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1.
Cardiovasc Intervent Radiol ; 41(4): 564-571, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29181605

ABSTRACT

PURPOSE: To assess the incidence of symptomatic heart failure (SHF) occurring after transjugular intrahepatic portosystemic shunt (TIPS) placement, identify potential predictors of SHF, and evaluate clinical presentation and outcomes in cases of post-TIPS SHF. MATERIALS AND METHODS: A prospectively maintained TIPS database was used to identify patients who underwent new TIPS placements at a large urban tertiary care center between 1995 and 2014. SHF was defined as otherwise unexplained new-onset dyspnea, hypoxemia, radiologic pulmonary edema, an increased need for diuretics, or need for intubation within 7 days after TIPS placement. Cases of deaths occurring within 7 days due to septic shock, continuing gastrointestinal bleed, or multi-organ failure were excluded. A control group consisting of a random sample of 40 patients from the same TIPS database was created. Uni-variable analysis was performed to assess differences between patients with and without post-TIPS SHF. RESULTS: Of the 934 TIPS procedures performed during the study period, 883 met the inclusion criteria. Eight (0.9%) patients developed SHF, usually manifested by hypoxemia (50%) or dyspnea (25%) within 48 h. Patients with SHF had higher pre-TIPS right atrial (p = 0.03) and portal vein (p = 0.01) pressures, higher albumin (p = 0.02), and higher prothrombin time (p = 0.02). CONCLUSION: Post-TIPS SHF is rare. Higher pre-TIPS right atrial and portal vein pressures are likely to predispose patients to this complication. Close monitoring may be warranted in these patients. In our eight patients, post-TIPS SHF did not result in poor outcomes.


Subject(s)
Heart Failure/etiology , Heart Failure/physiopathology , Portasystemic Shunt, Transjugular Intrahepatic/adverse effects , Case-Control Studies , Female , Humans , Hypertension, Portal/etiology , Hypertension, Portal/physiopathology , Incidence , Male , Middle Aged , Portal Vein/physiopathology , Portal Vein/surgery , Portasystemic Shunt, Transjugular Intrahepatic/methods , Prospective Studies , Retrospective Studies , Treatment Outcome
2.
Cardiovasc Intervent Radiol ; 40(11): 1723-1731, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28512687

ABSTRACT

PURPOSE: Transjugular intrahepatic portosystemic shunts (TIPS) were historically placed using uncovered bare-metal stents. Current practice has now shifted toward the use of polytetrafluoroethylene (PTFE)-covered stents, given the improved primary patency seen with these stents. The aim of this study was to determine whether there is any added value, such as overall survival or stent patency, when using covered stents versus uncovered stents in TIPS placement in a large cohort. MATERIALS AND METHODS: From April 1995 to June 2012, a total of 744 consecutive adult patients underwent de novo TIPS placement (378 receiving uncovered stents, 366 receiving covered stents). Information was obtained on demographics, baseline clinical variables, and outcomes after TIPS placement. Data were collected, compared, and analyzed to assess outcomes including mortality, primary patency (determined via repeat intervention), and secondary patency (determined via ultrasound parameters). RESULTS: Covered stents were associated with significantly improved primary patency (P < 0.001) and secondary patency (P < 0.001) when compared with uncovered stents in TIPS procedures. Additionally, covered stents were associated with higher estimated overall survival rates and higher survival rates when TIPS was performed emergently and in patients with higher Model for End-Stage Liver Disease (MELD) scores. For example, in patients with MELD scores between 11 and 18, there was a predicted survival of 59.2% with covered stents versus 42.8% with uncovered stents at 1 year. CONCLUSION: This study demonstrated that covered stents offer the additional value of higher estimated overall survival and higher estimated survival in patients undergoing TIPS emergently and in those with higher MELD scores when compared to uncovered stents.


