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991.
目的 评估跟骨塌陷性骨折手术治疗的效果。方法 1996年 5月~ 2 0 0 0年 6月共手术治疗跟骨塌陷性骨折 15例 ,8例内固定 ,7例植骨 ,平均随访 14个月 ,参照AOFAS评分对患者有否疼痛、步态、距下关节活动 ,是否支架辅助、术后X线照片等加以评估。结果 两组结果无明显差异。 2例手术切口皮缘坏死 ,6例疗效为优 ,9例为良。结论 跟骨塌陷性骨折手术解剖复位能取得好的效果 相似文献
992.
Chaikof EL Lin PH Brinkman WT Dodson TF Weiss VJ Lumsden AB Terramani TT Najibi S Bush RL Salam AA Smith RB 《Annals of surgery》2002,235(6):833-841
OBJECTIVE: The impact of co-morbid conditions on early and late clinical outcomes after endovascular treatment of abdominal aortic aneurysm (AAA) was assessed in concurrent cohorts of patients stratified with respect to risk for intervention. SUMMARY BACKGROUND DATA: As a minimally invasive strategy for the treatment of AAA, endovascular repair has been embraced with enthusiasm for all prospective patients who are suitable anatomical candidates because of the promise of achieving a durable result with a reduced risk of perioperative morbidity and mortality. METHODS: From April 1994 to March 2001, endovascular AAA repair was performed in 236 patients using commercially available systems. A subset of patients considered at increased risk for intervention (n = 123) were categorized, as such, based on a preexisting history of ischemic coronary artery disease, with documentation of myocardial infarction (60%) or congestive heart failure (35%), or due to the presence of chronic obstructive disease (21%), liver disease, or malignancy. RESULTS: Perioperative mortality (30-day) was 6.5% in the increased-risk patients as compared to 1.8% among those classified as low risk (P = NS). There was no difference between groups in age (74 +/- 9 years vs. 72 +/- 6 years; mean +/- SD), surgical time (235 +/- 95 minutes vs. 219 +/- 84 minutes), blood loss (457 +/- 432 mL vs. 351 +/- 273 mL), postoperative hospital stay (4.8 +/- 3.4 days vs. 4.0 +/- 3.9 days), or days in the ICU (1.3 +/- 1.8 days vs. 0.5 +/- 1.6 days). Patients at increased risk of intervention had larger aneurysms than low-risk patients (59 +/- 13 mm vs. 51 +/- 14 mm; P <.05). Stent grafts were successfully implanted in 116 (95%) increased-risk versus 107 (95%) low-risk patients (P = NS). Conversion rates to open operative repair were similar in increased-risk and low-risk groups at 3% and 5%, respectively. The initial endoleak rate was 22% versus 20%, based on the first CT performed (either at discharge or 1 month; P = NS). To date, increased-risk patients have been followed for 17.4 +/- 15 months and low-risk patients for 16.3 +/- 14 months. Kaplan-Meier analysis for cumulative patient survival demonstrated a reduced probability of survival among those patients initially classified as at increased risk for intervention (P <.05, Mantel-Cox test). Both cohorts had similar two-year primary and secondary clinical success rates of approximately 75% and 80%, respectively. CONCLUSIONS: Early and late clinical outcomes are comparable after endovascular repair of AAA, regardless of risk-stratification. Notably, 2 years after endovascular repair, at least one in five patients was classified as a clinical failure. Given the need for close life-long surveillance and the continued uncertainty associated with clinical outcome, caution is dictated in advocating endovascular treatment for the patient who is otherwise considered an ideal candidate for standard open surgical repair. 相似文献
993.
