Pub Date : 2026-01-26DOI: 10.1186/s42155-025-00640-0
Sandra Gad, Michael Mohnasky, Nima Kokabi, Zachary Schrank, Austin Evans, Benjamin Haithcock, Danielle O'Hara, Patrick Brown, Andrew Caddell, Christopher Goddard, Bahareh Gholami, Ali Afrasiabi, Alex Villalobos
Pulmonary sequestration (PS) is the second most common pulmonary congenital malformation, which involves non-functional lung tissue that lacks communication with the tracheobronchial tree and is supplied by aberrant systemic arteries, with venous drainage to either the pulmonary or systemic venous system. This anatomic malformation increases patients' risk of recurrent infection due to the lack of robust gas exchange. Hence, prompt intervention is warranted for favourable outcomes. Surgical resection is the gold standard treatment for PS. However, embolization of aberrant arteries prior to surgery is a promising adjunct to reduce the risk of intraoperative hemorrhage associated with the aberrant arterial supply. Here we report a case of a 47-year-old man with suspected symptomatic extralobar sequestration dual feeders from a subclavian common trunk with an anomalous pulmonary arterial connection. The patient underwent preoperative embolization of feeding and draining vessels using low-profile plug occluders. The patient tolerated embolization and surgical resection with < 50 ml blood loss. Two-month post-operative imaging demonstrated the stable position of plug occluders. This case highlights the role of preoperative embolization with low-profile plug occluders as a safe and effective strategy for achieving hemodynamic control and minimizing intraoperative bleeding risk in anatomically complex pulmonary sequestrations.
{"title":"Preoperative embolization of dual arterial supply in extralobar pulmonary sequestration: a case report and literature review.","authors":"Sandra Gad, Michael Mohnasky, Nima Kokabi, Zachary Schrank, Austin Evans, Benjamin Haithcock, Danielle O'Hara, Patrick Brown, Andrew Caddell, Christopher Goddard, Bahareh Gholami, Ali Afrasiabi, Alex Villalobos","doi":"10.1186/s42155-025-00640-0","DOIUrl":"10.1186/s42155-025-00640-0","url":null,"abstract":"<p><p>Pulmonary sequestration (PS) is the second most common pulmonary congenital malformation, which involves non-functional lung tissue that lacks communication with the tracheobronchial tree and is supplied by aberrant systemic arteries, with venous drainage to either the pulmonary or systemic venous system. This anatomic malformation increases patients' risk of recurrent infection due to the lack of robust gas exchange. Hence, prompt intervention is warranted for favourable outcomes. Surgical resection is the gold standard treatment for PS. However, embolization of aberrant arteries prior to surgery is a promising adjunct to reduce the risk of intraoperative hemorrhage associated with the aberrant arterial supply. Here we report a case of a 47-year-old man with suspected symptomatic extralobar sequestration dual feeders from a subclavian common trunk with an anomalous pulmonary arterial connection. The patient underwent preoperative embolization of feeding and draining vessels using low-profile plug occluders. The patient tolerated embolization and surgical resection with < 50 ml blood loss. Two-month post-operative imaging demonstrated the stable position of plug occluders. This case highlights the role of preoperative embolization with low-profile plug occluders as a safe and effective strategy for achieving hemodynamic control and minimizing intraoperative bleeding risk in anatomically complex pulmonary sequestrations.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"9"},"PeriodicalIF":1.5,"publicationDate":"2026-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12835465/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146054555","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-24DOI: 10.1186/s42155-025-00637-9
Fanyun Liu, Jianming Sun, Yikuan Chen, Xiaotong Qi, Hailong Luo
Background: To evaluate outcomes of Castor single-branched stent graft combined with in situ fenestration of the left subclavian artery for aortic arch disease.
Methods: A retrospective analysis of 30 patients undergoing TEVAR with Castor stent that was first implanted with the branch in the left common carotid artery (LCCA) followed by in situ fenestration of the left subclavian (LSA) between March 2022 and March 2024 was conducted. Perioperative and follow-up data were collected and analyzed.
Results: The study retrospective analysis of 30 patients comprised 16 (53.3%) with acute type B aortic dissections, 6 (20%) with thoracic aortic aneurysms, 2 (6.7%) with intramural hematoma, and 6 (20%) with penetrating aortic ulceration. The technical success rate was 96.7% (29/30). One patient required carotid-axillary bypass due to subclavian artery lateral wall opening. There were no cases of mortality, stroke, upper limb ischemia, paraplegia, or stent graft-induced new entry within the 30-day follow-up period. Median hospitalization was 11 (IQR, 9-14) days, with a median follow-up of 12 (IQR, 8-19) months. One patient (3.3%) suffered a fall-related cerebral hemorrhage unrelated to the procedure. Another (3.3%) developed left upper limb ischemia due to stent angulation, corrected with a cover stent. Subclavian artery patency was 96.6% (28/29), and carotid artery patency was 100%. No deaths, endoleaks, or stent migrations occurred.
Conclusion: The Castor stent combined with in situ fenestration is a feasible, effective, and safe strategy for aortic arch disease repair, especially in providing alternative approaches for aortic diseases that require reconstruction in both branches.
