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Clinical efficiency of orthotopic liver transplantation for advanced hepatic alveolar echinococcosis 原位肝移植治疗晚期肝泡包虫病的临床疗效观察
Pub Date : 2019-09-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.09.009
Aierken Yiliyaer, Lingxiang Kong, Lei Li, Bo Li
Objective To explore the indications and clinical value of orthotropic liver transplantation(OLT)in patients with advanced hepatic alveolar echinococcosis(HAE). Methods The clinical data of 12 patients with advanced HAE who received OLT from January 2001 to December 2017 were retrospectively analyzed. Among them, there were 7 males and 5 females, the age ranged from 16~58 years(median 42 years). The preoperative hepatic functions of 12 patients were 2 Child-Pugh class A, 3 class B and 7 class C, and the median model for end-stage liver disease(MELD)score was 19.5(8~23). Results The mean time of OLT procedure and anhepatic phase in 12 patients were 456.25(456.25±44.98)min and 79.17(79.17±10.01)min respectively. The median intraoperative blood loss and hospital stay times were 1000 ml(600~4000 ml), and 29.5(15±58)days respectively. All the patients were followed-up for 0 months to 207 months. Among the 12 patients who underwent OLT, 2 recipients died of incurable infection of pulmonary infection on day 23 post-OLT, and multiple organ failure on day 32 post-OLT, respectively. One case developed lung metastasis 2 years after operation, and brain metastasis was found in the same patient after 4 years. The recurrence occurred 3 years after OLT in another patient, no evidence of HAE recurrence or extrahepatic metastasis was found in the remaining 8 patients. Conclusions OLT can provide patients with advanced HAE the best chance for long term disease-free and overall survival who lost the opportunity for radical hepatectomy. Key words: Liver transplantation; Hepatic alveolar echinococcosis; Relapse
目的探讨晚期肝肺泡包虫病(HAE)患者原位各向异性肝移植(OLT)的适应证及临床价值。方法回顾性分析2001年1月至2017年12月12例晚期HAE患者行OLT治疗的临床资料。其中男性7例,女性5例,年龄16~58岁,中位42岁。12例患者术前肝功能Child-Pugh A级2例,B级3例,C级7例,终末期肝病模型(MELD)评分中位数为19.5分(8~23分)。结果12例患者的平均手术时间为456.25(456.25±44.98)min,平均无肝期时间为79.17(79.17±10.01)min。术中出血量中位数为1000 ml(600~4000 ml),住院时间中位数为29.5(15±58)d。随访0 ~ 207个月。12例接受OLT的患者中,有2例患者在OLT后第23天死于无法治愈的肺部感染,2例患者在OLT后第32天死于多器官衰竭。1例术后2年出现肺转移,4年后出现脑转移。另一例患者在肝移植后3年复发,其余8例患者未发现HAE复发或肝外转移的证据。结论:OLT可以为失去根治性肝切除术机会的晚期HAE患者提供长期无病生存和总生存的最佳机会。关键词:肝移植;肝肺泡包虫病;复发
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引用次数: 0
Preliminary study on the safety of liver transplantation recipients with Rh blood group mismatching Rh血型错配肝移植患者安全性的初步研究
Pub Date : 2019-09-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.09.010
Shao-hua Song, W. Yanling, Hao Liu, Junfeng Dong, Ke-Yan Sun, Jia-Yong Dong, F. Teng, Wen-Yuan Guo, Xiao-min Shi, Guoshan Ding
Objective To explore the safety of liver transplantation recipients with Rh blood group mismatchming. Methods From May 2005 to December 2018, 1 546 cases of liver transplantation in our hospital were retrospectively analyzed. Among these cases, 5 cases of Rh blood group mismatched were Rh(-) recipients receiving Rh(+ ) donor liver. For each Rh blood group mismatched liver transplantation, 5 patients received the same Rh blood group liver allograft were matched according to a certain principle and were defined as Rh-mismatch group and Rh-match group respectively. The serum alanine aminotransferase (ALT), aspartate aminotransferase(AST)and creatinine(SCr)were compared between two groups at Days 7 & 14 post-operation. Serum total