Complications during chest tube drainage for iatrogenic pneumothorax.

IF 1.8 Q3 RESPIRATORY SYSTEM European Clinical Respiratory Journal Pub Date : 2025-01-20 eCollection Date: 2025-01-01 DOI:10.1080/20018525.2025.2453255
Birgitte Siem Joensen, Uffe Bodtger, Christian B Laursen, Rob J Hallifax, Beenish Iqbal, Søren Helbo Skaarup
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Abstract

Background: Iatrogenic pneumothorax is a common complication of diagnostic and therapeutic pulmonary procedures. New guidelines on primary spontaneous pneumothorax suggest ambulatory approaches may be suitable. However, guidance on iatrogenic pneumothorax occurring in patients with impaired lung function, increased age, comorbidity and frailty is lacking, and the safety profile of ambulatory management is not known. The objective was to study the safety of iatrogenic pneumothorax treated with chest tubes and to identify the risks of life-threatening events.

Methods: In a retrospective cohort of patients admitted and treated with an adhesive valve-integrated chest tube system, we recorded the incidence of complications. The primary outcome was the incidence of life-threatening events that required urgent medical action. Incidences of serious adverse events, adverse events, serious device-related events and whether outpatient ambulatory treatment would be safe were recorded based on the review of the medical charts.

Results: In 97 patients, 6 (6%) life-threatening events occurred, including episodes of respiratory failure and an urgent need for new chest tube insertion. The event incidence was 21% in patients with pre-biopsy saturation below 95% and 1% in patients with saturation above 95%, p = 0.003, and greater if the lung had not expanded on the first radiograph, 25%, after insertion of the chest tube, than if the lung had fully expanded, 4%, or partially expanded, 2%, p = 0.009.

Conclusions: The incidence of life-threatening events during chest tube-treated iatrogenic pneumothorax is significant, but acceptable in patients without impaired lung function prior to the procedure and early response to treatment.

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医源性气胸胸管引流术中的并发症。
背景:医源性气胸是诊断和治疗肺部手术的常见并发症。关于原发性自发性气胸的新指南建议门诊方法可能是合适的。然而,缺乏关于肺功能受损、年龄增加、合并症和虚弱患者发生医源性气胸的指导,并且门诊治疗的安全性尚不清楚。目的是研究胸管治疗医源性气胸的安全性,并确定危及生命事件的风险。方法:在一个回顾性队列患者入院和治疗的粘接阀集成胸管系统,我们记录并发症的发生率。主要结果是需要紧急医疗行动的危及生命事件的发生率。严重不良事件发生率、不良事件发生率、严重器械相关事件发生率以及门诊门诊治疗是否安全均记录在病历回顾的基础上。结果:97例患者中有6例(6%)发生了危及生命的事件,包括呼吸衰竭发作和迫切需要插入新的胸管。活检前饱和度低于95%的患者的事件发生率为21%,饱和度高于95%的患者的事件发生率为1%,p = 0.003,如果在第一次x线片上肺未扩张,胸腔插管后肺未扩张的发生率为25%,高于肺完全扩张(4%)或部分扩张(2%)的发生率,p = 0.009。结论:在胸管治疗的医源性气胸中,危及生命事件的发生率是显著的,但对于术前无肺功能受损和对治疗早期反应的患者是可以接受的。
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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
15
审稿时长
16 weeks
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