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Dive into the research topics where Denton A. Cooley is active.

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Featured researches published by Denton A. Cooley.


Journal of the American College of Cardiology | 1985

Treatment of atrial automatic tachycardia by ablation procedures

Paul C. Gillette; Deborah G. Wampler; Arthur Garson; Alex Zinner; David A. Ott; Denton A. Cooley

Sixteen cases of atrial focus tachycardia are described clinically, electrophysiologically and hemodynamically. In each case multiple attempts at drug treatment (average 2.5 drugs) had failed. After delineation of the electrophysiologic mechanism, the patients were treated by surgical removal or cryoablation or catheter electroablation of the focus. In two of four patients catheter ablation was successful and without complication. Surgical treatment was successful in 13 of 14 patients. Left ventricular function, which had been abnormal in 10 patients, normalized in all but 1 patient whose echocardiographic shortening fraction improved from 10 to 27%. There have been no recurrences in a follow-up period of 6 months to 5 years (mean 2.2 years). It is recommended that any atrial automatic focus tachycardia that produces hemodynamic compromise undergo definitive treatment. Patients with chronic tachycardia rates of more than 140 beats/min should be followed up closely.


Annals of Surgery | 1987

The management of aortoduodenal fistula by in situ replacement of the infected abdominal aortic graft

William E. Walker; Denton A. Cooley; J M Duncan; Grady L. Hallman; David A. Ott; G J Reul

Conventional surgical wisdom dictates the complete removal of infected abdominal aortic graft, oversewing of the aorta, and restoration of lower limb bloodflow by extra-anatomic bypass grafting. Dissatisfied with this approach because of the high incidence of local complications, mortality, and loss of limb, 20 patients with secondary aortoduodenal fistula had duodenal repair, excision of the old graft, and placement of a new graft in the same location. A similar technique was used in three patients with erosion of an aortic graft into the jejunum. Length of follow-up averaged 5.2 years, and was more than 1 year in each instance. Of the eighteen patients who survived the repair, three have had early recurrent rupture or false aneurysm of the proximal aortic anastomosis, with consequent death in two, but fifteen patients (83%) have had no further related problem. There was no loss of limb. Use of greater omentum as a protective barrier seemed helpful. Optimal antibiotic usage, and the idea that varying degrees of graft infection require different approaches, require further definition. In conclusion, in situ graft replacement is the correct operative strategy in this challenging group of patients.


American Journal of Cardiology | 1972

Dysrhythmias after mustard's operation for transposition of the great arteries☆

Galal El-Said; Harvey S. Rosenberg; Charles E. Mullins; Hallman Gl; Denton A. Cooley; Dan G. McNamara

Abstract Dysrhythmias after Mustards operation for transposition of the great arteries were studied in 60 patients who survived the operation. Only 3 patients consistently had sinus rhythm after the operation. In 54 patients, low voltage atrial waves having the configuration of sinus P waves were seen at one time or another. The incidence of passive dysrhythmias remained nearly the same during the follow-up period. Eight patients showed at various times a specific pattern designated junctional rhythm with right inferior P axis. The mean P axis was directed downward, to the right and anteriorly, occurring either before or after the QRS complex with fixed Pue5f8R or Rue5f8P intervals. The characteristics of the junctional rhythm with right inferior P axis remained during subsequent attacks of supraventricular tachycardias. Whereas the incidence of sinus rhythm gradually decreased, the incidence of active dysrhythmias increased during follow-up study. There were no instances of second or third degree atrioventricular (A-V) block. Wolff-Parkinson-White syndrome, type A, developed and persisted in 1 patient. In 5 patients who died, presumably from rhythm disturbances, the histologie features of the sinoatrial (S-A) nodal area were examined. In a control group of normal hearts and 1 specimen with unoperated upon transposition, the S-A node and artery were readily identified. In the necropsy material from patients with transposition who had recently undergone Mustards operation, S-A nodal tissue was identified but fresh hemorrhage and acute inflammation were seen in and about the node. The S-A nodal artery in the 3 patients who died 4 months or more after operation was nearly or completely obliterated by intimai sclerosis and medial hypertrophy. The S-A node was replaced by dense connective tissue and fatty degeneration.


