Belinda Ireland
Saint Louis University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Belinda Ireland.
Chest | 2015
Gerard J. Criner; Jean Bourbeau; Rebecca L. Diekemper; Daniel R. Ouellette; Donna Goodridge; Paul Hernandez; Kristen Curren; Meyer Balter; Mohit Bhutani; Pat G. Camp; Bartolome R. Celli; Gail Dechman; Mark T. Dransfield; Stanley B. Fiel; Marilyn G. Foreman; Nicola A. Hanania; Belinda Ireland; Nathaniel Marchetti; Darcy Marciniuk; Richard A. Mularski; Joseph Ornelas; Jeremy Road; Michael K. Stickland
BACKGROUND COPD is a major cause of morbidity and mortality in the United States as well as throughout the rest of the world. An exacerbation of COPD (periodic escalations of symptoms of cough, dyspnea, and sputum production) is a major contributor to worsening lung function, impairment in quality of life, need for urgent care or hospitalization, and cost of care in COPD. Research conducted over the past decade has contributed much to our current understanding of the pathogenesis and treatment of COPD. Additionally, an evolving literature has accumulated about the prevention of acute exacerbations. METHODS In recognition of the importance of preventing exacerbations in patients with COPD, the American College of Chest Physicians (CHEST) and Canadian Thoracic Society (CTS) joint evidence-based guideline (AECOPD Guideline) was developed to provide a practical, clinically useful document to describe the current state of knowledge regarding the prevention of acute exacerbations according to major categories of prevention therapies. Three key clinical questions developed using the PICO (population, intervention, comparator, and outcome) format addressed the prevention of acute exacerbations of COPD: nonpharmacologic therapies, inhaled therapies, and oral therapies. We used recognized document evaluation tools to assess and choose the most appropriate studies and to extract meaningful data and grade the level of evidence to support the recommendations in each PICO question in a balanced and unbiased fashion. RESULTS The AECOPD Guideline is unique not only for its topic, the prevention of acute exacerbations of COPD, but also for the first-in-kind partnership between two of the largest thoracic societies in North America. The CHEST Guidelines Oversight Committee in partnership with the CTS COPD Clinical Assembly launched this project with the objective that a systematic review and critical evaluation of the published literature by clinical experts and researchers in the field of COPD would lead to a series of recommendations to assist clinicians in their management of the patient with COPD. CONCLUSIONS This guideline is unique because it provides an up-to-date, rigorous, evidence-based analysis of current randomized controlled trial data regarding the prevention of COPD exacerbations.
The Joint Commission Journal on Quality and Patient Safety | 2009
Katherine E. Henderson; Angela Recktenwald; Richard M. Reichley; Thomas C. Bailey; Brian Waterman; Rebecca L. Diekemper; Storey P; Belinda Ireland; Wm. Claiborne Dunagan
BACKGROUND The Agency for Healthcare Research and Quality (AHRQ) patient safety indicators (PSIs) screen for potentially preventable complications in hospitalized patients using hospital administrative data. The PSI for postoperative venous thromboembolism (VTE) relies on International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes for deep vein thrombosis (DVT) or pulmonary embolism (PE) in secondary diagnoses fields. In a clinical validation study of the PSI for postoperative VTE, natural language processing (NLP), supplemented by pharmacy and billing data, was used to identify VTE events missed by medical records coders. METHODS In a retrospective review of postsurgical discharges, charts were processed using the AHRQ PSI software. Cases were identified as possible false negatives by flagging charts for possible VTEs using pharmacy and billing data to identify all patients who were therapeutically anticoagulated or had placement of an inferior vena caval filter. All charts were reviewed by a physician blinded to screening results. Physician interpretation was considered the gold standard for VTE classification. RESULTS The AHRQ PSI had a positive predictive value (PPV) of .545 (95% confidence interval [CI], .453-.634) and a negative predictive value (NPV) of .997 (95% CI, .995-.999). Sensitivity was .87 and specificity was .98. Secondary coding review suggested that all 9 false-negative results were miscoded; if they had been properly coded, the sensitivity would increase to 1.00. Most false-positive cases resulted from superficial venous clots identified by the PSI due to coding ambiguity. DISCUSSION The VTE PSI performed well as a screening tool but generated a significant number of false-positive cases, a problem that could be substantially reduced with improved coding methods.
Chest | 2015
Gerard J. Criner; Jean Bourbeau; Rebecca L. Diekemper; Daniel R. Ouellette; Donna Goodridge; Paul Hernandez; Kristen Curren; Meyer Balter; Mohit Bhutani; Pat G. Camp; Bartolome R. Celli; Gail Dechman; Mark T. Dransfield; Stanley B. Fiel; Marilyn G. Foreman; Nicola A. Hanania; Belinda Ireland; Nathaniel Marchetti; Darcy Marciniuk; Richard A. Mularski; Joseph Ornelas; Jeremy Road; Michael K. Stickland
COPD is a common disease with substantial associated morbidity and mortality. Patients with COPD usually have a progression of airflow obstruction that is not fully reversible and can lead to a history of progressively worsening breathlessness, affecting daily activities and health-related quality of life.1-3 COPD is the fourth leading cause of death in Canada4 and the third leading cause of death in the United States where it claimed 133,965 lives in 2009.5 In 2011, 12.7 million US adults were estimated to have COPD.6 However, approximately 24 million US adults have evidence of impaired lung function, indicating an underdiagnosis of COPD.7 Although 4% of Canadians aged 35 to 79 years self-reported having been given a diagnosis of COPD, direct measurements of lung function from the Canadian Health Measures Survey indicate that 13% of Canadians have a lung function score indicative of COPD.4 COPD is also costly. In 2009, COPD caused 8 million office visits, 1.5 million ED visits, 715,000 hospitalizations, and 133,965 deaths in the United States.8 In 2010, US costs for COPD were projected to be approximately
Chest | 2017
Mark J. Rosen; Belinda Ireland; Mangala Narasimhan; Cynthia T. French; Richard S. Irwin; Todd M. Adams; Kenneth W. Altman; Alan F. Barker; Surinder S. Birring; Fiona Blackhall; Donald C. Bolser; Sidney S. Braman; Christopher E. Brightling; Priscilla Callahan-Lyon; Anne B. Chang; Andréanne Coté; Terrie Cowley; Paul W. Davenport; Satoru Ebihara; Ali A. El Solh; Patricio Escalante; Anthony Feinstein; Stephen K. Field; Dina Fisher; Peter G. Gibson; Philip Gold; Anthony Harnden; Adam T. Hill; Peter J. Kahrilas; Karina A. Keogh
49.9 billion, including
Chest | 2017
Mark A. Malesker; Priscilla Callahan-Lyon; Belinda Ireland; Richard S. Irwin; Todd M. Adams; Kenneth W. Altman; Elie Azoulay; Alan F. Barker; Surinder S. Birring; Fiona Blackhall; Donald C. Bolser; Louis-Philippe Boulet; Sidney S. Braman; Christopher E. Brightling; Anne B. Chang; Andréanne Coté; Terrie Cowley; Paul W. Davenport; Satoru Ebihara; Ali A. El Solh; Patricio Escalante; Stephen K. Field; Dina Fisher; Cynthia T. French; Cameron Grant; Peter G. Gibson; Philip Gold; Susan M. Harding; Anthony Harnden; Adam T. Hill
29.5 billion in direct health-care expenditures,
Chest | 2018
Stephen K. Field; Patricio Escalante; Dina Fisher; Belinda Ireland; Richard S. Irwin; Todd M. Adams; Kenneth W. Altman; Elie Azoulay; Alan F. Barker; Surinder S. Birring; Fiona Blackhall; Donald C. Bolser; Louis-Philippe Boulet; Sidney S. Braman; Christopher E. Brightling; Priscilla Callahan-Lyon; Anne B. Chang; Andréanne Coté; Terrie Cowley; Paul W. Davenport; Satoru Ebihara; Ali A. El Solh; Cynthia T. French; Peter G. Gibson; Philip Gold; Cameron Grant; Susan M. Harding; Anthony Harnden; Adam T. Hill; Peter J. Kahrilas
8.0 billion in indirect morbidity costs, and
Chest | 2018
Adam T. Hill; Philip Gold; Ali A. El Solh; Joshua P. Metlay; Belinda Ireland; Richard S. Irwin; Chest Expert Cough Panel
12.4 billion in indirect mortality costs.9 Exacerbations account for most of the morbidity, mortality, and costs associated with COPD. The economic burden associated with moderate and severe exacerbations in Canada has been estimated to be in the range of
Chest | 2018
Adam T. Hill; Alan F. Barker; Donald C. Bolser; Paul W. Davenport; Belinda Ireland; Anne B. Chang; Stuart B. Mazzone; Lorcan McGarvey
646 million to
Chest | 2017
Stephen K. Field; Patricio Escalante; Dina Fisher; Belinda Ireland; Richard S. Irwin; Todd M. Adams; Kenneth W. Altman; Elie Azoulay; Alan F. Barker; Surinder S. Birring; Fiona Blackhall; Donald C. Bolser; Louis-Philippe Boulet; Sidney S. Braman; Christopher E. Brightling; Priscilla Callahan-Lyon; Anne B. Chang; Andréanne Coté; Terrie Cowley; Paul W. Davenport; Satoru Ebihara; Ali A. El Solh; Cynthia T. French; Peter G. Gibson; Philip Gold; Cameron Grant; Susan M. Harding; Anthony Harnden; Adam T. Hill; Peter J. Kahrilas
736 million per annum.10 This value may be an underestimate given that the prevalence of moderate exacerbations is not well documented, COPD is underdiagnosed, and the rate of hospitalization due to COPD is increasing.11 Exacerbations are to COPD what myocardial infarctions are to coronary artery disease: They are acute, trajectory-changing, and often deadly manifestations of a chronic disease. Exacerbations cause frequent hospital admissions, relapses, and readmissions12; contribute to death during hospitalization or shortly thereafter12; reduce quality of life dramatically12,13; consume financial resources12,14; and hasten a progressive decline in pulmonary function, a cardinal feature of COPD. Hospitalization due to exacerbations accounts for > 50% of the cost of managing COPD in North America and Europe.15,16 COPD exacerbation has been defined as an event in the natural course of the disease characterized by a baseline change in the patient’s dyspnea, cough, and/or sputum that is beyond the normal day-to-day variations, is acute in onset, and may warrant a change in regular medication in a patient with underlying COPD.17,18 Exacerbation in clinical trials has been defined for operational reasons on the basis of whether an increase in treatment beyond regular or urgent care is required in an ED or a hospital. Exacerbation treatment in clinical trials usually is defined by the use of antibiotics, systemic corticosteroids, or both.19 The severity of the exacerbation is then ranked or stratified according to the outcome: mild, when the clinical symptoms are present but no change in treatment or outcome is recorded; moderate, when the event results in a change in medication, such as the use of antibiotics and systemic corticosteroids; or severe, when the event leads to a hospitalization.1 Two-thirds of exacerbations are associated with respiratory tract infections or air pollution, but one-third present without an identifiable cause.17 Exacerbations remain poorly understood in terms of not only cause but also treatment and prevention. Although the management of an acute exacerbation has been the primary focus of clinical trials, the prevention of acute exacerbations has not been a major focus until recently. Most current COPD guidelines focus on the general diagnosis and evaluation of the patient with COPD, the management of stable disease, and the diagnosis and management of acute exacerbations.1,20 Although current COPD guidelines state that prevention of exacerbations is possible, little guidance is provided to the clinician regarding current available therapies for the prevention of COPD exacerbations.1,20 Moreover, new therapies have promise in preventing acute exacerbations of COPD (AECOPD) and would benefit from critical review of their efficacy in the exacerbation prevention management.21-23 The American College of Chest Physicians (CHEST) and Canadian Thoracic Society (CTS) jointly commissioned this evidence-based guideline on the prevention of COPD exacerbations to fill this important void in COPD management. The overall objective of this CHEST and CTS joint evidence-based guideline (AECOPD Guideline) was to create a practical, clinically useful document describing the current state of knowledge regarding the prevention of AECOPD according to major categories of prevention therapies. We accomplished this by using recognized document evaluation tools to assess and choose the most appropriate studies and evidence to extract meaningful data and to grade the level of evidence supporting the recommendations in a balanced and unbiased fashion. The AECOPD Guideline is unique not only for its topic but also for the first-in-kind partnership between two of the largest thoracic societies in North America. The CHEST Guidelines Oversight Committee in partnership with the CTS COPD Clinical Assembly launched this project with the objective that a systematic review and critical evaluation of the published literature by clinical experts and researchers in the field of COPD would lead to a series of recommendations to assist clinicians in their management of the patient with COPD. This guideline is unique because a group of interdisciplinary clinicians who have special expertise in COPD clinical research and care led the development of the guideline process with the assistance of methodologists.
Chest | 2017
Mark A. Malesker; Priscilla Callahan-Lyon; Belinda Ireland; Richard S. Irwin; Todd M. Adams; Kenneth W. Altman; Elie Azoulay; Alan F. Barker; Surinder S. Birring; Fiona Blackhall; Donald C. Bolser; Louis-Philippe Boulet; Sidney S. Braman; Christopher E. Brightling; Anne B. Chang; Andréanne Coté; Terrie Cowley; Paul W. Davenport; Satoru Ebihara; Ali A. El Solh; Patricio Escalante; Stephen K. Field; Dina Fisher; Cynthia T. French; Cameron Grant; Peter G. Gibson; Philip Gold; Susan M. Harding; Anthony Harnden; Adam T. Hill
BACKGROUND: Cough is a common symptom prompting patients to seek medical care. Like patients in the general population, patients with compromised immune systems also seek care for cough. However, it is unclear whether the causes of cough in immunocompromised patients who are deemed unlikely to have a life‐threating condition and a normal or unchanged chest radiograph are similar to those in persons with cough and normal immune systems. METHODS: We conducted a systematic review to answer the question: What are the most common causes of cough in ambulatory immunodeficient adults with normal chest radiographs? Studies of patients ≥ 18 years of age with immune deficiency, cough of any duration, and normal or unchanged chest radiographs were included and assessed for relevance and quality. Based on the systematic review, suggestions were developed and voted on using the American College of Chest Physicians (CHEST) methodology framework. RESULTS: The results of the systematic review revealed no high‐quality evidence to guide the clinician in determining the likely causes of cough specifically in immunocompromised ambulatory patients with normal chest radiographs. CONCLUSIONS: Based on a systematic review, we found no evidence to assess whether or not the proper initial evaluation of cough in immunocompromised patients is different from that in immunocompetent persons. A consensus of the panel suggested that the initial diagnostic algorithm should be similar to that for immunocompetent persons but that the context of the type and severity of the immune defect, geographic location, and social determinants be considered. The major modifications to the 2006 CHEST Cough Guidelines are the suggestions that TB should be part of the initial evaluation of patients with cough and HIV infection who reside in regions with a high prevalence of TB, regardless of the radiographic findings, and that specific causes and immune defects be considered in all patients in whom the initial evaluation is unrevealing.