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Dive into the research topics where Richard A. Perryman is active.

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Featured researches published by Richard A. Perryman.


Anesthesia & Analgesia | 1997

Cardiopulmonary bypass in a patient with moyamoya disease.

Natalie Wang; John W. Kuluz; Michael Barron; Richard A. Perryman

M oyamoya disease (MMD) is a progressive cerebrovascular occlusive disease of the internal carotid arteries and anterior and middle cerebral arteries that affects children and young adults. Affected patients are pathophysiologically analogous to patients with bilateral internal carotid artery stenosis who are at very high risk of neurologic complications during cardiac surgery. Patients with MMD have not previously been reported to undergo cardiac surgery and cardiopulmonary bypass (CPB). We report a case of a patient with MMD and an atria1 septal defect (ASD) Gho underwent general anesthesia tempted device closure of an ASD followed eventful surgical closure with CPB.


The Annals of Thoracic Surgery | 1991

AUTOGENOUS ATRIAL TUNNEL FOR DIRECT CAVOPULMONARY CONNECTION IN INFANTS AND SMALL CHILDREN

Richard A. Perryman

A technique is described for construction of an autogenous right atrial tunnel for direct cavopulmonary connection in infants and small children requiring Fontan operation. Advantages, in this subset of patients, of this method over others previously described using prosthetic or growth-limited materials are suggested.


Asaio Journal | 1996

Emboli from an extraluminal blood Flow hollow fiber oxygenator with and without an arterial filter during cardiopulmonary bypass in a pig model

Mrinal K. Dewanjee; S. Wu; Mansoor Kapadvanjwala; D. De; Sumit Dewanjee; Lipton Gonzalez; Stana Novak; Li Chien Hsu; Richard A. Perryman; Robert Duncan; Aldo N. Serafini; George N. Sfakianakis; Allan F. Horton

&NA; The effect of an arterial filter on visceral emboli was quantified with autologous indium‐111 labeled platelets (INPLT) during cardiopulmonary bypass (CPB) in Yorkshire pigs. Biodistribution of INPLT was determined in 12 control pigs (30‐35 kg, unoperated control [n = 6] and sham operated control [n = 6]). CPB was carried out with (n = 6) and without (n = 6) an arterial filter in 12 pigs at a flow rate of 2.5‐3.5 L/min. Platelets labeled with In‐111 tropolone (650‐780 &mgr;Ci) were injected intravenously 24 hr before CPB. All pigs were systemically heparinized (activated coagulation time > 400 sec); CPB was instituted with a roller pump, an extraluminal blood flow oxygenator (Bentley Univox, 1.8 m2), and an arterial filter (0.25 m2) and continued for 3 hr. Platelet kinetics, pooling, and counts were monitored by a Geiger probe and a Coulter counter. The thrombi in the oxygenator and arterial filter and emboli in viscera and brain were imaged with a gamma camera and measured with an ion chamber and gamma counter. Percentage of INPLT (mean ± SD) in organs, tissues, and components of the circuit in four groups of pigs was calculated. Flow cytometry with antibodies to CD61 (GPIIIa) and CD62P (GMP‐140: control) of porcine platelets was carried out with blood samples taken before, during, and after CPB for estimation of circulating platelet aggregates and platelet microparticles. Pulmonary, renal, cardiac, and cerebral emboli in pigs undergoing CPB with and without a filter were similar (p < 0.1). The amount of filter adherent thrombi was small (0.04 ± 0.01%); oxygenator adherent thrombus in both groups was similar (p < 0.1). Emboli were found in the cerebral medulla, hippocampus, and posterior cerebral cortex in both groups. During CPB, the arterial filter functioned minimally as a trap for platelet thrombi detached from the oxygenator and circulating emboli. Flow cytometry of blood demonstrated the shift of equilibria from single platelets to platelet aggregates and microparticles during CPB and their gradual reversal to single platelets after CPB; the loosely adherent emboli dis‐aggregated and further shifted these equilibria to single platelets and smaller aggregates, probably through the action of endogenous nitric oxide and prostacyclin. The emboli were trapped in organs and tissues and microparticles were sequestered by the reticuloendothelial system. ASAIO Journal 1996;42:1010‐1018.


Annals of Surgery | 1992

Long-term surgical results in sudden death syndrome associated with cardiac dysfunction after myocardial infarction.