Annals of Surgery | 1952

Surgical Considerations of Intrathoracic Aneurysms of the Aorta and Great Vessels

Denton A. Cooley; Michael E. DeBakey

This was the first article that DeBakey and Cooley wrote together, and showed the rapid progress they were making in vascularn surgery.


American Heart Journal | 1982

Prolonged and decremental antograde conduction properties in right anterior accessory connections: Wide QRS antidromic tachycardia of left bundle branch block pattern without Wolff-Parkinson-White configuration in sinus rhythm

Paul C. Gillette; Arthur Garson; Denton A. Cooley; Dan G. McNamara

Four patients are described who had long conduction times and decremental conduction through right anterior accessory connections. None had Wolff-Parkinson-White syndrome on their ECG. Each had recurrent sustained wide QRS tachycardia due to antegrade conduction through the accessory connection. Three patients underwent epicardial mapping and successful surgical division of their accessory connection. Two of the three had a second accessory connection that was also divided surgically. Each of the three are free of tachycardia without medication. It is postulated that these accessory connections represent the remnants of anterior atrioventricular ring tissue described by Anderson.


American Heart Journal | 1985

Long-term follow-up of dysrhythmias following the Mustard procedure

Mark C. Duster; Margreet Th. E. Bink-Boelkens; Deborah G. Wampler; Paul C. Gillette; Dan G. McNamara; Denton A. Cooley

Earlier reports have suggested that the incidence of dysrhythmias after the Mustard procedure can be reduced if the sinoatrial node (SAN) is protected during surgery. To determine if these initial differences continue after longer follow-up, we examined all ECGs available for three groups of patients operated upon from January, 1965, through December, 1977. Group A included 37 patients who survived the operation prior to January, 1972, when surgical modifications were initiated to protect the SAN; group B included 44 patients available for follow-up who were operated upon from 1972 through 1974; and group C consisted of the 39 patients available for follow-up operated upon from 1975 to 1977. Dysrhythmias were classified as passive (failure of initiation or propagation of the SAN impulse), active (atrial flutter or supraventricular tachycardia), or atrioventricular (AV) conduction defects. Results were expressed as the incidence per number of different rhythms during follow-up intervals. The incidence of sinus rhythm in groups B and C (80%) was much greater than in group A (27%) during the first 2 years. However, after 8 years, less than 50% of the rhythms were sinus. Both brady- and tachydysrhythmias were common. Seven patients (6%) required pacemaker insertion for symptomatic sick sinus syndrome. Therefore despite efforts to protect the sinus node, late occurring dysrhythmias remain a significant problem in the postoperative Mustard patient.


Annals of Surgery | 1992

Intracavitary repair of ventricular aneurysm and regional dyskinesia.

Denton A. Cooley; O.H. Frazier; J M Duncan; G J Reul; Z Krajcer

Myocardial damage after infarction is a common sequela in patients with coronary occlusive disease. The extent of injury varies and may be localized or diffuse. Since March 1989, the authors have used a new surgical repair technique that employs an intracavitary patch of Dacron fabric or glutaraldehyde-treated pericardium to exclude the hypokinetic or fibrotic myocardial segment. An elliptical configuration preserves the contour and volume of the ventricular cavity. After securing the patch, the ventriculotomy is closed with a simple continuous suture. Through July 31, 1991, 136 patients underwent repair using this technique. Of these patients, 100 (group I) had neither sustained an acute myocardial infarction (within 30 days before surgery) nor had undergone previous cardiac surgery, whereas 36 (group II) had sustained an acute myocardial infarction or had undergone previous cardiac surgery. In group I, four (4%) died within 30 days of surgery, and seven died later, resulting in a 6-month survival of 90.5% and a 1-year survival of 85.3%. In group II, 11 (30.6%) died within 30 days of surgery, and three died later. Functional class improved after repair in 95.7% of patients in group I and all patients in group II. In both groups, ejection fraction improved significantly (p less than 0.0001, group I; p less than 0.0001, group II). By eliminating the need for epicardial buttresses to repair the ventriculotomy, myocardial revascularization has been possible in most patients. This method of intraventricular repair is also appropriate for patients with calcified aneurysms, acquired ventricular septal defects, and acute ventricular rupture.


