Communication with Fibromyalgia - Annotated Bibliography Example

Annotated Bibliography - Communication with Fibromyalgia 28/10/14 Bieber, C., Müller, K., Blumenstiel, K., Schneider, A.,Richter, A., Wilke, S., & ... Eich, W. (2006). Long-term effects of a shared decision-making intervention on physician–patient interaction and outcome in fibromyalgia: A qualitative and quantitative 1 year follow-up of a randomized controlled trial. Patient Education & Counselling, 63(3), 357-366. doi:10.1016/j.pec.2006.05.003. This article examines the role of a shared decision-making popularly referred to as the SDM. There is an existing syndrome linking a patient and the doctor that affects the communication among the two. The effect of lack of proper communication makes it difficult for the patient suffering from Fibromyalgia not to access the benefits of a specialist. The research was conducted to acknowledge that importance of a shared decision making in improving service delivery to the patient. The method was put in comparison with the information group. A total of sixty-seven patients were examined after being picked in a random procedure from the population. The patients were to choose the method they would like to follow in the essence of acquiring treatment. After the training the patients who underwent the shared decision making were eventually treated. The research that was conducted using both the qualitative and quantitate research showed that the shared decision making will prompt the patient to acquire the necessary treatment. A follow-up done on both parties for a period of three months (T2) and thereafter one year (T3) qualified the shared decision-making over the use of an information group. The result of this research shows that the shared decision making is an important tool that helps the patient to get the possible treatment. The reason is that of the improved integration that leads to a feasible relationship between the doctor and the patient. Therefore, the shared decision making can be used as a vital tool in the caring of the Fibromyalgia syndrome patients. The SDM is recommended as a method that can be used to search for a better relationship between the patient and the physicians. Briones-Vozmediano, E., Vives-Cases, C., Ronda-Pérez, E., & Gil-González, D. (2013). Patients’ and professionals’ views on managing fibromyalgia. Pain Research & Management: The Journal of the Canadian Pain Society = Journal De La Société Canadienne Pour Le Traitement De La Douleur, 18(1), 19-24. The study aims to explore the three ways are used to manage the FM syndrome. The three methods include; the diagnostic approach, therapeutic management and the health professional to the patient relationship. The study also entails establishing some areas concerning the relationship between the doctor and the patient that may not seem to be not satisfactory. The result of the study shows that there are a repeated occasions where the relationship between the patient and the caregivers seems unsatisfactory. The inclusive parties argued that there is a lack of satisfaction in the essence of the time used to get a diagnosis and acquiring effective treatment. The patients demand that they need a high level of moral support from the caregivers in the essence of quickening the healing process. The physicians, on the other hand, felt that they had inadequate support mechanisms that they could give to the patients. They agreed that there exist an uncertainty surrounding the two revelries. The study is useful in establishing the barriers present and the ineffectiveness of the current diagnosis system. The study analyses the importance of the support that the health providers need to practice in order to give the patients a beneficial attendance. The study recommends a proper patient to doctor relationship that will enhance the effectiveness in service provision. There is also a need to sensitize the public on matters relating to the identification and diagnosis of the fibromyalgia syndrome. Cohen, S. (2009). Overcoming obstacles: barriers to care in fibromyalgia treatment. Johns Hopkins Advanced Studies in Medicine, 9(4), 115-121. The article focuses on the difficulties that are common in the care giving to the fibromyalgia patients. The obstacles usually create a barrier between the patient and the caregivers leading to inefficiency in the treatment of the syndrome. There are however some ways that can be administered in the essence of overcoming such obstacles. Overcoming these obstructions means efficiency and adequate care to the patients. One of the barriers experienced relates to the affected people. The patient usually fails to acquire the necessary treatment that often disrupt their daily functions. The sick usually argue that the verdict of the FMS is hard to obtain. The patients also lack to identify whether they are suffering from the FMS as the symptoms associated with the disease can be similar to the normal backache. Studies have shown that this is the predominant factor that causes the lack of proper treatment. Physicians are also a barrier to the testing and curing of the FMS. The research has established