Parikh Sarthak, Howell Maryavis, Yeh Hung-Wen, Cheruvu Mani, Goodwin Robert, Shellenberger John
Trauma Institute, Saint Francis Health System, Tulsa, USA.
Department of Orthopedic Surgery, Oklahoma State University, Tulsa, USA.
Cureus. 2024 Mar 7;16(3):e55736. doi: 10.7759/cureus.55736. eCollection 2024 Mar.
A tension pneumothorax is a condition that results in elevated pressure within the pleural space. The effective management of tension pneumothorax relies on needle decompression, commonly performed at the second intercostal space (ICS) midclavicular line (MCL). However, some literature suggests that catheters placed in the second intercostal space midclavicular line are prone to higher failure rates compared to the fifth intercostal space midaxillary line (MAL) (42.5% versus 16.7%, respectively). In this study, we aim to identify and scrutinize the prevalence of prehospital needle decompression from one tertiary care center over eight years and examine their trends, efficacies, or pitfalls. It is hypothesized that preclinical providers are performing needle decompression prematurely and unnecessarily.
A set of 90 patient records obtained using the trauma registry at Saint Francis Hospital, Tulsa, Oklahoma, were retrospectively reviewed to evaluate the management and outcomes of tension pneumothorax, as well as the indications documented for needle decompression. Patient charts were reviewed via Epic Hyperspace (Epic, Madison, WI). The Oklahoma Emergency Medical Service Information System (OKEMSIS) also provided information contributing to the sample population.
The most documented indications for needle decompressions included diminished or absent breath sounds (52.70%), hypoxia (15.54%), hypotension, and hemodynamic instability (6.76%). Emergency medical services (EMS) reported improvements in 51 (56.67%) patients after needle thoracostomy. Improvements in vital signs after needle decompression were sporadic. The most common complication was catheter dislodging, which occurred most in the second intercostal space midclavicular line. Only nine patients had an oxygen saturation (SpO) below 92% and a systolic blood pressure (SBP) below 100 mm Hg prior to receiving needle decompression.
Current practices for tension pneumothorax show little improvement in vital signs before and after needle decompression. Vital signs prior to needle decompression often do not indicate tension pneumothorax physiology. Preclinical providers may be inappropriately performing needle decompressions, an invasive procedure with complications.
张力性气胸是一种导致胸膜腔内压力升高的病症。张力性气胸的有效治疗依赖于针减压,通常在锁骨中线第二肋间(ICS)进行。然而,一些文献表明,与腋中线第五肋间(MAL)相比,置于锁骨中线第二肋间的导管失败率更高(分别为42.5%和16.7%)。在本研究中,我们旨在确定并仔细审查一个三级护理中心八年来院前针减压的发生率,并检查其趋势、疗效或缺陷。据推测,临床前提供者过早且不必要地进行针减压。
回顾性审查了从俄克拉荷马州塔尔萨市圣弗朗西斯医院创伤登记处获得的90份患者记录,以评估张力性气胸的治疗和结果,以及记录的针减压指征。通过Epic Hyperspace(Epic,威斯康星州麦迪逊)审查患者病历。俄克拉荷马州紧急医疗服务信息系统(OKEMSIS)也提供了有助于样本人群的信息。
针减压最常见的记录指征包括呼吸音减弱或消失(52.70%)、缺氧(15.54%)、低血压和血流动力学不稳定(6.76%)。紧急医疗服务(EMS)报告称,51例(56.67%)患者在进行针胸造口术后情况有所改善。针减压后生命体征的改善是零星的。最常见的并发症是导管移位,最常发生在锁骨中线第二肋间。只有9例患者在接受针减压前血氧饱和度(SpO)低于92%,收缩压(SBP)低于100 mmHg。
目前张力性气胸的治疗方法在针减压前后生命体征方面几乎没有改善。针减压前的生命体征往往并不表明存在张力性气胸的生理状况。临床前提供者可能在不恰当地进行针减压,这是一种有并发症的侵入性操作。