Effect of mixed hematopoietic chimerism on cardiac allograft survival in cynomolgus monkeys 总被引:13,自引:0,他引:13
Kawai T Cosimi AB Wee SL Houser S Andrews D Sogawa H Phelan J Boskovic S Nadazdin O Abrahamian G Colvin RB Sach DH Madsen JC 《Transplantation》2002,73(11):1757-1764
BACKGROUND: We have previously reported the successful induction of mixed chimerism and long-term acceptance of renal allografts in MHC-mismatched nonhuman primates after nonmyeloablative conditioning and donor bone marrow transplantation. In this study, we extended our regimen to cardiac allotransplantation and compared the immunological responses of heart and kidney allograft recipients. METHODS: Five cynomolgus monkeys were conditioned with low-dose total body irradiation (1.5 Gy on days -6 and -5), supplemental thymic irradiation (7 Gy on day -1), antithymocyte globulin (50 mg/kg on days -2, -1, and 0), splenectomy (day 0), donor bone marrow transplantation (day 0), and a 4-week posttransplant course of cyclosporine. Heart allografts from MHC-mismatched donors were transplanted heterotopically on day 0. RESULTS: Two monkeys failed to develop multilineage chimerism and rejected their allografts soon after cyclosporine was stopped (postoperative days [PODs] 43 and 56). Three monkeys developed multilineage chimerism, which persisted 20 to 43 days posttransplant by flow cytometric analysis and to POD 124 by polymerase chain reaction analysis. Allograft survival in these recipients was prolonged to 138, 428, and 509 days, and in vitro mixed leukocyte reaction and cell-mediated lympholysis (CML) assays demonstrated donor-specific hyporesponsiveness. However, in contrast to kidney allograft recipients, long-term heart allograft recipients eventually developed humoral and cellular immunity against the donor and rejected the grafts. At the time of rejection, 1.3% to 9.5% of donor coronary arteries exhibited intimal proliferation. CONCLUSIONS: The induction of transient mixed hematopoietic chimerism leads to long-term heart allograft survival in MHC disparate monkeys without chronic immunosuppression. However, unlike kidney allografts, full tolerance to cardiac allografts was not achieved. Organ-specific modifications of the preparative regimen may be necessary to prevent the chronic cellular and humoral immune responses elicited by cardiac allografts. 相似文献
994.
995.
Early diagnosis of deep vein thrombosis in female patients who undergo total knee arthroplasty with measurement of P-selectin activation 总被引:9,自引:0,他引:9
BACKGROUND: Deep vein thrombosis (DVT) remains a leading cause of postoperative morbidity and mortality in patients who undergo total knee arthroplasty (TKA). Although patients with previous thrombotic episodes are inherently at a higher risk for subsequent episodes of DVT, it remains difficult to predict such an occurrence and to make a diagnosis in early stages. One potentially useful assay that can be used in the determination of changes of coagulation among patients who undergo arthroplasty is platelet activation. The goal of this study was to establish a predictive value for DVT with measurement of P-selectin levels that could help in planning appropriate perioperative management strategies for patients at high risk for DVT. METHODS: A total of 52 patients who underwent TKA with general anesthesia underwent contrast venography on the 5th postoperative day. Platelet activation before and after operation was measured with platelet surface expression of P-selectin with flow cytometry in these two groups of patients for TKA. None of the patients underwent any anticoagulation therapy. RESULTS: Nineteen of the 52 patients for TKA showed radiologic evidence of DVT, whereas 33 patients for TKA had no radiologic signs of DVT. There was no difference in platelet activation at baseline, which was 1 hour before induction of anesthesia, between the two groups (P >.05) as measured with P-selectin assays. Differences were noted between the two groups on the 5th day after operation, wherein P-selectin was expressed in only 2.72% +/- 0.9% (mean +/- standard deviation) of platelets in patients for TKA with healthy venogram results. This differed significantly from platelets in patients for TKA with DVT, who had P-selectin expression of 6.56% +/- 3.1% (mean +/- standard deviation; P <.01). Sensitivity for the diagnosis of DVT with P-selectin assay was calculated to be 74%, and specificity was found to be 94%. CONCLUSION: The findings showed that radiologically confirmed DVT in patients for TKA surgery with general anesthesia is associated with an elevated number of activated platelets. Perioperative assessment of P-selectin may predict the early onset of DVT in patients who undergo high risk surgical procedures like TKA. This laboratory assay may help prevent the occurrence of the fatal events caused by DVT with use of early therapeutic intervention, such as heparinization. 相似文献
996.
