ASSESSING MUSCULOSKELETAL DISORDERS

Published on 16/03/2015 by admin

Filed under Orthopaedics

Last modified 22/04/2025

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 0 (0 votes)

This article have been viewed 2537 times

CHAPTER ONE ASSESSING MUSCULOSKELETAL DISORDERS

INTRODUCTION

The evaluation for treatment consultation between a physician and a patient is at the center of all orthopedic practice activities.

From the moment of the first encounter with a patient, the physician is simultaneously observing and examining the movements and mannerisms of the patient, as well as listening to what is being said. The physician is trying to piece together the nature of the patient’s orthopedic problem.

The purpose of orthopedic evaluation is twofold. First, it allows the patient to present the problem, and second, it enables the physician to triage the nature of the problem and develop a course of action. In this context, the physician must always learn what has brought the patient to the consultation. In some cases a patient visits the orthopedic specialist because of referral by or on the advice of a third party. The diagnostic process is also complex, given that the physician needs to establish the physical issues that are of greatest importance to the patient and that are most disrupting to the activities of daily living, as well as try to differentiate the anatomic and pathologic aspects of any disease that might be present.

The history provides much information about the pathologic process involved and the impact of the condition on the patient, whereas the orthopedic physical examination is essential to define the anatomic structures involved; together these processes allow differentiation of orthopedic disorders into various categories.

Health care providers assess patients every day in clinical practice. Commonly, clinical practice is impossible without structured assessments and tests. Examination procedures look straightforward; results are either positive or negative. However, all assessment and testing in clinical practice is based on the assumption of uncertainty: Does the patient have a disease? The probability of a particular disease can be established only by performing a test from a chain of tests.

The accuracy of a test for detecting a disease or a condition is determined by sensitivity and specificity. A high sensitivity (or a high specificity) does not suffice to make a test useful in clinical practice; a test should be as sensitive as possible. The sensitivity and specificity of examination procedures and tests can often be found in the literature. Sensitivity and specificity are important characteristics of evidence-based physical assessment procedures but only in the context of a specific disease or condition.

The probability of a disease or condition after having performed a test (Bayes theorem) is dependent on two factors: (1) the specificity and sensitivity of the procedure (test characteristics) and (2) the probability of the disease or condition before conducting the procedure. Interpretation of Bayes theorem is that the probability of having a disease is not only dependent on the test or examination procedure result and the characteristics of the procedure, but also dependent on how likely the existence of the disease before the procedure is actually conducted. This factor is dependent on the prevalence of the disease.

The decision of whether to perform a new test depends on the result of the previous test. Procedures with the lowest burden, risk, and costs for the patient are performed first, and those with the highest burden, risk, or costs are reserved for certain patients in which the prior probability is highest. Examination procedures in the context of a low prior probability of disease are rarely, if ever, informative, with the yield of diagnostic testing that will increase the prior probability approximating 50%. Very experienced clinicians intuitively apply these rules and arrange their diagnostic process in such a way that the highest possible yield (a highly probable diagnosis) will be obtained at the lowest possible burden, risk, and cost for the patient. Less-experienced clinicians may learn from experienced colleagues by recalling Bayes theorem and implementing its principles in everyday clinical practice.

Health care providers cannot function adequately without physical examination procedures. In the real world, examiners accomplish clinical practice appropriately without a detailed knowledge of the principles of tests. However, the benefits from physical testing can be easily increased by recognizing that these tests do nothing more than increase the probability of a certain condition or diagnosis. Test results are never infallible.

From the moment of the first encounter with a patient, the examiner is simultaneously observing and examining the movements and mannerisms of the patient, as well as listening to what is being said. The diagnostic process is complex; the examiner needs to establish the physical issues that are of greatest importance to the patient (those most disrupting to the activities of daily living) and try to differentiate the anatomic and pathologic aspects of any disease or injury that might be present.

The history provides much information about what difficulties the patient is experiencing and the impact of these on the patient. Orthopedic examination is essential to define the structures involved; together, these processes allow differentiation of orthopedic disorders into various diagnostic categories (Box 1-1).

