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1.
Urol Case Rep ; 40: 101907, 2022 Jan.
Article in English | MEDLINE | ID: mdl-34745899

ABSTRACT

Testicular varicocele is a dilatation of the pampiniform plexus. It is a common clinical problem affecting 15% of adolescents and adults that may be associated with pain and discomfort, and can affect fertility. Varicocele treatment is associated with a significant improvement in sperm parameters, and pregnancy rate. For endovascular treatment Fibered embolization coils are commonly utilized. Complications associated with coil insertion are rare, but can have serious consequences. Here, we presenting the first reported case of a retroperitoneal abscess following testicular vein coil embolization. The patient underwent successful laparoscopic removal the infected coil followed by full recovery.

2.
Br J Radiol ; 93(1106): 20190781, 2020 Feb 01.
Article in English | MEDLINE | ID: mdl-31868522

ABSTRACT

OBJECTIVE: Sedation for pediatric patients undergoing interventional procedures in radiology is in increasing demand. Once only anesthesiology-performed, there is a demand for sedation services to perform sedations for these procedures. However, the safety of performing long sedations by non-anesthesiologists in interventional radiology has not been reported. This pilot study aimed at describing a single center's experience and outcome with sedation. METHODS: This study reviews the sedations performed at a single center by a pediatric emergency physician who performed the sedation. The results regarding safety and satisfaction were reviewed. RESULTS: A total of 52 sedations were documented. Four cases of significant adverse events and three adverse events occurred. In all cases, the procedures were completed. None of the patients required intubation or admission following the sedation. There was high satisfaction by the interventional radiologists. CONCLUSION: This small pilot study shows that sedations for procedures in interventional radiology can be performed safely and successfully by dedicated non-anesthesiology sedation services. This may be considered as an alternative when anesthesiology service is not available. ADVANCES IN KNOWLEDGE: This small, single center pilot study examines the safety of sedation by a non-anesthesiologist for interventional radiology procedures. This may offer an additional method of performing procedures in the pediatric population while anesthesia is not readily available.


Subject(s)
Conscious Sedation/methods , Emergency Medicine/statistics & numerical data , Vascular Malformations/surgery , Adolescent , Anesthesiologists , Child , Child, Preschool , Conscious Sedation/adverse effects , Emergency Medicine/standards , Epidemiologic Methods , Female , Humans , Infant , Male , Patient Safety
3.
J Vasc Interv Radiol ; 28(8): 1196-1197, 2017 08.
Article in English | MEDLINE | ID: mdl-28735939
4.
World J Hepatol ; 8(20): 858-62, 2016 Jul 18.
Article in English | MEDLINE | ID: mdl-27458506

ABSTRACT

The United States Food and Drug Administration recently warned that the direct acting antiviral (DAA) combination hepatitis C virus (HCV) treatment of Paritaprevir, Ombitasvir, Dasabuvir, Ritonavir, and Ribavirin (PODr + R) can cause severe liver injury in patients with advanced liver disease. Drug induced liver injury was observed in a small number of patients with decompensated cirrhosis treated with other DAAs, but has not been reported in patients with compensated cirrhosis. We report a case of a 74-year-old woman with chronic HCV and Child-Pugh class A cirrhosis (compensated cirrhosis) treated with PODr + R. The patient presented on day 14 of PODr + R therapy with jaundice and new-onset ascites. Her total bilirubin level increased to 23 mg/dL and international normalized ratio rose to 1.65, while aminotransferase levels remained relatively stable. Hepatitis C treatment was discontinued on day 24 and she gradually recovered. Follow-up testing showed that she achieved a sustained virologic response. In conclusion, hepatic decompensation developed within two weeks of starting treatment with PODr + R in a patient with Child-Pugh class A cirrhosis and was characterized by jaundice and ascites with stable aminotransferase levels. Careful monitoring is warranted in patients with HCV-related cirrhosis treated with PODr + R.

