肝移植术后胆道并发症的诊断与治疗

目的 探讨肝移植术后胆道并发症的诊断与治疗.方法 分析2007-2009年肝移植术后不同类型胆道并发症的患者的临床资料,评价胴道并发症的类型,处理方式及术后恢复情况.结果 肝移植术后胆道并发症患者23例,包括胆漏患者12例,计胆管吻合口漏7例,肝断面胆管漏3例,胆囊管漏1例,迷走胆管漏1例;移植术后胆管狭窄患者11例,其中吻合口狭窄4例,非吻合口性狭窄7例.7例吻合口漏患者中,胆管重建2例(Roux-en-Y吻合和胆肠襻式Warren吻合);胆道吻合口修补1例;单纯依靠外引流管引流1例,活体双供肝肝移植的患者剖腹探查纠正胆漏失败后行再次肝移植1例;行经内镜逆行胰胆管造影(endoscopic retrograde cholangiopancreatography,ERCP)植入支架2例.肝断面胆管漏3例中,行肝断面胆管缝扎1例,ERCP联合B超引导下穿刺引流2例,引流2个月后胆漏闭合,拔除引流管,但是随后又出现胆道狭窄,ERCP术后,病情好转.胆囊管漏1例,行胆囊管缝扎.迷走胆管漏1例,行胆囊床缝扎.吻合口狭窄的患者4例,3例经ERCP治愈,1例行胆肠吻合重建胆道后治愈.非吻合口性狭窄的7例,行ERCP治疗3例,ERCP失败后,行经皮肝穿刺胆管引流(percutaneous transhepatic cholangiographic drainage,PTCD)1例;再次肝移植3例,2例患者术后恢复良好,1例死于严重感染.结论 肝移植术后胆道并发症危害大,关键在于预防.     

肝移植术后胆道并发症的防治

目的探讨肝移植术后胆道并发症的防治措施。方法回顾性研究2002年4月至2007年2月我中心249例肝移植的临床资料。结果249例肝移植患者中,31例发生胆道并发症(12.45%),其中胆漏16例(早期14例、晚期2例),吻合口狭窄9例,非吻合口狭窄6例。并发胆漏患者中,3例经ERCP放置鼻胆管引流治愈,4例在B超引导下行腹腔穿刺置管引流治愈,7例轻度胆漏患者经延长腹腔引流管放置时间治愈,2例晚期胆漏患者充分引流后治愈。吻合口狭窄患者中,5例行PTCD球囊扩张术,4例行ERCP球囊扩张术,共有3例放置了胆道支架,现均存活良好。非吻合口狭窄患者中,2例二次肝移植后治愈,另4例行PTCD联合胆道镜治疗,2例治愈,2例恢复不佳。结论完善手术技术、缩短移植物冷热缺血时间及保护胆道血供是预防肝移植术后胆道并发症的重要措施,个体化治疗,多可取得良好疗效。     

经皮经肝胆道引流术联合胆道球囊扩张术治疗良性胆肠吻合口狭窄

目的评估经皮经肝胆道引流术联合胆道球囊扩张术治疗良性胆肠吻合口狭窄的有效性及安全性。方法回顾性分析经皮经肝胆道引流术联合胆道球囊扩张术治疗的良性胆肠吻合口狭窄患者14例,记录手术成功率、引流管拔除率、手术相关并发症,并随访胆肠吻合口长期开通情况。结果对所有患者均一次性成功实施经皮经肝胆道引流术,手术成功率100%(14/14),行胆道球囊扩张术1~6次,平均(3.0±1.8)次,胆道球囊直径8~10mm,单次球囊扩张时间1~3min。引流管拔除率85.71%(12/14),可夹闭引流管、但需间断开放引流管者占14.29%(2/14)。14例患者术后总胆红素、直接胆红素、丙氨酸氨基转移酶、天冬氨酸氨基转移酶、碱性磷酸酶、γ-谷胺酰转肽酶较术前均明显下降(P均0.05)。所有患者术中、术后生命体征平稳,1例患者因术中疼痛需静脉麻醉处理。随访6~54个月,中位随访时间17.5个月,吻合口开放良好。结论经皮经肝胆道引流术联合胆道球囊扩张术处理良性胆肠吻合口狭窄临床效果好,患者耐受性良好,手术并发症少。     

