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1.
J Clin Med ; 13(8)2024 Apr 20.
Article in English | MEDLINE | ID: mdl-38673677

ABSTRACT

The therapeutic management and short-term consequences of the coronavirus disease 2019 (COVID-19) are well known. However, COVID-19 post-acute sequelae are less known and represent a public health problem worldwide. Patients with COVID-19 who present post-acute sequelae may display immune dysregulation, a procoagulant state, and persistent microvascular endotheliopathy that could trigger microvascular thrombosis. These elements have also been implicated in the physiopathology of postural orthostatic tachycardia syndrome, a frequent sequela in post-COVID-19 patients. These mechanisms, directly associated with post-acute sequelae, might determine the thrombotic consequences of COVID-19 and the need for early anticoagulation therapy. In this context, heparin has several potential benefits, including immunomodulatory, anticoagulant, antiviral, pro-endothelial, and vascular effects, that could be helpful in the treatment of COVID-19 post-acute sequelae. In this article, we review the evidence surrounding the post-acute sequelae of COVID-19 and the potential benefits of the use of heparin, with a special focus on the treatment of postural orthostatic tachycardia syndrome.

3.
Front Endocrinol (Lausanne) ; 13: 851035, 2022.
Article in English | MEDLINE | ID: mdl-35813629

ABSTRACT

Background: The impact of glucagon-like peptide-1 receptor agonists on patients with heart failure has not been fully described. Our main objective was to evaluate the safety and clinical and glycemic efficacy of once-weekly semaglutide in obese patients with type 2 diabetes and heart failure. Methods: In this observational, retrospective, real-world study, we enrolled outpatients with type 2 diabetes, obesity, and heart failure who started semaglutide and were followed-up on at 3, 6, and 12 months. Results: A total of 136 patients were included. From baseline to 12 months, there was a significant improvement on the Kansas City Cardiomyopathy Questionnaire total symptom score (59.0 ± 24.1 vs 79.9 ± 28.4 points, p<0.01), a reduction in the proportion of patients with New York Heart Association functional class III (40.4% to 16.2%, p<0.01), and a reduction in N-terminal pro-brain natriuretic peptide levels (969.5 ± 653.5 vs 577.4 ± 322.1 pg/mL, p<0.01). Emergency department visits due to heart failure, hospitalizations due to heart failure, and all-cause hospitalizations also declined. Additionally, significant reductions in glycated hemoglobin (-1.4%) and body weight (-12.7 kilograms) were observed as well as a de-intensification of antidiabetic therapy. Moreover, semaglutide was safe and well-tolerated. Conclusion: In obese patients with type 2 diabetes and heart failure, the use of once-weekly semaglutide was safe and clinically efficacious, improving health and functional status. Nevertheless, more strong evidence on glucagon-like peptide-1 receptor agonists in heart failure is required.


Subject(s)
Diabetes Mellitus, Type 2 , Heart Failure , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/drug therapy , Glucagon-Like Peptide-1 Receptor/agonists , Glucagon-Like Peptides/therapeutic use , Heart Failure/complications , Heart Failure/drug therapy , Humans , Obesity/chemically induced , Obesity/complications , Obesity/drug therapy , Retrospective Studies
5.
J Neurol Sci ; 401: 37-42, 2019 Jun 15.
Article in English | MEDLINE | ID: mdl-31005763

ABSTRACT

Wearable technology used in Parkinson's disease (PD) research has become an increasing focus of interest in this field. Our group assessed the feasibility, clinical correlation, reliability, and acceptance of smartwatches in order to quantify arm resting tremors in PD patients. An Android application on a smartwatch was used to obtain raw data from the smartwatch's gyroscopes. Twenty-two PD patients were consecutively recruited and followed for 1 year. Arm rest tremors were video filmed and scored by two independent raters using the motor subscale of the Unified Parkinson's Disease Rating Scale (UPDRS-III). The tremor intensity parameter was defined by the root mean square of the angular speed measured by the smartwatch at the wrist. Sixty-four smartwatch evaluations were completed. The Spearman coefficient among the mean of the resting tremor (UPDRS-III) scores and smartwatch measurements for tremor intensity was 0.81 (p < .001); smartwatch reliability to quantify tremors was checked by intraclass reliability coefficient with a resting tremor = 0.89, minimum detectable change = 59.03%. Good acceptance of the system was shown. Smartwatch use for PD tremor analysis is possible, reliable, well-correlated with clinical scores, and well-accepted by patients for clinical follow-up. The results from these experiments suggest that this commodity hardware has the potential to quantify PD patients' tremors objectively in a consulting-room.


Subject(s)
Parkinson Disease/diagnosis , Parkinson Disease/physiopathology , Tremor/diagnosis , Tremor/physiopathology , Wearable Electronic Devices/standards , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Parkinson Disease/complications , Tremor/complications
6.
J Neurol Sci ; 390: 87-88, 2018 07 15.
Article in English | MEDLINE | ID: mdl-29801914

ABSTRACT

The interaction with electronic devices is crucial in our technological society. Hand kinetic tremor complicates mouse driving in Essential tremor patients. To solve this issue some technological solutions are available and accessible online. We present a 71-year-old patient with prominent mouse controlling tremor who improved with one of these systems.