bilirubin(TB), gamma-glutamyl transpeptidase(GGT)were compared between two groups at Month 1, 6 & 12 post-operation. Hemoglobin (Hb)were compared between two groups Month 1, 3 & 6 post-operation. The rates of infection, vascular complications and acute rejection was also compared. Indirect antiglobulin test (IAT)was used for detecting the production of anti-RhD antibody in patients in Rh-mismatch group at Month 1, 6 & 12 post-operation. Results At the mentioned time, no significant inter-group difference existed in serum ALT, AST, SCr, TB, GGT and blood Hb levels(all P>0.05); Also, no significant difference existed in the incidence of infection, vascular complications or acute rejection(all P>0.05). In Rhmismatch group, 4 recipients received Rh(+ )RBC transfusion during perioperative period and no hemolytic anemia occurred after operation. Rh(D) antibody was negative at all timepoints. Conclusions Taking into account the rarity of Rh-negative blood group in Chinese, it is safe and feasible to carry out Rh blood group mismatched liver transplantation when donor or recipient with the same Rh blood group is not available. Key words: Rh blood group system; Mismatching; Liver transplantation; Safety; Recipient
目的探讨Rh血型错配肝移植的安全性。方法回顾性分析我院2005年5月至2018年12月收治的1 546例肝移植病例。其中Rh血型错配5例为Rh(-)受体接受Rh(+)供体肝脏。每进行一次Rh血型错配肝移植,将5例接受相同Rh血型异体肝移植的患者按照一定的原则进行匹配,分别定义为Rh血型错配组和Rh血型匹配组。比较两组患者术后第7、14天血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和肌酐(SCr)水平。比较两组患者术后第1、6、12个月血清总胆红素(TB)、γ -谷氨酰转肽酶(GGT)水平。比较两组患者术后1、3、6个月血红蛋白(Hb)变化。比较两组的感染率、血管并发症和急性排斥反应的发生率。采用间接抗球蛋白试验(IAT)检测rh错配组患者术后1、6、12个月抗rhd抗体的产生。结果两组患者同期血清ALT、AST、SCr、TB、GGT、Hb水平差异均无统计学意义(P>0.05);两组间感染、血管并发症及急性排斥反应发生率差异无统计学意义(均P>0.05)。Rhmismatch组围手术期输注Rh(+)红细胞4例,术后无溶血性贫血发生。Rh(D)抗体在所有时间点均为阴性。结论考虑到我国Rh阴性血型的稀缺性,在无相同Rh血型供体或受体的情况下,进行Rh血型错配肝移植是安全可行的。关键词:Rh血型系统;错配;肝移植;安全;收件人
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引用次数: 0
Renal re-transplantation in a pre-sensitized small infant and literature review 预致敏小婴儿肾再移植及文献回顾
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.006
Lan Zhu, H. Feng, Yu Zhang, J. Jia, Xinyue Hu, Zheng-bin Lin, L. Qiu, Jianhua Zhou, Gang Chen
Objective To explore the feasibility and safety of kidney transplantation for pre-sensitized infants using deceased donors and summarize the relevant literature reports. Methods A second kidney transplantation was successfully performed for an 8-month-old pre-sensitized girl in July 2017. She had a low level of donor specific antibody (DSA) against human leucocyte antigen (HLA) B62 due to severe acute rejection (AR) after her first kidney transplantation. For desensitization, plasmapheresis and intravenous immunoglobulin plus anti-CD20 antibodies were offered on operative day. Clinical data and outcomes were retrospectively analyzed. Results Renal graft regained immediate function after transplantation. Preformed DSA could be detected at 1 week. However, there was no de novo DSA. At 1 year post-transplantation, preformed DSA turned negative. During a follow-up period of 2 years, renal graft showed an excellent function with a serum creatinine of 31 μmol/l and eGFR of 110 ml/min/1.73m2. No AR episode or proteinuria occurred. DSA stayed negative. Simultaneously physical development also caught up. Her height of 93 cm tall and weight of 13.5 kg at month 24 & 8 months corresponded to normal growth curve of her age. Conclusions Pre-sensitized infant could tolerate desensitization therapy well and achieve satisfactory outcomes. With surgical precisions and optimized managements, kidney transplantation provides excellent renal functions and survivals for infants with organs from deceased donors. Key words: Infant; Kidney transplantation; Pre-sensitization; Human leucocyte antigen; Donor specific antibodies
