Abstract:Background
Pneumothorax is a common complication of cardiac implantable electronic device (CIED) procedures. There is a paucity of data on the natural history and management of a CIED-associated pneumothorax.
Methods
This is a single-centre retrospective study of all consecutive patients with a CIED-associated pneumothorax between March 2010 and March 2020. Pneumothorax size was determined on all chest x-rays after device implantation and before chest tube insertion (if… Show more
“…Caudal imaging may also allow for rationalization in routine use of CXR following CIED insertion. In a recent review of the yield of CXR after CIED insertion, pneumothoraces were found to occur in 1.9% cases 21 . Given the markedly lower incidence of pneumothorax associated with caudal imaging in our study, it may be suitable to consider a more tailored approach to post‐procedural CXR, for instance only in the setting of operator‐reported access challenges or patient‐reported symptoms.…”
Section: Discussionmentioning
confidence: 69%
“…In a recent review of the yield of CXR after CIED insertion, pneumothoraces were found to occur in 1.9% cases. 21 Given the markedly lower incidence of pneumothorax associated with caudal imaging in our study, it may be suitable to consider a more tailored approach to post-procedural CXR, for instance only in the setting of operator-reported access challenges or patient-reported symptoms. One limitation of the caudal fluoroscopic (and other oblique) view is the potential for increased radiation scatter which results in greater radiation exposure to the proceduralist.…”
Section: Puncture Of the Extrathoracic Subclavian Vein (Subclavian Ve...mentioning
BackgroundPneumothorax is a well‐recognized complication of cardiac implantable electronic device (CIED) insertion. While AP fluoroscopy alone is the most commonly imaging technique for subclavian or axillary access, caudal fluoroscopy (angle 40°) is routinely used at our institution. The caudal view provides additional separation of the first rib and clavicle and may reduce the risk of pneumothorax. We assessed outcomes at our institution of AP and caudal fluoroscopic guided pacing lead insertion.MethodsRetrospective cohort study of consecutive patients undergoing transvenous lead insertion for pacemakers, defibrillators, and cardiac resynchronization therapy devices between 2011 and 2023. Both de novo and lead replacement/upgrade procedures were included. Data were extracted from operative, radiology, and discharge reports. All patients underwent postprocedure chest radiography.ResultsThree thousand two hundred fifty‐two patients underwent insertion of pacing leads between February 2011 and March 2023. Mean age was 71.1 years (range 16–102) and 66.7% were male. Most (n = 2536; 78.0%) procedures used caudal guidance to obtain venous access, while 716 (22.0%) procedures used AP guidance alone. Pneumothoraxes occurred in five (0.2%) patients in the caudal group and five (0.7%) patients in the AP group (p = .03). Subclavian contrast venography was performed less frequently in the caudal group (26.2% vs. 42.7%, p < .01).ConclusionCaudal fluoroscopy for axillary/subclavian access is associated with a lower rate of pneumothorax and contrast venography compared with an AP approach.
“…Caudal imaging may also allow for rationalization in routine use of CXR following CIED insertion. In a recent review of the yield of CXR after CIED insertion, pneumothoraces were found to occur in 1.9% cases 21 . Given the markedly lower incidence of pneumothorax associated with caudal imaging in our study, it may be suitable to consider a more tailored approach to post‐procedural CXR, for instance only in the setting of operator‐reported access challenges or patient‐reported symptoms.…”
Section: Discussionmentioning
confidence: 69%
“…In a recent review of the yield of CXR after CIED insertion, pneumothoraces were found to occur in 1.9% cases. 21 Given the markedly lower incidence of pneumothorax associated with caudal imaging in our study, it may be suitable to consider a more tailored approach to post-procedural CXR, for instance only in the setting of operator-reported access challenges or patient-reported symptoms. One limitation of the caudal fluoroscopic (and other oblique) view is the potential for increased radiation scatter which results in greater radiation exposure to the proceduralist.…”
Section: Puncture Of the Extrathoracic Subclavian Vein (Subclavian Ve...mentioning
BackgroundPneumothorax is a well‐recognized complication of cardiac implantable electronic device (CIED) insertion. While AP fluoroscopy alone is the most commonly imaging technique for subclavian or axillary access, caudal fluoroscopy (angle 40°) is routinely used at our institution. The caudal view provides additional separation of the first rib and clavicle and may reduce the risk of pneumothorax. We assessed outcomes at our institution of AP and caudal fluoroscopic guided pacing lead insertion.MethodsRetrospective cohort study of consecutive patients undergoing transvenous lead insertion for pacemakers, defibrillators, and cardiac resynchronization therapy devices between 2011 and 2023. Both de novo and lead replacement/upgrade procedures were included. Data were extracted from operative, radiology, and discharge reports. All patients underwent postprocedure chest radiography.ResultsThree thousand two hundred fifty‐two patients underwent insertion of pacing leads between February 2011 and March 2023. Mean age was 71.1 years (range 16–102) and 66.7% were male. Most (n = 2536; 78.0%) procedures used caudal guidance to obtain venous access, while 716 (22.0%) procedures used AP guidance alone. Pneumothoraxes occurred in five (0.2%) patients in the caudal group and five (0.7%) patients in the AP group (p = .03). Subclavian contrast venography was performed less frequently in the caudal group (26.2% vs. 42.7%, p < .01).ConclusionCaudal fluoroscopy for axillary/subclavian access is associated with a lower rate of pneumothorax and contrast venography compared with an AP approach.
