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Safety and Predictive Factors of Short-Term Efficacy of a Single Injection of Mannitol-Modified Cross-Linked Hyaluronic Acid in Patients with Trapeziometacarpal Osteoarthritis. Results of a Multicentre Prospective Open-Label Pilot Study (INSTINCT Trial). 单次注射甘露醇修饰交联透明质酸治疗梯形骨关节炎的安全性和短期疗效的预测因素。一项多中心前瞻性开放标签试点研究(INSTINCT试验)的结果。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-06-21 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118782901
Jérémy Dauvissat, Christophe Rizzo, Henri Lellouche, Jérôme Porterie, Sylvie Melac-Ducamp, Vincent Locquet, Vincent Travers, Bernard Maillet, Thierry Conrozier

Purpose: To assess safety and search predictive factors of efficacy of a single intra-articular injection of a mannitol-modified hyaluronic acid (HA) viscosupplement, in patients having trapeziometacarpal (TMC) osteoarthritis (OA).

Methods: Patients with symptomatic TMC OA, not adequately relieved by analgesic therapy and/or by the use of a thumb splint, were included in a 3-month prospective multicentre open-label trial. All underwent plain radiographs with the Kapandji incidences allowing the Dell radiological grade assessment (1-4). Primary end point was the variation between injection (D0) and day 90 (D90) of the thumb pain (11-point Likert scale). Treatment consisted in a single injection of 0.6 to 1 mL of a viscosupplement made of a cross-linked HA combined with mannitol. All injections were performed under imaging guidance. Predictive factors of pain decrease were studied in univariate and multivariate analysis.

Results: A total of 122 patients (76% women, mean age 60, mean disease duration 36 months) were included and 120 (98%) were assessed at 3 months. The TMC OA was of Dell's grade 1, 2, 3, and 4 in 23%, 36.8%, 36.8%, and 3.5% of cases, respectively. At D0, the average (SD) pain level was 6.5 ± 1.6 without significant difference between Dell groups (P = .21). At day 90, pain decreased from 6.5 ± 1.6 to 3.9 ± 2.5 (difference -2.7 ± 2.5; -42%; P < .0001) without significant difference between Dell grade (P = .055), despite a seemingly smaller number of responders in stage 2 patients. The average analgesic consumption decreased in more than 1 out of 2 patients. In multivariate analysis, no predictor of response was identified. There was no safety issue. All adverse events (11%) were transient increase in pain during or following HA administration and resolved without sequel within 1 to 7 days.

Conclusions: This study suggests that a single course of HANOX-M-XL injection is effective in relieving pain in patients with TMC OA, without safety concern. Patients with advanced stage of OA benefit the treatment as much as those with mild or moderate OA.

目的:评估单次关节内注射甘露醇修饰透明质酸(HA)粘胶补充剂治疗斜跖骨(TMC)骨关节炎(OA)患者的安全性并寻找其疗效的预测因素。方法:通过镇痛治疗和/或使用拇指夹板不能充分缓解的症状性TMC OA患者纳入了一项为期3个月的前瞻性多中心开放标签试验。所有患者均行平片检查,Kapandji发生率允许Dell放射分级评估(1-4)。主要终点是注射(D0)和第90天(D90)拇指疼痛(11点李克特量表)之间的变化。治疗包括单次注射0.6至1ml由交联透明质酸与甘露醇联合制成的黏液补充剂。所有注射均在影像学指导下进行。对疼痛减轻的预测因素进行单因素和多因素分析。结果:共纳入122例患者(76%为女性,平均年龄60岁,平均病程36个月),120例(98%)在3个月时进行评估。TMC OA为戴尔1级、2级、3级和4级的病例分别占23%、36.8%、36.8%和3.5%。D0时,平均(SD)疼痛水平为6.5±1.6,各组间差异无统计学意义(P = 0.21)。在第90天,疼痛从6.5±1.6下降到3.9±2.5(差值-2.7±2.5;-42%;P = .055),尽管在2期患者中应答者的数量似乎较少。2例患者中有1例以上的患者镇痛药平均用量下降。在多变量分析中,没有发现反应的预测因子。没有安全问题。所有不良事件(11%)是在给药期间或之后的短暂性疼痛增加,并在1至7天内解决,无后遗症。结论:本研究提示单疗程HANOX-M-XL注射对TMC OA患者疼痛的缓解是有效的,且无安全性问题。晚期OA患者与轻度或中度OA患者一样受益于治疗。
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引用次数: 12
Short-Term Outcomes in Treatment of Knee Osteoarthritis With 4 Bone Marrow Concentrate Injections. 骨髓浓缩液4次注射治疗膝骨性关节炎的近期疗效观察。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-06-18 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118781080
Brent Shaw, Marc Darrow, Armen Derian

Background: Preliminary research suggests that bone marrow concentrate (BMC), which contains mesenchymal stem cells and platelets, is a promising treatment for knee osteoarthritis. The aim of this study was to build on this preliminary research by reporting the short-term progress of 15 patients (20 knees) with knee osteoarthritis through 4 BMC treatments.