5.
Harefuah ; 154(3): 171-4, 212, 211, 2015 Mar.
Article in Hebrew | MEDLINE | ID: mdl-25962246

ABSTRACT

In this case report we describe a boy with extrahepatic biliary atresia who underwent a Kasai hepatoportoenterostomy at six weeks of age. Beginning several weeks post-op, he had recurrent cholangitis inadequately controlled by various antibiotic prophylaxis regimens. Imaging revealed the development of several bile lakes in the liver hilum. Due to the recurrent nature of his cholangitis, and some evidence of acutely impaired biliary drainage, he underwent a refashioning of his portoenterostomy with resultant improved drainage. However, shortly thereafter, the patient developed ongoing fever and anemia. Culture of the bile lake aspirate grew multiresistant Klebsiella and a 6 week course of parenteral meropenume controlled his fever and his anemia improved. Following treatment cessation his fever and anemia returned. A biliary drain was inserted into his larger bile lake and following another course of parenteral antibiotics he has remained free of clinically detected cholangitis despite ongoing contamination of drained bile fluid. The development of bile lakes after Kasai hepatoportoenterostomy is not an uncommon finding. This have been associated with worse prognosis including increased incidence of cholangitis. Often, conservative treatment with prophylactic antibiotics suffices, however, in rare cases, more aggressive intervention may be considered including percutaneous bile drainage or surgical management. The benefit of these management strategies must be balanced with the potential gain regarding quality of life and delaying transplant, on an individual basis.


Subject(s)
Bile , Biliary Atresia/surgery , Portoenterostomy, Hepatic/methods , Postoperative Complications/pathology , Anti-Bacterial Agents/therapeutic use , Cholangitis/etiology , Drug Resistance, Multiple, Bacterial , Humans , Infant , Klebsiella Infections/drug therapy , Klebsiella Infections/microbiology , Male , Meropenem , Thienamycins/therapeutic use
6.
J Vasc Surg ; 62(1): 115-22, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25770987

ABSTRACT

OBJECTIVE: Prosthetic grafts continue to be required for hemodialysis access when the options for native fistulas have been exhausted. The inferior long-term patency of grafts makes the possibility of preventing occlusion with heparin-bonded grafts an attractive alternative. We carried out a prospective randomized study to compare the patency of standard grafts with heparin-bonded grafts. METHODS: Patients with end-stage renal failure requiring a prosthetic access were randomized to receive either a standard expanded polytetrafluorethylene (ePTFE) graft or a heparin-bonded ePTFE graft. Patients were enrolled from June 2007 until November 2011 and were followed up until July 2013, when the study concluded. RESULTS: In this study, 160 patients were randomized and followed up for a median of 23.5 months. No patient was lost to follow-up. Primary patency was 35% and 14% for heparin-bonded grafts and 29% and 12% for standard ePTFE grafts at 6 and 12 months, respectively (P = .48). Assisted primary patency was 54%, 41%, and 27% for heparin-bonded grafts and 41%, 30%, and 23% for standard grafts at 12, 24, and 36 months, respectively (P = .12). Secondary patency was 83%, 83%, and 81% for heparin-bonded grafts and 81%, 73%, and 68% for standard grafts at 12, 24, and 36 months, respectively (P = .33). There were significantly fewer thromboses in heparin-bonded grafts during the first 5 months (P = .020). Of 80 standard grafts, 24 were eventually abandoned vs 17 heparin-bonded grafts (P = .188). Bleeding complications, infections, and intervention rates were similar in both groups. CONCLUSIONS: Heparin-bonded grafts demonstrated a trend to improved patency, but the difference was not statistically significant. Heparin-bonded grafts had a significantly lower early thrombosis rate that was sustained only for the first 5 months of follow-up.


Subject(s)
Anticoagulants/administration & dosage , Arteriovenous Shunt, Surgical/instrumentation , Blood Vessel Prosthesis Implantation/instrumentation , Blood Vessel Prosthesis , Coated Materials, Biocompatible , Heparin/administration & dosage , Kidney Failure, Chronic/therapy , Renal Dialysis , Adult , Aged , Aged, 80 and over , Arteriovenous Shunt, Surgical/adverse effects , Blood Vessel Prosthesis Implantation/adverse effects , Female , Graft Occlusion, Vascular/etiology , Graft Occlusion, Vascular/physiopathology , Graft Occlusion, Vascular/surgery , Humans , Israel , Male , Middle Aged , Polytetrafluoroethylene , Prospective Studies , Prosthesis Design , Reoperation , Risk Factors , Thrombosis/etiology , Thrombosis/physiopathology , Thrombosis/surgery , Time Factors , Treatment Outcome , Vascular Patency
7.
J Vasc Access ; 16 Suppl 9: S34-9, 2015.
Article in English | MEDLINE | ID: mdl-25751548