同种原位肝移植术的胆管重建及其术后并发症的防治

目的探讨同种原位肝移植(OLT)的胆管重建方式及其术后并发症的防治。方法回顾性分析1999年2月至2003年1月间103例终末期肝病患者施行OLT胆管重建及术后并发症的防治情况。103例患者中,75例采用经典式原位肝移植伴体外静脉转流、17例采用经典式原位肝移植不伴转流、11例采用背驮式原位肝移植。胆道重建过程中有94例行胆管端端吻合,9例行胆肠吻合。胆管端端吻合的患者中,62例带T管引流,32例不带T管,但11例经受者胆囊管置入小橡胶管引流。术后胆管并发症的诊断主要依据临床表现、B型超声波、磁共振胰胆管成像或逆行胰胆管造影检查。所有患者均随访1年以上。结果103例OLT患者术后胆管并发症发生率为7.8%(8/103)。62例带T管引流的患者中,6例(9.6%)发生胆管并发症,其中4例术后发生胆漏,2例拔除T管后发生局限性腹膜炎;32例不带T管引流的患者中,1例(3.1%)发生胆管狭窄。9例胆肠吻合中,1例(11.1%)术后发生胆漏。7例胆漏患者,2例经再次手术引流,其余继续保持引流胆漏自愈。不带T管引流的患者中的胆管狭窄为吻合口狭窄,经内镜取出异物、球囊扩张与安放内支架后治愈。1例患者因胆漏导致肝动脉吻合口假性动脉瘤及腹腔大出血,经介入法明确诊断并行栓塞治疗后治愈。患者中无胆管并发症而引起的死亡。结论胆管吻合口的胆漏与狭窄是OLT术后最常见的胆管并发症。良好的胆管血供与胆管吻合技术是防止胆管并发症发生的关键。及时的内镜检查与放射学技术是诊断和治疗胆管并发症的有效手段。     

逆行胰胆管造影在肝移植中的应用

目的探讨经内镜逆行胰胆管造影(ERCP)在诊断和治疗肝移植术后胆道并发症中的应用。方法对本院肝移植术后出现胆道并发症的16例患者进行ERCP检查,并根据情况分别行鼻胆管引流(ENBD)和/或内镜下乳头切开取石(EST)等治疗。结果ERCP确诊16例肝移植术后胆道并发症,发生率为9.47%,其中胆道结石6例,胆道狭窄3例,吻合口漏2例,胆道结石伴左肝管狭窄1例,吻合口胆漏伴胆道结石3例,1例示供受体胆管比例不一致,供体胆管相对狭窄,所有患者都得到有效治疗。结论内镜下ERCP是诊断和治疗肝移植术后胆道并发症的一种安全而有效的手段,可作为非手术治疗中的首选。     

原位肝脏移植术后胆道狭窄的病因分析与治疗方法

目的 探讨原位肝移植术后胆道狭窄的病因及治疗方法.方法 回顾性分析2006年5月至2008年9月间90例肝移植受者的临床资料,对术后发生胆道狭窄的病因和治疗方法进行了探讨.结果 90例肝移植受者中,术后有8例发生胆道狭窄并发症(8.89%),其中吻合口狭窄5例,非吻合口狭窄3例.吻合口狭窄中,有3例因炎症水肿引起狭窄,经内镜逆行胆管造影(ERC)球囊扩张或置入胆道支架治疗后痊愈;另2例因吻合口胆漏疤痕收缩导致狭窄,经ERC置入胆道塑料支架,1例狭窄消失,1例好转.3例非吻合口狭窄者,均为弥漫性肝内胆管狭窄,经ERC或经皮肝穿刺胆道造影(PTC),采用球囊扩张和胆道支架置入治疗效果不佳,2例行二次肝脏移植后获救,1例治疗无效死亡.结论 吻合口狭窄和非吻合口狭窄的病因对治疗的反应存在差异,因此,要重视肝移植术后胆道狭窄的病因诊断和分析.只要及时采取适当的治疗措施,均可有效地治疗肝移植术后胆道狭窄.     