that patients usually established negative perspectives towards the physicians during the curing processes. The physicians may also lack to identify the FMS symptoms on time making the diagnosis difficult. There are also barriers relating to the work and social life of the patient where the patient suffering from the FMS are seen as a burden to the society as well as the firms they where they work. Several measures can be used to break these hurdles. One of the methods that can be established is the use a proper education to both the physicians and the victims so that they can establish the symptoms of the disease at an early stage. The parties affected by the disease and the deliverers of medication should have a good communication that will avail a room for the treatment of the disease. The victims also need to be aware of the available medicines so that on recognizing the symptoms can look for this medicines. Counselling should also be offered to the patients suffering from FMS pre and post medication process for them to heal faster. Above all, the medical facilities offering diagnosis should be availed by the necessary institutions for quick access by the patients. The breaking of the barriers will be a big boost to the acquiring of the health facilities to the affected people. Quick interventions need to be formulated for effective realization and treatment of the disease. Nacu, A., & Benamouzig, D. (2010). Fibromyalgia: From public issue to the patient experience. Santé Publique (Vandoeuvre-lès-Nancy, France), 22(5), 551-562. The article draws the popularity that the FMS has grown and the sensitization that that is being done to the public about the syndrome. The component of the range of the disease is cannot be identified. There is new a biological nor a clinical method that can be used to specify the spread of the disease to the population. The community is hence called to the examination centre to establish the existence or not of the disease. The research conducted by stakeholders in the medical industry establishes that there is an excess of 1% of the world population suffers from the FMS syndrome. Of the one percent, more that 60% live with the syndrome without their knowledge. The article also examines some data in relation to the sociological field to examine the awareness of the existence of the syndrome. The findings show that even though the campaign the public to sensitize have been done since 1980, there is a common trend of the lack of knowledge over that time. The community remains ignorant of the presence of the disorder. Collective and individual efforts face some challenges in correcting this vice. P.K., G., K., H., & A., F. (2004). Communicating with Alexithymic and Non-Alexithymic Patients: An Experimental Study of the Effect of Psychosocial Communication and Empathy on Patient Satisfaction. Psychotherapy & Psychosomatics, 73(2), 92-100. The article presents the close relationship that exist between alexithymia and the pair of somatic and psychiatric conditions. Physician sometimes usually use psychosocial form of communication and the notion of empathy while communicating with their patients. The article is a research that tries to examine this behaviour of the doctors and how it affects the patients suffering from alexithymic and non-alexithymic syndrome. The research is accomplished by the use of seven doctors and 65 fibromyalgia patients who were all women. In order to compartmentalize the sick as either alexithymic or non-alexithymic, a Toronto alexithymia measure is put on the use. The patients were required to complete a questionnaire that was supposed to collect information regarding trait anxiety and satisfaction during their consultations. The doctors were given the task to disintegrate their communication in terms of psychosocial matters as well as an empathic response. The research applied Rotter International Research System to analyse the content of the result accrued. The result from the regression analysis portrayed that high empathic response from the doctors resulted to greater satisfaction to the alexithymic patients. High durations of the doctor to patient relationship during consultations was seen to be the satisfying factor towards the non-alexithymic patients. However, psychosocial communication was seen to be not important in the essence of satisfying the two categories of the patients, according to the statistics used in the research. The enquiry conclusion is in line with the response attained from the facts. Psychosocial communication that entails verbal exchange of ideas would be more effective in delivering the goals related to effective combating of the alexithymic complications. The research can also be used to determine the level of satisfaction towards the FMS infections, and it can be applied in offering counselling and other related treatments. Perrot, S., Choy, E., Petersel, D., Ginovker, A., & Kramer, K. (2012). Survey of physician experiences and perceptions about the diagnosis and treatment of fibromyalgia. BMC Health Services Research, 12(1), 356-363. doi: 10.1186/1472-6963-12-356. The survey aims at establishing the effectiveness