目的探讨预致敏婴儿肾移植的可行性和安全性,并总结相关文献报道。方法2017年7月,1例8月龄预致敏女童成功行第二次肾移植手术。她在第一次肾移植后由于严重急性排斥反应(AR),供体特异性抗体(DSA)抗人白细胞抗原(HLA) B62水平低。手术当天行血浆置换和静脉注射免疫球蛋白加抗cd20抗体进行脱敏治疗。回顾性分析临床资料和结果。结果移植肾术后即刻恢复功能。1周可检测到预形成的DSA。然而,没有新的DSA。移植后1年,预成形DSA变为阴性。随访2年,移植肾功能良好,血清肌酐31 μmol/l, eGFR 110 ml/min/1.73m2。未发生AR发作或蛋白尿。DSA保持负值。同时,身体发育也赶上了。24个月和8个月时身高93厘米,体重13.5公斤,符合正常年龄的生长曲线。结论预致敏婴儿对脱敏治疗耐受良好,效果满意。通过精确的手术和优化的管理,肾移植为婴儿提供了良好的肾脏功能和生存。关键词:婴幼儿;肾移植;Pre-sensitization;人白细胞抗原;供体特异性抗体
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引用次数: 0
Antibody mediated rejections: fighting an uphill battle 抗体介导的排斥反应:一场艰苦的战斗
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.001
Changxi Wang
抗体介导的排斥反应(AMR)是影响移植肾远期存活的重要疾病,其发病机理较明确但疾病异质性高,临床表型多,尚缺乏有效的治疗手段,特别是迟发或慢性AMR。细化AMR分型有助于实施针对性治疗和预估疗效。病理诊断标准和抗体检测技术有待进一步优化,分子病理和无创监测(如供者游离DNA)能辅助提高AMR的诊断和治疗。基于HLA Eplets错配建立免疫风险分层有助于指导个体化免疫抑制方案,降低新生供者特异性抗体(DSA)风险。
抗体介导的排斥反应(AMR)是影响移植肾远期存活的重要疾病,其发病机理较明确但疾病异质性高,临床表型多,尚缺乏有效的治疗手段,特别是迟发或慢性AMR。细化AMR分型有助于实施针对性治疗和预估疗效。病理诊断标准和抗体检测技术有待进一步优化,分子病理和无创监测(如供者游离DNA)能辅助提高AMR的诊断和治疗。基于HLA Eplets错配建立免疫风险分层有助于指导个体化免疫抑制方案,降低新生供者特异性抗体(DSA)风险。
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引用次数: 0
Desensitization strategies for ABO-incompatible living related kidney transplantation abo血型不相容活体相关肾移植的脱敏策略
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.007
J. Qiu, Guo-dong Chen, Hehuan Ruan, C. Deng, Jun Li, S. Deng, Gang Huang, Longshan Liu, Q. Fu, Changxi Wang, Lizhong Chen
Objective To explore the strategies of desensitization treatment for ABO incompatible (ABOi) related living-donor kidney transplantation. Methods A retrospective analysis was performed for 14 recipients undergoing ABOi related living kidney transplantation from July 2015 to December 2018. The clinical outcomes and expenditures of desensitization treatment before and after optimizing desensitization were compared. Results After desensitization treatment, 14 recipients successfully underwent ABOi-kidney transplantation. Within 2 weeks post-transplantation, blood group antibody rebounded to 1: 64 in only 1 recipient. Within 1 week post-transplantation, the serum creatinine levels decreased to 85-165 μmol/L in 14 recipients. Thirteen patients stabilized after 1 week while another patient had an elevated level of serum creatinine at Day 12 post-operation and renal allograft function recovered after treatment. Two cases of rejection were diagnosed by clinical manifestations and 1 case was confirmed by pathological biopsy. Five cases of programmed renal allograft biopsy indicated critical or suspected acute T-lymphocytic rejection within 1 year. Thirteen cases (92.6%) demonstrated varying degrees of peritubular capillary deposition of C4d. One case developed BK viral uropathy within 1 year and four patients of pulmonary infections requiring hospitalization were cured after treatment. During an early stage, the incidence of postoperative infection was 57.14% and declined to 14.29% after optimized desensitization. The expenditure of early desensitization treatment was (27004.86±10719.85) yuan and (10612.29±8143.05) yuan after optimization. And the expenditure of optimized desensitization was significantly lowered (P<0.05). During follow-ups, renal allograft function of 14 recipients remained decent. And the survival rate of recipient/allograft was 100% up to the statistical cut-off point. Conclusions Both desensitization strategies may achieve the goal of desensitization for ABOi kidney transplantation and the outcomes are excellent. The expenditure of desensitization treatment is significantly lowered after optimization. Key words: Kidney transplantation; Lving donor; ABO incompatibility; Blood group antibody; Desensitization therapy; Antibody-mediated rejection