{"title":"Outcomes of Castor single-branched stent graft combined with in situ fenestration left subclavian artery in aortic arch disease: a single-center experience.","authors":"Fanyun Liu, Jianming Sun, Yikuan Chen, Xiaotong Qi, Hailong Luo","doi":"10.1186/s42155-025-00637-9","DOIUrl":"10.1186/s42155-025-00637-9","url":null,"abstract":"<p><strong>Background: </strong>To evaluate outcomes of Castor single-branched stent graft combined with in situ fenestration of the left subclavian artery for aortic arch disease.</p><p><strong>Methods: </strong>A retrospective analysis of 30 patients undergoing TEVAR with Castor stent that was first implanted with the branch in the left common carotid artery (LCCA) followed by in situ fenestration of the left subclavian (LSA) between March 2022 and March 2024 was conducted. Perioperative and follow-up data were collected and analyzed.</p><p><strong>Results: </strong>The study retrospective analysis of 30 patients comprised 16 (53.3%) with acute type B aortic dissections, 6 (20%) with thoracic aortic aneurysms, 2 (6.7%) with intramural hematoma, and 6 (20%) with penetrating aortic ulceration. The technical success rate was 96.7% (29/30). One patient required carotid-axillary bypass due to subclavian artery lateral wall opening. There were no cases of mortality, stroke, upper limb ischemia, paraplegia, or stent graft-induced new entry within the 30-day follow-up period. Median hospitalization was 11 (IQR, 9-14) days, with a median follow-up of 12 (IQR, 8-19) months. One patient (3.3%) suffered a fall-related cerebral hemorrhage unrelated to the procedure. Another (3.3%) developed left upper limb ischemia due to stent angulation, corrected with a cover stent. Subclavian artery patency was 96.6% (28/29), and carotid artery patency was 100%. No deaths, endoleaks, or stent migrations occurred.</p><p><strong>Conclusion: </strong>The Castor stent combined with in situ fenestration is a feasible, effective, and safe strategy for aortic arch disease repair, especially in providing alternative approaches for aortic diseases that require reconstruction in both branches.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"7"},"PeriodicalIF":1.5,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12831746/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146042202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-17DOI: 10.1186/s42155-026-00649-z
Sooyeon Joy Kim, Natalie Layden, Scott Fleming, Hasan İlksen Hasan, Amin Bahabri, Sarah Louise Rylance, Gurjeet Singh Dulku
Background: Consistent with global trends, the incidence of placenta accreta spectrum (PAS) is increasing in Australia. Prophylactic internal iliac arterial balloon occlusion (PIIABO) is an endovascular intervention utilised to assist haemorrhage control during caesarean delivery in women with PAS, offering a potentially uterus-preserving alternative to hysterectomy. However, existing outcomes remain heterogeneous. This study aimed to evaluate the endovascular safety of PIIABO with immediate sheath removal in the management of PAS, with a secondary assessment of haemostatic and procedural outcomes.
Materials and methods: A 10-year retrospective, single-centre cohort study of all patients with suspected PAS who underwent PIIABO was conducted with data obtained from electronic medical records and Radiology Information System (RIS)/Picture Archiving and Communication System (PACS).
Results: Fifteen patients underwent PIIABO. The mean maternal age was 34.1 years, with a mean gravidity of 4.2 and a parity of 2.3; all had prior caesarean delivery and 93% had concurrent major placenta praevia (n = 14). Mean gestational age at delivery was 34.9 weeks. Diagnosis was established by MRI (n = 11, 87.5% concordance) and ultrasound (n = 4, 50% concordance). Twelve patients underwent hysterectomy, confirming 1 accreta, 3 increta, and 8 percreta; 3 patients preserved uterus, with intraoperative evidence of percreta (n = 2) or normal placentation (n = 1). Mean estimated blood loss was 2273 mL, and 11 patients received blood transfusions, including four who required ≥ 4 units of packed red blood cells. Mean balloon inflation time was 129.9 min, sheath dwell time 265.5 min, and operating theatre time 265.7 min. Mean dose-area product was 55.03 Gy.cm2 with a mean fluoroscopy time of 10.7 min. Radiation exposure decreased by approximately 90% over the study period with increasing institutional experience. No endovascular complications or reinterventions occurred, and all mothers and neonates were discharged without long-term morbidity.
Conclusion: PIIABO with immediate sheath removal demonstrated favourable procedural outcomes and a low complication rate in patients with PAS, supporting its safe implementation within a multidisciplinary care pathway.