that the physicians avail to their clients in the essence of diagnosing the fibromyalgia syndrome. The reason for the study is to capture the cause of the lack of proper treatment for the patients who visit the medical facilities. The research also aims at establishing why the doctors fail to establish proper medication to the patients on time. In order to complete this research, specialists from six European countries were supposed to fill a total of 1622 questionnaires. Specialists from Mexico and South Korea were also tested alongside those from the Europe. The survey included the primary care physicians with a total sample of 809, and the same sample was again used on rheumatologists, neurologists, psychiatrists and pain specialists. The research analysis found out that most of the doctors had contacted an FM patient in the past two years. The numeral is regarded to be over 80% of the aggregate doctors interviewed. The result implicates that most of the doctors have had a client’s case regarding the FM syndrome. 53% of the physicians who have come across an FM patient said that they experienced a lot of difficulty in treating the patient. 54% of the physicians acknowledged that the difficulty arose from improper training, therefore, had inadequate skills in handling the patient. Another group consisting a 32% said that they had no skills in diagnosing the FM syndrome. The result from the data analysis is a clear indication that the physicians face a lot of difficult in handling the patients. In other words, most of the doctors are not able to diagnose the patient and therefore the patients will still suffer in their hands. The result calls for proper training of doctors worldwide so that they can be able to offer effective diagnosis to their patients. There is also a need for improved communication between the patient and the client so that the FM syndrome can be managed. Salmon, P., Wissow, L., Carroll, J., Ring, A, Humphris, G., et al. (2007). Doctors’ responses to patients with medically unexplained symptoms who seek emotional support: Criticism or confrontation? Gen Hosp Psychiatry, 29(5), 454-460. The research investigates the respond of physicians who are contacted by patients undergoing some problems that do not have any medical explanation. The patients undergoing the medically unexplained symptoms MUSs may get the various respond from the doctors. Some of the responds may be encouraging while others seem to criticize their options. The research examined the incidence of guesses associated to the sick’s requests for expressive backing and the specialists’ sick-centred attitude and the style of the grown-up connection. The research involved 24 physicians were approached by 249 patients with the MUSs and recorded the aspect the traced of the patient-centred attitudes and also the adult attachment. The patients seemed to look for the emotional support before a consultation have been done. The consultation was noted to enable the analysis to be prepared on the experiences. The result of the research showed that there was a frequency of criticism concerning to the demands of the patients. The patients requested for the emotional support from the doctors, and there was a notion from the doctors who were seen to be positive in the sharing of information. The doctors’ responds to the demands of the patients are sometimes seen as a confrontation, but it is should be looked as a way of carrying out a therapeutic analysis. The patients are approaching the physicians for a MUSs need to understand the doctor’s explanation to their problems as they do not have adequate answers to their needs. Doctors also need to be motivated in various ways by those who are looking for an assistance from them by understanding their nature and scope of analysis. Silverman, S., Harnett, J., Zlateva, G., & Mardekian, J. (2010). Identifying fibromyalgia-associated symptoms and conditions from a clinical perspective: A step toward evaluating healthcare resource utilization in fibromyalgia. Pain Practice, 10(6), 520-529. The study aims at identifying the prescribed codes that can be utilized in enabling the doctors to identify the symptoms related to fibromyalgia syndrome. The symptoms are meant to help the physicians to attend the patients without difficulties. The outcome of the research generated the viable symptoms including muscle pain that reported a mean score of 8.7 of the total. Fatigue that also was identified as tiredness followed with 8.5 while insomnia came third at 8.0. Other symptoms accompanying the FM syndrome that were ranked include difficulty in remembering at a mean of 6.7, Nervousness at 6.0 depression at 7.8 and Muscle weakness and headache at 5.9 and 5.7 respectively. The conditions outcome was uniform to the patients that were interviewed. The signs are the common identification of a sick suffering from the FM syndrome. The physicians are encouraged to do a lot of investigation that will differentiate between the normal condition and the symptom that may lead to the actual identification of the syndrome. The doors are currently not closed for the research as the aim entails overcoming the FM