Response to the editor
Response to the editor
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对编辑的回应
DOI:
10.1016/j.chest.2021.07.044
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发表时间:
2021
期刊:
影响因子:
9.6
通讯作者:
Suda T.
中科院分区:
文献类型:
--
作者:
Hozumi H;Kono M;Hasegawa H;Yasui H;Suzuki Y;Karayama M;Furuhashi K;Enomoto N;Fujisawa T;Inui N;Nakamura Y;Yokomura K;Nakamura H;Suda T.
We read with great interest the work on the clinical significance of interstitial lung disease (ILD) and its acute exacerbation in microscopic polyangiitis (MPA) by Hozumi et al. published in the recent issue of Chest. 1 The authors provided convincing data supporting the existence of an MPA-ILD clinical phenotype with a poor prognosis that needs a different therapeutic approach. 2 However, we were surprised that treatment with antibiotics was not included as a covariate in the comparative analysis between MPA-ILD and MPA-non-ILD groups or the Cox proportional hazards regression analysis. Further, there is no description of therapy with antibiotics in the method section of the article. Patients with anti-neutrophil cytoplasmic antibody-associated vasculitis, including MPA, are generally at high risk of contracting an infection. 3 On this basis, international guidelines recommend the prophylactic prescription of antibiotics (eg, co-trimoxazole) and vaccination against infection in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis. 4 In agreement with this concept, a recent longitudinal matched-cohort study demonstrated that the risk of infection is up to seven times higher in patients with anti-neutrophil cytoplasmic