{"title":"Prophylactic bilateral internal iliac artery balloon occlusion with immediate sheath removal for placenta accreta spectrum.","authors":"Sooyeon Joy Kim, Natalie Layden, Scott Fleming, Hasan İlksen Hasan, Amin Bahabri, Sarah Louise Rylance, Gurjeet Singh Dulku","doi":"10.1186/s42155-026-00649-z","DOIUrl":"10.1186/s42155-026-00649-z","url":null,"abstract":"<p><strong>Background: </strong>Consistent with global trends, the incidence of placenta accreta spectrum (PAS) is increasing in Australia. Prophylactic internal iliac arterial balloon occlusion (PIIABO) is an endovascular intervention utilised to assist haemorrhage control during caesarean delivery in women with PAS, offering a potentially uterus-preserving alternative to hysterectomy. However, existing outcomes remain heterogeneous. This study aimed to evaluate the endovascular safety of PIIABO with immediate sheath removal in the management of PAS, with a secondary assessment of haemostatic and procedural outcomes.</p><p><strong>Materials and methods: </strong>A 10-year retrospective, single-centre cohort study of all patients with suspected PAS who underwent PIIABO was conducted with data obtained from electronic medical records and Radiology Information System (RIS)/Picture Archiving and Communication System (PACS).</p><p><strong>Results: </strong>Fifteen patients underwent PIIABO. The mean maternal age was 34.1 years, with a mean gravidity of 4.2 and a parity of 2.3; all had prior caesarean delivery and 93% had concurrent major placenta praevia (n = 14). Mean gestational age at delivery was 34.9 weeks. Diagnosis was established by MRI (n = 11, 87.5% concordance) and ultrasound (n = 4, 50% concordance). Twelve patients underwent hysterectomy, confirming 1 accreta, 3 increta, and 8 percreta; 3 patients preserved uterus, with intraoperative evidence of percreta (n = 2) or normal placentation (n = 1). Mean estimated blood loss was 2273 mL, and 11 patients received blood transfusions, including four who required ≥ 4 units of packed red blood cells. Mean balloon inflation time was 129.9 min, sheath dwell time 265.5 min, and operating theatre time 265.7 min. Mean dose-area product was 55.03 Gy.cm<sup>2</sup> with a mean fluoroscopy time of 10.7 min. Radiation exposure decreased by approximately 90% over the study period with increasing institutional experience. No endovascular complications or reinterventions occurred, and all mothers and neonates were discharged without long-term morbidity.</p><p><strong>Conclusion: </strong>PIIABO with immediate sheath removal demonstrated favourable procedural outcomes and a low complication rate in patients with PAS, supporting its safe implementation within a multidisciplinary care pathway.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"5"},"PeriodicalIF":1.5,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12811181/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145991715","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-17DOI: 10.1186/s42155-025-00644-w
Mohammad A Amarneh, Sara Amro, Kimberly Ferris, Mauricio Amoedo, Ahmad I Alomari
Background: Pelvic and groin lymphoceles and lymphatic leaks remain challenging postsurgical complications. Ethiodized-oil (lipiodol) lymphangiography has been increasingly utilized as a combined diagnostic and therapeutic modality, but published experience with lipiodol-only management in this setting is limited. While transnodal glue embolization is well established, evidence on its long-term outcomes and safety profile remains sparse, with particular concerns regarding the potential risk of lymphedema. These gaps highlight the need for further evaluation of lymphangiography alone as a minimally invasive treatment option.
Materials and methods: This retrospective study included patients who underwent lymphangiography between January 2019 and March 2023 for persistent symptomatic pelvic lymphoceles or groin lymphatic leaks. Imaging findings, drain output, prior interventions, and clinical outcomes were reviewed. Technical success was defined as adequate visualization of the targeted lymphatic vessels. Clinical success was defined as resolution or minimal residual leak without need for further treatment.
Results: Ten patients (5 males, median age, 69 years) underwent lymphangiography for pelvic lymphoceles (n = 7) or groin lymphatic leaks (n = 3). The median interval from surgery to INL was 67.5 days (range, 12-108). Three patients had previously undergone surgical interventions, and four patients had undergone sclerotherapy without clinical improvement before INL was performed. Technical success was achieved in all patients (100%) with identification of lymphatic leak in all patients. Clinical success was achieved in 7 patients (70%) following lymphangiography alone, with a median time to resolution of 5.5 days (range, 5-12 days) and no immediate adverse events.
Conclusions: Lymphangiography using ethiodized oil contrast is a safe, and potentially effective minimally invasive treatment for pelvic and groin lymphatic leaks. These findings support a stepwise management approach, using lymphangiography as a first-line intervention before escalating to intranodal glue embolization.
