Impact of drug reconciliation at discharge and communication between hospital and community pharmacists on drug-related problems: study protocol for a randomized controlled trial

被引:8
|
作者
Pourrat, Xavier
Roux, Clarisse [1 ]
Bouzige, Brigitte [2 ]
Garnier, Valerie [3 ]
Develay, Armelle [1 ]
Allenet, Benoit [4 ,8 ]
Fraysse, Martial [5 ]
Halimi, Jean-Michel [6 ,9 ]
Grassin, Jacqueline
Giraudeau, Bruno [7 ,10 ]
机构
[1] Univ Nimes Hosp, Dept Pharm, Pharm D, F-30029 Nimes, France
[2] Pharm Bouzige, Pharm D, Les Salles Du Gardon, France
[3] Pharm Garnier, Pharm D, F-30840 Meynes, France
[4] CHU Grenoble, Pharm D, Dept Pharm, F-38700 La Tronche, France
[5] Pharm D, F-94120 Fontenay Sous Bois, France
[6] Tours Univ Hosp, Dept Nephrol, F-37044 Tours 09, France
[7] CHRU Tours, Hop Bretonneau, INSERM CIC 1415, F-37044 Tours 09, France
[8] Univ Grenoble 1, Sch Med & Pharm, UMR CNRS 5525, ThEMAS TIMC IMAG, F-38041 St Martin Dheres, France
[9] Univ Tours, Sch Med, Dept Therapeut, F-37000 Tours, France
[10] Univ Tours, INSERM CIC 1415, F-37000 Tours, France
关键词
Community pharmacist; hospital pharmacist; drug-related problem; communication; cluster randomized crossover trial; hospital discharge; drug reconciliation; MEDICATION RECONCILIATION; DISCREPANCIES; SERVICE;
D O I
10.1186/1745-6215-15-260
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Patients are at risk of drug-related problems (DRPs) at transition points during hospitalization. The community pharmacist (CP) is often the first healthcare professional patients visit after discharge. CPs lack sufficient information about the patient and so they may be unable to identify problems in medications, which may lead to dispensing the wrong drugs or dosage, and/or giving wrong information. We aim to assess the impact of a complex intervention comprising of medication reconciliation performed at discharge by a hospital pharmacist (HP) with communication between the HP and CP on DRPs during the seven days following discharge. Methods/Design: The study is a cluster randomized crossover trial involving 46 care units (each unit corresponding to a cluster) in 22 French hospitals during two consecutive 14-day periods, randomly assigned as 'experimental' or 'control' (usual care) periods. We will recruit patients older than 18 years of age and visiting the same CP for at least three months. We will exclude patients with a hospital length of stay of more than 21 days, who do not return home or those in palliative care. During the experimental period, the HP will perform a medications reconciliation that will be communicated to the patient. The HP will inform the patient's CP about the patient's drug therapy (modification in home medication, acute drugs prescribed, nonprescription treatments, and/or lab results). The primary outcome will be a composite outcome of any kind of drug misuse during the seven days following discharge assessed at day seven (+/- 2) post-discharge by a pharmacist in charge of the study who will contact both patients and CPs by phone. The secondary outcome will be unplanned hospitalizations assessed by phone contact at day 35 (+/- 5) after discharge. We plan to recruit 1,176 patients. Discussion: This study will assess the impact of a reconciliation of medications performed at patient discharge followed by communication between the HP and the patient's CP. It will allow for identifying the type of patients in France for which the intervention is most relevant.
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收藏
页数:7
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