Division of Chest Surgery, Department of Surgery, Toho University School of Medicine, Tokyo, Japan.
Ann Thorac Cardiovasc Surg. 2022 Oct 20;28(5):329-333. doi: 10.5761/atcs.oa.22-00087. Epub 2022 Aug 2.
A pneumothorax occurs in 3%-8% of patients with idiopathic pulmonary fibrosis. A pneumothorax may predict a poor outcome in patients with interstitial lung disease (ILD), and it is difficult to treat patients with ILD and a pneumothorax.
We retrospectively studied data from all 12 patients with ILD and a pneumothorax who underwent surgical treatment at Toho University Omori Medical Center Hospital between 2009 and 2021.
Of the 12 patients, 2 had home oxygen therapy preoperatively and were classified with grade IV interstitial pneumonia (IP). Six patients had preoperative pleurodesis and two had postoperative one using auto-blood. Three patients (25%) had multi-step surgery ≥2, and 5 patients had surgical resection of bullae. No patients had postoperative acute exacerbations and all were discharged from the hospital in a stable condition. The 5-year overall survival rate for all patients was 70.0%. The median survival time was not reached. One patient with unclassified IP was doing well 116 months after surgery.
Patients with ILD and a pneumothorax were shown to require multi-step surgical treatment and can anticipate long-term survival.
特发性肺纤维化患者中,气胸的发生率为 3%-8%。气胸可能预示着间质性肺疾病(ILD)患者的预后不良,且ILD 合并气胸患者的治疗较为困难。
我们回顾性研究了 2009 年至 2021 年间在东京都立大冢医疗中心医院接受手术治疗的 12 例ILD 合并气胸患者的数据。
12 例患者中,术前有 2 例行家庭氧疗,且分类为 IV 级间质性肺炎(IP)。6 例行术前胸膜固定术,2 例行术后自体血。3 例(25%)患者行≥2 步手术,5 例行大疱切除术。无患者术后出现急性加重,且均病情稳定出院。所有患者的 5 年总生存率为 70.0%。中位生存时间尚未达到。1 例未分类的 IP 患者术后 116 个月仍情况良好。
ILD 合并气胸患者需要进行多步手术治疗,可预期长期生存。