Subject(s)
End Stage Liver Disease/complications , Hypertension, Portal/therapy , Polytetrafluoroethylene , Portasystemic Shunt, Transjugular Intrahepatic/methods , Stents , Female , Humans , Hypertension, Portal/etiology , Liver Function Tests , Male , Middle Aged , Retrospective Studies , Survival Analysis , Survival Rate , Treatment Outcome
3.
J Ultrasound Med ; 35(7): 1393-400, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27208197

ABSTRACT

OBJECTIVES: To retrospectively investigate the role of Doppler sonography in the early detection of splenic steal syndrome. METHODS: Fifty cases of splenic steal syndrome after orthotopic liver transplantation were identified. A control group was matched to the splenic steal syndrome group. Information was collected about the clinical presentation, liver enzyme levels, Doppler sonographic results, and follow-up after patients underwent splenic artery embolization. RESULTS: A persistent hepatic arterial diastolic reversal waveform was observed in 25 patients with splenic steal syndrome versus 0 control patients. The mean hepatic arterial resistive index (RI) values ± SD were 0.95 ± 0.09 in patients with splenic steal syndrome and 0.80 ± 0.10 in control patients (P < .0001). One week after orthotopic liver transplantation, the area under the receiver operating characteristic curve for the RI was 0.884 (95% confidence interval, 0.793-0.975; P = .001) for splenic steal syndrome diagnosis. After splenic artery embolization, there was normalization of the reversal waveform, with an average RI of 0.77 ± 0.11 (P < .0001). CONCLUSIONS: Dynamic changes in the hepatic arterial waveform and RI are keys to detecting splenic steal syndrome with Doppler sonography.


Subject(s)
Hepatic Artery/diagnostic imaging , Hepatic Artery/physiopathology , Liver Transplantation , Postoperative Complications/diagnostic imaging , Ultrasonography, Doppler/methods , Vascular Diseases/diagnostic imaging , Adolescent , Adult , Aged , Case-Control Studies , Child , Early Diagnosis , Female , Humans , Liver Circulation , Male , Middle Aged , Postoperative Complications/physiopathology , Retrospective Studies , Syndrome , Vascular Diseases/physiopathology , Young Adult
4.
J Vasc Interv Radiol ; 25(7): 1027-8, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24968725

ABSTRACT

Radiation recall is a rare side effect observed in patients treated with certain medications after radiation therapy. This effect mimics a radiation-induced tissue reaction in expression; however, it occurs outside of the traditional time course and only in the presence of a catalyzing agent. The authors report a case of radiation recall resulting from an interaction between radiation delivered during a fluoroscopically guided hepatic chemoembolization for treatment of metastatic carcinoid tumor and the oral chemotherapeutic agents capecitabine and temozolomide administered 7 weeks later.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/adverse effects , Carcinoid Tumor/drug therapy , Carcinoid Tumor/secondary , Chemoembolization, Therapeutic/adverse effects , Liver Neoplasms/drug therapy , Liver Neoplasms/secondary , Radiodermatitis/etiology , Radiography, Interventional/adverse effects , Administration, Oral , Capecitabine , Dacarbazine/administration & dosage , Dacarbazine/adverse effects , Dacarbazine/analogs & derivatives , Deoxycytidine/administration & dosage , Deoxycytidine/adverse effects , Deoxycytidine/analogs & derivatives , Drug Administration Schedule , Fluoroscopy , Fluorouracil/administration & dosage , Fluorouracil/adverse effects , Fluorouracil/analogs & derivatives , Humans , Male , Middle Aged , Radiodermatitis/diagnosis , Risk Factors , Temozolomide , Time Factors
5.
J Vasc Interv Radiol ; 23(12): 1557-63, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23177101

ABSTRACT

PURPOSE: To evaluate retrospectively the safety and retrievability of the Celect IVC filter. MATERIALS AND METHODS: All patients undergoing Celect filter placement and retrieval during the period 2007-2012 were assessed for complications and retrievability. RESULTS: Of 620 patients who underwent Celect filter placement, 120 presented for removal. The indwelling time in these patients was 158.1 days±103.0 (range, 2-518 d). There were 106 filters (88.3%) removed; 14 filters were left in situ for the following reasons: filter embedment (n=6), caval occlusion (n=3), retained thrombus (n=2), large floating thrombus in IVC (n=2), or tilt >15° (n=1). With filters in place, five patients developed new pulmonary embolism (PE), and two others presented with severe abdominal pain. The available 115 pairs of placement and removal cavagrams suggested limb penetration in 99 cases (86.1%), intracaval migration >2 cm in 5, secondary tilt >15° in 8, filter deformity in 10, retained thrombus within filters in 12, and IVC occlusion in 3. Among 38 available computed tomography (CT) scans, 9 scans (24%) showed asymptomatic limb penetration to the duodenum (n=6), aortic wall (n=2), or kidney (n=1). No filter fracture was found. CONCLUSIONS: This study showed a high penetration rate for Celect IVC filters, including penetrations that were symptomatic or involved adjacent structures. Penetration appears to correlate with indwelling time, suggesting that the filter should be removed as soon as PE protection is no longer indicated. Although most of the filters were removed, 5.8% of retrievals were unsuccessful because of technical failure.


