关节镜治疗难治性髌前滑囊炎30例临床分析

目的探讨改进关节镜下治疗难治性髌前滑囊炎的疗效。方法自2009年6月~2014年5月对我院30例复发髌前滑囊炎患者,男22例,女8例。囊肿最大为8cm×12cm,最小为4cm×5cm,全部病例均在关节镜下手术治疗,平均手术时间为30分钟,术后固定2周。膝关节疼痛评价按采用视觉模拟评分法(visual analogue scale,VAS)评分、膝关节关节活动度(ROM)对术前、术后3、6、12、24、36个月随访时功能进行评价。结果术后随访,全部患者均无感染,无肿胀,关节活动正常,全部病例术后膝关节疼痛显著缓解,活动显著改善。仅有1例患者残留有膝前疼痛,1例患者局部皮肤有麻木感。结论关节镜下保守治疗髌前滑囊炎,美容效果和功能效果满意,适合临床开展。     

Intra-articular morphine and postoperative analgesia after knee arthroscopy

The aim of this study was to evaluate the postoperative analgesic effect of intra-articular administration of a low- and a high-dose morphine solution after knee arthroscopy. Thirty patients who underwent diagnostic arthroscopy or arthroscopic meniscectomy were allocated in three groups. At the end of the arthroscopic procedure patients in Group A received intra-articularly 20 ml normal saline (N/S), Group B received 5 mg morphine in 20 ml N/S and Group C received 15 mg morphine in 20 ml N/S. The postoperative pain was assessed using a visual analogue scale for 24 h, while all the patients stayed at hospital. Side effects from the central action of opioids were not detected. Although the pain scores in the group of low-dose morphine were lower than in the control group, we failed to detect any significant differences in pain scores among the three groups. There was evidence that a high-dose can cause hyperalgesia.     

Intra-articular morphine versus bupivacaine for postoperative analgesia following knee arthroscopy

In a prospective, double blind, randomized study, 30 ASA I patients were allocated to three groups depending on the drug injected intra-articularly, in an attempt to establish the best postoperative analgesic protocol following knee arthroscopy. Group 1 received 3 mg of preservative-free morphine in 25 ml saline; group 2, 5 mg of preservative-free morphine in 25 ml saline; and group 3, 25 ml 0.25% bupivacaine. The degree of postoperative pain was evaluated by visual analogue scale and the need for additional analgesics at 1, 2, 3, 8 and 24 h. We conclude that bupivacaine 0.25% provides analgesia of early onset and of short duration. While 3 mg-preservative free morphine provides moderate postoperative analgesia with peak effect during the eighth postoperative hour, 5 mg preservative-free morphine provides effective and long lasting (more than 24 h) pain relief. No side effects were noted.     

Tourniquet inflation after intra-articular morphine and bupivacaine administration following knee arthroscopy

We performed a randomized doubled-blind study to evaluate whether there was a benefit in delay in tourniquet deflation with intra-articular administration of morphine and bupivacaine following operative arthroscopic surgery. In 34 patients the tourniquet was deflated immediately and in 38 patients the tourniquet remained inflated for 10 min following injection. The analgesic efficacy was assessed using pain scores and the amount of supplementary analgesia required. The results demonstrate no benefit in delay in tourniquet deflation.     

关节镜下自体骨软骨移植修复软骨缺损的临床研究

目的取非负重区软骨替代负重区病变软骨，探讨软骨缺损的修复方式。方法对膝关节负重面软骨缺损的患者采用关节镜下非负重面自体骨软骨移植，根据缺损大小选择不同大小的骨软骨移植物，术后行CPM功能锻炼1周，6周后负重行走。结果术后随访3～24月，所有患者膝关节活动良好，疼痛症状基本消失，复查MRI示原软骨缺损区软骨表面光滑，移植物位置良好。结论关节镜下自体骨软骨移植效果良好，创伤小，避免同种异体移植产生的排斥反应及疾病的传播，是修复软骨缺损的好方式。     

