Pub Date : 2017-05-01DOI: 10.1016/j.rbre.2016.09.013
Mariana de Almeida Lourenço , Izabela Roma , Marcos Renato de Assis
Objective
To evaluate the occurrence of falls reported by rheumatoid arthritis patients and its relation to disease activity, functional capacity and physical fitness.
Materials and methods
A cross-sectional study constituted by a sample of 97 rheumatoid arthritis patients from the city of Marília (SP) from 2012 to 2013, were assessed for disease activity. Instruments validated for Brazilian population in order to evaluate physical and functional capacity were used. Data analysis was carried out with descriptive statistics, Spearman correlation and Chi-squared test, considering p < 0.05.
Results
88.7% were female subjects with a mean age of 56 (±11.7) years. The median duration of rheumatoid arthritis was 10 years (P25 = 6 and P75 = 17) and the mean of disease activity was 3.6 (±1.3), what was considered a moderate activity. In the last 12 months 37.1% of patients experienced at least one fall, with a total of 52 episodes, and fear of falling was reported by 74.2% of them, but this was not associated to the occurrence of a fall (χ2 = 1.19, p = 0.27). Gender, number of medications, age, disease activity, duration of rheumatoid arthritis, functional capacity, and physical tests showed no associations with history of falls in the past year.
Conclusion
It was observed that the occurrence of falls and the fear of falling are quite common in this population. The occurrence of falls in this sample of rheumatoid arthritis patients bears no relation to disease activity, functional capacity, or physical fitness tests.
{"title":"Falls and their association with physical tests, functional capacity, clinical and demographic factors in patients with rheumatoid arthritis","authors":"Mariana de Almeida Lourenço , Izabela Roma , Marcos Renato de Assis","doi":"10.1016/j.rbre.2016.09.013","DOIUrl":"10.1016/j.rbre.2016.09.013","url":null,"abstract":"<div><h3>Objective</h3><p>To evaluate the occurrence of falls reported by rheumatoid arthritis patients and its relation to disease activity, functional capacity and physical fitness.</p></div><div><h3>Materials and methods</h3><p>A cross-sectional study constituted by a sample of 97 rheumatoid arthritis patients from the city of Marília (SP) from 2012 to 2013, were assessed for disease activity. Instruments validated for Brazilian population in order to evaluate physical and functional capacity were used. Data analysis was carried out with descriptive statistics, Spearman correlation and Chi-squared test, considering <em>p</em> <!--><<!--> <!-->0.05.</p></div><div><h3>Results</h3><p>88.7% were female subjects with a mean age of 56 (±11.7) years. The median duration of rheumatoid arthritis was 10 years (P25<!--> <!-->=<!--> <!-->6 and P75<!--> <!-->=<!--> <!-->17) and the mean of disease activity was 3.6 (±1.3), what was considered a moderate activity. In the last 12 months 37.1% of patients experienced at least one fall, with a total of 52 episodes, and fear of falling was reported by 74.2% of them, but this was not associated to the occurrence of a fall (<em>χ</em><sup>2</sup> <!-->=<!--> <!-->1.19, <em>p</em> <!-->=<!--> <!-->0.27). Gender, number of medications, age, disease activity, duration of rheumatoid arthritis, functional capacity, and physical tests showed no associations with history of falls in the past year.</p></div><div><h3>Conclusion</h3><p>It was observed that the occurrence of falls and the fear of falling are quite common in this population. The occurrence of falls in this sample of rheumatoid arthritis patients bears no relation to disease activity, functional capacity, or physical fitness tests.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 3","pages":"Pages 217-223"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.09.013","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35020910","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-05-01DOI: 10.1016/j.rbre.2017.01.001
Ellen Luz Pereira Caires , Mailze Campos Bezerra , Ana Flávia Torquato de Araújo Junqueira , Sheila Márcia de Araújo Fontenele , Silvana Cristina de Albuquerque Andrade , Catarina Brasil d’Alva
Bisphosphonates are considered first-line agents in the treatment of postmenopausal osteoporosis based on extensive experience of use, safety, and proven efficacy in reducing vertebral, non-vertebral and femur fractures. However, post-marketing reports based on the treatment of millions of patients/year over lengthy periods of time have revealed the occurrence of initially unexpected adverse effects, such as osteonecrosis of the jaw and atypical femoral fracture, leading to the restriction of treatment duration with bisphosphonates by global regulatory agencies. However, despite the association between these effects and bisphosphonates, this risk should be analyzed in the context of osteoporosis treatment, alongside the benefit of preventing osteoporotic fractures and their clinical consequences. Therefore, we consider it plausible to discuss the restriction to the use of bisphosphonates, possible indications for prolonged treatment and alternative therapies following the suspension of this drug class for patients with persistent high risk of fracture after initial treatment, especially considering the problems of public health funding in Brazil and the shortage of drugs provided by the government. Thus, to standardize the treatment of osteoporosis in the public health care system, we aim to develop a proposal for a scientifically-based pharmacological treatment for postmenopausal osteoporosis, establishing criteria for indication and allowing the rational use of each pharmacological agent. We discuss the duration of the initial bisphosphonate treatment, the therapeutic options for refractory patients and potential indications of other classes of drugs as first-choice treatment in the sphere of public health, in which assessing risk and cost effectiveness is a priority.
