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Dive into the research topics where Douglas Gregory is active.

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Featured researches published by Douglas Gregory.


Circulation | 2004

Randomized, Controlled Evaluation of Short- and Long-Term Benefits of Heart Failure Disease Management Within a Diverse Provider Network The SPAN-CHF Trial

Carey Kimmelstiel; Daniel M. Levine; Kathleen Perry; Ara Sadaniantz; Noreen Gorham; Margaret Cunnie; Lynne Duggan; Linda Cotter; Patricia Shea-Albright; Athena Poppas; Kenneth LaBresh; Daniel E. Forman; David Brill; William M. Rand; Douglas Gregory; James E. Udelson; Beverly H. Lorell; Varda Konstam; Kathleen Furlong; Marvin A. Konstam

Background—Several trials support the usefulness of disease management (DM) for improving clinical outcomes in heart failure (HF). Most of these studies are limited by small sample size; absence of concurrent, randomized controls; limited follow-up; restriction to urban academic centers; and low baseline use of effective medications. Methods and Results—We performed a prospective, randomized assessment of the effectiveness of HF DM delivered for 90 days across a diverse provider network in a heterogeneous population of 200 patients with high baseline use of approved HF pharmacotherapy. During a 90-day follow-up, patients randomized to DM experienced fewer hospitalizations for HF [primary end point, 0.55±0.15 per patient-year alive versus 1.14±0.22 per patient-year alive in control subjects; relative risk (RR), 0.48, P=0.027]. Intervention patients experienced reductions in hospital days related to a primary diagnosis of HF (4.3±0.4 versus 7.8±0.6 days hospitalized per patient-year; RR, 0.54; P<0.001), cardiovascular hospitalizations (0.81±0.19 versus 1.43±0.24 per patient-year alive; RR, 0.57; P=0.043), and days in hospital per patient-year alive for cardiovascular cause (RR, 0.64; P<0.001). Intervention patients showed a trend toward reduced all-cause hospitalizations and total hospital days. On long-term (mean, 283 days) follow-up, there was substantial attrition of the 3-month gain in outcomes, with sustained significant reduction only in days in hospital for cardiac cause. Conclusions—In a population with high background use of standard HF therapy, a DM intervention, uniformly delivered across varied clinical sites, produced significant short-term improvement in HF-related clinical outcomes. Longer-term benefit likely requires more active chronic intervention, even among patients who appear clinically stable.


American Heart Journal | 2011

CD34+ cell infusion after ST elevation myocardial infarction is associated with improved perfusion and is dose dependent

Arshed A. Quyyumi; Edmund K. Waller; Jonathan R. Murrow; Fabio Esteves; James R. Galt; John N. Oshinski; Stamatios Lerakis; Salman Sher; Douglas E. Vaughan; Emerson C. Perin; James T. Willerson; Bernard J. Gersh; Douglas Gregory; Astrid Werner; Thomas J. Moss; Wai Shun Chan; Robert A. Preti; Andrew L. Pecora

BACKGROUND the objective of the study was to determine whether the effects of infarct-related artery (IRA) infusion of autologous bone marrow-derived CD34(+) cells after ST elevation myocardial infarction (STEMI) are dependent on the dose (quantity and mobility) of the cells infused. Beneficial effects of IRA infusion of mononuclear cells after STEMI have been inconsistent, possibly because of differences in timing, cell type, quantity, and mobility of infused cells. METHODS patients were randomized to bone marrow harvest (n = 16) or control (n = 15). At a median of 8.3 days after coronary stenting for STEMI, CD34(+) cells were infused via the IRA at 3 dose levels (5, 10, and 15 × 10(6)) in cohorts of 5 patients each. Baseline and follow-up imaging and ex vivo CD34(+) cell mobility were performed. RESULTS Cell harvest and infusion were safe. Quantitative rest hypoperfusion score measured by single-photon emission computed tomography improved at 6 months in the ≥ 10 million cohorts compared with controls (-256 vs +14, P = .02). There was a trend toward improved ejection fraction at 6 months (+4.5%) in the ≥ 10 million cohorts compared with no change in the controls and 5 million cohort (+0.7%). Improved perfusion and infarct size reduction correlated with the quantity and mobility of the infused CD34(+) cells. CONCLUSIONS the effects of CD34(+) cell IRA infusion during the repair phase after STEMI are dose dependent and, at a threshold dose of 10 million CD34(+) cells, associated with a significant improvement in perfusion that may limit deterioration in cardiac function (IRA infusion of CD34(+) cells in patients with acute myocardial infarction [AMR-01] NCT00313339).


