Kayikci Hazal, Cimen Pinar, Katgi Nuran
Department of Pulmonology, Dr. Suat Seren Chest Diseases and Surgery Training and Research Hospital, Izmir, Türkiye.
Sisli Etfal Hastan Tip Bul. 2023 Dec 29;57(4):506-512. doi: 10.14744/SEMB.2023.06767. eCollection 2023.
In the past years, surgery has been used for the non-medical treatment of severe emphysema. However, in recent years, bronchoscopic lung volume reduction (LVR) treatment has become more preferred because it is less invasive. Bronchoscopic coil treatment is the most frequently applied technique among these methods. The aim of the investigation was to determine the efficacy and safety of bronchoscopic volume reduction coil treatment for patients with severe emphysema.
The patients who were performed bronchial volume reduction coil treatment between 2015 and 2017 and were followed in our outpatient clinic were retrospectively examined. They were followed for 1 year at quarterly intervals after the procedure. All the safety and efficacy of the patient's records, including the modified Medical Research Council (MRC) dyspnea score, the St. George's Respiratory Questionnaire (SGRQ) quality of life scale, the 6 min walk distance (6-MWT), pulmonary function tests, and adverse events, were evaluated.
Sixteen patients were included in the study. The mean of the preoperative mMRC clinic dyspnea score was 3.38, the mean of the 3rd month's mMRC score was 2.62 (p=0.007), and the mean of the 12th month's mMRC was 2.37 (p=0.003). The preoperative SGRQ quality of life parameter was 71.95±15.7, the 3 month was 66.7±16.2 (p=0.007), and the 12 month was 62.9±16.4 (p=0.003). Preoperative mean of 6-MWT was 247.25±112.36 m, 3 month 264.25±95 m (p=0.148), and 12 month 317±122.9 m (p=0.034). Patients' preoperative residual volume was 5.28±1.96 L, 3 month 4.52±1.35 L (p=0.023), and 12 month 4.545±1.83 L (p=0.163). Patients' preoperative forced expiratory volume in one second, respectively, was 0.79±0.29 L, 3 month 0.79±0.3 L (p=0.917), and 12 month 0.86±0.3 L (p=0.756).
It seems that bronchoscopic LVR coil treatment, which is an effective and reliable procedure that reduces shortness of breath rather than respiratory function test parameters and improves the quality of daily life, will become even more widespread.
在过去几年中,手术已被用于重度肺气肿的非药物治疗。然而,近年来,支气管镜肺减容(LVR)治疗因其侵入性较小而更受青睐。支气管镜线圈治疗是这些方法中应用最频繁的技术。本研究的目的是确定支气管镜减容线圈治疗重度肺气肿患者的疗效和安全性。
回顾性研究2015年至2017年间接受支气管减容线圈治疗并在我们门诊随访的患者。术后每季度随访1年。评估患者记录的所有安全性和疗效,包括改良医学研究委员会(MRC)呼吸困难评分、圣乔治呼吸问卷(SGRQ)生活质量量表、6分钟步行距离(6-MWT)、肺功能测试和不良事件。
16例患者纳入研究。术前mMRC临床呼吸困难评分平均为3.38,第3个月的mMRC评分平均为2.62(p = 0.007),第12个月的mMRC评分平均为2.37(p = 0.003)。术前SGRQ生活质量参数为71.95±15.7,3个月时为66.7±16.2(p = 0.007),12个月时为62.9±16.4(p = 0.003)。术前6-MWT平均为247.25±112.36米,3个月时为264.25±95米(p = 0.148),12个月时为317±122.9米(p = 0.034)。患者术前残气量为5.28±1.96升,3个月时为4.52±1.35升(p = 0.023),12个月时为4.545±1.83升(p = 0.163)。患者术前一秒用力呼气量分别为0.79±0.29升,3个月时为0.79±0.3升(p = 0.917),12个月时为0.86±0.3升(p = 0.756)。
支气管镜LVR线圈治疗似乎是一种有效且可靠的方法,它可减轻呼吸急促而非呼吸功能测试参数,并改善日常生活质量,这种治疗方法将变得更加普遍。