Methods: Patients underwent four sequential BMC treatments with mean injection times of 13.80 days after the first treatment, 21.40 days after the second treatment, and 33.50 days after the third treatment. The last follow-up was conducted a mean 86 days after the first treatment. Baseline and posttreatment outcomes of resting pain, active pain, lower functionality scale, and overall improvement percentage were compared after each treatment.

Results: Patients experienced statistically significant improvements in active pain and functionality score after the first treatment. Additionally, patients experienced a mean decrease in resting pain after the first treatment, yet outcomes were not statistically significant until after the second treatment. On average, patients experienced an 84.31% decrease in resting pain, a 61.95% decrease in active pain, and a 55.68% increase in functionality score at the final follow-up. Patients also reported a mean 67% total overall improvement at study conclusion. Outcomes at the final follow-up after the fourth treatment were statistically significant compared to outcomes at baseline, after first treatment, after second treatment, and after third treatment.

Conclusions: These results are promising, and additional research with a larger sample size and longer follow-up is needed to further examine the treatment effectiveness of multiple BMC injections for knee osteoarthritis.

背景:初步研究表明,骨髓浓缩液(BMC)含有间充质干细胞和血小板,是治疗膝关节骨关节炎的一种很有前景的方法。本研究的目的是在此初步研究的基础上,报告15例膝关节骨性关节炎患者(20个膝关节)通过4种BMC治疗的短期进展。方法:患者连续4次接受BMC治疗,平均注射次数分别为第一次治疗后13.80天、第二次治疗后21.40天、第三次治疗后33.50天。最后一次随访在第一次治疗后平均86天进行。每次治疗后比较静息疼痛、活动性疼痛、低功能量表和总改善百分比的基线和治疗后结果。结果:患者在第一次治疗后活性疼痛和功能评分有统计学意义的改善。此外,患者在第一次治疗后静息疼痛平均减少,但直到第二次治疗后,结果才有统计学意义。平均而言,在最后的随访中,患者静息疼痛减少了84.31%,活动疼痛减少了61.95%,功能评分增加了55.68%。在研究结束时,患者还报告了平均67%的总体改善。与基线、第一次治疗后、第二次治疗后和第三次治疗后的结果相比,第四次治疗后最后随访的结果具有统计学意义。结论:这些结果是有希望的,需要更多的样本量更大、随访时间更长的研究来进一步检验多次BMC注射对膝关节骨关节炎的治疗效果。
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引用次数: 23
Retrocalcaneal Bursitis Precedes or Accompanies Achilles Tendon Enthesitis in the Early Phase of Rheumatoid Arthritis. 在类风湿关节炎的早期阶段,跟骨后滑囊炎先于跟腱炎或伴随跟腱炎。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-06-05 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118781094
Takeshi Suzuki, Yuka Hidaka, Yu Seri

The consecutive reports and stored images of ultrasound examinations for 100 symptomatic ankles of 74 patients with rheumatoid arthritis (RA) were reviewed for the presence or absence of retrocalcaneal bursitis (RCB) and Achilles tendon enthesitis (ATE). The ankles were classified into 4 categories based on the presence or absence of RCB or ATE. The number of RCB(-)/ATE(-), RCB(+)/ATE(-), RCB(+)/ATE(+), and RCB(-)/ATE(+) ankles was 62, 16, 12, and 10, respectively. When classifying patients into early RA and established RA, the percentage of RCB(-)/ATE(+) ankles with early RA was significantly lower than that with established RA (P = .00595). The disease duration was significantly longer in the RCB(-)/ATE(+) ankles than in the RCB(+)/ATE(-) ankles (median [interquartile range]: 15.29 [8.69] months vs 3.6 [3.06] months, P = .0247). It was speculated that RCB precedes or accompanies ATE in the early phase of RA, which suggests that entheseal inflammation in RA arises from synovial tissues.

回顾性分析74例类风湿性关节炎(RA)患者100例有症状的踝关节超声检查的连续报告和存储图像,分析其是否存在跟骨后滑囊炎(RCB)和跟腱粘连炎(ATE)。根据有无RCB或ATE将踝关节分为4类。RCB(-)/ATE(-)、RCB(+)/ATE(-)、RCB(+)/ATE(+)、RCB(+)/ATE(+)、RCB(-)/ATE(+)踝关节分别为62、16、12、10个。将患者分为早期RA和确诊RA时,早期RA患者RCB(-)/ATE(+)踝关节比例明显低于确诊RA患者(P = 0.00595)。RCB(-)/ATE(+)踝关节组的病程明显长于RCB(+)/ATE(-)踝关节组(中位数[四分位数间距]:15.29[8.69]个月vs 3.6[3.06]个月,P = 0.0247)。推测RCB在RA早期先于ATE发生或伴随ATE发生,提示RA的骨膜炎症起源于滑膜组织。
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引用次数: 5
A Pooled Analysis of Two Multicenter, Randomized Controlled Trials of a Single Intra-articular Injection of Gel-200 for Treatment of Osteoarthritis of the Knee. 单次关节内注射凝胶-200治疗膝关节骨性关节炎的两项多中心随机对照试验的汇总分析
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-05-09 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118773068
Junko Takamura, Takayuki Seo, Vibeke Strand

Background and objective: To perform an integrated analysis of 2 randomized controlled trials (RCTs) to assess the efficacy and safety of a single intra-articular injection of Gel-200 compared with phosphate buffered saline (PBS) for treatment of osteoarthritis of the knee.

