Satisfacción y calidad asistencial de la Telefarmacia durante la pandemia por COVID-19 en un hospital de primer nivel / Satisfaction with and quality of Telepharmacy care in a top-tier hospital during the COVID-19 pandemic

Objetivo: Conocer el grado de satisfacción de los pacientes o sus familiares/cuidadores con respecto a la atención recibida mediante Telefarmacia desde la Consulta de Atención Farmacéutica a Pacientes Externos de un Servicio de Farmacia Hospitalaria de primer nivel. Métodos: Estudio transversal de 5 meses de duración. Se incluyeron todos los pacientes atendidos en las Consultas de Atención Farmacéutica de manera telemática con dispensación informada de la medicación entre los meses de mayo y septiembre de 2020. Para medir el grado de satisfacción se utilizó una encuesta tipo Likert de 10 niveles. Los datos de pacientes se obtuvieron a partir del aplicativo Historia Clínica electrónica (IANUS®) y del software Silicon®. Para comparaciones entre grupos se utilizó el test t de Student de comparación de medias y el test ANOVA. Resultados: Se realizaron un total de 392 encuestas de satisfacción a 209 mujeres (53,3%) y 183 hombres (46,7%) de edad media 59,8 años (s.d. 18,5), de las cuáles 231 (58,9%) eran pacientes y 161 (41,1%) cuidadores/familiares. Se observó una puntuación de satisfacción global de 9,88 (s.d. 0,4). No se observaron diferencias estadísticamente significativas entre la puntuación obtenida de los pacientes o cuidadores/familiares (p=0,102). Conclusiones: La consulta telemática de atención farmacéutica constituye una valiosa herramienta que satisface las necesidades asistenciales de los pacientes y sus familiares y supone una oportunidad de mejora en la atención sanitaria integrada a distancia. Desde nuestra experiencia, la telefarmacia se posiciona como una importante estrategia para evitar desplazamientos al centro sanitario, con la consecuente mejoría en la calidad de vida de nuestros pacientes. (AU)

Objective: To ascertain the degree of satisfaction of patients or their relatives/caregivers with the care received via Telepharmacy at the Outpatient Pharmaceutical Care Clinic of a top-tier Hospital Pharmacy Service. Methods: Cross-sectional study lasting 5 months. All patients cared for online by the Pharmaceutical Care Clinics with informed dispensation of medication between May and September 2020 were included. A 10-point Likert-type survey was used to measure the level of satisfaction. Patient data was obtained from the electronic medical record program (IANUS®) and the Silicon® software. Student’s mean comparison t-test and ANOVA test were used for comparisons between groups. Results: A total of 392 satisfaction surveys were conducted on 209 women (53.3%) and 183 men (46.7%) with an average age of 59.8 (s.d. 18.5), of whom 231 (58.9%) were patients and 161 (41.1%) caregivers/relatives. An overall satisfaction score of 9.88 (s.d. 0.4) was observed. No statistically significant differences were observed between the score obtained from patients and that obtained from caregivers/relatives (p=0.102). Conclusions: The online pharmaceutical care clinic is a valuable tool that meets the care needs of patients and their relatives and is an opportunity for improvement in remote comprehensive healthcare. From our experience, telepharmacy is an important strategy in avoiding travel to the health centre, with the subsequent improvement in the quality of life of our patients. (AU)

Aplicabilidad de la herramienta “Prácticas seguras en pacientes con medicamentos de uso crónico” en el ámbito sociosanitario / Applicability of the tool “Safe practices in patients with chronic medicines” in social healthcare

Objetivo: Describir la aplicabilidad de la herramienta “Prácticas seguras en pacientes con medicamentos de uso crónico” en el ámbito de la atención sociosanitaria. Métodos: Estudio observacional transversal (junio 2018) de pacientes institucionalizados en residencia de pacientes asistidos, cuya atención sociosanitaria se realiza desde el Servicio de Farmacia de un hospital de primer nivel. Se aplicaron 18 prácticas seguras a cada tratamiento. Resultados: 153 pacientes incluidos, 69,3% mujeres, mediana edad 83 años (51-101), mediana medicamentos prescritos 12 (1-28). No fueron de aplicación a nuestra población 4 criterios de 18: PG10 (bifosfonatos), PO2 (fentanilo liberación rápida), PG11 (teriparatida por un tiempo superior a 2 años) y PG03 (buprenorfina como deshabituación en pacientes a tratamiento con otros opioides). 14 criterios de 18 detectan prescripciones relacionadas con los criterios de seguridad (monitorizar) y 8 de 18 criterios detectan prescripciones de riesgo en la población, siguiendo la siguiente distribución: 3 PG2 (AAS dosis >150 mg), 2 PG5 (AINE+antitrombótico), 2 PG6 (Triple Whammy), 3 PG7 (2 SRRA), 4 PG8 (2 o más anticolinérgicos), 1 PG9.1 (R/G/D+ anticolinérgicos), 2 PG9.2 (memantina+anticolinérgicos), 1 PO1 (opioide menor+mayor).Conclusiones: La utilización de esta herramienta garantiza la continuidad asistencial de los pacientes, constituye un punto de partida para el desarrollo de un programa de atención farmacéutica sociosanitaria y fomenta la colaboración entre los diferentes niveles asistenciales. A la vista de los resultados, existe una oportunidad de mejora a la hora de rediseñar estos criterios para ser aplicados a esta población institucionalizada.(AU)

