The Experts below are selected from a list of 39840 Experts worldwide ranked by ideXlab platform
Elizabeth A Ashley - One of the best experts on this subject based on the ideXlab platform.
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Competing Risk events in antimalarial drug trials in uncomplicated plasmodium falciparum malaria a worldwide antimalarial resistance network individual participant data meta analysis
Malaria Journal, 2019Co-Authors: Prabin Dahal, Julie A Simpson, Salim Abdulla, Jane Achan, Ishag Adam, Aarti Agarwal, Richard Allan, Anupkumar R Anvikar, Emmanuel Arinaitwe, Elizabeth A AshleyAbstract:Background: Therapeutic efficacy studies in uncomplicated Plasmodium falciparum malaria are confounded by new infections, which constitute Competing Risk events since they can potentially preclude/ ...
Prabin Dahal - One of the best experts on this subject based on the ideXlab platform.
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Competing Risk events in antimalarial drug trials in uncomplicated plasmodium falciparum malaria a worldwide antimalarial resistance network individual participant data meta analysis
Malaria Journal, 2019Co-Authors: Prabin Dahal, Julie A Simpson, Salim Abdulla, Jane Achan, Ishag Adam, Aarti Agarwal, Richard Allan, Anupkumar R Anvikar, Emmanuel Arinaitwe, Elizabeth A AshleyAbstract:Background: Therapeutic efficacy studies in uncomplicated Plasmodium falciparum malaria are confounded by new infections, which constitute Competing Risk events since they can potentially preclude/ ...
Antoine Pariente - One of the best experts on this subject based on the ideXlab platform.
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Comparison of Treatment Persistence with Dabigatran or Rivaroxaban versus Vitamin K Antagonist Oral Anticoagulants in Atrial Fibrillation Patients: A Competing Risk Analysis in the French National Health Care Databases
Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 2018Co-Authors: Géric Maura, C. Billionnet, Francois Alla, J. J. Gagne, Antoine ParienteAbstract:BACKGROUND: Direct oral anticoagulants (DOACs) have been proposed as a more convenient alternative to vitamin K antagonists (VKAs), which are commonly associated with poor treatment persistence in nonvalvular atrial fibrillation (nv-AF). METHODS: Using data from the French National Healthcare databases (Regime General, 50 million beneficiaries), a cohort study was conducted to compare the 1-year non-persistence rates in nv-AF patients initiating dabigatran (N=11,141) or rivaroxaban (N=11,126) versus VKA (N=11,998). Treatment discontinuation was defined as a switch between oral anticoagulant (OAC) classes or a 60-day gap with no medication coverage, with the additional criterion of no reimbursement for international normalized ratio monitoring during this gap for VKA patients. Considering death as a Competing Risk, differences between 1-year discontinuation rates were used to compare each DOAC versus VKA. 95% confidence intervals [CIs] were estimated via bootstrapping. Baseline patient characteristics were adjusted using inverse probability of treatment weighting. Subgroup analyses considered DOAC dose at initiation, age, Risk of stroke, and bleeding. RESULTS: Adjusted 1-year discontinuation rates were higher for dabigatran than for VKA new users (36.8% vs 30.2%; difference: 6.6% [95% CI, 5.5 to 7.6]) and for rivaroxaban versus VKA new users (33.4% vs 30.4%; 3.0% [1.9 to 4.1]). Similar differences were found in all subgroup analyses, except in dabigatran and rivaroxaban patients
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comparison of treatment persistence with dabigatran or rivaroxaban versus vitamin k antagonist oral anticoagulants in atrial fibrillation patients a Competing Risk analysis in the french national health care databases
Pharmacotherapy, 2018Co-Authors: Géric Maura, C. Billionnet, Francois Alla, J. J. Gagne, Antoine ParienteAbstract:Background Direct oral anticoagulants (DOACs) have been proposed as a more convenient alternative to vitamin K antagonists (VKAs), which are commonly associated with poor treatment persistence in nonvalvular atrial fibrillation (nv-AF). Methods Using data from the French National Healthcare databases (Regime General, 50 million beneficiaries), a cohort study was conducted to compare the 1-year non-persistence rates in nv-AF patients initiating dabigatran (N=11,141) or rivaroxaban (N=11,126) versus VKA (N=11,998). Treatment discontinuation was defined as a switch between oral anticoagulant (OAC) classes or a 60-day gap with no medication coverage, with the additional criterion of no reimbursement for international normalized ratio monitoring during this gap for VKA patients. Considering death as a Competing Risk, differences between 1-year discontinuation rates were used to compare each DOAC versus VKA. 95% confidence intervals [CIs] were estimated via bootstrapping. Baseline patient characteristics were adjusted using inverse probability of treatment weighting. Subgroup analyses considered DOAC dose at initiation, age, Risk of stroke, and bleeding. Results Adjusted 1-year discontinuation rates were higher for dabigatran than for VKA new users (36.8% vs 30.2%; difference: 6.6% [95% CI, 5.5 to 7.6]) and for rivaroxaban versus VKA new users (33.4% vs 30.4%; 3.0% [1.9 to 4.1]). Similar differences were found in all subgroup analyses, except in dabigatran and rivaroxaban patients <75 y (dabigatran vs VKA: 0.3% [-1.4 to 1.8]; rivaroxaban vs VKA: -2.6% [-4.3 to -0.9]) and dabigatran 150 mg new users (-1.1% [-3.1 to 0.7]). Consistent results were obtained when considering both switches between OAC classes and death as Competing Risks of treatment discontinuation. Conclusion Results from this nationwide cohort study showed high non-persistence levels with all OACs and suggest that persistence with both dabigatran and rivaroxaban therapy is not better than persistence with VKA therapy. Hospitalizations for bleeding among non-persistent patients were unlikely to explain these high non-persistence rates. This article is protected by copyright. All rights reserved.