Subject(s)
Computers , Essential Tremor/rehabilitation , Self-Help Devices , Aged , Hand , Humans , Male , Motor Skills
7.
J Neurosci Methods ; 303: 95-102, 2018 06 01.
Article in English | MEDLINE | ID: mdl-29481820

ABSTRACT

BACKGROUND: The use of wearable technology is an emerging field of research in movement disorders. This paper introduces a clinical study to evaluate the feasibility, clinical correlation and reliability of using a system based in smartwatches to quantify tremor in essential tremor (ET) patients and check its acceptance as clinical monitoring tool. NEW METHOD: The system is based on a commercial smartwatch and an Android smartphone. An investigational Android application controls the process of recording raw data from the smartwatch three-dimensional gyroscopes. Thirty-four ET patients were consecutively enrolled in the experiments and assessed along one year. Arm tremor was videofilmed and scored using the Fahn-Tolosa-Marin Tremor Rating Scale (FTM-TRS). Tremor intensity was quantified with the root mean square of angular velocity measured in the patients' wrists. RESULTS: Eighty-two assessments with smartwatches were performed. Spearman's correlation coefficients (ρ) between clinical tremor (FTM-TRS) scores and smartwatch measures for tremor intensity were 0.590 at rest; ρ = 0.738 in steady posture; ρ = 0.189 in finger-to-nose maneuvers; and ρ = 0.652 in pouring water task. Smartwatch reliability was checked by intraclass realiability coefficients: 0.85, 0.95, 0.91, 0.95 respectively. Most of patients showed good acceptance of the system. COMPARISON WITH EXISTING METHOD(S): This commodity hardware contributes to quantify tremor objectively in a consulting-room by customized Android smart devices as clinical monitoring tool. CONCLUSIONS: The NetMD system for tremor analysis is feasible, well-correlated with clinical scores, reliable and well-accepted by patients to tremor follow-up. Therefore, it could be an option to objectively quantify tremor in ET patients during their regular follow-up.


Subject(s)
Essential Tremor/diagnosis , Mobile Applications , Smartphone , Wearable Electronic Devices , Aged , Female , Humans , Male , Middle Aged , Mobile Applications/standards , Patient Acceptance of Health Care , Reproducibility of Results
8.
Biomed Eng Online ; 16(Suppl 1): 74, 2017 Aug 18.
Article in English | MEDLINE | ID: mdl-28830552

ABSTRACT

BACKGROUND: This paper presents the preliminary results of a novel rehabilitation therapy for cervical and trunk control of children with cerebral palsy (CP) based on serious videogames and physical exercise. MATERIALS: The therapy is based on the use of the ENLAZA Interface, a head mouse based on inertial technology that will be used to control a set of serious videogames with movements of the head. METHODS: Ten users with CP participated in the study. Whereas the control group (n = 5) followed traditional therapies, the experimental group (n = 5) complemented these therapies with a series of ten sessions of gaming with ENLAZA to exercise cervical flexion-extensions, rotations and inclinations in a controlled, engaging environment. RESULTS: The ten work sessions yielded improvements in head and trunk control that were higher in the experimental group for Visual Analogue Scale, Goal Attainment Scaling and Trunk Control Measurement Scale (TCMS). Significant differences (27% vs. 2% of percentage improvement) were found between the experimental and control groups for TCMS (p < 0.05). The kinematic assessment shows that there were some improvements in the active and the passive range of motion. However, no significant differences were found pre- and post-intervention. CONCLUSIONS: Physical therapy that combines serious games with traditional rehabilitation could allow children with CP to achieve larger function improvements in the trunk and cervical regions. However, given the limited scope of this trial (n = 10) additional studies are needed to corroborate this hypothesis.


Subject(s)
Cerebral Palsy/physiopathology , Cerebral Palsy/therapy , Cervical Cord/physiopathology , Head Movements , Physical Therapy Modalities , Posture , Video Games , Biomechanical Phenomena , Child , Child, Preschool , Female , Humans , Male , Recovery of Function
9.
Ginecol. obstet. Méx ; 58: 43-6, feb. 1990. tab
Article in Spanish | LILACS | ID: lil-95456

ABSTRACT

Las prostaglandinas se han usado para favorecer, la maduración cervical, la expulsión del producto y diminuir el número de maniobras obstétricas quirúrgicas. En el trabajo se pretende demostrar la utilidad de este fármaco administrado por vía tópica vaginal; en 40 pacientes con embarazo a término, sin trabajo de parto, con un índice de Bishop de 2 (rango o 4) que acudieron al Servicio de Obstetricia, distribuidas en dos grupos de 20 c/u que recibieron prostaglandinas 0.70 mg. por vía intracervical, y 20 con oxitocina 2 ml. unidad por minuto hasta obtener respuesta, se realizó un estudio longitudinal prospectivo y abierto; se excluyó del grupo de pacientes de alto riesgo; en ambos grupos se registraron partogramas en forma cuidadosa, los resultados se validaron obteniendo un promedio y desviación stándar; la edad promedio 25.15 años, edad gestacional 39.4 semanas. Indice de Bishop 2, en el grupo I y en grupo testigo la edad promedio 24.9 años, edad gestacional 40.4 semans y un índice de Bishop de 3.7ñ el tiempo de inducción del ler. grupo fué de 4.65 horas; en el grupo II 7.9 horas P< 0.05, condicionando en 40% menos tiempo de inducción de la maduración cervical, y el trabajo de parto. No se presentaron accidentes fetoplacentarios. La cesárea se redujo, en el grupo de prostaglandinas, un caso contra 6 del grupo testigo, el número de fórceps fué de mayor en este ler. grupo (7 casos contra 2 casos) del testigo. El estado de los poductos no tuvo diferencias significativas. Se puede concluir que es un fármaco de gran ayuda en la práctica obstétrica manejando cuidadosamente considerándolo como un medicamento de elección para la maduración cervical.


Subject(s)
Humans , Pregnancy , Female , Labor, Induced , Prostaglandins E , Vagina
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