Pub Date : 2025-12-13DOI: 10.1186/s42155-025-00619-x
Simone Hammer, Anna Dorn, Michael Christian Doppler, Florian Zeman, Christian Stroszczynski, Dirk Grothues, Birgit Knoppke, Stefan M Brunner, Hans Jürgen Schlitt, Wibke Uller
Background: Portal vein (PV) stenosis (PVS) is a common issue after pediatric liver transplantation (LT) and may be associated with severe morbidity. The purpose of this retrospective matched cohort study was to compare graft and patient survival after percutaneous angioplasty (PTA) for PVS in pediatric patients under 7 years with a control cohort without PVS and a cohort with chronic portal vein thrombosis (PVT).
Methods: This study included 31 patients with PVS (intervention group) and 62 patients without PVS (control group). Furthermore, 9 patients with chronic PVT were evaluated (negative control group). Primary endpoints were graft and patient survival. Secondary endpoints were comparison of liver function and clinical course (signs of portal hypertension), procedure-related complications, and long-term patency after PTA.
Results: Graft survival was comparable between the intervention and control group (p = 0.380), with 7-year survival rates of 93% (95% confidence interval [CI]: 84%, 100%) and 88% (95% CI: 80%, 97%), respectively. Graft survival was significantly higher in the intervention group compared to the negative control group p = 0.032; 7-year graft survival was 75% (95% CI: 50%, 100%). Patient survival was significantly higher in the intervention group (p = 0.034), with a 100% 7-year survival rate (95% CI: 100%, 100%) compared to 86% (95% CI: 78%, 96%) in the control group. Survival was reduced in the negative control group compared to the intervention group (p = 0.053). Seven-year patient survival in the negative control group was 88% (95% CI: 67%, 100%). There was one minor procedure-related complication (1/31 [3%]); long-term patency was 100%.
Conclusions: Seven-year graft and patient survival after PTA for PVS were on par with that of patients without PVS. Graft survival was lower for patients with chronic PVT. Clinical course and liver function after PTA were comparable to patients without PVS. These findings, together with the low complication rate and high long-term patency, provide additional evidence supporting the efficacy of PTA in the management of PVS.
{"title":"Graft and patient survival following angioplasty for post-transplant portal vein stenosis in children under 7 years: a matched case-control study.","authors":"Simone Hammer, Anna Dorn, Michael Christian Doppler, Florian Zeman, Christian Stroszczynski, Dirk Grothues, Birgit Knoppke, Stefan M Brunner, Hans Jürgen Schlitt, Wibke Uller","doi":"10.1186/s42155-025-00619-x","DOIUrl":"10.1186/s42155-025-00619-x","url":null,"abstract":"<p><strong>Background: </strong>Portal vein (PV) stenosis (PVS) is a common issue after pediatric liver transplantation (LT) and may be associated with severe morbidity. The purpose of this retrospective matched cohort study was to compare graft and patient survival after percutaneous angioplasty (PTA) for PVS in pediatric patients under 7 years with a control cohort without PVS and a cohort with chronic portal vein thrombosis (PVT).</p><p><strong>Methods: </strong>This study included 31 patients with PVS (intervention group) and 62 patients without PVS (control group). Furthermore, 9 patients with chronic PVT were evaluated (negative control group). Primary endpoints were graft and patient survival. Secondary endpoints were comparison of liver function and clinical course (signs of portal hypertension), procedure-related complications, and long-term patency after PTA.</p><p><strong>Results: </strong>Graft survival was comparable between the intervention and control group (p = 0.380), with 7-year survival rates of 93% (95% confidence interval [CI]: 84%, 100%) and 88% (95% CI: 80%, 97%), respectively. Graft survival was significantly higher in the intervention group compared to the negative control group p = 0.032; 7-year graft survival was 75% (95% CI: 50%, 100%). Patient survival was significantly higher in the intervention group (p = 0.034), with a 100% 7-year survival rate (95% CI: 100%, 100%) compared to 86% (95% CI: 78%, 96%) in the control group. Survival was reduced in the negative control group compared to the intervention group (p = 0.053). Seven-year patient survival in the negative control group was 88% (95% CI: 67%, 100%). There was one minor procedure-related complication (1/31 [3%]); long-term patency was 100%.</p><p><strong>Conclusions: </strong>Seven-year graft and patient survival after PTA for PVS were on par with that of patients without PVS. Graft survival was lower for patients with chronic PVT. Clinical course and liver function after PTA were comparable to patients without PVS. These findings, together with the low complication rate and high long-term patency, provide additional evidence supporting the efficacy of PTA in the management of PVS.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"113"},"PeriodicalIF":1.5,"publicationDate":"2025-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12701888/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145745369","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 : 2025-12-10DOI: 10.1186/s42155-025-00625-z
Warren Clements, Abigail Chenoweth, Salam Findakly, Tuan D Phan, Mark Bolger, William P L Bradley, William Kemp, Stuart K Roberts, Matthew W Lukies, Gerard S Goh, Tim Joseph, Christine Ball, Jim Koukounaras
Background: After a gastric variceal rupture, clinical practice guidelines recommend either transjugular intrahepatic portosystemic shunt (TIPS) or balloon-occluded retrograde transvenous obliteration (BRTO) as interventional options for secondary prevention. This study aimed to generate and compare TIPS and BRTO costing data to calculate the secondary prevention cost following gastric variceal bleeding, to encourage consideration of resource cost within decision-making.
