Penetrating thoracic trauma injuries and the use of Pneumofix Respiration, Thoracic Trauma | Safeguard Medical 08/12/2021 As mentioned on our previous blog about thoracic trauma and chest seals, tension pneumothorax is a life-threatening condition, which, left untreated can be fatal within a matter of minutes. Studies suggest that tension pneumothorax is the second most common cause of preventable death on the battlefield1,2,3. Standard clinical management of a suspected tension pneumothorax includes insertion of a cannula into the pleural cavity1. When a patient has a tension pneumothorax, needle chest decompression can be life-saving. There have been widespread reports of complications following needle chest decompression5,6. Commonly used devices, such as intravenous cannula, may not be long enough to reach the pleural space or they may kink and occlude. There are a number of important aspects to consider when performing a needle decompression for the treatment of tension pneumothorax. These include the size of the individual chest wall, the product chosen to perform the procedure and also how certain the individual is of the tension pneumothorax diagnosis. These three criteria include: Chest wall thickness Decompression failure Diagnosis and safety 1. Chest wall thickness Using an unsuitable product to perform needle chest decompression may lead to complications or be ineffective all together. Studies have shown a failure rate of standard needle chest compression using an intravenous cannula in the pre-hospital environment of up to 40%1. The length of the needle or catheter used can be too short to reach the pleural space to release the tensioned air. The published literature suggests that adult chest wall thickness varies quite considerably. A mean of >4 cm depth is often quoted. However, any product that is to be used for needle decompression would need to be able to treat all the population and not just those mean chest wall thickness of 4cm or less. Harcke8 et al reported a mean chest wall thickness of 5.36 cm in US military personnel but with some individuals having a greater chest wall thickness and a maximum of 9.35 cm. While this might seem like an extremely large chest wall thickness, military personnel are a significant market for needle decompression products due to the potential requirement for needle decompression on the battlefield. Therefore, any product hoping to be used for the treatment of tension pneumothorax will need to be able to treat most if not all of military personnel. 2. Decompression failure The failure rate of an needle chest decompression to effectively decompress a tension pneumothorax is well known. Smith & Harris catheter kinking as a leading cause of failure, together with obstruction and occlusion[1]. In the military setting, these failures have also been recognised, especially during prolonged field care and medical evacuation2. The previous gold standard, needle chest decompression, has a failure rate of up to 64% (Lubin D 2013). Lubin et al13 (Lubin D 2013) then demonstrated superiority of a modified veress needle over a standard angiocatheter for chest decompression. Real et al (Real 2015) demonstrated the success of the Russell PneumoFixTM over a modified angiocatheter commonly used in the UK for needle decompression. Hatch et al. (Hatch Q 2014) demonstrated safe and effective chest decompression with 5-mm laparoscopic trocars. Summarising the literature detailing failure mechanisms, it can be concluded that any product to be used for needle decompression must address the following concerns; Be long enough to reach the pleural space in the majority of the population. Data from military personnel and obese individuals indicates the need for longer devices. The device should not kink and occlude. A device made from material that can kink increases the likelihood of failure. A mechanism to reduce potential for occlusion by blood, fats, tissue etc should be included. To prevent having to continually repeat the procedure the incorporation of a one valve would allow for prolong transport and continual decompression maintenance especially if the patency of the device is maintained 3. Safety A study by Leigh-Smith et al (Leigh-Smith S 2005) found that any pleural injury communicating with the atmosphere via a one-way valve that opens on inspiration and closes on expiration will lead to an expanding pneumothorax. For clinical purposes they suggest that a pneumothorax is considered to be under tension when it results in ‘‘significant respiratory or haemodynamic compromise. In trauma a clear diagnosis can be in doubt and the study lists the diagnosis signs and symptoms of tension pneumothorax (Table 1). Table 1. Symptoms of tension pneumothorax (Leigh-Smith S 2005) As can be seen from the list of potential symptoms of tension pneumothorax, these can be difficult to appreciate in the pre-hospital setting. Although needle decompression should only be used in patients with tension pneumothorax, one series of trauma needle decompression placements established that only about 5% of patients had tension pneumothorax (Wernick B 2015). This suggests that in the field needle decompression can be performed when it is not always needed. Ball (Ball CG 2010) also states that it should be realised it is easier for a physician in a controlled trauma bay to diagnose tension pneumothorax, compared with paramedics with field challenges that include suboptimal sedation, environment, vital sign monitoring and the potential pulmonary effects of altitude. This results in decompression devices being placed with greater frequency by paramedics or field doctors than their hospital-based colleagues. The insertion of a needle decompressing device when a tension pneumothorax is not present does create a safety issue for some products. If a tension pneumothorax is not present, then it is likely that the lung surface is adjacent to the pleural cavity wall. Many commonly used devices have unprotected sharp tips. In the case of such a sharp ended product being inserted through the chest wall when a tension pneumothorax is not present, there is a significant danger of piercing the lung and then causing a tension pneumothorax which was the condition the procedure was designed to treat. A Veress needle contains a spring-loaded inner section that pushes back in contact with stiffer material such as skin or muscle and exposes the sharp cutting edge. When in contact with less dense tissues such as lung tissue or vascular structures, the spring-loaded inner section does not retract and thereby limits any damage. Therefore, it is logical that any product used as a needle decompression device should have a safety tip such as that on a Veress needle. Safeguard Medical offers a variety of solutions for the Respiratory element of the MARCH mnemonic. The Russell PneumoFixTM chest decompression needle is composed of a Veress-tipped needle inserted through an 11cm or 8cm catheter, with a one-way low-pressure release valve. The Veress tip and indicator device assist with the safe insertion with a minimal risk of injuring the underlying lung, whilst the low-pressure, one-way release valve permits the release of tension pneumothorax with minimal potential of subsequent air re-entry. Summary Needle Length – the needle should be long enough to reach the pleural space in an increasingly overweight civilian population and increasingly muscular military population. Most current devices do not meet this requirement Kinking – any product used for needle decompression should be kink resistant. Kinking can cause occlusion and render the device non-functional. Most current devices do not meet this requirement Occlusion – Occlusion by blood, tissue or other materials can block the catheter/cannula and render the device non-functional. Addition of fenestrations/holes in the catheter/cannula will enable the device to be functional even if the primary channel is blocked. Most current devices do not meet this requirement Air entrainment – air influx into the pleural cavity should be avoided. Attached of a one-way valve and capped product would allow air and fluid out of the pleural space but would not allow any air influx. Most current devices do not have this feature Safety tip – the addition of a Veress tipped needle to the device or similar would provide and extra safety dimension to a needle decompression product. Most current devices do not have this feature Learn more about our variety of solutions in the Respiration category. References: [1] Committee on Trauma, ATLS Manual 2012, 9th Edition, American College of Surgeons [2] Zengerink , et al. 2008; [3] Leigh Smith & Harris., 2014; [4] Beckett, A. et al. 2011 Previous Article Next Article