78 research outputs found

    Estudio prospectivo de intervenciĂłn sobre comorbilidades, interacciones farmacolĂłgicas y su manejo en pacientes con cĂĄncer

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    Introduction: Drug-Drug interactions (DDI) may cause considerable adverse drug reactions and potentially lead to an increased or decreased clinical effect of a given drug and increases the cost of management. Cancer patients are at high risk of such DDIs because they commonly receive a high number of drugs concomitantly, including other cytotoxic agents, hormonal agents, targeted agents, and supportive care agents among medication prescribed to treat comorbidities, especially for elderly patients. The objective of this study is to evaluate the incidence of comorbidities and the role of clinical pharmacist in preventing DDIs in a group of cancer patients. Materials and Methods: A prospective – observational study was conducted in a multispecialty hospital for a period of 8 months among 100 cancer inpatients of oncology department. DDIs were analyzed using Medscape Drug Interaction checker. Results: In this study, 65 DDIs were identified from 100 patients. Of all DDIs, 33.85% were major, 60% were moderate, and 6.15% were minor DDIs. Clinically significant (55.38 %) DDIs were reported and 69.44% of those were accepted and modified accordingly. Furthermore, we observed 50.77% of DDIs between co administered drugs. Elderly people (48%) have more co-morbidity such as diabetes (30%) and hypertension (17.81%). Conclusion: This study concluded that DDIs are very common in cancer patients, particularly people with more co morbidities and using multiple medicines. Clinical pharmacist and physicians must work together to extend the practice of preventing DDIs on individual patient management to improve their quality of life.IntroducciĂłn: Las interacciones medicamentosas (DDI) pueden causar reacciones adversas considerables a los medicamentos y, potencialmente, pueden provocar un aumento o disminuciĂłn del efecto clĂ­nico de un medicamento dado y aumentan los costos de administraciĂłn. Los pacientes con cĂĄncer tienen un alto riesgo de tales interacciones porque comĂșnmente reciben una gran cantidad de medicamentos concomitantes, incluidos otros agentes citotĂłxicos, agentes hormonales, agentes dirigidos y agentes de atenciĂłn de apoyo entre los medicamentos prescritos para tratar las comorbilidades, especialmente en pacientes ancianos. El objetivo de este estudio es evaluar la incidencia de comorbilidades y el papel del farmacĂ©utico clĂ­nico en la prevenciĂłn de interacciones entre medicamentos en un grupo de pacientes con cĂĄncer. Materiales y mĂ©todos: se realizĂł un estudio prospectivo - observacional en un hospital de mĂșltiples especialidades durante un perĂ­odo de 8 meses entre 100 pacientes hospitalizados con cĂĄncer del departamento de oncologĂ­a. Las interacciones de fĂĄrmaco y fĂĄrmaco se analizaron utilizando el comprobador de interacciĂłn de medicamentos de Medscape. Resultados: En este estudio, se identificaron 65 interacciones de 100 pacientes. De todas las interacciones entre medicamentos, 33,85% fueron mayores, 60% fueron moderadas y 6,15% fueron interacciones menores. Se informaron interacciones clĂ­nicamente significativas (55,38%) y el 69,44% de ellas se aceptaron y modificaron en consecuencia. AdemĂĄs, observamos el 50,77% de las interacciones entre los fĂĄrmacos coadministrados. Las personas mayores (48%) tienen mĂĄs comorbilidad, como diabetes (30%) e hipertensiĂłn (17,81%). ConclusiĂłn: este estudio concluyĂł que las interacciones entre medicamentos son muy comunes en pacientes con cĂĄncer, especialmente en personas con mĂĄs comorbilidades y que usan mĂșltiples medicamentos. El farmacĂ©utico clĂ­nico y los mĂ©dicos deben trabajar juntos para ampliar la prĂĄctica de prevenciĂłn de interacciones entre medicamentos en el manejo individual del paciente para mejorar su calidad de vida

    Study on the adoption and integration of OER materials in selfInstructional course development