Methods: Data from the intention-to-treat (ITT) populations of both RCTs were pooled for this integrated analysis. Mean changes from baseline in Western Ontario and McMaster Universities Arthritis Index (WOMAC) pain subscores were assessed using a longitudinal model; treatment differences were compared between intra-articular Gel-200 and PBS injections. Analyses included secondary outcome measures repeated at individual time points. The safety populations of both RCTs were pooled for an integrated safety analysis to compare adverse events (AEs).

Results: The pooled ITT population included 1184 subjects (649 Gel-200; 535 PBS); demographic characteristics were similar between treatment groups. Mean improvements in pain subscores from baseline to week 12 were -24.7 mm in Gel-200 and -21.8 mm in PBS groups, a statistically significant treatment group difference of -2.9 mm (P = .047). From weeks 3 to 26, mean improvements from baseline in pain subscores were -23.8 mm with Gel-200 and -20.8 mm with PBS; this treatment group difference of -3.0 mm was statistically significant (P = .017). The rate of AEs was similar between Gel-200 and PBS treatment groups.

Conclusion: This integrated analysis demonstrated the efficacy of a single intra-articular injection of Gel-200 compared with PBS for treatment of osteoarthritis of the knee over 26 weeks without major safety concerns.

Trial registration: NCT00449696 and NCT00450112.

背景和目的:对2项随机对照试验(RCTs)进行综合分析,以评估单次关节内注射Gel-200与磷酸盐缓冲盐水(PBS)治疗膝关节骨关节炎的疗效和安全性。方法:将两项随机对照试验的意向治疗(ITT)人群的数据汇总进行综合分析。使用纵向模型评估西安大略省和麦克马斯特大学关节炎指数(WOMAC)疼痛评分与基线的平均变化;比较关节内注射Gel-200和PBS的治疗差异。分析包括在个别时间点重复的次要结果测量。对两项随机对照试验的安全人群进行综合安全性分析,以比较不良事件(ae)。结果:ITT人群共纳入1184名受试者(649名Gel-200;535 PBS);治疗组间的人口学特征相似。从基线到第12周,凝胶-200组疼痛评分的平均改善为-24.7 mm, PBS组为-21.8 mm,治疗组差异有统计学意义-2.9 mm (P = 0.047)。从第3周到第26周,Gel-200组疼痛评分较基线的平均改善为-23.8 mm, PBS组为-20.8 mm;治疗组-3.0 mm差异有统计学意义(P = 0.017)。凝胶-200治疗组和PBS治疗组的ae发生率相似。结论:这项综合分析表明,与PBS相比,单次关节内注射Gel-200治疗膝关节骨关节炎的疗效超过26周,没有重大的安全性问题。试验注册号:NCT00449696和NCT00450112。
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引用次数: 4
Late Presentation of Infected Silicone Granulomas in the Lower Limb. 下肢感染性硅胶肉芽肿的晚期表现。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-02-22 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118759020
Zita M Jessop, Matthew Welck, Emily Zinser, Nicholas Garlick, Susan Hopkins

Introduction: Dermal fillers are used for multiple cosmetic indications including gluteal and thigh augmentation. Complications, although infrequent, are increasing due to the dramatic growth of dermal filler use. Our aim was to describe how the complication of infected silicone granulomas can present following lower limb augmentation.

Methods: Two cases presented with pain, oedema, and erythema at the site of previous silicone filler injection, following a considerable delay after the last injection (range 4-7 years). We collected data on their biochemistry, haematology, histology, microbiology, and imaging at the time of presentation.

Results: Complications included prolonged cellulitis with recurrent abscesses at sites of previous silicone dermal filler injection. Histology revealed infiltration of chronic inflammatory cells suggestive of silicone granuloma in both cases. Patients were reluctant to divulge use of cosmetic fillers or failed to recognise their significance given the time delay making diagnosis difficult. Delayed or recurring infections can suggest the presence of atypical organisms and we present the first reported case of silicone granuloma infection with Propionibacterium acnes.

Conclusions: Microorganisms can induce immune-mediated hypersensitivity and are believed to be the trigger for delayed activation of a quiescent foreign body to a granulomatous reaction. The substantial time delay between injection and reaction must be recognised and may be attributable to atypical microorganisms or biofilm formation. Previous antibiotic use can affect expedient microbiological diagnosis and treatment requires close collaboration with microbiologists. It is important that clinicians are aware of these important complications which are becoming more common with increased use of filler augmentation.

