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The localization of agents for collaborative tasks is crucial to maintain the quality of the communication link for successful data transmission between the base station and agents. Power-domain Non-Orthogonal Multiple Access (P-NOMA) is an emerging multiplexing technique that enables the base station to accumulate signals for different agents using the same time-frequency channel. The environment information such as distance from the base station is required at the base station to calculate communication channel gains and allocate suitable signal power to each agent. The accurate estimate of the position for power allocation of P-NOMA in a dynamic environment is challenging due to the changing location of the end-agent and shadowing. In this paper, we take advantage of the two-way Visible Light Communication (VLC) link to (1) estimate the position of the end-agent in a real-time indoor environment based on the signal power received at the base station using machine learning algorithms and (2) allocate resources using the Simplified Gain Ratio Power Allocation (S-GRPA) scheme with the look-up table method. In addition, we use the Euclidean Distance Matrix (EDM) to estimate the location of the end-agent whose signal was lost due to shadowing. The simulation results show that the machine learning algorithm is able to provide an accuracy of 0.19 m and allocate power to the agent.
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Noma , Humanos , Algoritmos , Comunicação , Luz , Aprendizado de MáquinaRESUMO
Due to the growing number of users, power, and spectral effectiveness, most communication systems are complex and difficult to implement on a large scale. Artificial Intelligence (AI) has played an outstanding role in the implementation of theoretical systems in the real world, with less complexity achieving better results. In this direction, we compare the Non-Orthogonal Multiple Access (NOMA) technique for a multiuser Visible Light Communication (VLC) system with Successive Interference Cancellation (SIC) for two types of detectors: (1) the deep learning-based system and (2) the traditional maximum likelihood (ML) decoder-based system. For multiplexing, we compare the variations of novel Orbital Angular Momentum (OAM) multiplexing and Orthogonal Frequency Division Multiplexing (OFDM) with Index Modulation (IM). In this article, we implement OFDM-IM and OAM-IM for four users for the Gaussian fading MIMO Line-of-Sight (LoS) and Non-Line-of-Sight (NLoS) VLC channels. The suggested systems' bit error rate (BER) performances are compared in simulations for a wide range of Signal-to-Noise Ratios (SNRs), which shows that deep learning-based systems outperform the ML-based system for both users to ensure better decoding at the receiver end, especially at higher SNR values. The detection error is lower in a deep learning-based system at around 20% and around 30% for low SNR and high SNR values, respectively.
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In the condition of anemia, kidneys produce less erythropoietin hormone to stimulate the bone marrow to make red blood cells (RBC) leading to a reduced hemoglobin (Hgb) level, also known as chronic kidney disease (CKD). External recombinant human erythropoietin (EPO) is administrated to maintain a healthy level of Hgb, i.e., 10 - 12 g/dl. The semi-blind robust model identification method is used to obtain a personalized patient model using minimum dose-response data points. The identified patient models are used as predictive models in the model predictive control (MPC) framework. The simulation results of MPC for different CKD patients are compared with those obtained from the existing clinical method, known as anemia management protocol (AMP), used in hospitals. The in-silico results show that MPC outperforms AMP to maintain healthy levels of Hgb without over-or-under- shoots. This offers a considerable performance improvement compared to AMP which is unable to stabilize EPO dosage and shows oscillations in Hgb levels throughout the treatment.Clinical Relevance-This research work provides a framework to help clinicians in decision-making for personalized EPO dose guidance using MPC with semi-blind robust model identification using minimum clinical patient dose-response data.
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Anemia , Eritropoetina , Insuficiência Renal Crônica , Humanos , Anemia/tratamento farmacológico , Modelagem Computacional Específica para o Paciente , Eritropoetina/uso terapêutico , RimRESUMO
Warfarin is a challenging drug to administer due to the narrow therapeutic index of the International Normalized Ratio (INR), the inter- and intra-variability of patients, limited clinical data, genetics, and the effects of other medications. Goal: To predict the optimal warfarin dosage in the presence of the aforementioned challenges, we present an adaptive individualized modeling framework based on model (In)validation and semi-blind robust system identification. The model (In)validation technique adapts the identified individualized patient model according to the change in the patient's status to ensure the model's suitability for prediction and controller design. Results: To implement the proposed adaptive modeling framework, the clinical data of warfarin-INR of forty-four patients has been collected at the Robley Rex Veterans Administration Medical Center, Louisville. The proposed algorithm is compared with recursive ARX and ARMAX model identification methods. The results of identified models using one-step-ahead prediction and minimum mean squared analysis (MMSE) show that the proposed framework effectively predicts the warfarin dosage to keep the INR values within the desired range and adapt the individualized patient model to exhibit the true status of the patient throughout treatment. Conclusion: This paper proposes an adaptive personalized patient modeling framework from limited patientspecific clinical data. It is shown by rigorous simulations that the proposed framework can accurately predict a patient's doseresponse characteristics and it can alert the clinician whenever identified models are no longer suitable for prediction and adapt the model to the current status of the patient to reduce the prediction error.
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Administration of drugs requires sophisticated methods to determine the drug quantity for optimal results, and it has been a challenging task for the number of diseases. To solve these challenges, in this paper, we present the semi-blind robust model identification technique to find individualized patient models using the minimum number of clinically acquired patient-specific data to determine optimal drug dosage. To ensure the usability of these models for dosage predictability and controller design, the model (In)validation technique is also investigated. As a case study, the patients treated with warfarin are studied to demonstrate the semi-blind robust identification and model (In)validation techniques. The performance of models is assessed by calculating minimum means squared error (MMSE).Clinical Relevance- This work establishes a general framework for adaptive individualized drug-dose response models from a limited number of clinical patient-specific data. This work will help clinicians in decision-making for improved drug dosing, patient care, and limiting patient exposure to agents with a narrow therapeutic range.
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Preparações Farmacêuticas , Varfarina , Anticoagulantes , HumanosRESUMO
Warfarin belongs to a medication class called anticoagulants or blood thinners. It is used for the treatment to prevent blood clots from forming or growing larger. Patients with venous thrombosis, pulmonary embolism, or who have suffered a heart attack, have an irregular heartbeat, or prosthetic heart valves are prescribed with warfarin. It is challenging to find optimal doses due to inter-patient and intra-patient variabilities and narrow therapeutic index. This work presents an individualized warfarin dosing method by utilizing the individual patient model generated using limited clinical data of the patients with chronic conditions under warfarin anticoagulation treatment. Then, the individual precise warfarin dosing is formalized as an optimal control problem, which is solved using the DORBF control approach. The efficiency of the proposed approach is compared with results obtained from practiced clinical protocol.