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Nationwide survey of adult patients with pulmonary alveolar proteinosis using the National Database of designated intractable diseases of Japan.
- Source :
-
Respiratory investigation [Respir Investig] 2023 May; Vol. 61 (3), pp. 364-370. Date of Electronic Publication: 2023 Apr 10. - Publication Year :
- 2023
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Abstract
- Background: Autoimmune pulmonary alveolar proteinosis (APAP) and congenital/hereditary PAP were labeled intractable diseases in Japan in 2015. Since then, patients registered in the National Database of Designated Incurable Diseases (NDDID) who met certain requirements became eligible for medical subsidies. Epidemiological studies using recent data are needed for the development of management protocols for patients with PAP.<br />Methods: We conducted the first nationwide study describing the epidemiology and characteristics of PAP using data for patients registered in the Japanese NDDID between 2015 and 2020. We focused on patient demographics, diagnosis, disease severity score (DSS), symptoms, test results, and treatment.<br />Results: We identified 110 patients with PAP, among whom 96.4% had APAP/idiopathic PAP (IPAP). The median age was 58 years, with a slight male predominance. Most patients had a DSS ≥3 (64.5%) and reported symptoms (e.g., dyspnea on exertion). High-resolution computed tomography typically revealed ground glass opacity and crazy paving appearances. Pulmonary function was relatively preserved, except for carbon monoxide diffusing capacity. Only 27.4% of patients underwent therapeutic whole-lung lavage and/or bronchoalveolar lavage, while 25% required long-term oxygen therapy. Serum Krebs von den Lungen-6, surfactant protein D, and lactate dehydrogenase levels significantly and positively correlated with the DSS.<br />Conclusions: Most patients registered in the NDDID have APAP/IPAP with a DSS ≥3, and about one-quarter require long-term oxygen therapy and infrequent lavages. Our results provide important details of the current prevalence and clinical practice related to APAP/IPAP with a DSS ≥3 in Japan.<br />Competing Interests: Conflict of Interest K.M. has no conflict of interest. H.H. has no conflict of interest. Y.I. received honoraria for lecture fees and for serving as a steering committee board member from Boehringer Ingelheim (none of which are related to this manuscript). T. Suzuki. belongs to endowed departments sponsored by Nippon Boehringer Ingelheim Co., Ltd., and AstraZeneca K.K. T. Suda. has no conflict of interest.<br /> (Copyright © 2023 The Japanese Respiratory Society. Published by Elsevier B.V. All rights reserved.)
Details
- Language :
- English
- ISSN :
- 2212-5353
- Volume :
- 61
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Respiratory investigation
- Publication Type :
- Academic Journal
- Accession number :
- 37043919
- Full Text :
- https://doi.org/10.1016/j.resinv.2023.02.011