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CHaPtEr 57  Spondyloarthritis             781



            TABLE 57.6  Measurements of Disease                   Radiographic Imaging of Spondyloarthritis
            Outcome in spondyloarthritis                          Axial Spondyloarthritis
                                                                  The bottom line in the diagnosis of AS is the demonstration of
            ankylosing spondylitis                                radiographic sacroiliitis (Fig. 57.5).  Two outcome instruments
                                                                                              4
            1) Disease activity                                   have been introduced in the assessment of disease damage and
              (a) Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)  progression in AS: the Bath Ankylosing Spondylitis Radiographic
              (b) Ankylosing Spondylitis Disease Activity Score (ASDAS)  Index (BASRI) and the modified Stokes Ankylosing Spondylitis
              (c)  Patient and Physician Global Assessments                            31
            2) Function                                           Scoring System (mSASSS).  As a rule, these instruments have
              (a) Bath Ankylosing Spondylitis Functional Index (BASFI)  a low sensitivity to change (7.5% over 2 years), have been validated
              (b) Dougados Functional Index                       in long-duration disease only, and their predictive effect for
            3) Quality of Life                                    disease activity is not yet ascertained.
              (a) SF-36                                             One problem with radiographic imaging is the average decade-
              (b) Ankylosing Spondylitis Quality of Life Index (ASQOL)  long interval from the onset of inflammatory back pain to the
              (c)  ASAS Health Index                                                            5
            4) Metrometry                                         appearance of radiographic sacroiliitis.  The introduction of MRI
              (a) Schober test (lumbar flexion)                   imaging of the spine and entheses has allowed not only correct
              (b) Chest expansion                                 anatomical description of spinal structures but also differentiation
              (c)  Occiput-to-wall distance                       of AS-related and unrelated inflammatory spinal lesions earlier
              (d) Lateral bending                                 than is possible with standard radiography.  MRI of the sacroiliac
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              (e) Bath Ankylosing Spondylitis Metrology Index (BASMI) lateral   joints and spine is currently the only imaging tool to localize
                ending
            5) Imaging                                            and quantify spinal inflammation accurately (Fig. 57.6) and is
              (a) Standard radiography                            being developed as a measure of disease activity and treatment
              (b) Computed tomography                             response.
              (c)  Magnetic resonance imaging
            6) Assessment in Ankylosing Spondylitis (ASAS) 20     Psoriatic Arthritis
              (a) An improvement of 20% and absolute improvement of 10 units   PsA has some characteristic radiographic manifestations, including
                on a 0–100 scale in three of the following four domains:
                i.  Patient global assessment (by visual analogue scale [VAS]   asymmetrical involvement, involvement of the DIP joints, and
                  global assessment)                              the classic “pencil-in-cup” deformities. Also seen are periostitis,
                ii.  Pain assessment (the average of VAS total and nocturnal pain   bony ankylosis, and bony erosions with new bone formation.
                  scores)                                         Radiographic severity is quantitated by the modified Sharp scoring
                iii. Function (represented by BASFI)              method used in RA.
                iv. Inflammation (the average of the BASDAI’s last two VAS   The measures used in PsA to assess disease severity include
                  concerning morning stiffness, intensity, and duration)  the ACR response criteria, the Psoriatic Arthritis Response Criteria
                v.  Absence of deterioration in the potential remaining domain
                  (deterioration is defined as 20% worsening)     (PsARC), which entail improvement in at least two of the fol-
                                                                  lowing four criteria: (i) physician; and (ii) patient global assess-
            Psoriatic arthritis                                   ments (on 0–5 visual analogue scales); (iii) tender and swollen
            1) Arthritis                                          joint scores (>30% improvement), with improvement in at least
              (a) ACR response criteria                           one of these two joint scales; and (iv) no worsening in any criteria.
              (b) Psoriatic Arthritis Response Criteria (PsARC)   The Ritchie Articular Index is also used. The Psoriasis Area and
              (c)  Ritchie Articular Index                        Severity Index (PASI) is used to assess the extent of skin involve-
            2) Skin response                                      ment, as well as general measures, such as the target lesion score,
              (a) Psoriasis Area and Severity Index (PASI)
              (b) Target lesion score                             and the static global assessment. The PASI is a composite index
              (c)  Static global assessment                       of skin disease severity, including an overall evaluation and
            3) Quality of life (HAQ, SF-36, DLQI)                 quantitation of the extent of scaling, erythema, and induration
            4) Radiographic                                       weighted: (i) by severity; and (ii) by body surface area. A target
                                                                  lesion is a single lesion >2 cm in diameter that is evaluated over
                                                                  time by a dermatologist and is graded for size, elevation, erythema,
               CLiNiCaL rELEVaNCE                                 and scaling.
            Utility of Human Leukocyte Antigen (HLA)-B27          DISEASE COURSE AND PROGNOSIS
            Testing in the Evaluation of Inflammatory Back
            Pain and Spondyloarthritis                            Ankylosing Spondylitis
                                                                  AS significantly impacts the lives of those affected. Recent data
            •  Not indicated where the diagnosis is unquestionable, as it has little   suggest that patients with AS are more likely to be work disabled or
              value in prognosis.                                 even not participate in the labor force compared with population
            •  Although patients with spondyloarthritis of African and Middle Eastern
              ancestry are more likely to be HLA-B27 negative, the finding of HLA-B27   controls, especially in older patients and in those with longer
              in these patients has higher predictive value.      disease duration. Moreover, in the same study, patients with AS
            •  Most useful in patients with either inflammatory back pain without   were more likely to have never married or to be divorced. Women
              radiographic changes or with other features of spondyloarthritis   with AS were less likely than expected to have had children. 32
              (unexplained lower extremity arthritis in a young adult, uveitis, etc.).  Although AS is a chronic condition that can frequently have
            •  If serological testing is used to ascertain HLA-B27, it must be ensured   an unpredictable course, some studies suggest that those with
              that the blood sample arrives in the laboratory within 24 hours of
              being drawn (false negatives will be caused by cell death).  higher levels of disease activity early in the course of the disease
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                                                                  are more likely to have active disease in the future (Fig 57.7).
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