原位肝脏移植术后胆道狭窄的病因分析与治疗方法

目的 探讨原位肝移植术后胆道狭窄的病因及治疗方法.方法 回顾性分析2006年5月至2008年9月间90例肝移植受者的临床资料,对术后发生胆道狭窄的病因和治疗方法进行了探讨.结果 90例肝移植受者中,术后有8例发生胆道狭窄并发症(8.89%),其中吻合口狭窄5例,非吻合口狭窄3例.吻合口狭窄中,有3例因炎症水肿引起狭窄,经内镜逆行胆管造影(ERC)球囊扩张或置入胆道支架治疗后痊愈;另2例因吻合口胆漏疤痕收缩导致狭窄,经ERC置入胆道塑料支架,1例狭窄消失,1例好转.3例非吻合口狭窄者,均为弥漫性肝内胆管狭窄,经ERC或经皮肝穿刺胆道造影(PTC),采用球囊扩张和胆道支架置入治疗效果不佳,2例行二次肝脏移植后获救,1例治疗无效死亡.结论 吻合口狭窄和非吻合口狭窄的病因对治疗的反应存在差异,因此,要重视肝移植术后胆道狭窄的病因诊断和分析.只要及时采取适当的治疗措施,均可有效地治疗肝移植术后胆道狭窄.     

原位肝脏移植术后胆道狭窄的病因分析与治疗方法

目的 探讨原位肝移植术后胆道狭窄的病因及治疗方法.方法 回顾性分析2006年5月至2008年9月间90例肝移植受者的临床资料,对术后发生胆道狭窄的病因和治疗方法进行了探讨.结果 90例肝移植受者中,术后有8例发生胆道狭窄并发症(8.89%),其中吻合口狭窄5例,非吻合口狭窄3例.吻合口狭窄中,有3例因炎症水肿引起狭窄,经内镜逆行胆管造影(ERC)球囊扩张或置入胆道支架治疗后痊愈;另2例因吻合口胆漏疤痕收缩导致狭窄,经ERC置入胆道塑料支架,1例狭窄消失,1例好转.3例非吻合口狭窄者,均为弥漫性肝内胆管狭窄,经ERC或经皮肝穿刺胆道造影(PTC),采用球囊扩张和胆道支架置入治疗效果不佳,2例行二次肝脏移植后获救,1例治疗无效死亡.结论 吻合口狭窄和非吻合口狭窄的病因对治疗的反应存在差异,因此,要重视肝移植术后胆道狭窄的病因诊断和分析.只要及时采取适当的治疗措施,均可有效地治疗肝移植术后胆道狭窄.     

原位肝脏移植术后胆道狭窄的病因分析与治疗方法

目的 探讨原位肝移植术后胆道狭窄的病因及治疗方法.方法 回顾性分析2006年5月至2008年9月间90例肝移植受者的临床资料,对术后发生胆道狭窄的病因和治疗方法进行了探讨.结果 90例肝移植受者中,术后有8例发生胆道狭窄并发症(8.89%),其中吻合口狭窄5例,非吻合口狭窄3例.吻合口狭窄中,有3例因炎症水肿引起狭窄,经内镜逆行胆管造影(ERC)球囊扩张或置入胆道支架治疗后痊愈;另2例因吻合口胆漏疤痕收缩导致狭窄,经ERC置入胆道塑料支架,1例狭窄消失,1例好转.3例非吻合口狭窄者,均为弥漫性肝内胆管狭窄,经ERC或经皮肝穿刺胆道造影(PTC),采用球囊扩张和胆道支架置入治疗效果不佳,2例行二次肝脏移植后获救,1例治疗无效死亡.结论 吻合口狭窄和非吻合口狭窄的病因对治疗的反应存在差异,因此,要重视肝移植术后胆道狭窄的病因诊断和分析.只要及时采取适当的治疗措施,均可有效地治疗肝移植术后胆道狭窄.     

劈离式肝移植术后胆管并发症

目的 探讨体外劈离式肝移植术后胆管并发症的危险因素及其防治措施.方法 2006年6月至2010年9月,我院共施行劈离式肝移植术33例,其中1例于术后10 d死亡,予以排除.其余32例患者中男性18例,女性14例,平均年龄33.4岁(6个月～65岁).胆管重建方式胆管端端吻合20例,胆肠吻合12例.胆管并发症的诊断依靠T管造影、经皮经肝胆管造影(PTC)、经内镜逆行胆胰管造影、磁共振胰胆管造影(MRCP)等方法.胆管并发症定义为存在需要外科、介入、内镜等方法治疗的胆漏或胆管狭窄.结果 受者中位随访时间13.5个月(3～54个月).32例患者中11例患者发生12次胆管并发症(37.5％),其中肝断面胆漏3例(9.3％),胆管吻合口漏4例(12.5％),左肝管残端漏1例(3.1％),胆管吻合口狭窄1例(3.1％),缺血性胆管狭窄3例(9.3％).8例发生胆漏的受者中6例经手术或穿刺放置引流后痊愈,2例因腹腔内感染死亡.单因素分析表明,移植物类型、胆管重建方式等均不是肝断面胆漏的危险因素.结论 与全肝移植和活体肝移植相比,劈离式肝移植术后胆管并发症尤其是胆漏更为常见.进一步防治胆管并发症是改善劈离式肝移植预后的重要因素.     