{"title":"Diagnostic and therapeutic utility of ethiodized oil-based lymphangiography in pelvic and groin lymphatic leaks.","authors":"Mohammad A Amarneh, Sara Amro, Kimberly Ferris, Mauricio Amoedo, Ahmad I Alomari","doi":"10.1186/s42155-025-00644-w","DOIUrl":"10.1186/s42155-025-00644-w","url":null,"abstract":"<p><strong>Background: </strong>Pelvic and groin lymphoceles and lymphatic leaks remain challenging postsurgical complications. Ethiodized-oil (lipiodol) lymphangiography has been increasingly utilized as a combined diagnostic and therapeutic modality, but published experience with lipiodol-only management in this setting is limited. While transnodal glue embolization is well established, evidence on its long-term outcomes and safety profile remains sparse, with particular concerns regarding the potential risk of lymphedema. These gaps highlight the need for further evaluation of lymphangiography alone as a minimally invasive treatment option.</p><p><strong>Materials and methods: </strong>This retrospective study included patients who underwent lymphangiography between January 2019 and March 2023 for persistent symptomatic pelvic lymphoceles or groin lymphatic leaks. Imaging findings, drain output, prior interventions, and clinical outcomes were reviewed. Technical success was defined as adequate visualization of the targeted lymphatic vessels. Clinical success was defined as resolution or minimal residual leak without need for further treatment.</p><p><strong>Results: </strong>Ten patients (5 males, median age, 69 years) underwent lymphangiography for pelvic lymphoceles (n = 7) or groin lymphatic leaks (n = 3). The median interval from surgery to INL was 67.5 days (range, 12-108). Three patients had previously undergone surgical interventions, and four patients had undergone sclerotherapy without clinical improvement before INL was performed. Technical success was achieved in all patients (100%) with identification of lymphatic leak in all patients. Clinical success was achieved in 7 patients (70%) following lymphangiography alone, with a median time to resolution of 5.5 days (range, 5-12 days) and no immediate adverse events.</p><p><strong>Conclusions: </strong>Lymphangiography using ethiodized oil contrast is a safe, and potentially effective minimally invasive treatment for pelvic and groin lymphatic leaks. These findings support a stepwise management approach, using lymphangiography as a first-line intervention before escalating to intranodal glue embolization.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"6"},"PeriodicalIF":1.5,"publicationDate":"2026-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12811176/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145991639","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: Removal of an adhered indwelling catheter in a totally implantable venous access device (TIVAD) can occasionally be challenging, particularly after prolonged implantation. The purpose of this paper is to present a modified endovascular technique for difficult TIVAD removal and to highlight its clinical relevance in cases where the catheter is firmly adhered to the vessel wall, making standard removal methods challenging.
Materials and methods: Between December 2015 and April 2025, a total of 3347 TIVADs were implanted, and 367 removal procedures were conducted. Among these, 355 (96.7%) catheters were successfully removed using the standard technique. Three (0.8%) were removed using the push-in techniques, and one (0.3%) was removed using the contralateral pull-through combined with the sheath-twist technique. In 8 (2.2%), the ipsilateral pull-through technique was required after failure of the initial approaches. The ipsilateral pull-through technique was performed using an introducer sheath and a handmade loop-snare constructed from a guidewire and a seeking catheter. Patient characteristics and procedural data were collected for analysis.
Results: The ipsilateral pull-through technique was successfully used to remove difficult-to-remove TIVADs in 7 of 8 patients. In the remaining patient, the indwelling catheter was firmly adhered to the segment extending from the innominate vein to the superior vena cava, where antegrade flow was absent and numerous collateral vessels were present. Although the occlusion was successfully crossed, catheter removal was aborted due to severe pain and concerns about potential superior vena cava rupture. One procedure-related complication was observed: catheter fracture on follow-up computed tomography in one of the seven successful cases. No other complications were observed. The subclavian vein, innominate vein, and superior vena cava were patent on follow-up computed tomography performed for cancer evaluation. The median indwelling duration in this cohort was 2473 days (interquartile range [IQR], 2017-3002 days), and the median procedure time was 60 min (IQR, 45.8-74.8 min).
Conclusion: The ipsilateral pull-through technique is a useful method to detach adhered catheters during difficult TIVAD removal.
{"title":"Ipsilateral pull-through technique using a handmade loop snare catheter for difficult port catheter removal.","authors":"Tomomasa Matsuo, Atsushi Saiga, Rui Sato, Kazuhisa Asahara, Takeshi Aramaki","doi":"10.1186/s42155-025-00646-8","DOIUrl":"10.1186/s42155-025-00646-8","url":null,"abstract":"<p><strong>Purpose: </strong>Removal of an adhered indwelling catheter in a totally implantable venous access device (TIVAD) can occasionally be challenging, particularly after prolonged implantation. The purpose of this paper is to present a modified endovascular technique for difficult TIVAD removal and to highlight its clinical relevance in cases where the catheter is firmly adhered to the vessel wall, making standard removal methods challenging.</p><p><strong>Materials and methods: </strong>Between December 2015 and April 2025, a total of 3347 TIVADs were implanted, and 367 removal procedures were conducted. Among these, 355 (96.7%) catheters were successfully removed using the standard technique. Three (0.8%) were removed using the push-in techniques, and one (0.3%) was removed using the contralateral pull-through combined with the sheath-twist technique. In 8 (2.2%), the ipsilateral pull-through technique was required after failure of the initial approaches. The ipsilateral pull-through technique was performed using an introducer sheath and a handmade loop-snare constructed from a guidewire and a seeking catheter. Patient characteristics and procedural data were collected for analysis.