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Randomized Controlled Trial
. 2005 Oct 31;36(7):367-72.
doi: 10.1157/13080299.

[Efficacy of educational sessions to modify the prescription of new drugs]

[Article in Spanish]
Affiliations
Randomized Controlled Trial

[Efficacy of educational sessions to modify the prescription of new drugs]

[Article in Spanish]
T Molina López et al. Aten Primaria. .

Abstract

Objective: To evaluate the efficacy of an educational intervention to minimise the prescription of those new medicines whose therapeutic effects are of little benefit.

Design: Controlled and randomised experimental study.

Setting: 27 health centres in the province of Sevilla, Spain.

Participants: 376 general practitioners. The 264 who worked in the same posts were randomised for the 6 pre-intervention months. 10 of them did not complete the post-intervention period.

Interventions: Four 45-minute training sessions in a 2-month period, given by health team doctors, with a critical reading of the studies available on recently marketed drugs, plus personal feed-back on prescription and bulletins on therapeutic novelties. The control group received only the feed-back and bulletins.

Main measurements: Prescription of new medication of little benefit, measured as the number of packages out of the total. Second, the amount of coxib and eprosartan measured as defined daily doses.

Results: In the 6 months after the educational sessions, the doctors in the intervention group prescribed proportionately fewer therapeutic novelties of little benefit than those allocated to the control group (1.34% vs 1.62%; P<.001). The coxib and eprosartan prescribed showed only a non-significant trend towards less prescription by the intervention group.

Conclusions: The group educational sessions, run by doctors trained in aspects of evidence-based medicine and prepared jointly with the pharmacy unit, reduced discreetly the prescription of new medicines that were not very innovative.

Objetivo: Evaluar la eficacia de una intervención educativa para minimizar la prescripción de medicamentos nuevos cuya aportación terapéutica es poco relevante.

Diseño: Estudio experimental, controlado y aleatorizado.

Emplazamiento: El estudio se realizó en 27 centros de salud de la provincia de Sevilla.

Participantes: Participaron 376 médicos de familia generalistas. Se aleatorizó a los 264 que trabajaron en una misma plaza los 6 meses preintervención; 10 de ellos no completaron el período postintervención.

Intervenciones: Se realizaron 4 sesiones formativas de 45 minutos en un intervalo de 2 meses, impartidas por médicos de equipos de salud, sobre lectura crítica de los estudios disponibles de medicamentos de reciente comercialización, además de retroinformación personalizada de la prescripción y los boletines sobre novedades terapéuticas. El grupo control recibió sólo la retroinformación y los boletines.

Mediciones principales: Prescripción de medicamentos nuevos poco relevantes, medida como la proporción de envases respecto al total de medicamentos.

Secundariamente, se midió la proporción de coxib y eprosartán medida como dosis diarias definidas.

Resultados: En los 6 meses posteriores a las sesiones educativas, los médicos del grupo intervención prescribieron proporcionalmente menos novedades terapéuticas no relevantes que los asignados al grupo control (el 1,34 frente al 1,62%, respectivamente; p < 0,001). La proporción de coxib y eprosartán sólo muestra una tendencia no significativa hacia una menor prescripción por el grupo intervención.

Conclusiones: Las sesiones educativas grupales, mediadas por médicos formados en elementos de medicina basada en la evidencia y preparadas de manera conjunta con la unidad de farmacia, disminuyen de manera discreta la prescripción de medicamentos nuevos escasamente innovadores.

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References

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