syndrome. Thorne, S., McGuinness, L., McPherson, G., Con, A., Cunningham, M., et al. (2004). Health care communication issues in fibromyalgia: An interpretive description. Physiotherapy Canada, 56(1), 31 The aim of the study in the article is to establish desirable patterns of communication during a patient to doctor interaction. The interaction between the doctors and their FM clients is vital in establishing a viable relationship that will benefit all of them. The patterns identified should then be encouraged to be put in use by the professionals in the occasions of giving care to the patients. The results of the study got that the best communication practices are those that would encourage patients to live with the disease. The talks that will enable the patients to accept themselves as the FM patients would be beneficial. They also need to be encouraged and be involved in performing practices that would help them recover from the syndrome. Ullrich, A., Hauer, J., & Farin, E. (2014). Communication preferences in patients with fibromyalgia syndrome: Descriptive results and patient characteristics as predictors. Patient Preference and Adherence, 8, 135-145 The study in the article entails the challenges the faced by the FM patients in the event of seeking a proper guidance towards their search for treatment. The challenges accrued by these patients is put into a comparison with those that are faced by a different group of other chronic diseases. The study aims at establishing the possible means that the patients can use confidently to channel their needs to the relevant institutions. The study established that the patients undergoing an FM syndrome prefers an open system of communication that is centred towards their concerns. They do prefer some communications that support them emotionally meaning that they need to be encouraged by the talks. The communications are supposed to touch on their personal situations that they are undergoing through, although the level of personality differs from one patient to the other. The variables between the patients in terms of communications are minimal. The variables that have been discussed ranges between 3.1% and 9.7%, showing that the level of disagreement is minimal. The psychological variables have been picked as predictors in conjunction with all the communication preferences. The study concludes by offering the doctors to practice an open, patient centred form of communication when looking for the facts regarding the wellbeing of the patient. The so doing will encourage the patients to be corporative when it comes to the diagnosis schedule. The patients will be able to give their feeling and conditions that will enable the doctors to capture the symptoms of the FM as portrayed by the patient. References Bieber, C., Müller, K., Blumenstiel, K., Schneider, A., Richter, A., Wilke, S., & ... Eich, W. (2006). Long-term effects of a shared decision-making intervention on physician–patient interaction and outcome in fibromyalgia: A qualitative and quantitative 1 year follow-up of a randomized controlled trial. Patient Education & Counselling, 63(3), 357-366. doi:10.1016/j.pec.2006.05.003. Briones-Vozmediano, E., Vives-Cases, C., Ronda-Pérez, E., & Gil-González, D. (2013). Patients’ and professionals’ views on managing fibromyalgia. Pain Research & Management: The Journal of the Canadian Pain Society = Journal De La Société Canadienne Pour Le Traitement De La Douleur, 18(1), 19-24. Cohen, S. (2009). Overcoming obstacles: barriers to care in fibromyalgia treatment. Johns Hopkins Advanced Studies in Medicine, 9(4), 115-121. Nacu, A., & Benamouzig, D. (2010). Fibromyalgia: From public issue to the patient experience. Santé Publique (Vandoeuvre-lès-Nancy, France), 22(5), 551-562 P.K., G., K., H., & A., F. (2004). Communicating with Alexithymic and Non-Alexithymic Patients: An Experimental Study of the Effect of Psychosocial Communication and Empathy on Patient Satisfaction. Psychotherapy & Psychosomatics, 73(2), 92-100. Perrot, S., Choy, E., Petersel, D., Ginovker, A., & Kramer, K. (2012). Survey of physician experiences and perceptions about the diagnosis and treatment of fibromyalgia. BMC Health Services Research, 12(1), 356-363. doi: 10.1186/1472-6963-12-356. Salmon, P., Wissow, L., Carroll, J., Ring, A, Humphris, G., et al. (2007). Doctors’ responses to patients with medically unexplained symptoms who seek emotional support: Criticism or confrontation? Gen Hosp Psychiatry, 29(5), 454-460. Silverman, S., Harnett, J., Zlateva, G., & Mardekian, J. (2010). Identifying fibromyalgia-associated symptoms and conditions from a clinical perspective: A step toward evaluating healthcare resource utilization in fibromyalgia. Pain Practice, 10(6), 520-529. Thorne, S., McGuinness, L., McPherson, G., Con, A., Cunningham, M., et al. (2004). Health care communication issues in fibromyalgia: An interpretive description. Physiotherapy Canada, 56(1), 31 Ullrich, A., Hauer, J., & Farin, E. (2014). Communication preferences in patients with fibromyalgia syndrome: Descriptive results and patient characteristics as predictors. Patient Preference and Adherence, 8, 135-145 Read More