Objetive: To describe the applicability of the tool “Safe practices in patients with chronic medicines” in social healthcare.Method: Cross-sectional observational study (June 2018) that included all patients admitted to a care home, whose social healthcare is provided by the Pharmacy Service at a top-tier hospital. Results: The study included 153 patients, 69.3% of whom were female. The average age was 38 (51-101) years. The mean medicines prescribed were 12 (1-28). A total of 4 criteria out of 18 did not apply to our study population: PG10 (biphosphonates), PO2 (rapid release fentanyl), PG11 (teriparatide for a period greater than 2 years) and PG03 (buprenorphine as detoxification in patients treated with other opioids). 14 criteria out of 18 detect treatments related to safety criteria (monitor) and 8 of 18 criteria detect high-risk prescriptions in the population according to the following distribution: 3 PG2 (AAS dose >150 mg), 2 PG5 (NSAID + antithrombotic), 2 PG6 (Triple Whammy), 3 PG7 (2 SSRI), PG8 (2 or more anticholinergics), 1 PG9.1 (R/G/D+anticholinergics), 2 PG9.2 (memantine+anticholinergics), 1 PO1 (strong+weak opioids). Conclusions: The use of this tool guarantees the continuity of care of patients, constitutes a starting point for the development of a pharmaceutical care programme in care homes. and encourages collaboration between the different levels of care. In view of the results, there is an opportunity for improvement when it comes to redesigning these criteria to be applied to this institutionalized population.(AU)

Influencia psicoemocional de la pandemia por COVID-19 en la experiencia farmacoterapéutica de los pacientes con patologías reumáticas / Psycho-emotional influence of COVID-19 pandemic on medication experience of patients with rheumatic diseases

Objetivo: Realizar una revisión bibliográfica para conocer el impacto de la influencia psicoemocional de la pandemia sobre la experiencia farmacoterapéutica de pacientes con patologías reumáticas tratados con fármacos antirreumáticos modificadores de la enfermedad. Métodos: Se seleccionaron artículos con metodología cualitativa, cuantitativa o mixta disponibles en inglés o castellano. Las bases de datos consultadas fueron Medline, Cochrane Library y PsycInfo. Se eligieron como términos MeSH para realizar la búsqueda: “COVID-19”, “Rheumatic Diseases”, “Qualitative”. Resultados: Se localizaron 8 publicaciones. Se examinaron títulos y resúmenes incluyendo 3 artículos y excluyendo 5. Emergieron otros 3 artículos que cumplían criterios de inclusión pero carecían de los términos MeSH seleccionados. Se analizaron un total de 6 artículos. Conclusiones: La pandemia y el aislamiento social han impactado en la salud mental de los pacientes con patologías reumáticas desencadenando como respuestas emocionales ansiedad, fatiga y estrés. En la mayoría de casos éstos han mantenido su tratamiento. Se distingue su autogestión y conocimiento de la enfermedad y la conciencia acerca de la importancia de continuar con su tratamiento para mantener la estabilidad de su patología. (AU)

Objective: To review the scientific literature concerning psycho-emotional impact of the COVID-19 pandemic on the medication experience of patients with rheumatic diseases treated with disease-modifying antirheumatic drugs. Methods: Articles selected were qualitative, quantitative or mixed methodology available in English or Spanish. Databases consulted were Medline, Cochrane Library and PsycInfo. «COVID-19», «Rheumatic Diseases», «Qualitative» MeSH terms were chosen to perform the search. Results: 8 publications were located. Titles and abstracts were examined including 3 articles and excluding 5. Another 3 articles emerged that met the inclusion criteria but lacked the selected MeSH terms. A total of 6 articles were analyzed. Conclusions: Pandemic and social isolation have impacted on mental health of patients with rheumatic diseases, triggering anxiety, fatigue and stress as emotional responses. In most cases they maintained their treatment. Self-management and knowledge about their disease and awareness of the importance of continuing treatments to maintain the stability of their pathology are distinguished. (AU)

Platform for automatic patient quality assurance via Monte Carlo simulations in proton therapy.