真皮填充物用于多种美容适应症,包括臀部和大腿增大。并发症虽然不常见,但由于真皮填充物使用的急剧增长,并发症正在增加。我们的目的是描述感染硅胶肉芽肿如何在下肢隆胸后出现并发症。方法:2例患者在最后一次注射硅胶填充物后相当长的时间(范围4-7年)出现先前注射部位的疼痛,水肿和红斑。我们收集了他们的生物化学、血液学、组织学、微生物学和影像学资料。结果:并发症包括长期蜂窝织炎和复发性脓肿在以前的硅胶真皮填充物注射部位。组织学显示慢性炎性细胞浸润提示硅胶肉芽肿。患者不愿透露使用化妆品填充物或未能认识到其重要性,因为时间延迟使得诊断困难。延迟或反复感染可以提示非典型生物体的存在,我们提出硅酮肉芽肿感染痤疮丙酸杆菌的第一例报告。结论:微生物可以诱导免疫介导的超敏反应,并被认为是触发静止异物延迟激活肉芽肿反应的触发器。必须认识到注射和反应之间的大量时间延迟,这可能归因于非典型微生物或生物膜的形成。以前使用抗生素会影响微生物诊断和治疗需要与微生物学家密切合作。重要的是,临床医生意识到这些重要的并发症,这些并发症随着填充物增加的使用变得越来越普遍。
{"title":"Late Presentation of Infected Silicone Granulomas in the Lower Limb.","authors":"Zita M Jessop,&nbsp;Matthew Welck,&nbsp;Emily Zinser,&nbsp;Nicholas Garlick,&nbsp;Susan Hopkins","doi":"10.1177/1179544118759020","DOIUrl":"https://doi.org/10.1177/1179544118759020","url":null,"abstract":"<p><strong>Introduction: </strong>Dermal fillers are used for multiple cosmetic indications including gluteal and thigh augmentation. Complications, although infrequent, are increasing due to the dramatic growth of dermal filler use. Our aim was to describe how the complication of infected silicone granulomas can present following lower limb augmentation.</p><p><strong>Methods: </strong>Two cases presented with pain, oedema, and erythema at the site of previous silicone filler injection, following a considerable delay after the last injection (range 4-7 years). We collected data on their biochemistry, haematology, histology, microbiology, and imaging at the time of presentation.</p><p><strong>Results: </strong>Complications included prolonged cellulitis with recurrent abscesses at sites of previous silicone dermal filler injection. Histology revealed infiltration of chronic inflammatory cells suggestive of silicone granuloma in both cases. Patients were reluctant to divulge use of cosmetic fillers or failed to recognise their significance given the time delay making diagnosis difficult. Delayed or recurring infections can suggest the presence of atypical organisms and we present the first reported case of silicone granuloma infection with <i>Propionibacterium acnes</i>.</p><p><strong>Conclusions: </strong>Microorganisms can induce immune-mediated hypersensitivity and are believed to be the trigger for delayed activation of a quiescent foreign body to a granulomatous reaction. The substantial time delay between injection and reaction must be recognised and may be attributable to atypical microorganisms or biofilm formation. Previous antibiotic use can affect expedient microbiological diagnosis and treatment requires close collaboration with microbiologists. It is important that clinicians are aware of these important complications which are becoming more common with increased use of filler augmentation.</p>","PeriodicalId":10443,"journal":{"name":"Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders","volume":"11 ","pages":"1179544118759020"},"PeriodicalIF":2.6,"publicationDate":"2018-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1179544118759020","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35889048","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}
引用次数: 3
Is It the Age at Disease Onset or the Disease Radiological Severity That Affects Cervical Spine Involvement in Patients With Rheumatoid Arthritis? 类风湿关节炎患者的颈椎受累与发病年龄或疾病放射学严重程度有关吗?
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-02-20 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118759688
Hanan Sayed M Abozaid, Reham Alaa El-Din Hassan, Waleed A Elmadany, Mohamed Aly Ismail, Dalia S Elgendy, Sahar A Elsayed, Rania M Gamal, Osama S Daifallah, Esam M Abu Alfadl

Background: Cervical spine involvement in patients with rheumatoid arthritis (RA) can cause pain and disability, with a variety of neurologic signs and symptoms.

Objectives: To investigate the relationship between structural cervical spine involvement in patients with RA with the age at disease onset and the degree of radiologic severity of RA measured by Larsen scoring.

Patients and methods: This cross-sectional study included 50 adult patients with RA. Patients who complained or not complained from symptoms of cervical spine involvement in RA were included; we did X-ray of the cervical spine, hands, and feet; Larsen scoring method; disease activity score (DAS28); and Neck Disability Index.

Results: The results revealed that patients with cervical involvement tend to be younger at their disease onset than those with no cervical involvement, as detected by cervical X-ray. The relation was significant P < .05 regarding all cervical involvements except for basilar invagination. Disease radiological severity (measured by Larsen score) significantly increases the risk for subaxial subluxation, P = .040. All other cervical complications of RA tend to have nonsignificant relation with disease severity. Using univariate binary regression analysis for risk factors for cervical involvement showed that the only probable risk factor for cervical involvement (detected by X-ray) in patients with RA is age at disease onset.

