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Nature and Treatment Received for Psoriasis and Co-morbidities in Patients with Psoriatic Arthritis. A Multi-centre Observational Study from Western India 银屑病的性质和治疗方法以及银屑病关节炎患者的并发症。印度西部的一项多中心观察研究
IF 0.7 Q4 Medicine Pub Date : 2024-02-19 DOI: 10.1177/09733698241229943
Soham Kadam, P. Jadhav, Asna Shaikh, Sushant Shinde, Varsha Bagul, J. Oak, Nilesh Nolkha, C. Balakrishnan, Priti Nagnur Mehta, Shubhada Kalke, K. Bhojani, Rohini Samant
Many recent studies have suggested a changing paradigm of management of psoriatic disease. One of the main concerns is the lost opportunity of controlling ‘psoriatic disease’ during the early phase, especially when the disease is limited to the skin. The study’s main aim was to determine psoriasis (PsO) treatment before the patient’s presentation to the rheumatologist. We also studied the associated comorbidities in these patients. This was a cross-sectional study done at eight centres. Data was collected from 375 patients with psoriatic arthritis (PsA) about their demography, details of psoriatic lesions, treatment taken for them, additional co-morbidities and pattern of PsA. Only 22.4% of patients had received oral methotrexate for PsO: the majority for less than a year. Plaque and scalp PsO were the most common, and 75% of patients had body surface area involvement greater than 5%. There was a significantly higher prevalence of type II diabetes mellitus (T2DM) (24% vs. 9.1%) and obesity as compared to the general population. Few patients received sustained systemic treatment for PsO prior to the development of arthritis. There was a significant association of co-morbidities such as T2DM and obesity with PsA.
最近的许多研究表明,银屑病的治疗模式正在发生变化。其中一个主要问题是,在早期阶段失去了控制 "银屑病 "的机会,尤其是当疾病局限于皮肤时。这项研究的主要目的是在患者向风湿免疫科医生求诊之前确定银屑病(PsO)的治疗方法。我们还研究了这些患者的相关合并症。这是一项在八个中心进行的横断面研究。我们从 375 名银屑病关节炎(PsA)患者中收集了有关其人口统计学、银屑病皮损详情、所接受的治疗、其他并发症和 PsA 模式的数据。只有 22.4% 的患者接受过口服甲氨蝶呤治疗银屑病,其中大多数患者的治疗时间不到一年。斑块型和头皮型PsO最为常见,75%的患者体表受累面积超过5%。与普通人群相比,II型糖尿病(T2DM)(24%对9.1%)和肥胖症的发病率明显更高。很少有患者在出现关节炎之前接受过持续的系统治疗。T2DM和肥胖等并发症与PsA有明显关联。
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引用次数: 0
Prevalence and Clinical Associations of Anti-C1q Antibodies in Paediatric Systemic Lupus Erythematosus in Indian Children 抗 C1q 抗体在印度儿童系统性红斑狼疮中的患病率和临床关联性
IF 0.7 Q4 Medicine Pub Date : 2024-02-19 DOI: 10.1177/09733698241229918
G. Vettiyil, Anu Punnen K., J. Prakash, V. Jayaseelan, Sathish Kumar
Paediatric systemic lupus erythematosus (pSLE) is a heterogeneous, chronic autoimmune disease characterised by multi-system inflammation and the production of antibodies-directed self-antigens. Anti-C1q has been associated with SLE as well as other connective tissue diseases. They have been considered as a marker for disease activity and the presence of nephritis. To determine the prevalence of anti-C1q antibodies in the paediatric SLE and to determine clinical associations of elevated anti-C1q antibody levels, especially with lupus nephritis. All consecutive children with SLE on treatment with immunosuppressive drugs attending our clinic were recruited. After obtaining informed consent, blood samples were tested for anti-C1q antibodies by a commercially available ELISA kit. The prevalence of anti-C1q and its association with lupus nephritis were determined. Out of a total 150 children with SLE, anti-C1q positivity was present in 95 children (64%), at a cut-off value of 20 U/mL. Children with proteinuria, low C3, low C4 and anti-dsDNA positivity had significantly more anti-C1q antibody positivity. Children with lupus nephritis were significantly more likely to have anti-C1q antibody positivity than children without renal involvement (74% vs. 51%, p = .02). Among the children with lupus nephritis, children with active renal disease were more likely to have anti-C1q positivity than in children with quiescent disease (88% vs. 53%, p = .002). Anti-C1q antibodies had a sensitivity of 74% and specificity of 54% at a cut-off value of 22 U/L for renal disease in pSLE. In our study, children with lupus nephritis were significantly associated with elevated anti-C1q antibodies, and children with active renal disease had higher anti-C1q positivity than those with quiescent disease. Anti-C1q levels showed significant associations with low C3, low C4 and anti-dsDNA positivity. Anti-C1q levels did not show significant associations with clinical features of SLE like malar rash, arthritis and CNS involvement. Anti-C1q antibody titres were found to have a positive correlation with renal disease and hence could be used as an adjunctive biomarker in monitoring the disease activity in children with lupus nephritis.
