TITLE: 
                        
                            Understanding Health Care Professional-Patient Interactions in Multiple Sclerosis: A Systematic Review and Thematic Synthesis
                                
                                
                                    AUTHORS: 
                                            Andrew Soundy, Carolyn Roskell, Rachel Adams, Tracey Elder, Helen Dawes 
                                                    
                                                        KEYWORDS: 
                        Qualitative, Meta-Synthesis, Interaction, Communication, Therapeutic  Relationships, Health Care Professionals, Neurology, Multiple Sclerosis 
                                                    
                                                    
                                                        JOURNAL NAME: 
                        Open Journal of Therapy and Rehabilitation,  
                        Vol.4 No.4, 
                        November
                                                        7,
                        2016
                                                    
                                                    
                                                        ABSTRACT: Aim: To examine the experiences of health care professional (HCP)-patient interactions in Multiple Sclerosis (MS), identifying factors that can influence these interactions. Methods: A three-stage systematic review and thematic synthesis of qualitative and quantitative research was undertaken. Stage 1: the systematic literature search; Stage 2: methodological appraisal of the qualitative papers; Stage 3: thematic synthesis of all qualitative papers and the integration of quantitative findings into the synthesis. Results: Forty-nine qualitative studies were identified. This included 1014 individuals with MS (244 male, 755 female and 15 unknown) and 106 carers and 86 HCPs. Seventeen quantitative studies were identified which included 7680 (2008 male, 5812 females, and 40 unknown) participants as well as 224 carers. Two themes are discussed: 1) The expectations, experiences and perceptions of interactions with HCPs, and 2) The factors that influenced interactions and relationships. Discussion: There is need for improvement in the content and provision of information to patients with MS from HCPs. Specific strategies are suggested and implications for patients and health care providers are considered.