OBSERVATION AND INSPECTION

A useful approach in clinical examination of the neuromusculoskeletal system is to seek answers to the Critical 5 questions for an orthopedic specialist. Once all five questions are answered, a differential diagnosis can usually be established (Box 1-2).

The physician needs to learn what exacerbates or relieves the symptom pattern. Equally important is how long the complaints have existed (Table 1-1).

NEUROLOGIC EVALUATION

The neurologic evaluation involves locating the lesion; testing deep tendon, superficial, and pathologic reflexes; testing cranial nerve and brainstem function; measuring body parts (mensuration); grading muscular strength; and testing the gross sensory modalities.

STABILITY TESTING

Because clinical examination reveals the degree of ligamentous or joint sprain (Table 1-2), the examiner must be able to test accurately for joint instability. Stability testing moves joint and periarticular structures through their respective arcs and end-range motions. Stability testing involves stressing ligamentous tissues and joint capsules.

CLINICAL LABORATORY

For the examiner concerned with musculoskeletal disorders, differential diagnosis becomes a challenge. Complete blood and urine tests can help determine a diagnosis (Box 1-3). Diseases of the heart, liver, kidney, pancreas, and prostate can mimic back pain of spinal origin.

BOX 1-3 CLINICAL LABORATORY TESTS

Most laboratory testing has limited utility for orthopedic diagnosis (Table 1-3). As an example, in rheumatoid arthritis, the diagnosis is often established from the history and physical examination; for systemic lupus erythematosus, from the laboratory test antinuclear antibody (ANA); for gout, from a synovial fluid examination; and for ankylosing spondylitis, from a radiograph. In common disorders such as osteoarthritis, fibromyalgia, or muscular strains and sprains, in essence, only a limited diagnostic role exists for laboratory tests, primarily to exclude other diagnostic possibilities.

TABLE 1-3 LABORATORY STUDIES USEFUL IN DIAGNOSING LOW BACK SYNDROMES

Test Measurement Low Back Implication

Alkaline phosphatase Enzyme associated with bone formation; therefore, elevation implies increased bone formation May be elevated in primary or secondary osseous neoplasms. Acid phosphatase An enzyme associated with tumors metastatic to bone Increased in prostatic tumors.

HLA, Human leukocyte antigen.

Adapted from Pope ML: Occupational low back pain, assessment, treatment and prevention, St Louis, 1991, Mosby.

The simplest orthopedic screen includes rheumatoid factor, ANA, and uric acid, although more elaborate screens are available, which may include erythrocyte sedimentation rate, C-reactive protein (CRP), antistreptolysin O titer, protein electrophoresis, quantitative immunoglobulins, and ANA subsets such as anti-Ro and anti-La, anti-Sm, and anticentromere antibodies.

Synovial Fluid Testing

Normal synovial fluid is a hypocellular, avascular connective tissue. In disease, the synovial fluid increases in volume and can be aspirated. Synovial fluid is a transudate of plasma supplemented with high–molecular-weight, saccharide-rich molecules. The most notable of these is hyaluronan, which is produced by fibroblast-derived type B synoviocyte (Box 1-4). Variation in the volume and composition of synovial fluid reflects pathologic processes within the joint.

BOX 1-4 NORMAL SYNOVIAL FLUID

Adapted from Klippel JH, Dieppe PA: Rheumatology, vol 1-2, ed 2, London, 1998, Mosby

Osmolarity 296 mOsm/L
pH 7.44
Carbon dioxide pressure 6.0 kPa (range 4.7–7.3)
Oxygen pressure <4.0 kPa
Potassium 4.0 mmol/L
Sodium 136 mmol/L
Calcium 1.8 mmol/L
Urea 2.5 mmol/L
Uric acid 0.23 mmol/L
Glucose 100 mmol/L
Chondroitin sulfate 40 mg/L
Hyaluronate 2.14 g/L
Cholesterol Small amounts
Total protein ∼25 g/L
Albumin ∼8 g/L
α1-antitrypsin 0.78 mcg/L
Ceruloplasmin ∼43 mg/L
Haptoglobin ∼90 mg/L
α2-macroglobin 0.31 g/L
Lactoferrin 0.44 mg/L
IgG 2.62 g/L
IgA 0.85 g/L
IgM 0.14 g/L
IL-1β 20 pg/mL
IL-2 15.1 U/mL
TNF-α 1.38 hg/mL
INF-α 350 U/mL
INF-δ 13.7 U/mL

IgA, Immunoglobulin A; IgG, immunoglobulin G; IgM, immunoglobulin M; IL, interleukin; INF, interferon; TNF, tumor-necrosis factor.

