4 results on '"Ashton, R. C."'
Search Results
2. Circulatory resuscitation with left ventricular assist device support reduces interleukins 6 and 8 levels.
- Author
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Goldstein DJ, Moazami N, Seldomridge JA, Laio H, Ashton RC Jr, Naka Y, Pinsky DJ, and Oz MC
- Subjects
- Biomarkers blood, Female, Follow-Up Studies, Humans, Male, Middle Aged, Resuscitation, Shock therapy, Heart-Assist Devices, Interleukin-6 blood, Interleukin-8 blood, Shock blood, Tumor Necrosis Factor-alpha metabolism
- Abstract
Background: Elevated tumor necrosis factor serum levels have been reported in patients with severe congestive heart failure. This study was designed to characterize the cytokine profile in patients with acute circulatory collapse., Methods: Blood drawn from 14 consecutive patients within 24 hours before undergoing left ventricular assist device placement and after at least 30 days of mechanical assistance or before transplantation was assayed for levels of interleukin 6, interleukin 8, and tumor necrosis factor-alpha., Results: Interleukin 6 level was elevated in 11 (79%), interleukin 8 in 10 (71%), and tumor necrosis factor in 2 (14%) of the 14 patients. After hemodynamic recovery, interleukin 6 levels decreased from 33.6 +/- 9 pg/mL to 11.3 +/- 4 pg/mL (p = 0.05) and interleukin 8 levels decreased from 122 +/- 34 pg/mL to 19.7 +/- 8 pg/mL (p = 0.005). Tumor necrosis factor-alpha levels did not vary significantly; they were associated with infection in 2 left ventricular assist device recipients and normalized after left ventricular assist device support. All patients had resolution of circulatory shock after mechanical support and had improvement in parameters of end-organ function., Conclusions: Circulatory shock treated with left ventricular assist device placement is associated with a proinflammatory response similar to that seen in septic shock. The decrease in cytokine serum levels that follows hemodynamic recovery suggests that these cytokines may be markers of tissue damage and may modulate cardiac dysfunction.
- Published
- 1997
- Full Text
- View/download PDF
3. Right-to-left veno-arterial shunting for right-sided circulatory failure.
- Author
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Slater JP, Goldstein DJ, Ashton RC Jr, Levin HR, Spotnitz HM, and Oz MC
- Subjects
- Animals, Cattle, Coronary Circulation, Femoral Artery surgery, Hemodynamics, Oxygen blood, Pulmonary Artery, Ventricular Function, Right, Arteriovenous Shunt, Surgical, Assisted Circulation methods, Cardiac Output, Low physiopathology, Cardiac Output, Low surgery
- Abstract
Background: Right-sided circulatory failure, a complication of heart transplantation and left ventricular assist device use, results in decreased cardiac output due to diminished flow across the pulmonary circuit. We hypothesized that creation of a controlled right-to-left shunt would result in decompression of the right ventricle and improved systemic cardiac output at tolerable oxygen saturations. We also hypothesized that a peripheral veno-arterial shunt is physiologically superior to a central shunt., Methods: Right atrial-femoral artery and right atrial-left atrial shunts were created in a large animal model (calf). Right-sided circulatory failure was induced by banding the pulmonary artery. Hemodynamic measures and blood gas determinations were obtained during nonshunted and shunted states., Results: Peripheral and central shunts resulted in decreased right-sided pressures and increased cardiac output. Arterial oxygen saturation remained greater than 90% during shunting. The peripheral shunt had the added advantage of decreasing left ventricular end-diastolic pressure and left ventricular stroke work., Conclusions: A controlled right-to-left shunt improved hemodynamics and cardiac output in a large animal model with right-sided circulatory failure. This strategy may be useful in the management of transplant and left ventricular assist device recipients with perioperative right-sided circulatory failure. Our studies also indicate that creation of a peripheral shunt has both physiologic and technical advantages over a central shunt.
- Published
- 1995
- Full Text
- View/download PDF
4. Sutureless ring graft replacement of ascending aorta and aortic arch.
- Author
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Oz MC, Ashton RC Jr, McNicholas KW, and Lemole GM
- Subjects
- Adolescent, Adult, Aged, Aorta surgery, Aorta, Thoracic surgery, Aortic Valve Insufficiency surgery, Arteriosclerosis surgery, Female, Follow-Up Studies, Heart Valve Prosthesis, Humans, Male, Middle Aged, Postoperative Complications, Retrospective Studies, Suture Techniques, Aortic Dissection surgery, Aortic Aneurysm surgery, Blood Vessel Prosthesis
- Abstract
Complications after aortic replacement that result from prolonged graft insertion time and technical difficulties with suturing through friable, diseased aortic tissue can be addressed with use of the sutureless intraluminal ring graft. Between 1978 and 1989, we replaced the ascending aorta or aortic arch with this device in 49 patients. At no time were we unable to use a sutureless graft during a procedure. Twenty-eight cases of aneurysmal disease and 21 cases of acute or chronic dissection were treated. Twenty-six patients required replacement of the aortic valve, with annuloartic ectasia being the most common indication (71%). Ten patients underwent concomitant coronary artery bypass grafting. The operative mortality rate for ascending aortic aneurysm repairs was 4%, and that for dissections was 18%. Five of 8 patients requiring aortic arch replacement survived. Most patients were studied angiographically before discharge. No complications were related to anastomotic hemorrhage, pseudoaneurysm formation, graft migration, or thromboemboli. Individual cases of phrenic nerve palsy, acute tubular necrosis, and transient ischemic attack, all of which resolved completely, were identified. The actuarial 5-year survival rate is 64%. We conclude that modification of the sutureless intraluminal ring graft to suit the pathology encountered at operation allows the quickest repair with the least chance of anastomotic complication.
- Published
- 1990
- Full Text
- View/download PDF
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