Zobrazeno 1 - 10
of 10
pro vyhledávání: '"L Borràs Trias"'
Publikováno v:
Section 7: Post Congress additions.
Autor:
A Sosa-Pons, P Monzó Gallo, R Rodriguez Mauriz, N Rudi Sola, AA Villagrasa Vilella, L Borràs Trias, N Almendros-Abad
Publikováno v:
Section 4: Clinical pharmacy services.
Background and importance Human serum albumin (HSA) is widely used in clinical practice, although many indications are still being debated. Aim and objectives To analyse the clinical indications for HSA and the level of evidence for them. Material an
Autor:
N Almendros-Abad, L Borràs Trias, R Rodriguez Mauriz, C Seguí Solanes, N Rudi Sola, MA Pérez-Quirós, MA Aldirra-Taha, A Planas-Giner
Publikováno v:
Section 5: Patient Safety and Quality Assurance.
Background Neutropaenia is one of the most common adverse effects of paclitaxel. It is dose-dependent and has dose-limiting toxicity. However, the American Society of Clinical Oncology (ASCO) guideline recommends the use of real bodyweight for chemot
Autor:
Aldirra-Taha, N Almendros Abad, C Seguí Solanes, L Borràs Trias, N Rudi Sola, MA Pérez-Quirós, R Rodriguez Mauriz, A Planas-Giner
Publikováno v:
Section 5: Patient Safety and Quality Assurance.
Background The use of panitumumab in the treatment of metastatic colorectal cancer (mCRC) remains controversial because of its risk/benefit profile. Purpose The aim of this study was to investigate the efficacy and safety of panitumumab in patients w
Autor:
M Gómez-Valent, M Cirera i Perich, L Borràs Trias, S Ortonobes Roig, B Mañé Velilla, MQ Gorgas Torner
Publikováno v:
Patient safety and risk management.
Background Chronic treatment revisions optimise drug treatment and prevent potential drug related problems. Therefore, we started a new healthcare model based on multidisciplinary team work, integrated and focused on the patient. This programme is a
Autor:
Milagros García-Peláez, L Borràs Trias, MQ Gorgas Torner, M Florit Sureda, G Puig Comas, P Miralles Albors
Publikováno v:
Patient safety and risk management.
Background One of the objectives of the Health Department of Catalonia (Spain) is the clinical review of medications in chronic complex patients (CCP) and patients with advanced disease (PAD). The reconciliation and validation of treatments to detect
Publikováno v:
European Journal of Hospital Pharmacy. 23:A80.2-A81
Background Hospital pharmacists validate many treatments per day, mostly not knowing the hospitalised patient’s current situation and with little interaction with the medical team and nurses who care for these patients. Purpose To describe differen
Autor:
MQ Gorgas Torner, L Ortiz Ruiz, A Estefanell Tejero, E Oliver Ferrer, L Borràs Trias, C. Pontes García, N Rudi Sola, L Raich Montiu, M De Castro Julve
Publikováno v:
European Journal of Hospital Pharmacy. 22:A109.1-A109
Background Tenofovir/emtricitabine/rilpivirine (TDF/FTC/RPV) is a recently-marketed fixed-dose combination of antiretrovirals with which there is little clinical experience as yet. Purpose To describe our clinical experience with TDF/FTC/RPV, in term
Autor:
M. García Argelaguet, MQ Gorgas Torner, L Borràs Trias, L Raich Montiu, C. Pontes García, M De Castro Julve
Publikováno v:
European Journal of Hospital Pharmacy. 22:A108.2-A109
Background It has been repeatedly reported that up to 7% of patients have serious adverse drug reactions (ADR) during hospital admissions. Hospital-based pharmacovigilance aims to detect previously unknown serious ADRs arising during differential dia
Autor:
Milagros García-Peláez, MQ Gorgas Torner, M. Cabré Serres, L Borràs Trias, M Gómez-Valent, L Raich Montiu, ML Iglesias Lepine, M De Castro Julve, M Payés Peich
Publikováno v:
European Journal of Hospital Pharmacy. 21:A145.2-A145
Background Clinical safety is an essential component of health care quality. The EVADUR study showed that 12% of patients who were in the emergency department (ED) had adverse events (AE). 70% of them were considered avoidable. Purpose To describe ph