Methods: All costs were included for patients treated between 1 January 2017 and 1 January 2024. Data on procedure, non-procedure, and ward costs were collected. Ward costs were only calculated for elective admissions to reduce bias from inpatient emergency procedures. All costs were measured from a healthcare system perspective and included direct and indirect expenses where relevant. A 5% indexation for inflation was applied to non-fixed costs from 2017 to the 2024 cost year. The cost to prevent gastric re-bleeding was then calculated by adjusting the costing data generated based on existing outcome data in the literature, utilising the largest existing meta-analysis on the efficacy of TIPS and BRTO in preventing re-bleeding.
Results: There were 38 patients in the study cohort, with a mean age 56.8 years (SD 12.0), and 25 patients (66%) were male. TIPS was performed in 27 patients (71%). The TIPS and BRTO groups had similar mean age, proportion of male sex, CP grading, and proportions of elective admissions. The median total cost for TIPS was AUD$11,922 (range $6307-$53,432), while the median total cost for BRTO was AUD$3632 (range $1818-$5174), p < 0.001. The adjusted cost to prevent future gastric re-bleed using TIPS was AUD$14,803, while the cost to prevent re-bleed using BRTO was AUD$3896.
Conclusion: The cost magnitude of both TIPS and BRTO was both low in an Australian model, and both remain good options for patients. However, the use of BRTO was associated with significantly lower upfront procedural costs than for TIPS for secondary prevention of gastric variceal bleeding. Costs should form a key component of the value of IR to modern healthcare.
{"title":"A comparative cost analysis of TIPS and BRTO for secondary prophylaxis in gastric variceal bleeding.","authors":"Warren Clements, Abigail Chenoweth, Salam Findakly, Tuan D Phan, Mark Bolger, William P L Bradley, William Kemp, Stuart K Roberts, Matthew W Lukies, Gerard S Goh, Tim Joseph, Christine Ball, Jim Koukounaras","doi":"10.1186/s42155-025-00625-z","DOIUrl":"10.1186/s42155-025-00625-z","url":null,"abstract":"<p><strong>Background: </strong>After a gastric variceal rupture, clinical practice guidelines recommend either transjugular intrahepatic portosystemic shunt (TIPS) or balloon-occluded retrograde transvenous obliteration (BRTO) as interventional options for secondary prevention. This study aimed to generate and compare TIPS and BRTO costing data to calculate the secondary prevention cost following gastric variceal bleeding, to encourage consideration of resource cost within decision-making.</p><p><strong>Methods: </strong>All costs were included for patients treated between 1 January 2017 and 1 January 2024. Data on procedure, non-procedure, and ward costs were collected. Ward costs were only calculated for elective admissions to reduce bias from inpatient emergency procedures. All costs were measured from a healthcare system perspective and included direct and indirect expenses where relevant. A 5% indexation for inflation was applied to non-fixed costs from 2017 to the 2024 cost year. The cost to prevent gastric re-bleeding was then calculated by adjusting the costing data generated based on existing outcome data in the literature, utilising the largest existing meta-analysis on the efficacy of TIPS and BRTO in preventing re-bleeding.</p><p><strong>Results: </strong>There were 38 patients in the study cohort, with a mean age 56.8 years (SD 12.0), and 25 patients (66%) were male. TIPS was performed in 27 patients (71%). The TIPS and BRTO groups had similar mean age, proportion of male sex, CP grading, and proportions of elective admissions. The median total cost for TIPS was AUD$11,922 (range $6307-$53,432), while the median total cost for BRTO was AUD$3632 (range $1818-$5174), p < 0.001. The adjusted cost to prevent future gastric re-bleed using TIPS was AUD$14,803, while the cost to prevent re-bleed using BRTO was AUD$3896.