“…A similar result was reported by Faruqi et al, and the mean pain scores for simple aspiration and intercostal tube drainage were 1.6 and 4.0 respectively [ 17 ]. Moreover, the lack of indwelling catheter not only alleviated the irritable sensation that occurred owning to the presence of a foreign body object inside the body, which enabled patients to mobilize freely without limitation or fear of tube dislodgement, but also reduced the clinical burden of tube care on the nursing stuff and the medical costs [ 23 ]. Finally, no complication occurred in patients who underwent vacuum bottle plus non-tunneled catheter drainage in this study.…”
Background
Iatrogenic pneumothorax is common after thoracic procedures. For patients with pneumothorax larger than 15%, simple aspiration is suggested. Although vacuum bottle plus non-tunneled catheter drainage has been performed in many institutions, its safety and efficacy remain to be assessed.
Methods
Through this prospective cohort study (NCT03724721), we evaluated the safety and efficacy of vacuum bottle plus non-tunneled catheter drainage. Patients older than 20 years old who developed post-procedural pneumothorax were enrolled. A non-tunneled catheter was placed at the intersection of the midclavicular line and the second intercostal space. A 3-way stopcock, a drainage set, and a digital pressure gauge were connected. The stopcock was manipulated to connect the pleural space to the pressure gauge for measurement of end-expiration intrapleural pressure or to the vacuum bottle for air drainage. The rate of successful drainage, the end-expiration intrapleural pressure before, during, and after the procedure and the duration of hospitalization were recorded.
Results
From August 2018 to February 2020, 21 patients underwent vacuum bottle plus catheter drainage (intervention group) and 31 patients received conservative treatment (control group). The end-expiration intrapleural pressure of all patients remained less than − 20 cmH2O during drainage. No procedure related complication was observed. Large pneumothorax (≥ 15%) was associated with higher risk of persistent air leak (Odds ratio 12, 95% CI 1.2–569.7). Vacuum bottle assisted air drainage yielded shorter event-free duration than that of conservative treatment (2 days vs 5 days [interquartile range 1–4 days vs 3–7 days], p < .05). Vacuum bottle assisted air drainage also help identifying patients with persistent pneumothorax and necessitate the subsequent management. The event-free duration of persistent air leak in the intervention group was also comparable with that of conservative treatment (5 days vs 5 days [interquartile range 5–8 days vs 3–7 days], p = .45).
Conclusions
Vacuum bottle plus catheter drainage of iatrogenic pneumothorax is a safe and efficient procedure. It may be considered as an alternative management of stable post-procedural pneumothorax with size larger than 15%.
Trial registration The study protocol was approved by the Research Ethics Committee of National Taiwan University Hospital (No. 201805105DINA) on 6th August, 2018. The first participant was enrolled on 23rd August, 2018 after Research Ethics Committee approval. This clinical trial complete registration at U.S. National Library of Medicine clinicaltrials.gov with identifier NCT03724721 and URL: https://clinicaltrials.gov/ct2/show/NCT03724721 on 30th October, 2018.
“…A patient can manifest signs and symptoms during the procedure or up to 72 hours after implantation ( 20 ). Every patient should receive a chest x-ray within 4 h post-procedure ( 30 ). Patients discharged from the hospital shortly after outpatient procedures should remain in contact with the CIED center ( 17 ).…”
Cardiac implantable electronic devices (CIED) including pacemakers (PM), implantable cardioverter defibrillators (ICD), and cardiac resynchronized therapy (CRT) have become the mainstay of therapy for many cardiac conditions, consequently drawing attention to the risks and benefits of these procedures. Although CIED implantation is usually a safe procedure, pneumothorax remains an important complication and may contribute to increased morbidity, mortality, length of stay, and hospital costs. On the other hand, pneumopericardium and pneumomediastinum are rare but potentially fatal complications. Accordingly, a high degree of awareness about these complications is important. Pneumothorax almost always occurs on the ipsilateral side of implantation. The development of contralateral pneumothorax is uncommon and may be undetected on an initial chest radiograph. Contralateral pneumothorax with concurrent pneumopericardium and pneumomediastinum is much rarer. We describe a rare case of concurrent right-sided pneumothorax with pneumopericardium and pneumomediastinum after left-sided pacemaker implantation and highlight the risk factors, management, and possible ways to prevent the complications.
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