小儿系统性红斑狼疮(pSLE)是一种异质性慢性自身免疫性疾病,其特点是多系统炎症和产生抗体指向自身抗原。抗 C1q 与系统性红斑狼疮和其他结缔组织疾病有关。它们被认为是疾病活动和肾炎存在的标志物。目的:确定抗 C1q 抗体在儿童系统性红斑狼疮中的流行率,并确定抗 C1q 抗体水平升高的临床关联,尤其是与狼疮肾炎的关联。我们招募了所有在本诊所接受免疫抑制剂治疗的系统性红斑狼疮患儿。在获得知情同意后,使用市售的酶联免疫吸附试剂盒对血样进行抗C1q抗体检测。测定抗C1q抗体的流行率及其与狼疮肾炎的关系。在总共 150 名系统性红斑狼疮患儿中,95 名患儿(64%)的抗 C1q 阳性,临界值为 20 U/mL。蛋白尿、低C3、低C4和抗dsDNA阳性的儿童抗C1q抗体阳性率明显更高。狼疮性肾炎患儿抗 C1q 抗体阳性率明显高于无肾脏受累的患儿(74% 对 51%,P = 0.02)。在狼疮肾炎患儿中,活动性肾病患儿的抗C1q抗体阳性率高于静止期患儿(88% 对 53%,P = .002)。以22 U/L为临界值,抗C1q抗体对狼疮肾病的敏感性为74%,特异性为54%。在我们的研究中,狼疮肾炎患儿的抗C1q抗体升高与活动性肾病患儿的抗C1q抗体阳性率显著相关,且活动性肾病患儿的抗C1q抗体阳性率高于静止期患儿。抗C1q水平与低C3、低C4和抗dsDNA阳性率有明显相关性。抗C1q水平与系统性红斑狼疮的临床特征(如鳞状皮疹、关节炎和中枢神经系统受累)无明显关联。研究发现,抗 C1q 抗体滴度与肾脏疾病呈正相关,因此可用作监测狼疮肾炎患儿疾病活动的辅助生物标志物。
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引用次数: 0
Clinical and Serological Associations of Subclinical Atherosclerosis in Spondyloarthropathy 脊柱关节病亚临床动脉粥样硬化的临床和血清学相关性
IF 0.7 Q4 Medicine Pub Date : 2024-02-18 DOI: 10.1177/09735984241229873
M. Rai, N. Jain, N. Mohindra, Sudeep Kumar, V. Agarwal, D. Misra
Patients with spondyloarthropathy (SpA) have a higher risk of subclinical atherosclerosis (SCA). We assessed clinical and serological determinants of SCA in Indian SpA patients. Patients with SpA (fulfilling ASAS 2010 criteria; n = 104) attending our hospital were recruited; mean carotid intima-media thickness (CIMT) was performed by carotid ultrasonography, along with clinical assessment and traditional risk factor evaluation. Microparticles were extracted from plasma and total, as well as endothelial microparticles (EMP), platelet microparticles, T lymphocyte microparticles and B lymphocyte microparticles, were analysed by flow cytometry. Serum samples were analysed for inflammatory cytokines previously implicated in atherosclerosis, namely interleukin 1β (IL-1β), IL-6, IL-17, IL-27, IL-33 and tumour necrosis factor-alpha. Thirty-eight healthy controls were used for comparison. Subgroup analyses compared parameters between SpA with SCA (i.e., with carotid plaque or more than 75th percentile of CIMT for that age and sex in the Indian population) versus those without SCA. Ethical approval and written, informed consent were obtained. Despite significantly younger age, lower body mass index and higher total cholesterol in controls compared to SpA, those with SpA had higher CIMT. Traditional cardiovascular risk factors (older age, higher waist-hip ratio) and novel markers of inflammation (serum IL-1β, IL-6) were associated with SCA. While total microparticles, EMP, T lymphocyte and B lymphocyte microparticles were increased in SpA than in healthy controls, they were not associated with SCA. Traditional risk factors and serum inflammatory cytokines IL-1β and IL-6 are associated with higher SCA in Indian SpA patients.