ABSTRACT

Arteriovenous (AV) grafts are required for hemodialysis access when options for native fistulas have been fully exhausted, where they continue to play an important role in hemodialysis patients, offering a better alternative to central vein catheters. When planning autogenous accesses using Doppler ultrasound, adequate arterial inflow and venous outflow must be consciously preserved for future access creation with grafts. Efforts to improve graft patency include changing graft configuration, graft biology and hemodynamics. Industry offers early cannulation grafts to reduce central catheter use and a bioengineered graft is undergoing clinical studies. Although the outcome of AV grafts is inferior to fistulas, grafts can provide long-term hemodialysis access that is a better alternative to central venous catheters. AV grafts have significant drawbacks, mainly poor patency, infection and cost but also have some advantages: early maturation, ease of creation and needling and widespread availability. The outcome of AV graft surgery is variable from center to center. The primary patency rate for AV grafts is 58% at 6 months and the secondary patency rate is 76% at 6 months and 55% at 18 months. There are centers of excellence that report a 1 year secondary patency rate of up to 91%. In this review of the use of AV grafts for hemodialysis access in the upper extremities, technical issues involved in planning the access and performing the surgery in its different configurations are discussed and the role of surveillance and maintenance with their attendant surgical and radiological interventions is described.


Subject(s)
Arteriovenous Shunt, Surgical/methods , Blood Vessel Prosthesis Implantation/methods , Kidney Failure, Chronic/therapy , Renal Dialysis , Upper Extremity/blood supply , Arteriovenous Shunt, Surgical/adverse effects , Arteriovenous Shunt, Surgical/instrumentation , Blood Vessel Prosthesis , Blood Vessel Prosthesis Implantation/adverse effects , Blood Vessel Prosthesis Implantation/instrumentation , Graft Occlusion, Vascular/etiology , Graft Occlusion, Vascular/physiopathology , Humans , Kidney Failure, Chronic/diagnosis , Prosthesis Design , Risk Factors , Time Factors , Treatment Outcome , Vascular Patency
8.
Eur Radiol ; 25(6): 1639-45, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25523457

ABSTRACT

OBJECTIVES: To investigate the effect of a radiation reduction program on total dose, fluoroscopy dose per second corrected for body habitus and degree of collimation in left varicocele embolizations (LVE). METHODS: A radiation reduction program for LVE was implemented, consisting of a technique minimizing fluoroscopy time, using low-dose presets, virtual collimation, and virtual patient positioning. Height, weight, fluoroscopy time, kerma area product (KAP) and reference air kerma (Ka,r) were recorded for 100 consecutive cases satisfying the inclusion criteria. For each patient, a device specific dose correction factor, determined using a phantom, was used to standardize the KAP to that of the cylindrical diameter of the standard man and a collimation index was derived from the KAP and Ka,r. RESULTS: Median fluoroscopy time was 3 minutes (mean 4.5, range 1-23.8). Median KAP was 0.54 Gy/cm(2) (mean 0.82, range 0.12-6.52). There was a significant decrease in KAP/second corrected for cylindrical diameter (p < 0.001) and the collimation index (p < 0.001) over time. CONCLUSIONS: This study shows that a dedicated dose reduction program can achieve very low total radiation dose rates for LVE. The significant decrease in collimation index and standardized KAP per second during this study suggest a learning curve for collimation. KEY POINTS: • Left varicocele embolization can be performed with very low radiation doses. • The most effective real time radiation reduction measure is collimation. • There is a learning curve to achieving optimal collimation.


