ERJ Open Research (May 2020)

Prognostic impact of pre-existing interstitial lung disease in non-HIV patients with Pneumocystis pneumonia

  • Shohei Hamada,
  • Hidenori Ichiyasu,
  • Megumi Inaba,
  • Hiroshi Takahashi,
  • Tomoki Sadamatsu,
  • Kimitaka Akaike,
  • Aiko Masunaga,
  • Yasumasa Tashiro,
  • Naomi Hirata,
  • Takeshi Yoshinaga,
  • Takuro Sakagami

DOI
https://doi.org/10.1183/23120541.00306-2019
Journal volume & issue
Vol. 6, no. 2

Abstract

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Background The increasing incidence of life-threatening Pneumocystis pneumonia (PCP) in non-HIV immunocompromised patients is a global concern. Yet, no reports have examined the prognostic significance of pre-existing interstitial lung disease (ILD) in non-HIV PCP. Methods We retrospectively reviewed the medical records of non-HIV PCP patients with (ILD group) or without (non-ILD group) pre-existing ILD. The clinical features and outcomes of the ILD group were compared with those of the non-ILD group. Cox regression models were constructed to identify prognostic factors. Results 74 patients were enrolled in this study. The 90-day mortality was significantly higher in the ILD group than in the non-ILD group (62.5% versus 19.0%, p<0.001). In the ILD group, patients with a higher percentage of bronchoalveolar lavage fluid neutrophils had worse outcomes compared to those having a lower percentage (p=0.026). Multivariate analyses revealed that pre-existing ILD (p=0.002) and low levels of serum albumin (p=0.009) were independent risk factors for 90-day mortality. Serum levels of β-d-glucan were significantly reduced after treatment of PCP in both groups, whereas levels of Krebs von den Lungen-6 (KL-6) significantly increased in the ILD group. In the ILD group, the 90-day mortality of patients with increasing KL-6 levels after treatment was significantly higher than those with decreasing levels (78.9% versus 0%, p=0.019). Conclusion In non-HIV PCP patients, pre-existing ILD is associated with a poorer prognosis. Prophylaxis for PCP is needed in patients with pre-existing ILD under immunosuppression.