Fibrosing alveolitis in patients with rheumatoid arthritis as assessed by high resolution computed tomography, chest radiography, and pulmonary function tests
J K Dawsona, H E Fewinsd, J Desmondb, M P Lyncha, D R Grahamc
a Department of
Rheumatology, St Helens and Knowsley Trust Hospitals, Liverpool, UK, b Department
of Radiology, St Helens and Knowsley Trust Hospitals, c Department of Respiratory Medicine, St Helens
and Knowsley Trust Hospitals, d Department
of Radiology, Cardiothoracic Centre, Liverpool, UK
Correspondence to: Dr J K Dawson, Department of Rheumatology, Southport and Formby District General Hospital, Southport, Merseyside PR8 6PN, UK twodocs{at}doctors.org.uk
Received 20 September 2000; Returned to authors 1 March 2001; Revised version received 2 April 2001; Accepted for publication 17 May 2001
BACKGROUND
Fibrosing
alveolitis (FA) is a common and serious complication of rheumatoid
arthritis (RA). Before the availability of high resolution computed
tomographic (HRCT) scanning, it was difficult to diagnose accurately
without recourse to biopsy. Prospective studies have reported a
prevalence of interstitial lung disease (ILD) of 19-44%. The term ILD
used by these authors encompasses a variety of appearances on HRCT
scans. This prospective study used HRCT scanning to determine the true
prevalence of FA in hospital outpatients with RA, and to study
associated clinical characteristics.
METHODS
One
hundred and fifty consecutive patients with RA were selected from a
hospital outpatient department, irrespective of the presence or absence
of chest disease. All underwent a detailed clinical assessment, chest
HRCT scanning, and conventional chest radiography within 4 weeks of
full pulmonary function tests.
RESULTS
Seventy
percent of patients were current or reformed cigarette smokers. Twenty
eight (19%) had FA, most frequently of reticular pattern, and 12 of
this group (43%) also had emphysematous bullae. None of the previously
suggested risk factors for developing FA were confirmed. Fifty four
percent of patients with HRCT evidence of FA had bilateral basal chest
crackles, 82% had a reduced carbon monoxide transfer factor
(TLCO), 14% had restrictive pulmonary function tests, and
14% had bilateral chest radiographic signs of FA.
CONCLUSIONS
HRCT
evidence of FA was present in 19% of hospital outpatients with RA.
Abnormalities on chest examination or on full pulmonary function tests,
even without restrictive changes or chest radiographic abnormalities,
should prompt physicians to request a chest HRCT scan when
investigating dyspnoea in patients with RA.
Keywords: fibrosing alveolitis; rheumatoid arthritis; high resolution computed tomography
© 2001 by Thorax
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