Hooshang Bolooki; Michael D. Horowitz; Alberto Interian; Richard J. Thurer; George M. Palatianos; Eduardo DeMarchena; Richard A. Perryman; Robert J. Myerburg

To evaluate the surgical results in patients with inducible ventricular tachyarrhythmias due to coronary disease and left ventricular dysfunction, the authors reviewed their experience in 170 patients who had survived one or more cardiac arrests after myocardial infarction and were unresponsive to drug therapy based on electrophysiologic studies (EPS). There were nine operative deaths (5%). Based on intraoperative EPS, surgical remodeling of left ventricular dysfunction (aneurysm resection, infarct debulking, and septal reinforcement) with map-guided cryoablation and coronary artery bypass graft was performed in 34 patients (group A), and left ventricular remodeling and coronary artery bypass graft without guided endocardial resection was performed in 25 patients (group B). Forty-three patients (group C) had coronary artery bypass graft with implantation of an automatic implantable cardioverter defibrillator (AICD). Group D (68 patients) received AICD only. After operation, based on EPS results, four patients in group A (12%) and three patients in Group B (15%) required AICD implantation. Overall survival at 6 years was 65%, 48%, 85%, and 58% in patient groups A, B, C, and D, respectively (p = not significant). During follow-up in group A patients, none died suddenly and none needed AICD. In group B, two patients required AICD 3 and 5 years later, and five patients died suddenly. The incidence of sudden death was 2.3%/patient/year and 3.5%/patient/year after AICD implantation (groups C and D). At 6 years, cardiac-event-free survival was 80% and 70% for groups A and B and 38% and 24% for groups C and D, respectively (p less than 0.001). Patients receiving map-guided ablative procedures had significantly improved cardiac-event-free survival rates.


Pediatric Cardiology | 1991

Bull-Worker syncopy: Congenital subclavian steal syndrome following isometric exercise

Richard A. Perryman; Edward Bayne; Robert H. Miller

SummaryA patient with congenital great artery abnormality facilitating subclavian steal is presented. Sustained isometric upper body exercise, using a “Bull-Worker,” resulted in vertebrobasilar steal symptoms (subclavian steal syndrome) shortly after exercise. A mechanism for the timing of symptoms following isometric exercise is suggested.


Obstetrics & Gynecology | 1998

Fetal tissue typing in anticipation of neonatal heart transplantation

Jerry M. Gilles; Gene Burkett; Richard A. Perryman; Peter L. Ferrer

Background Hypoplastic left heart syndrome is among the most common major congenital cardiac anomalies. Fetuses with this anomaly survive but require either reconstructive surgery or heart transplantation postnatally. Case A woman whose fetus was diagnosed with hypoplastic left heart syndrome underwent funipuncture for fetal tissue typing. The fetus then was listed for heart transplantation. Once an ABO-compatible donor heart was procured, the fetus was delivered and immediately underwent transplantation. Conclusion In candidates for neonatal heart transplantation, fetal tissue typing allows the search for an ABO-compatible donor heart to begin earlier. This approach minimizes the morbidity associated with postnatal waiting and allows transplantation to take place while the neonate is less immunocompetent.


Asaio Journal | 1996

Reduction of neutrophil margination by L-arginine during hypothermic cardiopulmonary bypass in a pig model.

Mrinal K. Dewanjee; S. Wu; D. De; Stana Novak; W. Ganz; Li-Chien Hsu; Richard A. Perryman; A. H. Serafini; George N. Sfakianakis

Nitric oxide generation by L-arginine (2 mg/kg/min) infusion during cardiopulmonary bypass (CPB) increases blood flow to all organs and reduces cytokine induced organ damage by reducing the level of marginating neutrophils (Ns). The N-trapping in the oxygenator (OX), arterial filter (AF), cardiotomy reservoir (CR), and N-margination were quantified with indium 111 labeled autologous neutrophils (INN) in nine groups of 40 Yorkshire pigs (30-35 kg). Cardiopulmonary bypass (180 min or 90 min CPB, 90 min reperfusion) was carried out at 2.5-3.5 L/min and at two temperatures (18 degrees C, 28 degrees C). The INN (650-780 microCi) was administered intravenously 15 mins before CPB. All pigs received heparin systemically (activated coagulation time > 400 secs); CPB was instituted with a roller pump, OX (Univox 1.8 m2), AF (0.25 m2), and CR (BCR-3500, Bentley Lab, Irvine, CA). The INN distribution in the device (OX, AF, CR) and organs was imaged with a gamma camera and measured with an ion chamber and a gamma counter. The LA infusion decreased N-trapping, estimated as the percent of injected INN (mean +/- standard deviation), in OX from control (2.7 +/- 2.02)% to (0.94 +/- 0.29)%, and margination in lung from control (48 +/- 4)% to minimal levels (23 +/- 2)% (p < 0.01). In the CPB reperfusion group, a beneficial effect was observed at LA low dose and toxicity of higher N-margination at 15 mg/ kg/min. Neither CPB temperature nor Leumedin affected N-margination significantly.