Subject(s)
Device Removal/statistics & numerical data , Postoperative Complications/epidemiology , Postoperative Complications/prevention & control , Pulmonary Embolism/epidemiology , Pulmonary Embolism/prevention & control , Vena Cava Filters/statistics & numerical data , Venous Thrombosis/epidemiology , Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Ohio/epidemiology , Prevalence , Retrospective Studies , Risk Factors , Treatment Outcome , Venous Thrombosis/prevention & control , Young Adult
6.
J Vasc Interv Radiol ; 23(2): 199-205.e1, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22188776

ABSTRACT

PURPOSE: To report the occurrence of fracture of the Recovery filter and incidence of potentially life-threatening complications associated with fractured fragment migration. MATERIALS AND METHODS: A retrospective study of images obtained after placement of Recovery inferior vena cava (IVC) filters from 2003 to 2006 was conducted at a single tertiary-care center. Images were reevaluated for fracture and migration; complications related to filter fracture were investigated. Kaplan-Meier survival analysis was performed to investigate the relationship between time in situ and fracture. RESULTS: A total of 363 Recovery filters were placed; 97 were retrieved, leaving 266 filters in situ (135 patients subsequently died of other causes). The following images were evaluated: 130 chest computed tomography (CT) scans, 153 abdominal CT scans, 254 chest radiographs, 148 radiographs of the abdomen/pelvis, and 106 cavagrams. Mean imaging follow-up interval was 18.4 months (maximum, 81.3 mo). No en bloc migration occurred outside the IVC. Twenty-six limb fractures (all short limbs) were identified in 20 patients; the earliest occurred at 4.1 months. Eight fragment migrations occurred into pulmonary arteries, seven into iliac/femoral veins, one into the right ventricle, and one into the renal vein. Seven fragments were intracaval near the filter, one was extracaval, and one could not be located. Kaplan-Meier survival estimates predicted a fracture rate of 40% at 5.5 years. Of the 20 patients with filter fractures, three died of unrelated causes and 17 remain asymptomatic. CONCLUSIONS: Recovery filter fractures occurred at the short limb only, with a suggested 5.5-year fracture risk of 40%. No life-threatening events occurred in patients with filter fracture.


Subject(s)
Device Removal/mortality , Equipment Failure/statistics & numerical data , Foreign-Body Migration/mortality , Postoperative Complications/mortality , Vena Cava Filters/statistics & numerical data , Venous Thromboembolism/mortality , Comorbidity , Female , Foreign-Body Migration/diagnostic imaging , Humans , Male , Middle Aged , Ohio/epidemiology , Postoperative Complications/diagnostic imaging , Prevalence , Radiography , Risk Assessment , Risk Factors , Treatment Outcome , Venous Thromboembolism/diagnostic imaging
7.
J Vasc Interv Radiol ; 22(6): 806-12, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21482140

ABSTRACT

PURPOSE: To evaluate the retrievability and safety of the G2 filter. MATERIALS AND METHODS: A retrospective study of all G2 filter retrievals at a single institution was conducted. Hospital records and imaging studies were reviewed for complications, and factors affecting retrieval were analyzed. RESULTS: From 2005 to 2009, a total of 139 patients presented for retrieval of their G2 filter, and 131 pairs of pre- and post-placement cavagrams and 39 computed tomography scans were available for analysis. The following findings were recorded: limb penetration (n = 33), tilt greater than 15° (n = 22), local migration greater than 2 cm (n = 17), retained thrombus within the filter (n = 16), deformity (n = 10), inferior vena cava (IVC) occlusion (n = 3), fracture (n = 2), and pulmonary embolism breakthrough (n = 2). A total of 118 filters were removed, with a mean indwelling time of 131.8 days (range, 3-602 d). Indwell time (< 90, 90-180, or > 180 d) did not affect retrieval (P = .4). There were 21 filters (15.1%) left in situ as a result of severe tilt (n = 9), significant thrombus in the filter (n = 5), IVC occlusion (n = 3), filter incorporation into the caval wall (n = 3), or lack of central venous access (n = 1). There was a strong relationship between penetration and caudal migration (P < .0001). Severe tilt was associated with prolonged fluoroscopic times for retrieval (P = .003). CONCLUSIONS: The majority of G2 filters can be removed without difficulty. The most common factor affecting retrieval was severe tilting. The indwelling time had no impact on retrieval. G2 filter-related complications were frequent but most, including fractures, were clinically insignificant.