</p><p><strong>Conclusion: </strong>The cost magnitude of both TIPS and BRTO was both low in an Australian model, and both remain good options for patients. However, the use of BRTO was associated with significantly lower upfront procedural costs than for TIPS for secondary prevention of gastric variceal bleeding. Costs should form a key component of the value of IR to modern healthcare.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"109"},"PeriodicalIF":1.5,"publicationDate":"2025-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12696224/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145716703","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 : 2025-12-09DOI: 10.1186/s42155-025-00636-w
Robert A Morgan
{"title":"The journey continues to make CVIR Endovascular THE open-access journal for all endovascular specialists: a few words from the new editor in chief.","authors":"Robert A Morgan","doi":"10.1186/s42155-025-00636-w","DOIUrl":"10.1186/s42155-025-00636-w","url":null,"abstract":"","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"108"},"PeriodicalIF":1.5,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12690021/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145709920","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 : 2025-12-09DOI: 10.1186/s42155-025-00623-1
Qian Yu, Patrick Tran, Ethan Ungchusri, Kunal Karani, Abdul Khan, Mikin Patel, Osman Ahmed, Thuong Van Ha, Jonathan Lorenz, Steven Zangan, Brian Funaki, Rakesh Navuluri
Purpose: To evaluate the safety and effectiveness of microfibrillar collagen paste (MCP), coils, and coils combined with gelatin sponge for transhepatic access tract embolization following portal vein islet cell transplant.
Methods: A retrospective review was conducted at a single institution between January 2008 and October 2024, including 20, 28, and 21 consecutive islet cell transplant procedures requiring transhepatic access embolization with MCP, coils, and coil plus gelatin sponge, respectively. All procedures were performed via a right portal vein branch. MCP was performed using Avitene (BD). The average number of coils required in the coil plus gelatin sponge and coil-only groups were 1.8 and 1.6 coils per procedure, respectively. All patients were placed on therapeutic anticoagulation during the procedure and for at least two weeks post-transplant. Medical records were reviewed to compare laboratory results, portal venous pressures, post-procedure liver ultrasounds, and 30-day hemorrhagic events across the three groups.
Results: All procedures were technically successful. However, one instance of coil migration into a portal vein branch occurred in the coil plus gelatin sponge group (1/28, 3.5%). Baseline hemoglobin, platelet counts, and partial thromboplastin time did not differ significantly between groups (p > 0.05). A statistically significant lower international normalized ratio (INR) was observed in the MCP group compared to the gelatin sponge and coil-only groups (1.0 vs. 1.1 vs. 1.1, p = 0.0036 and 0.004). No statistically significant differences were found in hemoglobin changes, post-transplant portal venous pressures, or post-embolization hemorrhagic events (p > 0.05). One patient in the coil plus gelatin sponge group developed a large subcapsular hematoma (1/27, 3.7%), while another in the MCP group experienced a large right hemothorax (1/20, 5.0%).
Conclusion: MCP, coils, and coil plus gelatin sponge are similarly effective for transhepatic access closure following islet cell transplant in anticoagulated patients. However, coil embolization may require multiple coils and carries a risk of migration.