</p><p><strong>Results: </strong>The ipsilateral pull-through technique was successfully used to remove difficult-to-remove TIVADs in 7 of 8 patients. In the remaining patient, the indwelling catheter was firmly adhered to the segment extending from the innominate vein to the superior vena cava, where antegrade flow was absent and numerous collateral vessels were present. Although the occlusion was successfully crossed, catheter removal was aborted due to severe pain and concerns about potential superior vena cava rupture. One procedure-related complication was observed: catheter fracture on follow-up computed tomography in one of the seven successful cases. No other complications were observed. The subclavian vein, innominate vein, and superior vena cava were patent on follow-up computed tomography performed for cancer evaluation. The median indwelling duration in this cohort was 2473 days (interquartile range [IQR], 2017-3002 days), and the median procedure time was 60 min (IQR, 45.8-74.8 min).</p><p><strong>Conclusion: </strong>The ipsilateral pull-through technique is a useful method to detach adhered catheters during difficult TIVAD removal.</p><p><strong>Level of evidence: </strong>Level 3, Retrospective Study.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"3"},"PeriodicalIF":1.5,"publicationDate":"2026-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12807998/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145985874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-15DOI: 10.1186/s42155-025-00647-7
Erbil Arik, Efe Soydemir, Baris Yer, Onur Taydas, Omer Faruk Topaloglu, Mustafa Ozdemir, Volkan Tasci, Mehmet Halil Ozturk, Bulent Arslan
<p><strong>Background: </strong>Spontaneous abdominal wall hematomas (AWH), typically involving the iliopsoas or rectus sheath, are most often seen in elderly or anticoagulated patients. Their nonspecific presentation can mimic other acute abdominal conditions, delaying diagnosis and management. Computed tomography angiography (CTA), particularly when performed in a multiphasic manner, including venous and delayed phases, provides high sensitivity and specificity in detecting active bleeding. Although subtle arterial bleeding may not always be detectable on arterial-phase imaging alone, this can potentially result in false-negative findings. Treatment options include conservative management, endovascular embolization, and surgical intervention. Identification of the bleeding source on CTA guides targeted embolization during digital subtraction angiography (DSA). In cases where CTA fails to identify the bleeding source, DSA is employed for further assessment and potential embolization. There is no standardized approach in the literature for planning DSA in patients with negative active bleeding signs on preprocedural CTA. This narrative review discusses the clinical presentation, pathophysiology, imaging characteristics, and endovascular treatment options for AWH, with particular emphasis on our procedural approach in patients with negative preprocedural CTA findings.</p><p><strong>Methods: </strong>We conducted a literature search in PubMed and Google Scholar from inception to December 2024, including studies on spontaneous AWH treated with endovascular embolization. Traumatic hematomas and cases managed exclusively with conservative or surgical methods were excluded. Data from four publications (two systematic reviews and two retrospective studies, totaling 460 patients) were synthesized, and our institutional approach to managing CTA-negative AWH was also summarized.</p><p><strong>Results: </strong>A total of 460 patients were identified across 4 publications, including 2 systematic reviews (accounting for 408 patients) and 2 retrospective studies. Technical success rates were 100%. In retrospective studies, clinical success rates ranged from 77 to 100%, whereas in two systematic reviews, the reported rates were 56.3% to 89.5% and 93.1%, respectively. Bleeding detection rates were 47% to 82% for CTA and 79% to 85% for DSA. Targeted arteries for embolization were reported, in order of frequency, as follows: lumbar artery, iliolumbar artery, and deep circumflex iliac artery for posterior AWH and deep inferior epigastric artery for anterior AWH.</p><p><strong>Conclusion: </strong>Endovascular embolization is an effective and safe treatment for spontaneous AWH. DSA remains essential for localization and embolization. In cases with negative CTA, catheterization of arteries anatomically supplying the hematoma is recommended for both diagnostic and therapeutic purposes. Our stepwise, experience-based protocol for CTA-negative cases offers a practical
{"title":"Management of spontaneous abdominal wall hematomas: a narrative review with a focus on CTA-negative endovascular cases.","authors":"Erbil Arik, Efe Soydemir, Baris Yer, Onur Taydas, Omer Faruk Topaloglu, Mustafa Ozdemir, Volkan Tasci, Mehmet Halil Ozturk, Bulent Arslan","doi":"10.1186/s42155-025-00647-7","DOIUrl":"10.1186/s42155-025-00647-7","url":null,"abstract":"<p><strong>Background: </strong>Spontaneous abdominal wall hematomas (AWH), typically involving the iliopsoas or rectus sheath, are most often seen in elderly or anticoagulated patients. Their nonspecific presentation can mimic other acute abdominal conditions, delaying diagnosis and management. Computed tomography angiography (CTA), particularly when performed in a multiphasic manner, including venous and delayed phases, provides high sensitivity and specificity in detecting active bleeding. Although subtle arterial bleeding may not always be detectable on arterial-phase imaging alone, this can potentially result in false-negative findings. Treatment options include conservative management, endovascular embolization, and surgical intervention. Identification of the bleeding source on CTA guides targeted embolization during digital subtraction angiography (DSA). In cases where CTA fails to identify the bleeding source, DSA is employed for further assessment and potential embolization. There is no standardized approach in the literature for planning DSA in patients with negative active bleeding signs on preprocedural CTA. This narrative review discusses the clinical presentation, pathophysiology, imaging characteristics, and endovascular treatment options for AWH, with particular emphasis on our procedural approach in patients with negative preprocedural CTA findings.</p><p><strong>Methods: </strong>We conducted a literature search in PubMed and Google Scholar from inception to December 2024, including studies on spontaneous AWH treated with endovascular embolization. Traumatic hematomas and cases managed exclusively with conservative or surgical methods were excluded. Data from four publications (two systematic reviews and two retrospective studies, totaling 460 patients) were synthesized, and our institutional approach to managing CTA-negative AWH was also summarized.