Conclusions: The early age at disease onset tends to affect cervical spine involvement in patients with RA more than the disease radiological severity.

背景:类风湿性关节炎(RA)患者颈椎受累可引起疼痛和残疾,并伴有多种神经系统体征和症状。目的:探讨RA患者结构性颈椎受累与发病年龄及Larsen评分法测定RA放射学严重程度的关系。患者和方法:这项横断面研究包括50名成年RA患者。包括主诉或不主诉RA颈椎受累症状的患者;我们给颈椎、手和脚做了x光检查;拉森评分法;疾病活动评分(DAS28);和颈部残疾指数。结果:宫颈x线检查显示,有宫颈受累的患者发病时比无宫颈受累的患者更年轻。P = 0.040。RA的其他颈椎并发症与病情严重程度无显著相关性。对宫颈受累危险因素的单变量二元回归分析显示,RA患者唯一可能的宫颈受累危险因素(x线检测)是发病年龄。结论:早期发病年龄对RA患者颈椎受累的影响大于疾病放射学严重程度。
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引用次数: 1
An Observational 1-Month Trial on the Efficacy and Safety of Promerim for Improving Knee Joint. Promerim改善膝关节的疗效和安全性的1个月观察性试验。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-02-11 eCollection Date: 2018-01-01 DOI: 10.1177/1179544118757496
Bekir Eray Kilinc, Yunus Oc, Gungor Alibakan, Emre Bilgin, Muharrem Kanar, Osman Tugrul Eren

Objective: This study was conducted to evaluate the efficacy and tolerability of the oral intake of promerim in the elimination of acute pain and discomfort associated with knee osteoarthritis (OA).

Methods: Single-center, 1-month, prospective, observational clinical trial. A total of 92 patients not older than 70 years were included. Patients were offered to use 720-mg promerim for the first 15 days after admission after breakfast and then 360 mg for the second 15 days. All patients were analyzed with the visual analog scale (VAS) for pain, which ranges from 0 to 10, and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score before the start of treatment and 1 month after the start. Statistical analysis was performed by SPSS 15.0 software. An α level of P < .05 was assumed to be statistically significant.

Results: This study comprised 92 patients (69 women and 23 men) with a mean age of 51.5 (range: 40-69) years. Before treatment, the mean VAS score was 5.6 ± 1.1, and after treatment, the mean VAS score was 2.6 ± 1.7. Treatment with promerim consistently showed a significant decrease in the VAS score (P < .001). The mean WOMAC score of the patients was 46.4 ± 8.2 before treatment. After treatment, the mean WOMAC score was 72.1 ± 14.4. Treatment with promerim consistently showed a significant increase in the WOMAC score (P < .001).

Conclusions: The results of this single-center, open-label clinical study demonstrate that promerim is a viable natural treatment option for treating knee OA. We recommend that 720-mg promerim taken once daily for the first 15 days after admission and 360 mg taken once daily for the next 15 days significantly and rapidly reduced composite pain and stiffness in the knee OA within 1 month.

目的:本研究旨在评估口服promerim消除膝骨关节炎(OA)相关急性疼痛和不适的疗效和耐受性。方法:单中心、1个月、前瞻性、观察性临床试验。共纳入92例年龄不超过70岁的患者。患者在入院后的前15天早餐后服用720毫克promerim,后15天服用360毫克promerim。所有患者在治疗开始前和治疗开始后1个月采用视觉模拟疼痛评分(VAS)(0 ~ 10分)和Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)评分进行分析。采用SPSS 15.0软件进行统计学分析。结果:本研究纳入92例患者(女性69例,男性23例),平均年龄51.5岁(范围:40-69岁)。治疗前平均VAS评分为5.6±1.1分,治疗后平均VAS评分为2.6±1.7分。结论:这项单中心、开放标签的临床研究结果表明,promerim是治疗膝关节OA的一种可行的天然治疗选择。我们建议在入院后的前15天每天服用一次720毫克的promerim,在接下来的15天每天服用一次360毫克,在1个月内显著并迅速地减少膝关节OA的复合疼痛和僵硬。
{"title":"An Observational 1-Month Trial on the Efficacy and Safety of Promerim for Improving Knee Joint.","authors":"Bekir Eray Kilinc,&nbsp;Yunus Oc,&nbsp;Gungor Alibakan,&nbsp;Emre Bilgin,&nbsp;Muharrem Kanar,&nbsp;Osman Tugrul Eren","doi":"10.1177/1179544118757496","DOIUrl":"https://doi.org/10.1177/1179544118757496","url":null,"abstract":"<p><strong>Objective: </strong>This study was conducted to evaluate the efficacy and tolerability of the oral intake of promerim in the elimination of acute pain and discomfort associated with knee osteoarthritis (OA).</p><p><strong>Methods: </strong>Single-center, 1-month, prospective, observational clinical trial. A total of 92 patients not older than 70 years were included. Patients were offered to use 720-mg promerim for the first 15 days after admission after breakfast and then 360 mg for the second 15 days. All patients were analyzed with the visual analog scale (VAS) for pain, which ranges from 0 to 10, and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score before the start of treatment and 1 month after the start. Statistical analysis was performed by SPSS 15.0 software. An α level of <i>P</i> < .05 was assumed to be statistically significant.</p><p><strong>Results: </strong>This study comprised 92 patients (69 women and 23 men) with a mean age of 51.5 (range: 40-69) years. Before treatment, the mean VAS score was 5.6 ± 1.1, and after treatment, the mean VAS score was 2.6 ± 1.7. Treatment with promerim consistently showed a significant decrease in the VAS score (<i>P</i> < .001). The mean WOMAC score of the patients was 46.4 ± 8.2 before treatment. After treatment, the mean WOMAC score was 72.1 ± 14.4. Treatment with promerim consistently showed a significant increase in the WOMAC score (<i>P</i> < .001).</p><p><strong>Conclusions: </strong>The results of this single-center, open-label clinical study demonstrate that promerim is a viable natural treatment option for treating knee OA. We recommend that 720-mg promerim taken once daily for the first 15 days after admission and 360 mg taken once daily for the next 15 days significantly and rapidly reduced composite pain and stiffness in the knee OA within 1 month.</p>","PeriodicalId":10443,"journal":{"name":"Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders","volume":"11 ","pages":"1179544118757496"},"PeriodicalIF":2.6,"publicationDate":"2018-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1179544118757496","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35851846","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}
引用次数: 7
A Preliminary Evaluation of the Ability of Keratotic Tissue to Act as a Prognostic Indicator of Hip Fracture Risk. 角化组织作为髋部骨折风险预后指标能力的初步评估。
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-01-16 eCollection Date: 2018-01-01 DOI: 10.1177/1179544117754050
J Renwick Beattie, Diane Feskanich, M Clare Caraher, Mark R Towler

