled trial. Lancet. 2011;378:1560-1571.
104. Maina CJ, Sowdena G, Hill JC, et al. Integrating physical and psychological approaches to treatment in low back pain: the development and content of the STarT Back trial’s high-risk’ intervention. Physiotherapy. 2012;98:110-116.
SECTION
13
CHAPTER
Multiple imaging methods with tremendous technologic complexity and sophistication can be used to evaluate spinal pathology. Magnetic resonance imaging (MRI) quickly emerged as the study of choice for many disorders of the spine, with computed tomography (CT) continuing to play a key role, bolstered by newer innovations such as helical scanning and multidetector arrays allowing isotropic voxels and multiplanar reformatting without loss of resolution. is
chapter reviews the basic imaging approaches to the spine and their usefulness, both in specic disease states, and in
the context of the anatomic categories of spine pathology (extradural, intradural extramedullary, and intramedullary).

Modalities

Radiographs
Routine plain lms are universally available and inexpensive, but are limited by an inability to directly visualize neural structures and nerve root or cord compression. Ionizing radia­tion is used to obtain the radiographic image, which despite the relatively fast time of acquisition, can still be susceptible to motion.1 Radiographs can be used for evaluation of alignment, status of hardware in the postoperative patient, intraoperative localization, and motion with exion-extension views.
Radiographs can visualize osseous structures and sur-
rounding so tissues (i.e., extradural pathology). A routine
examination of the spine includes frontal or anteroposterior and lateral views, with additional views such as oblique or
exion-extension also available.
Orthogonal conventional radiography is the rst line of evaluation in an instrumented postoperative patient, and plain radiographs are usually obtained at 6 weeks and 3, 6, and 12 months postoperatively.3 Regardless of which fusion approach is taken, the presence or absence of demonstrable motion or evidence of hardware failure or loosening is a key factor in the evaluation. In the case of posterolateral fusion, arthrodesis is deemed successful if follow-up radio­graphs show continuity in the fusion mass between the cephalad and the caudal transverse processes. Instrumented
2

Spine Imaging

Todd M. Emch
Jerey S. Ross
Gordon R. Bell
interbody fusion is considered fused if any of the following is present:
1. Increased or maintained bony density within the cage implant because of the presence of mature bony trabeculae bridging the interbody space
2. Absence of a halo or a periprosthetic lucency around the implant
3. A sclerotic line between the cage and the vertebral bone because of bone remodeling and new bone formation
4. Resorption of anterior vertebral traction spurs or the pres­ence of bone gra anterior to an intervertebral implant
(sentinel sign)
5. Lack of motion on exion-extension views
Pseudarthrosis or failure of fusion is indicated by progres-
sive loss of disc height, vertebral displacement, broken or loose hardware, and loss of position of the implant or resorption of the bone gra. Flexion and extension views are useful for
assessing stability or functional fusion, but the central x-ray beam should pass through the same area in both views.
Myelography
Myelography involves instillation of the contrast agent through either lumbar puncture (midline or oblique approaches) or lateral C1–C2 puncture with subsequent radiographic and CT imaging of the region of interest. e diagnosis of extradural
neural compression by myelography is inferred indirectly by changes in the contour of normal contrast agent–lled thecal sac
and root sleeves rather than by direct visualization of the lesion.5 Expansion of the spinal cord (Fig. 13.1) can be visualized as well as intradural extramedullary lesions; however nonexpansile cord pathology cannot be detected with myelography.
e major disadvantage of myelography is its invasive
nature and lack of diagnostic specicity.7 e use of less toxic second-generation, water-soluble nonionic agents has obviated the need for overnight hospitalization aer the
procedure. Routine postprocedural monitoring of 2 to 4 hours is usually sucient. Multiple water-soluble agents are
available that provide excellent contrast and lower rates of side
eects, such as iohexol (Omnipaque) and iopamidol (Isovue).
4
6
II
201
202 DIAGNOSIS
BC
A
FIG. 13.1 Computed tomographic myelogram demonstrating an intramedullary mass lesion. (A) Axial image
demonstrates normal diameter of the thoracic spinal cord. (B) Axial and (C) sagittal images demonstrate fusiform expansion of the mid-thoracic spinal cord in this patient with an ependymoma.
Current water-soluble agents are associated with less toxicity, and their absorption through the theca and arachnoid villi makes their removal unnecessary.8 Newer nonionic water­soluble agents generally produce mild side eects, although
signicant adverse reactions can still rarely occur, such as hallucinations, confusion, or seizures. Considerations before myelography include obtaining screening laboratory tests such as platelets, prothrombin time/international normalized ratio, and partial thromboplastin time; medication history of the patients, especially metformin; psychiatric medications, which can lower seizure threshold; and anticoagulants.
9,10
Computed Tomography
CT permits direct visualization of potential neural compress­ing structures and provides better visualization of lateral pathology, such as foraminal stenosis. from a surgical perspective is the ability of CT to distinguish neural compression due to so tissue from compression from bone pathology.
12,14-16
Disadvantages of CT include radiation exposure, the eects of partial volume averaging, streak artifacts in the cervical spine caused by the dense bone of the shoulder girdle, and changes in conguration of the spine that occur between
11-13
An important benet
successive motion segments.17 Many of the limitations can be obviated by obtaining multiple thin sections (1.5 to 3 mm) with the gantry tilted to permit imaging parallel to the plane of the disc. Further accuracy is obtained by routinely imaging the spine by CT aer the introduction of water-soluble con­trast agents (intrathecal contrast medium–enhanced CT).
Reported accuracy rates for CT range from 72% to 91%.
7,12,14,15
Agreement rates between contrast medium–enhanced CT and myelography have been reported to range from 75% to 96%.
12,14
When a discrepancy exists between myelographic and CT nd­ings, postcontrast CT is invariably the more accurate study (Fig.
13.2). Current multirow detector technology is now available
that allows for extremely rapid thin-slice acquisitions over long body segments. With this technology, contiguous 3-mm slices can be obtained from L1 to S1 in less than 30 seconds. e acquisition of isotropic voxels allows for multiplanar reformation of the CT data with no loss in spatial resolution. Changes in the windowing and leveling of the images can change the focus onto either osseous structures or so tissues.
1
Magnetic Resonance Imaging
MRI can readily evaluate the extradural, intradural extramed­ullary, and intramedullary spaces and is also the only modality