{"title":"Treatment of postmenopausal osteoporosis: a literature-based algorithm for use in the public health care system","authors":"Ellen Luz Pereira Caires , Mailze Campos Bezerra , Ana Flávia Torquato de Araújo Junqueira , Sheila Márcia de Araújo Fontenele , Silvana Cristina de Albuquerque Andrade , Catarina Brasil d’Alva","doi":"10.1016/j.rbre.2017.01.001","DOIUrl":"10.1016/j.rbre.2017.01.001","url":null,"abstract":"<div><p>Bisphosphonates are considered first-line agents in the treatment of postmenopausal osteoporosis based on extensive experience of use, safety, and proven efficacy in reducing vertebral, non-vertebral and femur fractures. However, post-marketing reports based on the treatment of millions of patients/year over lengthy periods of time have revealed the occurrence of initially unexpected adverse effects, such as osteonecrosis of the jaw and atypical femoral fracture, leading to the restriction of treatment duration with bisphosphonates by global regulatory agencies. However, despite the association between these effects and bisphosphonates, this risk should be analyzed in the context of osteoporosis treatment, alongside the benefit of preventing osteoporotic fractures and their clinical consequences. Therefore, we consider it plausible to discuss the restriction to the use of bisphosphonates, possible indications for prolonged treatment and alternative therapies following the suspension of this drug class for patients with persistent high risk of fracture after initial treatment, especially considering the problems of public health funding in Brazil and the shortage of drugs provided by the government. Thus, to standardize the treatment of osteoporosis in the public health care system, we aim to develop a proposal for a scientifically-based pharmacological treatment for postmenopausal osteoporosis, establishing criteria for indication and allowing the rational use of each pharmacological agent. We discuss the duration of the initial bisphosphonate treatment, the therapeutic options for refractory patients and potential indications of other classes of drugs as first-choice treatment in the sphere of public health, in which assessing risk and cost effectiveness is a priority.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 3","pages":"Pages 254-263"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2017.01.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35021351","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-05-01DOI: 10.1016/j.rbre.2017.01.002
Hatice Isik , Metin Isik , Oner Aynioglu , Deniz Karcaaltincaba , Ahmet Sahbaz , Tugba Beyazcicek , Mehmet Ibrahim Harma , Nejat Demircan
Objective
Females with Sjögren's Syndrome (SS) often experience vaginal dryness and dyspareunia, along with glandular and extraglandular symptoms. We aimed to evaluate sexual function and life quality in women with SS.
Methods
Forty-six premenopausal women with SS and 47 age-matched controls were studied. Age, duration of the disease, medications, and comorbid diseases were noted. Participants completed 36-Item Short Form Health Survey (SF-36) and Female Sexual Function Index (FSFI). Patients were asked about vaginal discharge and itching in the last month, and if they informed their rheumatologists about any sexual problems. Gynecologic examinations were performed and vaginal smears were taken on each participant.
Results
The median total scores of FSFI were significantly lower in the SS group than the controls [17.12 (2.4–27.8) and 27.4 (16.9–36.0), respectively, p < 0.001]. In the SS group, 37 (80.4%) and in the control group 18 (38.3%) of patients were sexually dissatisfied (p < 0.001). Vaginal dryness and lubricant use were significantly increased in patients with SS compared to controls (p < 0.001). Life quality scores were significantly lower in patients with SS than the controls (p < 0.001). Vaginal dryness was negatively correlated with FSFI total (r = −0.312, p = 0.035) and subscores except desire and arousal. Physical functioning, role physical and role emotional scores were positively correlated with total FSFI scores (r = 0.449, p = 0.002, r = 0.371, p = 0.011, r = 0.299, p = 0.043, respectively).
Conclusions
Women with SS experience less satisfaction with sexual activity, which can be affected by age, vaginal dryness, physical pain, and impaired function due to the disease. Therefore, rheumatologists should pay attention to these symptoms and management.
