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Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?

BACKGROUND: Lack of adherence to medication is a trigger of graft rejection in solid-organ transplant (SOT) recipients. OBJECTIVE: This exploratory study aimed to assess whether a biopsychosocial evaluation using the INTERMED instrument before transplantation could identify SOT recipients at risk of...

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Autores principales: Michaud, Laurent, Ludwig, Gundula, Berney, Sylvie, Rodrigues, Stéphanie, Niquille, Anne, Santschi, Valérie, Favre, Anne-Sophie, Lange, Anne-Catherine, Michels, Annemieke A., Vrijens, Bernard, Bugnon, Olivier, Pilon, Nathalie, Pascual, Manuel, Venetz, Jean-Pierre, Stiefel, Friedrich, Schneider, Marie-Paule
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centro de Investigaciones y Publicaciones Farmaceuticas 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5184375/
https://www.ncbi.nlm.nih.gov/pubmed/28042353
http://dx.doi.org/10.18549/PharmPract.2016.04.822
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author Michaud, Laurent
Ludwig, Gundula
Berney, Sylvie
Rodrigues, Stéphanie
Niquille, Anne
Santschi, Valérie
Favre, Anne-Sophie
Lange, Anne-Catherine
Michels, Annemieke A.
Vrijens, Bernard
Bugnon, Olivier
Pilon, Nathalie
Pascual, Manuel
Venetz, Jean-Pierre
Stiefel, Friedrich
Schneider, Marie-Paule
author_facet Michaud, Laurent
Ludwig, Gundula
Berney, Sylvie
Rodrigues, Stéphanie
Niquille, Anne
Santschi, Valérie
Favre, Anne-Sophie
Lange, Anne-Catherine
Michels, Annemieke A.
Vrijens, Bernard
Bugnon, Olivier
Pilon, Nathalie
Pascual, Manuel
Venetz, Jean-Pierre
Stiefel, Friedrich
Schneider, Marie-Paule
author_sort Michaud, Laurent
collection PubMed
description BACKGROUND: Lack of adherence to medication is a trigger of graft rejection in solid-organ transplant (SOT) recipients. OBJECTIVE: This exploratory study aimed to assess whether a biopsychosocial evaluation using the INTERMED instrument before transplantation could identify SOT recipients at risk of suboptimal post-transplantation adherence to immunosuppressant drugs. We hypothesized that complex patients (INTERMED>20) might have lower medication adherence than noncomplex patients (INTERMED≤20). METHODS: Each patient eligible for transplantation at the University Hospital of Lausanne, Switzerland, has to undergo a pre-transplantation psychiatric evaluation. In this context the patient was asked to participate in our study. The INTERMED was completed pre-transplantation, and adherence to immunosuppressive medication was monitored post-transplantation by electronic monitors for 12 months. The main outcome measure was the implementation and persistence to two calcineurin inhibitors, cyclosporine and tacrolimus, according to the dichotomized INTERMED score (>20 or ≤20). RESULTS: Among the 50 SOT recipients who completed the INTERMED, 32 entered the study. The complex (N=11) and noncomplex patients (N=21) were similar in terms of age, sex and transplanted organ. Implementation was 94.2% in noncomplex patients versus 87.8% in complex patients (non-significant p-value). Five patients were lost to follow-up: one was non-persistent, and four refused electronic monitoring. Of the four patients who refused monitoring, two were complex and withdrew early, and two were noncomplex and withdrew later in the study. CONCLUSION: Patients identified as complex pre-transplant by the INTERMED tended to deviate from their immunosuppressant regimen, but the findings were not statistically significant. Larger studies are needed to evaluate this association further, as well as the appropriateness of using a nonspecific biopsychosocial instrument such as INTERMED in highly morbid patients who have complex social and psychological characteristics.
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spelling pubmed-51843752016-12-30 Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence? Michaud, Laurent Ludwig, Gundula Berney, Sylvie Rodrigues, Stéphanie Niquille, Anne Santschi, Valérie Favre, Anne-Sophie Lange, Anne-Catherine Michels, Annemieke A. Vrijens, Bernard Bugnon, Olivier Pilon, Nathalie Pascual, Manuel Venetz, Jean-Pierre Stiefel, Friedrich Schneider, Marie-Paule Pharm Pract (Granada) Original Research BACKGROUND: Lack of adherence to medication is a trigger of graft rejection in solid-organ transplant (SOT) recipients. OBJECTIVE: This exploratory study aimed to assess whether a biopsychosocial evaluation using the INTERMED instrument before transplantation could identify SOT recipients at risk of suboptimal post-transplantation adherence to immunosuppressant drugs. We hypothesized that complex patients (INTERMED>20) might have lower medication adherence than noncomplex patients (INTERMED≤20). METHODS: Each patient eligible for transplantation at the University Hospital of Lausanne, Switzerland, has to undergo a pre-transplantation psychiatric evaluation. In this context the patient was asked to participate in our study. The INTERMED was completed pre-transplantation, and adherence to immunosuppressive medication was monitored post-transplantation by electronic monitors for 12 months. The main outcome measure was the implementation and persistence to two calcineurin inhibitors, cyclosporine and tacrolimus, according to the dichotomized INTERMED score (>20 or ≤20). RESULTS: Among the 50 SOT recipients who completed the INTERMED, 32 entered the study. The complex (N=11) and noncomplex patients (N=21) were similar in terms of age, sex and transplanted organ. Implementation was 94.2% in noncomplex patients versus 87.8% in complex patients (non-significant p-value). Five patients were lost to follow-up: one was non-persistent, and four refused electronic monitoring. Of the four patients who refused monitoring, two were complex and withdrew early, and two were noncomplex and withdrew later in the study. CONCLUSION: Patients identified as complex pre-transplant by the INTERMED tended to deviate from their immunosuppressant regimen, but the findings were not statistically significant. Larger studies are needed to evaluate this association further, as well as the appropriateness of using a nonspecific biopsychosocial instrument such as INTERMED in highly morbid patients who have complex social and psychological characteristics. Centro de Investigaciones y Publicaciones Farmaceuticas 2016 2016-12-15 /pmc/articles/PMC5184375/ /pubmed/28042353 http://dx.doi.org/10.18549/PharmPract.2016.04.822 Text en Copyright: © Pharmacy Practice http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY-NC-ND 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Michaud, Laurent
Ludwig, Gundula
Berney, Sylvie
Rodrigues, Stéphanie
Niquille, Anne
Santschi, Valérie
Favre, Anne-Sophie
Lange, Anne-Catherine
Michels, Annemieke A.
Vrijens, Bernard
Bugnon, Olivier
Pilon, Nathalie
Pascual, Manuel
Venetz, Jean-Pierre
Stiefel, Friedrich
Schneider, Marie-Paule
Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title_full Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title_fullStr Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title_full_unstemmed Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title_short Immunosuppressive therapy after solid-organ transplantation: does the INTERMED identify patients at risk of poor adherence?
title_sort immunosuppressive therapy after solid-organ transplantation: does the intermed identify patients at risk of poor adherence?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5184375/
https://www.ncbi.nlm.nih.gov/pubmed/28042353
http://dx.doi.org/10.18549/PharmPract.2016.04.822
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