Subject(s)
Device Removal , Pulmonary Embolism/prevention & control , Vena Cava Filters/adverse effects , Vena Cava, Inferior , Venous Thrombosis/therapy , Adult , Aged , Aged, 80 and over , Chi-Square Distribution , China , Female , Foreign-Body Migration/etiology , Humans , Male , Middle Aged , Phlebography/methods , Prosthesis Design , Prosthesis Failure , Pulmonary Embolism/diagnostic imaging , Pulmonary Embolism/etiology , Retrospective Studies , Risk Assessment , Risk Factors , Time Factors , Tomography, X-Ray Computed , Treatment Outcome , Vena Cava, Inferior/diagnostic imaging , Venous Thrombosis/complications , Venous Thrombosis/diagnostic imaging , Young Adult
9.
Cardiovasc Intervent Radiol ; 34(3): 522-31, 2011 Jun.
Article in English | MEDLINE | ID: mdl-20700592

ABSTRACT

PURPOSE: To retrospectively evaluate the role of the Amplatzer Vascular Plug (AVP) in proximal splenic artery embolization (SAE) compared with coils. MATERIALS AND METHODS: Forty patients had proximal SAE performed with AVP(s) or coils as the primary embolic agent for splenic artery steal syndrome (n=23), trauma (n=5), portal hypertension (n=5), bleeding due to pancreatic pathology (n=4), and pre-splenectomy (n=3). Comparisons were made of occlusion and procedure time, cost, and radiation dose. RESULTS: Eighteen proximal SAE procedures were successfully performed with AVP. Twenty-two procedures were performed with coils, including one failed AVP attempt, which was completed with coils. Precise deployment without migration was achieved in all 18 AVP cases. Seven of 22 (31.8%) coil procedures had distal migration without consequence. There was no statistically significant difference in mean occlusion time (24.4 min for AVP vs. 31.5 min for coils, P=0.13), procedure time (43.7 min for AVP vs. 53.8 min for coils, P=0.16), or cost ($1474.13 for AVP vs. $1722.51 for coils, P=0.69). There was significant difference in radiation dose (842 mGy for AVP vs. 1,309 mGy for coils, P=0.04). Fourteen of the 18 (78%) AVP devices required additional embolic material. CONCLUSIONS: AVP with additional embolic agents is a useful alternative for proximal SAE because of precise deployment, resistance to migration, and radiation reduction. AVP use may be limited by vessel tortuosity. The occlusion time, procedure time, and cost were reduced but this was not statistically significant due to the need for additional embolic material.


Subject(s)
Embolization, Therapeutic/instrumentation , Septal Occluder Device , Splenic Artery , Adolescent , Adult , Aged , Aged, 80 and over , Analysis of Variance , Chi-Square Distribution , Female , Humans , Linear Models , Male , Middle Aged , Radiation Dosage , Radiography, Interventional , Retreatment , Retrospective Studies , Treatment Outcome
10.
11.
J Vasc Interv Radiol ; 20(11): 1449-53, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19875062

ABSTRACT

PURPOSE: To assess the technical success and safety for retrieval of the G2 filter. MATERIALS AND METHODS: The authors performed a prospective, multicenter study of 100 patients with temporary indication for caval interruption. Patients were enrolled consecutively between December 2005 and July 2006. There were 67 men and 33 women with a mean age of 52.1 years (range, 19-82 years). Indications for filter placement were trauma (n = 56), perioperative risk (n = 16), and medical indications (n = 28). Forty-two patients had venous thromboembolism at filter placement. Fifty-eight filters were placed prophylactically. RESULTS: Retrieval was attempted in 61 patients. Fifty-eight of the 61 filters (95%) were successfully retrieved after a mean dwell time of 140 days (range, 5-300 days). In all failed retrievals, the filter tip was against the caval wall. There was no difference in dwell times between successful and unsuccessful retrievals. Although there were no cases of cranial migration, caudal migrations were observed in 12% of cases (10 of 85 patients with a complete data set). Other device-related complications included filter fracture (1/85, 1.2%), filter tilt of more than 15 degrees (15/85, 18%), and leg penetration (16/61, 26%). The recurrent pulmonary embolism (PE) rate was 2%, with no PE in the 30-day period after filter retrieval. CONCLUSIONS: Retrieval of the Recovery G2 filter was safe and successful in most patients. Caudal migration was observed as an unexpected phenomenon.