目的:患有Sjögren综合征(SS)的女性经常经历阴道干燥和性交困难,并伴有腺和腺外症状。方法对46例绝经前SS患者和47例年龄匹配的对照组进行研究。记录了年龄、病程、药物和合并症。参与者完成了36项简短健康调查(SF-36)和女性性功能指数(FSFI)。研究人员询问患者上个月的阴道分泌物和瘙痒情况,以及他们是否向风湿病医生报告了任何性问题。对每位参与者进行妇科检查和阴道涂片检查。结果SS组FSFI总分中位数显著低于对照组[分别为17.12(2.4 ~ 27.8)和27.4 (16.9 ~ 36.0)],p <0.001]。SS组37例(80.4%),对照组18例(38.3%)性不满意(p <0.001)。与对照组相比,SS患者阴道干燥和润滑剂的使用显著增加(p <0.001)。SS患者的生活质量评分显著低于对照组(p <0.001)。阴道干燥与FSFI总分呈负相关(r = - 0.312, p = 0.035),除性欲和性兴奋外,其余各分项得分均呈负相关。身体功能、角色身体和角色情绪得分与FSFI总分呈显著正相关(r = 0.449, p = 0.002, r = 0.371, p = 0.011, r = 0.299, p = 0.043)。结论SS女性对性活动的满意度较低,这可能与年龄、阴道干燥、身体疼痛和疾病导致的功能受损有关。因此,风湿病学家应注意这些症状和管理。
{"title":"Are the women with Sjögren's Syndrome satisfied with their sexual activity?","authors":"Hatice Isik , Metin Isik , Oner Aynioglu , Deniz Karcaaltincaba , Ahmet Sahbaz , Tugba Beyazcicek , Mehmet Ibrahim Harma , Nejat Demircan","doi":"10.1016/j.rbre.2017.01.002","DOIUrl":"10.1016/j.rbre.2017.01.002","url":null,"abstract":"<div><h3>Objective</h3><p>Females with Sjögren's Syndrome (SS) often experience vaginal dryness and dyspareunia, along with glandular and extraglandular symptoms. We aimed to evaluate sexual function and life quality in women with SS.</p></div><div><h3>Methods</h3><p>Forty-six premenopausal women with SS and 47 age-matched controls were studied. Age, duration of the disease, medications, and comorbid diseases were noted. Participants completed 36-Item Short Form Health Survey (SF-36) and Female Sexual Function Index (FSFI). Patients were asked about vaginal discharge and itching in the last month, and if they informed their rheumatologists about any sexual problems. Gynecologic examinations were performed and vaginal smears were taken on each participant.</p></div><div><h3>Results</h3><p>The median total scores of FSFI were significantly lower in the SS group than the controls [17.12 (2.4–27.8) and 27.4 (16.9–36.0), respectively, <em>p</em> <!--><<!--> <!-->0.001]. In the SS group, 37 (80.4%) and in the control group 18 (38.3%) of patients were sexually dissatisfied (<em>p</em> <!--><<!--> <!-->0.001). Vaginal dryness and lubricant use were significantly increased in patients with SS compared to controls (<em>p</em> <!--><<!--> <!-->0.001). Life quality scores were significantly lower in patients with SS than the controls (<em>p</em> <!--><<!--> <!-->0.001). Vaginal dryness was negatively correlated with FSFI total (<em>r</em> <!-->=<!--> <!-->−0.312, <em>p</em> <!-->=<!--> <!-->0.035) and subscores except desire and arousal. Physical functioning, role physical and role emotional scores were positively correlated with total FSFI scores (<em>r</em> <!-->=<!--> <!-->0.449, <em>p</em> <!-->=<!--> <!-->0.002, <em>r</em> <!-->=<!--> <!-->0.371, <em>p</em> <!-->=<!--> <!-->0.011, <em>r</em> <!-->=<!--> <!-->0.299, <em>p</em> <!-->=<!--> <!-->0.043, respectively).</p></div><div><h3>Conclusions</h3><p>Women with SS experience less satisfaction with sexual activity, which can be affected by age, vaginal dryness, physical pain, and impaired function due to the disease. Therefore, rheumatologists should pay attention to these symptoms and management.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 3","pages":"Pages 210-216"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2017.01.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35020911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-05-01DOI: 10.1016/j.rbre.2017.01.009
José Cleosmaque Leite Júnior , Regina Terse Trindade Ramos , Teresa Cristina Martins Vicente Robazzi
Introduction
Children and adolescents with rheumatic diseases receiving TNF blockers are at risk for the activation of latent Mycobacterium tuberculosis infection (LTBI). Although LTBI treatment is indicated in this group, there are different therapeutic regimens in the literature, without a definite consensus.
Objectives
To review in the literature therapeutic schemes used and indicated for the treatment of LTBI in these patients.
Methods
Systematic review of the literature, using health databases, selecting studies that addressed the treatment of LTBI in patients with juvenile rheumatic diseases using TNF blockers, from 1990 to 2015. All study designs were considered.
