移植人羊膜细胞对大鼠创伤性脑损伤的实验研究

目的 探究大鼠TBI后脑内移植人羊膜细胞（HACs）对大鼠运动功能的影响。方法 HACs经分离、Hoechst33342标记后重悬调整细胞浓度为10^5/μl；采用改进的Feeney自由落体法打击大鼠脑皮层后肢运动区域，损伤后24h经微量注射器和立体定向仪将Hoechst33342标记的HACs 10μl分别移植于挫伤灶中心和挫伤灶边缘；在TBI后的28d内采用钉板平衡木行走测试大鼠运动功能变化，运动功能检测结束后取出脑组织行组织学检测。结果 治疗组滑落脚步数明显少于对照组（P〈0．05）；移植的HACs呈蓝色荧光；部分移植HACs可见MAP-2阳性表达。结论 移植HACs使大鼠TBI后运动功能明显改善。     

后路椎体间融合术后融合器脱出的原因及其翻修术

目的：探讨后路椎体间融合术后融合器脱出的原因及其翻修方法。方法：10例后路椎体间融合术后融合器脱出行翻修术的病例，其中腰椎滑脱症5例，腰椎管狭窄症3例，腰椎间盘突出症2例。手术节段为L4／54例，L5／S1 3例，L4／5＋L5／S1 3例；融合器应用BAK（旋入型）7例，聚醚醚酮矩形融合器（PEEK）2例，钛金属矩形融合器1例。于首次术后1～90d内行翻修术。就其脱出原因，再次手术方法及疗效进行分析。结果：融合器脱出的原因：矩形融合器中2例型号太小，1例放置位置偏后；旋入型融合器1例定位错误，其余大都因两枚融合器之间发生碰撞挤压所致。翻修术后获得完整随访资料者8例，随访时间10-36个月，平均17个月，均得到融合，无融合器再次移位或脱出以及内同定的断裂，1例伴有足下垂者遗留患足背伸肌力减弱，其余病例神经症状消除。结论：后路腰椎椎体间融合术后融合器脱出的可能原因有融合器型号偏小导致椎间隙撑开不够，放置位置偏后，两枚融合器不对称或距离太近发生碰撞等。早期、积极的手术翻修能取得较好的疗效。     

TCD观察动脉瘤性SAH后脑血管痉挛的血流动力学改变

目的探讨动脉瘤性蛛网膜下腔出血(SAH)后脑血管痉挛的血流动力学改变。方法经CT、DSA证实为动脉瘤性SAH患者179例,床旁经颅超声多谱勒(TCD)在术前、术后1~3d、5~7d、9~11d、12~14d记录并分析大脑中动脉(M CA)的血流参数及频谱改变。结果M CA平均血流速度(Vm)于SAH后1~3d开始升高,5~7d、9~11d达到高峰;L I(血管痉挛指数)为3~6时预后良好;>6时可以出现神经系统功能损害,颅内压增高且有脑血管痉挛(CV S)者预后较差。结论TCD能无创、实时评价SAH后CV S的动态变化,可以推断SAH后CV S的严重程度及临床转归。     

血小板β-淀粉样肽前体蛋白免疫强度及异构体比率对Alzheimer病的诊断价值

目的 探讨血小板β淀粉样肽前体蛋白（APP）免疫强度及异构体比率对Alzheimer病（AD）的诊断价值。方法 应用流式细胞术和Western Blot方法分别检测31例AD患者、22例血管性痴呆（VD）患者、28例神经变性病患者及30名健康老年人血小板APP免疫强度和APP异构体比率。结果 APP免疫活性各组间差异无统计学意义；APP130／APP106比率AD组明显低于VD组、神经变性病组和健康老年组（均P〈0．05）；AD组APP130／APP、06比率与其简易智力状态量表（MMSE）评分呈正相关（r=0．607，P〈0．01）。结论 血小板APP异构体比率降低可用于临床对AD的诊断。     