Journal of Cardiac Failure | 2008

The Heart Failure Clinic: A Consensus Statement of the Heart Failure Society of America

Paul J. Hauptman; Michael W. Rich; Paul A. Heidenreich; John Chin; Nancy Cummings; Mark E. Dunlap; Michelle Edwards; Douglas Gregory; Christopher M. O'Connor; Stephen M. Pezzella; Edward F. Philbin

BACKGROUND Outpatient care accounts for a significant proportion of total heart failure (HF) expenditures. This observation, plus an expanding list of treatment options, has led to the development of the disease-specific HF clinic. METHODS AND RESULTS The goals of the HF clinic are to reduce mortality and rehospitalization rates and improve quality of life for patients with HF through individualized patient care. A variety of staffing configurations can serve to meet these goals. Successful HF clinics require an ongoing commitment of resources, the application of established clinical practice guidelines, an appropriate infrastructure, and a culture of quality assessment. CONCLUSIONS This consensus statement will identify the components of HF clinics, focusing on systems and procedures most likely to contribute to the consistent application of guidelines and, consequently, optimal patient care. The domains addressed are: disease management, functional assessment, quality of life assessment, medical therapy and drug evaluation, device evaluation, nutritional assessment, follow-up, advance planning, communication, provider education, and quality assessment.


Journal of Cardiac Failure | 2010

A Multicenter Randomized Controlled Evaluation of Automated Home Monitoring and Telephonic Disease Management in Patients Recently Hospitalized for Congestive Heart Failure: The SPAN-CHF II Trial

Andrew Weintraub; Douglas Gregory; Daniel M. Levine; David M. Venesy; Kathleen Perry; Christine Delano; Marvin A. Konstam

BACKGROUND We performed a prospective, randomized investigation assessing the incremental effect of automated health monitoring (AHM) technology over and above that of a previously described nurse directed heart failure (HF) disease management program. The AHM system measured and transmitted body weight, blood pressure, and heart rate data as well as subjective patient self-assessments via a standard telephone line to a central server. METHODS AND RESULTS A total of 188 consented and eligible patients were randomized between intervention and control groups in 1:1 ratio. Subjects randomized to the control arm received the Specialized Primary and Networked Care in Heart Failure (SPAN-CHF) heart failure disease management program. Subjects randomized to the intervention arm received the SPAN-CHF disease management program in conjunction with the AHM system. The primary end point was prespecified as the relative event rate of HF hospitalization between intervention and control groups at 90 days. The relative event rate of HF hospitalization for the intervention group compared with controls was 0.50 (95%CI [0.25-0.99], P = .05). CONCLUSIONS Short-term reductions in the heart failure hospitalization rate were associated with the use of automated home monitoring equipment. Long-term benefits in this model remain to be studied.


Health Services Research | 2003

Hospital economics of the hospitalist.

Douglas Gregory; Walter Baigelman; Ira B. Wilson

OBJECTIVE To determine the economic impact on the hospital of a hospitalist program and to develop insights into the relative economic importance of variables such as reductions in mean length of stay and cost, improvements in throughput (patients discharged per unit time), payer methods of reimbursement, and the cost of the hospitalist program. DATA SOURCES The primary data source was Tufts-New England Medical Center in Boston. Patient demographics, utilization, cost, and revenue data were obtained from the hospitals cost accounting system and medical records. STUDY DESIGN The hospitalist admitted and managed all patients during a six-week period on the general medical unit of Tufts-New England Medical Center. Reimbursement, cost, length of stay, and throughput outcomes during this period were contrasted with patients admitted to the unit in the same period in the prior year, in the preceding period, and in the following period. PRINCIPAL FINDINGS The hospitalist group compared with the control group demonstrated: length of stay reduced to 2.19 days from 3.45 days (p<.001); total hospital costs per admission reduced to 1,775 dollars from 2,332 dollars (p<.001); costs per day increased to 811 dollars from 679 dollars (p<.001); no differences for readmission within 30 days of discharge to extended care facilities. The hospitals expected incremental profitability with the hospitalist was -1.44 dollars per admission excluding incremental throughput effects, and it was most sensitive to changes in the ratio of per diem to case rate reimbursement. Incremental throughput with the hospitalist was estimated at 266 patients annually with an associated incremental profitability of 1.3 million dollars. CONCLUSION Hospital interventions designed to reduce length of stay, such as the hospitalist, should be evaluated in terms of cost, throughput, and reimbursement effects. Excluding throughput effects, the hospitalist program was not economically viable due to the influence of per diem reimbursement. Throughput improvements occasioned by the hospitalist program with high baseline occupancy levels are substantial and tend to favor a hospitalist program.