Results
A total of 162 studies were identified through the electronic databases and one was found through a manual search by the author, totaling 163 articles. We excluded studies that did not meet the mentioned inclusion criteria, and included a retrospective cohort study and two prospective cohort studies. The three studies addressed treatment with isoniazid (INH) for 9 months and one of them also addressed INH treatment associated with rifampicin for 3 months.
Conclusions
Only one case of LTBI activation was observed; there was good treatment adherence and absence of complications during follow-up. More studies are necessary to evaluate the response to the other available therapeutic regimens, with better tolerability assessment and a larger sample. However, the results showed that INH therapy for 9 months and INH therapy plus rifampicin for 3 months had a low rate of LTBI activation and complications.
{"title":"Treatment of latent tuberculosis in patients with juvenile rheumatic diseases: a systematic review","authors":"José Cleosmaque Leite Júnior , Regina Terse Trindade Ramos , Teresa Cristina Martins Vicente Robazzi","doi":"10.1016/j.rbre.2017.01.009","DOIUrl":"10.1016/j.rbre.2017.01.009","url":null,"abstract":"<div><h3>Introduction</h3><p>Children and adolescents with rheumatic diseases receiving TNF blockers are at risk for the activation of latent <em>Mycobacterium tuberculosis</em> infection (LTBI). Although LTBI treatment is indicated in this group, there are different therapeutic regimens in the literature, without a definite consensus.</p></div><div><h3>Objectives</h3><p>To review in the literature therapeutic schemes used and indicated for the treatment of LTBI in these patients.</p></div><div><h3>Methods</h3><p>Systematic review of the literature, using health databases, selecting studies that addressed the treatment of LTBI in patients with juvenile rheumatic diseases using TNF blockers, from 1990 to 2015. All study designs were considered.</p></div><div><h3>Results</h3><p>A total of 162 studies were identified through the electronic databases and one was found through a manual search by the author, totaling 163 articles. We excluded studies that did not meet the mentioned inclusion criteria, and included a retrospective cohort study and two prospective cohort studies. The three studies addressed treatment with isoniazid (INH) for 9 months and one of them also addressed INH treatment associated with rifampicin for 3 months.</p></div><div><h3>Conclusions</h3><p>Only one case of LTBI activation was observed; there was good treatment adherence and absence of complications during follow-up. More studies are necessary to evaluate the response to the other available therapeutic regimens, with better tolerability assessment and a larger sample. However, the results showed that INH therapy for 9 months and INH therapy plus rifampicin for 3 months had a low rate of LTBI activation and complications.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 3","pages":"Pages 245-253"},"PeriodicalIF":0.0,"publicationDate":"2017-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2017.01.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35020916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.07.009
Renan Bazuco Frittoli , Barbara Sugui Longhi , Amanda Meireles Silva , Antônio de Azevedo Barros Filho , Maria Ângela Reis de Góes Monteiro , Simone Appenzeller
Introduction
Children with juvenile idiopathic arthritis (JIA) often have impaired growth and short stature. There is evidence that the therapeutic use of growth hormone (GH) is useful and safe in these patients.
Objective
To analyze the effects of GH use in patients with JIA.
Method
A systematic review of the literature over the last 18 years in Medline and Embase databases. The criteria were analyzed independently by the researchers. We used the following keywords: “growth hormone”, “arthritis, juvenile”, “arthritis, rheumatoid”, “child” and “adolescent”.
Results
Among the 192 identified articles, 20 corresponded to the inclusion criteria. Seventeen longitudinal studies and 3 case reports were found. Most studies analyzed observed increased growth, muscle mass and bone mass using GH. Adverse effects observed were glucose intolerance, diabetes, bone deformities, osteonecrosis, reactivation of the disease and low final height.
Conclusion
The majority of studies reported positive effects after the therapeutic use of GH, but some variability in response to treatment was observed. The combination of growth hormone with other drugs seems to be a good option.
{"title":"Effects of the use of growth hormone in children and adolescents with juvenile idiopathic arthritis: a systematic review","authors":"Renan Bazuco Frittoli , Barbara Sugui Longhi , Amanda Meireles Silva , Antônio de Azevedo Barros Filho , Maria Ângela Reis de Góes Monteiro , Simone Appenzeller","doi":"10.1016/j.rbre.2016.07.009","DOIUrl":"10.1016/j.rbre.2016.07.009","url":null,"abstract":"<div><h3>Introduction</h3><p>Children with juvenile idiopathic arthritis (JIA) often have impaired growth and short stature. There is evidence that the therapeutic use of growth hormone (GH) is useful and safe in these patients.</p></div><div><h3>Objective</h3><p>To analyze the effects of GH use in patients with JIA.</p></div><div><h3>Method</h3><p>A systematic review of the literature over the last 18 years in Medline and Embase databases. The criteria were analyzed independently by the researchers. We used the following keywords: “growth hormone”, “arthritis, juvenile”, “arthritis, rheumatoid”, “child” and “adolescent”.</p></div><div><h3>Results</h3><p>Among the 192 identified articles, 20 corresponded to the inclusion criteria. Seventeen longitudinal studies and 3 case reports were found. Most studies analyzed observed increased growth, muscle mass and bone mass using GH. Adverse effects observed were glucose intolerance, diabetes, bone deformities, osteonecrosis, reactivation of the disease and low final height.</p></div><div><h3>Conclusion</h3><p>The majority of studies reported positive effects after the therapeutic use of GH, but some variability in response to treatment was observed. The combination of growth hormone with other drugs seems to be a good option.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 100-106"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.07.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34855735","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.03.012
Saime Ay , Hatice Ecem Konak , Deniz Evcik , Sibel Kibar
Objective
The aim of this study was to investigate the effectiveness of Kinesio Taping and sham Kinesio Taping on pain, pressure pain threshold, cervical range of motion, and disability in cervical myofascial pain syndrome patients (MPS).
