Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where W. David Watkins is active.

Publication


Featured researches published by W. David Watkins.


Journal of Clinical Anesthesia | 1998

Benchmarking the perioperative process: III. Effects of regional anesthesia clinical pathway techniques on process efficiency and recovery profiles in ambulatory orthopedic surgery☆

Brian A. Williams; Barbara M DeRiso; Chiara M Figallo; Joel W Anders; Lori B Engel; Kari A Sproul; Hakan Ilkin; Christopher D. Harner; Freddie H. Fu; Nandu J. Nagarajan; John H. Evans; W. David Watkins

STUDY OBJECTIVES (1) To incorporate regional anesthesia options for common outpatient orthopedic surgery into clinical pathways; (2) to use the clinical pathway format and the Procedural Times Glossary published by the Association of Anesthesia Clinical Directors (AACD) as management tools to measure postoperative same-day surgery processes and discharge outcomes; and (3) to determine the effects of general, regional, and combined general-regional anesthesia on these processes and outcomes. DESIGN Hospital database and patient chart review of consecutive patients undergoing anterior cruciate ligament reconstruction (ACLR) during academic years (AY) 1995-1996 and 1996-1997. Patient data from AY 1995-1996, during which no intraoperative anesthesia clinical pathway existed, served as historical controls. Data from AY 1996-1997, during which intraoperative anesthesia clinical pathways were used, served as the treatment group. SETTING Ambulatory surgery center in a teaching hospital. MEASUREMENTS AND MAIN RESULTS The records of 503 ASA physical status I and II patients were reviewed. 1996-1997 patients selected general anesthesia (+/- femoral nerve block) or epidural anesthesia, after which the remainder of the perioperative anesthesia process was standardized with respect to the drugs and equipment used. 1995-1996 patients did not necessarily have a choice in anesthesia technique and did not have a standardized perioperative anesthetic course with respect to specific drugs and supplies. Intervals described in the AACD Procedural Times Glossary, anesthesia drug and supply costs, and patient outcome variables (postoperative nursing interventions required and unexpected admissions), as influenced by anesthesia technique used, were measured. Combined general-regional anesthesia care for ACLR in 1996-1997, when compared with general anesthesia alone, led to increased pharmacy and materials costs and increased turnover time. However, patients with the combined technique showed improved recovery profiles and lower unexpected admission rates, and they required fewer nursing interventions for common postoperative symptoms. Patients receiving epidural anesthesia showed discharge outcomes similar to those patients receiving general anesthesia with femoral nerve block. Postanesthesia care unit bypass (fast-tracking) was more likely in clinical pathway regional anesthesia patients, when compared with the clinical pathway general anesthesia used. CONCLUSIONS Clinical pathway regional anesthesia care for outpatient orthopedics may have a significant role in simultaneously containing costs and improving both process efficiency and patient outcomes.


Advances in pharmacology | 1995

Nitric Oxide and Intracellular Heme

Young-Myeong Kim; Hector A. Bergonia; Claudia Müller; Bruce R. Pitt; W. David Watkins; Jack R. Lancaster

Figure 2 depicts a working hypothesis for these results. Activation of .NO synthesis results in nitrogen oxide-induced loss of protein-bound heme from CYP proteins, which remain relatively intact. This heme liberation results in a decrease in heme synthesis (decreased ALAS) and an increase in heme degradation (increased HO). In addition, .NO synthesis results in direct inhibition of ferrochelatase, which further contributes to inhibition of heme synthesis. There also appears to be a mechanism to repair or resynthesize CYP after .NO synthesis is inhibited. Finally, a result of this effect may be protection against cellular injury, since increased HO is an important response against cellular injury from a variety of insults.


Journal of Hepatology | 1998

Superoxide-induced changes in endothelin (ET) receptors in hepatic stellate cells

Adelheid Gabriel; R Kuddus; Abdul S. Rao; W. David Watkins; Chandrashekhar R. Gandhi

BACKGROUND/AIMS Reactive oxygen species are mediators of various pathophysiologic events, including postischemic reperfusion injury and inflammation. Generation of reactive oxygen species and consequent organ injury are associated with increased levels of a powerful vasoconstrictor peptide endothelin-1. Current evidence suggests that actions of endothelin-1 on the contractile and fibrogenic transdifferentiated stellate cells may play a critical role in hepatic pathophysiology. The aim of this investigation was to determine whether reactive oxygen species modulate the synthesis of endothelin-1 and its receptors in stellate cells. METHODS Primary cultures of transdifferentiated stellate cells were exposed to reactive oxygen species-generating system, hypoxanthine/xanthine oxidase, before determination of endothelin-1 and its receptors. RESULTS The treatment caused an initial decrease in ET-1 receptor density (about 30% at 30 min), followed by a significant increase over the basal level at 6 h. The increase in the receptors, which occurred specifically in the ET(B) subtype, progressed thereafter up to 24 h and was accompanied by an augmented functional response, as indicated by an enhanced endothelin-1-induced release of [3H]arachidonic acid from the prelabeled cells. Furthermore, treatment of cells for 24 h but not 30 min caused increased expression of ET(B) mRNA as determined by semi-quantitative polymerase chain reaction. The release of endothelin-1 in the culture medium was also enhanced by hypoxanthine/xanthine oxidase treatment. These effects of hypoxanthine/xanthine oxidase were inhibited by superoxide dismutase and dimethyl sulfoxide. ET-1-induced [3H]arachidonic acid release was also inhibited by the ET(B) receptor antagonist BQ788, but not by the ET(A) receptor antagonist BQ123. CONCLUSIONS These findings indicate that interactions between ET-1 and stellate cells during episodes of the generation of reactive oxygen species can be an important mechanism in the pathophysiology of hepatic disorders.