目的:评价微纤维胶原蛋白膏(MCP)、线圈、线圈联合明胶海绵在门静脉胰岛细胞移植后经肝通路栓塞中的安全性和有效性。方法:回顾性回顾2008年1月至2024年10月在一家机构进行的一项研究,包括20例、28例和21例连续的胰岛细胞移植手术,分别需要经肝通道栓塞MCP、线圈和线圈加明胶海绵。所有手术均通过右门静脉分支进行。采用Avitene (BD)进行MCP。在线圈加明胶海绵组和仅线圈组中,每个程序所需的平均线圈数分别为1.8和1.6线圈。所有患者在手术过程中和移植后至少两周内都接受治疗性抗凝治疗。回顾医疗记录,比较三组患者的实验室结果、门静脉压、术后肝脏超声检查和30天出血事件。结果:所有手术在技术上均成功。然而,线圈向门静脉分支迁移的一例发生在线圈加明胶海绵组(1/ 28,3.5%)。基线血红蛋白、血小板计数和部分凝血活酶时间在两组间无显著差异(p < 0.05)。MCP组的国际标准化比率(INR)较明胶海绵组和纯软糖组有统计学意义的降低(1.0 vs. 1.1 vs. 1.1, p = 0.0036和0.004)。两组在血红蛋白变化、移植后门静脉压力或栓塞后出血事件方面无统计学差异(p < 0.05)。线圈加明胶海绵组1例患者出现大的包膜下血肿(1/ 27,3.7%),而MCP组1例患者出现大的右侧血胸(1/ 20,5.0%)。结论:MCP、线圈和线圈加明胶海绵对抗凝患者胰岛细胞移植后经肝通道关闭的效果相似。然而,线圈栓塞可能需要多个线圈,并有迁移的风险。
{"title":"Transhepatic access closure for islet cell transplant in anticoagulated patients: a comparison of microfibrillar collagen paste, coils, and coil plus gel foam.","authors":"Qian Yu, Patrick Tran, Ethan Ungchusri, Kunal Karani, Abdul Khan, Mikin Patel, Osman Ahmed, Thuong Van Ha, Jonathan Lorenz, Steven Zangan, Brian Funaki, Rakesh Navuluri","doi":"10.1186/s42155-025-00623-1","DOIUrl":"10.1186/s42155-025-00623-1","url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the safety and effectiveness of microfibrillar collagen paste (MCP), coils, and coils combined with gelatin sponge for transhepatic access tract embolization following portal vein islet cell transplant.</p><p><strong>Methods: </strong>A retrospective review was conducted at a single institution between January 2008 and October 2024, including 20, 28, and 21 consecutive islet cell transplant procedures requiring transhepatic access embolization with MCP, coils, and coil plus gelatin sponge, respectively. All procedures were performed via a right portal vein branch. MCP was performed using Avitene (BD). The average number of coils required in the coil plus gelatin sponge and coil-only groups were 1.8 and 1.6 coils per procedure, respectively. All patients were placed on therapeutic anticoagulation during the procedure and for at least two weeks post-transplant. Medical records were reviewed to compare laboratory results, portal venous pressures, post-procedure liver ultrasounds, and 30-day hemorrhagic events across the three groups.</p><p><strong>Results: </strong>All procedures were technically successful. However, one instance of coil migration into a portal vein branch occurred in the coil plus gelatin sponge group (1/28, 3.5%). Baseline hemoglobin, platelet counts, and partial thromboplastin time did not differ significantly between groups (p > 0.05). A statistically significant lower international normalized ratio (INR) was observed in the MCP group compared to the gelatin sponge and coil-only groups (1.0 vs. 1.1 vs. 1.1, p = 0.0036 and 0.004). No statistically significant differences were found in hemoglobin changes, post-transplant portal venous pressures, or post-embolization hemorrhagic events (p > 0.05). One patient in the coil plus gelatin sponge group developed a large subcapsular hematoma (1/27, 3.7%), while another in the MCP group experienced a large right hemothorax (1/20, 5.0%).</p><p><strong>Conclusion: </strong>MCP, coils, and coil plus gelatin sponge are similarly effective for transhepatic access closure following islet cell transplant in anticoagulated patients. However, coil embolization may require multiple coils and carries a risk of migration.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"107"},"PeriodicalIF":1.5,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12690018/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145710030","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 : 2025-11-29DOI: 10.1186/s42155-025-00628-w
Jonathan Hanly, Hugo C Temperley, Christopher O'Loughlin, Niall O'Sullivan, Marliza O'Dwyer, Richard Sweeney, Nazia Kahn, Robert Craig, Kevin P Sheahan
Introduction: The field of interventional radiology (IR) has witnessed rapid advancements, with an increasing emphasis on complex and high-risk procedures. Increasingly, new IR treatments are becoming both available and indicated for patients with complex comorbidities. As a result, anaesthetic expertise has become essential to ensure patient safety, optimise procedural outcomes, and manage perioperative complications. Despite this growing demand, dedicated anaesthetic teams in IR remain limited, which leads to concerns regarding patient safety and procedural efficiency.
