TY - JOUR
T1 - The Risk Factors of Exacerbation in Interstitial Pneumonia With Autoimmune Features
T2 - A Single-Center Observational Cohort Study
AU - Murata, Okinori
AU - Suzuki, Katsuya
AU - Takeuchi, Tsutomu
AU - Maemondo, Makoto
N1 - Funding Information:
We express our gratitude to all the participants in this study. This work was supported by the Division of Pulmonary Medicine, Allergy, and Rheumatology, Department of Internal Medicine, Iwate Medical University School of Medicine. The journal's Rapid Service Fee was funded by a special research grant from the Division of Pulmonary Medicine, Allergy, and Rheumatology, Department of Internal Medicine, Iwate Medical University School of Medicine. We thank Editage Corp. (www.editage.com) for editing the manuscript drafts. All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. O.M. designed the study, had full access to all the data used for analyses in this study, contributed to the acquisition, analysis, and interpretation of data, and wrote the initial draft of the manuscript. K.S. designed the study, contributed to the analysis and interpretation of data, and assisted in drafting the manuscript. T.T. and M.M. contributed to the analysis and interpretation of data. Katsuya Suzuki and Tsutomu Takeuchi have nothing to disclosure. Okinori Murata has changed affiliation: Division of Allergy and Rheumatology, Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Japan. Makoto Maemondo has changed affiliation: Division of Pulmonary Medicine, Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Japan. All procedures were approved by the Medical Ethics Committee of Iwate Medical University Hospital (registration no. MH2018-505) and adhered to the tenets of the Declaration of Helsinki. This is a retrospective study and written consent is not required. The method of disclosure to patients is as follows. The method of disclosure to patients will be explained in writing at the outpatient clinic of the Department of Respiratory, Allergy, and Collagen Diseases, and subjects will be given the opportunity to refuse the use of their data. All data generated or analyzed during this study are included in this published article or as supplementary information files.
Funding Information:
This work was supported by the Division of Pulmonary Medicine, Allergy, and Rheumatology, Department of Internal Medicine, Iwate Medical University School of Medicine. The journal's Rapid Service Fee was funded by a special research grant from the Division of Pulmonary Medicine, Allergy, and Rheumatology, Department of Internal Medicine, Iwate Medical University School of Medicine.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Objectives: To investigate the long-term outcomes, including risk factors, for exacerbation between monotherapy and combination therapy in patients with interstitial pneumonia with autoimmune features (IPAF). Methods: We assessed 672 patients between April 2009 and March 2019 who were evaluated using high-resolution computed tomography (HRCT) of the chest. We applied the IPAF criteria. Fifty-two patients who visited our department for at least 6 months were diagnosed with IPAF. Clinical, laboratory, and imaging data were collected from medical records and statistically analyzed. Results: Among the 52 cases of IPAF, we compared the characteristics at diagnosis between treated (n = 28) and untreated patients (n = 24). The exacerbation rates were 42.9% (n = 12) and 8.3% (n = 2) (P = 0.0051), respectively. Among the treated patients, smoking history, high titer of KL-6, and the duration from diagnosis to the start of treatment were significant risk factors for exacerbation (P = 0.0062, 0.011, and 0.019, respectively). The number of risk factors was significantly and positively associated with exacerbation rate (P = 0.0053). Among the treated patients, glucocorticoid (GC) monotherapy was used in 13 cases, and GC and immunosuppressant (IS) combination therapy was used in 14 patients. There was no significant difference in the treatment methods between patients with and without risk factors (P = 0.47). When comparing the long-term outcomes between the monotherapy and combination therapy groups, the 3-year non-exacerbation rates were 72.9 and 45.9% (P = 0.020), respectively. Conclusions: IPAF patients with risk factors had a high exacerbation rate, regardless of the type of treatment. New interventions aimed at preventing exacerbations in these patients are required.
AB - Objectives: To investigate the long-term outcomes, including risk factors, for exacerbation between monotherapy and combination therapy in patients with interstitial pneumonia with autoimmune features (IPAF). Methods: We assessed 672 patients between April 2009 and March 2019 who were evaluated using high-resolution computed tomography (HRCT) of the chest. We applied the IPAF criteria. Fifty-two patients who visited our department for at least 6 months were diagnosed with IPAF. Clinical, laboratory, and imaging data were collected from medical records and statistically analyzed. Results: Among the 52 cases of IPAF, we compared the characteristics at diagnosis between treated (n = 28) and untreated patients (n = 24). The exacerbation rates were 42.9% (n = 12) and 8.3% (n = 2) (P = 0.0051), respectively. Among the treated patients, smoking history, high titer of KL-6, and the duration from diagnosis to the start of treatment were significant risk factors for exacerbation (P = 0.0062, 0.011, and 0.019, respectively). The number of risk factors was significantly and positively associated with exacerbation rate (P = 0.0053). Among the treated patients, glucocorticoid (GC) monotherapy was used in 13 cases, and GC and immunosuppressant (IS) combination therapy was used in 14 patients. There was no significant difference in the treatment methods between patients with and without risk factors (P = 0.47). When comparing the long-term outcomes between the monotherapy and combination therapy groups, the 3-year non-exacerbation rates were 72.9 and 45.9% (P = 0.020), respectively. Conclusions: IPAF patients with risk factors had a high exacerbation rate, regardless of the type of treatment. New interventions aimed at preventing exacerbations in these patients are required.
KW - Interstitial pneumonia with autoimmune features
KW - Long-term outcomes
KW - Prognosis
KW - Risk factors
KW - Treatment methods
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U2 - 10.1007/s40744-021-00371-3
DO - 10.1007/s40744-021-00371-3
M3 - Article
AN - SCOPUS:85115171620
SN - 2198-6576
VL - 8
SP - 1693
EP - 1710
JO - Rheumatology and Therapy
JF - Rheumatology and Therapy
IS - 4
ER -