</p><p><strong>Results: </strong>A total of 460 patients were identified across 4 publications, including 2 systematic reviews (accounting for 408 patients) and 2 retrospective studies. Technical success rates were 100%. In retrospective studies, clinical success rates ranged from 77 to 100%, whereas in two systematic reviews, the reported rates were 56.3% to 89.5% and 93.1%, respectively. Bleeding detection rates were 47% to 82% for CTA and 79% to 85% for DSA. Targeted arteries for embolization were reported, in order of frequency, as follows: lumbar artery, iliolumbar artery, and deep circumflex iliac artery for posterior AWH and deep inferior epigastric artery for anterior AWH.</p><p><strong>Conclusion: </strong>Endovascular embolization is an effective and safe treatment for spontaneous AWH. DSA remains essential for localization and embolization. In cases with negative CTA, catheterization of arteries anatomically supplying the hematoma is recommended for both diagnostic and therapeutic purposes. Our stepwise, experience-based protocol for CTA-negative cases offers a practical ","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"4"},"PeriodicalIF":1.5,"publicationDate":"2026-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12808008/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145985845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: This report describes an embolization technique using a steerable sheath and an Amplatzer vascular plug 2 (AVP 2) to treat a wide-necked aneurysm located at the ostium of the renal artery. Given this particular location, directly attached to the aortic wall, similar to a saccular aneurysm of the abdominal aorta, stent placement or embolization using coils or liquid agents was not feasible.
Case presentation: A 45-year-old patient with a long medical history including heterozygous SC sickle cell disease, systemic lupus erythematosus, and a left iliac fossa kidney transplant presented with a partially thrombosed right renal artery aneurysm of 45-mm diameter. The aneurysm was located at the ostium of the renal artery that was occluded downstream. The aneurysm was directly attached to the aortic wall with a wide neck measured at 8 mm. Use of coils or liquid agents was not possible because of a very high risk of extra-target embolization. Lack of a patent right renal artery downstream precluded placement of a covered stent. Following multidisciplinary discussion, and due to the patient's high risk for aortic abdominal surgery, endovascular management with embolization was decided. Embolization was performed under local anesthesia, using fluoroscopic guidance and a cone-beam computed tomography three-dimensional road map. Following common right femoral artery access, a 7F steerable sheath was used to catheterize the aneurysm. An AVP 2 was then passed through the sheath in the aneurysm. Particular attention was paid to deploying the last disc of the AVP 2 in the aortic lumen to ensure closure of the aneurysm neck. Final aortic angiogram confirmed exclusion of the aneurysm. There were no intraoperative or postoperative complications. At computed tomography performed 7 months later, the AVP 2 remained in position, and the aneurysm was excluded and partially decreased in size.
Conclusions: In an anatomical presentation that was not a candidate for stent placement or classic embolization techniques, deployment of an AVP 2 using a steerable sheath successfully excluded the aneurysm. This procedure, performed under local anesthesia, obviated the need for abdominal aortic surgical repair or for an aortic stent graft.
{"title":"Embolization of a wide-necked aneurysm of the renal artery ostium using an Amplatzer vascular plug 2: a case report.","authors":"Mario Ghosn, Haytham Derbel, Youssef Zaarour, Félix Wei, Vania Tacher, Hicham Kobeiter","doi":"10.1186/s42155-025-00607-1","DOIUrl":"10.1186/s42155-025-00607-1","url":null,"abstract":"<p><strong>Background: </strong>This report describes an embolization technique using a steerable sheath and an Amplatzer vascular plug 2 (AVP 2) to treat a wide-necked aneurysm located at the ostium of the renal artery. Given this particular location, directly attached to the aortic wall, similar to a saccular aneurysm of the abdominal aorta, stent placement or embolization using coils or liquid agents was not feasible.</p><p><strong>Case presentation: </strong>A 45-year-old patient with a long medical history including heterozygous SC sickle cell disease, systemic lupus erythematosus, and a left iliac fossa kidney transplant presented with a partially thrombosed right renal artery aneurysm of 45-mm diameter. The aneurysm was located at the ostium of the renal artery that was occluded downstream. The aneurysm was directly attached to the aortic wall with a wide neck measured at 8 mm. Use of coils or liquid agents was not possible because of a very high risk of extra-target embolization. Lack of a patent right renal artery downstream precluded placement of a covered stent. Following multidisciplinary discussion, and due to the patient's high risk for aortic abdominal surgery, endovascular management with embolization was decided. Embolization was performed under local anesthesia, using fluoroscopic guidance and a cone-beam computed tomography three-dimensional road map. Following common right femoral artery access, a 7F steerable sheath was used to catheterize the aneurysm. An AVP 2 was then passed through the sheath in the aneurysm. Particular attention was paid to deploying the last disc of the AVP 2 in the aortic lumen to ensure closure of the aneurysm neck. Final aortic angiogram confirmed exclusion of the aneurysm. There were no intraoperative or postoperative complications. At computed tomography performed 7 months later, the AVP 2 remained in position, and the aneurysm was excluded and partially decreased in size.</p><p><strong>Conclusions: </strong>In an anatomical presentation that was not a candidate for stent placement or classic embolization techniques, deployment of an AVP 2 using a steerable sheath successfully excluded the aneurysm. This procedure, performed under local anesthesia, obviated the need for abdominal aortic surgical repair or for an aortic stent graft.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"1"},"PeriodicalIF":1.5,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12779785/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145913906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-07DOI: 10.1186/s42155-025-00622-2
Robert Terzis, Robert Wawer Matos Reimer, David Maintz, Erkan Celik
Background: Intravascular lithotripsy (IVL) is an emerging technique for modifying heavily calcified arterial lesions, with primary application in peripheral arteries. We report the use of IVL for lesion preparation prior to stenting in a patient with severely calcified superior mesenteric artery (SMA) stenosis.