目的探讨ABO血型不合(ABOi)相关活体肾移植脱敏治疗策略。方法对2015年7月至2018年12月14例ABOi相关活体肾移植患者进行回顾性分析。比较优化脱敏前后脱敏治疗的临床效果和费用。结果经脱敏治疗后,14例受者成功行aboi肾移植。在移植后2周内,只有1名受者的血型抗体反弹至1:64。14例移植后1周内血清肌酐水平降至85 ~ 165 μmol/L。13例患者术后1周稳定,1例患者术后第12天血清肌酐升高,治疗后肾功能恢复。2例经临床表现诊断为排斥反应,1例经病理活检证实。5例同种异体肾移植活检1年内提示急性或疑似急性t淋巴细胞排斥反应。13例(92.6%)C4d表现为不同程度的管周毛细血管沉积。1例1年内发生BK病毒性尿路病变,4例需住院治疗的肺部感染患者经治疗均痊愈。术后早期感染发生率为57.14%,优化脱敏后感染发生率降至14.29%。优化后的早期脱敏治疗费用分别为(27004.86±10719.85)元和(10612.29±8143.05)元。优化后的脱敏费用显著降低(P<0.05)。随访期间,14例受者肾功能保持良好。受体/同种异体移植成活率达到统计分界点100%。结论两种脱敏策略均可达到ABOi肾移植的脱敏目的,且效果良好。优化后的脱敏处理费用显著降低。关键词:肾移植;住捐赠;ABO血型不相容;血型抗体;脱敏治疗;抗体介入拒绝
{"title":"Desensitization strategies for ABO-incompatible living related kidney transplantation","authors":"J. Qiu, Guo-dong Chen, Hehuan Ruan, C. Deng, Jun Li, S. Deng, Gang Huang, Longshan Liu, Q. Fu, Changxi Wang, Lizhong Chen","doi":"10.3760/CMA.J.ISSN.0254-1785.2019.08.007","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.0254-1785.2019.08.007","url":null,"abstract":"Objective \u0000To explore the strategies of desensitization treatment for ABO incompatible (ABOi) related living-donor kidney transplantation. \u0000 \u0000 \u0000Methods \u0000A retrospective analysis was performed for 14 recipients undergoing ABOi related living kidney transplantation from July 2015 to December 2018. The clinical outcomes and expenditures of desensitization treatment before and after optimizing desensitization were compared. \u0000 \u0000 \u0000Results \u0000After desensitization treatment, 14 recipients successfully underwent ABOi-kidney transplantation. Within 2 weeks post-transplantation, blood group antibody rebounded to 1: 64 in only 1 recipient. Within 1 week post-transplantation, the serum creatinine levels decreased to 85-165 μmol/L in 14 recipients. Thirteen patients stabilized after 1 week while another patient had an elevated level of serum creatinine at Day 12 post-operation and renal allograft function recovered after treatment. Two cases of rejection were diagnosed by clinical manifestations and 1 case was confirmed by pathological biopsy. Five cases of programmed renal allograft biopsy indicated critical or suspected acute T-lymphocytic rejection within 1 year. Thirteen cases (92.6%) demonstrated varying degrees of peritubular capillary deposition of C4d. One case developed BK viral uropathy within 1 year and four patients of pulmonary infections requiring hospitalization were cured after treatment. During an early stage, the incidence of postoperative infection was 57.14% and declined to 14.29% after optimized desensitization. The expenditure of early desensitization treatment was (27004.86±10719.85) yuan and (10612.29±8143.05) yuan after optimization. And the expenditure of optimized desensitization was significantly lowered (P<0.05). During follow-ups, renal allograft function of 14 recipients remained decent. And the survival rate of recipient/allograft was 100% up to the statistical cut-off point. \u0000 \u0000 \u0000Conclusions \u0000Both desensitization strategies may achieve the goal of desensitization for ABOi kidney transplantation and the outcomes are excellent. The expenditure of desensitization treatment is significantly lowered after