Studies have shown that Raman spectroscopic analysis of fingernail clippings can help differentiate between post-menopausal women who have and who have not suffered a fracture. However, all studies to date have been retrospective in nature, comparing the proteins in nails sourced from women, post-fracture. The objective of this study was to investigate the potential of a prospective test for hip fracture based on spectroscopic analysis of nail tissue. Archived toenail samples from post-menopausal women aged 50 to 63 years in the Nurses' Health Study were obtained and analysed by Raman spectroscopy. Nails were matched case-controls sourced from 161 women; 82 who underwent a hip fracture up to 20 years after nail collection and 81 age-matched controls. A number of clinical risk factors (CRFs) from the Fracture Risk Assessment (FRAX) tool had been assessed at toenail collection. Using 80% of the spectra, models were developed for increasing time periods between nail collection and fracture. Scores were calculated from these models for the other 20% of the sample and the ability of the score to predict hip fracture was tested in model with and without the CRFs by comparing the odds ratios (ORs) per 1 SD increase in standardised predictive values. The Raman score successfully distinguished between hip fracture cases and controls. With only the score as a predictor, a statistically significant OR of 2.2 (95% confidence interval [CI]: 1.5-3.1) was found for hip fracture for up to 20 years after collection. The OR increased to 3.8 (2.6-5.4) when the CRFs were added to the model. For fractures limited to 13 years after collection, the OR was 6.3 (3.0-13.1) for the score alone. The test based on Raman spectroscopy has potential for identifying individuals who may suffer hip fractures several years in advance. Higher powered studies are required to evaluate the predictive capability of this test.

研究表明,指甲剪的拉曼光谱分析可以帮助区分绝经后妇女谁有和谁没有遭受骨折。然而,迄今为止所有的研究都是回顾性的,比较了女性骨折后指甲中的蛋白质。本研究的目的是探讨基于指甲组织光谱分析的髋部骨折前瞻性测试的潜力。从护士健康研究中获得50至63岁绝经后妇女的存档趾甲样本,并通过拉曼光谱进行分析。指甲与来自161名女性的病例对照相匹配;其中82人在收集指甲20年后髋部骨折,81人作为对照组。在收集趾甲时,通过骨折风险评估(FRAX)工具评估了许多临床危险因素(CRFs)。利用80%的光谱,建立了从钉采集到断裂的时间间隔增加的模型。根据这些模型计算其他20%样本的评分,并通过比较标准化预测值每增加1 SD的优势比(or),在有和没有CRFs的模型中测试评分预测髋部骨折的能力。拉曼评分成功地区分了髋部骨折病例和对照组。仅以评分作为预测因子,收集后长达20年的髋部骨折的OR为2.2(95%可信区间[CI]: 1.5-3.1),具有统计学意义。当CRFs加入到模型中时,OR增加到3.8(2.6-5.4)。对于取骨后局限于13年的骨折,仅评分的OR为6.3(3.0-13.1)。基于拉曼光谱的测试有可能提前几年识别可能遭受髋部骨折的个体。需要更有力的研究来评估该测试的预测能力。
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引用次数: 3
Total Knee Arthroplasty: Does Day of Surgery Matter? 全膝关节置换术:手术日期重要吗?
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-01-15 eCollection Date: 2018-01-01 DOI: 10.1177/1179544117754067
Azeem Tariq Malik, Shahid Khan, Arif Ali, Syed Hamza Mufarrih, Shahryar Noordin

Introduction: There has been an influx of research studies aimed at identifying all factors that contribute to minimizing cost and maximizing postoperative care after total knee arthroplasty (TKA). Length of stay (LOS) has been defined as a significant factor that contributes to increased burden. We aimed at looking whether day of surgery has any significant effect on the LOS and postoperative complications following total knee arthroplasty (TKA).