Methods: A comprehensive literature search was conducted across multiple databases, including PubMed, Embase, and the Cochrane Library, to identify studies published up to September 2024 that examined the expanding scope of IR, with a focus on the increasing need for anaesthetic support. This commentary draws on the existing literature to discuss the interaction between anaesthesia and interventional radiology, with particular attention to procedural sedation, pain management, and the care of high-risk patients. This commentary also evaluates workforce limitations, logistical challenges, and potential benefits of increased anaesthetic involvement in IR.
Findings: Existing literature demonstrates the significant benefits of anaesthetic involvement in IR. The presence of an anaesthesiologist was associated with reduced procedural risks, enhanced patient satisfaction, and quicker postoperative recovery times. Despite these benefits, many IR departments remain under-resourced in terms of dedicated anaesthetic staff. Furthermore, training programmes for anaesthesiologists rarely focus on the unique demands of IR, creating a gap in specialist care. The growing complexity and risk associated with IR procedures underscore the need for expanded anaesthetic support in this field. Hospitals and healthcare systems should prioritise the integration of anaesthetic teams into IR, investing in specialist training and workforce expansion. Doing so can improve patient outcomes and the overall efficiency of IR procedures, reducing procedural risks, increasing patient satisfaction, and facilitating quicker postoperative recovery times.
{"title":"Highlighting the increasing need for anaesthetic support in interventional radiology.","authors":"Jonathan Hanly, Hugo C Temperley, Christopher O'Loughlin, Niall O'Sullivan, Marliza O'Dwyer, Richard Sweeney, Nazia Kahn, Robert Craig, Kevin P Sheahan","doi":"10.1186/s42155-025-00628-w","DOIUrl":"10.1186/s42155-025-00628-w","url":null,"abstract":"<p><strong>Introduction: </strong>The field of interventional radiology (IR) has witnessed rapid advancements, with an increasing emphasis on complex and high-risk procedures. Increasingly, new IR treatments are becoming both available and indicated for patients with complex comorbidities. As a result, anaesthetic expertise has become essential to ensure patient safety, optimise procedural outcomes, and manage perioperative complications. Despite this growing demand, dedicated anaesthetic teams in IR remain limited, which leads to concerns regarding patient safety and procedural efficiency.</p><p><strong>Methods: </strong>A comprehensive literature search was conducted across multiple databases, including PubMed, Embase, and the Cochrane Library, to identify studies published up to September 2024 that examined the expanding scope of IR, with a focus on the increasing need for anaesthetic support. This commentary draws on the existing literature to discuss the interaction between anaesthesia and interventional radiology, with particular attention to procedural sedation, pain management, and the care of high-risk patients. This commentary also evaluates workforce limitations, logistical challenges, and potential benefits of increased anaesthetic involvement in IR.</p><p><strong>Findings: </strong>Existing literature demonstrates the significant benefits of anaesthetic involvement in IR. The presence of an anaesthesiologist was associated with reduced procedural risks, enhanced patient satisfaction, and quicker postoperative recovery times. Despite these benefits, many IR departments remain under-resourced in terms of dedicated anaesthetic staff. Furthermore, training programmes for anaesthesiologists rarely focus on the unique demands of IR, creating a gap in specialist care. The growing complexity and risk associated with IR procedures underscore the need for expanded anaesthetic support in this field. Hospitals and healthcare systems should prioritise the integration of anaesthetic teams into IR, investing in specialist training and workforce expansion. Doing so can improve patient outcomes and the overall efficiency of IR procedures, reducing procedural risks, increasing patient satisfaction, and facilitating quicker postoperative recovery times.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"105"},"PeriodicalIF":1.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662969/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145642629","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 : 2025-11-27DOI: 10.1186/s42155-025-00624-0
George Rahmani
{"title":"Comment on \"Underreporting of inferior vena cava filter characteristics in diagnostic radiology reports: a call for standardization\".","authors":"George Rahmani","doi":"10.1186/s42155-025-00624-0","DOIUrl":"https://doi.org/10.1186/s42155-025-00624-0","url":null,"abstract":"","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"102"},"PeriodicalIF":1.5,"publicationDate":"2025-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12657689/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145642642","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: Femoropopliteal diffuse calcified occlusions (FPDCOs) are challenging, especially in high-bleeding-risk patients for whom a stentless strategy is preferred. We introduce FRAP-CROSS, combining Fracking and Rendezvous-PIERCE, to achieve intracalcium guidewire crossing and facilitate stentless revascularization.
