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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centro de Investigaciones y Publicaciones Farmaceuticas
2016
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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. |
format | Online Article Text |
id | pubmed-5184375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Centro de Investigaciones y Publicaciones Farmaceuticas |
record_format | MEDLINE/PubMed |
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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