维生素D受体在糖尿病肾病足细胞损伤及蛋白尿缓解中的作用

目的探讨维生素D受体(VDR)在糖尿病肾病(DKD)足细胞中的表达水平及在足细胞损伤及蛋白尿缓解中的作用。方法(1)本研究纳入了65例诊断患有2型糖尿病(伴或不伴蛋白尿)的患者,并纳入了25例年龄和性别相匹配的健康体检者为对照组。根据白蛋白/肌酐(ACR)的尿排泄比例对2型糖尿病患者进行分组,分别为无蛋白尿(ACR<30 mg/g,n=24)、微量白蛋白尿(ACR 30~300 mg/g,n=18)和临床蛋白尿(ACR>300 mg/g,n=23)。另选择25例经肾活检确诊的DKD患者作为DKD组。正常肾脏组织标本均取自泌尿外科同一时期肾脏肿瘤切除患者10例。将各组检测指标进行对比,同时采用实时定量PCR、ELISA法和免疫组化法检测VDR在各组患者的血液、尿液样本和肾脏组织中的表达情况,以及使用Pearson相关分析分析VDR与尿蛋白的相关性。(2)在2型糖尿病肾病小鼠模型中对上述结果进行验证,将遗传背景均为C57BLKs/J的雄性db/db小鼠及同窝出生的db/m小鼠,随机分为正常对照组(A组)、DKD对照组(B组)、DKD二甲基亚砜处理组(C组)、DKD帕立骨化醇(VDR激动剂)处理组(D组),C、D组连续腹腔注射处理8周,对照组不做任何处理。小鼠10周龄时开始连续干预8周,在小鼠22周龄(开始干预后12周)检测各组小鼠体重、血、尿生化指标对比;Western印迹法检测β⁃catenin、VDR的变化;免疫荧光观察足细胞标志蛋白podocin及足细胞损伤蛋白α⁃SMA的表达变化。结果(1)与正常健康对照组相比,无蛋白尿组、微量白蛋白尿组和临床蛋白尿组的糖尿病患者血浆中VDR的mRNA和蛋白水平均较低(均P<0.05);与无蛋白尿组的糖尿病患者相比,微量白蛋白尿组和临床蛋白尿组的糖尿病患者血浆中VDR的mRNA和蛋白水平均较低(均P<0.05)。(2)与正常健康对照组相比,无蛋白尿糖尿病组和DKD组患者血浆中VDR的mRNA和蛋白水平均较低(均P<0.05);与无蛋白尿糖尿病组患者相比,DKD组患者血浆中VDR的mRNA和蛋白水平亦较低(均P<0.05)。(3)免疫组化结果显示,DKD组肾组织中VDR的表达明显少于正常对照组。(4)DKD患者血浆中VDR mRNA相对水平与ACR呈负相关(r=-0.342,P<0.05)。(5)各组尿液上清液中VDR的水平与血浆中的水平呈相反趋势。(6)Western印迹结果显示,B组、C组肾小球足细胞β⁃catenin蛋白表达高于D组(均P<0.05),VDR蛋白的表达低于D组(均P<0.05);免疫荧光结果显示,B组、C组肾小球足细胞podocin的表达低于D组(均P<0.05),α⁃SMA的表达高于D组(均P<0.05)。结论VDR高表达缓解DKD足细胞损伤及蛋白尿。     

Anterior Interosseous Nerve Palsy After Shoulder Arthroscopy Treated With Surgical Decompression: A Case Series and Systematic Review of the Literature