Materials and methods: When bidirectional intracalcium wiring fails across dense calcification in FPDCO, FRAP-CROSS is applied. Fracking is initially performed by inserting a 20-gauge metal needle into a guidewire-uncrossable plaque and applying hydraulic pressure to create microfractures, facilitating subsequent guidewire crossing. If device tracking remains unsuccessful after guidewire passage, Rendezvous-PIERCE is employed. An 18-gauge needle is advanced toward the intralesional guidewire tip, and the guidewire is externalized through the needle (Needle Rendezvous). A 20-gauge needle is then advanced over the externalized guidewire to create a lumen within the calcification (inner PIERCE). After successful all-intracalcium crossing, balloon angioplasty is performed. Inadequate expansion prompts additional Fracking alone or with Jetstream atherectomy (JET-Frack). Drug-coated balloon (DCB) angioplasty completes the stentless strategy.
Results: A 90-year-old man at high bleeding risk with bilateral FPDCOs underwent FRAP-CROSS. The right limb required three Fracking and two Rendezvous-PIERCE; the left required four Fracking and two Rendezvous-PIERCE, respectively, with adjunctive JET-Frack. Following DCB-based stentless treatment, final angiography and intravascular ultrasound confirmed adequate luminal expansion and blood flow in both limbs, without major complications.
Conclusion: FRAP-CROSS provides a practical approach to achieve all-intracalcium guidewire crossing and stentless revascularization in complex FPDCOs. Further studies should assess its safety and long-term outcomes.
{"title":"FRAP-CROSS technique: Fracking and Rendezvous-PIERCE for intracalcium crossing in femoropopliteal diffuse calcified occlusions.","authors":"Takuya Haraguchi, Masanaga Tsujimoto, Ricky Wang-Hei Leung, Yaowen Chang, Yuhei Kasai, Daisuke Hachinohe, Yoshifumi Kashima","doi":"10.1186/s42155-025-00626-y","DOIUrl":"https://doi.org/10.1186/s42155-025-00626-y","url":null,"abstract":"<p><strong>Background: </strong>Femoropopliteal diffuse calcified occlusions (FPDCOs) are challenging, especially in high-bleeding-risk patients for whom a stentless strategy is preferred. We introduce FRAP-CROSS, combining Fracking and Rendezvous-PIERCE, to achieve intracalcium guidewire crossing and facilitate stentless revascularization.</p><p><strong>Materials and methods: </strong>When bidirectional intracalcium wiring fails across dense calcification in FPDCO, FRAP-CROSS is applied. Fracking is initially performed by inserting a 20-gauge metal needle into a guidewire-uncrossable plaque and applying hydraulic pressure to create microfractures, facilitating subsequent guidewire crossing. If device tracking remains unsuccessful after guidewire passage, Rendezvous-PIERCE is employed. An 18-gauge needle is advanced toward the intralesional guidewire tip, and the guidewire is externalized through the needle (Needle Rendezvous). A 20-gauge needle is then advanced over the externalized guidewire to create a lumen within the calcification (inner PIERCE). After successful all-intracalcium crossing, balloon angioplasty is performed. Inadequate expansion prompts additional Fracking alone or with Jetstream atherectomy (JET-Frack). Drug-coated balloon (DCB) angioplasty completes the stentless strategy.</p><p><strong>Results: </strong>A 90-year-old man at high bleeding risk with bilateral FPDCOs underwent FRAP-CROSS. The right limb required three Fracking and two Rendezvous-PIERCE; the left required four Fracking and two Rendezvous-PIERCE, respectively, with adjunctive JET-Frack. Following DCB-based stentless treatment, final angiography and intravascular ultrasound confirmed adequate luminal expansion and blood flow in both limbs, without major complications.</p><p><strong>Conclusion: </strong>FRAP-CROSS provides a practical approach to achieve all-intracalcium guidewire crossing and stentless revascularization in complex FPDCOs. Further studies should assess its safety and long-term outcomes.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"103"},"PeriodicalIF":1.5,"publicationDate":"2025-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12657688/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145642644","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 : 2025-11-27DOI: 10.1186/s42155-025-00620-4
Kimberly Wei, Susan Shamimi-Noori, Theodore G Drivas, Scott O Trerotola
Background: To assess how patients interpret and adhere to the International HHT Guidelines' recommendation to avoid intravenous (IV) air and to evaluate whether misinterpretation of this guidance as a strict requirement for in-line bubble filters may inadvertently hinder access to care. An anonymous 15-question survey was distributed to 7000 members of the HHT Research Network. The survey assessed awareness of the guideline, perceived necessity of bubble filter use, and the practical consequences of filter use. Responses were excluded if incomplete or submitted by individuals under 18 years old.