脊柱关节病(SpA)患者发生亚临床动脉粥样硬化(SCA)的风险较高。我们评估了印度SpA患者SCA的临床和血清学决定因素。我们招募了在本医院就诊的 SpA 患者(符合 ASAS 2010 标准;n = 104);通过颈动脉超声波检查了平均颈动脉内膜中层厚度 (CIMT),同时进行了临床评估和传统风险因素评估。从血浆中提取微粒,并通过流式细胞术分析总微粒、内皮微粒(EMP)、血小板微粒、T淋巴细胞微粒和B淋巴细胞微粒。血清样本中的炎症细胞因子,即白细胞介素 1β (IL-1β)、IL-6、IL-17、IL-27、IL-33 和肿瘤坏死因子-α,以前曾与动脉粥样硬化有关。38名健康对照者被用来进行比较。亚组分析比较了伴有SCA的SpA(即伴有颈动脉斑块或CIMT超过印度人口中该年龄和性别的第75百分位数)和不伴有SCA的SpA之间的参数。该研究获得了伦理批准和书面知情同意。尽管与SpA患者相比,对照组患者的年龄明显更小、体重指数更低且总胆固醇更高,但SpA患者的CIMT更高。传统的心血管风险因素(年龄较大、腰臀比较高)和新型炎症标记物(血清IL-1β、IL-6)与SCA相关。与健康对照组相比,SpA 患者的总微粒、EMP、T 淋巴细胞和 B 淋巴细胞微粒均有所增加,但它们与 SCA 无关。传统风险因素和血清炎性细胞因子 IL-1β 和 IL-6 与印度 SpA 患者较高的 SCA 相关。
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引用次数: 0
Distinguishing Between IgG4-related Disease and Erdheim-Chester Disease: A Challenging Diagnostic Journey 区分 IgG4 相关疾病与埃尔德海姆-切斯特病:充满挑战的诊断之旅
IF 0.7 Q4 Medicine Pub Date : 2024-02-18 DOI: 10.1177/09733698241229797
Dogga Prasanna Kumar, K. Chandwar, D. Ekbote, J. Dixit, K. Kishor, Puneet Kumar, U. Dhakad
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引用次数: 0
Clinical Profile of Acute Methotrexate Toxicity in Rheumatic Diseases: A Series of 15 Cases 风湿病急性甲氨蝶呤中毒的临床概况:15 例系列病例
IF 0.7 Q4 Medicine Pub Date : 2024-02-18 DOI: 10.1177/09733698241229913
Prakashini Mruthyunjaya, D. Maikap, Biswajit Bhuyan, Sakir Ahmed, Ramnath Misra, Ratikanta Tripathy, P. Padhan
Methotrexate (MTX) at a dose of ≤25 mg/week is one of the most prescribed disease-modifying anti-rheumatic drugs (DMARDs) in a variety of rheumatic diseases. It can potentially cause life-threatening neutropenic sepsis, and acute renal and hepatotoxicity when taken inadvertently at high doses. We aim to analyse the clinical profile and risk factors of patients who presented with acute MTX toxicity. All patients presenting to the Rheumatology department with a history of inadvertent consumption of higher doses of MTX (>25 mg/week), from July 2021 to May 2023 were included. Additional data was extracted from hospital electronic medical health records. The clinical profile, risk factors, and outcome of patients with MTX toxicity were analysed. The median age of the patients in our cohort was 52 IQR (40–62.5) years, with 80% females. The median cumulative dose of MTX was 120 mg (IQR 95–150). The reason for overdose in our cohort was medication error in comprehending once-weekly dosing. The most common major adverse event was neutropenia (80%). All our patients had stomatitis, with half of them having oral bleeding. Gastrointestinal adverse events like vomiting and diarrhoea were seen in 60% and 13% of the patients, respectively. Our cohort had two patients who succumbed to the complications due to neutropenic sepsis. The dose of MTX did not correlate with the severity of the disease or duration of hospital stay; however, the latter was significantly influenced by lower absolute neutrophil count (ANC). Acute MTX toxicity is one of the severe rheumatological emergencies and the toxicity profile includes haematological, gastrointestinal, hepatic, and renal adverse events. Severe neutropenia leading to sepsis can be fatal if not intervened early.