Background: Anterior interosseous nerve (AIN) palsy is a very uncommon cause of upper extremity pain and weakness that comprises less than 1% of all upper extremity nerve palsies. Rarely reported but also mentioned in the literature is AIN palsy after shoulder arthroscopy. Methods: A systematic review of the literature to date using PubMed was conducted to identify patients who suffered AIN palsy after shoulder arthroscopy procedures. Articles included met the following criteria: (1) published in English; (2) primary presentation of the data; (3) patients had undergone shoulder arthroscopy before developing symptoms of AIN palsy; and (4) diagnosis was confirmed with clinical symptoms of AIN palsy. Measured outcomes included patient demographics, specific shoulder procedure, anesthesia procedure, intra-operative patient positioning, intra-operative compressive dressing, intra-operative traction, surgical versus conservative treatment, abnormal findings during decompression procedure, proposed mechanism of injury, and follow-up. Results: The search yielded 6 articles, of which 4 (13 cases) met inclusion criteria. An additional 2 cases were included in this report totaling 15 cases. The average patient age was 49 years (range: 31-64) with 73% males. At average follow-up of 24 months, 67% of patients experienced complete resolution of symptoms—more than half of which underwent surgical decompression. Patients who failed to progress experienced weakness of the flexor digitorum profundus and flexor pollicis longus muscles. Conclusions: Proposed injury mechanisms for AIN palsy after shoulder arthroscopy range from mechanical trauma, compressive hematoma, and direct anesthetic neurotoxicity. Management should be directed by clinical symptoms, imaging, and patient factors with majority of patients expected to have excellent clinical outcomes.     

不同尿钙水平的Gitelman综合征患者临床特点比较

目的观察不同尿钙水平Gitelman综合征(GS)患者的临床特点,探讨尿钙在GS疾病临床分型中的价值。方法收集2016—2018年来自中国国家罕见病注册系统(NRSC)、在北京协和医院行SLC12A3基因检测诊断为GS患者的临床资料,分析其尿钙特点,比较不同尿钙水平患者的临床和实验室检查指标。氢氯噻嗪试验按照标准操作流程进行,测定患者基线和用药后3 h内氯离子排泄分数改变量的最大值(ΔFECl)。结果共有83例GS患者被纳入研究,其中低尿钙患者53例(63.86%)。低尿钙组尿钙/肌酐比明显低于非低尿钙组[(0.085±0.058)mmol/mmol比(0.471±0.284)mmol/mmol,t=7.349,P<0.001]。两组患者在年龄、性别、估算肾小球滤过率、血压、血尿电解质水平、代谢性碱中毒方面差异均无统计学意义。低尿钙组患者乏力(χ2=4.595,P=0.032)及多尿(χ2=5.778,P=0.016)发生比例低于非低尿钙组,两组患者在其他临床症状方面差异无统计学意义。低尿钙和非低尿钙组各有16例患者行氢氯噻嗪试验,中位ΔFECl结果分别为0.539%(0.430%,1.283%)和0.829%(0.119%,1.298%),均提示对氢氯噻嗪无反应,组间差异无统计学意义(U=130.000,P=0.956)。结论GS患者中低尿钙比例为63.86%,尿钙水平与疾病临床表型、NCC功能损伤严重程度之间均无明确相关性。     

Role of Conventional and Diffusion-Weighted Magnetic Resonance Imaging of Spinal Treatment Protocol for Hydatid Disease

Objective:

To demonstrate the role of magnetic resonance imaging (MRI) in determining the treatment protocol for hydatid disease of the spine.

Design:

Case report; literature review.

Findings:

Diffusion-weighted MRI can help differentiate complicated infected hydatidosis from abscesses, epidermoid cysts from arachnoid cysts, and benign from malignant vertebral compression fractures. It is also helpful in differentiating between abscesses and necrotic tumors.

Conclusion:

Diffusion-weighted MRI can help differentiate between infections requiring immediate surgery and those that can be treated medically with antihelmintic treatment.     

Fibrinogen-thrombin collagen patch reinforcement of highrisk colonic anastomoses in rats