Methods
This study was designed as a randomized, double-blind placebo controlled study. Sixty-one patients with MPS were randomly assigned into two groups. Group 1 (n = 31) was treated with Kinesio Taping and group 2 (n = 30) was treated sham taping five times by intervals of 3 days for 15 days. Additionally, all patients were given neck exercise program. Patients were evaluated according to pain, pressure pain threshold, cervical range of motion and disability. Pain was assessed by using Visual Analog Scale, pressure pain threshold was measured by using an algometer, and active cervical range of motion was measured by using goniometry. Disability was assessed with the neck pain disability index disability. Measurements were taken before and after the treatment.
Results
At the end of the therapy, there were statistically significant improvements on pain, pressure pain threshold, cervical range of motion, and disability (p < 0.05) in both groups. Also there was a statistical difference between the groups regarding pain, pressure pain threshold, cervical flexion-extension (p < 0.05); except cervical rotation, cervical lateral flexion and disability (p > 0.05).
Conclusion
This study shows that Kinesio Taping leads to improvements on pain, pressure pain threshold and cervical range of motion, but not disability in short time. Therefore, Kinesio Taping can be used as an alternative therapy method in the treatment of patients with MPS.
{"title":"The effectiveness of Kinesio Taping on pain and disability in cervical myofascial pain syndrome","authors":"Saime Ay , Hatice Ecem Konak , Deniz Evcik , Sibel Kibar","doi":"10.1016/j.rbre.2016.03.012","DOIUrl":"10.1016/j.rbre.2016.03.012","url":null,"abstract":"<div><h3>Objective</h3><p>The aim of this study was to investigate the effectiveness of Kinesio Taping and sham Kinesio Taping on pain, pressure pain threshold, cervical range of motion, and disability in cervical myofascial pain syndrome patients (MPS).</p></div><div><h3>Methods</h3><p>This study was designed as a randomized, double-blind placebo controlled study. Sixty-one patients with MPS were randomly assigned into two groups. Group 1 (<em>n</em> <!-->=<!--> <!-->31) was treated with Kinesio Taping and group 2 (<em>n</em> <!-->=<!--> <!-->30) was treated sham taping five times by intervals of 3 days for 15 days. Additionally, all patients were given neck exercise program. Patients were evaluated according to pain, pressure pain threshold, cervical range of motion and disability. Pain was assessed by using Visual Analog Scale, pressure pain threshold was measured by using an algometer, and active cervical range of motion was measured by using goniometry. Disability was assessed with the neck pain disability index disability. Measurements were taken before and after the treatment.</p></div><div><h3>Results</h3><p>At the end of the therapy, there were statistically significant improvements on pain, pressure pain threshold, cervical range of motion, and disability (<em>p</em> <!--><<!--> <!-->0.05) in both groups. Also there was a statistical difference between the groups regarding pain, pressure pain threshold, cervical flexion-extension (<em>p</em> <!--><<!--> <!-->0.05); except cervical rotation, cervical lateral flexion and disability (<em>p</em> <!-->><!--> <!-->0.05).</p></div><div><h3>Conclusion</h3><p>This study shows that Kinesio Taping leads to improvements on pain, pressure pain threshold and cervical range of motion, but not disability in short time. Therefore, Kinesio Taping can be used as an alternative therapy method in the treatment of patients with MPS.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 93-99"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.03.012","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34856575","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.11.008
Vanessa Patricia L. Pereira , Teresa Cristina Martins Vicente Robazzi
Juvenile rheumatic diseases affect the musculoskeletal system and begin before the age of 18. These conditions have varied, identifiable or unknown etiologies, but those of an autoimmune inflammatory nature have been associated with an increased risk of development of cancer, regardless of treatment. This study aims to assess, through a systematic review of the literature according to Prisma (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) quality criteria, the risk of cancer in patients with juvenile rheumatic disease, and its association with biological agents. The criteria described by the Strengthening the Reporting of Observational Studies in Epidemiology initiative were used in order to assess the methodological quality of those individual items selected in this study. We analyzed nine publications, from a total of 251 papers initially selected. There was an increase in cancer risk in the population with juvenile rheumatic disease versus the general population. Most specified cancers were of a lymphoproliferative nature. Seven studies did not specify the treatment or not defined an association between treatment and cancer risk. Only one study has suggested this association; in it, their authors observed high risk in patients diagnosed in the last 20 years, a period of the advent of new therapies. One study found an increased risk in a population not treated with biological agents, suggesting a disease in its natural course, and not an adverse effect of therapy. Studies have shown an increased risk of malignancy associated with juvenile rheumatic disease, and this may be related to disease activity and not specifically to the treatment with biological agents.