Subject(s)
Device Removal/statistics & numerical data , Prosthesis Failure , Pulmonary Embolism/epidemiology , Pulmonary Embolism/prevention & control , Registries/statistics & numerical data , Vena Cava Filters/statistics & numerical data , Adolescent , Adult , Aged , Aged, 80 and over , Female , Humans , Incidence , Longitudinal Studies , Male , Middle Aged , Therapeutics , United States/epidemiology , Young Adult
12.
J Vasc Interv Radiol ; 20(4): 461-6, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19328425

ABSTRACT

PURPOSE: To determine whether the effectiveness of arterial embolization in patients with acute upper gastrointestinal hemorrhage is related to the visualization of contrast medium extravasation at angiography. MATERIALS AND METHODS: Transcatheter embolization was performed in 108 patients who experienced acute upper gastrointestinal hemorrhage during a 5-year period. Patient charts were retrospectively reviewed. Thirty-six patients who underwent embolization after angiography demonstrated active contrast medium extravasation from an involved artery. Seventy-two patients underwent embolization in the absence of contrast medium extravasation into a bowel lumen. Embolization technique, requirement for further blood products, need for further surgery, and 30-day mortality were recorded. RESULTS: The gastroduodenal artery (GDA) was embolized in 26 of the 36 patients (72%) with extravasation, and the left gastric artery was embolized in 10 (28%). The GDA was embolized in 64 of the 72 patients (89%) without extravasation, and the left gastric artery was embolized in 13 (18%). After embolization, 23 of the 36 patients (64%) with extravasation and 44 of the 72 (61%) without extravasation required additional blood product transfusions. Seven of the 36 patients (19%) with extravasation and 16 of the 72 (22%) without extravasation required subsequent surgery secondary to bleeding. Thirty-day hemorrhage-related mortality was 17% (six of 36 patients) in the positive extravasation group and 22% (16 of 72 patients) in the negative extravasation group. The treatment success rate was 44% (16 of 36 patients) in the positive extravasation group and 44% (32 of 72 patients) in the negative extravasation group. CONCLUSIONS: In patients with acute upper gastrointestinal hemorrhage, arterial embolization is equally effective in patients who demonstrate active contrast medium extravasation at angiography as in those who do not show contrast extravasation.


Subject(s)
Angiography/methods , Embolization, Therapeutic/instrumentation , Embolization, Therapeutic/methods , Gastrointestinal Hemorrhage/diagnostic imaging , Gastrointestinal Hemorrhage/therapy , Upper Gastrointestinal Tract/radiation effects , Aged , Female , Humans , Male , Retrospective Studies , Sensitivity and Specificity , Treatment Outcome
13.
Eur J Cardiothorac Surg ; 33(3): 435-9, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18207415

ABSTRACT

OBJECTIVE: Because chylothorax complicating thoracic surgery is difficult to diagnose and failure of nonoperative management necessitates further surgery, we critically evaluated an evolving percutaneous strategy for diagnosing and treating chylothorax. METHODS: After thoracic surgery, 37 patients with a clinical diagnosis of chylothorax were referred for lymphangiography for definitive diagnosis and percutaneous treatment. Successful localization of the cisterna chyli by lymphangiogram facilitated percutaneous cannulation of the thoracic duct and its embolization. In patients in whom cannulation was not possible, the thoracic duct was percutaneously disrupted. DIAGNOSIS: Lymphangiography was successful in 36 of the 37 patients (97%). Contrast extravasation, confirming clinical diagnosis, was present in 21 of the 36 (58%). MANAGEMENT: Twenty-one of 36 patients underwent 22 lymphangiographically directed percutaneous interventions: 12 embolizations and 10 disruptions. Mortality was zero, with two manageable complications. Patients without percutaneous intervention were discharged a median of 7 days (range 4-58) after first lymphangiography, 8 days (range 2-19) after percutaneous embolization, and 19 days (range 6-48) after first disruption. Eight patients had nine subsequent reoperations for chylothorax, two with negative lymphangiograms; no embolization patient required reoperation. CONCLUSIONS: There is a discrepancy between the clinical diagnosis of chylothorax after thoracic surgery and the presumed gold standard of diagnosis, contrast extravasation at lymphangiogram. Percutaneous treatment by thoracic duct embolization or disruption is safe and may obviate reoperation, but embolization of the thoracic duct is preferable to its disruption.