DIAGNOSTIC IMAGING MODALITIES IN ORTHOPEDICS

Imaging procedures are important to the diagnosis and management of an orthopedic condition. The decision to use any diagnostic imaging procedure, especially ionizing imaging procedures, should be based on a demonstrated need and should be used only after an adequate medical history is obtained and a physical examination is conducted. The decision to use any imaging procedure must also be based on the assumption that the results of the examination, even if negative, will significantly affect the treatment of the patient. The value of the information gained from the imaging examination must be worth the possible detrimental effects of the procedure. In imaging modalities that use ionizing radiation (plain-film radiography, fluoroscopy, and computed tomography [CT]), the possible effect of radiation on the patient or future offspring must be considered.

Cervical spine Thoracic spine Lumbar spine Sacrum Chest Ribs Shoulder Humerus Clavicle Anteroposterior or posteroanterior (to include both joints with and without weight bearing) Sternum, sternoclavicular joints Radioulnar joints (forearm) Wrist and hand Pelvis, acetabulum Hip, proximal part of femur Femur Distal part of femur and knee Tibia, fibula Ankle Calcaneus Foot

From Gustilo RB, Kyle RF, Templeman DC: Fractures and dislocations, vol 1, St Louis, 1993, Mosby.

Care must be taken to investigate the possibility of associated injuries in trauma victims (Table 1-6). Patients may not realize that such injuries have occurred.

TABLE 1-6 INJURIES ASSOCIATED WITH SKELETAL TRAUMA

Fracture Associated Injury
Bone and Bone
Spine Remote additional spinal fracture
Chest wall Scapula fracture
Anterior pelvic arch Sacrum fracture or dislocated sacroiliac joint
Femoral shaft Fracture or fracture-dislocation of hip
Tibia (severe) Dislocated hip
Calcaneus Fractured thoracolumbar spine
Bone and Viscera
Chance fracture of spine Ruptured mesentery or small bowel
Lower ribs Laceration of liver, spleen, kidney, or diaphragm
Pelvis  
Pelvis Ruptured bladder or urethra
  Ruptured diaphragm
Bone and Vascular
Ribs 1, 2, or 3 Ruptured aorta
Sternum Myocardial contusion
Pelvis Laceration of pelvic arterial tree
Distal third femur Laceration of femoral artery
Knee dislocation Popliteal artery laceration

Adapted from Rogers LF, Hendrix RW: Evaluating the multiple injured patient radiographically, Orthop Clin North Am 21(3):444, 1990.

ORTHOPEDIC GAMUT 1-23 ARTHRITIDES: DIAGNOSIS AND CLINICAL PROGRESSION ASSESSMENT STEPS IN RHEUMATOID ARTHRITIS, PSORIATIC ARTHRITIS, ANKYLOSIS SPONDYLITIS, AND OSTEOARTHRITIS

Adapted from Ory PA: Radiography in the assessment of musculoskeletal conditions, Best Pract Res Clin Rheumatol 17(3):495-512, 2003.

Rheumatoid arthritis

Psoriatic arthritis

Ankylosing spondylitis

Osteoarthritis

Magnetic Resonance Imaging

MRI is a computerized, thin-section imaging procedure that uses a magnetic field and radio-frequency waves rather than ionizing radiation. MRI can produce thin-section images in the sagittal, coronal, or axial planes, as well as any other oblique plane desired. The MRI can image neurologic structures and other soft tissues and can reveal disc degeneration before any other imaging method. Indications for MRI are similar to those for CT. MRI is superior to CT for evaluating possible spinal cord tumors or damage, intracranial disease, and various types of central nervous system disease (e.g., multiple sclerosis). MRI is especially useful in identifying small differences among similar soft tissues and surpasses CT in this regard.

