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Home » Fibromyalgia

Consultant. Vol. 43 No. 10
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Fibromyalgia: Making a Firm Diagnosis, Understanding Its Pathophysiology

By SULE ARSLAN, MD
Gaziosmanpasa University
MUHAMMAD B. YUNUS, MD
University of Illinois | September 1, 2003

Dr Arslan is assistant professor of physical medicine and rehabilitation at Gaziosmanpasa University Medical School in Tokat, Turkey. Dr Yunus is professor of medicine in the section of rheumatology at the University of Illinois College of Medicine at Peoria.

ABSTRACT: Fibromyalgia syndrome (FMS) is a common condition that causes chronic pain and disability. It should be diagnosed by its own clinical characteristics of widespread musculoskeletal pain and multiple tender points. American College of Rheumatology criteria guidelines are most helpful in diagnosing FMS. The major symptoms are pain, stiffness, fatigue, poor sleep, and those of other associated conditions, for example, irritable bowel syndrome, headaches, restless legs syndrome, chronic fatigue syndrome, and depression. The pathophysiology of FMS is thought to involve central sensitization and neuroendocrine aberrations, triggered or aggravated by genetic predisposition; trauma; psychosocial distress; sleep deprivation; and peripheral nociception.

 

Fibromyalgia syndrome (FMS) is characterized by chronic musculoskeletal aches and pains as well as multiple tender points on palpation by an examiner. It is more common in women than men; about 90% of patients are women. The most common age of presentation is between 30 and 60 years.1-3 However, FMS has been well described among juveniles.4,5

FMS is a common condition. It is encountered among 2.1%, 5%, and 10% to 20% of patients seen in a family practice, internal medicine clinic, and rheumatic disease clinic, respectively.6 The prevalence of FMS in a community was found to be between 2% in Wichita, Kan,7 and 3.3% in London, Ontario.8 The prevalence increases with age until 65 to 79 years.7,8 More than 7% of women had FMS in the 55 to 64 age group in a Canadian study8 and in the 60 to 79 age group in a US study.7

The term "primary fibromyalgia" is used when a significant underlying or concomitant condition that may contribute to pain is absent. FMS may be classified as "concomitant" when another condition, such as rheumatoid arthritis (RA), osteoarthritis, or hypothyroidism is present and may contribute to pain or fatigue of FMS. However, currently the term FMS, or fibromyalgia, is collectively applied to both primary and concomitant types.

We describe clinical features, diagnosis, and pathophysiology in this article. Management is discussed in a future article.

CLINICAL FEATURES

Symptoms. Besides widespread pain, patients complain of many other symptoms, such as fatigue, poor sleep, a subjective swelling of soft tissues (and sometimes of the joints), paresthesia, cognitive dysfunction, and symptoms of other associated conditions, such as irritable bowel syndrome (IBS), headaches, restless legs syndrome, and temporomandibular dysfunction (Table 1).2,3,9 There is no significant correlation between subjective swelling or subjective numbness and psychological status.9 Common sites of pain or stiffness are low back, neck, shoulder region, arms, hands, knees, hips, thighs, legs, and feet. Chest pain is not uncommon and is accompanied by tender points in the chest wall (also see differential diagnosis). Fatigue is common in FMS and may be the presenting feature in some cases because of its severity. Several factors may contribute to, or aggravate, fatigue and pain in FMS, such as nonrestorative sleep, deconditioning, overwork, psychological factors, and poor coping skills.10 Patients are also sensitive to environmental stimuli, such as noise.9

Signs. Patients with FMS look healthy, but often they seem fatigued and in pain. Examination of the joints shows no objective swelling (unless there is concomitant arthritis), but some patients have marked joint tenderness on palpation. Despite neurologic symptoms, such as weakness and numbness, neurologic examination in FMS perseis normal. The most significant physical finding in FMS is the presence of multiple tender points in a widespread distribution. For the purpose of diagnosis (see below), one needs to examine 18 specified sites (Box, Figure 1), by application of a force of approximately 4 kg (roughly the pressure one needs to whiten the nail bed when pressing against a firm surface), using the index finger or the thumb. Note that the proper way of examining a tender point needs to be learned, as in the case of examining other physical signs in medicine, such as hepatomegaly or splenomegaly. An underestimation of the number of tender points in a patient with FMS is the most important reason for missing a diagnosis of this disorder.
 