Subject(s)
Embolization, Therapeutic , Models, Biological , Radiation Dosage , Varicocele/diagnostic imaging , Varicocele/therapy , Adolescent , Adult , Fluoroscopy , Humans , Male , Middle Aged , Phantoms, Imaging , Time Factors , Young Adult
9.
J Vasc Interv Radiol ; 24(9): 1280-7; quiz 1288, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23806382

ABSTRACT

PURPOSE: To assess long-term outcomes of stent grafts in patients with symptomatic central venous stenoses and occlusions ipsilateral to hemodialysis grafts or fistulas. MATERIALS AND METHODS: The study included 52 of 55 consecutive patients with symptomatic stenoses of the central veins draining upper limb dialysis access grafts or fistulas treated with stent grafts. Indications for stent grafts were poor angioplasty results, rapid recurrence, or total occlusion. Endpoints were lesion patency and access patency following intervention. Mean follow-up was 25 months with a median of 24 months and 1.25 additional procedures per patient year. Patency rates were calculated using Kaplan-Meier analysis. RESULTS: All stent grafts were successfully deployed. The lesion patency rates at 6, 12, 24, and 36 months after intervention were 60%, 40%, 28%, and 28%. The access patency rates at 6, 12, 24, and 36 months after intervention were 96%, 94%, 85%, and 72%. There was one major complication and no minor complications. In 40 patients (77%), the internal jugular vein confluence was covered by the stent graft. In five patients, the dialysis circuits became occluded, with no clinical sequelae in four; one patient was lost to follow-up. The contralateral brachiocephalic vein was covered in three patients (6%), preventing contralateral access construction in one patient. CONCLUSIONS: Central vein stent graft placement in patients with hemodialysis access is associated with prolonged access patency. Coverage of major vein confluences, which occurred in 83% of the patients in this series, can compromise future access and should be avoided whenever possible by careful technique.


Subject(s)
Blood Vessel Prosthesis/statistics & numerical data , Cerebral Veins/surgery , Cerebrovascular Disorders/epidemiology , Cerebrovascular Disorders/surgery , Renal Dialysis/statistics & numerical data , Stents/statistics & numerical data , Adult , Aged , Aged, 80 and over , Cerebral Veins/diagnostic imaging , Cerebrovascular Disorders/diagnostic imaging , Female , Humans , Israel/epidemiology , Male , Middle Aged , Prevalence , Radiography , Risk Factors , Treatment Outcome
10.
J Vasc Surg ; 54(4): 1088-94, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21658886

ABSTRACT

BACKGROUND: Aneurysms that develop in arteriovenous accesses as a result of repeated punctures are sometimes complicated by infection or ischemia causing sloughing of the overlying skin, which may endanger the access and risk major bleeding and other complications. Surgical revision may necessitate the temporary use of a central venous catheter until dialysis can be resumed via the access. We used stent grafts in selected patients for the exclusion of access aneurysms. METHODS: Twenty of 63 patients requiring access revision for complication of an aneurysm from February 2005 to December 2009 underwent ambulatory endovascular stent graft deployment. Indications included signs of impending rupture, questionable viability of overlying skin, pain, infection, and limitation of cannulation sites by the size or number of the aneurysms. Endovascular treatment always included angioplasty of associated outflow or central vein stenoses at the same ambulatory session. RESULTS: Twenty patients with complicated access aneurysms were treated by endovascular stent graft exclusion at an average of 4.8 ± 4.3 years (range, 0.2 to 16.1 years) after access construction: nine graft pseudoaneurysms, nine native vein aneurysms, and two acute iatrogenic pseudoaneurysms. Six patients had skin erosion over the aneurysm, and 12 had painful aneurysms and clinical signs of compromised blood supply to the skin. Another two patients with an acute giant false aneurysm occurring during endovascular procedures were treated in the same interventional session by the stenting technique to control bleeding. All the aneurysms underwent endovascular exclusion without complications. Only one infected puncture site failed to heal within 2 months of stenting and was closed surgically 10 months later due to persistent localized graft infection, but with no further bleeding episodes. Only one aneurysm did not reabsorb within 3 months. Patients with painful skin ischemia had immediate pain relief. All patients also had stenosis in the draining veins necessitating additional percutaneous transluminal angioplasty. Only one patient required hospitalization (for intravenous antibiotic treatment of staphylococcal sepsis). No patients required a central catheter for hemodialysis. One access occluded due to cephalic arch stenosis in a noncompliant patient. Functional patency was 87% at 12 months, with a median follow-up of 15 months (range, 6.3 to 55.5 months). CONCLUSION: Endovascular treatment with stent grafts in complicated access aneurysms is a simple, safe and rapid ambulatory procedure that enables treatment of both the aneurysm and its accompanying draining vein stenosis. It enables continued cannulation of the existing access and avoids the use of central catheters.


