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1.
Ann Pharm Fr ; 72(3): 178-83, 2014 May.
Article in English | MEDLINE | ID: mdl-24780833

ABSTRACT

UNLABELLED: Concerns have recently emerged about the quality of generic vancomycin products. Our aim is to analyze serum vancomycin concentrations measured 48 hours after the start of an empirical treatment regimen in patients with acute myeloid leukemia (AML) who received one of the two generic vancomycin products available in France. PATIENTS AND METHODS: Seventy-nine AML patients treated with vancomycin during two study periods were included in the study. Our vancomycin dosing regimen was based on the patients' total body weight adjusted for renal clearance. RESULTS: A total of 93 serum vancomycin concentrations were collected: 31 in period 1 and 62 in period 2. In bivariate analysis, the mean serum vancomycin concentrations were not significantly different (19.9 ± 11.2 mg/L in period 1 vs 18.9 ± 6.0 mg/L in period 2, P=0.64). In the final generalized estimating equations model, serum vancomycin concentrations correlated statistically with a positive coefficient for age (P<0.001) and with negative coefficients for male sex (P=0.001) and hemoglobin level (P=0.021). CONCLUSION: Serum vancomycin concentrations measured 48 hours after the start of an empirical treatment were not influenced by the nature of the generic product but correlated with age, sex and hemoglobin level in AML patients.


Subject(s)
Anti-Bacterial Agents/blood , Leukemia, Myeloid, Acute/metabolism , Vancomycin/blood , Adolescent , Adult , Aged , Anti-Bacterial Agents/pharmacokinetics , Drugs, Generic , Female , Humans , Kidney/metabolism , Male , Middle Aged , Retrospective Studies , Vancomycin/pharmacokinetics , Young Adult
2.
Ann Fr Anesth Reanim ; 32(11): 760-5, 2013 Nov.
Article in French | MEDLINE | ID: mdl-24135730

ABSTRACT

OBJECTIVES: Ephedrine is an emergency drug available in ampules and syringes need to be prepared in advance according to one of two strategies in our establishment: strategy 1 (S1: 1 ampule per patient) and strategy 2 (S2: 1 ampule per operating room). There are also prefilled syringes. Because of their high cost and conflicting results in the literature, we assessed the economic interest of using prefilled syringes compared with strategies S1 and S2. TYPE OF STUDY: This was a prospective observational study. PATIENTS AND METHODS: The consumption of ephedrine was recorded over two periods of 14 days: P1 with syringes prepared in advance according to S1 or S2 and P2 with the on-demand use of prefilled syringes. RESULTS: The cost of a syringe of ephedrine prepared in advance (nurse time preparation included) was evaluated at €1.65 vs. €3.57 for a prefilled syringe. In operating rooms using S1, the use of prefilled syringes reduced overall the cost per patient about €1.22 and global annual costs by 72% (€2830), while the decrease was about €0.32 for the cost per patient and about 47% (€2760) for global annual costs for operating rooms using S2. CONCLUSION: The interest of our study is that we investigated different supply strategies for ephedrine within a large number of operating rooms. In our establishment, it was decided to use prefilled syringes in operating rooms that used S1. As well as the economic interest, prefilled syringes contributed to improved safety and saved nursing time.


Subject(s)
Ephedrine/administration & dosage , Ephedrine/economics , Syringes/economics , Vasoconstrictor Agents/administration & dosage , Vasoconstrictor Agents/economics , Drug Compounding/economics , Drug Costs , Drug Utilization , France , Humans , Nurses , Operating Rooms/economics , Operating Rooms/organization & administration , Prospective Studies
3.
Diagn Interv Imaging ; 94(1): 53-9, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23146417

ABSTRACT

PURPOSE: The aim of our study was to assess the results and cost of a treatment strategy involving transarterial chemoembolisation with drug eluting beads (DEB-TACE) in patients with unresectable non-metastatic hepatocellular carcinoma (HCC). PATIENTS AND METHODS: This study included all patients treated with DEB-TACE in our hospital between January 2009 and December 2010. All patients received DEB-TACE on demand and were evaluated after each session. RESULTS: Twenty-one patients received an average of 1.3 sessions. The median time to treatment discontinuation and median progression-free survival was 181 days and 295 days, respectively. Toxicity caused treatment discontinuation in three patients (14%). For the hospital, the average direct cost of treatment was €6,033 according to the analytical accounting system vs. €4,558 according to the official tariffs from the new French Diagnosis-Related Group prospective payment system (P=0.002). CONCLUSION: In the treatment of HCC, on-demand DEB-TACE stabilises the disease in some patients but has not yet been thoroughly evaluated.


Subject(s)
Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/economics , Chemoembolization, Therapeutic/economics , Drug Delivery Systems/economics , Liver Neoplasms/drug therapy , Liver Neoplasms/economics , Aged , Aged, 80 and over , Costs and Cost Analysis , Female , Humans , Male , Microspheres , Middle Aged , Retrospective Studies , Treatment Outcome
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