Journal of Cardiac Failure | 2011

Health-Related Quality of Life in a Multicenter Randomized Controlled Comparison of Telephonic Disease Management and Automated Home Monitoring in Patients Recently Hospitalized With Heart Failure: SPAN-CHF II Trial

Varda Konstam; Douglas Gregory; Jie Chen; Andrew Weintraub; Daniel M. Levine; David M. Venesy; Kathleen Perry; Christine Delano; Marvin A. Konstam

BACKGROUND Although disease management programs have been shown to provide a number of clinical benefits to patients with heart failure (HF), the incremental impact of an automated home monitoring (AHM) system on health-related quality of life (HRQL) is unknown. METHODS AND RESULTS We performed a prospective randomized investigation, examining the additive value of AHM to a previously described nurse-directed HF disease management program (SPAN-CHF), with attention to HRQL, in patients with a recent history of decompensated HF. A total of 188 patients were randomized to receive the SPAN-CHF intervention for 90 days, either with (AHM group) or without (NAHM, standard-care group) AHM, with a 1:1 randomization ratio after HF-related hospitalization. HRQL, measured by the Minnesota Living With Heart Failure Questionnaire (MLHFQ) (Physical, Emotional, and Total scores on MLHFQ) was assessed at 3 time points: baseline, 45 days, and 90 days. Although both treatments (AHM and NAHM) improved HRQL at 45 and 90 days compared with baseline with respect to Physical, Emotional, and Total domain scales, no significant difference emerged between AHM and NAHM groups. CONCLUSIONS AHM and NAHM treatments demonstrated improved HRQL scores at 45 and 90 days after baseline assessment. When comparing 2 state-of the-art disease management programs regarding HRQL outcomes, our results did not support the added value of AHM.


The American Journal of Medicine | 2001

Economic impact of beta blockade in heart failure

Douglas Gregory; James E. Udelson; Marvin A. Konstam

We reviewed the literature on clinical trials of beta-adrenergic blockade for treatment of heart failure, seeking evidence of reductions in hospital admissions. To analyze the economic implications of six clinical trials, we developed a stochastic cost model to generate estimates of total medical costs resulting from heart failure and related causes. The model includes inpatient, outpatient, and professional cost estimates based on Medicare claims data, and it is driven by traditional endpoint statistics reported in the clinical trial literature. It provides a common framework for comparing cost effectiveness across clinical trials in the absence of detailed cost information collected in the trial. The incremental expected cost per year of life saved is


International Journal of Cardiology | 2014

Incident hyperkalemia may be an independent therapeutic target in low ejection fraction heart failure patients: Insights from the HEAAL study

Patrick Rossignol; Daniela Dobre; Douglas Gregory; Joe Massaro; Michael S. Kiernan; Marvin A. Konstam; Faiez Zannad

3,300 for bisoprolol,


Circulation-heart Failure | 2015

Tolvaptan in Patients Hospitalized With Acute Heart Failure Rationale and Design of the TACTICS and the SECRET of CHF Trials

G. Michael Felker; Robert J. Mentz; Kirkwood F. Adams; Robert T. Cole; Gregory F. Egnaczyk; Chetan B. Patel; Mona Fiuzat; Douglas Gregory; Patricia Wedge; Christopher M. O’Connor; James E. Udelson; Marvin A. Konstam

2,500 for metoprolol, and


Journal of Cardiac Failure | 2012

HFSA and AAHFN Joint Position Statement: Advocating for a Full Scope of Nursing Practice and Leadership in Heart Failure

Christopher S. Lee; Barry H. Greenberg; Ann S. Laramee; Susan E. Ammon; Marilyn A. Prasun; Marie Galvao; Lynn V. Doering; M. Eugene Sherman; Lynne Warner Stevenson; Douglas Gregory; Paul A. Heidenreich; Navin K. Kapur; John B. O’Connell; Anne L. Taylor; Joseph A. Hill; Linda S. Baas; Ashley Gibbs; Kismet Rasmusson; Connie M. Lewis; Peggy Kirkwood; Juanita Reigle; Lisa D. Rathman; Cynthia Bither

6,700 for carvedilol. The cost per year of life saved for each compound is well below accepted standards for cost effectiveness. These results are sensitive to the cost of drug therapy and the relative mortality rate for the experimental group. For example, if the relative mortality rate of the experimental group were to increase from the reported 40% to 82%, and if the annual cost of the drug were to decrease from

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Paul A. Heidenreich

American College of Physicians

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