甲氨蝶呤(MTX)的剂量≤25 毫克/周,是治疗各种风湿性疾病的最常用抗风湿药(DMARDs)之一。如果不慎大剂量服用,有可能导致危及生命的中性粒细胞败血症以及急性肾毒性和肝毒性。我们旨在分析出现 MTX 急性中毒的患者的临床特征和风险因素。我们纳入了 2021 年 7 月至 2023 年 5 月期间所有到风湿病科就诊并无意中服用过大剂量 MTX(>25 毫克/周)的患者。其他数据来自医院电子医疗健康记录。分析了MTX毒性患者的临床概况、风险因素和预后。队列中患者的中位年龄为52 IQR(40-62.5)岁,80%为女性。MTX累积剂量的中位数为120毫克(IQR 95-150)。在我们的队列中,用药过量的原因是理解每周一次的剂量时出现用药错误。最常见的主要不良反应是中性粒细胞减少(80%)。所有患者都患有口腔炎,其中半数患者有口腔出血。分别有 60% 和 13% 的患者出现呕吐和腹泻等胃肠道不良反应。我们的队列中有两名患者因中性败血症并发症而死亡。MTX的剂量与疾病的严重程度或住院时间无关;但住院时间则受中性粒细胞绝对计数(ANC)降低的显著影响。MTX急性毒性是严重的风湿病急症之一,其毒性特征包括血液、胃肠道、肝脏和肾脏不良反应。如果不及早干预,导致败血症的严重中性粒细胞减少症可能是致命的。
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引用次数: 0
The Epidemiology of Rheumatic Diseases in India 印度的风湿病流行病学
IF 0.7 Q4 Medicine Pub Date : 2024-02-18 DOI: 10.1177/09733698241229779
DurgaPrasanna Misra, Aman Sharma, B. Dharmanand, S. Chandrashekara
Epidemiological studies, referred to as the Community Oriented Program for Control of Rheumatic Diseases (COPCORD) studies, have been conducted under the aegis of the International League against Rheumatism and the World Health Organization to evaluate the epidemiology of rheumatic and musculoskeletal (RMSK) diseases in India. These COPCORD studies conducted in rural Bhigwan and urban Pune in Maharashtra, rural Calicut and rural Trivandrum in Kerala and rural and urban Lucknow in Uttar Pradesh, along with data from the Global Burden of Diseases study have helped to understand the burden of rheumatic diseases in the community. Based on these studies, RMSK diseases, which are amongst the top 25 causes of disability in the Indian population, are prevalent in nearly 25%–30% of the Indian population. The common rheumatic diseases in the community are soft tissue rheumatism, neck and back pain, fibromyalgia and unspecified pains and osteoarthritis (most commonly affecting the knee). These diseases most commonly affect young persons between the third to the fifth decade of life, more often affect females, are prevalent in both rural and urban populations, and account for considerable disability in up to one-fifth of individuals leading to loss of livelihood and dependence on others for self-care. Community-based national healthcare programs to manage RMSK diseases at the community level are urgently needed. There also remains an unmet need to train more doctors to diagnose and manage rheumatic diseases at the primary, secondary and tertiary levels of care.