AIM To evaluate the effectiveness of human fibrinogenthrombin collagen patch(TachoSil~?) in the reinforcement of high-risk colon anastomoses.METHODS A quasi-experimental study was conducted in Wistar rats(n = 56) that all underwent high-risk anastomoses(anastomosis with only two sutures) after colectomies. The rats were divided into two randomized groups: Control group(24 rats) and treatment group(24 rats). In the treatment group, high-risk anastomosis was reinforced with TachoSil~? (a piece of Tacho Sil? was applied over this high-risk anastomosis, covering the gap). Leak incidence, overall survival, intra-abdominal adhesions, and histologic healing of anastomoses were analyzed. Survivors were divided into two subgroups and euthanized at 15 and 30 d after intervention in order to analyze the adhesions and histologic changes. RESULTS Overall survival was 71.4% and 57.14% in the TachoSil~? group and control group, respectively(P = 0.29); four rats died from other causes and six rats in the treatment group and 10 in the control group experienced colonic leakage(P 0.05). The intra-abdominal adhesion score was similar in both groups, with no differences between subgroups. We found non-significant differences in the healing process according to the histologic score used in both groups(P = 0.066).CONCLUSION In our study, the use of TachoSil~? was associated with a non-statistically significant reduction in the rate of leakage in high-risk anastomoses. TachoSil~? has been shown to be a safe product because it does not affect the histologic healing process or increase intra-abdominal adhesions.     

Fluorescence in the Sclera,Nails, and Teeth Secondary to Favipiravir Use for COVID-19 Infections

Favipiravir, an antiviral agent originally used for influenza infections, has become popular due to its beneficial signals in coronavirus disease. It is currently used in some countries within COVID-19 treatment protocols. This is an initial report of favipiravir-related fluorescence observed in three healthcare providers working in the same ward in our hospital. All three individuals had been diagnosed with COVID-19 two months earlier and were treated with favipiravir. None of the three individuals received hydroxychloroquine or tetracyclines. Wood’s light examination led to an incidental discovery of favipiravir-induced fluorescence involving the sclera, nails, and teeth. In all patients, white linear, square, and band-like specks of fluorescence were noticed on the sclera of both eyes, some teeth, and the proximal part of all fingernails and toenails. Exposure of the eyes to the Wood’s light was for a brief duration of 3 to 5 seconds during examination and photodocumentation. Favipiravir might cause bright white fluorescence of nails, sclera, and teeth, detectable by Wood’s light even two months after its cessation.     

Safety and tolerability of single intravenous doses of sugammadex administered simultaneously with rocuronium or vecuronium in healthy volunteers

BACKGROUND: Sugammadex rapidly reverses rocuronium- and vecuronium-induced neuromuscular block. To investigate the effect of combination of sugammadex and rocuronium or vecuronium on QT interval, it would be preferable to avoid the interference of anaesthesia. Therefore, this pilot study was performed to investigate the safety, tolerability, and plasma pharmacokinetics of single i.v. doses of sugammadex administered simultaneously with rocuronium or vecuronium to anaesthetized and non-anaesthetized healthy volunteers. METHODS: In this phase I study, 12 subjects were anaesthetized with propofol/remifentanil and received sugammadex 16, 20, or 32 mg kg(-1) combined with rocuronium 1.2 mg kg(-1) or vecuronium 0.1 mg kg(-1); four subjects were not anaesthetized and received sugammadex 32 mg kg(-1) with rocuronium 1.2 mg kg(-1) or vecuronium 0.1 mg kg(-1) (n=2 per treatment). Neuromuscular function was assessed by TOF-Watch SX monitoring in anaesthetized subjects and by clinical tests in non-anaesthetized volunteers. Sugammadex, rocuronium, and vecuronium plasma concentrations were measured at several time points. RESULTS: No serious adverse events (AEs) were reported. Fourteen subjects reported 23 AEs after study drug administration. Episodes of mild headache, tiredness, cold feeling (application site), dry mouth, oral discomfort, nausea, increased aspartate aminotransferase and gamma-glutamyltransferase levels, and moderate injection site irritation were considered as possibly related to the study drug. The ECG and vital signs showed no clinically relevant changes. Rocuronium/vecuronium plasma concentrations declined faster than those of sugammadex. CONCLUSIONS: Single-dose administration of sugammadex 16, 20, or 32 mg kg(-1) in combination with rocuronium 1.2 mg kg(-1) or vecuronium 0.1 mg kg(-1) was well tolerated with no clinical evidence of residual neuromuscular block, confirming that these combinations can safely be administered simultaneously to non-anaesthetized subjects. Rocuronium and vecuronium plasma concentrations decreased faster than those of sugammadex, reducing the theoretical risk of neuromuscular block developing over time.     

