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1.
Biomed Eng Lett ; 10(4): 555-578, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33194248

RESUMO

In the anesthesia automation, an automatic propofol infusion system uses Bi-spectral Index Signal (BIS) as a primary feedback signal to manipulate propofol dose. However, the BIS signal may be suspended for some time due to poor EEG signal quality, noise, and many other factors. Therefore, BIS signal failure may be the main cause of inadequate propofol infusion. This fact motivates the need for integration of multivariable fault tolerance module (MFTM) and fractional-order Smith predictor controller to avoid adverse reactions of inadequate propofol dosing during BIS failure. Smith Predictor control strategy is sufficiently robust to predict feedback BIS during BIS failure via patient pharmacological modeled BIS. However, modeled BIS may not provide a guarantee of adequate propofol infusion during BIS failure and especially in the presence of hypotension and hypertension. Thus, the proposed control strategy is designed with MFTM to detect BIS sensor fault and to estimate feedback BIS during BIS failure. Further, the proposed control strategy is designed with a multivariable pharmacological patient model to analyze the cross effect of propofol infusion on BIS and hemodynamic variables. The robustness of the proposed control strategy is tested in the presence of noxious surgical stimulation, BIS sensor fault and heavy hemodynamic disturbance. The pharmacological parameters and recorded signals of 30 patients during various surgeries have been used to validate simulated results. The performance of the proposed control strategy assures optimization and smooth propofol infusion during BIS failure. The proposed system provides stability for a wide range of physiological parameters range. The proposed scheme maintains smooth BIS and MAP signal despite the delay, BIS sensor fault, and surgical disturbances.

2.
Biomed Eng Lett ; 9(1): 127-144, 2019 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-30956886

RESUMO

Anesthetic agent propofol needs to be administered at an appropriate rate to prevent hypotension and postoperative adverse reactions. To comprehend more suitable anesthetic drug rate during surgery is a crucial aspect. The main objective of this proposal is to design robust automated control system that work efficiently in most of the patients with smooth BIS and minimum variations of propofol during surgery to avoid adverse post reactions and instability of anesthetic parameters. And also, to design advanced computer control system that improves the health of patient with short recovery time and less clinical expenditures. Unlike existing research work, this system administrates propofol as a hypnotic drug to regulate BIS, with fast bolus infusion in induction phase and slow continuous infusion in maintenance phase of anesthesia. The novelty of the paper lies in possibility to simplify the drug sensitivity-based adaption with infusion delay approach to achieve closed-loop control of hypnosis during surgery. Proposed work uses a brain concentration as a feedback signal in place of the BIS signal. Regression model based estimated sensitivity parameters are used for adaption to avoid BIS signal based frequent adaption procedure and large offset error. Adaptive smith predictor with lead-lag filter approach is applied on 22 different patients' model identified by actual clinical data. The actual BIS and propofol infusion signals recorded during clinical trials were used to estimate patient's sensitivity parameters EC 50 and λ. Simulation results indicate that patient's drug sensitivity parameters based adaptive strategy facilitates optimal controller performance in most of the patients. Results are obtained with proposed scheme having less settling time, BIS oscillations and small offset error leads to adequate depth of anesthesia. A comparison with manual control mode and previously reported system shows that proposed system achieves reduction in the total variations of the propofol dose. Proposed adaptive scheme provides better performance with less oscillation in spite of computation delay, surgical stimulations and patient variability. Proposed scheme also provides improvement in robustness and may be suitable for clinical practices.

3.
Ann Card Anaesth ; 21(2): 167-172, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29652278

RESUMO

BACKGROUND: The prevalence of diabetes mellitus in patients requiring coronary artery bypass grafting (CABG) is noticeably high (20%-30%). These patients have inferior perioperative outcome, reduced long-term survival, and high risk of recurrent episodes of angina. To improve perioperative outcome surgical unit defined satisfactory glycemic control is desired during this period. Hence, the aim of our study is to compare the efficacy of glargine insulin combination with continuous human insulin infusion for perioperative glycemic control in patients with diabetes undergoing CABG. MATERIALS AND METHODS: Fifty Patients, who were posted for off-pump CABG with diabetes mellitus type II, were randomized in two group, Group I normal saline + human insulin infusion during the perioperative period, Group II (glargine group): Glargine + human insulin infusion during perioperative period. RESULTS: During surgery and in the postoperative period, random blood sugar and human insulin requirement are significantly higher in control group than glargine group. Other infection, step-up antibiotics, intensive care unit (ICU) stay, and hospital stay were significantly higher in control groups in postoperative period. CONCLUSION: Our study results suggest that glargine effectively manages blood glucose level with significantly greater control over postoperative morbidity.


Assuntos
Glicemia , Ponte de Artéria Coronária sem Circulação Extracorpórea/métodos , Diabetes Mellitus Tipo 2/tratamento farmacológico , Hipoglicemiantes/uso terapêutico , Insulina Glargina/uso terapêutico , Idoso , Cuidados Críticos/estatística & dados numéricos , Diabetes Mellitus Tipo 2/sangue , Feminino , Humanos , Infusões Intravenosas , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Assistência Perioperatória , Complicações Pós-Operatórias/epidemiologia , Complicações Pós-Operatórias/prevenção & controle , Estudos Prospectivos
4.
Ann Pediatr Cardiol ; 10(1): 26-30, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28163425

RESUMO

BACKGROUND: We sought to compare the effectiveness of oxygen (O2) treatment administered by an O2 mask and nasal continuous positive airway pressure (NCPAP) in infants after congenital cardiac surgery. METHODS: In this retrospective observational study, 54 infants undergoing corrective cardiac surgery were enrolled. According to the anesthesiologist's preference, the patients ventilated for more than 48 h were either put on NCPAP or O2 mask immediately after extubation. From pre-extubation to 24 h after treatment, arterial blood gas and hemodynamic data were measured. RESULTS: After 24 h of NCPAP institution, the patients showed a significant improvement in oxygenation compared to O2 mask group. Respiratory rate (per minute) decreased from 31.67 ± 4.55 to 24.31 ± 3.69 (P < 0.0001), PO2 (mmHg) increased from 112.12 ± 22.83 to 185.74 ± 14.81 (P < 0.0001), and PCO2 (mmHg) decreased from 42.88 ± 5.01 to 37.00 ± 7.22 (P < 0.0076) in patients on NCPAP. In this group, mean pediatric cardiac surgical Intensive Care Unit (PCSICU) stay was 4.72 ± 1.60 days, with only 2 (11.11%) patients requiring re-intubation. CONCLUSION: NCPAP can be used safely and effectively in infants undergoing congenital cardiac surgery to improve oxygenation/ventilation. It also reduces the work of breathing, PCSICU stay, and may reduce the likelihood of re-intubation.

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