For patients who have sustained head trauma with skull fractures, MRI is an efficient way to identify the early signs of cerebral edema. The test procedure of choice for diagnosing metastatic disease is an MRI scan (Table 1-7).

TABLE 1-7 MAGNETIC RESONANCE IMAGING VERSUS COMPUTED TOMOGRAPHY

Anatomic Area Indications Recommended Procedure
Brain (including brainstem)

Ear, nose, throat, and eye Musculoskeletal spine Hips Extremities Chest Abdomen and pelvis

CT, Computed tomography; MRI, magnetic resonance imaging; US, ultrasonography.

* Consult radiologist for imaging options.

From Brier SR: Primary care orthopedics, St Louis, 1999, Mosby; originally courtesy of Robert Goodman, MD, South Suffolk MRI, PC, Bayshore, New York.

Contrast Arthrography

The conventional use of arthrography in musculoskeletal disease involves the use of air to distend a synovial joint and a radiopaque contrast agent to outline anatomic structures. The injection of contrast material into the joint space results in a radiographic outline of the cartilage, menisci, ligaments, or synovium. Conventional arthrography is used in diagnosis of the scope and magnitude of orthopedic trauma to the shoulder, wrist, knee, and ankle (Table 1-8).

TABLE 1-8 JOINTS TYPICALLY STUDIED WITH COMPUTED TOMOGRAPHIC ARTHROGRAPHY AFTER TRAUMA

Joint To Observe
Knee Meniscus, cruciate and collateral ligaments, hyaline cartilage tears, osteochondral defects
Shoulder Rotator cuff, glenoid labrum disruption
Hip Hyaline cartilage integrity and tears, prosthetic joint loosening
Wrist Triangular fibrocartilage, intercarpal ligament integrity
Elbow Hyaline cartilage integrity, osteochondral defects
Ankle Ligamentous tears, osteochondral defects
Temporomandibular Disc and condylar integrity

Adapted from Gustilo RB, Kyle RF, Templeman DC: Fractures and dislocations, vol 1, St Louis, 1993, Mosby.

Electrodiagnostic Testing

Although electrodiagnostic testing provides valuable information, it does not stand alone as a diagnostic entity (Table 1-9). The data obtained must be correlated with the physical examination findings and case history.

TABLE 1-9 STRENGTHS AND LIMITATIONS OF ELECTRODIAGNOSTIC TESTING

Testing Modality Strengths Limitations
Nerve conduction velocity Helpful in ruling out peripheral entrapment neuropathic conditions (e.g., prolonged latencies exhibited in carpal tunnel syndrome, tarsal tunnel syndrome) and ulnar neuropathic variations Provides imperfect sensitivity; limited localization and determination of injury severity; timing of study an important factor
F waves Provides screening for late motor response with distal sweeps starting at the foot Evaluates motor reflex only; possibly evaluates abnormal findings only in the presence of multiple-level injury
H reflex Equivalent of ankle joint reflex; evaluates monosynaptic reflex with sensory and motor S1 function Provides assessment of S1 nerve root only
SSEPs Helpful in documenting sensory pathway disturbances in proximal neural injury and central conduction delays, as in myopathies and multiple sclerosis Offers imperfect localization; findings are rarely abnormal if results of other electrodiagnostic tests are within normal limits
Needle EMG Useful in assessing conductivity of neural tissues; helpful in determining site and severity of lesion; may be helpful in early assessment of recovery, screening for fibrillation potentials, and signs of denervation from nerve root compression disorders Unable to detect denervation potentials for 14 to 28 days after injury; provides imperfect sensitivity; study timing an important factor; proximal lesions sometimes inaccessible anatomically; effectiveness reduced after surgery

EMG, Electromyography; SSEPs, somatosensory-evoked potentials. Adapted from Brier SR: Primary care orthopedics, St Louis, 1999, Mosby.