慢性移植物抗宿主病相关性肌炎一例

目的总结1例异基因造血干细胞移植后并发与慢性移植物抗宿主病(cGVHD)相关的多发性肌炎的诊治体会。方法1例急性淋巴细胞白血病患者在处于完全缓解状态下接受同胞间供髓异基因造血干细胞移植,移植后采用环孢素A和甲氨蝶呤预防移植物抗宿主病(GVHD)。结果移植后11 d,WBC＞0．5×10~9/L,移植后13 d,血小板＞20×10~9/L；27 d时,骨髓细胞染色体分析显示99%为供者型。移植后17 d,发生Ⅰ度急性皮肤型GVHD,经静脉注射地塞米松及甲氨蝶呤后,GVHD被完全控制。移植后8个月,患者发生轻度肝脏cGVHD,经他克莫司及硫唑嘌呤治疗,效果不佳,血清肝酶升高,后改为他克莫司和西罗莫司治疗,血清肝酶逐渐下降,但肌酸激酶从9 U/L上升至272 U/L,随后患者出现全身乏力,并逐渐加重,上下肢近端处活动出现障碍,肌酸激酶升至3010 U/L,股四头肌、肱二头肌的肌电图表现为肌源性损害,双侧大腿磁共振成像符合多发性肌炎表现,给予甲泼尼龙、血浆置换治疗,但无显著效果,患者突发阵发性呼吸困难,经抢救无效,患者死亡,死亡时肌酸激酶为21 010 U/L。结论多发性肌炎为cGVHD的一种较少见形式,累及重要肌组织者预后较差。     

滤膜法与涂抹法检测血液透析相关用水微生物的效果

目的 探讨滤膜法和涂抹法检测血液透析相关用水微生物的效果,为选择合适的检测方法提供依据。方法 回顾性收集某三级甲等综合性医院2018年1-12月同时采用滤膜法和涂抹法检测血液透析相关用水微生物的结果,对比分析滤膜法和涂抹法检测细菌检出率、单位菌落数、超干预值检出率和微生物合格率。结果 共收集274份血液透析相关用水微生物检测结果,其中透析液131份,反渗水39份,B浓缩液（下简称B液）14份,置换液34份,其他透析用水56份。滤膜法细菌检出率均高于涂抹法,其中透析液、反渗水、置换液、其他透析用水标本使用两种方法的细菌检出率比较,差异有统计学意义（均P<0.05）。透析液、B液、其他透析用水标本单位菌落数滤膜法数值上低于涂抹法,但仅其他透析用水标本使用两种方法检测结果单位菌落数差异有统计学意义（t=-3.011,P=0.004）。超干预值检出率其他透析用水滤膜法低于涂抹法,差异有统计学意义（χ²=6.596,P=0.010）。置换液、反渗水标本微生物合格率滤膜法数值上低于涂抹法,但仅置换液标本微生物合格率差异有统计学意义（χ²=18.987,P<0.001）。结论 滤膜法检出细菌的能力高于涂抹法,但其在血液透析相关用水微生物检测中存在一定局限性,除用于置换液比较适合外,应用在其余血液透析相关用水微生物的检测效果并不优于涂抹法。     

Closed reduction of glenohumeral dislocations with associated tuberosity fracture in the emergency department is safe

AimA fracture of the tuberosity is associated with 16% of glenohumeral dislocations. Extension of the fracture into the humeral neck can occur during closed manipulation, leading some to suggest that all such injures should be managed under general anaesthesia in the operating theatre. The purpose of this study was to establish the safety of reduction of glenohumeral dislocations with tuberosity fractures in the emergency department (ED).Patients and methodsWe reviewed 188 consecutive glenohumeral dislocations with associated tuberosity fractures identified from a prospective orthopaedic trauma database. Patient demographics, injury details, emergency department management and complications were recorded. The method of reduction, sedation, grade of clinician and outcome were documented.ResultsThe mean age was 61 years (range 18–96 years) with 79 males and 109 females. The majority of injuries (146, 78%) occurred after a fall from standing height. Closed reduction under sedation in the ED was successful in 162 (86%) cases. Of the remainder, 22 (11%) failed closed reduction under sedation and subsequently went to theatre and 6 (3%) were deemed not suitable for ED manipulation. At presentation 35 (19%) patients had a nerve injury, of which 29 (90%) resolved spontaneously. Two iatrogenic fractures occurred during close manipulation, one in the ED and the other in the operating theatre. Therefore, the risk of iatrogenic propagation of the fracture into the proximal humerus neck was 0.5% if the reduction was performed in the ED, and 1% over-all. More than two attempted reductions predicted a failed ED reduction (P = 0.001).ConclusionClosed reduction of glenohumeral dislocations with associated tuberosity fractures in the ED is safe, with a rate of iatrogenic fracture of 1%. These injuries should be managed by those with appropriate experience only after two adequate radiographic views. In cases where there is ambiguity over the integrity of the humeral neck, reduction should be delayed until multiplanar CT imaging has been obtained.     