在国际风湿病联盟和世界卫生组织的支持下,印度开展了流行病学研究,即风湿病控制社区导向计划(COPCORD)研究,以评估印度风湿病和肌肉骨骼疾病(RMSK)的流行病学情况。COPCORD 在马哈拉施特拉邦的比格旺农村和浦那城市、喀拉拉邦的卡利卡特农村和特里凡得琅农村以及北方邦的勒克瑙农村和城市进行了研究,这些研究以及全球疾病负担研究的数据有助于了解风湿病在社区造成的负担。根据这些研究,印度人口中有近 25%-30% 的人患有风湿性关节炎疾病,这些疾病是导致印度人口残疾的 25 大原因之一。社区中常见的风湿病包括软组织风湿病、颈部和背部疼痛、纤维肌痛和不明原因的疼痛以及骨关节炎(最常影响膝关节)。这些疾病最常见于三至五十年代的年轻人,多发于女性,在农村和城市人口中都很普遍,造成多达五分之一的人严重残疾,导致他们失去生计并依赖他人进行自我护理。目前急需开展以社区为基础的国家医疗保健计划,在社区一级管理 RMSK 疾病。此外,培训更多医生在初级、二级和三级医疗机构诊断和管理风湿性疾病的需求仍未得到满足。
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引用次数: 0
Clinical and Serological Associations of Subclinical Atherosclerosis in Systemic Sclerosis 系统性硬化症亚临床动脉粥样硬化的临床和血清学相关性
IF 0.7 Q4 Medicine Pub Date : 2024-02-18 DOI: 10.1177/09733698241229901
H. Gangadharan, M. Rai, N. Jain, N. Mohindra, Sudeep Kumar, Vikas Agarwal, D. Misra
While patients with systemic sclerosis (SSc) are predisposed to cardiovascular events, data regarding this from India is sparse. We analysed correlates of subclinical atherosclerosis in Indian patients with SSc. Patients with SSc fulfilling the 2013 classification criteria ( n = 61) were recruited after obtaining written informed consent. Clinical risk factors for cardiovascular disease (CVD) were assessed. A carotid ultrasound was performed to assess the mean carotid intima-media thickness (CIMT). Total and endothelial microparticles (EMP, positive for CD31 and CD146) were estimated from plasma. Serum cytokines known to play a role in atherosclerosis (interleukin-1β [IL-1β], tumour necrosis factor-alpha, IL-6 and IL-17) were assessed. Forty-one age- and sex-similar healthy controls were recruited for comparison. Clinical and serological risk factors for CVD were compared between SSc with and without carotid plaque. Linear regression analyses were conducted to identify predictors of CIMT and carotid plaque in SSc. Patients with SSc had lower body-mass index than healthy controls, however, had higher CIMT, higher serum IL-1β, IL-6, total microparticles and EMP than control subjects. SSc with carotid plaque ( n = 13) were older, and more likely to be male, but demonstrated no differences in serological markers of CVD. On multivariable-adjusted regression analyses, age was the only significant predictor of CIMT in SSc and male sex was the only significant predictor of carotid plaque in SSc. Carotid plaques were present in one-fifth of young patients with SSc. Older age and male sex predicted a higher risk of subclinical atherosclerosis in SSc.
虽然系统性硬化症(SSc)患者容易发生心血管事件,但印度的相关数据却很少。我们分析了印度 SSc 患者亚临床动脉粥样硬化的相关因素。在获得书面知情同意后,我们招募了符合 2013 年分类标准的 SSc 患者(n = 61)。评估了心血管疾病(CVD)的临床风险因素。进行颈动脉超声检查以评估平均颈动脉内膜中层厚度(CIMT)。从血浆中估算出总微粒和内皮微粒(EMP,CD31和CD146阳性)。对已知在动脉粥样硬化中发挥作用的血清细胞因子(白细胞介素-1β [IL-1β]、肿瘤坏死因子-α、IL-6 和 IL-17)进行了评估。同时还招募了 41 名年龄和性别相似的健康对照者进行对比。比较了有颈动脉斑块和无颈动脉斑块的 SSc 患者的心血管疾病临床和血清学风险因素。进行了线性回归分析,以确定SSc患者CIMT和颈动脉斑块的预测因素。与健康对照组相比,SSc患者的体重指数较低,但CIMT、血清IL-1β、IL-6、总微粒和EMP均高于对照组。患有颈动脉斑块的SSc(n = 13)年龄更大,更可能是男性,但在心血管疾病血清学标志物方面没有表现出差异。在多变量调整回归分析中,年龄是预测 SSc 患者 CIMT 的唯一重要因素,男性是预测 SSc 患者颈动脉斑块的唯一重要因素。五分之一的年轻 SSc 患者存在颈动脉斑块。年龄越大、性别越男,SSc亚临床动脉粥样硬化的风险越高。
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引用次数: 0
Evolving Trends in Rheumatoid Arthritis Care: A Two-decade Analysis From Single Tertiary Health Care Centre 类风湿关节炎护理的演变趋势:来自单一三级医疗保健中心的二十年分析