Results: Of the 596 responses received (9% response rate), 446 met inclusion criteria. Most respondents (79%) were aware of the guideline, and 66% interpreted it as requiring use of an IV bubble filter. Notably, 16% of respondents reported refusing care, and 25% reported delaying treatment-most often patient-initiated-due to perceived filter requirements. The interventions affected included essential and, in some cases, urgent care. In total, 20 respondents (4%) reported experiencing a transient ischemic attack (TIA) during IV therapy; two of these occurred despite filter use, and none resulted in permanent deficits. Patients who did not use filters were significantly less likely to report difficulty accessing care (p < 0.05).
Conclusions: Although the guideline advises caution in avoiding IV air, many patients interpret it as mandating bubble filter use. This misunderstanding has been linked to delays in necessary care, increased patient frustration, and limited treatment access. These findings underscore the importance of clearer communication and education around guideline intent to mitigate unintended consequences.
{"title":"Patient interpretation and implementation of air embolism prevention guidelines in hereditary hemorrhagic telangiectasia (HHT): a survey-based study.","authors":"Kimberly Wei, Susan Shamimi-Noori, Theodore G Drivas, Scott O Trerotola","doi":"10.1186/s42155-025-00620-4","DOIUrl":"https://doi.org/10.1186/s42155-025-00620-4","url":null,"abstract":"<p><strong>Background: </strong>To assess how patients interpret and adhere to the International HHT Guidelines' recommendation to avoid intravenous (IV) air and to evaluate whether misinterpretation of this guidance as a strict requirement for in-line bubble filters may inadvertently hinder access to care. An anonymous 15-question survey was distributed to 7000 members of the HHT Research Network. The survey assessed awareness of the guideline, perceived necessity of bubble filter use, and the practical consequences of filter use. Responses were excluded if incomplete or submitted by individuals under 18 years old.</p><p><strong>Results: </strong>Of the 596 responses received (9% response rate), 446 met inclusion criteria. Most respondents (79%) were aware of the guideline, and 66% interpreted it as requiring use of an IV bubble filter. Notably, 16% of respondents reported refusing care, and 25% reported delaying treatment-most often patient-initiated-due to perceived filter requirements. The interventions affected included essential and, in some cases, urgent care. In total, 20 respondents (4%) reported experiencing a transient ischemic attack (TIA) during IV therapy; two of these occurred despite filter use, and none resulted in permanent deficits. Patients who did not use filters were significantly less likely to report difficulty accessing care (p < 0.05).</p><p><strong>Conclusions: </strong>Although the guideline advises caution in avoiding IV air, many patients interpret it as mandating bubble filter use. This misunderstanding has been linked to delays in necessary care, increased patient frustration, and limited treatment access. These findings underscore the importance of clearer communication and education around guideline intent to mitigate unintended consequences.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"104"},"PeriodicalIF":1.5,"publicationDate":"2025-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12657698/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145642637","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 : 2025-11-13DOI: 10.1186/s42155-025-00615-1
Jack M Bell, Hugo C Temperley, Benjamin M Mac Curtain, Nicholas A Clausen, Robert S Doyle, Noel E Donlon, Kevin Sheahan, Michael J Lee
Background: Parastomal varices are a rare but serious complication in patients with portal hypertension, characterised by bleeding that can be life-threatening in a predominantly comorbid population. Traditional surgical approaches to managing parastomal varices are associated with high morbidity and recurrence rates, prompting increased interest in minimally invasive techniques. This systematic review aims to evaluate the efficacy and safety of interventional radiology (IR) procedures, including transjugular intrahepatic portosystemic shunt (TIPS), sclerotherapy and embolisation, in managing parastomal varices.
Methods: A comprehensive literature search was conducted across multiple databases, including MEDLINE, EMBASE and Web of Science, to identify studies published up to January 2025 that reported IR interventions for parastomal varices. Data were extracted on patient demographics, procedural success, recurrence rates and complications. A pooled proportions meta-analysis was performed.