Bertram L Kasiske - One of the best experts on this subject based on the ideXlab platform.
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beyond median waiting time development and validation of a Competing Risk model to predict outcomes on the kidney transplant waiting list
Transplantation, 2016Co-Authors: Allyson Hart, Nicholas Salkowski, Jon J Snyder, Ajay K Israni, Bertram L KasiskeAbstract:BackgroundMedian historical time to kidney transplant is misleading because it does not convey the Competing Risks of death or removal from the waiting list. We developed and validated a Competing Risk model to calculate likelihood of outcomes for kidney transplant candidates and demonstrate how thi
Meijie Zhang - One of the best experts on this subject based on the ideXlab platform.
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instrumental variable with Competing Risk model
Statistics in Medicine, 2017Co-Authors: Cheng Zheng, Ran Dai, Parameswaran Hari, Meijie ZhangAbstract:In this paper, we discuss causal inference on the efficacy of a treatment or medication on a time-to-event outcome with Competing Risks. Although the treatment group can be randomized, there can be confoundings between the compliance and the outcome. Unmeasured confoundings may exist even after adjustment for measured covariates. Instrumental variable methods are commonly used to yield consistent estimations of causal parameters in the presence of unmeasured confoundings. On the basis of a semiparametric additive hazard model for the subdistribution hazard, we propose an instrumental variable estimator to yield consistent estimation of efficacy in the presence of unmeasured confoundings for Competing Risk settings. We derived the asymptotic properties for the proposed estimator. The estimator is shown to be well performed under finite sample size according to simulation results. We applied our method to a real transplant data example and showed that the unmeasured confoundings lead to significant bias in the estimation of the effect (about 50% attenuated). Copyright © 2017 John Wiley & Sons, Ltd.
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instrumental variable with Competing Risk model
arXiv: Methodology, 2016Co-Authors: Cheng Zheng, Ran Dai, Parameswaran Hari, Meijie ZhangAbstract:In this paper, we discuss causal inference on the efficacy of a treatment or medication on a time-to-event outcome with Competing Risks. Although the treatment group can be randomized, there can be confoundings between the compliance and the outcome. Unmeasured confoundings may exist even after adjustment for measured co- variates. Instrumental variable (IV) methods are commonly used to yield consistent estimations of causal parameters in the presence of unmeasured confoundings. Based on a semi-parametric additive hazard model for the subdistribution hazard, we pro- pose an instrumental variable estimator to yield consistent estimation of efficacy in the presence of unmeasured confoundings for Competing Risk settings. We derived the asymptotic properties for the proposed estimator. The estimator is shown to be well per- formed under finite sample size according to simulation results. We applied our method to a real transplant data example and showed that the unmeasured confoundings lead to significant bias in the estimation of the effect (about 50% attenuated).
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analyzing Competing Risk data using the r timereg package
Journal of Statistical Software, 2011Co-Authors: Thomas H Scheike, Meijie ZhangAbstract:In this paper we describe flexible Competing Risks regression models using the comp.Risk() function available in the timereg package for R based on Scheike et al. (2008). Regression models are specified for the transition probabilities, that is the cumulative incidence in the Competing Risks setting. The model contains the Fine and Gray (1999) model as a special case. This can be used to do goodness-of-fit test for the subdistribution hazards’ proportionality assumption (Scheike and Zhang 2008). The program can also construct confidence bands for predicted cumulative incidence curves.We apply the methods to data on follicular cell lymphoma from Pintilie (2007), where the Competing Risks are disease relapse and death without relapse. There is important non-proportionality present in the data, and it is demonstrated how one can analyze these data using the flexible regression models.