Subject(s)
Aneurysm, False/therapy , Aneurysm/therapy , Angioplasty/instrumentation , Arteriovenous Shunt, Surgical/adverse effects , Renal Dialysis , Stents , Adolescent , Adult , Aged , Aged, 80 and over , Ambulatory Care , Aneurysm/etiology , Aneurysm/physiopathology , Aneurysm, False/etiology , Aneurysm, False/physiopathology , Angioplasty/adverse effects , Child , Child, Preschool , Female , Humans , Israel , Male , Middle Aged , Pain/etiology , Pain Management , Prosthesis-Related Infections/etiology , Prosthesis-Related Infections/therapy , Punctures/adverse effects , Stents/adverse effects , Time Factors , Treatment Outcome , Vascular Patency , Young Adult
11.
Anticancer Drugs ; 21(7): 704-7, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20517148

ABSTRACT

Indwelling central venous catheters and implantable port systems are widely used in the care of patients with cancer. Bevacizumab, a humanized monoclonal antibody against vascular endothelial growth factor, significantly prolongs survival when added to intravenous 5-fluorouracil-based chemotherapy as first-line treatment for metastatic colorectal cancer. It has also been shown to be of value in a range of other malignant diseases. Some elements of the toxicity profile of bevacizumab, however, such as bleeding and impaired wound healing, could interfere with surgical procedures involved in the treatment of the diseases. The aim of this study was to evaluate the possible effect of bevacizumab in increasing the morbidity associated with an indwelling central venous access port in patients currently receiving the drug, or those who had received it in the preoperative run-up to surgery. An analysis of the medical records of 57 patients with a variety of cancers, who had received an indwelling central venous access port, either during the course of treatment with bevacizumab or in the 4-week period before the commencement of therapy was carried out, with particular emphasis on periprocedural complications. Eight of the patients also had diabetes mellitus. There were no instances of delay in wound healing, abnormal bleeding, or wound infection in any of the patients and no episodes of skin ulceration during bevacizumab treatment. Although this is a relatively small study, and no definitive conclusions can be drawn at this stage, our data suggest that an indwelling central venous access port insertion may be carried out shortly before or during bevacizumab treatment without increasing periprocedural morbidity.


Subject(s)
Angiogenesis Inhibitors/adverse effects , Antibodies, Monoclonal/adverse effects , Catheterization, Central Venous , Catheters, Indwelling , Adult , Aged , Aged, 80 and over , Angiogenesis Inhibitors/administration & dosage , Angiogenesis Inhibitors/therapeutic use , Antibodies, Monoclonal/administration & dosage , Antibodies, Monoclonal/therapeutic use , Antibodies, Monoclonal, Humanized , Bevacizumab , Female , Humans , Male , Middle Aged , Retrospective Studies
12.
Surg Laparosc Endosc Percutan Tech ; 19(4): e113-8, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19692859

ABSTRACT

INTRODUCTION: Aggressive surgical pancreatic debridement remains the standard of care, may require multiple abdominal explorations and is associated with high mortality. We have introduced the stepped technique of percutaneous treatment of infected peripancreatic fluid collections. METHODS: We performed a retrospective review of patients with severe infected necrotizing pancreatitis who were managed percutaneously. Culture results, number of radiological interventions, length of stay, and complications were recorded. RESULTS: There were 8 patients with a median number of Ranson's criteria of 4.5. Sixty invasive procedures were performed. A median number of two separate catheter sites per patient were necessary for the removal of necrotic material. Median duration of percutaneous intervention was 71.5 days with complete removal of necrotic material and resolution of infected collections in all patients. CONCLUSIONS: Surgeons and interventional radiologists should be familiar with this evolving technique which is less invasive then surgery, but may prolong the time necessary for complete resolution.


Subject(s)
Debridement/methods , Drainage/methods , Pancreatitis, Acute Necrotizing/therapy , Adult , Aged , Aged, 80 and over , Catheterization , Female , Humans , Male , Middle Aged , Necrosis , Pancreatitis, Acute Necrotizing/pathology , Retrospective Studies , Therapeutic Irrigation
13.
World J Gastroenterol ; 14(25): 4091-2, 2008 Jul 07.
Article in English | MEDLINE | ID: mdl-18609697

ABSTRACT

In this case report, we present a patient who suffered from gastrointestinal bleeding. The bleeding source was a gastric arterio-venous malformation emerging from the splenic artery. Attempts to stop the bleeding failed and therapeutic angiography succeeded in occluding the vessel. A search at the literature has not yielded any other case report describing this anatomical anomaly.


