Predictive Factors for Recurrent Hemoptysis After Bronchial Artery Embolization in Patients with Lung Cancer

医学 支气管动脉 栓塞 放射科 肺癌 血管造影 肺动脉 外科 内科学
作者
Clément Hanotin,Raphael SALVAYRE,Louis Lassalle,Muriel Fartoukh,Raphael Lehrer,Aude Gibelin,Matthias Barral
出处
期刊:Journal of Vascular and Interventional Radiology [Elsevier BV]
标识
DOI:10.1016/j.jvir.2024.05.017
摘要

•Hemoptysis recurrence risk in lung cancer patients within one month post-Bronchial Artery Embolization (BAE) is 34.7%, requiring a second embolization in 33% of cases. •SAPS II, massive hemoptysis, Terlipressin use, necrosis/cavitation, and pulmonary artery lesions on MDCTA is associated with hemoptysis recurrence. •Massive hemoptysis and pulmonary artery lesions identified by MDCTA independently predict hemoptysis recurrence in lung cancer patients post-BAE. Purpose Severe hemoptysis (SH) in lung cancer patients admitted to the intensive care unit (ICU) treated with bronchial artery embolization (BAE) is associated with a high risk of recurrent hemoptysis. The purpose of this study was to identify clinical, radiological and angiographic characteristics associated with recurrent hemoptysis Materials and Methods 144 consecutive lung cancer patients who underwent BAE for life-threatening hemoptysis admitted in the ICU between 2014 and 2022 were retrospectively included. Demographics, laboratory values, clinical course, and radiological/angiographic features were compared between those with and without recurrent hemoptysis within one-month post-embolization. Results Of the 144 patients (mean age of 60.2 ± 10.9 years, 15.3% females), 34.7% (50/144) experienced significant recurrent hemoptysis within one month, among them 29/50 (58.0%) necessitated a second embolization. Massive hemoptysis was observed in 54.2%, with 16.7% receiving Terlipressin. The mean volume of hemoptysis and SAPS 2 score were 235 ± 214.3ml and 31.2 ± 18.6, respectively. Multidetector computed tomographic angiography (MDCTA) revealed pulmonary artery injury (11.5%), necrosis/cavitation (25.8%), and pulmonary artery embolization was performed in 15.3% of cases. Technical success was 92%. SAPS 2 (p = 0.01), massive hemoptysis (p < 0.001), Terlipressin use (p = 0.01), necrosis/cavitation (p = 0.01), and pulmonary artery injury on MDCTA (p < 0.001) were associated with recurrent hemoptysis. Independent predictors on multivariate analysis were massive hemoptysis (p = 0.016) and pulmonary artery injury on MDCTA (p = 0.001). Conclusion In patients with lung cancer and life-threatening hemoptysis treated by BAE, massive hemoptysis and pulmonary artery injury identified on MDCTA are independent predictors of recurrent hemoptysis. Severe hemoptysis (SH) in lung cancer patients admitted to the intensive care unit (ICU) treated with bronchial artery embolization (BAE) is associated with a high risk of recurrent hemoptysis. The purpose of this study was to identify clinical, radiological and angiographic characteristics associated with recurrent hemoptysis 144 consecutive lung cancer patients who underwent BAE for life-threatening hemoptysis admitted in the ICU between 2014 and 2022 were retrospectively included. Demographics, laboratory values, clinical course, and radiological/angiographic features were compared between those with and without recurrent hemoptysis within one-month post-embolization. Of the 144 patients (mean age of 60.2 ± 10.9 years, 15.3% females), 34.7% (50/144) experienced significant recurrent hemoptysis within one month, among them 29/50 (58.0%) necessitated a second embolization. Massive hemoptysis was observed in 54.2%, with 16.7% receiving Terlipressin. The mean volume of hemoptysis and SAPS 2 score were 235 ± 214.3ml and 31.2 ± 18.6, respectively. Multidetector computed tomographic angiography (MDCTA) revealed pulmonary artery injury (11.5%), necrosis/cavitation (25.8%), and pulmonary artery embolization was performed in 15.3% of cases. Technical success was 92%. SAPS 2 (p = 0.01), massive hemoptysis (p < 0.001), Terlipressin use (p = 0.01), necrosis/cavitation (p = 0.01), and pulmonary artery injury on MDCTA (p < 0.001) were associated with recurrent hemoptysis. Independent predictors on multivariate analysis were massive hemoptysis (p = 0.016) and pulmonary artery injury on MDCTA (p = 0.001). In patients with lung cancer and life-threatening hemoptysis treated by BAE, massive hemoptysis and pulmonary artery injury identified on MDCTA are independent predictors of recurrent hemoptysis.
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