optimization. \u0000 \u0000 \u0000Key words: \u0000Kidney transplantation; Lving donor; ABO incompatibility; Blood group antibody; Desensitization therapy; Antibody-mediated rejection","PeriodicalId":9885,"journal":{"name":"Chineae Journal of Organ Transplantation","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84269939","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Influencing factors of quality-of-life for donors undergoing pediatric living related liver transplantation: a qualitative approach 影响儿童活体肝移植供体生活质量的因素:一种定性方法
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2014.00.011
Yaqi Huang, Yuexian Shi, Yue Zhao
Objective To explore the life experiences of donors undergoing pediatric living related liver transplantation and elucidate it’s the influencing factors of quality-of-life. Methods A qualitative study was performed with a phenomenological-hermeneutic approach. Twelve living related liver transplantation donors were face-to-face interviewed by a semi-structured interview and 7-step Colaizzi method was applied for data analysis. Results Four domains and 9 sub-domains were summarized as follows: body disturbance (pain, discomfort & physical changes), sense of uncertainty (recipient-dependent sensitive, self-doubt & confusion under family pressure), role conflict (patient-carer & family-social) and contentment & gratitude (willing to sacrifice, living in the present & benefiting from social funds). Conclusions The levels of quality-of-life vary greatly in different donors. Body disturbance, sense of uncertainty, role conflict, contentment and gratitude are the major influencing factors of quality-of-life for donors undergoing pediatric living related transplantation. Key words: Child; Liver transplantation; Lving donor; Quality of life
目的探讨儿童活体肝移植供者的生活经历,探讨影响其生活质量的因素。方法采用现象学-解释学方法进行定性研究。采用半结构化访谈法对12例在世亲属肝移植供者进行面对面访谈,采用7步Colaizzi法进行数据分析。结果共分为4个领域和9个子领域,分别是身体障碍(疼痛、不适和生理变化)、不确定感(受助者依赖敏感、自我怀疑和家庭压力下的困惑)、角色冲突(患者-照顾者和家庭-社会)和满足与感恩(愿意牺牲、活在当下和受益于社会资金)。结论不同献血者的生活质量水平差异较大。躯体障碍、不确定感、角色冲突、满足和感激是影响儿童活体相关移植供体生活质量的主要因素。关键词:儿童;肝移植;住捐赠;生活质量
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引用次数: 0
Liver transplantation in acute-on-chronic liver failure patients: a single center experience of 159 consecutive cases 急性慢性肝功能衰竭患者的肝移植:一个连续159例病例的单中心经验
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2014.00.010
Jiequn Li, Zhen‐jie Zhou, Yangyang Bin, Guangshun Chen, Qiang Li, Haizhi Qi
Objective To evaluate the outcome of 1iver transplantation for acute-on-chronic liver failure (ACLF) patients. Methods We included 453 consecutive patients with previously cirrhosis who underwent liver transplantation between January 2013 and December 2017. Patients were categorized as no ACLF (n=294) and ACLF(n=159) according to EASL-CLIF consortium criteria. Furthermore, we used ACLF grades to categorize the ACLF patients. Their clinical data were reviewed and their 90-days survival outcomes were compared. Results Compared with the no ACLF group, the length of stay in the ICU was significantly prolonged for all patients with ACLF, and the 90-days survival rate after transplantation was significantly reduced in ACLF group. The length of stay in the ICU was shorter in Grade 1 and Grade 2 group when compared to Grade 3 group. The 90-days survival rate of no ACLF, Grade 1, Grade 2 and Grade 3 group were 93.20%, 92.59%, 93.33% and 73.68%, respectively. There were no statistically significant differences in 90-days survival rate among the no ACLF, Grade 1 and Grade 2 group. However, the 90-days survive rate of Grade 3 group was lower than that of other groups. Conclusions Liver transplantation has been shown to be safe and effective with good outcome in patients with ACLF and should be offered in early course of ACLF before onset of multi-organ failure. Key words: Acute-on-chronic liver failure; Liver transplantation; Outcome; Diagnosis criteria; Prognostic Score