Subject(s)
Chylothorax/diagnostic imaging , Embolization, Therapeutic/methods , Postoperative Complications/diagnostic imaging , Thoracic Duct/diagnostic imaging , Catheterization/methods , Chylothorax/etiology , Chylothorax/surgery , Humans , Lymphography/methods , Postoperative Complications/surgery , Thoracic Duct/surgery , Thoracic Surgery
14.
JPEN J Parenter Enteral Nutr ; 30(1 Suppl): S57-64, 2006.
Article in English | MEDLINE | ID: mdl-16387912

ABSTRACT

The dependence of IV hyperalimentation programs on the achievement and maintenance of reliable vascular access in the home infusion patient population has necessitated a review of the current methods used to establish and maintain adequate long-term vascular access. Vascular access device-related complications are significant contributors to the medical course and costs associated with the care of home parenteral nutrition (HPN) patients. The purpose of this manuscript is to review current thoughts on the establishment of long-term vascular access for HPN with regard to techniques used, device selection, and associated complications.


Subject(s)
Catheterization, Peripheral , Catheters, Indwelling , Parenteral Nutrition, Home , Patient Selection , Adult , Humans , Infusions, Intravenous , Parenteral Nutrition, Home/adverse effects , Parenteral Nutrition, Home/instrumentation , Parenteral Nutrition, Home/methods , Safety
15.
Semin Vasc Surg ; 17(2): 66-82, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15185173

ABSTRACT

In clinical diagnostic imaging there has been a rapid evolution of nuclear magnetic resonance techniques. A subset of these has proven particularly powerful when applied to the arena of noninvasive vascular imaging. This article will serve as a primer for practitioners with little prior background in magnetic resonance angiography (MRA). It will develop the first principles of magnetic resonance image creation, and establish familiarity with current imaging applications of the thoracic, abdominal, and peripheral vasculature.


Subject(s)
Magnetic Resonance Imaging/methods , Humans , Magnetic Resonance Angiography/methods
16.
Dis Colon Rectum ; 46(2): 260-3, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12576900

ABSTRACT

PURPOSE: Gastrointestinal bleeding in patients with Crohn's disease presents both a diagnostic and therapeutic challenge. The bleeding site may be difficult to localize preoperatively and multiple segments of gross disease can lead to uncertainty as to the precise source at the time of laparotomy. METHODS: We describe a patient with Crohn's disease and recurrent gastrointestinal bleeding in whom the combined use of provocative angiography and highly selective methylene blue injection was used preoperatively to accurately identify the site of hemorrhage and direct bowel resection. RESULTS: Provocative angiography identified the bleeding point in the jejunum. Methylene blue, which had been injected distally into the bleeding vessel during angiography, stained the bowel wall at the bleeding site. Segmental bowel resection was subsequently performed and no further bleeding occurred during the 18-month follow-up period. CONCLUSIONS: The combined use of provocative angiography and highly selective methylene blue injection may aid in the preoperative and intraoperative localization of occult bleeding sites in patients with Crohn's disease. This allows the bleeding lesion to be removed with a limited resection, thus preserving bowel length.


Subject(s)
Gastrointestinal Hemorrhage/diagnosis , Jejunal Diseases/diagnosis , Jejunum/blood supply , Methylene Blue , Adult , Crohn Disease/complications , Crohn Disease/surgery , Gastrointestinal Hemorrhage/surgery , Humans , Injections , Jejunal Diseases/surgery , Jejunum/diagnostic imaging , Laparotomy/methods , Male , Mesenteric Arteries/diagnostic imaging , Mesenteric Arteries/drug effects , Mesenteric Arteries/pathology , Preoperative Care , Radiography , Treatment Outcome
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