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. 2021 Aug 25;10(17):3806. doi: 10.3390/jcm10173806

Table 1.

HRCT patterns and prognosis of RA-ILD.

Authors Year No. of Patients HRCT Patterns Reference to Criteria of HRCT Classification 5-Year Survival Rate (%) Median Survival
Kim et al. [23] 2010 82 24% (UIP)
23% (NSIP)
51% (Indeterminate)
2% (Others)
2002 ATS/ERS classification of the IIPs N/A 3.2 years (UIP)
6.6 years (Non-UIP)
Tsuchiya et al. [42] 2011 94 61% (UIP)
17% (NSIP)
22% (Others)
2002 ATS/ERS classification of the IIPs 36.6% (UIP)
93.8% (NSIP)
3.9 years (UIP)
17 years (NSIP)
Kelly et al. [25] 2014 230 65% (UIP)
24% (NSIP)
11% (Others)
N/A N/A N/A
Solomon et al. [26] 2016 137 79% (Definite + Possible UIP) 21% (NSIP) 2011 IPF guideline N/A 10.2 years (Definite+Possible UIP)
13.6 years (NSIP)
Morisset et al. [43] 2017 309 24% (Definite UIP)
16% (Possible UIP)
60% (Inconsistent with UIP)
2011 IPF guideline N/A N/A
Zamora-Legoff et al. [20] 2017 181 54% (UIP)
40% (NSIP)
6% (OP)
N/A 55.2% (UIP)
65.0% (NSIP)
47.4% (OP)
N/A
Yunt et al. [44] 2017 158 63% (Definite UIP)
15% (Possible UIP)
22% (NSIP)
2011 IPF guideline N/A 8.3 years (Definite UIP)
6.1 years (Possible UIP)
Incalculable (NSIP)
Fu et al. [45] 2019 266 17% (Definite UIP)
20% (Possible UIP)
32% (Unclassifiable)
30% (Others)
2011 IPF guideline 69.7% (All) N/A
Jacob et al. [46] 2019 157 35% (Definite UIP)
36% (Probable UIP)
29% (Inconsistent with UIP)
2018 Diagnostic criteria for IPF:
Fleischner Society
<6-year survival rate >
45% (Definite UIP)
58% (Probable UIP)
N/A
Yamakawa et al. [47] 2019 112 21% (Definite UIP)
20% (Probable UIP)
27% (Mixed NSIP/UIP)
29% (Alternative)
2018 IPF guideline 70.2% (Definite UIP)
90.9% (Probable UIP)
80.0% (Mixed NSIP/UIP)
90.0% (NSIP)
6.8 years (Definite UIP)
9.1 years (Probable UIP)
8.6 years (Mixed NSIP/UIP)
7.8 years (NSIP)
Kakutani et al. [5] 2020 261 46% (Definite + Possible UIP)
54% (Non-UIP)
2011 IPF guideline N/A N/A

Abbreviations: ATS = American Thoracic Society; ERS = European Respiratory Society; HRCT = high-resolution computed tomography; IPF = idiopathic pulmonary fibrosis; NSIP = nonspecific interstitial pneumonia; OP = organizing pneumonia; RA-ILD = rheumatoid arthritis-associated interstitial lung disease; UIP = usual interstitial pneumonia.