Ishiwata Tsukasa, Abe Mitsuhiro, Kasai Hajime, Ikari Jun, Kawata Naoko, Terada Jiro, Sakao Seiichiro, Tada Yuji, Tanabe Nobuhiro, Tatsumi Koichiro
Department of Respirology, Graduate School of Medicine, Chiba University, 1-8-1, Inohana, Chuo-ku, Chiba 260-8670, Japan.
Respir Investig. 2019 Jan;57(1):73-78. doi: 10.1016/j.resinv.2018.08.009. Epub 2018 Oct 24.
The presence of pulmonary hypertension (PH) and treatment with anticoagulant agents could potentially increase the risk for bleeding/hemodynamic complications associated with bronchoscopic procedures. The aim of this study was to assess the safety of diagnostic flexible bronchoscopy (FB) in patients with PH.
A retrospective review of clinical records of patients with echocardiographic evidence of PH (right ventricular systolic pressure [RVSP] > 40 mm Hg) who underwent diagnostic FB between 2004 and 2016 at a single facility in Japan was conducted. Patients with no clinical evidence suggestive of PH who underwent FB during the same period were enrolled as a pairwise-matched control group; factors used in matching included age, sex, and performed procedures.
Overall, there were 45 patients in the PH group and 90 patients in the control group. Six (13%) patients in the PH group had severe PH (RVSP > 61 mm Hg). Forceps biopsies and transbronchial needle aspirations were performed in 62% and 13% of patients, respectively, in the PH group, and 58% and 13% of patients, respectively, in the control group. The total incidence of bleeding during FB was not significantly different between the two groups (18% versus 16%; p = 0.742). Vital signs recorded 2 h after FB were also not significantly different between the two groups. There were no episodes of cardiac arrhythmias or deaths associated with the FB procedures.
The data suggest that diagnostic FB procedures can be performed safely in patients with echocardiographic evidence of PH.
肺动脉高压(PH)的存在以及抗凝剂治疗可能会增加与支气管镜检查相关的出血/血流动力学并发症的风险。本研究的目的是评估诊断性柔性支气管镜检查(FB)在PH患者中的安全性。
对2004年至2016年期间在日本一家机构接受诊断性FB且有超声心动图证据显示PH(右心室收缩压[RVSP]>40 mmHg)的患者的临床记录进行回顾性分析。将同期接受FB且无PH临床证据的患者纳入配对对照组;匹配因素包括年龄、性别和所进行的操作。
总体而言,PH组有45例患者,对照组有90例患者。PH组中有6例(13%)患者患有重度PH(RVSP>61 mmHg)。PH组分别有62%和13%的患者进行了钳取活检和经支气管针吸活检,对照组分别有58%和13%的患者进行了上述操作。两组FB期间出血的总发生率无显著差异(18%对16%;p = 0.742)。FB后2小时记录的生命体征在两组之间也无显著差异。没有与FB操作相关的心律失常或死亡事件。
数据表明,对于有超声心动图证据显示PH的患者,可以安全地进行诊断性FB操作。