For radiation therapy, it is crucial to ensure that the delivered dose matches the planned dose. Errors in the dose calculations done in the treatment planning system (TPS), treatment delivery errors, other software bugs or data corruption during transfer might lead to significant differences between predicted and delivered doses. As such, patient specific quality assurance (QA) of dose distributions, through experimental validation of individual fields, is necessary. These measurement based approaches, however, are performed with 2D detectors, with limited resolution and in a water phantom. Moreover, they are work intensive and often impose a bottleneck to treatment efficiency. In this work, we investigated the potential to replace measurement-based approach with a simulation-based patient specific QA using a Monte Carlo (MC) code as independent dose calculation engine in combination with treatment log files. Our developed QA platform is composed of a web interface, servers and computation scripts, and is capable to autonomously launch simulations, identify and report dosimetric inconsistencies. To validate the beam model of independent MC engine, in-water simulations of mono-energetic layers and 30 SOBP-type dose distributions were performed. Average Gamma passing ratio 99 ± 0.5% for criteria 2%/2 mm was observed. To demonstrate feasibility of the proposed approach, 10 clinical cases such as head and neck, intracranial indications and craniospinal axis, were retrospectively evaluated via the QA platform. The results obtained via QA platform were compared to QA results obtained by measurement-based approach. This comparison demonstrated consistency between the methods, while the proposed approach significantly reduced in-room time required for QA procedures.

Neurohormonal Imbalance: A Neglected Problem-And Potential Therapeutic Target-In Acute Heart Failure.

Decompensated or acute heart failure (AHF) is characterized by increased ventricular and atrial pressures which may lead to and be caused by circulatory congestion. Unless due to a primary decrease in cardiac function, congestion arises from volume expansion or vasoconstriction. In turn, volume expansion and vasoconstriction are due to neurohormonal imbalance since both result from activation of the sympathetic nervous system, the renin-angiotensin-aldosterone axis and excess secretion of arginine vasopressin. Outcomes in AHF remain dismal. Loop diuretics are the mainstay of therapy for AHF and may themselves aggravate neurohormonal imbalance. No adjunctive pharmacotherapy has yielded improvement in outcomes in AHF despite many attempts with various vasodilators and inotropes. We, therefore, propose that insufficient attention has been paid to neurohormonal imbalance in AHF. As in chronic HF, rectifying the effects of neurohormonal imbalance may lead to better outcomes. The use of alternative decongestive strategies or adjunctive pharmacotherapy directed at neurohormonal activation could yield benefit.

[Are we controlling the sedation in ICU? A multicenter study results].

The aim of this study is to evaluate the issues of sedation and analgesia in all-purpose ICUs in Russia. To obtain that, a single-day observational survey was performed in 55 ICUs of Ural and Siberia regions. This work enabled to describe the targets, instruments of control and patterns of sedative and analgetics and sedatives prescription, as well as to make conclusions about issues in this area and possibilities of creation and necessity of analgesia and sedation standards. The study has shown a decent percentage of use of standardized scales evaluating pain in ICU and predominance of effectivae drugs and analgesia patterns, which leads to "formalization" of analgesia and decrease of it's effectiveness. Sedation indications do not satisfy the modern concept, sedation level evaluation scores are used only in 13%, schemes and drugs are traditional. The results of this study may serve as a reason for discussion of necessity of introducing of sedative and analgetic therapy in ICU standarts.

Presente de la historia clínica electrónica en nefrología ambulatoria / Present of the electronic clinical record in outpatient nephrology

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The use of immobilized enzyme reactors in continuous-flow analyzers for the determination of glucose, urea, and uric acid.

We describe the use of immobilized enzymes in assay methods for the determination of glucose with glucose oxidase, uric acid with uricase, and urea with urease in serum samples. The enzyme reactor tubes were adapted to continuous-flow analyzers (Technicon AA II, SMA 12/60, and SMAC) used in routine laboratory determinations, and results with their use were compared to those from assays involving soluble enzymes. We substituted the reactors for the free enzyme reagents in the respective channels of the SMA 12/60 and SMAC, without modifying the parameters of the remaining channels. We compared assay sensitivity, precision, and carryover for immobilized and conventional liquid enzymes. Immobilized enzyme reactors provide accurate, reliable, convenient, and economical alternatives to the use of free enzyme reagents in these systems.