目的评价急性伴慢性肝衰竭(ACLF)患者肝移植的疗效。方法:我们纳入了2013年1月至2017年12月期间连续接受肝移植的453例既往肝硬化患者。根据EASL-CLIF联盟标准,将患者分为无ACLF(n= 294)和ACLF(n=159)两组。此外,我们使用ACLF分级对ACLF患者进行分类。回顾他们的临床资料,比较他们90天的生存结果。结果与无ACLF组相比,所有ACLF患者的ICU住院时间均明显延长,ACLF组移植后90天生存率明显降低。与3级组相比,1级组和2级组在ICU的住院时间较短。无ACLF组、1级组、2级组、3级组90天生存率分别为93.20%、92.59%、93.33%、73.68%。无ACLF组、1级组和2级组90天生存率比较,差异无统计学意义。但3级组90天存活率低于其他组。结论肝移植治疗ACLF安全有效,预后良好,应在ACLF发生多器官功能衰竭前进行肝移植治疗。关键词:急性-慢性肝衰竭;肝移植;结果;诊断标准;预后评分系统
{"title":"Liver transplantation in acute-on-chronic liver failure patients: a single center experience of 159 consecutive cases","authors":"Jiequn Li, Zhen‐jie Zhou, Yangyang Bin, Guangshun Chen, Qiang Li, Haizhi Qi","doi":"10.3760/CMA.J.ISSN.0254-1785.2014.00.010","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.0254-1785.2014.00.010","url":null,"abstract":"Objective \u0000To evaluate the outcome of 1iver transplantation for acute-on-chronic liver failure (ACLF) patients. \u0000 \u0000 \u0000Methods \u0000We included 453 consecutive patients with previously cirrhosis who underwent liver transplantation between January 2013 and December 2017. Patients were categorized as no ACLF (n=294) and ACLF(n=159) according to EASL-CLIF consortium criteria. Furthermore, we used ACLF grades to categorize the ACLF patients. Their clinical data were reviewed and their 90-days survival outcomes were compared. \u0000 \u0000 \u0000Results \u0000Compared with the no ACLF group, the length of stay in the ICU was significantly prolonged for all patients with ACLF, and the 90-days survival rate after transplantation was significantly reduced in ACLF group. The length of stay in the ICU was shorter in Grade 1 and Grade 2 group when compared to Grade 3 group. The 90-days survival rate of no ACLF, Grade 1, Grade 2 and Grade 3 group were 93.20%, 92.59%, 93.33% and 73.68%, respectively. There were no statistically significant differences in 90-days survival rate among the no ACLF, Grade 1 and Grade 2 group. However, the 90-days survive rate of Grade 3 group was lower than that of other groups. \u0000 \u0000 \u0000Conclusions \u0000Liver transplantation has been shown to be safe and effective with good outcome in patients with ACLF and should be offered in early course of ACLF before onset of multi-organ failure. \u0000 \u0000 \u0000Key words: \u0000Acute-on-chronic liver failure; Liver transplantation; Outcome; Diagnosis criteria; Prognostic Score","PeriodicalId":9885,"journal":{"name":"Chineae Journal of Organ Transplantation","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2019-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90631345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects ofWeChat-based peer supports upon medication adherence in liver transplant recipients 微信同伴支持对肝移植受者药物依从性的影响
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.008
Jia Liu, Jianfei Xie, Lifang Liu, Ying Niu, Y. Ming, Ke Chen