{"title":"Biological therapy and development of neoplastic disease in patients with juvenile rheumatic disease: a systematic review","authors":"Vanessa Patricia L. Pereira , Teresa Cristina Martins Vicente Robazzi","doi":"10.1016/j.rbre.2016.11.008","DOIUrl":"10.1016/j.rbre.2016.11.008","url":null,"abstract":"<div><p>Juvenile rheumatic diseases affect the musculoskeletal system and begin before the age of 18. These conditions have varied, identifiable or unknown etiologies, but those of an autoimmune inflammatory nature have been associated with an increased risk of development of cancer, regardless of treatment. This study aims to assess, through a systematic review of the literature according to Prisma (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) quality criteria, the risk of cancer in patients with juvenile rheumatic disease, and its association with biological agents. The criteria described by the Strengthening the Reporting of Observational Studies in Epidemiology initiative were used in order to assess the methodological quality of those individual items selected in this study. We analyzed nine publications, from a total of 251 papers initially selected. There was an increase in cancer risk in the population with juvenile rheumatic disease <em>versus</em> the general population. Most specified cancers were of a lymphoproliferative nature. Seven studies did not specify the treatment or not defined an association between treatment and cancer risk. Only one study has suggested this association; in it, their authors observed high risk in patients diagnosed in the last 20 years, a period of the advent of new therapies. One study found an increased risk in a population not treated with biological agents, suggesting a disease in its natural course, and not an adverse effect of therapy. Studies have shown an increased risk of malignancy associated with juvenile rheumatic disease, and this may be related to disease activity and not specifically to the treatment with biological agents.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 174-181"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.11.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34857179","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.09.012
José Eduardo Martinez , Eduardo S. Paiva , Marcelo C. Rezende , Roberto E. Heymann , Milton Helfenstein Jr. , Aline Ranzolin , Jose Roberto Provenza , Luiz Severiano Ribeiro , Eduardo J.R. Souza , Daniel P. Feldman , Marcos Renato de Assis
Introduction
EpiFibro (Brazilian Epidemiological Study of Fibromyalgia) was created to study Fibromyalgia patients. Patients were included since 2011 according to the 1990 American College of Rheumatology Classification Criteria for Fibromyalgia (ACR1990).
Objectives
To determine how many patients still fulfill the ACR1990 and the ACR2010 criteria in 2014; to determine the correlation between the impact of FM and to describe data on the follow-up evaluation.
Methods
This is a cross sectional study in a multicenter cohort of patients. The data was collected between 2013 and 2015. Physician included patients that fulfilled the ACR1990 criteria on the date of entry. The follow-up data were considered only for patients with at least two evaluations. A minimally significant change was considered to be a 30% variation of parameters scores.
Results
810 patients’ data were analyzed. Patients presented a mean age of 51.8 ± 11.5 years old. There were 786 female. Most patients met both criteria. There was a greater fulfilling of the ACR2010. There was a moderate correlation between Polysymptomatic Distress Scale and Fibromyalgia Impact Questionnaire. Three hundred fourteen patients with more than one assessment were found, but 88 patients were excluded. Thus, 226 patients with one follow-up monitoring parameter were considered (Fibromyalgia Impact Questionnaire: 222; Polysymptomatic Distress Scale: 199; both: 195). The mean follow-up time was 9.1 ± 7.5 months (1–44). Most patients became stable.
Conclusion
InEpiFibro, most patients fulfill simultaneously the ACR1990 and ACR2010. A larger number of patients fulfill the ACR2010 at the time of the evaluation. There was a moderate correlation between the Polysymptomatic Distress Scale and the Fibromyalgia Impact Questionnaire. Most patients remained stable over time.