Materials and methods: Retrospective cohort study done at the Aga Khan University Hospital, Pakistan, from January 2007 to December 2015. A total of 611 patients who underwent a unilateral or bilateral total knee arthroplasty (TKA) were included in study: 269 (44.0%) patients underwent unilateral TKA and 342 (56.0%) underwent a bilateral TKA.

Results: Kruskal-Wallis test and post hoc pairwise comparisons showed that unilateral TKAs performed on Tuesday, Saturday, and Sunday resulted in a lower median LOS (P < .05). No significant association was seen in bilateral TKA group. Day of surgery was not associated with postoperative complications.

Conclusions: Unilateral TKAs performed earlier during the week and later on the weekend are associated with a significantly lower LOS. It is highly probable that patch ancillary services during the latter part of the week and a higher workload for the staff are important reasons for this phenomenon.

导论:有大量的研究旨在确定全膝关节置换术(TKA)后成本最小化和术后护理最大化的所有因素。停留时间被定义为造成负担增加的一个重要因素。我们的目的是观察手术日期是否对全膝关节置换术(TKA)后LOS和术后并发症有显著影响。材料和方法:2007年1月至2015年12月在巴基斯坦阿迦汗大学医院进行回顾性队列研究。研究共纳入611例接受单侧或双侧全膝关节置换术(TKA)的患者:269例(44.0%)患者接受单侧全膝关节置换术,342例(56.0%)患者接受双侧全膝关节置换术。结果:Kruskal-Wallis检验和事后两两比较显示,在周二、周六和周日进行的单侧tka导致较低的中位LOS (P结论:在本周早些时候和周末晚些时候进行的单侧tka与显著较低的LOS相关。造成这种现象的重要原因很可能是一周后半段的补丁辅助服务和工作人员的工作量增加。
{"title":"Total Knee Arthroplasty: Does Day of Surgery Matter?","authors":"Azeem Tariq Malik,&nbsp;Shahid Khan,&nbsp;Arif Ali,&nbsp;Syed Hamza Mufarrih,&nbsp;Shahryar Noordin","doi":"10.1177/1179544117754067","DOIUrl":"https://doi.org/10.1177/1179544117754067","url":null,"abstract":"<p><strong>Introduction: </strong>There has been an influx of research studies aimed at identifying all factors that contribute to minimizing cost and maximizing postoperative care after total knee arthroplasty (TKA). Length of stay (LOS) has been defined as a significant factor that contributes to increased burden. We aimed at looking whether day of surgery has any significant effect on the LOS and postoperative complications following total knee arthroplasty (TKA).</p><p><strong>Materials and methods: </strong>Retrospective cohort study done at the Aga Khan University Hospital, Pakistan, from January 2007 to December 2015. A total of 611 patients who underwent a unilateral or bilateral total knee arthroplasty (TKA) were included in study: 269 (44.0%) patients underwent unilateral TKA and 342 (56.0%) underwent a bilateral TKA.</p><p><strong>Results: </strong>Kruskal-Wallis test and post hoc pairwise comparisons showed that unilateral TKAs performed on Tuesday, Saturday, and Sunday resulted in a lower median LOS (<i>P</i> < .05). No significant association was seen in bilateral TKA group. Day of surgery was not associated with postoperative complications.</p><p><strong>Conclusions: </strong>Unilateral TKAs performed earlier during the week and later on the weekend are associated with a significantly lower LOS. It is highly probable that patch ancillary services during the latter part of the week and a higher workload for the staff are important reasons for this phenomenon.</p>","PeriodicalId":10443,"journal":{"name":"Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders","volume":"11 ","pages":"1179544117754067"},"PeriodicalIF":2.6,"publicationDate":"2018-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1179544117754067","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35768482","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}
引用次数: 6
The Protein Tyrosine Phosphatase Nonreceptor 22 (PTPN22) R620W Functional Polymorphism in Psoriasis. 蛋白酪氨酸磷酸酶非受体22 (PTPN22) R620W在银屑病中的功能多态性
IF 2.6 Q2 ORTHOPEDICS Pub Date : 2018-01-11 eCollection Date: 2018-01-01 DOI: 10.1177/1179544117751434
Ghaleb Bin Huraib, Fahad Al Harthi, Misbahul Arfin, Sadaf Rizvi, Abdulrahaman Al-Asmari

Background: Psoriasis is a complex autoimmune disease caused by the interaction of genetic and environmental factors. PTPN22 gene polymorphism has been reported to affect psoriasis susceptibility; however, no data are available for Middle Eastern populations.