Subject(s)
Arteriovenous Malformations/diagnostic imaging , Gastrointestinal Hemorrhage/etiology , Splenic Artery/abnormalities , Stomach/blood supply , Adult , Arteriovenous Malformations/complications , Arteriovenous Malformations/therapy , Embolization, Therapeutic , Gastrointestinal Hemorrhage/diagnostic imaging , Gastrointestinal Hemorrhage/therapy , Humans , Male , Radiography , Splenic Artery/diagnostic imaging , Treatment Outcome
14.
J Neurol Sci ; 272(1-2): 151-7, 2008 Sep 15.
Article in English | MEDLINE | ID: mdl-18649895

ABSTRACT

Penetrating injuries may infrequently cause pseudoaneurysms, lacerations and arteriovenous fistulas involving the subclavian artery. These injuries present with life-threatening bleedings, associated regional injuries and critical limb ischemia and although surgery has been considered the treatment of choice, subclavian injuries pose a real surgical challenge. We prospectively examined data of six patients presenting with penetrating subclavian artery injuries that were treated by urgent endovascular stent-graft placements. All stent-grafts were deployed successfully achieving complete exclusion of the pseudoaneurysm, control of bleeding and reconstruction of the injured artery. No procedural complications, stent thrombosis or stent infections occurred during hospitalization. One patient developed stenosis at 7 months, which required angioplasty. The series mean clinical and ultrasound-CTA follow-up is 38+/-19.7 months (range 11-60 months) and 28+/-19.1 months (range 6-58 months), respectively. This series shows the feasibility of endovascular repair by means of stent-grafts for selected patients with acute penetrating injuries of the subclavian arteries. This approach proved to be safe and effective in restoring the arterial lumen and patency, excluding the pseudoaneurysms and controlling the bleeding caused by subclavian lacerations. Mid-term follow-up on stent-graft patency rates are encouraging.


Subject(s)
Blood Vessel Prosthesis Implantation/methods , Carotid Artery Injuries/surgery , Stents , Subclavian Artery/surgery , Wounds, Penetrating/surgery , Adolescent , Adult , Angiography , Carotid Artery Injuries/complications , Female , Follow-Up Studies , Humans , Male , Prospective Studies , Subclavian Artery/injuries , Ultrasonics , Wounds, Penetrating/complications
15.
World J Gastroenterol ; 14(11): 1797-9, 2008 Mar 21.
Article in English | MEDLINE | ID: mdl-18350614

ABSTRACT

Fibro-muscular dysplasia (FMD) is a rare but well documented disease with multiple arterial aneurysms. The patients, usually women, present with various clinical manifestations according to the specific arteries that are affected. Typical findings are aneurysmatic dilatations of medium-sized arteries. The renal and the internal carotid arteries are most frequently affected, but other anatomical sites might be affected too. The typical angiographic picture is that of a "string of beads". Common histological features are additionally described. Here we present a case of a 47-year-old woman, who was hospitalized due to intractable abdominal pain. A routine work-up revealed a liver mass near the portal vein. Before a definite diagnosis was reached, the patient developed massive upper gastrointestinal bleeding. In order to control the hemorrhage, celiac angiography was performed revealing features of FMD in several arteries, including large aneurysms of the hepatic artery. Active bleeding from one of these aneurysms into the biliary tree indicated selective embolization of the hepatic artery. The immediate results were satisfactory, and the 5 years follow-up revealed absence of any clinical symptoms.