The American College of Rheumatology
1990 Criteria for the Classification of FMS*

1. History of widespread pain (for at least 3 months)
Definition: Pain is considered widespread when all of the following are present: pain in the left side of the body, pain in the right side of the body, pain above the waist, pain below the waist. In addition, axial skeletal pain (cervical spine or anterior chest or thoracic spine or low back) must be present. In this definition, shoulder and buttock pain are considered as pain for each involved side. "Low back" pain is considered lower segment pain. Thus, pain at 3 widespread sites (for example, right arm, low back, and left leg) will satisfy the criterion of widespread pain.

2. Pain in 11+ of 18 tender point sites on digital palpation with an approximate force of 4 kg
Definition: Pain (mild or greater) on digital palpation must be present in at least 11 of the following 18 tender point sites:</P><P><em>Occiput:</em>bilateral, at the suboccipital muscle insertions.
Low cervical: bilateral, at the anterior aspects of the intertransverse spaces at C5-7.
Trapezius: bilateral, at the midpoint of the upper border.
Supraspinatus: bilateral, at origins above the scapula spine near the medial border.
Second rib: bilateral, at the second costochondral junctions, just lateral to the junctions on upper surfaces.
Lateral epicondyle: bilateral, 2 cm distal to the epicondyles.
Gluteal: bilateral, in upper outer quadrants of buttocks in anterior fold of muscle.
Greater trochanter: bilateral, posterior to the trochanteric prominence.
Knee: bilateral, at the medial fat pad proximal to the joint line.
FMS, fibromyalgia syndrome.

*For classification purposes, patients will be said to have FMS if both criteria (1 and 2) are satisfied. The presence of a second clinical disorder does not exclude the diagnosis of FMS.                                                                             From Wolfe F et al. Arthritis Rheum. 1990.2

LABORATORY INVESTIGATIONS

It may surprise many physicians to learn that a diagnosis of FMS does not require any specific laboratory testing, since "ruling out" does not apply to FMS. Laboratory tests, including radiology, should be requested only if another concomitant condition is suspected by careful history taking and physical examination.There is no reason to order tests of antinuclear antibodies or rheumatoid factor unless clinically indicated. However, a complete blood count and a chemistry panel with blood urea(Drug information on urea) nitrogen, creatinine, and hepatic enzymes are useful to monitor side effects of drugs either for FMS or a concomitant condition. Although the prevalence of hypothyroidism does not seem increased in FMS compared with the normal population, we obtain T4 and thyroid-stimulating hormone levels in patients with significant fatigue, even in the absence of other features of hypothyroidism.

DIAGNOSIS

Despite a common notion, diagnosis of FMS is disarmingly simple. It can, and should, be diagnosed by its own characteristics of widespread pain and multiple tender points; another concomitant condition, such as arthritis or hypothyroidism, does not exclude the diagnosis of FMS, as stated by the American College of Rheumatology (ACR) criteria.2 Putting it another way, if a patient has FMS as well as RA, this patient has both FMS and RA. Although the ACR criteria (see Box, Figure 1) were developed for classification of FMS (so that researchers can use a uniform set of criteria for patient selection), these criteria have been found to be very useful for the diagnosis of FMS in clinical practice. A patient with FMS may have many symptoms, but he or she needs only present with widespread pain (as defined in the Box) and 11 or more tender points among the 18 sites specified in ACR criteria. Note that a patient with FMS may be tender in many more sites (including bones) besides these 18. Some patients have diffuse tenderness "everywhere" on palpation. Such a phenomenon does not necessarily imply high psychological distress. Such diffuse tenderness on palpation or a significant psychiatric disease does not influence a diagnosis of FMS (as long as a patient satisfies the ACR criteria).

Now, a frequent question we hear from practicing physicians is: "Should one diagnose FMS if a patient has widespread pain but not 11 tender points?" For a clinical purpose, we suggest that a patient who has otherwise characteristic symptoms of FMS (eg, fatigue, poor sleep, morning fatigue, and 1 or more associated conditions; see Table 1), but only 6 to 10 tender points, should be treated for FMS.

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