罗伊适应模式对腹股沟疝无张力疝修补术后恢复情况的影响

目的探讨罗伊适应模式对患者腹股沟疝无张力疝修补术后恢复情况的影响。 方法将2016年1月至2019年5月在秦皇岛市第二医院择期进行无张力修补术治疗的120例腹股沟疝患者，按照随机数字法分为对照组和观察组，每组各60例。对照组采用常规护理治疗，观察组在对照组的基础上采用罗伊适应模式。比较2组患者的术后临床指标、心理状态、围手术期并发症发生情况及满意度。 结果术后观察组患者的首次排气时间、恢复正常饮食时间、离床活动时间和术后住院时间均低于对照组（P<0.05）；术后观察组患者的抑郁自评量表（SDS）和焦虑自评量表（SAS）评分显著低于对照组（P<0.05）；术后2组患者均无切口感染发生，2组患者尿潴留、急性疼痛、认知功能障碍、发热、血肿等发生率相比无统计学差异（P>0.05）；术后观察组患者护理满意度为96.67%，显著高于对照组的83.33%（P<0.05）。 结论在常规护理的基础上，罗伊适应模式用于患者腹股沟疝无张力修补围手术期，能有效改善术后患者的焦虑/抑郁情绪，不增加围手术期并发症，促进术后患者的恢复及提高治疗满意度。     

Factors Associated With Reoperation After Silicone Proximal Interphalangeal Joint Arthroplasty

Background: Silicone proximal interphalangeal (PIP) joint arthroplasty has a high revision rate. It has been suggested that persistent ulnar deviation and joint instability influence the durability of PIP silicone arthroplasties. The goal of this study was to evaluate what factors are associated with reoperation after silicone PIP arthroplasty. Methods: We retrospectively evaluated all adult patients who underwent PIP silicone arthroplasty between 2002 and 2016 at one institutional system for inflammatory-, posttraumatic-, and primary degenerative arthritis. After manual chart review, we included 91 patients who underwent 114 arthroplasties. Fingers operated included 14 index, 41 middle, 38 ring, and 21 small fingers. Results: The overall reoperation rate was 14% (n = 16). Non-Caucasian race (P = .040), smoking (P = .022) and PIP silicone arthroplasty for post-traumatic osteoarthritis (P = .021) were associated with reoperation. The 1-, 5- and 10-year implant survival rates were 87%, 85%, and 85%, respectively. Conclusion: Caution should be exercised when considering PIP silicone arthroplasty of the index finger or in patients with post-traumatic osteoarthritis. It may be worthwhile addressing smoking behavior before pursuing silicone PIP arthroplasty.     

血浆凝血因子VIII水平与IgA肾病患者临床病理改变及预后的关系

目的探讨血浆凝血因子VIII(factor VIII,FVIII)水平与IgA肾病(IgAN)患者临床参数及预后的关系。方法收集2016年1月至2016年12月中南大学湘雅二医院确诊的IgAN患者的临床资料。按照时间依赖的受试者工作特征曲线(ROC)得出的血浆FVIII预测IgAN预后的临界值,将患者分为高FVIII组(FVIII>140.50%)和低FVIII组(FVIII≤140.50%),比较两组患者肾活检时基线临床参数的差异。以估算肾小球滤过率(eGFR)下降≥30%或进入终末期肾脏病(ESRD)为终点事件,采用Kaplan-Meier生存曲线及Cox回归方程法分析血浆FVIII水平对IgAN患者预后的影响。结果共93例IgAN患者纳入本研究,中位随访时间为35.15(33.77,36.76)个月,12例(12.90%)患者发生终点事件。高FVIII组患者年龄、血肌酐、尿素氮、血三酰甘油、血总胆固醇、血浆纤维蛋白原、D-二聚体、24 h尿蛋白量、蛋白C、蛋白S和eGFR下降速率高于低FVIII组(均P<0.05);eGFR、血白蛋白、中位随访时间低于低FVIII组(均P<0.05)。Kaplan-Meier生存分析结果显示,与低FVIII组比较,高FVIII组患者肾脏累积生存率降低(χ2=5.635,P=0.018)。在校正收缩压、eGFR、尿蛋白、肾小管萎缩/间质纤维化程度等因素后,多因素Cox回归分析结果显示,高血浆FVIII水平是IgAN患者肾脏预后不良的独立危险因素(HR=4.147,95%CI 1.055~16.308,P=0.042)。结论血浆FVIII水平与IgAN患者临床指标及预后相关,高血浆FVIII水平是IgAN患者肾脏预后不良的独立危险因素。