{"title":"EpiFibro (Brazilian Fibromyalgia Registry): data on the ACR classification and diagnostic preliminary criteria fulfillment and the follow-up evaluation","authors":"José Eduardo Martinez , Eduardo S. Paiva , Marcelo C. Rezende , Roberto E. Heymann , Milton Helfenstein Jr. , Aline Ranzolin , Jose Roberto Provenza , Luiz Severiano Ribeiro , Eduardo J.R. Souza , Daniel P. Feldman , Marcos Renato de Assis","doi":"10.1016/j.rbre.2016.09.012","DOIUrl":"10.1016/j.rbre.2016.09.012","url":null,"abstract":"<div><h3>Introduction</h3><p>EpiFibro (Brazilian Epidemiological Study of Fibromyalgia) was created to study Fibromyalgia patients. Patients were included since 2011 according to the 1990 American College of Rheumatology Classification Criteria for Fibromyalgia (ACR1990).</p></div><div><h3>Objectives</h3><p>To determine how many patients still fulfill the ACR1990 and the ACR2010 criteria in 2014; to determine the correlation between the impact of FM and to describe data on the follow-up evaluation.</p></div><div><h3>Methods</h3><p>This is a cross sectional study in a multicenter cohort of patients. The data was collected between 2013 and 2015. Physician included patients that fulfilled the ACR1990 criteria on the date of entry. The follow-up data were considered only for patients with at least two evaluations. A minimally significant change was considered to be a 30% variation of parameters scores.</p></div><div><h3>Results</h3><p>810 patients’ data were analyzed. Patients presented a mean age of 51.8<!--> <!-->±<!--> <!-->11.5 years old. There were 786 female. Most patients met both criteria. There was a greater fulfilling of the ACR2010. There was a moderate correlation between Polysymptomatic Distress Scale and Fibromyalgia Impact Questionnaire. Three hundred fourteen patients with more than one assessment were found, but 88 patients were excluded. Thus, 226 patients with one follow-up monitoring parameter were considered (Fibromyalgia Impact Questionnaire: 222; Polysymptomatic Distress Scale: 199; both: 195). The mean follow-up time was 9.1<!--> <!-->±<!--> <!-->7.5 months (1–44). Most patients became stable.</p></div><div><h3>Conclusion</h3><p>InEpiFibro, most patients fulfill simultaneously the ACR1990 and ACR2010. A larger number of patients fulfill the ACR2010 at the time of the evaluation. There was a moderate correlation between the Polysymptomatic Distress Scale and the Fibromyalgia Impact Questionnaire. Most patients remained stable over time.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 129-133"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.09.012","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34855737","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.07.008
Javier Fernández-Torres , Gabriela Angélica Martínez-Nava , María Concepción Gutiérrez-Ruíz , Luis Enrique Gómez-Quiroz , Marwin Gutiérrez
Osteoarthritis (OA) is the most common form of arthritis and is frequently diagnosed and managed in primary care; it is characterized by loss of articular hyaline cartilage, which is a unique connective tissue that physiologically lacks blood vessels. Articular cartilage survives in a microenvironment devoid of oxygen, which is regulated by hypoxia inducible factor (HIF-1α). HIF-1α is considered the main transcriptional regulator of cellular and developmental response to hypoxia. To date, the relevance of HIF-1α in the assessment of cartilage has increased since its participation is essential in the homeostasis of this tissue. Taking into account the new emerging insights of HIF-1α in the scientific literature in the last years, we focused the present review on the potential role of HIF-1α signaling pathway in OA development, especially in how some genetic factors may influence the maintenance or breakdown of articular cartilage.
{"title":"Role of HIF-1α signaling pathway in osteoarthritis: a systematic review","authors":"Javier Fernández-Torres , Gabriela Angélica Martínez-Nava , María Concepción Gutiérrez-Ruíz , Luis Enrique Gómez-Quiroz , Marwin Gutiérrez","doi":"10.1016/j.rbre.2016.07.008","DOIUrl":"10.1016/j.rbre.2016.07.008","url":null,"abstract":"<div><p>Osteoarthritis (OA) is the most common form of arthritis and is frequently diagnosed and managed in primary care; it is characterized by loss of articular hyaline cartilage, which is a unique connective tissue that physiologically lacks blood vessels. Articular cartilage survives in a microenvironment devoid of oxygen, which is regulated by hypoxia inducible factor (HIF-1α). HIF-1α is considered the main transcriptional regulator of cellular and developmental response to hypoxia. To date, the relevance of HIF-1α in the assessment of cartilage has increased since its participation is essential in the homeostasis of this tissue. Taking into account the new emerging insights of HIF-1α in the scientific literature in the last years, we focused the present review on the potential role of HIF-1α signaling pathway in OA development, especially in how some genetic factors may influence the maintenance or breakdown of articular cartilage.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 162-173"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.07.008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34857173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-03-01DOI: 10.1016/j.rbre.2016.11.010
Rosa Weiss Telles, Luciana Costa-Silva, Luciana A.C. Machado, Rodrigo Citton Padilha dos Reis, Sandhi Maria Barreto
Objective
To describe the performance of a non-fluoroscopic fixed-flexion PA radiographic protocol with a new positioning device, developed for the assessment of knee osteoarthritis (OA) in Brazilian Longitudinal Study of Adult Health Musculoskeletal Study (ELSA-Brasil MSK).