Case presentation: A 66-year-old man with type I adenocarcinoma of the esophagogastric junction (AEG Type I) and neoadjuvant FLOT chemotherapy was scheduled for Ivor Lewis esophagectomy. Preoperative CT angiography (CTA) revealed a high-grade ostial SMA stenosis due to extensive atherosclerotic calcification. To mitigate the risk of postoperative mesenteric hypoperfusion, percutaneous endovascular revascularization was performed. Following initial predilatation, IVL using a Shockwave 5.5 × 60 mm balloon catheter was employed for lesion preparation. Subsequently, an 8.0 × 24 mm balloon-expandable stent was successfully deployed with low-grade residual stenosis and no complications.
Conclusion: This case demonstrates that IVL represents a feasible and effective adjunct in the management of severely calcified visceral arterial lesions. It facilitates adequate lesion preparation and enables full stent expansion, even when the IVL balloon diameter is notably smaller than the stent diameter. This potentially represents a less traumatic approach to the vessel than alternative techniques. IVL may therefore be considered a therapeutic option in selected patients.
{"title":"Pre-stenting lesion preparation using shockwave intravascular lithotripsy in severely calcified superior mesenteric artery stenosis.","authors":"Robert Terzis, Robert Wawer Matos Reimer, David Maintz, Erkan Celik","doi":"10.1186/s42155-025-00622-2","DOIUrl":"10.1186/s42155-025-00622-2","url":null,"abstract":"<p><strong>Background: </strong>Intravascular lithotripsy (IVL) is an emerging technique for modifying heavily calcified arterial lesions, with primary application in peripheral arteries. We report the use of IVL for lesion preparation prior to stenting in a patient with severely calcified superior mesenteric artery (SMA) stenosis.</p><p><strong>Case presentation: </strong>A 66-year-old man with type I adenocarcinoma of the esophagogastric junction (AEG Type I) and neoadjuvant FLOT chemotherapy was scheduled for Ivor Lewis esophagectomy. Preoperative CT angiography (CTA) revealed a high-grade ostial SMA stenosis due to extensive atherosclerotic calcification. To mitigate the risk of postoperative mesenteric hypoperfusion, percutaneous endovascular revascularization was performed. Following initial predilatation, IVL using a Shockwave 5.5 × 60 mm balloon catheter was employed for lesion preparation. Subsequently, an 8.0 × 24 mm balloon-expandable stent was successfully deployed with low-grade residual stenosis and no complications.</p><p><strong>Conclusion: </strong>This case demonstrates that IVL represents a feasible and effective adjunct in the management of severely calcified visceral arterial lesions. It facilitates adequate lesion preparation and enables full stent expansion, even when the IVL balloon diameter is notably smaller than the stent diameter. This potentially represents a less traumatic approach to the vessel than alternative techniques. IVL may therefore be considered a therapeutic option in selected patients.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"9 1","pages":"2"},"PeriodicalIF":1.5,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12779857/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145913922","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1186/s42155-025-00638-8
Leonardo Pasquetti, Edoardo Pasqui, Giuseppe Galzerano, Elisa Lazzeri, Bruno Gargiulo, Gianmarco de Donato
{"title":"Salvage of undeflatable intra-stent angioplasty-balloon-catheter with direct percutaneous needle puncture.","authors":"Leonardo Pasquetti, Edoardo Pasqui, Giuseppe Galzerano, Elisa Lazzeri, Bruno Gargiulo, Gianmarco de Donato","doi":"10.1186/s42155-025-00638-8","DOIUrl":"10.1186/s42155-025-00638-8","url":null,"abstract":"","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"119"},"PeriodicalIF":1.5,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12756208/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145865980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-31DOI: 10.1186/s42155-025-00639-7
Ruben Geevarghese, Stephen B Solomon, Francois H Cornelis
Background: This study evaluates the current evidence on the use of cone-beam computed tomography (CBCT) combined with advanced planning and guidance (APG) software in transarterial embolization for acute hemorrhage and reviews our institution's preliminary experience of use in emergency settings.