Results: Five studies, encompassing 45 patients, met the inclusion criteria. The pooled technical success rate of IR procedures was 91.3%, with a clinical success rate of 80.5% over a mean follow-up of 618.4 days. The pooled mean proportion of rebleeding, predominantly minor and non-life-threatening, was 36.4%. TIPS showed the highest efficacy, but is traditionally associated with increased procedural risks compared to other interventional radiology methods.
Conclusion: IR offers a highly effective and safe alternative to traditional surgical management for parastomal varices in contemporary terms. The low recurrence and complication rates highlight the potential of IR ab initio as a first-line treatment; consequently, we advocate for its use, particularly in patients unsuitable for surgery in the minimally invasive era.
背景:造口旁静脉曲张是门静脉高压患者的一种罕见但严重的并发症,其特征是出血,在主要合并症人群中可危及生命。传统的手术方法治疗造口旁静脉曲张具有较高的发病率和复发率,这促使人们对微创技术的兴趣增加。本系统综述旨在评估介入放射学(IR)治疗的有效性和安全性,包括经颈静脉肝内门静脉系统分流术(TIPS)、硬化治疗和栓塞治疗吻合口旁静脉曲张。方法:对多个数据库(包括MEDLINE、EMBASE和Web of Science)进行全面的文献检索,以确定截至2025年1月发表的关于口旁静脉曲张IR干预的研究。提取患者人口统计学、手术成功率、复发率和并发症的数据。进行合并比例荟萃分析。结果:5项研究,包括45例患者,符合纳入标准。IR手术的总技术成功率为91.3%,临床成功率为80.5%,平均随访618.4天。再出血的合并平均比例为36.4%,主要是轻微的和不危及生命的。TIPS显示出最高的疗效,但与其他介入放射学方法相比,传统上与手术风险增加有关。结论:相对于传统手术治疗造口旁静脉曲张,IR是一种高效、安全的治疗方法。低复发率和并发症率突出了从头开始IR作为一线治疗的潜力;因此,我们提倡使用它,特别是在微创时代不适合手术的患者。系统评价注册:PROSPERO CRD42024627470。
{"title":"The contemporary management of parastomal varices by interventional radiology: a systematic review.","authors":"Jack M Bell, Hugo C Temperley, Benjamin M Mac Curtain, Nicholas A Clausen, Robert S Doyle, Noel E Donlon, Kevin Sheahan, Michael J Lee","doi":"10.1186/s42155-025-00615-1","DOIUrl":"10.1186/s42155-025-00615-1","url":null,"abstract":"<p><strong>Background: </strong>Parastomal varices are a rare but serious complication in patients with portal hypertension, characterised by bleeding that can be life-threatening in a predominantly comorbid population. Traditional surgical approaches to managing parastomal varices are associated with high morbidity and recurrence rates, prompting increased interest in minimally invasive techniques. This systematic review aims to evaluate the efficacy and safety of interventional radiology (IR) procedures, including transjugular intrahepatic portosystemic shunt (TIPS), sclerotherapy and embolisation, in managing parastomal varices.</p><p><strong>Methods: </strong>A comprehensive literature search was conducted across multiple databases, including MEDLINE, EMBASE and Web of Science, to identify studies published up to January 2025 that reported IR interventions for parastomal varices. Data were extracted on patient demographics, procedural success, recurrence rates and complications. A pooled proportions meta-analysis was performed.</p><p><strong>Results: </strong>Five studies, encompassing 45 patients, met the inclusion criteria. The pooled technical success rate of IR procedures was 91.3%, with a clinical success rate of 80.5% over a mean follow-up of 618.4 days. The pooled mean proportion of rebleeding, predominantly minor and non-life-threatening, was 36.4%. TIPS showed the highest efficacy, but is traditionally associated with increased procedural risks compared to other interventional radiology methods.</p><p><strong>Conclusion: </strong>IR offers a highly effective and safe alternative to traditional surgical management for parastomal varices in contemporary terms. The low recurrence and complication rates highlight the potential of IR ab initio as a first-line treatment; consequently, we advocate for its use, particularly in patients unsuitable for surgery in the minimally invasive era.</p><p><strong>Systematic review registration: </strong>PROSPERO CRD42024627470.</p>","PeriodicalId":52351,"journal":{"name":"CVIR Endovascular","volume":"8 1","pages":"101"},"PeriodicalIF":1.5,"publicationDate":"2025-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12615892/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145508054","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}