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    In spite of a few studies on reusability of open educational content in different contexts, there is insufficient information and understanding about the processes involved in Open Educational Resources (OER) integration and contextualisation. This study investigates the processes involved in reusing online OER for developing an entire course in an e-Learning environment as part of OER implementation in the Wawasan Open University. Study results relate to three variables: findability, reusability and cost-time efficiency, of adoption and integration of OER materials for course development

    Oyster depuration display unit for high-end restaurants

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    Considerable interest has been generated recently on consumption of live oysters in high-end restaurants in cities such as Kochi. A major lacuna in this lucrative and emerging enterprise is the lack of consumer confidence on quality of live oysters, particularly purity of oysters with respect to microorganisms. In a meeting with a large number of chefs of star hotels in Kochi at David Hall on 9th June 2010 organized by the CGH Earth group, scientists of CMFRI gave an exposition on farming of oysters and methods of its purification. A consensus that emerged during the meeting was that oyster purification should be done in a manner which is visible to the restaurant clients. Accordingly the CMFRI is proposing a model ULTRA-PURE DEPURATION DIPLAY UNIT (DDU) the details of which are presented in this manual

    A phase II trial of an alternative schedule of palbociclib and embedded serum TK1 analysis

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    Palbociclib 3-weeks-on/1-week-off, combined with hormonal therapy, is approved for hormone receptor positive (HR+)/HER2-negative (HER2-) advanced/metastatic breast cancer (MBC). Neutropenia is the most frequent adverse event (AE). We aim to determine whether an alternative 5-days-on/2-days-off weekly schedule reduces grade 3 and above neutropenia (G3 + ANC) incidence. In this single-arm phase II trial, patients with HR+/HER2- MBC received palbociclib 125 mg, 5-days-on/2-days-off, plus letrozole or fulvestrant per physician, on a 28-day cycle (C), as their first- or second-line treatment. The primary endpoint was G3 + ANC in the first 29 days (C1). Secondary endpoints included AEs, efficacy, and serum thymidine kinase 1 (sTK1) activity. At data-cutoff, fifty-four patients received a median of 13 cycles (range 2.6-43.5). The rate of G3 + ANC was 21.3% (95% CI: 11.2-36.1%) without G4 in C1, and 40.7% (95% CI: 27.9-54.9%), including 38.9% G3 and 1.8% G4, in all cycles. The clinical benefit rate was 80.4% (95% CI: 66.5-89.7%). The median progression-free survival (mPFS) (95% CI) was 19.75 (12.11-34.89), 33.5 (17.25-not reached [NR]), and 11.96 (10.43-NR) months, in the overall, endocrine sensitive or resistant population, respectively. High sTK1 at baseline, C1 day 15 (C1D15), and C2D1 were independently prognostic for shorter PFS (p = 9.91 × 1

    Dual effect of thiol addition on fluorescent polymeric micelles: ON-to-OFF emissive switch and morphology transition

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    YesThe morphology transition from micelles to vesicles of a solution-state self-assembled block copolymer, containing a fluorescent dye at the core–shell interface, has been induced by an addition–elimination reaction using a thiol, and has been shown to be coupled to a simultaneous ON-to-OFF switch in particle fluorescence.EPSRC and the IAS at the University of Warwic

    Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease

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    Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1ÎČ, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1ÎČ innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.

    Impact of infection on proteome-wide glycosylation revealed by distinct signatures for bacterial and viral pathogens

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    Mechanisms of infection and pathogenesis have predominantly been studied based on differential gene or protein expression. Less is known about posttranslational modifications, which are essential for protein functional diversity. We applied an innovative glycoproteomics method to study the systemic proteome-wide glycosylation in response to infection. The protein site-specific glycosylation was characterized in plasma derived from well-defined controls and patients. We found 3862 unique features, of which we identified 463 distinct intact glycopeptides, that could be mapped to more than 30 different proteins. Statistical analyses were used to derive a glycopeptide signature that enabled significant differentiation between patients with a bacterial or viral infection. Furthermore, supported by a machine learning algorithm, we demonstrated the ability to identify the causative pathogens based on the distinctive host blood plasma glycopeptide signatures. These results illustrate that glycoproteomics holds enormous potential as an innovative approach to improve the interpretation of relevant biological changes in response to infection
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