IF 0.7 Q4 Medicine Pub Date : 2024-02-15 DOI: 10.1177/09733698241229939
P. Sagdeo, S. Yadav, C. Balakrishnan
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引用次数: 0
Tongue Ulcer as the Presenting Feature of Granulomatosis with Polyangiitis 舌溃疡是肉芽肿伴多血管炎的表现特征
IF 0.7 Q4 Medicine Pub Date : 2024-02-13 DOI: 10.1177/09733698241229802
Prakashini Mruthyunjaya, D. Maikap, Lipsa Bhuyan, P. Padhan
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引用次数: 0
Delay in Referral to Specialty Care in Patients with Spondyloarthropathy and Psoriatic Arthritis in India: IRA Database Report 印度脊柱关节病和银屑病患者转诊专科治疗的延迟:IRA 数据库报告
IF 0.7 Q4 Medicine Pub Date : 2024-02-13 DOI: 10.1177/09733698241229759
Chandrashekara S, Padmanabha D. Shenoy, Uma Kumar, S. Pandya, Alakendu Ghosh, Apurva Khare, R. Dudam, D. Danda, R. Goswami
The present study is intended to evaluate the factors influencing the diagnostic and rheumatology care referral delay in patients with spondyloarthropathy (SpA) and psoriatic arthritis (PsA) in India. The independent prospective, multicentre, observational study collected data from 8 centres across India through the database created by the Indian Rheumatology Association (IRA). Modified Prasad scale was used for socio-economic classification based on the patient’s income. The data of PsA and SpA were analysed separately, and the causes were compared using t-test for continuous variables and chi-square and Fisher’s exact tests for categorical variables. The mean referral delay noted for PsA and SpA subjects were 16.3±34.35 and 17.48±33.59 (IQR 24 and 34) months, respectively. Majority of the PsA patients and about 65% of SpA subjects reported a lack of awareness of the rheumatology specialty as the major reason for the delay. Another major reason was management by other specialists instead of rheumatologists (65% and 74% respectively). Approximately 8% of patients in both disease groups had no faith in modern care due to perceived elevated risk of adverse effects. SpA patients with improved socio-economic status had a higher proportion of subjects seeking specialty care. A direct association was noted between professional skill and early access to specialty care for both PsA and SpA patients. The lack of awareness of rheumatology as a specialty and patients being managed by other specialties are the two major reasons for delayed referral of SpA and PsA. Additionally, a patient’s economic and skill level can influence their ability to access specialty care.
本研究旨在评估影响印度脊柱关节病(SpA)和银屑病关节炎(PsA)患者诊断和风湿病治疗转诊延迟的因素。这项独立的前瞻性多中心观察研究通过印度风湿病学协会(IRA)建立的数据库收集了印度8个中心的数据。根据患者的收入,采用改良普拉萨德量表进行社会经济分类。PsA和SpA的数据分别进行分析,连续变量采用t检验,分类变量采用卡方检验和费雪精确检验。PsA和SpA受试者的平均转诊延迟时间分别为16.3±34.35和17.48±33.59(IQR为24和34)个月。大多数 PsA 患者和约 65% 的 SpA 患者表示,对风湿病专科缺乏了解是延误转诊的主要原因。另一个主要原因是由其他专科医生而不是风湿免疫科医生进行治疗(分别占 65% 和 74%)。两组疾病中约有 8% 的患者因认为不良反应风险较高而对现代医疗失去信心。社会经济地位较高的 SpA 患者寻求专科治疗的比例较高。研究发现,PsA 和 SpA 患者的专业技能与尽早获得专科治疗有直接关系。缺乏对风湿病学这一专科的认识以及患者由其他专科管理是导致 SpA 和 PsA 转诊延迟的两个主要原因。此外,患者的经济和技术水平也会影响他们获得专科治疗的能力。
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引用次数: 0
期刊
Indian Journal of Rheumatology
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