超声清创联合重组人表皮生长因子治疗肛周脓肿合并感染的效果

目的探讨超声清创联合重组人表皮生长因子对肛周脓肿合并感染患者表皮细胞生长因子(Epidermal growth factor,EGF)、激活素A(Activin A,ACTA)水平及创面血流量的影响。方法选取2018年2月-2020年1月承德医学院附属医院肛周脓肿合并感染患者117例,依据随机数字表法分为对照A组(n=39)、对照B组(n=39)、联合组(n=39)。常规干预基础上对照A组采取超声清创,对照B组采取重组人表皮生长因子,联合组采取超声清创及重组人表皮生长因子。统计三组治疗情况、治疗前后疼痛程度评分、创面血流量及经皮氧分压、EGF、转化生长因子-β(Transforming growth factor-β,TGF-β)、ACTA、C-反应蛋白(C-reactive protein,CRP)水平及临床疗效。结果联合组创面愈合时间、感染控制时间、住院时间分别为(12.39±2.01)d、(5.22±1.56)d、(13.91±2.51)d短于对照A组、对照B组,创面细菌清除率为(89.13±4.64)%高于对照A组、对照B组(P<0.001);治疗后1 d、3 d、7 d、14 d三组VAS评分较治疗前降低,且联合组低于对照A组、对照B组(P<0.05);治疗后1 d联合组创面血流量及经皮氧分压分别为(0.92±0.25)PU、(35.69±3.20)mmHg大于对照A组、对照B组(P<0.05);治疗后1 d联合组血清EGF、TGF-β分别为(0.70±0.11)μg/L、(0.68±0.12)μg/L高于对照A组、对照B组(P<0.05);治疗后1 d联合组血清ACTA、CRP分别为(9.45±3.58)μg/L、(5.71±2.68)mg/L低于对照A组、对照B组(P<0.05);联合组疗效优于A组和B组(P<0.05)。结论联合采取超声清创及重组人表皮生长因子治疗肛周脓肿合并感染,可改善创面愈合及感染控制情况,缓解疼痛程度,增加创面血流量及经皮氧分压,调节EGF、ACTA等水平,提高整体治疗效果。     

多重耐药菌感染患者清创术后内镜灭菌方法研究

 目的 探讨过氧乙酸和环氧乙烷两种不同方法对胰腺包裹性坏死(WON)并多重耐药菌(MDRO)感染(经皮/经胃)内镜下清创术内镜的灭菌效果。方法 选取江西省某三级甲等医院WON并MDRO感染(经皮/经胃)内镜下清创术患者使用带副送水功能的内镜,采用随机数字表法将其分为两组:A组采用过氧乙酸浸泡灭菌,B组采用环氧乙烷低温灭菌。滤膜法采集内镜的钳子管道、送气/送水管道和副送水管道3个位点标本进行微生物培养,比较两组内镜灭菌合格率、菌落数和检出MDRO情况。结果 共采集78条副送水内镜,A组和B组各39条,共234份标本,A组和B组内镜灭菌合格率分别为61.54%、100%。A组钳子管道灭菌合格率为82.05%,送气/送水管道灭菌合格率为89.74%, 副送水管道灭菌合格率为74.36%,B组3个位点灭菌合格率均为100%。A组钳子管道、送气/送水管道和副送水管道菌落总数范围分别为0~6、0~112、0~23 CFU,分离MDRO 36株,以多重耐药铜绿假单胞菌、耐甲氧西林金黄色葡萄球菌和多重耐药肺炎克雷伯菌为主。将A组15条不合格的内镜转为环氧乙烷低温灭菌后,微生物学监测合格率达100%。结论 对于WON并MDRO感染(经皮/经胃)内镜下清创术的内镜,环氧乙烷低温灭菌方法更有效。对内镜的微生物学监测不能仅局限于钳子管道的监测,带副送水功能的内镜需监测副送水管道,以降低感染风险。     

Outcome of Debridement,Antibiotics, and Implant Retention With Modular Component Exchange in Acute Culture-Negative Periprosthetic Joint Infections

BackgroundModular component exchange and culture-directed antibiotic treatment is routinely employed for acute periprosthetic joint infection (PJI). However, as many as 7%-23% of PJIs have been reported to yield negative culture results. The efficacy of debridement, antibiotics, and implant retention (DAIR) with modular component exchange in the setting of acute culture negative PJI remains largely unknown. The aim of our study is to evaluate the outcomes of DAIR with modular component exchange in acute culture-positive and culture-negative PJI.MethodsA total of 149 consecutive patients with primary total joint replacements (90 total knee arthroplasties and 59 total hip arthroplasties) who underwent DAIR with modular component exchange for acute PJI with at least 3 years of follow-up were evaluated: (1) 46 culture-negative PJI patients and (2) 103 culture-positive PJI patients. Reinfection and aseptic revision rates along with complication rates were compared.ResultsThe reinfection rate for DAIR in acute culture-negative PJI was 13.0% compared to 19.4% in culture-positive PJI (P = .48). Mean survival time from reinfection between culture-negative (7.7 ± 0.4 years) and culture-positive (7.4 ± 0.3 years) PJI groups did not differ significantly (P = .40). Aseptic revision rates were 8.7% and 4.9% (P = .46), respectively, with loosening being the primary reason for implant failure in both cohorts.ConclusionsDespite lack of an identifying organism to guide postoperative antibiotic therapy, DAIR with modular component exchange for acute culture-negative PJI was associated with similar reinfection rates compared to acute culture-positive PJI, suggesting that culture negativity may not be a contraindication to DAIR in patients with acute PJI.