Subject(s)
Aneurysm/etiology , Fibromuscular Dysplasia/diagnosis , Hemobilia/etiology , Hepatic Artery , Abdominal Pain/etiology , Aneurysm/complications , Aneurysm/diagnostic imaging , Aneurysm/therapy , Cholangiopancreatography, Endoscopic Retrograde , Embolization, Therapeutic , Female , Fibromuscular Dysplasia/complications , Fibromuscular Dysplasia/diagnostic imaging , Hemobilia/diagnostic imaging , Hemobilia/therapy , Hepatic Artery/diagnostic imaging , Humans , Middle Aged , Pain, Intractable/etiology , Tomography, X-Ray Computed , Treatment Outcome
16.
Vasc Endovascular Surg ; 42(2): 173-5, 2008.
Article in English | MEDLINE | ID: mdl-18362125

ABSTRACT

Since the introduction of laparoscopic-assisted ileocolic resection for Crohn disease more than 15 years ago, it has become established as a challenging but feasible and safe procedure. A crucial step in the operation is the division of the thick and chronically inflamed mesentery, which in many cases is performed extracorporeally. We report a case of a 32-year-old man with a 14-year history of Crohn ileitis who underwent elective laparoscopic-assisted ileocolic resection. His procedure and the postoperative course were uneventful. A computed tomography scan 2 weeks later revealed a 3-cm-diameter asymptomatic mesenteric pseudoaneurysm, which was successfully treated by transcatheter coil embolization. Pseudoaneurysm of mesenteric arteries has not been documented before in relation to bowel resection by conventional or minimally invasive approaches. It is likely that the thick vascular mesentery of this patient with Crohn disease was a contributing factor to this complication.


Subject(s)
Aneurysm, False/therapy , Crohn Disease/surgery , Digestive System Surgical Procedures/adverse effects , Embolization, Therapeutic , Laparoscopy/adverse effects , Mesenteric Arteries , Adult , Aneurysm, False/diagnostic imaging , Aneurysm, False/etiology , Humans , Male , Mesenteric Arteries/diagnostic imaging , Tomography, X-Ray Computed , Treatment Outcome
17.
J Vasc Res ; 42(1): 29-37, 2005.
Article in English | MEDLINE | ID: mdl-15627784

ABSTRACT

We here propose an alternative cell therapy approach to induce angiogenesis. We prepared small organ fragments whose geometry allows preservation of the natural epithelial/mesenchymal interactions and ensures appropriate diffusion of nutrients and gases to all cells. Fragments derived from lung are shown to behave as fairly independent units, to undergo a marked upregulation of angiogenic factors and to continue to function for several weeks in vitro in serum-free media. When implanted into hosts, they transcribe a similar array of angiogenic factors that specifically induce the formation of a potent vascular network. The angiogenic induction capacity of these fragments was also tested in a mouse and rat model of limb ischemia. We report that such fragments, when implanted in the vicinity of the ischaemic area, induce an angiogenic response which can rescue the ischaemia-induced damage. The approach presented differs from single factor application, gene therapy and other cell therapy methods in that it exploits the complex behaviour of autologous cells in their near to normal environment in order to achieve secretion of a whole range of angiogenic stimuli continuously and in an apparently coordinated fashion.


Subject(s)
Lung/physiology , Neovascularization, Physiologic , Animals , Extremities/blood supply , Fibroblast Growth Factor 2/genetics , Ischemia/therapy , Mice , Mice, Inbred C57BL , Rats , Rats, Inbred Lew , Reverse Transcriptase Polymerase Chain Reaction , Vascular Endothelial Growth Factor A/genetics
18.
BJOG ; 111(8): 880-4, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15270943

ABSTRACT

Arterial embolisation is a recognised treatment for postpartum haemorrhage (PPH). In this retrospective study, we evaluate its use in the management of persistent PPH. Records of all births during a 54 month period at a university hospital were analysed. Two sub-groups were identified. Group I (n= 5), underwent embolisation after hysterectomy and Group II (n= 4), had embolisation as a first-line theraphy without hysterectomy. Of 20,215 births, there were 636 cases of PPH (3.1%). Nine required embolisation to control bleeding (1.4%). Group I needed multiple surgical procedures, had a larger pre- and post-operative blood requirement (12-100, median 22 units, vs. 6-12, median 8.5 units), longer embolisation (33-93, median 54 minutes, vs 20-66, 47 minutes) with a larger radiation exposure (5194-9067, median 6301 dGy, vs. 269-3862, median 950 dGy), a longer intensive care stay (3-7, median four days vs. 0-1.5, median one day), and more complications, when compared with Group II. Three of four women from Group II resumed menstrual function. Embolisation prior to hysterectomy may be preferable to embolisation after hysterectomy for the control of PPH.


