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. 2019 Dec 4;20:275. doi: 10.1186/s12931-019-1242-4

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — Flow chart. 329 Adult patients (> 18 years old) diagnosed with non-CF bronchiectasis were retrospectively identified. In order to evaluate clinical and functional course, only patients with an available medical follow up of more than 5 years and at least 4 pulmonary functional tests were selected. Finally, patients were divided into three groups according to the cause of bronchiectasis: PID, idiopathic/post-infectious and all other causes. PID: Primary Immunodeficiency; HSCT: Hematopoietic Stem Cell Transplantation; PFT: Pulmonary Functional Test