How a Patient Personalised Clinical Pharmacy Programme Can Secure Therapeutic Care in an Orthogeriatric Care Pathway (5P Project)?

clinical relevance frail elderly hip fracture medication errors pharmaceutical services

Journal

Clinical interventions in aging
ISSN: 1178-1998
Titre abrégé: Clin Interv Aging
Pays: New Zealand
ID NLM: 101273480

Informations de publication

Date de publication:
2021
Historique:
received: 19 06 2021
accepted: 23 09 2021
entrez: 28 10 2021
pubmed: 29 10 2021
medline: 26 11 2021
Statut: epublish

Résumé

A new model was developed for integrating a personalised clinical pharmacy programme (5P project) into the orthogeriatric care pathway. To secure the therapeutic care of orthogeriatric patients. Prospective descriptive study in a multisite teaching hospital from June 2019 to January 2020. Patients aged ≥75 years admitted for hip fracture. A prescription review was performed for all patients at inclusion. Other clinical pharmacy activities (additional prescription review, pharmaceutical interviews, medication reconciliation) were dedicated to "high-risk" patients. Potential medication errors (ME), either pharmaceutical interventions (PI) or unintentional discrepancies (UID), were recorded. The potential clinical impact of PI was evaluated by a pluriprofessional expert panel using a validated tool. In the 455 patients included, 955 potential ME were detected, that is ≥1 potential ME for 324/455 (71%) patients. In acute care, 561 PI were formulated during prescription review for 440/455 (97%) patients and 348/561 (62%) were accepted by physicians. Medication reconciliation was performed for 213 patients, 316 UID were identified. In rehabilitation units, a second prescription review was performed for 112/122 (92%) "high-risk" patients, leading to 61 PI. The clinical impact was evaluated for 519/622 (83%) PI. A consensus was obtained for 310/519 (60%) PI: 147/310 (47%) were rated as having minor clinical impact, 138/310 (45%) moderate, 22/310 (7%) major, 2/310 (0.6%) vital, and 1/310 (0.3%) null. The 5P project secured the orthogeriatric care pathway by detecting a great number of potential ME, including PI mostly considered as having a significant clinical impact.

Sections du résumé

BACKGROUND BACKGROUND
A new model was developed for integrating a personalised clinical pharmacy programme (5P project) into the orthogeriatric care pathway.
OBJECTIVE OBJECTIVE
To secure the therapeutic care of orthogeriatric patients.
DESIGN AND SETTING METHODS
Prospective descriptive study in a multisite teaching hospital from June 2019 to January 2020.
SUBJECTS METHODS
Patients aged ≥75 years admitted for hip fracture.
METHODS METHODS
A prescription review was performed for all patients at inclusion. Other clinical pharmacy activities (additional prescription review, pharmaceutical interviews, medication reconciliation) were dedicated to "high-risk" patients. Potential medication errors (ME), either pharmaceutical interventions (PI) or unintentional discrepancies (UID), were recorded. The potential clinical impact of PI was evaluated by a pluriprofessional expert panel using a validated tool.
RESULTS RESULTS
In the 455 patients included, 955 potential ME were detected, that is ≥1 potential ME for 324/455 (71%) patients. In acute care, 561 PI were formulated during prescription review for 440/455 (97%) patients and 348/561 (62%) were accepted by physicians. Medication reconciliation was performed for 213 patients, 316 UID were identified. In rehabilitation units, a second prescription review was performed for 112/122 (92%) "high-risk" patients, leading to 61 PI. The clinical impact was evaluated for 519/622 (83%) PI. A consensus was obtained for 310/519 (60%) PI: 147/310 (47%) were rated as having minor clinical impact, 138/310 (45%) moderate, 22/310 (7%) major, 2/310 (0.6%) vital, and 1/310 (0.3%) null.
CONCLUSION CONCLUSIONS
The 5P project secured the orthogeriatric care pathway by detecting a great number of potential ME, including PI mostly considered as having a significant clinical impact.

Identifiants

pubmed: 34707352
doi: 10.2147/CIA.S325035
pii: 325035
pmc: PMC8544550
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1857-1867

Informations de copyright

© 2021 Barral et al.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest in this work.

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Auteurs

Marine Barral (M)

Pharmacie, Hospices Civils de Lyon, Lyon, France.

Julie Martin (J)

Pharmacie, Hospices Civils de Lyon, Lyon, France.

Emmanuelle Carre (E)

Pharmacie Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Audrey Janoly-Dumenil (A)

Pharmacie Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
6-EA 4129 P2S Parcours Santé Systémique- Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.

Florence Ranchon (F)

Pharmacie Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.
Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
EA3738, CICLY Centre pour l'Innovation en cancérologie de Lyon, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.

Stéphanie Parat (S)

Pharmacie Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Catherine Rioufol (C)

Pharmacie Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.
Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
EA3738, CICLY Centre pour l'Innovation en cancérologie de Lyon, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.

Sylvain Goutelle (S)

Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
Pharmacie Hôpital Pierre Garraud, Hospices Civils de Lyon, Lyon, France.
CNRS, UMR 5558, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.

Laurent Bourguignon (L)

Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
Pharmacie Hôpital Pierre Garraud, Hospices Civils de Lyon, Lyon, France.
CNRS, UMR 5558, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.

Teddy Novais (T)

Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
Pharmacie Hôpital des Charpennes, Hospices Civils de Lyon, Villeurbanne, France.
Université Claude Bernard Lyon 1, Research on Healthcare Performance (RESHAPE), INSERM U1290, Lyon, France.

Sebastien Doh (S)

Service de Gériatrie Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Matthieu Malatray (M)

Service de Chirurgie Orthopédique Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Philippe Chaudier (P)

Service de Chirurgie Orthopédique Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Jerome Gauthier (J)

Service d'anesthésie et réanimation Hôpital Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Christine Pivot (C)

Pharmacie Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.

Christelle Mouchoux (C)

Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
Pharmacie Hôpital des Charpennes, Hospices Civils de Lyon, Villeurbanne, France.
Lyon Neuroscience Research Center, INSERM U1028, CNRS UMR5292, Lyon, France.

Delphine Hoegy (D)

Pharmacie, Hospices Civils de Lyon, Lyon, France.
Institut des Sciences Pharmaceutiques et Biologiques, Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.
6-EA 4129 P2S Parcours Santé Systémique- Univ Claude Bernard Lyon 1, Univ Lyon 1, Lyon, France.

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