Outcomes following quadriceps tendon repair using transosseous tunnels versus suture anchors: A systematic review

IntroductionTwo major techniques are used to repair complete quadriceps tendon ruptures, transosseous tunnel (TT) and the suture anchor (SA). There are multiple studies comparing the biomechanical outcomes of repairs performed with TT or SA. Our purpose was to compare the clinical outcomes following quadriceps tendon repair using SA and TT fixation techniques.MethodsThree major search engines were used with predetermined keyword searches to perform a systematic review of literature. These studies were independently scanned by two reviewers using PRISMA criterion. All included studies had to include at least one of the following outcome measures: range of motion (ROM), Lysholm score, complications, and/or re-ruptures.ResultsUsing three major search engines, 1039 articles were identified. After removing duplicates and screening for inclusion, 49 articles were reviewed. Two independent reviewers searched the studies to meet the inclusion criteria, and eight studies were selected. These eight studies included 156 knees in the TT group and 54 knees in the SA group. The TT group had a significantly better ROM after QT repair (132.5° versus 127.0°, p = 0.02). There was no significant difference in Lysholm scores between the TT group (92.6) and SA group (91.0, p = 0.11). There were significantly more complications in SA groups (9.3% versus 1.3%, p = 0.013), but not a significant difference in re-rupture rate between those undergoing SA vs. TT repair (3.7% versus 0%, p = 0.065). The SA group had a significantly higher age at time of surgery (63.62 vs. 54.32)ConclusionThe current study suggests that, following quadriceps tendon rupture, there are no significant differences in functional outcome between TT and SA techniques. Those undergoing TT repair attained a statistically significantly greater final ROM but this difference may not be clinically relevant. There was a statistically significantly higher rate of post-operative complications using SA technique.     

SARS病毒膜融合抑制剂的鉴定

目的：用分子对接技术预测HIV融合抑制剂是否能对SAILS起作用。方法：搜寻HIVsp41融合抑制剂，用DOCK软件分析其与SAILS蛋白的S2结构域HRl三聚体晶体结构的亲和力。结果：预测了23个小分子。ADS-J1、ADS-J2、XTYFormazan等几个小分子得分较高，提示与S2结构域有亲和力。结论：发现抗HIV的融合抑制剂有可能对SARS起作用。     

“Impact of Nociception Level (NOL) index intraoperative guidance of fentanyl administration on opioid consumption,postoperative pain scores and recovery in patients undergoing gynecological laparoscopic surgery. A randomized controlled trial”

Study objectiveThe Nociception Level (NOL) index uses a multiparametric approach to measure the balance between sympathetic and parasympathetic systems activity. Recently, a strong correlation between the NOL index response to nociceptive stimuli and the level of opioid analgesia during surgery was reported. Others observed that intraoperative doses of remifentanil and sufentanil were reduced when the NOL index was used. So far, no study has evaluated the impact of NOL-guided fentanyl antinociception in laparoscopic gynecological surgery. The primary hypothesis of this present study was to evaluate whether intraoperative NOL-guided fentanyl administration would reduce intra-operative opioid consumption. Secondary hypotheses were to assess whether this would lead to lower postoperative opioid consumption and pain scores, as well as improved postoperative outcomes.SettingUniversity hospital, operating room.Patients70 adult patients, ASA 1–3, scheduled for total laparoscopic hysterectomy.InterventionsPatients were randomized into 2 groups: SOC (standardization of care) and NOL (using the NOL index to guide the administration of fentanyl). The depth of anesthesia was monitored with BIS™. Intraoperative fentanyl boluses were administered based on heart rate and mean arterial pressure variations in the SOC group, and NOL index for the NOL group.MeasurementsFentanyl total intraoperative dose administered was collected and also averaged per hour. Pain scores and hydromorphone consumption were assessed in the post-anesthesia care unit and up to 24 h.Main resultsSixty-six patients completed the study, 33 in each group. Total intraoperative fentanyl administration was not different between the two groups (217 (70) in the NOL group vs 280 (210) in the SOC group (P = 0.11)). Nevertheless, intraoperative fentanyl administration per hour was reduced by 25% in the NOL-guided group compared to the SOC group: 81 (24) vs 108 (66) μg.h⁻¹, respectively (P = 0.03). Hydromorphone consumption and pain scores in the post-anesthesia care unit and at 24 h were not significantly different between the two groups.ConclusionNOL-guided analgesia allowed for a 22% reduction of the total amount of intraoperative fentanyl which was not significant. Nevertheless, results reported a significant reduction by 25% in the doses of fentanyl averaged per hour of surgery and administered in the NOL-guided group compared with the standardized practice in laparoscopic gynecological surgery. The pain measured postoperatively was similar in the two groups while the average postoperative consumption of opioids to achieve the same level of pain scores in post-anesthesia care unit and at 24 h was not significantly reduced. Further larger multicenter studies centered towards postoperative outcomes are needed.