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Abstract Number: 1881

Is the Presence of Esophageal Dilation a Poor Prognostic Factor in Dilated Interstitial Lung Disease Associated with Systemic Sclerosis?

Javier Narváez1, Sergi Heredia2, Helena Borrell Paños2, Eulalia Armengol2, Eugenia De Lama3 and Jose Antonio Narvaez3, 1Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 2Department of Rheumatology, Hospital Universitario de Bellvitge, Barcelona, Spain, 3Department of Radiology. Hospital Universitario de Bellvitge, Barcelona, Spain

Meeting: 2015 ACR/ARHP Annual Meeting

Date of first publication: September 29, 2015

Keywords: Gastrointestinal complications and systemic sclerosis, Lung Disease

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Session Information

Date: Monday, November 9, 2015

Title: Systemic Sclerosis, Fibrosing Syndromes and Raynaud's - Clinical Aspects and Therapeutics Poster II

Session Type: ACR Poster Session B

Session Time: 9:00AM-11:00AM

Background/Purpose: Several studies have shown that gastroesophageal reflux disease (GERD) is a risk factor in the progression of idiopathic pulmonary fibrosis. In systemic sclerosis (SSc), esophageal involvement is common; however, it does not generate symptoms in 50% of patients. Therefore, the presence of esophageal dilation and GERD may be a poor prognostic factor in patients with systemic sclerosis and diffuse interstitial lung disease (ILD-SSc) as a result of recurrent episodes of micro-aspiration. Our objective was to analyze whether the presence of esophageal dilation is a poor prognostic factor in ILD-SSc.

Methods: Thirty-one patients with SSc (ACR/EULAR 2013 criteria) and secondary symptomatic ILD, as confirmed by thoracic HRCT, were studied. HRCT images performed at the time of ILD diagnosis were reviewed with particular attention to: a)the presence of dilation in the lower two-thirds of the esophagus and b) the extent of ground glass areas and fibrotic changes (honeycombing areas, thickening of the interlobular septa and traction bronchiectasis with architectural distortion). The extent of HRCT lung abnormalities were scored in 3 categories: 1 = involvement of < 25% of total pulmonary parenchyma, 2 = 25-30%, and 3 = > 50%.   

Results: Esophageal dilation was detected in the HRCT of 15 (48%) patients. The main clinical characteristics of the patients and the results from the comparative study between groups are shown in the following table:

Esophageal dilation in the HRCT
N= 15

No esophageal dilation in the HRCT

N=16

 p

Age  (mean±SD), yrs

54 ± 16

63 ± 15

0.120

SSc Types

Limited :5

Diffuse:  9

SSc sine escleroderma 1

Limited: 12

Difuse:  2

SSc sine escleroderma:2

0.022

SSc disease duration (median ±SD), months

102 ± 143

112 ± 95

0.812

ILD type

NSIP: 12

UIP: 3

NSIP:12

UIP:4

0.095

ILD disease duration (median ±SD), months

35 ± 27

70 ± 44

0.014

Baseline HRCT

Ground glass areas

Score 1:  6

Score 2:  6

Score 3:   0

Score 1:  10

Score 2:   1

Score 3:  0

0.033

Fibrotic changes

Score 1:  2

Score 2:  4

Score  3:  0

Score 1:  4

Score 2:  0

Score 3:  0

0.035

Baseline PFT

FVC% (mean ± SD)

83.9 ± 22.1

103.4 ± 19.5

0.015

TLC%

87.9 ± 25.7

110.7 ± 33.9

0.116

DLCO%

57.4 ± 17.9

71.3 ± 24.3

0.095

PFT at the end of the follow-up period

FVC%

79 ± 20.8

98.3 ± 26

0.031

TLC%

79 ±19.2

98.5 ± 26.8

0.067

DLCO%

48.8 ±15.7

62.2 ±18.3

0.046

Treatment with CYC and/or rituximab

10 (67%)

 

5 (31%)

0.049

Treatment with proton pump inhibitors

14 (93%) 11 (69%) 0.172

At the time of ILD-SSc diagnosis, patients with esophageal dilation showed a greater extent of ground glass areas (P = 0.033) and fibrotic changes (P = 0.035) in the HRCT. A relatively common finding in these patients was an asymmetry in injury severity with greater involvement in one of the two lungs. In addition, patients with esophageal dilation showed greater deterioration of lung function parameters, although the differences were only statistically significant for baseline (P = 0.015) and final (P = 0.031) FVC measurements and for the final DLCO measurement (P= 0.046). These patients also received more frequent treatment with CYC or rituximab.

Conclusion: The presence of esophageal dilation appears to be a poor prognostic factor in ILD-SSc, which relates to a greater extent of HRCT lung abnormalities and further deterioration in baseline pulmonary function tests (PFT)


Disclosure: J. Narváez, None; S. Heredia, None; H. Borrell Paños, None; E. Armengol, None; E. De Lama, None; J. A. Narvaez, None.

To cite this abstract in AMA style:

Narváez J, Heredia S, Borrell Paños H, Armengol E, De Lama E, Narvaez JA. Is the Presence of Esophageal Dilation a Poor Prognostic Factor in Dilated Interstitial Lung Disease Associated with Systemic Sclerosis? [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/is-the-presence-of-esophageal-dilation-a-poor-prognostic-factor-in-dilated-interstitial-lung-disease-associated-with-systemic-sclerosis/. Accessed .
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