TY - JOUR
T1 - Challenges in multiple sclerosis care
T2 - Results from an international mixed-methods study
AU - Péloquin, Sophie
AU - Schmierer, Klaus
AU - Leist, Thomas P.
AU - Oh, Jiwon
AU - Murray, Suzanne
AU - Lazure, Patrice
N1 - Funding Information:
This study was financially supported with an unrestricted education research grant from Merck KGaA , Darmstadt, Germany.
Funding Information:
The authors would like to acknowledge the support provided by Morgan Peniuta, Sara Labbé, Sacha Zahabi and Monica Augustyniak (researchers), as well as Olivier Jacob and Randa Dalle (project managers) who supported data collection, communications and other aspects of the research. The authors would also like to thank Olga Salvidio and Maged Saleh (Merck KGaA) who helped identify relevant literature to inform the areas of investigation at the onset of the project. The authors would like to thank all those who took part in this study.
Funding Information:
TPL has received consultancy fees or clinical research grants from Biogen, EMDSerono, Novartis, Genentech, and Abbvie.
Funding Information:
KS is a member of the MAGNIFY-MS steering committee and the MS Global Advisory Network of Merck KGaA. He is the Chief Investigator of ChariotMS, a multi-center trial supported by the National Institute of Health Research, the MS Society of Great Britain & Northern Ireland, National MS Society (US), Barts Charity and Merck. KS has received further research support from Biogen, the European Medicines Agency, Lipomed, the Morris-Saady Charitable Trust, Novartis and the Royal College of Radiologists. He has received speaking honoraria from, and/or served in an advisory role for, Biogen, Guidepoint, Merck KGaA, Novartis, Roche, Sanofi-Genzyme and Teva; and has received remuneration for teaching activities from EXCEMED and the Neurology Academy.
Publisher Copyright:
© 2021
PY - 2021/5
Y1 - 2021/5
N2 - Background: Disease-modifying treatment (DMT) selection for people with multiple sclerosis (MS) is challenging. Neurologists and advanced practice nurses (APNs) in MS care may be facing knowledge and confidence gaps when screening patients to initiate or switch between DMTs, assessing the safety of new DMTs and monitoring for adverse events. Healthcare providers are required to demonstrate enhanced patient communication skills, to share treatment decisions and assess treatment adherence. To better inform educational interventions, there is a need to better understand these challenges and uncover their causalities. We undertook an international study across seven countries to identify challenges for neurologists and APNs that may impact DMT choices and optimum care for people with MS (pwMS). Methods: This mixed methods study involved two concurrent data collection phases, a qualitative phase with semi-structured interviews and a quantitative phase using an online survey. Neurologists (n=333) and APNs (n=135) were recruited from Canada, France, Germany, Italy, Spain, United Kingdom and the United States. All participants had to have a minimum of two years’ experience in the care of pwMS and be currently active in clinical practice. Results: A triangulated analysis of qualitative and quantitative data identified multiple challenges. For APNs, these mainly related to diagnosing MS, integrating new agents in their practice, sequential DMT selection, treatment monitoring and providing personalized care. Specifically, two-thirds of APNs reported no or basic knowledge of the 2017 McDonald criteria and over half reported a knowledge gap of new DMTs available (51%) and a skill gap when integrating them into practice (58%). APNs expressed a knowledge gap of treatment sequencing (46%) and a skill gap in making decisions about sequencing (62%). Forty-four percent of APNs reported a gap in their skills of integrating patient's goals into treatment recommendations. For neurologists, the main challenges included managing side effects, aligning care to their patient's personal goals and quality of life (QoL). Specifically, over a third of neurologists reported no or basic knowledge of the characteristics of treatment failure (35%), and 32% reported no or basic skills identifying treatment failure. Skills needed to integrate patient's individual goals into treatment recommendations were reported as none or low by 39% of neurologists. In addition, there were significant differences according to years of practice in the majority (9 out of 14) of confidence items with respect to discussing specific MS-related topics with patients. Significant differences between countries were also identified. Conclusion: The complexity of diagnosing MS and the variety of available DMTs for pwMS lead to uncertainties, even among specialized healthcare professionals. These should be addressed through focused education and training to optimize care for pwMS.
AB - Background: Disease-modifying treatment (DMT) selection for people with multiple sclerosis (MS) is challenging. Neurologists and advanced practice nurses (APNs) in MS care may be facing knowledge and confidence gaps when screening patients to initiate or switch between DMTs, assessing the safety of new DMTs and monitoring for adverse events. Healthcare providers are required to demonstrate enhanced patient communication skills, to share treatment decisions and assess treatment adherence. To better inform educational interventions, there is a need to better understand these challenges and uncover their causalities. We undertook an international study across seven countries to identify challenges for neurologists and APNs that may impact DMT choices and optimum care for people with MS (pwMS). Methods: This mixed methods study involved two concurrent data collection phases, a qualitative phase with semi-structured interviews and a quantitative phase using an online survey. Neurologists (n=333) and APNs (n=135) were recruited from Canada, France, Germany, Italy, Spain, United Kingdom and the United States. All participants had to have a minimum of two years’ experience in the care of pwMS and be currently active in clinical practice. Results: A triangulated analysis of qualitative and quantitative data identified multiple challenges. For APNs, these mainly related to diagnosing MS, integrating new agents in their practice, sequential DMT selection, treatment monitoring and providing personalized care. Specifically, two-thirds of APNs reported no or basic knowledge of the 2017 McDonald criteria and over half reported a knowledge gap of new DMTs available (51%) and a skill gap when integrating them into practice (58%). APNs expressed a knowledge gap of treatment sequencing (46%) and a skill gap in making decisions about sequencing (62%). Forty-four percent of APNs reported a gap in their skills of integrating patient's goals into treatment recommendations. For neurologists, the main challenges included managing side effects, aligning care to their patient's personal goals and quality of life (QoL). Specifically, over a third of neurologists reported no or basic knowledge of the characteristics of treatment failure (35%), and 32% reported no or basic skills identifying treatment failure. Skills needed to integrate patient's individual goals into treatment recommendations were reported as none or low by 39% of neurologists. In addition, there were significant differences according to years of practice in the majority (9 out of 14) of confidence items with respect to discussing specific MS-related topics with patients. Significant differences between countries were also identified. Conclusion: The complexity of diagnosing MS and the variety of available DMTs for pwMS lead to uncertainties, even among specialized healthcare professionals. These should be addressed through focused education and training to optimize care for pwMS.
KW - Advanced practice nurse
KW - Continuing health education
KW - Continuing medical education
KW - Needs assessment
KW - Neurologist
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U2 - 10.1016/j.msard.2021.102854
DO - 10.1016/j.msard.2021.102854
M3 - Article
C2 - 33690086
AN - SCOPUS:85101959380
SN - 2211-0348
VL - 50
JO - Multiple Sclerosis and Related Disorders
JF - Multiple Sclerosis and Related Disorders
M1 - 102854
ER -