Objective: The aim of this study was to investigate the association of PTPN22 (1858C/T) R620W polymorphism with psoriasis in a Saudi cohort.

Methods: Saudi subjects (n = 306) including patients with psoriasis (n = 106) and matched controls (n = 200) were studied for PTPN22 variants using tetra-primer amplification refractory mutation system-polymerase chain reaction method. The frequencies of alleles and genotypes of PTPN22 (1858C/T) polymorphism were compared between patients and controls.

Results: The frequency of CT genotype of PTPN22 (1858C/T) polymorphism was significantly higher, whereas that of CC genotype was lower in patients with psoriasis than in controls (P < .001, relative risk [RR] = 7.151). The homozygous genotype TT was absent in both the patients and healthy controls. The frequency of allele T encoding tryptophan (W) was significantly increased (P < .001, RR = 5.76), whereas that of allele C encoding arginine (R) decreased in psoriasis cases as compared with controls (P < .001, RR = 0.173) indicating that individuals carrying allele T are more susceptible to psoriasis than noncarriers.

Conclusions: PTPN22 (1858C/T) polymorphism is positively associated with susceptibility of psoriasis in Saudis and can be developed as biomarker for evaluating psoriasis risk. However, further studies on PTPN22 polymorphism in larger samples from different geographical areas and ethnicity are warranted.

背景:银屑病是遗传和环境因素共同作用下的一种复杂的自身免疫性疾病。PTPN22基因多态性与银屑病易感性有关;然而,没有关于中东人口的数据。目的:本研究的目的是研究沙特队列中PTPN22 (1858C/T) R620W多态性与牛皮癣的关系。方法:采用四引物扩增难解突变系统-聚合酶链反应法对沙特受试者(306例)进行PTPN22变异检测,其中包括牛皮癣患者(106例)和匹配对照(200例)。比较两组患者PTPN22 (1858C/T)多态性的等位基因频率和基因型。结果:银屑病患者PTPN22 (1858C/T)基因型的CT基因型频率显著高于对照组,而CC基因型的频率明显低于对照组(P P P)结论:PTPN22 (1858C/T)基因型多态性与银屑病易感性呈正相关,可作为评价银屑病风险的生物标志物。然而,PTPN22多态性的进一步研究需要来自不同地理区域和种族的更大样本。
{"title":"The Protein Tyrosine Phosphatase Nonreceptor 22 (<i>PTPN22</i>) R620W Functional Polymorphism in Psoriasis.","authors":"Ghaleb Bin Huraib,&nbsp;Fahad Al Harthi,&nbsp;Misbahul Arfin,&nbsp;Sadaf Rizvi,&nbsp;Abdulrahaman Al-Asmari","doi":"10.1177/1179544117751434","DOIUrl":"https://doi.org/10.1177/1179544117751434","url":null,"abstract":"<p><strong>Background: </strong>Psoriasis is a complex autoimmune disease caused by the interaction of genetic and environmental factors. <i>PTPN22</i> gene polymorphism has been reported to affect psoriasis susceptibility; however, no data are available for Middle Eastern populations.</p><p><strong>Objective: </strong>The aim of this study was to investigate the association of PTPN22 (1858C/T) R620W polymorphism with psoriasis in a Saudi cohort.</p><p><strong>Methods: </strong>Saudi subjects (n = 306) including patients with psoriasis (n = 106) and matched controls (n = 200) were studied for <i>PTPN22</i> variants using tetra-primer amplification refractory mutation system-polymerase chain reaction method. The frequencies of alleles and genotypes of PTPN22 (1858C/T) polymorphism were compared between patients and controls.</p><p><strong>Results: </strong>The frequency of CT genotype of PTPN22 (1858C/T) polymorphism was significantly higher, whereas that of CC genotype was lower in patients with psoriasis than in controls (<i>P </i>< .001, relative risk [RR] = 7.151). The homozygous genotype TT was absent in both the patients and healthy controls. The frequency of allele T encoding tryptophan (W) was significantly increased (<i>P </i>< .001, RR = 5.76), whereas that of allele C encoding arginine (R) decreased in psoriasis cases as compared with controls (<i>P </i>< .001, RR = 0.173) indicating that individuals carrying allele T are more susceptible to psoriasis than noncarriers.</p><p><strong>Conclusions: </strong>PTPN22 (1858C/T) polymorphism is positively associated with susceptibility of psoriasis in Saudis and can be developed as biomarker for evaluating psoriasis risk. However, further studies on PTPN22 polymorphism in larger samples from different geographical areas and ethnicity are warranted.</p>","PeriodicalId":10443,"journal":{"name":"Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders","volume":"11 ","pages":"1179544117751434"},"PeriodicalIF":2.6,"publicationDate":"2018-01-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1179544117751434","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35749426","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}
引用次数: 9
期刊
Clinical Medicine Insights. Arthritis and Musculoskeletal Disorders
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