Methods: A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. PubMed, SCOPUS, and Embase were searched to identify studies using CBCT with software for transarterial embolization of hemorrhage. Inclusion criteria focused on studies utilizing CBCT and APG software for hemorrhage management, with data extracted on demographics, hemorrhage locations, equipment/software specifications, technical success and procedural metrics. Additionally, we report a single-center review of patient outcomes using CBCT with multi-organ APG software (EmboASSIST with Virtual Injection, GE HealthCare, Chicago, IL, USA).
Results: Nine studies met the inclusion criteria, including 71 patients. The most common site of bleeding was the lower gastrointestinal (GI) tract (62%). The mean technical success rate of embolization utilizing CBCT with APG was 94.3% (range: 82-100%). Three studies reported procedure time (mean 98.9 min, range 50-146 min), and two studies reported fluoroscopy time (mean 27.1 min, range 25-29.1 min). In our initial experience, all six cases were technically successful with favorable outcomes.
Conclusions: CBCT with APG software is a feasible and effective tool for hemorrhage embolization in emergency settings. Its potential ability to improve bleeding detection compared to digital subtraction angiography (DSA) may lead to reduced procedure time, lower radiation exposure, and enhanced patient outcomes.
背景:本研究评估了锥束计算机断层扫描(CBCT)结合先进计划和指导(APG)软件在急性出血经动脉栓塞治疗中的应用的现有证据,并回顾了我院在急诊情况下使用CBCT的初步经验。方法:按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行系统评价。检索PubMed, SCOPUS和Embase,以确定使用CBCT软件进行经动脉栓塞出血的研究。纳入标准侧重于利用CBCT和APG软件进行出血管理的研究,并提取了人口统计学、出血位置、设备/软件规格、技术成功和程序指标等数据。此外,我们报告了使用CBCT和多器官APG软件(EmboASSIST with Virtual Injection, GE HealthCare, Chicago, IL, USA)对患者结果的单中心回顾。结果:9项研究符合纳入标准,包括71例患者。最常见的出血部位是下胃肠道(62%)。应用CBCT联合APG栓塞的平均技术成功率为94.3%(范围:82-100%)。3项研究报告了手术时间(平均98.9分钟,范围50-146分钟),2项研究报告了透视时间(平均27.1分钟,范围25-29.1分钟)。在我们最初的经验中,所有六个病例在技术上都是成功的,结果良好。结论:CBCT配合APG软件是急诊出血栓塞的一种可行、有效的工具。与数字减影血管造影(DSA)相比,其改善出血检测的潜在能力可能会缩短手术时间,降低辐射暴露,并提高患者的预后。系统评价注册:NIHR-PROSPERO CRD 42024619227。
{"title":"Emergency embolization of acute hemorrhage: cone-beam computed tomography with advanced planning and guidance software-a systematic review and case series.","authors":"Ruben Geevarghese, Stephen B Solomon, Francois H Cornelis","doi":"10.1186/s42155-025-00639-7","DOIUrl":"10.1186/s42155-025-00639-7","url":null,"abstract":"<p><strong>Background: </strong>This study evaluates the current evidence on the use of cone-beam computed tomography (CBCT) combined with advanced planning and guidance (APG) software in transarterial embolization for acute hemorrhage and reviews our institution's preliminary experience of use in emergency settings.</p><p><strong>Methods: </strong>A systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. PubMed, SCOPUS, and Embase were searched to identify studies using CBCT with software for transarterial embolization of hemorrhage. Inclusion criteria focused on studies utilizing CBCT and APG software for hemorrhage management, with data extracted on demographics, hemorrhage locations, equipment/software specifications, technical success and procedural metrics. Additionally, we report a single-center review of patient outcomes using CBCT with multi-organ APG software (EmboASSIST with Virtual Injection, GE HealthCare, Chicago, IL, USA).</p><p><strong>Results: </strong>Nine studies met the inclusion criteria, including 71 patients. The most common site of bleeding was the lower gastrointestinal (GI) tract (62%). The mean technical success rate of embolization utilizing CBCT with APG was 94.3% (range: 82-100%). Three studies reported procedure time (mean 98.9 min, range 50-146 min), and two studies reported fluoroscopy time (mean 27.1 min, range 25-29.1 min). In our initial experience, all six cases were technically successful with favorable outcomes.</p><p><strong>Conclusions: </strong>CBCT with APG software is a feasible and effective tool for hemorrhage embolization in emergency settings. Its potential ability to improve bleeding detection compared to digital subtraction angiography (DSA) may lead to reduced procedure time, lower radiation exposure, and enhanced patient outcomes.</p><p><strong>Systematic review registration: </strong>NIHR-PROSPERO CRD 42024619227.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"120"},"PeriodicalIF":1.5,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12756198/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145866489","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}