Journal of Thrombosis and Thrombolysis | 1996

Reduction of platelet thrombi and emboli by L-arginine during cardiopulmonary bypass in a pig model

Mrinal K. Dewanjee; S. Wu; Mansoor Kapadvanjwala; D. De; Sumit Dewanjee; Stana Novak; Li Chien Hsu; Richard A. Perryman; Aldo N. Serafini; George N. Sfakianakis; Robert Duncan; W. Dalton Dietrich; Allan F. Horton

We wanted to test the hypothesis that NO generation by L-arginine (LA) infusion will be beneficial in increasing blood flow to all organs to counteract the process of global ischemia during cardiopulmonary bypass (CPB) and to reduce platelet emboli by platelet inhibition. The effect of LA infusion on NO formation, vasodilation, and reduction of thromboembolic burden in organs and tissues after CPB was quantified with In-111-labeled autologous platelets in two major groups: 180 minutes CPB (CPB) and 90 minutes CPB plus 90 minutes reperfusion (RP). Platelets labeled with In-111 tropolone (650–780 μCi) were administered 24 hours before CPB and LA infusion (bolus, 10 mg/kg and infusion at 2 mg/kg/min, 21 pigs for 180 minutes CPB) in 8 groups of 30 Yorkshire pigs (30–35 kg, 6 pigs; LA 2 mg/kg/min, 3 pigs; sham-thoracotomy control, 6 pigs; unoperated control, 6 pigs). Two groups of 9 pigs (control CPB, 6 pigs; LA 2 mg/ kg/min, 3 pigs) underwent 90 minutes of CPB and 90 minutes of reperfusion. All pigs were heparinized (ACT >400 seconds); CPB was instituted with a roller pump, an oxygenator (OX: Bentley Univox, 1.8 m2), and an arterial filter (AF: 0.25 m2, Bentley) at a blood flow of 2.5–3.5 1/min. Radioactive thrombi in OX and AF and emboli in viscera, brain, and connective tissues were imaged with a gamma camera and were finally measured with an ion chamber and a gamma counter. The percent of injected platelets (mean ± SD) in the organs and tissues of all pigs was calculated. Cerebral emboli were mapped in 25 regions of both hemispheres of pig brain. Flow cytometry with antibodies to CD61 (GPIIIa) and CD62P (GMP-140: control) of porcine platelets was carried out with blood samples taken before, during, and after CPB. Coronary bypass with LA infusion decreased the amount of adherent thrombi in OX and AF (p < 0.07). The embolic burden in brain and lung also decreased. Regional cerebral mapping of In-111 platelets showed reduced emboli in almost all regions, including the medulla, hippocampus, and posterior cerebral cortex in both LA-treated groups. Flow cytometry of blood samples demonstrated the shift of equilibria from single platelet to platelet-aggregate-microparticle during CPB and steady-state level after the first 5–10 minutes of initiation of CPB. The L-arginine infusion reduced thrombi and emboli during CPB in the pig model.


The Annals of Thoracic Surgery | 1997

Atrially Based Pericardial Tunnel for Central Pulmonary Artery Construction

Richard A. Perryman; Robert D.B. Jaquiss

Discontinuity of central intrapericardial pulmonary arteries requires reconstruction of a pulmonary artery confluence before cavopulmonary connection, whether this connection be by bidirectional Glenn or Fontan procedure. Reconstruction of the central pulmonary arteries has previously been described using material of poor or no growth potential. A method is described for central pulmonary artery reconstruction that provides growth potential and is based on previous experience with Fontan lateral tunnel construction.


The Annals of Thoracic Surgery | 1997

Rapid Safe Central Venous Access in Children and Adults Undergoing Open Cardiac Operations

Robert D.B. Jaquiss; Richard A. Perryman

A technique is described for percutaneous placement of central venous catheters under direct vision in children and adults undergoing open heart operations. The method is reliable, rapid, and safe, and avoids blind attempts at obtaining vascular access.

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D. De

University of Miami

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S. Wu

University of Miami

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