Objective To explore the effects of WeChat-based peer supports upon medication adherence and quality-of-life in liver transplant recipients. Methods A total of 63 patients with liver transplantation were conveniently divided into intervention group (n=32) and control group (n=31) depending upon their different follow-up periods. In control group, routine outpatient health guidance was offered while intervention group received 6-week WeChat-based peer supports. Medication compliance and quality-of-life of two groups were evaluated at Month 3/6/12 post-intervention. Results At Month 3 post-intervention, as compared with control group, only non-punctual medication improved significantly in intervention group (P 0.05). However, inter-group quality-of-life was not statistically significant at Month 3/6/12 post-intervention. Conclusions WeChat-based peer supports may partially improve the immediate compliance of patients with liver transplantation. However, long-term outcomes and effects on quality-of-life are worth further researches. Key words: Liver transplantation; Medication; Adherence; WeChat; Peer supports; Quality of life
目的探讨微信同伴支持对肝移植受者药物依从性和生活质量的影响。方法63例肝移植患者根据随访时间不同分为干预组(n=32)和对照组(n=31)。对照组给予常规门诊健康指导,干预组给予为期6周的微信同伴支持。于干预后3/6/12个月对两组患者的用药依从性和生活质量进行评估。结果干预后第3个月,与对照组相比,干预组只有不按时用药情况有明显改善(P < 0.05)。然而,干预后3/6/12个月组间生活质量差异无统计学意义。结论微信同伴支持可部分提高肝移植患者的即时依从性。然而,长期结果和对生活质量的影响值得进一步研究。关键词:肝移植;药物治疗;依从性;微信;同伴支持;生活质量
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引用次数: 0
Therapeutic efficacy of plasmapheresis and intravenous immunoglobulin plus Rituximab for antibody-mediated rejection after kidney transplantation 血浆置换联合静脉注射免疫球蛋白联合利妥昔单抗治疗肾移植后抗体介导性排斥反应的疗效观察
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.005
Lixiang Zhao, Z. Huang, Jinfeng Li, Lei Liu, Keke Zhang, Hongchang Xie, Yong-hua Feng, X. Pang, G. Feng
Objective To compare the therapeutic efficacy of plasmapheresis (PP) and intravenous immunoglobulin (IVIG) plus Rituximab for antibody-mediated rejection (AMR) after kidney transplantation. Methods From May 2015 to November 2018, a single-center retrospective cohort study was conducted for 540 recipients with high-resolution HLA undergoing kidney transplantation. According to the criteria of diagnosing AMR and patient selection, 20 patients were selected for PP+ IVIG (group A, n=12), PP+ IVIG+ Rituximab (group B, n=8). The efficacies and outcomes of two groups were compared. Results During a follow-up period of (12.0±5.8) months, no significant inter-group differences existed in basic profiles (P>0.05). After AMR treatment, serum creatinine levels decreased significantly from 283.4 to 226.4 μmol/L in group A (P=0.001) and from 289.4 to 166.6 μmol/L in group B (P=0.049). And the magnitude of decline was more marked in group B (P=0.023). Meanwhile, antibody MFI (log10) decreased from 3.73 to 3.62 in group A (P=0.012) and from 3.57 to 3.02 in group B (P=0.043). At months 3 and 6, serum creatinine level was lower in group B than that in group A (125.0 vs. 166.1 μmol/L, P=0.03; 127.0 vs. 169.0 μmol/L, P=0.048). The serum creatinine levels of AMR patients were 249.8 and 233.8 μmol/L respectively (P=0.182). Serum creatinine levels were 176.1 and 120.3 μmol/L (P=0.045) and 180.2 and 114.8 μmol/L at months 3 and 6 (P=0.044) respectively. Serum creatinine levels were 202.8 and 122.5 μmol/L (P=0.049) in group A and 142.7 and 107.0 μmol/L (P=0.046) in group B respectively. Four recipients developed allograft failure. At month 6 post-operation, AMR occurred in group A (n=3, 25%) and group B (n=1, 12.5%). And the incidence of leucopenia was 37.5% and 0 (P=0.049) in groups A and B respectively. Conclusions PP and IVIG plus rituximab is more efficacious for AMR. The earlier occurring time, the better prognosis. Key words: Kidney transplantation; Antibody-mediated rejection; Plasmapheresis; Intravenous immunoglobulin; Rituximab