Subject(s)
Embolization, Therapeutic/methods , Hysterectomy/methods , Postoperative Care/methods , Postpartum Hemorrhage/therapy , Preoperative Care/methods , Adolescent , Adult , Arteries , Female , Humans , Postpartum Hemorrhage/diagnostic imaging , Radiography , Retrospective Studies
19.
Clin Ther ; 26(3): 407-14, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15110133

ABSTRACT

BACKGROUND: Hepatic grafr-versus-host disease (GVHD) is associated with significant morbidity and mortality. Standard therapy includes systemically administered immunosuppressive drugs. More recent reports have described catheter-directed intrahepatic arterial (IHA) delivery of low-dose methotrexate (MTX) and methylprednisolone in the treatment of corticosteroid-resistant severe hepatic GVHD. OBJECTIVE: This article reports on MTX toxicity and the variability in plasma drug concentrations after IHA administration of low-dose MTX in patients with severe hepatic GVHD. METHODS: In this open-label, uncontrolled pilot study, MTX and methylprednisolone were administered via the hepatic artery in patients with corticosteroid-resistant grade III or IV GVHD of the liver. Patients also received standard therapy. MTX concentrations were measured in the hepatic artery 5 and 10 minutes after injection and in peripheral venous blood at 1, 2, and 24 hours. RESULTS: Six patients (5 males [83.3%], I female [16.7%]; median age, 32 years; range, 8-42 years) were enrolled in the study. No hepatotoxicity was observed after IHA administration of MTX. In 5 patients with normal renal function, plasma drug concentrations 24 hours after administration of MTX ranged from 0.01 to 0.12 micromol/L (mean [SD], 0.043 [0.042] micromol/L). In 1 patient with renal failure, plasma MTX concentrations were 1.0 micromol/L 24 hours after administration and 0.07 micromol/L 5 days after administration. The severe hematologic and renal toxicity observed in this patient may have contributed to his death. Adverse events in patients with GVHD and normal renal function, who had normal plasma MTX concentrations, were comparable to those that have been reported after administration of an intravenous infusion. CONCLUSIONS: In patients with GVHD and normal renal function, IHA administration of low-dose MTX was not associated with liver or bone marrow toxicity. Further study is needed to determine the optimal protocols for treating corticosteroid-resistant hepatic GVHD.


Subject(s)
Graft vs Host Disease/drug therapy , Immunosuppressive Agents/administration & dosage , Methotrexate/administration & dosage , Adolescent , Adult , Child , Drug Resistance , Female , Hepatic Artery , Humans , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/therapeutic use , Infusions, Intra-Arterial , Male , Methotrexate/adverse effects , Methotrexate/therapeutic use , Methylprednisolone/therapeutic use , Renal Insufficiency/physiopathology
20.
Cardiovasc Intervent Radiol ; 26(1): 58-64, 2003.
Article in English | MEDLINE | ID: mdl-12522643

ABSTRACT

PURPOSE: To report our results for the placement of central venous stents in patients undergoing hemodialysis. METHODS: Ten Wallstents (Schneider, Bülach, Switzerland) were placed in 10 patients with shunt thrombosis, shunt dysfunction or arm swelling associated with central vein stenosis or occlusion. Technical success, patency and complications were evaluated. RESULTS: Stent deployment was successful in all cases. In seven cases (70%) there was significant delayed stent shortening. In two of these cases there was also stent migration. All these cases required additional stents. Primary patency rates at 6, 12 and 24 months were 66%, 25% and 0. Twenty-three additional procedures (percutaneous transluminal angioplasty or stenting) were required to achieve secondary patency rates at 6, 12 and 24 months of 100%, 75% and 57%. CONCLUSION: Stent placement in the central veins of dialysis patients has a high technical success rate resulting in symptomatic relief and preservation of access. Repeat interventions are required to maintain patency. Significant delayed shortening of the Wallstent occurred in 70% of patients which may have affected the patency rates. Strategies are suggested to avoid this problem.


Subject(s)
Catheterization, Central Venous , Graft Occlusion, Vascular/therapy , Renal Dialysis/instrumentation , Stents , Subclavian Vein , Aged , Female , Foreign-Body Migration , Graft Occlusion, Vascular/diagnostic imaging , Humans , Male , Middle Aged , Radiography , Treatment Outcome , Vascular Patency
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