Husain Syed A, Finch David, Ahmed Manzoor, Morgan Anthony, Hetzel Martin R
Department of Respiratory Medicine, Bristol Royal Infirmary, Bristol, United Kingdom.
Ann Thorac Surg. 2007 Apr;83(4):1251-6. doi: 10.1016/j.athoracsur.2006.11.066.
We report experience with Ultraflex metallic stents (Boston Scientific, Natick, MA) inserted at rigid bronchoscopy under general anesthesia for palliation of benign and malignant upper airway obstruction.
Notes of all patients treated with Ultraflex stents from 1999 to 2003 were reviewed for symptomatic response, spirometric data, and any complications before discharge home. Long-term outcome was assessed by questionnaires sent to patients' general practitioners.
Recruited were 66 patients (12 benign, 54 malignant airway obstructions). Before discharge home, breathlessness improved in 11 of 12 patients with benign obstruction and in 39 of 54 with malignancies. Postoperative complications in 10 patients with malignant obstructions and in 2 patients with benign obstruction were successfully controlled. It was not possible to perform preoperative pulmonary function tests in most of the patients who presented as emergencies. Mean improvement in forced expiratory volume in 1 second was 0.88 liters in 3 patients with benign obstruction and 0.28 liters in 14 patients with malignant obstruction, and mean peak expiratory flow rate improved by 109 L/min and 97 L/min, respectively. General practitioners completed questionnaires for 12 benign patients and 46 of 54 patients with malignancies. At a mean follow-up of 1017 days (range, 46 to 1120 days), 10 of the 12 patients with benign disease were alive and 7 of 46 patients with malignant airway obstruction were alive, with a median survival of 128 days (mean, 361; range, 3 to 1859 days). Most survivors had Medical Research Council grade III breathlessness or better, with few stent-related symptoms.
Ultraflex stents proved safe and effective in prolonged palliation of benign and malignant airways obstruction.
我们报告了在全身麻醉下经硬质支气管镜插入Ultraflex金属支架(波士顿科学公司,马萨诸塞州纳蒂克)以缓解良性和恶性上气道梗阻的经验。
回顾了1999年至2003年所有接受Ultraflex支架治疗患者的病历,以了解症状缓解情况、肺功能数据以及出院前的任何并发症。通过向患者的全科医生发送问卷来评估长期预后。
招募了66例患者(12例良性气道梗阻,54例恶性气道梗阻)。出院前,12例良性梗阻患者中有11例呼吸困难得到改善,54例恶性梗阻患者中有39例得到改善。10例恶性梗阻患者和2例良性梗阻患者的术后并发症得到成功控制。大多数作为急诊就诊的患者无法进行术前肺功能测试。3例良性梗阻患者的一秒用力呼气量平均改善0.88升,14例恶性梗阻患者平均改善0.28升,平均呼气峰值流速分别提高109升/分钟和97升/分钟。全科医生完成了12例良性患者和54例恶性患者中46例的问卷。平均随访1017天(范围46至1120天),12例良性疾病患者中有10例存活,46例恶性气道梗阻患者中有7例存活,中位生存期为128天(平均361天;范围3至1859天)。大多数幸存者的医学研究委员会呼吸困难分级为III级或更好,很少有与支架相关的症状。
Ultraflex支架在长期缓解良性和恶性气道梗阻方面被证明是安全有效的。