American Journal of Cardiology | 1980

Surgical treatment of supraventricular tachycardia in infants and children

Paul C. Gillette; Arthur Garson; John D. Kugler; Denton A. Cooley; Alex Zinner; Dan G. McNamara

The technique, indications and results of surgical division of accessory atrioventricular connections in 10 infants and children with drug-resistant supraventricular tachycardia are described. The patients ranged in age from 6 months to 15 years. Four patients had associated congenital heart disease. Division of accessory connections were performed on free wall pathways in nine patients (seven right atrial, two left atrial) and on a septal pathway in one patient. Four patients had both anterograde and retrograde conduction over the accessory connection (manifest Wolff-Parkinson-White conduction) whereas six had only retrograde conduction (concealed Wolff-Parkinson-White conduction). The manifst Wolff-Parkinson-White conduction was abolished by surgical division in all four patients. In 8 of the 10 patients the procedure stopped the attacks of paroxysmal supraventricular tachycardia for follow-up periods ranging from 9 months to 3 1/2 years; no patient receives medication to date.


Circulation | 1972

Atresia of the Left Coronary Artery Ostium Repair by Saphenous Vein Graft

Charles E. Mullins; Galal El-Said; Dan G. McNamara; Denton A. Cooley; B. Treistman; E. Garcia

Symptoms and electrocardiographic changes of acute myocardial ischemia in a 10-year-old boy resulted from congenital atresia of the ostium of the left coronary artery. At 14 years of age persistence of symptoms and a positive exercise test prompted surgical treatment by aortocoronary artery saphenous vein bypass graft. Two months postoperatively, the symptoms and the abnormal findings on exercise test had subsided and forward flow through the graft to the left coronary artery was demonstrated by contrast angiography.


American Journal of Cardiology | 1979

Management of surgical complete atrioventricular block in children

David J. Driscoll; Paul C. Gillette; Hallman Gl; Denton A. Cooley; Dan G. McNamara

Because there is disagreement concerning the efficacy of and indication for permanent pacemaker implantation in children with postoperative complete (third degree) atrioventricular (A-V) block, experience in the management of this problem at one institution was reviewed. Thirty-four patients with postoperative complete atrioventricular block were identified. They ranged in age from 4 months to 22 years and in weight from 4 to 60 kg and were evaluated from 1 month to 20 years postoperatively. Complete A-V block developed within 24 hours of operation in 28 of the 34 patients. A permanent pacemaker was implanted in 13 of the 28. Death occurred in 4 of these 13 patients and in 5 of the remaining 15 patients who did not have an artificial permanent pacemaker. Complete A-V block developed later than 1 day (2 days to 4 months) postoperatively in 6 of the 34 patients; all 6 of these patients survived, and only 3 required permanent pacemaker implantation. Intracardiac electrophysiologic studies were performed by 14 of the 34 patients. The site of complete block was above the His bundle in 5, within the His bundle in 2, and below the His bundle in 4; it was undetermined in 3. The results of intracardiac electrophysiologic studies are important in delineating the natural history of surgically induced complete A-V block and in the clinical management of this lesion. Permanent pacemaker implantation is indicated if complete A-V block persists longer than 2 weeks postoperatively and if the site of the block is within or below the bundle of His.

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Dan G. McNamara

Baylor College of Medicine

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Paul C. Gillette

Medical University of South Carolina

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Hallman Gl

Baylor College of Medicine

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Galal El-Said

Baylor College of Medicine

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David A. Ott

Baylor College of Medicine

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Michael R. Nihill

Baylor College of Medicine

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