Journal of Clinical Anesthesia | 1998

Benchmarking the perioperative process: II. Introducing anesthesia clinical pathways to improve processes and outcomes and to reduce nursing labor intensity in ambulatory orthopedic surgery

Brian A. Williams; Barbara M DeRiso; Lori B Engel; Chiara M Figallo; Joel W Anders; Kari A Sproul; Hakan Ilkin; Christopher D. Harner; Freddie H. Fu; Nandu J. Nagarajan; John H. Evans; W. David Watkins

STUDY OBJECTIVES (1) To introduce anesthesia clinical pathways as a management tool to improve the quality of care; (2) to use the Procedural Times Glossary published by the Association of Anesthesia Clinical Directors (AACD) as a template for data collection and analysis; and (3) to determine the effects of anesthesia clinical pathways on surgical processes, outcomes, and costs in common ambulatory orthopedic surgery. DESIGN Hospital database and patient chart review of consecutive patients undergoing anterior cruciate ligament reconstruction (ACLR) during academic years (AY) 1995-1996 and 1996-1997. Patient data from AY 1995-1996, during which no intraoperative anesthesia clinical pathways existed, served as historical controls. Data from AY 1996-1997, during which intraoperative anesthesia clinical pathways were used, served as the treatment group. Regional anesthesia options were routinely offered to patients in the clinical pathway. SETTING Ambulatory surgery center in a teaching hospital. MEASUREMENTS AND MAIN RESULTS The records of 503 ASA physical status I and II patients were reviewed. 1996-1997 patients underwent clinical pathway anesthesia care in which the intraoperative and postoperative anesthesia process was standardized with respect to symptom management, drugs, and equipment used. 1995-1996 patients did not have a standardized intraoperative and postoperative anesthetic course with respect to the management of common symptoms or to specific drugs and supplies used. Intervals described in the AACD Procedural Times Glossary, anesthesia drug and supply costs, and patient outcome variables (postoperative nursing interventions required and unexpected admissions), as influenced by the use of the anesthesia clinical pathway, were measured. Clinical pathway anesthesia care of ACLR in 1996-1997, which actively incorporated regional anesthesia options, reduced pharmacy and materials cost variability; slightly increased turnover time; improved intraoperative anesthesia and surgical efficiency, recovery times, and unexpected admission rates; and decreased the number of required nursing interventions for common postoperative symptoms. CONCLUSIONS Clinical pathway patient management systems in anesthesia care are likely to produce useful outcome data of current practice patterns when compared with historical controls. This management tool may be useful in simultaneously containing costs and improving process efficiency and patient outcomes.


Current Opinion in Anesthesiology | 1994

Mechanisms and modulators of opioid analgesia

Brett R. Stacey; W. David Watkins

Three general avenues of recent research serve to advance the basis of understanding of opioid analgesia: (1) the characterization of opioid receptors; (2) the definition of endogenous substances that mediate or modulate opioid receptor function; (3) an improved understanding of opioid tolerance and dependence. Advances in each area are revealing treatment and pharmacologic strategies which promise safer and more effective treatment of pain.


Journal of Biological Chemistry | 1995

Loss and Degradation of Enzyme-bound Heme Induced by Cellular Nitric Oxide Synthesis

Young-Myeong Kim; Hector A. Bergonia; Claudia Müller; Bruce R. Pitt; W. David Watkins; Jack R. Lancaster


Anesthesiology | 1994

Endothelins. Biochemistry and pathophysiologic actions.

Chandrashekhar R. Gandhi; Dan E. Berkowitz; W. David Watkins


Journal of Clinical Anesthesia | 1997

Benchmarking the perioperative process. I. Patient routing systems: A method for continual improvement of patient flow and resource utilization

Armando J. Rotondi; Charles Brindis; Kimberly K. Cantees; Barbara M DeRiso; Hakan Ilkin; Jeffrey S. Palmer; Helena B. Gunnerson; W. David Watkins


Journal of Hepatology | 2000

A scenario-based stochastic programming model for water supplies from the highland lakes

W. David Watkins; Daene C. McKinney; Leon S. Lasdon; Søren Saxmose Nielsen; Quentin W. Martin


Archive | 1995

Nitric Oxide and Intracellular Heme 1 1 This chapter is dedicated to Professor Lawrence H. Piette, who died on November 17,1992.

Young-Myeong Kim; Hector A. Bergonia; Claudia Müller; Bruce R. Pitt; W. David Watkins; Jack R. Lancaster

Collaboration


Dive into the W. David Watkins's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar

Bruce R. Pitt

University of Pittsburgh

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Hakan Ilkin

University of Pittsburgh

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Jack R. Lancaster

University Medical Center New Orleans

View shared research outputs
Top Co-Authors

Avatar

Young-Myeong Kim

Kangwon National University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Chandrashekhar R. Gandhi

Cincinnati Children's Hospital Medical Center

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge