125 results on '"Tarek A. Hammad"'
Search Results
2. Exploring the scientific underpinnings of investigating safety signals: analytical insights in deciphering drug safety evidence
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Tarek A. Hammad, Simon Davis, and Salman Afsar
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drug safety ,pharmacovigilance ,analytical insights ,evidence interpretation ,safety signals assessment ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Ensuring the safety of drugs is a critical aspect of healthcare. Accurate interpretation of drug safety evidence is vital to understand the safety profile and to evaluate the benefits and risks of the medicinal product. However, validity of this evidence has numerous challenges that must be carefully considered, highlighting the need for a heightened appreciation of data interpretation pitfalls. This paper aims to delve into the intricacies of analytic considerations in drug safety data interpretation aiming at providing insights into the safety profile of pharmaceutical interventions. The applicability of these analytic considerations extends to controlled and observational data as well as spontaneously reported individual case reports. Increasing the understanding of scientific underpinnings of evidence interpretation empowers Pharmacovigilance professionals to grasp fundamental concepts, use appropriate terminology, engage in meaningful discussions with colleagues conducting analyses, and critically evaluate evidence. These skills and knowledge enable them to make informed decisions and enhance their expertise in drug safety. By correct utilization of analytic approaches while appreciating their strengths and limitations, one can advance drug safety and benefit-risk research using evidence-based decision-making and ultimately ensure better healthcare outcomes for patients.
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- 2024
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3. Navigating a transforming landscape: the evolving role of pharmacovigilance physicians in drug development and implications for future challenges and training requirements
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Tarek A. Hammad, Salman Afsar, Herve Le-Louet, and Veronique F. Kugener
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pharmacovigilance ,role of pharmacovigilance physicians ,safety physicians ,evidence-based medicine ,enhanced safety surveillance technologies ,pharmacovigilance physician training requirements ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Contrary to the famous quote from Voltaire, “The art of medicine consists in amusing the patient, while nature cures the disease”, medicine has evolved since the 17th century into a multi-faceted scientific field facilitating healing and improving overall wellbeing. One rapidly evolving area within this field is drug safety, also known as pharmacovigilance (PV). PV identifies and evaluates potential risks throughout the life cycle of the drug, minimizing patient exposure to harmful effects and guiding appropriate risk mitigation and management strategies. Timely identification and mitigation of risks not only contribute to patient safety but also allows maximum therapeutic benefits while curtailing economic burden associated with adverse events. In the evolving landscape of drug safety, the role of the PV physicians has emerged as an integral component of drug development. This paper aims to explore the evolving nature of PV physicians’ roles in drug development, highlighting changing landscape in drug development and safety monitoring and attendant changes and advancements in responsibilities, scope, and training implications. To be well-rounded, PV physicians are encouraged to strive to undergo relevant training and education. This would enable them to leverage pertinent complementary fields of science by developing the proficiency to ask the right questions, acknowledge multidisciplinary perspectives, and interpret the overall evidence. While on-the-job training is valuable for gaining experience, building a future safety workforce necessitates more targeted efforts, especially considering that medical school curricula may not readily emphasize the development of skills required for successful PV physician roles. Therefore, academic centers, pharmaceutical companies, and regulatory agencies should increase collaboration to establish hands-on training opportunities through post-doctoral, internship, and fellowship programs, in order to meet the growing demand for well-trained PV physicians.
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- 2023
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4. How can patient preferences be used and communicated in the regulatory evaluation of medicinal products? Findings and recommendations from IMI PREFER and call to action
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Rosanne Janssens, Liese Barbier, Mireille Muller, Irina Cleemput, Isabelle Stoeckert, Chiara Whichello, Bennett Levitan, Tarek A. Hammad, Charis Girvalaki, Juan-Jose Ventura, Karin Schölin Bywall, Cathy Anne Pinto, Elise Schoefs, Eva G. Katz, Ulrik Kihlbom, and Isabelle Huys
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patient preferences ,patient experience data ,regulatory evaluation ,scientific advice ,benefit-risk assessment ,clinical trial endpoint selection ,Therapeutics. Pharmacology ,RM1-950 - Abstract
Objective: Patients have unique insights and are (in-)directly affected by each decision taken throughout the life cycle of medicinal products. Patient preference studies (PPS) assess what matters most to patients, how much, and what trade-offs patients are willing to make. IMI PREFER was a six-year European public-private partnership under the Innovative Medicines Initiative that developed recommendations on how to assess and use PPS in medical product decision-making, including in the regulatory evaluation of medicinal products. This paper aims to summarize findings and recommendations from IMI PREFER regarding i) PPS applications in regulatory evaluation, ii) when and how to consult with regulators on PPS, iii) how to reflect PPS in regulatory communication and iv) barriers and open questions for PPS in regulatory decision-making.Methods: PREFER performed six literature reviews, 143 interviews and eight focus group discussions with regulators, patient representatives, industry representatives, Health Technology Assessment bodies, payers, academics, and clincians between October 2016 and May 2022.Results: i) With respect to PPS applications, prior to the conduct of clinical trials of medicinal products, PPS could inform regulators’ understanding of patients’ unmet needs and relevant endpoints during horizon scanning activities and scientific advice. During the evaluation of a marketing authorization application, PPS could inform: a) the assessment of whether a product meets an unmet need, b) whether patient-relevant clinical trial endpoints and outcomes were studied, c) the understanding of patient-relevant effect sizes and acceptable trade-offs, and d) the identification of key (un-)favorable effects and uncertainties. ii) With respect to consulting with regulators on PPS, PPS researchers should ideally have early discussions with regulators (e.g., during scientific advice) on the PPS design and research questions. iii) Regarding external PPS communication, PPS could be reflected in the assessment report and product information (e.g., the European Public Assessment Report and the Summary of Product Characteristics). iv) Barriers relevant to the use of PPS in regulatory evaluation include a lack of PPS use cases and demonstrated impact on regulatory decision-making, and need for (financial) incentives, guidance and quality criteria for implementing PPS results in regulatory decision-making. Open questions concerning regulatory PPS use include: a) should a product independent broad approach to the design of PPS be taken and/or a product-specific one, b) who should optimally be financing, designing, conducting, and coordinating PPS, c) when (within and/or outside clinical trials) to perform PPS, and d) how can PPS use best be operationalized in regulatory decisions.Conclusion: PPS have high potential to inform regulators on key unmet needs, endpoints, benefits, and risks that matter most to patients and their acceptable trade-offs. Regulatory guidelines, templates and checklists, together with incentives are needed to foster structural and transparent PPS submission and evaluation in regulatory decision-making. More PPS case studies should be conducted and submitted for regulatory assessment to enable regulatory discussion and increase regulators’ experience with PPS implementation and communication in regulatory evaluations.
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- 2023
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5. Aspects to consider in causality assessment of safety signals: broadening the thought process
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Tarek A. Hammad, Salman Afsar, Laura B. McAvoy, and Hervé Le Louet
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drug safety ,causality assessment ,evidence-based medicine ,structured framework for causality ,holistic safety signal assessment approach ,pharmacovigilance ,Therapeutics. Pharmacology ,RM1-950 - Abstract
In the field of drug safety, causality assessment aims to determine the level of plausibility of the relationship between an adverse event and exposure to a particular product. It is after the causality assessment process that we will be able to point out a product adverse reaction. While regulators often require pharmaceutical companies to use a structured approach for assessing the causality of their products, the available methods are challenged by a number of procedural differences, even when drawing from the same domain of elements. To mitigate these inconsistencies, as well as the additional challenges associated with incomplete information and differences in the application of clinical judgments at the individual case level, this paper proposes a holistic framework for causality assessment that utilizes a combination of expert judgment/global introspection, evidence-based medicine, and probabilistic method. The goal of the presented approach is to provide a guide of clues to causality reminding medical safety assessors to seek and examine all available streams of evidence in totality and to assess this evidence in a qualitative, structured way.
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- 2023
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6. Predictors and potential advantages of PERT and advanced therapy use in acute pulmonary embolism
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Robert Schilz, Tarek A. Hammad, Leben Tefera, Nicole M Chahine, Mehdi H. Shishehbor, Melanie Parikh, Teresa Carman, and Jun Li
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medicine.medical_specialty ,medicine.medical_treatment ,Hemorrhage ,030204 cardiovascular system & hematology ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Heart rate ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,030212 general & internal medicine ,Oxygen saturation (medicine) ,Patient Care Team ,business.industry ,General Medicine ,Thrombolysis ,Bleed ,medicine.disease ,Pulmonary embolism ,Catheter ,Treatment Outcome ,Blood pressure ,Acute Disease ,Cohort ,Pulmonary Embolism ,Cardiology and Cardiovascular Medicine ,business - Abstract
We sought to examine predictors of pulmonary embolism response team (PERT) utilization and identify those who could benefit from advanced therapy.PERT and advanced therapy use remain low. Current risk stratification tools heavily weight age and comorbidities, which may not always correlate with presentation's severity.We prospectively studied patients with CT-confirmed PE between January 2019 and December 2019 at our hospital. PERT activation was left to the treating physician. Multivariable analyses were utilized to identify predictors of PERT activation and advanced therapy. Using the log odd ratio of each significant predictor of advanced therapy, we created a scoring system and a score of 2 was associated with the highest use. Primary outcomes were 30- and 90-day all-cause mortality, readmission, and major bleed.Of the 307 patients, PERT was activated in 22.5%. While abnormal vital signs and right ventricular (RV) strain were associated with PERT activation, pulmonary embolism severity index (PESI) was not. Advanced therapy use was significantly higher in the PERT cohort (35% vs 2%). Predictors of advanced therapy use were composite variable (heart rate 110 or systolic blood pressure 100 or respiratory rate 30 or oxygen saturation 90%) and right-to-left ventricular ratio 0.9. PERT patients with advanced therapy use, when compared to the no-PERT patients who could have qualified (score of 2), had significantly lower 30- and 90-day mortality and 30-day readmission without difference in major bleed.PERT has important therapeutic impact, yet no guidelines to direct activation. We recommend a multidisciplinary approach for higher acuity pulmonary embolism cases and physician education regarding PERT and the scope of advanced therapy use.
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- 2021
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7. ECONOMIC FEASIBILITY STUDY AS AN INPUT TO RATIONALIZE FISHERIES MANAGEMENT SYSTEMS
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Ahmed M. A. Shaaban, Tarek A. Hammad, and Mahmoud A Mahmoud
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Public economics ,Order (exchange) ,Agriculture ,business.industry ,Production (economics) ,Organizational culture ,Business ,Fisheries management ,Descriptive research ,Element (criminal law) ,Economic problem - Abstract
The study aims to identify the current situation of fisheries in the Arab Republic of Egypt. The study dealt with the organizational culture and its impact on economic feasibility, the most important factors affecting economic feasibility, and in order to achieve the objectives of the study, the descriptive approach was used. This is to ensure the validity of the study hypotheses. The study found the following results: There is statistical indication that there is a difference in the opinions of the respondents about the influence of the organizational culture (the focus of researchers and research in fisheries management) on the economics of fisheries, as the first hypothesis is confirmed. There is statistical indication that there is a difference in the opinions of the respondents about the effect of organizational culture (an axis related to employees in fisheries management) on the economics of fisheries, as the second hypothesis is confirmed. There is statistical indication that there is a discrepancy in the opinions of the respondents about the most important factors affecting the economic viability of fisheries, as the third hypothesis is confirmed. Among the most important recommendations made by researchers are the following: Attention must be paid to the organizational culture of fisheries management and focus on the human element (employees, researchers and workers) in order to streamline and flow production processes and raise the organizational efficiency of fisheries management. Research authorities must be consulted as they help solve economic problems and have a positive impact on the economic viability of fisheries and research bodies such as the Institute of Marine Sciences, colleges of fish wealth and others. It is imperative to distinguish those who obtained degrees, both materially and morally, which encourages researchers to make more efforts to develop the fisheries sector in the Arab Republic of Egypt. Paying attention to the organizational culture elements that positively affect the economic viability of fisheries, such as cooperation between leaders and researchers, cooperation between various disciplines, the assistance of Egyptian researchers and specialists, support of specialists for fisheries guidance, and employee support through specialists in the field of fisheries. There is no doubt that the study and analysis of economic feasibility related to fisheries can be used to develop the features of strategies that benefit policy makers and aim to rationalize fisheries management systems by focusing on the main and pivotal role of the economy, as dispensing with it when planning is considered an economic suicide for fisheries management (Food and Agriculture Organization) 2016.
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- 2021
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8. THE IMPACT OF FLOATING EXCHANGE RATE ON THE SOCIAL RESPONSIBILITY AN APPLIED STUDY ON BUSINESS SECTOR COMPANIES IN EGYPT
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Ayman, S. Abdel Kader, primary, Tarek, A. Hammad, additional, and Wael, Fawzy, additional
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- 2022
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9. THE ROLE OF MANAGEMENT ACCOUNTING METHODS IN MINIMIZING THE RISK OF STRATEGIC DECISIONS IN THE ENVIRONMENTS OF EGYPTIAN BUSINESS ORGANIZATIONS A FIELD STUDY
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Mahmoud A. M. Amin, Tarek A. Hammad, and Shaimaa M. M. Elmansoury
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Knowledge management ,Accounting method ,business.industry ,Process (engineering) ,Field (Bourdieu) ,Management accounting ,Statistical analysis ,Sample (statistics) ,Effective management ,business ,Conceptual study - Abstract
The study aims to study the role of management accounting methods in reducing the risks of strategic decisions in the business organization environment. For achieve the study goals the extrapolation method was used in the conceptual study and prepare the field aspect on the questionnaire list that directed to the items sampled which amount to 106 item sample and the statistical analysis is used in ascertain the veracity of the study assumptions. The study reached the following results: 1) There are enough statistical evidences ascertain the invalidity of the first subsidiary assumption, it means that there is an intangible relationship between the use of effective management accounting methods to reduce the risks associated with strategic decisions. 2) There are enough statistical evidences ascertain the invalidity of the second subsidiary assumption, it means that there is an intangible relationship between the environment surrounding business organizations (internal or external environment) and effective decision-making in organizations. 3) There are enough statistical evidences ascertain the invalidity of the third subsidiary assumption, it means that there is an intangible relationship between the use of effective management accounting methods to increase efficiency in business organizations. The most important recommendations of the researcher include the following: 1) Attention to use management accounting methods when making strategic decisions. 2) Attention to the environmental factors surrounding the organizationbefore starting to make strategic decisions. 3) Attention to the strategic decision-making process because it leads to risks that threaten the organization.
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- 2020
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10. THE IMPACT OF LOGISTIC AND ENVIRONMENTAL FACTORS ON ACTIVITY OF SUPPLYING SHIPS WITH FUEL (BUNKERING) IN THE SUEZ CANAL REGION
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Rasheed A. M. Hoteaba, Osama I. Abulhassan, and Tarek A. Hammad
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Computer assistance ,Order (business) ,Suez canal ,Sample (statistics) ,Business ,Environmental economics ,Inefficiency ,Port (computer networking) ,Corporation ,Work environment - Abstract
The study aims to improve the activity of supplying ships with fuel (Bunkering) in the ports located on the axis of the Suez Canal region, attracting local and foreign investments and developing the necessary logistic services that are compatible with environmental requirements, which is considered one of the most important factors in the development of this activity like followed by the largest international ports (operating) working in bunkering activity, In order to achieve the objectives of the study, the descriptive approach was used to prepare the theoretical framework for the study and prepare the field study by preparing a questionnaire list that was directed to the sample items which amounted to 384 sample that workers in the bunkering activity in each of the Egyptain General Petroleum Corporation and companies working in the bunkering activity and the response rate reached 356 sample with 92.7%, and various statistical analysis methods and computer assistance were used through the SPSS program. The study reached the following results: Storage warehouse spaces cause a hindrance to the development bunkering activity in the port. Barges is one of the reasons for the deterioration of bunkering activity, in terms of efficiency and performance . Companies suffering from inefficiency and accordance of marine barges with environmental requirements. The role of environmental management in encouraging workers to innovation new methods reducing pollution . The most important recommendations reached by the researchers : Interesting to the efficiency of the storage warehouses to improve the bunkering activity and increasing their storage areas. Interesting to barges and increasing their capabilities in terms of: the storage area, pumping rate, heating and mixing, to become competitive, modern and competitive with followed in the global competing ports. Warning about workers using protective masks during charging and discharging operations. Attention to the procedures of continuous monitoring and follow-up in the various locations to protect the work environment and the surrounding environment from pollution. Interesting to the efficiency and conformity of the "barges" marine supply to environmental requirements and IMO regulations.
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- 2020
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11. Stromal Cell–Derived Factor-1 Plasmid Treatment for Patients With Peripheral Artery Disease (STOP-PAD) Trial: Six-Month Results
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Timothy D. Henry, Saihari Sadanandan, Mehdi H. Shishehbor, Vikram S. Kashyap, Joseph M. Pastore, Leslie W. Miller, Parag D Patel, Tarek A Hammad, Matthew C. Bunte, John H. Rundback, and Michael L. Fitzgerald
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Male ,medicine.medical_specialty ,Time Factors ,Stromal cell ,medicine.medical_treatment ,Neovascularization, Physiologic ,030204 cardiovascular system & hematology ,Revascularization ,Amputation, Surgical ,law.invention ,Microcirculation ,Peripheral Arterial Disease ,03 medical and health sciences ,0302 clinical medicine ,Double-Blind Method ,Randomized controlled trial ,Ischemia ,law ,Humans ,Medicine ,Radiology, Nuclear Medicine and imaging ,Stromal cell-derived factor 1 ,Aged ,Wound Healing ,biology ,business.industry ,Genetic Therapy ,Recovery of Function ,Limb Salvage ,Chemokine CXCL12 ,United States ,Surgery ,Treatment Outcome ,Amputation ,Regional Blood Flow ,Chronic Disease ,Toe Brachial Index ,biology.protein ,Female ,Cardiology and Cardiovascular Medicine ,business ,Wound healing ,Vascular Surgical Procedures ,030217 neurology & neurosurgery ,Plasmids - Abstract
Purpose: To present the 6-month results of the Stromal Cell–Derived Factor-1 Plasmid Treatment for Patients with Peripheral Artery Disease (STOP-PAD) trial. The trial was an attempt to alter the course of chronic limb-threatening ischemia (CLTI) with a biological agent vs placebo after successful arterial revascularization at or below the knee. Materials and Methods: The multicenter, randomized, double-blinded, placebo-controlled, phase 2B STOP-PAD trial ( ClinicalTrials.gov identifier NCT02544204) randomized 109 patients (mean age 71 years; 68 men) with Rutherford category 5 or 6 CLTI and evidence of persistent impaired forefoot perfusion following recent successful revascularization to 8- (n=34) or 16-mg (n=36) intramuscular injections of a non-viral DNA plasmid–based treatment vs placebo (n=34). The primary efficacy outcome was the 6-month wound healing score evaluated by an independent wound core laboratory; the primary safety endpoint was major adverse limb events (MALE), a composite of major amputation plus clinically-driven target lesion revascularization at 6 months. Results: Only one-third of the patients had complete wound healing at 6 months in the placebo (31%), 8-mg injection (33%), and 16-mg injection (33%) groups. In addition, the observed increase in the toe-brachial index from baseline to 6 months was statistically significant in each group; however, this did not result in lower rates of MALE at 6 months (24% in the placebo, 29% in the 8-mg injection, and 11% in the 16-mg injection groups). During the 6-month period, 6 patients (6%) died, and 24 patients (23%) had an amputation [only 4 (4%) major]. Conclusion: Combining revascularization and biological therapy failed to improve outcomes in CLTI at 6 months. STOP-PAD has provided insights for future trials to evaluate biological therapy.
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- 2020
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12. Impact of Interdisciplinary System-Wide Limb Salvage Advisory Council on Lower Extremity Major Amputation
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Mehdi H. Shishehbor, Tarek A. Hammad, Tonia J. Rhone, Ahmad Younes, Norman Kumins, Abdullah Abdullah, Jun Li, Karem Harth, Teresa L. Carman, Heather L. Gornik, Peter J. Pronovost, and Vikram S. Kashyap
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Treatment Outcome ,Lower Extremity ,Humans ,Limb Salvage ,Cardiology and Cardiovascular Medicine ,Amputation, Surgical ,Retrospective Studies - Published
- 2022
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13. ENVIRONMENTAL IMPACTS OF THE INVESTMENTS AND FOREIGN AIDS ON INFRASTRUCTURE PROJECTS WITHIN EGYPT – WATER SECTOR
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Bassant, M. Mattar, primary, Tarek, A. Hammad, additional, Mamood, AbuZeid, additional, and Yossry, Abo El-Ela, additional
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- 2022
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14. Novel intracardiac echocardiography-guided catheter-based removal of inoperable tricuspid valve vegetation
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Yasir Abu-Omar, Tarek A Hammad, and Mehdi H. Shishehbor
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medicine.medical_specialty ,Percutaneous ,Catheters ,Intracardiac injection ,medicine ,Endocarditis ,Humans ,Radiology, Nuclear Medicine and imaging ,cardiovascular diseases ,Tricuspid valve ,business.industry ,General Medicine ,Endocarditis, Bacterial ,medicine.disease ,Surgery ,Catheter ,medicine.anatomical_structure ,Treatment Outcome ,Echocardiography ,Infective endocarditis ,Heart failure ,cardiovascular system ,Tricuspid Valve ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,Vegetation (pathology) - Abstract
With the ongoing intravenous drug abuse (IVDA) epidemic, the number of IVDA patients with infective endocarditis is increasing. These cases are often characterized by large vegetations complicated by valvular dysfunction, heart failure, and recurrent septic pulmonary emboli demanding surgical intervention. Latter cannot be offered in a good proportion of the patients due to challenging medical and social complexities. Hence, AngioVac system has been used as an alternative therapy; however, it is associated with high procedural mortality. In this document, we describe in detail the successful treatment of a case of large tricuspid valve vegetation, with prohibitive risk for surgery, using a percutaneous catheter-based system, the Triever aspiration catheter with FLEX technology, with the guidance of intracardiac echocardiogram.
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- 2021
15. MEASURE THE EFFECTS OF ENVIRONMENTAL COSTS AND BENEFITS ON THE QUALITY OF FINANCIAL STATEMENTS IN EGYPTIAN PHARMACEUTICAL COMPANIES
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Doaa, M. Harhash, primary, Tarek, A. Hammad, additional, and Mahmoud, A. Amin, additional
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- 2021
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16. ROOTING THE ARCHITECTURAL VALUES OF HERITAGE IN THE CONTEMPORARY ARCHITECTURE (AN ANALYTICAL STUDY OF THE ARCHITECTURE HERITAGE AT AL-BAHA IN THE KINGDOM OF SAUDI ARABIA IN ORDER TO BE STABILIZEDWITHIN THE CONTEMPORARY ARCHITECTURE)
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Mahmoud Tarek Mohamed Hammad and Ali Saied Bokhary
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Civilization ,Urban heritage ,media_common.quotation_subject ,Sociology ,Social science ,Architecture ,Sense of belonging ,media_common - Abstract
A rich cultural and urban heritage has been accumulated through successive ages andgenerations on the land of Kingdom of Saudi Arabia, especially in Al-Baha Area, whosefeatures are still clear and its impacts are existing nowadays. Such heritage is reflecting thesociety's features, physical, environmental, and social merits, and as a result of the rapidchanges in all aspects of life, architectural trends and ideas are emerged, which not muchconsistent with the values of society known with the civilization history. Hence, and to linkthe values of the past with the present, it is required to study the values of this local heritageand rooting it in the contemporary buildings by a deepen and balanced local vision matchingwith the present capacities and the past authenticity, so this study aims to draw out and studythese values which including many systems of environmental treatments that could be rootedin contemporary architectural works that keep with age potentials and culture of the society. Italso emphasized the continuity of Al Baha civilization identity, as well it provides andembodies certain architectural templates, which represent attempts of intellectual integrationbetween heritage and contemporary in an attempt to create a sense of belonging andemphasize the architectural identity of Al Baha city. Furthermore, the study has adopted theanalytical inductive methodology, progressive from the theoretical approach for studying theconcepts related to heritage, contemporary, and their relevant concepts of values.Then, the study adopted the empirical approach through analyzing the contemporary conceptsand trends in Al Baha to analyzing the most significant characteristics and values of Al Bahaheritage architecture. The research concludes in identifying the architectural values that couldbe rooted at Al Baha contemporary architecture, providing a proposal enables us to solve thedilemma of local urbanization and architecture, besides arising the functionality ofconstruction for achieving the contemporary architectural identity to Al Baha City. تراکم على ارض المملکة العربية السعودية وخاصة في منطقھ الباحة عبر العصور و الأجيال المتعاقبة موروث ثقافيعمراني ثري لاتزال ملامحھ واضحة وأثاره قائمھ حتى اليوم وتعکس خصائص المجتمع ومزاياه المادية و البيئية والاجتماعية ، ونتيجة للتغيرات المتسارعة في کافھ أوجھ الحياة ظھرت توجھات معماريھ وأفکار کثيرا لا تنسجم مع قيمالمجتمع ذو التاريخ الحضاري وعلي ذلک لربط قيم الماضي بالحاضر فان الأمر يتطلب دراسة القيم ھذا التراث المحلي وتأصيلھ في المباني المعاصرة وذلک برؤية محليھ ذات عمق وتوازن مع إمکانيات الحاضر وآصالھ الماضي ، لذا فان ھدفھذه الدراسة ھو استنباط ودراسة لھذه القيم التي تتضمن العديد من نظم المعالجات البيئية والتي يمکن تأصيلھا في إعمالمعماريھ معاصره تواکب إمکانات العصر وثقافة المجتمع وتضمن الاستمرارية لھوية مدينھ الباحة الحضارية کما يعرضو يجلل بعض النماذج المعمارية التي تمثل محاولات للدمج الفکري بين التراث و المعاصرة في محاولھ لخلق الإحساسبالانتماء وتأکيد الھوية المعمارية لمدينھ الباحة ، وانتھج البحث المنھج الاستقرائي التحليلي والمتدرج من المنھج النظريالخاص بدراسة المفاھيم المتعلقة بالتراث و المعاصرة ومفاھيم القيم المرتبطة يھما ثم المنھج التطبيقي عن طريق تحليلللأفکار و التوجھات المعاصرة بالباحة إلى تحليل لأھم الخصائص و القيم الخاصة بعماره الباحة التراثية ،ويخلص البحثبتحديد القيم المعمارية التي يمکن تأصيلھا في عماره الباحة المعاصرة وتقديم مقترح يمکنا من حل مشکلات الطابعالعمراني و المعماري المحلي ويرفع الأداء الوظيفي للمباني للوصول للھويھ المعمارية المعاصرة. لمدينھ الباحة.
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- 2020
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17. SDF-1 plasmid treatment for patients with peripheral artery disease (STOP-PAD): Randomized, double-blind, placebo-controlled clinical trial
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Mehdi H. Shishehbor, Timothy D. Henry, Vikram S. Kashyap, Tarek A. Hammad, Matthew C. Bunte, Parag D Patel, Michael L. Fitzgerald, John H. Rundback, Joseph M. Pastore, Leslie Miller, and Saihari Sadanandan
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Male ,medicine.medical_specialty ,Time Factors ,medicine.medical_treatment ,Hemodynamics ,Placebo ,Revascularization ,Peripheral Arterial Disease ,Double-Blind Method ,Diabetes mellitus ,Humans ,Medicine ,Ankle Brachial Index ,Peripheral artery disease (PAD) ,Aged ,Aged, 80 and over ,Wound Healing ,business.industry ,Microcirculation ,Genetic Therapy ,Critical limb ischemia ,Middle Aged ,medicine.disease ,Chemokine CXCL12 ,United States ,Surgery ,Clinical trial ,Treatment Outcome ,Amputation ,Regional Blood Flow ,Female ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,Plasmids - Abstract
The efficacy of biologic therapies in critical limb ischemia (CLI) remains elusive, in part, due to limitations in trial design and patient selection. Using a novel design, we examined the impact of complementing revascularization therapy with intramuscular JVS-100 – a non-viral gene therapy that activates endogenous regenerative repair pathways. In this double-blind, placebo-controlled, Phase 2B trial, we randomized 109 patients with CLI (Rutherford class V or VI) to 8 mg or 16 mg intramuscular injections of placebo versus JVS-100. Patients were eligible if they persistently had reduced forefoot perfusion, by toe–brachial index (TBI) or skin perfusion pressure (SPP), following successful revascularization with angiographic demonstration of tibial arterial flow to the ankle. The primary efficacy end point was a 3-month wound healing score assessed by an independent wound core laboratory. The primary safety end point was major adverse limb events (MALE). Patients’ mean age was 71 years, 33% were women, 79% had diabetes, and 8% had end-stage renal disease. TBI after revascularization was 0.26, 0.27, and 0.26 among the three groups (placebo, 8 mg, and 16 mg injections, respectively). Only 26% of wounds completely healed at 3 months, without any differences between the three groups (26.5%, 26.5%, and 25%, respectively). Similarly, there were no significant changes in TBI at 3 months. Three (2.8%) patients died and two (1.8%) had major amputations. Rates of MALE at 3 months were 8.8%, 20%, and 8.3%, respectively. While safe, JVS-100 failed to improve wound healing or hemodynamic measures at 3 months. Only one-quarter of CLI wounds healed at 3 months despite successful revascularization, highlighting the need for additional research in therapies that can improve microcirculation in these patients. ClinicalTrials.gov Identifier: NCT02544204
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- 2019
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18. The utility of geriatric nutritional risk index to predict outcomes in chronic limb-threatening ischemia
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Mehdi H. Shishehbor, Justin Smith, Kuniyasu Ikeoka, Jun Li, Tarek A. Hammad, Shilpkumar Arora, Haytham Mously, Vikram S. Kashyap, Siddhartha Dash, and Stephen Kimura
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Chronic Limb-Threatening Ischemia ,medicine.medical_specialty ,Population ,Ischemia ,Target vessel revascularization ,Cardiovascular care ,Context (language use) ,Amputation, Surgical ,Peripheral Arterial Disease ,Risk Factors ,Internal medicine ,Nutritional risk index ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Risk factor ,Adverse effect ,education ,Aged ,Retrospective Studies ,education.field_of_study ,business.industry ,General Medicine ,medicine.disease ,Limb Salvage ,Treatment Outcome ,Chronic Disease ,Cardiology and Cardiovascular Medicine ,business - Abstract
OBJECTIVES To assess geriatric nutritional risk index (GNRI) in patients with chronic limb-threatening ischemia (CLTI). BACKGROUND The prevalence of CLTI continues to rise, with major amputation and mortality remaining prominent. Frailty is a vital risk factor for adverse outcomes in cardiovascular care. The GNRI is a nutrition-based surrogate for frailty that has been utilized in Southeast Asia to predict adverse events in CLTI. It has not yet been evaluated in a primarily Western population, nor in the context of wound healing. METHODS Between 8August 2017 and April 2019, we identified patients undergoing endovascular interventions for CLTI at our institution, categorized into low GNRI (≤ 94, frail) versus normal GNRI (> 94, reference). We analyzed the risks of major adverse limb events (MALE), its individual components [mortality, major amputation, and target vessel revascularization (TVR)], amputation free survival (AFS), and wound healing using Kaplan-Meier and multivariate cox-proportional hazard regression analyses. RESULTS A total of 255 patients were included in the analysis, with follow up of 14 ± 9.1 months. Lower GNRI was associated with higher cumulative event rates for MALE (71.0% vs. 43.3%, p < 0.001), mortality (34.3% vs. 15.2%, p
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- 2021
19. Advances in chronic limb-threatening ischemia
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Tarek A. Hammad and Mehdi H. Shishehbor
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Chronic Limb-Threatening Ischemia ,medicine.medical_specialty ,business.industry ,medicine.medical_treatment ,Endovascular Procedures ,Ischemia ,medicine.disease ,Revascularization ,Limb Salvage ,Amputation, Surgical ,Peripheral Arterial Disease ,Treatment Outcome ,Risk Factors ,Internal medicine ,medicine ,Cardiology ,Humans ,Peripheral artery disease (PAD) ,Cardiology and Cardiovascular Medicine ,business ,Retrospective Studies - Published
- 2021
20. Prospective Experience of Pulmonary Embolism Management and Outcomes
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Matthew J, Lacey, Tarek A, Hammad, Melanie, Parikh, Leben, Tefera, Pallavi, Sharma, Rebecca, Kahl, Amanda, Zemko, Jun, Li, Teresa, Carman, Robert, Schilz, and Mehdi H, Shishehbor
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Cohort Studies ,Patient Care Team ,Humans ,Hemorrhage ,Prospective Studies ,Pulmonary Embolism - Abstract
We sought to evaluate the impact of pulmonary embolism (PE) response teams (PERTs) on all consecutive patients with PE.Multidisciplinary PERTs have been promoted for the management and treatment of (PE); however, the impact of PERTs on clinical outcomes has not been prospectively evaluated.We prospectively studied 220 patients with computed tomography (CT)-confirmed PE between January, 2019 and August, 2019. Baseline characteristics, as well as medical, interventional, and operational care, were captured. The total population was divided into 2 groups, ie, those with PERT activation and those without PERT activation. PERT activation was left at the discretion of the primary team. Our primary outcome was 90-day composite endpoint (rate of readmission, major bleeds, and mortality). Using 2:1 propensity-matched and multivariable-adjusted Cox proportional hazard analyses, we examined the impact of PERT activation on primary outcome, treatment approach, and length of stay.Of the total 220 patients, PERT was activated in 47 (21.4%). The PERT cohort, as compared with the non-PERT cohort, was more likely to present with dyspnea, syncope, lower systolic blood pressure, higher heart rate, higher respiratory rate, lower oxygen saturation, higher troponin levels, and higher right ventricular to left ventricular ratio. PERT activation was associated with increased use of advanced therapies (36.2% vs 1.2%; P.001) and catheter-directed inventions (25.5% vs 0.6%; P.001). In multivariable-adjusted analysis of propensity-matched cohorts, PERT activation was associated with lower 90-day outcomes (hazard ratio, 0.40; 95% confidence interval, 0.21-0.75; P.01).At our institution, PERT had a clinically significant impact on therapeutic strategies and 90-day outcomes in patients with PE.
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- 2021
21. IMPACT OF ISLAMIC VALUES AND CONCEPTS IN ARCHITECTURE: A CASE STUDY OF ISLAMIC COMMUNITIES
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Mahmoud Tarek Mohamed Hammad, Djamel Beggas, and Ali Bokhari
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Social change ,Islam ,Sociology ,Social science ,Architecture - Published
- 2020
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22. Abstract 14286: Significance of Nutritional Status in Patients With Chronic Limb Threatening Ischemia
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Mehdi H. Shishehbor, Siddhartha Dash, Kuniyasu Ikeoka, Jun Li, Stephen Kimura, and Tarek A. Hammad
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medicine.medical_specialty ,business.industry ,Ischemia ,Nutritional status ,medicine.disease ,Pathogenesis ,Physiology (medical) ,Internal medicine ,medicine ,In patient ,Peripheral artery disease (PAD) ,Cardiology and Cardiovascular Medicine ,Wound healing ,business ,Vascular Medicine - Abstract
Introduction: The nutrition status plays a key role in the pathogenesis of frailty, and is strongly associated with the prognosis of patients with chronic limb-threatening ischemia (CLTI). The Geriatric Nutritional Risk Index (GNRI) is a widely used, simple, and well established nutritional status screening method. The association between the GNRI and wound healing in patients with CLTI has not been established. Hypothesis: We assessed the hypothesis that GNRI is associated with wound healing in patients with CLTI. Methods: We conducted a single-center retrospective analysis for 172 consecutive CLTI patients who were admitted to our hospital from August 2017 to April 2019 (age 70±14 years; men 62.2%). The GNRI on admission was calculated as follows: [14.89 х albumin (g/dL)] + [41.7 х (bodyweight/ideal body weight)]. According to the GNRI values, 4 grades of nutrition-related risk are defined as major risk (GNRI:98). The amputation-free survival (AFS) and the cumulative wound healing rate are calculated by the log-rank test. The receiver operating characteristic curve was used to obtain a cutoff value for wound heal. Cox proportional hazards regression analysis was performed to explore the independent association between the GNRI and wound heal. Results: The follow-up period was 12±6.7 months. The 1-year AFS in no risk, low risk, moderate risk, and major risk groups were 90%, 74%, 66%, and 62%, respectively ( P =0.045). GNRI was significantly associated with WIfI wound score (W1, 95±8.8; W2, 87±8.0; W3, 84±9.3, P P =0.036). GNRI=95 was selected as cutoff value with maximum discriminative power for wound healing (sensitivity 70%, specificity 60%; Area under the curve, 0.67; 95% confidence interval, 0.59-0.76). GNRI>95 was an independent predictor of wound healing (Hazard ratio, 1.9; 95% confidence interval, 1.0-3.7; P =0.046). Conclusions: The GNRI was significantly associated with AFS and wound healing in patients with CLTI. GNRI=95 is a novel cutoff value to predict wound healing during follow-up.
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- 2020
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23. Impact of COVID ‐19 pandemic on ST‐elevation myocardial infarction in a non‐COVID ‐19 epicenter
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Nour Tashtish, Melanie Parikh, Mehdi H. Shishehbor, Cynthia M Lowry, Diane Gorbey, Tarek A Hammad, Farshad Forouzandeh, Marco A. Costa, William M Wolf, Daniel I. Simon, and Steven J Filby
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medicine.medical_specialty ,Ejection fraction ,biology ,business.industry ,General Medicine ,medicine.disease ,Troponin ,Intensive care unit ,law.invention ,Blood pressure ,law ,Radiology Nuclear Medicine and imaging ,Statistical significance ,Internal medicine ,Heart rate ,Cardiology ,Door-to-balloon ,biology.protein ,Medicine ,Radiology, Nuclear Medicine and imaging ,Myocardial infarction ,business ,Cardiology and Cardiovascular Medicine - Abstract
Objectives We sought to study the impact of COVID-19 pandemic on the presentation delay, severity, patterns of care, and reasons for delay among patients with ST-elevation myocardial infarction (STEMI) in a non-hot-spot region. Background COVID-19 pandemic has significantly reduced the activations for STEMI in epicenters like Spain. Methods From January 1, 2020, to April 15, 2020, 143 STEMIs were identified across our integrated 18-hospital system. Pre- and post-COVID-19 cohorts were based on March 23rd, 2020, whenstay-at-home orders were initiated in Ohio. We used presenting heart rate, blood pressure, troponin, new Q-wave, and left ventricle ejection fraction (LVEF) to assess severity. Duration of intensive care unit stay, total length of stay, door-to-balloon (D2B) time, and radial versus femoral access were used to assess patterns of care. Results Post-COVID-19 presentation was associated with a lower admission LVEF (45 vs. 50%, p = .015), new Q-wave, and higher initial troponin; however, these did not reach statistical significance. Among post-COVID-19 patients, those with >12-hr delay in presentation 31(%) had a longer average D2B time (88 vs. 53 min, p = .033) and higher peak troponin (58 vs. 8.5 ng/ml, p = .03). Of these, 27% avoided the hospital due to fear of COVID-19, 18% believed symptoms were COVID-19 related, and 9% did not want to burden the hospital during the pandemic. Conclusions COVID-19 has remarkably affected STEMI presentation and care. Patients' fear and confusion about symptoms are integral parts of this emerging public health crisis.
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- 2020
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24. EVALUATING THE ENVIRONMENTAL COMMITMENT TO FINANCING INVESTMENT PROJECTS AN APPLIED STUDY ON A COMMERCIAL BANK
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Enas, H. Ahmed, primary, Tarek, A. Hammad, additional, Muhammad, A. Khalifa, additional, and Wael, F. Abdul Basit, additional
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- 2021
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25. The utility of real-world evidence for benefit-risk assessment, communication, and evaluation of pharmaceuticals: Case studies
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Ariel E. Arias, Christine Radawski, Meredith Y. Smith, Susan Colilla, Paul Coplan, Dimitri Bennett, Emily Freeman, Rachel E. Sobel, Tarek A. Hammad, Priya Bahri, and Kenneth Hornbuckle
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Data collection ,Epidemiology ,business.industry ,Communication ,Novelty ,Stakeholder engagement ,Health technology ,Real world evidence ,030226 pharmacology & pharmacy ,Risk Assessment ,Application lifecycle management ,03 medical and health sciences ,0302 clinical medicine ,Risk analysis (engineering) ,Pharmaceutical Preparations ,Research Design ,Medicine ,Benefit risk assessment ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Product (category theory) ,business - Abstract
PURPOSE In recent years, novel types of real-world evidence (RWE) have played a role in various decision-making processes relating to medicinal products, including regulatory approval, patient access, health technology assessment, safety monitoring, clinical use, and post-approval lifecycle management. We therefore reviewed the potential utility of RWE in the cycle of medicinal product benefit-risk (BR) assessment, communication/risk minimization and evaluation ("BRACE"). METHODS A convenience sample of illustrative studies was drawn from the published literature and examined. Specifically, we examined the purpose for using RWE, the type of RWE used, its novelty and how it might be integrated with other data and activities of the BRACE cycle, and how it contributed to regulatory decision-making. RESULTS Eight studies were selected with each illustrating a different activity in the BRACE cycle ranging from BR assessment in the preapproval setting, post-approval assessment of safety or effectiveness, communicating BR information to patients and healthcare professionals, and evaluating the effectiveness of risk minimization initiatives to support a positive BR balance. CONCLUSIONS RWE has an important role in informing regulatory decision-making regarding the BR management of medicines. With increasing digitalization, facilitating data collection and stakeholder engagement in health, this role is only expected to expand in the future. To reach the full potential of RWE, both regulators and sponsors will need to be familiar with a range of existing and emerging methods for generating and analyzing such evidence appropriately and achieve convergence regarding how different types of RWE can best be used to inform BR management and decision-making.
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- 2019
26. Cardiovascular, electrophysiologic, and hematologic effects of omega-3 fatty acids beyond reducing hypertriglyceridemia: as it pertains to the recently published REDUCE-IT trial
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Robert J. Chilton, Anthony G. Vande Hei, Omar Sheikh, Tarek A. Hammad, Ayman Battisha, and Son V. Pham
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Male ,medicine.medical_specialty ,lcsh:Diseases of the circulatory (Cardiovascular) system ,Heart disease ,Endocrinology, Diabetes and Metabolism ,Down-Regulation ,030209 endocrinology & metabolism ,Hemorrhage ,Review ,030204 cardiovascular system & hematology ,Risk Assessment ,03 medical and health sciences ,0302 clinical medicine ,Diabetes mellitus ,Risk Factors ,Internal medicine ,Atrial Fibrillation ,medicine ,Clinical endpoint ,Humans ,Myocardial infarction ,Triglycerides ,Randomized Controlled Trials as Topic ,chemistry.chemical_classification ,Hypertriglyceridemia ,Unstable angina ,business.industry ,Omega-3 polyunsaturated fatty acids ,Incidence ,Absolute risk reduction ,medicine.disease ,Eicosapentaenoic acid ,Treatment Outcome ,Hyperlipidemia ,chemistry ,Eicosapentaenoic Acid ,lcsh:RC666-701 ,Cardiovascular Diseases ,Dietary Supplements ,Female ,Cardiology and Cardiovascular Medicine ,business ,Biomarkers ,Polyunsaturated fatty acid - Abstract
Heart disease continues to affect health outcomes globally, accounting for a quarter of all deaths in the United States. Despite the improvement in the development and implementation of guideline-directed medical therapy, the risk of adverse cardiac events remains substantially high. Historically, it has been debated whether omega-3 polyunsaturated fatty acids provide clinical benefit in cardiac disease. The recently published REDUCE-IT trial demonstrated a statistically significant absolute risk reduction of 4.8% in its primary endpoint (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina) with the use of icosapent ethyl, which is a highly purified eicosapentaenoic acid (EPA) ethyl ester. However, the mechanism of action of omega-3 fatty acids is not commonly discussed. Moreover, the use of EPA was not without risk, as the incidence of atrial fibrillation was increased along with a trend towards increased bleeding risk. Thus, our aim is to help explain the function of purified EPA ethyl ester, especially at the molecular level, which will ultimately lead to a better understanding of their clinically observable effects.
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- 2019
27. THE GERIATRIC NUTRITIONAL RISK INDEX PREDICTS THE PROGNOSIS IN PATIENTS WITH CHRONIC LIMB-THREATENING ISCHEMIA
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Stephen Kimura, Shilpkumar Arora, Siddartha Dash, Jun Li, Tarek A. Hammad, Kuniyasu Ikeoka, and Mehdi H. Shishehbor
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medicine.medical_specialty ,business.industry ,Internal medicine ,Nutritional risk index ,Ischemia ,medicine ,In patient ,Cardiology and Cardiovascular Medicine ,medicine.disease ,business - Published
- 2021
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28. Renal denervation: What happened, and why?
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Tarek A. Hammad, Mehdi H. Shishehbor, and George Thomas
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Denervation ,medicine.medical_specialty ,Kidney ,business.industry ,medicine.medical_treatment ,Resistant hypertension ,MEDLINE ,Urology ,Blood Pressure ,General Medicine ,030204 cardiovascular system & hematology ,03 medical and health sciences ,0302 clinical medicine ,Blood pressure ,medicine.anatomical_structure ,Sympathectomy ,Hypertension ,medicine ,Humans ,030212 general & internal medicine ,business - Abstract
Despite promising results in initial trials, renal denervation failed to achieve its efficacy end points as a treatment for resistant hypertension in the SYMPLICITY HTN-3 trial, the largest trial of this treatment to date (N Engl J Med 2014; 370:1393-1401). Is renal denervation dead, or will future trials and newer technology revive it?
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- 2017
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29. Key Changes in Benefit–Risk Assessment Guidelines and Implications for Data Analysis in Drug Development
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Tarek A. Hammad and Cathy Anne Pinto
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Statistics and Probability ,Operationalization ,Management science ,Pharmaceutical Science ,Harmonization ,Legislature ,030204 cardiovascular system & hematology ,Marketing authorization ,03 medical and health sciences ,0302 clinical medicine ,Risk analysis (engineering) ,Drug development ,Key (cryptography) ,Spite ,Common Technical Document ,030212 general & internal medicine ,Business - Abstract
The number and complexity of regulatory and legislative policy initiatives for benefit–risk (B-R) assessments and the challenges associated with operationalizing and integrating these initiatives in the drug development process have increased exponentially in the last 10 years. Although there are some similarities in the approaches being used among regions, there are no unifying principles for a consistent approach to address various regulatory agency requirements. Therefore, some sponsors might end up with marketing authorization in one region but not in another, in spite of using the same available benefits and risks evidence without obvious differences between regions. Fortunately, however, there has been a recent global effort by the International Conference on Harmonization (ICH) to develop guidance which provides greater specificity on the format and structure of B-R evidence that is submitted with marketing applications in Module 2 of the Common Technical Document (CTD). The guidance was fi...
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- 2016
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30. An analysis of IN.PACT DEEP randomized trial on the limitations of the societal guidelines-recommended hemodynamic parameters to diagnose critical limb ischemia
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Iris Baumgartner, Tarek A. Hammad, Thomas Zeller, Mehdi H. Shishehbor, Dierk Scheinert, and Krishna J. Rocha-Singh
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Male ,medicine.medical_treatment ,Hemodynamics ,Blood Pressure ,030204 cardiovascular system & hematology ,Balloon ,Severity of Illness Index ,law.invention ,0302 clinical medicine ,Randomized controlled trial ,Ischemia ,law ,030212 general & internal medicine ,Aged, 80 and over ,Angiography ,Middle Aged ,Prognosis ,medicine.anatomical_structure ,Lower Extremity ,Practice Guidelines as Topic ,Female ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,medicine.medical_specialty ,Critical Illness ,Peripheral Arterial Disease ,03 medical and health sciences ,Predictive Value of Tests ,medicine.artery ,Angioplasty ,medicine ,Humans ,Ankle Brachial Index ,Vascular Patency ,Aged ,Chi-Square Distribution ,business.industry ,Reproducibility of Results ,Blood Pressure Determination ,Critical limb ischemia ,Surgery ,body regions ,Logistic Models ,Blood pressure ,Plantar arch ,Multivariate Analysis ,Ankle ,business - Abstract
Recent small single-center data indicate that the current hemodynamic parameters used to diagnose critical limb ischemia are insensitive. We investigated the validity of the societal guidelines-recommended hemodynamic parameters against core laboratory-adjudicated angiographic data from the multicenter IN.PACT DEEP (RandomIzed AmPhirion DEEP DEB vs StAndard PTA for the treatment of below the knee Critical limb ischemia) Trial.Of the 358 patients in the IN.PACT DEEP Trial to assess drug-eluting balloon vs standard balloon angioplasty for infrapopliteal disease, 237 had isolated infrapopliteal disease with an available ankle-brachial index (ABI), and only 40 of the latter had available toe pressure measurements. The associations between ABI, ankle pressure, and toe pressure with tibial runoff, Rutherford category, and plantar arch were examined according to the cutoff points recommended by the societal guidelines. Abnormal tibial runoff was defined as severely stenotic (≥70%) or occluded and scored as one-, two-, or three-vessel disease. A stenotic or occluded plantar arch was considered abnormal.Only 14 of 237 patients (6%) had an ABI 0.4. Abnormal ankle pressure, defined as 50 mm Hg if Rutherford category 4 and 70 mm Hg if Rutherford category 5 or 6, was found only in 37 patients (16%). Abnormal toe pressure, defined as 30 mm Hg if Rutherford category 4 and 50 mm Hg if Rutherford category 5 or 6, was found in 24 of 40 patients (60%) with available measurements. Importantly, 29% of these 24 patients had an ABI within normal reference ranges. A univariate multinomial logistic regression found no association between the above hemodynamic parameters and the number of diseased infrapopliteal vessels. However, there was a significant paradoxic association where patients with Rutherford category 6 had higher ABI and ankle pressure than those with Rutherford category 5. Similarly, there was no association between ABI and pedal arch patency.The current recommended hemodynamic parameters fail to identify a significant portion of patients with lower extremity ulcers and angiographically proven severe disease. Toe pressure has better sensitivity and should be considered in all patients with critical limb ischemia.
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- 2016
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31. A PROPOSED MODEL FOR MEASURING COST AND BENEFIT IN WATER INSTITUTIONS TO EVALUATE THE ENVIRONMENTAL PERFORMANCE AN APPLIED STUDY ON TOSHKA PROJECT
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Ezzat M. Soliman, Tarek A. Hammad, M. S. M Hassanin, and M. A Abou Zaid
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Balance (accounting) ,Cost–benefit analysis ,Agriculture ,business.industry ,media_common.quotation_subject ,Accounting information system ,Revenue ,Environmental pollution ,Sample (statistics) ,Quality (business) ,Environmental economics ,business ,media_common - Abstract
The environment kept its miraculous balance due to God's power till man, intentionally or non-intentionally, started to corrupt God's creation. This led to a huge problem, namely damaging the environment. Hence, the researcher decided to study and analyze costs, environmental returns of water industrial facilities of Toshka project of agricultural expansion under the title " A proposed Model to Measure Cost & Return in Water Facilities with the aim of Assessing Environmental Performance- Applied Study on Toshka Project" . This is due to the importance quality of accounting information for decision-making and conducting a research study of the opinions of a sample of those responsible for industrial facilities of Toshka Project. For the theoretical part of the studyk, light was shed on care of these facilities of environmental issues and nature of environmental costs borne by these facilities. The researcher also examined concept and nature of environmental costs and means of approaching them. As for the applied part, it is the research study and building a measurement model of cost & return. Through a questionnaire form distributed on those working at industrial facilities at Toshka Project, results and recommendations to achieve goals of the research were attained, the most important of which are: Firstly, Results: There is no moral relationship of statistically significance between rationalizing costs in water facilities and the results of the environmental performance of these facilities. There is no moral- relationship of statistically significance between cost rationalization, revenue of water facilities & the amount of environmental pollution. There is no moral relationship of statistically significance among the results of suggested model for measuring the cost & revenue of water facilities & rationalizing environmental performance of Toshka Project. Secondly: Recommendations: Paying attention to laying out qualified cadres in the accountant units & operational ones related to environment. Activating the laws that make the facilities conform to their responsibilities towards the environment & paying attention to research & study for indicating the role of environmental legislations & their effects on environmental costs. Paying attention to evaluation as a tool for improving the facilities performance periodically as well as research and study of accountancy information in evaluating environmental performance .
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- 2016
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32. PROSPECTIVE SINGLE CENTER EXPERIENCE OF PULMONARY EMBOLISM MANAGEMENT AND OUTCOMES IN THE ERA OF PULMONARY EMBOLISM RESPONSE TEAMS
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Mehdi H. Shishehbor, Robert Schilz, Matthew J. Lacey, Amanda Zemko, Leben Tefera, Teresa Carman, Jun Li, Tarek A. Hammad, and Rebecca Kahl
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High morbidity ,medicine.medical_specialty ,business.industry ,medicine ,Cardiology and Cardiovascular Medicine ,medicine.disease ,Single Center ,business ,Intensive care medicine ,Pulmonary embolism - Abstract
Pulmonary Embolism (PE) is associated with high morbidity and mortality; however, with the advent of multidisciplinary Pulmonary Embolism Response Teams (PERT) and advanced therapies, those may be preventable. We evaluated the treatment and 30-day outcomes of all PE admitted to our hospital. We
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- 2020
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33. Personalized benefit-risk assessments combining clinical trial and real-world data provide further insights into which patients may benefit most from therapy: Demonstration for a new oral antiplatelet therapy
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Andrew M. Tershakovec, Kevin Marsh, Thibaud Prawitz, Tarek A. Hammad, Cathy Anne Pinto, Dimitra Lambrelli, Anna Schultze, Tommi Tervonen, and Johanna Hyacinthe
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Male ,medicine.medical_specialty ,Databases, Factual ,Epidemiology ,Pyridines ,Clinical Decision-Making ,Myocardial Infarction ,Normal Distribution ,Hemorrhage ,Comorbidity ,030226 pharmacology & pharmacy ,Risk Assessment ,Placebos ,03 medical and health sciences ,Lactones ,0302 clinical medicine ,Sex Factors ,Risk Factors ,Secondary Prevention ,Medicine ,Humans ,Pharmacology (medical) ,030212 general & internal medicine ,Intensive care medicine ,Disease burden ,Aged ,Randomized Controlled Trials as Topic ,Aged, 80 and over ,business.industry ,Proportional hazards model ,Patient Selection ,Hazard ratio ,Age Factors ,Pharmacoepidemiology ,Middle Aged ,United Kingdom ,Clinical trial ,Treatment Outcome ,Platelet aggregation inhibitor ,Feasibility Studies ,Female ,Metric (unit) ,business ,Risk assessment ,Platelet Aggregation Inhibitors - Abstract
Purpose Quantitative benefit-risk (B-R) assessments are used to characterize treatment by combining key benefits and risks into a single metric but have historically been done for the "average" patient. Our aim was to conduct an individualized assessment for the oral antiplatelet vorapaxar by combining trial and real-world data to further personalize the treatment profiles. Methods Using linked UK health care databases, we developed risk prediction equations for key ischemic and bleeding events using Cox proportional hazards models. Trial hazard ratios, relative to placebo, were applied to baseline risk estimates to compute expected attributable risks, summed to derive a per-patient net clinical benefit (NCB). High risk subgroups were defined a priori, and Gaussian mixture models (GMM) were fit to characterize the NCB distribution and identify subgroups with similar NCBs. Results NCB was consistently positive for all subgroups, likely due to the outcome correlation, and would remain positive with a 12-fold increase in bleeding risk. GMMs identified three distinct NCB subgroups. Compared with the middle/lower NCB subgroups, those with a higher NCB tended to be older, female, and have higher CV disease burden. Conclusions Personalized B-R assessments are feasible and clinically valuable and can be used to better predict who would benefit most from therapy.
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- 2018
34. Patient Engagement at a Tipping Point-The Need for Cultural Change Across Patient, Sponsor, and Regulator Stakeholders: Insights From the DIA Conference, 'Patient Engagement in Benefit Risk Assessment Throughout the Life Cycle of Medical Products'
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Rebecca Noel, Anne M. Wolka, F. Reed Johnson, Debra L. Michaels, Marilyn Metcalf, Meredith Smith, Tarek A. Hammad, and Bennett Levitan
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Value (ethics) ,business.industry ,Process (engineering) ,030503 health policy & services ,Best practice ,Public Health, Environmental and Occupational Health ,Foundation (evidence) ,Pharmacy ,Public relations ,Tipping point (climatology) ,03 medical and health sciences ,0302 clinical medicine ,Work (electrical) ,Order (business) ,Medicine ,Pharmacology (medical) ,030212 general & internal medicine ,0305 other medical science ,business ,Pharmacology, Toxicology and Pharmaceutics (miscellaneous) - Abstract
Benefit-risk assessment is the foundation for decision making throughout the life cycle of medical products. Because patients are the beneficiaries of the efficacy of medical treatments and also bear their possible risks, their perspectives and judgments about value and the relative importance of benefits and risks should be at the heart of the medical decision-making process. Patient engagement is now at a tipping point; there have been a growing number of patient engagement initiatives over the past several years, but there remains the need for a common language, alignment on engagement approaches and best practices, and a shared vision regarding a desired future state. This article discusses insights gleaned from the DIA conference, "Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products" (September 2015). It highlights the changes that will need to occur within the patient, medical-product sponsor, and regulatory cultures in order for patient engagement to become integrated into the medical-product development process and life cycle maintenance. Furthermore, it emphasizes that reaching the desired future state will require a conscious commitment from all stakeholders to work collaboratively to develop shared solutions and to map a common path forward.
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- 2018
35. Associations of exercise ankle-brachial index, pain-free walking distance and maximum walking distance with the Peripheral Artery Questionnaire: Finding from the PORTRAIT PAD Registry
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Kim G. Smolderen, John A. Spertus, Mehdi H. Shishehbor, Tarek A. Hammad, and Philip G. Jones
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Male ,Percentile ,medicine.medical_specialty ,Health Status ,Walk Test ,Disease ,Walking ,030204 cardiovascular system & hematology ,Logistic regression ,03 medical and health sciences ,Peripheral Arterial Disease ,0302 clinical medicine ,Vascular Stiffness ,Quality of life ,Predictive Value of Tests ,Surveys and Questionnaires ,medicine ,Humans ,Ankle Brachial Index ,030212 general & internal medicine ,Peripheral artery disease (PAD) ,Registries ,Aged ,Netherlands ,Exercise Tolerance ,business.industry ,Australia ,Odds ratio ,Intermittent Claudication ,Middle Aged ,medicine.disease ,United States ,Test (assessment) ,body regions ,Physical therapy ,Quality of Life ,Female ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,Claudication ,business ,human activities - Abstract
An exercise ankle–brachial index (ABI) test can provide further insight into the functional significance of peripheral artery disease (PAD). The variability in its use, associated patient factors and its relation to patients’ symptoms are unknown. From the international PORTRAIT registry, we identified 1131 patients with PAD. We fit a hierarchical logistic regression model, adjusting for patient factors, country and site, to examine predictors of and variation in ordering exercise ABI testing. We also examined the associations between test components and health status as quantified by the Peripheral Artery Questionnaire (PAQ) using semi-parametric regression methods. Testing was ordered in 22% in the United States versus 80% in the Netherlands and 90% in Australia. Testing was likely to be performed if the patient was male, younger, had typical symptoms and a higher resting ABI, with substantial variability across sites (median odds ratio=5.9, 95% CI: 3.2–19.5). Adjusting for country and site, the resting ABI and all exercise ABI metrics were associated with the PAQ Physical Limitation score. In addition, important components of the test, namely time to onset of claudication, pain-free walking distance (PFWD), and maximum walking distance (MWD), were also associated with PAQ Symptoms and Summary scores. More importantly, even after adjusting for resting ABI, a patient with a post-exercise ABI of 0.29 (25th percentile), compared to 0.61 (75th percentile), achieved 4.4 (95% CI: 0.4–8.4, p=0.031) points less on the PAQ Physical Limitation score. Exercise ABI test use is remarkably variable, and less used in the United States. Its data, specifically PFWD and MWD, might help in objectively assessing the impact of PAD on patients’ functioning and quality of life.
- Published
- 2018
36. Myocarditis Associated with Immune Checkpoint Inhibitors: An Expert Consensus on Data Gaps and a Call to Action
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Tomas G, Neilan, Mace L, Rothenberg, Laleh, Amiri-Kordestani, Ryan J, Sullivan, Richard M, Steingart, William, Gregory, Subramanian, Hariharan, Tarek A, Hammad, JoAnn, Lindenfeld, Martin J, Murphy, Javid J, Moslehi, and Ming, Zhou
- Subjects
Cancer Research ,medicine.medical_specialty ,Myocarditis ,Consensus ,Side effect ,business.industry ,Immune checkpoint inhibitors ,Normal tissue ,Expert consensus ,030204 cardiovascular system & hematology ,medicine.disease ,Call to action ,03 medical and health sciences ,0302 clinical medicine ,Oncology ,Risk Factors ,030220 oncology & carcinogenesis ,medicine ,Humans ,In patient ,Immunotherapy ,Intensive care medicine ,Adverse effect ,business - Abstract
Immune checkpoint inhibitors (ICIs) have transformed the treatment landscape for cancer. Due to the mechanism of action of ICIs, inflammatory reactions against normal tissue were an anticipated side effect of these agents; these immune-related adverse events have been documented and are typically low grade and manageable. Myocarditis has emerged as an uncommon but potentially life-threatening adverse reaction in patients treated with ICIs. Assessment and characterization of ICI-associated myocarditis is challenging because of its low incidence and protean manifestations. Nevertheless, the seriousness of ICI-associated myocarditis justifies a coordinated effort to increase awareness of this syndrome, identify patients who may be at risk, and enable early diagnosis and appropriate treatment. The “Checkpoint Inhibitor Safety Working Group,” a multidisciplinary committee of academic, industry, and regulatory partners, convened at a workshop hosted by Project Data Sphere, LLC, on December 15, 2017. This meeting aimed to evaluate the current information on ICI-associated myocarditis, determine methods to collect and share data on this adverse reaction, and establish task forces to close the identified knowledge gaps. In this report, we summarize the workshop findings and proposed steps to address the impact of ICI-associated myocarditis in patients with cancer.
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- 2018
37. The Effect of Post-Exercise Ankle-Brachial Index on Lower Extremity Revascularization
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Mehdi H. Shishehbor, Tarek A. Hammad, Heather L. Gornik, Grant W. Reed, Ashley M. Lowry, Sridhar Venkatachalam, John R. Bartholomew, Paul Zellers, Jason A. Strefling, and Eugene H. Blackstone
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Male ,medicine.medical_specialty ,medicine.medical_treatment ,Kaplan-Meier Estimate ,Revascularization ,Peripheral Arterial Disease ,Predictive Value of Tests ,Risk Factors ,Internal medicine ,medicine ,Clinical endpoint ,Humans ,Ankle Brachial Index ,cardiovascular diseases ,Propensity Score ,Aged ,Proportional Hazards Models ,Retrospective Studies ,Aged, 80 and over ,Chi-Square Distribution ,Proportional hazards model ,business.industry ,Hazard ratio ,Endovascular Procedures ,Middle Aged ,Confidence interval ,Surgery ,body regions ,Treatment Outcome ,Lower Extremity ,Predictive value of tests ,Multivariate Analysis ,Cardiology ,Exercise Test ,Female ,business ,Cardiology and Cardiovascular Medicine ,human activities ,Chi-squared distribution ,Vascular Surgical Procedures ,Mace - Abstract
The purpose of this study was to investigate the effect of post-exercise ankle-brachial index (ABI) on the incidence of lower extremity (LE) revascularization, cardiovascular outcomes, and all-cause mortality in patients with normal and abnormal resting ABI.The clinical and prognostic value of post-exercise ABI in the setting of normal or abnormal resting ABI remains uncertain.A total of 2,791 consecutive patients with ABI testing between September 2005 and January 2010 were classified into group 1: normal resting (NR)/normal post-exercise (NE); group 2: NR/abnormal post-exercise (AE); group 3: abnormal resting (AR)/NE; and group 4: AR/AE. Abnormal post-exercise ABI was defined as a drop of20% from resting ABI as per the American College of Cardiology/American Heart Association guidelines. The primary endpoint was incidence of LE revascularization. Secondary endpoints were major adverse cardiovascular events (MACE) and all-cause mortality. Associations between post-exercise ABI and outcomes were adjusted using multivariable Cox proportional hazard and propensity analyses.Compared with group 1 (NR/NE), group 2 (NR/AE) had increased LE revascularization (propensity-matched adjusted hazard ratio [HR]: 6.63, 95% confidence interval [CI]: 3.13 to 14.04; p0.001) but no differences in MACE or all-cause mortality. When resting ABI was abnormal, group 4 (AR/AE) compared with group 3 (AR/NE), abnormal post-exercise ABI was still associated with increased LE revascularization (adjusted HR: 1.59, 95% CI: 1.11 to 2.28; p = 0.01), which persisted after propensity matching (adjusted HR: 2.32, 95% CI: 1.52 to 3.54; p0.001). Compared with group 1 (NR/NE) and after propensity matching, group 4 (AR/AE) had a significant increase in MACE (adjusted HR: 1.44, 95% CI: 1.09 to 1.90; p = 0.009) and a trend toward increased all-cause mortality (adjusted HR: 1.37, 95% CI: 0.99 to 1.88; p = 0.052); however, group 3 (AR/NE) did not.Post-exercise ABI appears to offer both clinical (lower extremity revascularization) and prognostic information in those with normal and abnormal resting ABI.
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- 2015
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38. Regulatory and Legislative Policy and Science Considerations in the Era of Patient-Centeredness, Big Data, and Value
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Tarek A. Hammad and George A. Neyarapally
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- 2017
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39. Analysis of IN.PACT DEEP trial on the association between changes in perfusion from pre- to postrevascularization and clinical outcomes in critical limb ischemia
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Mehdi H. Shishehbor, Tarek A. Hammad, Iris Baumgartner, Thomas Zeller, Krishna J. Rocha-Singh, and Dierk Scheinert
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Male ,medicine.medical_specialty ,medicine.medical_treatment ,Ischemia ,Hemodynamics ,030204 cardiovascular system & hematology ,Revascularization ,03 medical and health sciences ,0302 clinical medicine ,Risk Factors ,Internal medicine ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Ankle Brachial Index ,Arterial Pressure ,030212 general & internal medicine ,610 Medicine & health ,Aged ,business.industry ,Endovascular Procedures ,Angiography ,Ultrasonography, Doppler ,General Medicine ,Critical limb ischemia ,Toes ,medicine.disease ,Surgery ,body regions ,Tibial Arteries ,Blood pressure ,medicine.anatomical_structure ,Treatment Outcome ,Amputation ,Lower Extremity ,Toe Brachial Index ,Cardiology ,Female ,medicine.symptom ,Ankle ,Cardiology and Cardiovascular Medicine ,business ,Vascular Surgical Procedures - Abstract
Objectives To quantify changes in ankle and toe pressure from pre- to post-endovascular revascularization for critical limb ischemia (CLI) and examine their association with major adverse limb events (MALE). Background Despite societal guidelines recommendation of routine hemodynamic surveillance following revascularization, little is known about hemodynamic assessment in CLI. Methods Among the 358 patients with CLI from the international multicenter IN.PACT DEEP trial, ankle and toe pressures measurements were available at both baseline and after intervention in 270 and 44 patients, respectively. The change in ankle and toe pressures in response to endovascular revascularization and its association with 1-year MALE (target limb revascularization, amputation, or death) were examined using Kaplan–Meier curves and multivariable Cox proportional hazard analyses. Corresponding optimal cutoff points were also identified. Results The mean increase in ankle and toe pressures following revascularization was 33 and 13 mmHg, respectively. Patients with an improvement of ankle pressure >73 mmHg or toe pressure >1 mmHg had similarly the lowest incidence of MALE (23%), while the highest rate of MALE (50%) was found in those whose toe pressure failed to improve by at least 1 mmHg following intervention. In addition, an increase in ankle pressure >73 mmHg was numerically protective against MALE, and more importantly, an increase in toe pressure of >1 mmHg provided statistically significant protection from MALE (adjusted HR = 0.15, 95% CI: 0.04–0.57, P = 0.005). Conclusions Improvements in toe pressure post revascularization are incremental and rarely normalize. Toe pressure, compared to ankle pressure, is more useful in CLI and predicts future MALE.
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- 2017
40. The Contemporary Role of Stents and Angioplasty for the Treatment of Infrapopliteal Disease in Critical Limb Ischemia
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Tarek A. Hammad and Anand Prasad
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medicine.medical_specialty ,Atherectomy ,medicine.medical_treatment ,Ischemia ,030204 cardiovascular system & hematology ,Revascularization ,Balloon ,03 medical and health sciences ,0302 clinical medicine ,Drug Delivery Systems ,Angioplasty ,medicine ,Humans ,cardiovascular diseases ,030212 general & internal medicine ,Leg ,business.industry ,Stent ,Critical limb ischemia ,medicine.disease ,Limb Salvage ,Surgery ,body regions ,Stents ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,Claudication ,Angioplasty, Balloon - Abstract
Critical limb ischemia (CLI) is associated with significant morbidity, mortality, and increased health care expenses. Revascularization has a central role in the treatment of CLI. Following publication of BASIL (bypass versus angioplasty in severe ischemia of the leg) trial a decade ago, an "endovascular first" approach had gained momentum and the technologies available for endovascular therapy have exponentially increased. Both the development of technology and technique, highlighted in this review, have allowed operators to treat complex infrapopliteal lesions which are central to CLI pathology.The role of atherectomy remains controversial but for calcified lesions it has become an accepted adjunctive tool for plaque modification. The place of drug delivery technologies requires further trials. The use of a drug-coated balloon (DCB) makes intuitive sense; however, choice of excipient, lower limit of vessel size, and impact on remodeling and thrombosis remain uncertain. The optimal treatment of infrapopliteal disease remains an area of active investigation. The endpoints in CLI trials continue to be challenging and calibration of patency in relation to wound healing remains a moving target. In addition, unaccounted variables continue to confound interpretation of CLI trials-including quality and nature of wound care, status of pedal-plantar loop patency, and management of underlying diabetes and other comorbidities. In summary, these challenges will also need to be addressed as the CLI field continues to mature in the twenty-first century.
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- 2017
41. Cancer recording in patients with type 2 diabetes in primary care and hospital admission data
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Tjeerd van Staa, Frank de Vries, Rachael Williams, Tarek A. Hammad, B Leufkens, and Arlene M. Gallagher
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education.field_of_study ,medicine.medical_specialty ,Pediatrics ,Type 1 diabetes ,Information Systems and Management ,business.industry ,Concordance ,Cancer ,Health Informatics ,medicine.disease ,Read codes ,Internal medicine ,Cohort ,medicine ,Medical prescription ,Skin cancer ,education ,Stomach cancer ,business ,Information Systems ,Demography - Abstract
ObjectiveElectronic health records are increasingly used to investigate associations between antidiabetic therapy and cancer. Misclassification can impact results, especially if differential between comparators. The objective of this study was to estimate cancer misclassification when using primary care or hospital data alone. ApproachAdults aged ≥40 years with an insulin or oral antidiabetic prescription in Clinical Practice Research Datalink (CPRD) primary care data at least a year after start of data collection, and no record of type 1 diabetes, were included. Patients were matched by year of birth (stepwise within 5 years), sex and GP practice to up to 1 non-diabetic patient. The cohort was restricted to those eligible for Hospital Episode Statistics (HES) linkage with follow-up during the study period (01/04/97-31/12/06). Follow-up started at the maximum of the registration date with the practice, practice up-to-standard date (a CPRD quality metric), and start of study period. Follow-up ended at the minimum of when the patient left the practice, the date CPRD last collected data from the practice, and end of study period. Cancer was identified in CPRD via Read codes and in HES via ICD10 codes. For each cancer case in CPRD, analysis evaluated whether there was a corresponding record in HES coded with same, different or unspecified site. Analysis was repeated for cancers identified in HES. Results53,585 diabetic patients were matched to 47,435 non-diabetic patients. 83% of cancer cases in CPRD had a corresponding record in HES (78% with the same type). Misclassification varied by cancer site, ranging from 3% (stomach cancer) to 57% (nonmelanoma skin cancer). 83% of cancer cases in HES had a corresponding record in CPRD, with all misclassification rates
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- 2017
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42. Evaluating the validity of clinical codes to identify cataract and glaucoma in the UK Clinical Practice Research Datalink
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Adel Abou-Ali, Simone P. Pinheiro, Tarek A. Hammad, and Elizabeth M. Kang
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education.field_of_study ,Pediatrics ,medicine.medical_specialty ,genetic structures ,Epidemiology ,Clinical events ,business.industry ,Glaucoma ,Pharmacoepidemiology ,medicine.disease ,eye diseases ,Clinical Practice ,Read codes ,medicine ,Optometry ,Eye disorder ,Pharmacology (medical) ,sense organs ,Code algorithm ,Medical diagnosis ,education ,business - Abstract
Purpose The aim of this study is to determine (i) the positive predictive value (PPV) of an algorithm using clinical codes to identify incident glaucoma and cataract events in the Clinical Practice Research Datalink (CPRD) and (ii) the ability to capture the correct timing of these clinical events. Methods A total of 21 339 and 5349 potential cataract and glaucoma cases, respectively, were identified in CPRD between 1 January 1990 and 31 December 2010. Questionnaires were sent to the general practitioners (GP) of 1169 (5.5%) cataract and 1163 (21.7%) glaucoma cases for validation. GPs were asked to verify the diagnosis and the timing of the diagnosis and to provide other supporting information. Results A total of 986 (84.3%) valid cataract questionnaires and 863 (74.2%) glaucoma questionnaires were completed. 92.1% and 92.4% of these used information beyond EMR to verify the diagnosis. Cataract and glaucoma diagnoses were confirmed in the large majority of the cases. The PPV (95% CI) of the cataract and glaucoma Read code algorithm were 92.0% (90.3–93.7%) and 84.1% (81.7–86.6%), respectively. However, timing of diagnosis was incorrect for a substantial proportion of the cases (20.3% and 32.8% of the cataract and glaucoma cases, respectively) among whom 30.4% and 49.2% had discrepancies in diagnosis timing greater than 1 year. Conclusions High PPV suggests that the algorithms based on the clinical Read codes are sufficient to identify the cataract and glaucoma cases in CPRD. However, these codes alone may not be able to accurately identify the timing of the diagnosis of these eye disorders. Copyright © 2014 John Wiley & Sons, Ltd.
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- 2014
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43. ABO phenotype and sepsis in very low birth infants
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An N. Massaro, Ceyda Acun, Mohamed A. Mohamed, Tarek A. Hammad, Hany Aly, Asra Tanveer, and Elsie Lee
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medicine.medical_specialty ,Pediatrics ,Neonatal sepsis ,Obstetrics ,business.industry ,Birth weight ,Incidence (epidemiology) ,Prevalence ,Gestational age ,medicine.disease ,Sepsis ,Low birth weight ,Infectious Diseases ,ABO blood group system ,Pediatrics, Perinatology and Child Health ,medicine ,medicine.symptom ,business - Abstract
An association between infection and an individual's blood group has been reported in the adult medical literature. This association has so far not been investigated in the neonate, and may be reflected in the differences in susceptibilities of neonates to bacterial sepsis. The aim of this study is to investigate the association between ABO phenotype and the incidence of sepsis in very low birth weight infants. This is a retrospective data analysis. All very low birth weight infants admitted to The George Washington University Medical Center between November 1997 and March 2003 were classified according to blood groups into group 1: Phenotype O and A (possible B-antibody (ab)); and group 2: Phenotype B and AB (without B-ab). Multivariate regression analysis was performed to determine statistically significant differences in sepsis between the two groups. Data on 164 infants was analyzed. One hundred and twenty five infants (76.2%) had blood group A or O and 39 infants (23.8%) had blood group B or AB. Mean gestational age was 27.6 ± 2.4 weeks and mean birth weight was 984.5 ± 295 g. Groups were not significantly different in gestational age, birth weight, gender, and race. After controlling for confounding variables, there was no difference between the groups in the incidence of sepsis (34% vs. 33%, P = 0.24). ABO blood group phenotype was not correlated with sepsis in the very low birth weight infants in our unit.
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- 2015
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44. Determining the predictive value of Read codes to identify congenital cardiac malformations in the UK Clinical Practice Research Datalink
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Yulan Ding, Tarek A. Hammad, Holly Epperly, Andrea V. Margulis, and Marian M. Strazzeri
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Data source ,Response rate (survey) ,education.field_of_study ,Pediatrics ,medicine.medical_specialty ,Epidemiology ,business.industry ,Pharmacoepidemiology ,medicine.disease ,Predictive value ,Clinical Practice ,Read codes ,medicine ,Pharmacology (medical) ,Medical emergency ,Medical diagnosis ,Congenital cardiac malformations ,education ,business - Abstract
Purposes The purposes of this study were to determine (i) the positive predictive value (PPV) of multiple Read codes used to identify congenital cardiac malformation (CCM) cases in the UK Clinical Practice Research Datalink (CPRD); (ii) the accuracy of the diagnosis date; and (iii) the source of information that the general practitioners (GPs) use for validating the diagnosis suggested by the code. Methods Eight hundred eighty-eight records with Read diagnostic and procedures codes for CCM, between January 1996 and November 2010, were identified from CPRD. Questionnaires were sent to GPs to verify the diagnoses and date of the code-identified events. Results A total of 719 questionnaires were returned (81% response rate). The PPV of the CCM codes was 93% (670/719). Thirty-one percent of cases had a different event date than the one recorded in the electronic medical record (EMR); 10% of these differing dates were within 30days of the code-identified CCM date. GPs used a variety of data sources to confirm CCM diagnoses. Although the EMR was the most frequently used data source (70%), 66% reported using consultation letters, 9% reported using clinical notes or paper charts, and 35% of GPs reported using the hospital record to confirm the CCM diagnosis. Conclusions Clinical Practice Research Datalink Read codes for CCMs have 93% PPV and most likely point to true cases. However, the accuracy of diagnosis dates and the age at diagnosis may not be as reliable. The findings of this study indicate that GPs use information beyond what is available for researchers in the EMR to confirm clinical diagnoses when responding to validation questionnaires. Published 2013. This article is a U.S. Government work and is in the public domain in the USA. key words—Clinical Practice Research Datalink; Read/OXMIS codes; validation of congenital cardiac malformation; heart defects; congenital abnormalities; pharmacoepidemiology
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- 2013
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45. Antidepressant medication dispensing among montelukast initiators
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Yute Wu, Yulan Ding, Tarek A. Hammad, Sigal Kaplan, Andrew D. Mosholder, Esther H. Zhou, Solomon Iyasu, and David Moeny
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Cyclopropanes ,Male ,Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,Adolescent ,medicine.drug_class ,Pharmacy ,Acetates ,Sulfides ,Young Adult ,Internal medicine ,medicine ,Humans ,Immunology and Allergy ,Anti-Asthmatic Agents ,Medical prescription ,Young adult ,Adverse effect ,Montelukast ,Asthma ,Fluticasone ,Depression ,business.industry ,medicine.disease ,Antidepressive Agents ,Anesthesia ,Pediatrics, Perinatology and Child Health ,Quinolines ,Corticosteroid ,Female ,business ,hormones, hormone substitutes, and hormone antagonists ,medicine.drug - Abstract
This study investigates the potential association between montelukast use and psychiatric adverse events by monitoring changes in antidepressant medication dispensing rates before and after initiating montelukast.The primary study group of montelukast initiators was identified using the Wolters Kluwer's SOURCE Lx® pharmacy claims database (WK). This group included 232,159 patients ≤45 years old who had at least two montelukast prescriptions from 2003 to 2007. Comparison groups comprised of 264,704 fluticasone initiators and 89,635 long-acting β-agonist corticosteroid (LABA/ICS) initiators were also identified. Antidepressant medication dispensing rates in these three groups were determined using WK, and changes in rates before and after the first asthma controller medication prescription date were evaluated using interrupted time-series analysis (ITS). ITS was performed separately for four age categories, with a focus on youth (12-17 years) and young adult (18-24 years).For patients 18-24 years old, antidepressant medication dispensing rates increased significantly after initiating montelukast [1.93% (1.55-2.32%, p 0.001)] but also after initiating fluticasone and LABA/ICS [1.72% (1.30-2.15%, p 0.001) and 2.76% (2.35-3.17%, p 0.001)]. Similar patterns were observed across the three medication groups for other age categories but these differences were not all significant.Small increases in antidepressant medication dispensing rates occurred after initiating montelukast. However, similar increases were observed in the fluticasone and LABA/ICS comparison groups. The results of this study cannot support a specific association between initiation of montelukast treatment and an increase in psychiatric adverse effects.
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- 2013
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46. Concomitant use of isotretinoin and contraceptives before and after iPledge in the United States
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Laura A. Governale, Elizabeth M. Kang, Clara Y. Kim, Simone P. Pinheiro, Esther H. Zhou, and Tarek A. Hammad
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education.field_of_study ,Pediatrics ,medicine.medical_specialty ,Epidemiology ,business.industry ,Population ,Pharmacology ,Pharmacoepidemiology ,medicine.disease ,Family planning ,Concomitant ,medicine ,Pharmacology (medical) ,Medical prescription ,skin and connective tissue diseases ,education ,business ,Isotretinoin ,Developed country ,Acne ,medicine.drug - Abstract
PURPOSE: The major concern associated with isotretinoin treatment is its high teratogenic potential. Therefore ensuring use of contraception while on therapy is an important strategy for at-risk patients and has been emphasized in all risk management programs. iPledge the latest and most rigorous isotretinoin program requires among other stipulations monthly assessments of contraceptive use for patients undergoing isotretinoin treatment. The purpose of this study is to evaluate isotretinoin usage patterns and assess concomitant use of isotretinoin and contraceptives before and after iPledge. METHODS: Female patients aged 13-45 years with a new prescription for isotretinoin products during 2004-2008 were identified in the IMS Health longitudinal prescription claims database. Monthly concomitant use of isotretinoin and contraceptives was estimated. Segmented regression analysis of interrupted time series data was used to assess changes in monthly proportion of concomitant use in the 24 months preceding versus following iPledge implementation. RESULTS: The number of isotretinoin prescriptions decreased after iPledge implementation. A small but significant increase in monthly proportion of patients concomitantly using isotretinoin and contraceptive therapies was observed immediately after iPledge implementation (1.3% p-value = 0.02) particularly among younger patients (2.5% p-value < 0.01). No changes in the proportion of concomitancy over time (i.e. slope) between the periods before and after iPledge implementation were observed. CONCLUSION: The findings of this pharmacy prescription claims-based study suggest a small increase in concomitant use of isotretinoin and contraceptives coincident with the time of implementation of iPledge particularly among younger women. Published 2013. This article is a U. S. Government work and is in the public domain in the USA.
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- 2013
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47. Use of selective serotonin reuptake inhibitors in pregnancy and cardiac malformations: a propensity-score matched cohort in CPRD
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Adel Abou-Ali, Fatmatta Kuyateh, Andrea V. Margulis, Mark Levenson, Yulan Ding, Tarek A. Hammad, Marian M. Strazzeri, and Eric Y. Frimpong
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medicine.medical_specialty ,Pregnancy ,Epidemiology ,Offspring ,business.industry ,Obstetrics ,Serotonin reuptake inhibitor ,Odds ratio ,Pharmacoepidemiology ,medicine.disease ,Surgery ,Cohort ,Propensity score matching ,Medicine ,Pharmacology (medical) ,Live birth ,business - Abstract
Purpose Research on the association of maternal selective serotonin reuptake inhibitor (SSRI) use and cardiac malformations in the offspring has yielded conflicting findings. We therefore sought to further investigate the association using data from a large population-based cohort in the UK. Methods The study population consisted of 149464 pregnancies ending in a live birth between January/1996 and November/2010 from the Clinical Practice Research Datalink’s Mother Baby Link. We created propensity-score matched cohorts of first-trimester SSRI users who did not use other antidepressants in the same gestational period (‘SSRI users’, n=3046) and non-antidepressant users (no use from the 3 months before pregnancy through the second trimester of pregnancy, ‘non-users’; n=8991). Weighted logistic regression was used to estimate the odds ratio (OR) and 95% confidence interval (CI) of cardiac malformations overall and septal defects diagnosed in the first year of life, or in the first 6 years of life. Results Sixteen infants with cardiac malformations were identified among SSRI users; 10 of them were septal defects. Among non-users, there were 48 infants with cardiac malformations, 26 of whom had septal defects. The OR (95% CI) for cardiac malformations was 1.00 (0.50; 2.00), and for septal defects was 1.15 (0.46; 2.87). Results were similar for cardiac malformations diagnosed in the first 6 years of life, and in several sensitivity analyses that were also implemented. Conclusions The results of this study are most compatible with no association between maternal use of SSRIs in early pregnancy and cardiac malformations or septal defects in the offspring. Published 2013. This article is a U.S. Government work and is in the public domain in the USA. key words—congenital abnormalities; heart defects; propensity score; SSRIS; weighted logistic regression; mother–baby link; pharmacoepidemiology
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- 2013
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48. Methods of linking mothers and infants using health plan data for studies of pregnancy outcomes
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Pamala A. Pawloski, Inna Dashevsky, David H. Smith, Katherine Haffenreffer, Sascha Dublin, Sengwee Toh, T. Craig Cheetham, Susan E. Andrade, De Kun Li, Pamela E. Scott, Sarah J. Beaton, William O. Cooper, Tarek A. Hammad, Robert L. Davis, Marsha A. Raebel, and Karin E. Johnson
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medicine.medical_specialty ,education.field_of_study ,Pediatrics ,Pregnancy ,Epidemiology ,business.industry ,Medical record ,Population ,Context (language use) ,Birth certificate ,Pharmacoepidemiology ,medicine.disease ,Family medicine ,medicine ,Pharmacology (medical) ,education ,business ,Medicaid - Abstract
Purpose Research on medication safety in pregnancy often utilizes health plan and birth certificate records. This study discusses methods used to link mothers with infants, a crucial step in such research. Methods We describe how eight sites participating in the Medication Exposure in Pregnancy Risk Evaluation Program created linkages between deliveries, infants and birth certificates for the 2001–2007 birth cohorts. We describe linkage rates across sites, and for two sites, we compare the characteristics of populations linked using different methods. Results Of 299260 deliveries, 256563 (86%; range by site, 74–99%) could be linked to infants using a deterministic algorithm. At two sites, using birth certificate data to augment mother–infant linkage increased the representation of mothers who were Hispanic or non-White, younger, Medicaid recipients, or had low educational level. A total of 236460 (92%; range by site, 82–100%) deliveries could be linked to a birth certificate. Conclusions Tailored approaches enabled linking most deliveries to infants and to birth certificates, even when data systems differed. The methods used may affect the composition of the population identified. Linkages established with such methods can support sound pharmacoepidemiology studies of maternal drug exposure outside the context of a formal registry. Copyright © 2013 John Wiley & Sons, Ltd. key words—birth certificates; Medicaid; pregnancy outcome/epidemiology; medical record linkage; pharmacoepidemiology
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- 2013
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49. Prevalence and trends in the use of antipsychotic medications during pregnancy in the U.S., 2001–2007: a population-based study of 585,615 deliveries
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William O. Cooper, Simone P. Pinheiro, Katherine Haffenreffer, De Kun Li, Pamela E. Scott, Inna Dashevsky, Sascha Dublin, T. Craig Cheetham, William V. Bobo, Lyndsay A. Avalos, Qian Li, Jean M. Lawrence, Marsha A. Raebel, Tarek A. Hammad, Sengwee Toh, Susan E. Andrade, Pamala A. Pawloski, David H. Smith, and Robert L. Davis
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Adult ,Pediatrics ,medicine.medical_specialty ,Adolescent ,medicine.drug_class ,medicine.medical_treatment ,Atypical antipsychotic ,Prenatal care ,Birth certificate ,Article ,Young Adult ,International Classification of Diseases ,Pregnancy ,Prevalence ,medicine ,Humans ,Antipsychotic ,Depression (differential diagnoses) ,business.industry ,Obstetrics and Gynecology ,Gestational age ,Prenatal Care ,Middle Aged ,medicine.disease ,Typical antipsychotic ,Drug Utilization ,United States ,Psychiatry and Mental health ,Prescriptions ,Socioeconomic Factors ,Health Care Surveys ,Population Surveillance ,Schizophrenia ,Female ,business ,Antipsychotic Agents - Abstract
This study aims to estimate the prevalence of and temporal trends in prenatal antipsychotic medication use within a cohort of pregnant women in the U.S. We identified live born deliveries to women aged 15–45 years in 2001–2007 from 11 U.S. health plans participating in the Medication Exposure in Pregnancy Risk Evaluation Program. We ascertained prenatal exposure to antipsychotics from health plan pharmacy dispensing files, gestational age from linked infant birth certificate files, and ICD-9-CM diagnosis codes from health plan claims files. We calculated the prevalence of prenatal use of atypical and typical antipsychotics according to year of delivery, trimester of pregnancy, and mental health diagnosis. Among 585,615 qualifying deliveries, 4,223 (0.72 %) were to women who received an atypical antipsychotic and 548 (0.09 %) were to women receiving a typical antipsychotic any time from 60 days before pregnancy through delivery. There was a 2.5-fold increase in atypical antipsychotic use during the study period, from 0.33 % (95 % confidence interval: 0.29 %, 0.37 %) in 2001 to 0.82 % (0.76 %, 0.88 %) in 2007, while the use of typical antipsychotics remained stable. Depression was the most common mental health diagnosis among deliveries to women with atypical antipsychotic use (63 %), followed by bipolar disorder (43 %) and schizophrenia (13 %). The number and proportion of pregnancies exposed to atypical antipsychotics has increased dramatically in recent years. Studies are needed to examine the comparative safety and effectiveness of these medications relative to other therapeutic options in pregnancy.
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- 2013
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50. Validation of an algorithm to estimate gestational age in electronic health plan databases
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Inna Dashevsky, William O. Cooper, Pamala A. Pawloski, Pamela E. Scott, Sengwee Toh, Sascha Dublin, David H. Smith, Katherine Haffenreffer, Tarek A. Hammad, Susan E. Andrade, Robert L. Davis, Simone P. Pinheiro, Karin E. Johnson, Marsha A. Raebel, and Qian Li
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Pregnancy ,Pediatrics ,medicine.medical_specialty ,Database ,Epidemiology ,Singleton ,business.industry ,Gestational age ,Birth certificate ,Pharmacoepidemiology ,computer.software_genre ,medicine.disease ,Predictive value of tests ,medicine ,Pharmacology (medical) ,Diagnosis code ,Young adult ,business ,computer ,Algorithm - Abstract
Purpose To validate an algorithm that uses delivery date and diagnosis codes to define gestational age at birth in electronic health plan databases. Methods Using data from 225 384 live born deliveries to women aged 15–45 years in 2001–2007 within eight of the 11 health plans participating in the Medication Exposure in Pregnancy Risk Evaluation Program, we compared (1) the algorithm-derived gestational age versus the “gold-standard” gestational age obtained from the infant birth certificate file and (2) the prenatal exposure status of two antidepressants (fluoxetine and sertraline) and two antibiotics (amoxicillin and azithromycin) as determined by the algorithm-derived versus the gold-standard gestational age. Results The mean algorithm-derived gestational age at birth was lower than the mean obtained from the birth certificate file among singleton deliveries (267.9 vs 273.5 days) but not among multiple-gestation deliveries (253.9 vs 252.6 days). The algorithm-derived prenatal exposure to the antidepressants had a sensitivity and a positive predictive value of ≥95%, and a specificity and a negative predictive value of almost 100%. Sensitivity and positive predictive value were both ≥90%, and specificity and negative predictive value were both >99% for the antibiotics. Conclusions A gestational age algorithm based upon electronic health plan data correctly classified medication exposure status in most live born deliveries, but trimester-specific misclassification may be higher for drugs typically used for short durations. Copyright © 2013 John Wiley & Sons, Ltd.
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- 2013
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