Material and methods
A test–retest design including 19 adults (38 knee images) was conducted. Feasibility of the radiographic protocol was assessed by image quality parameters and presence of radioanatomic alignment according to intermargin distance (IMD) values. Repeatability was assessed for IMD and joint space width (JSW) measured at three different locations.
Results
Approximately 90% of knee images presented excellent quality. Frequencies of nearly perfect radioanatomic alignment (IMD ≤1 mm) ranged from 29% to 50%, and satisfactory alignment was found in up to 71% and 76% of the images (IMD ≤1.5 mm and ≤1.7 mm, respectively). Repeatability analyses yielded the following results: IMD [SD of mean difference = 1.08; coefficient of variation (%CV) = 54.68%; intraclass correlation coefficient (ICC) (95%CI) = 0.59 (0.34–0.77)]; JSW [SD of mean difference = 0.34–0.61; %CV = 4.48%–9.80%; ICC (95%CI) = 0.74 (0.55–0.85)–0.94 (0.87–0.97)]. Adequately reproducible measurements of IMD and JSW were found in 68% and 87% of the images, respectively.
Conclusions
Despite the difficulty in achieving consistent radioanatomic alignment between subsequent radiographs in terms of IMD, the protocol produced highly repeatable JSW measurements when these were taken at midpoint and 10 mm from the medial extremity of the medial tibial plateau. Therefore, measurements of JSW at these locations can be considered adequate for the assessment of knee OA in ELSA-Brasil MSK.
{"title":"Fixed-flexion knee radiography using a new positioning device produced highly repeatable measurements of joint space width: ELSA-Brasil Musculoskeletal Study (ELSA-Brasil MSK)","authors":"Rosa Weiss Telles, Luciana Costa-Silva, Luciana A.C. Machado, Rodrigo Citton Padilha dos Reis, Sandhi Maria Barreto","doi":"10.1016/j.rbre.2016.11.010","DOIUrl":"10.1016/j.rbre.2016.11.010","url":null,"abstract":"<div><h3>Objective</h3><p>To describe the performance of a non-fluoroscopic fixed-flexion PA radiographic protocol with a new positioning device, developed for the assessment of knee osteoarthritis (OA) in Brazilian Longitudinal Study of Adult Health Musculoskeletal Study (ELSA-Brasil MSK).</p></div><div><h3>Material and methods</h3><p>A test–retest design including 19 adults (38 knee images) was conducted. Feasibility of the radiographic protocol was assessed by image quality parameters and presence of radioanatomic alignment according to intermargin distance (IMD) values. Repeatability was assessed for IMD and joint space width (JSW) measured at three different locations.</p></div><div><h3>Results</h3><p>Approximately 90% of knee images presented excellent quality. Frequencies of nearly perfect radioanatomic alignment (IMD ≤1<!--> <!-->mm) ranged from 29% to 50%, and satisfactory alignment was found in up to 71% and 76% of the images (IMD ≤1.5<!--> <!-->mm and ≤1.7<!--> <!-->mm, respectively). Repeatability analyses yielded the following results: IMD [SD of mean difference<!--> <!-->=<!--> <!-->1.08; coefficient of variation (%CV)<!--> <!-->=<!--> <!-->54.68%; intraclass correlation coefficient (ICC) (95%CI)<!--> <!-->=<!--> <!-->0.59 (0.34–0.77)]; JSW [SD of mean difference<!--> <!-->=<!--> <!-->0.34–0.61; %CV<!--> <!-->=<!--> <!-->4.48%–9.80%; ICC (95%CI)<!--> <!-->=<!--> <!-->0.74 (0.55–0.85)–0.94 (0.87–0.97)]. Adequately reproducible measurements of IMD and JSW were found in 68% and 87% of the images, respectively.</p></div><div><h3>Conclusions</h3><p>Despite the difficulty in achieving consistent radioanatomic alignment between subsequent radiographs in terms of IMD, the protocol produced highly repeatable JSW measurements when these were taken at midpoint and 10<!--> <!-->mm from the medial extremity of the medial tibial plateau. Therefore, measurements of JSW at these locations can be considered adequate for the assessment of knee OA in ELSA-Brasil MSK.</p></div>","PeriodicalId":101096,"journal":{"name":"Revista Brasileira de Reumatologia (English Edition)","volume":"57 2","pages":"Pages 154-161"},"PeriodicalIF":0.0,"publicationDate":"2017-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rbre.2016.11.010","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34857174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}