目的比较血浆置换(PP)与静脉注射免疫球蛋白(IVIG)联合利妥昔单抗(Rituximab)治疗肾移植术后抗体介导性排斥反应(AMR)的疗效。方法2015年5月至2018年11月,对540例高分辨率HLA肾移植受者进行单中心回顾性队列研究。根据AMR诊断标准及患者选择,选择PP+ IVIG组(A组,n=12)、PP+ IVIG+利妥昔单抗组(B组,n=8)患者20例。比较两组患者的疗效和转归。结果在(12.0±5.8)个月的随访期间,两组患者基本情况差异无统计学意义(P < 0.05)。经AMR治疗后,A组血清肌酐水平由283.4 μmol/L降至226.4 μmol/L (P=0.001), B组由289.4 μmol/L降至166.6 μmol/L (P=0.049)。B组下降幅度更明显(P=0.023)。抗体MFI (log10)由A组的3.73降至3.62 (P=0.012),由B组的3.57降至3.02 (P=0.043)。第3、6个月时,B组血清肌酐水平低于A组(125.0 vs. 166.1 μmol/L, P=0.03;127.0 vs. 169.0 μmol/L, P=0.048)。AMR患者血清肌酐水平分别为249.8 μmol/L和233.8 μmol/L (P=0.182)。第3个月和第6个月血清肌酐水平分别为176.1和120.3 μmol/L (P=0.045)和180.2和114.8 μmol/L (P=0.044)。A组和B组血清肌酐水平分别为202.8和122.5 μmol/L (P=0.049)和142.7和107.0 μmol/L (P=0.046)。4名受者发生同种异体移植失败。术后6个月,A组(n=3, 25%)和B组(n=1, 12.5%)发生AMR。A组和B组的白细胞减少率分别为37.5%和0 (P=0.049)。结论PP和IVIG联合利妥昔单抗治疗AMR更有效。发病时间越早,预后越好。关键词:肾移植;抗体介入拒绝;血浆置换;静脉注射免疫球蛋白;利妥昔单抗
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引用次数: 0
De novo donor specific antibody affect the prognosis of kidney transplant recipients: retrospective study 新供者特异性抗体影响肾移植受者预后的回顾性研究
Pub Date : 2019-08-20 DOI: 10.3760/CMA.J.ISSN.0254-1785.2019.08.003
Z. Sun, Xiaodong Zhang, Xinuo Zhang, Peng Cao, Xing-han Li, Xiang Zheng, Baozhong Yu
Objective To explore the relationship between positive rate of de novo donor specific antibody (dnDSA) and human leukocyte antigen (HLA) mismatch after kidney transplantation and explore the impact of dnDSA upon long-term graft survival and rejection. Methods Retrospective analysis was conducted for clinical data of 101 kidney transplant recipients. Based upon HLA antibody and dnDSA, they were divided into three groups of HLA- (n=70), dnDSA- (n=23) and dnDSA+ (n=8). Rejection and graft survival were recorded for evaluating the impact of dnDSA on rejection and graft survival and observing the differences among all groups. Results The mismatchs of HLA-A/B and HLA-DR were more frequent than HLA- and dnDSA- groups(P=0.047, P=0.010)and graft survival was lower in dnDSA+ group than HLA- and dnDSA- groups (P=0.001). The rejection rate was higher in dnDSA+ group (62.5%) than HLA- group (8.57%) and dnDSA- group (8.69%). The difference was statistically significant (P=0.013). Pathological examination indicated microcirculatory inflammation (glomerulonephritis & trichodangiitis) and damage (multilayer change of capillary basement membrane) occurred frequently in dnDSA+ group and C4d remained positive. However, scar, arterial fibrosis or tubulointerstitial inflammation was not correlated with dnDSA. Conclusions HLA mismatch is correlated with dnDSA positivity. And dnDSA may reduce graft survival and enhance rejection rate. Rejection mediated by dnDSA is often accompanied by microcirculatory inflammation and C4d positivity. Key words: Kidney transplantation; Donor specific antibody; Rejection; Graft Survival
目的探讨肾移植术后新生供体特异性抗体(dnDSA)阳性率与人白细胞抗原(HLA)错配的关系,并探讨dnDSA对移植体长期存活和排斥反应的影响。方法对101例肾移植受者的临床资料进行回顾性分析。根据HLA抗体和dnDSA分为HLA-组(n=70)、dnDSA-组(n=23)和dnDSA+组(n=8)。记录排斥反应和移植物存活,评价dnDSA对排斥反应和移植物存活的影响,观察各组间差异。结果HLA- a /B和HLA- dr错配发生率高于HLA-组和dnDSA-组(P=0.047, P=0.010),且dnDSA+组移植物存活率低于HLA-组和dnDSA-组(P=0.001)。dnDSA+组的排异率(62.5%)高于HLA-组(8.57%)和dnDSA-组(8.69%)。差异有统计学意义(P=0.013)。病理检查显示dnDSA+组微循环炎症(肾小球肾炎、毛纤支炎)及损伤(毛细血管基底膜多层改变)多发,C4d阳性。然而,疤痕、动脉纤维化或小管间质炎症与dnDSA无关。结论HLA错配与dnDSA阳性相关。dnDSA可能降低移植物存活率,提高排异率。dnDSA介导的排斥反应常伴有微循环炎症和C4d阳性。关键词:肾移植;供体特异性抗体;拒绝;移植物存活率
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引用次数: 0
期刊
Chineae Journal of Organ Transplantation
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