目的 研究重度恶性梗阻性黄疸术前经皮肝穿刺胆管引流术(PTCD)的应用价值。方法 接受根治性胰十二指肠切除术的41例重度恶性梗阻性黄疸病人(血清总胆红素>350umol/L)进行回顾分析。按术前是否行PTCD将患者分为两组。A组21例,术前在超声引导下行PTCD,引流2~3周,待血清总胆红素降至100umol/L左右即行根治性胰十二指肠切除术。B组20例,术前未行PTCD而直接行根治性胰十二指肠切除术。对比研究两组病人术后的临床结果。结果 术后1、3、7、14天APACHE Ⅱ评分系统的 APS分值,A组明显低于B组(P<0.01)。A组术后发生并发症 12例次,B组 33例次(P<0.01)。A组无手术死亡,B组死亡4例(P<0.01)。结论 对于重度恶性梗阻黄疸行根治性胰十二指肠切除术的病人,术前PTCD能明显减少术后应激反应的程度和期限,降低并发症发生和手术死亡率,提高手术疗效。 相似文献
997.
经内镜胆管引流对恶性胆管梗阻术前肝功能恢复的疗效观察 总被引:5,自引:0,他引:5
目的 比较经内镜胆管引流术对梗阻性黄疸术前肝功能恢复的疗效。方法 腹壶周围癌、胰头癌共 76例 ,引流组 3 6例 ,其中行内置管引流 2 9例 ,鼻胆管引流 7例 ;对照组 40例 ,未做任何方式的胆管减压引流。结果 入院后第 14 d丙氨酸氨基转移酶 (ALT)、凝血酶原时间 (PT)和血清总胆红素 (TBIL)水平下降幅度分别为 :引流组 71.46± 11.81% ,2 3 .0 9±9.5 6% ,81.5 8± 7.5 0 % ;对照组 48.87± 19.3 2 % ,18.3 7± 9.3 1% ,5 .88± 3 .65 %。结论 经内镜胆管引流术能迅速改善梗阻性黄疸病的肝功能 ,为后续治疗创造良好的条件 相似文献
998.
999.
门静脉激素疗法在改善肝切除术后肝功能的价值研究 总被引:1,自引:1,他引:1
叶林 《中华肝胆外科杂志》2002,8(7):399-401
目的 探讨门静脉激素疗法对肝切除术后肝功能改善的价值。方法 对照组 (n =70 )给予常规护肝处理。研究组 (n =70 )增加肝门阻断前及术后 1~ 3d经门静脉注射地塞米松治疗 ,两组于术前第 4天及术后第 4天分别测试口服葡萄糖耐量试验 (OGTT)及 15min血清吲哚氰绿潴留(retentionforindocyaninegreenat 15minutes ,R15ICG)。结果 对照组OGTT术前呈抛物线型 (P型 )4 4例中有 17例于术后变成线型 (L型 )。R15ICG由术前 2 3%± 5 %增加至术后的 2 7%± 8%。术后肝衰 2 0例 ,死亡 7例。研究组OGTT术前呈抛物线型 4 0例增加至术后的 6 1例 ,R15ICG由术前的 2 4 %± 7%下降至 14 %± 3% ,术后肝衰 5例 ,无死亡病例。两组术后的差异有显著性 (P <0 0 5 )。结论 门静脉激素疗法能显著改善术后肝功能及预防肝衰 ,OGTT及R15ICG能早期灵敏地反映肝储备功能 相似文献
1000.
细胞毒药物(Gemcitabine)治疗人胰腺癌裸鼠胰腺原位移植癌的实验研究 总被引:2,自引:0,他引:2
目的 探讨细胞毒药物(Gemcitabine)对胰腺癌裸鼠原位移植模型(SOI)生长,转移的抑制作用。方法 SOI模型分为Ⅰ组(Gemcitabine 100mg/kg),Ⅱ组(Gemcitabine50mg/kg)和对照组。Gemcitabine于术后第2,3,6,9天给药,ip,术后第10周处死裸鼠;并对肿瘤组织的增殖指数(PI),凋亡指数(AI)以及PI/AI进行分析。结果 (1)Ⅰ组能显著抑制胰腺癌生长,Ⅱ组则无显著的肿瘤抑制作用,但两者对胰腺癌转移和预后均无显著疗效;(2)Ⅰ组可显著降低肿瘤增殖指数(PI),增大凋亡指数(AI),PI/AI显著降低。结论 Gemcitabine单用能有效抑制胰腺癌生长,但对肿瘤转移无显著抑制作用。 相似文献