• 【分离牛心肌细胞用于基于核转移的重编程研究。】 复制标题 收藏 收藏
    DOI:10.1089/clo.2006.8.150 复制DOI
    作者列表:Schwarzer M,Carnwath JW,Lucas-Hahn A,Lemme E,Kues WA,Wachsmann B,Haverich A,Martin U,Niemann H
    BACKGROUND & AIMS: :The goal of this study was to establish and validate a protocol for preparing bovine cardiomyocytes from slaughterhouse material for nuclear transfer experiments. The cardiomyocyte was selected because it is a terminally differentiated cell and strongly expresses a unique subset of genes which can be monitored during the reprogramming period. A total of 39 trials were conducted, and an optimized protocol was developed yielding individual contractile cardiomyocytes from 3-5-month-old bovine fetuses The basic protocol involves stabilization of bovine heart tissue for transportation from the slaughterhouse to the laboratory by perfusion with Custodiol. This was followed by an enzymatic dissociation with collagenase in calcium-free medium and yielded individual contractile rod-shaped cardiomyocytes. Subsequent addition of Ca2+ caused the cardiomyocytes to round up which was an essential pre-condition for drawing them into glass transfer pipettes for delivery into the perivitelline space and for efficient electrofusion with cytoplasts derived from in vitro matured bovine oocytes. The use of cardiomyocytes maintained at 37 degrees C in nuclear transfer, resulted in a significantly reduced proportion of blastocysts compared to adult fibroblasts (14.0% versus 32.7%). Storage of cardiomyocytes at 4 degrees C prior to nuclear transfer was not compatible with blastocyst development. It is expected that this system will be valuable for investigating the reprogramming of gene expression which occurs after somatic cell nuclear transfer.
    背景与目标: :这项研究的目的是建立和验证从屠宰场材料制备牛心肌细胞用于核移植实验的方案。选择心肌细胞是因为它是终末分化细胞,并且强烈表达可以在重编程期间监测的独特基因子集。总共进行了39次试验,并开发了优化的方案,以从3-5个月大的牛胎儿中产生单个可收缩的心肌细胞。基本方案涉及稳定牛心脏组织,以便通过灌注邻苯二酚从屠宰场运送到实验室。然后在无钙培养基中用胶原酶进行酶解,产生单个可收缩的杆状心肌细胞。随后添加Ca2导致心肌细胞聚集,这是将它们吸引到玻璃移液管中以递送到玻璃体腔中并与源自体外成熟牛卵母细胞的细胞质进行有效电融合的必要先决条件。与成年成纤维细胞相比,使用维持在37摄氏度的心肌细胞进行核移植,导致胚泡的比例大大降低(分别为14.0%和32.7%)。核移植前将心肌细胞储存在4摄氏度下与胚泡发育不兼容。预期该系统对于研究在体细胞核转移后发生的基因表达的重编程将是有价值的。
  • 【神经性贪食症的危险因素。基于社区的病例对照研究。】 复制标题 收藏 收藏
    DOI:10.1001/archpsyc.1997.01830180015003 复制DOI
    作者列表:Fairburn CG,Welch SL,Doll HA,Davies BA,O'Connor ME
    BACKGROUND & AIMS: BACKGROUND:Many apparently disparate risk factors have been implicated as causes of eating disorders. This study was designed to test the hypothesis that 2 broad classes of risk factors exist for bulimia nervosa: those that increase the risk for development of a psychiatric disorder in general and those that increase the risk of dieting. It was predicted that the latter are especially common among persons with bulimia nervosa.

    METHODS:A case-control design was used involving 2 integrated comparisons. First, 102 subjects with bulimia nervosa were compared with 204 healthy control subjects without an eating disorder. Second, the same 102 subjects with bulimia nervosa were compared with 102 subjects with other psychiatric disorders. To reduce sampling bias, the subjects were recruited directly from the community. A broad range of putative risk factors was assessed.

    RESULTS:The subjects with bulimia nervosa and the healthy control subjects differed in their rates of exposure to most of the putative risk factors. Far fewer differences were evident between the subjects with bulimia nervosa and the control subjects with other psychiatric disorders, although exposure to factors that were likely to increase the risk of dieting and to negative self-evaluation and certain parental problems (including alcohol use disorder) were substantially more common among those with bulimia nervosa.

    CONCLUSIONS:The findings support the hypothesis that bulimia nervosa is the result of exposure to general risk factors for psychiatric disorder and risk factors for dieting. An unexpected finding was the particularly high rates of premorbid negative self-evaluation and certain parental problems among those with bulimia nervosa.

    背景与目标: 背景:许多明显不同的危险因素被认为是饮食失调的原因。这项研究旨在检验以下假设:存在2种广泛的神经性贪食症危险因素:那些通常会增加患精神病的风险,以及那些会增加节食的风险的因素。预计后者在神经性贪食症患者中尤为常见。

    方法:采用病例对照设计,涉及2个综合比较。首先,将102例神经性贪食症患者与204例无饮食失调的健康对照者进行了比较。其次,将相同的102名神经性贪食症患者与102名其他精神疾病患者进行了比较。为了减少抽样偏差,直接从社区招募了受试者。评估了广泛的推定危险因素。

    结果:神经性贪食症患者和健康对照组的暴露于大多数推定危险因素的比率有所不同。神经性贪食症患者与其他精神病患者的对照对象之间的差异要小得多,尽管接触可能会增加节食风险和自我评估为负面因素的因素以及某些父母问题(包括饮酒障碍)结论

    结论:这些发现支持以下假设:神经性贪食症是暴露于精神疾病的一般危险因素和饮食风险因素的结果。一个出乎意料的发现是神经性贪食症患者的病前阴性自我评估率特别高,并且存在某些父母问题。

  • 【紫杉醇在患有晚期胃癌的血液透析患者中​​的药代动力学:一例报告。】 复制标题 收藏 收藏
    DOI:10.3748/wjg.v12.i32.5237 复制DOI
    作者列表:Kawate S,Takeyoshi I,Morishita Y
    BACKGROUND & AIMS: :We report for the first time the possibility of weekly paclitaxel chemotherapy for a patient with advanced, nonresectable gastric cancer undergoing hemodialysis. A 50-year-old man with chronic renal failure due to bilateral polycystic kidneys, who had undergone hemodialysis three times a week for 5 years, presented with hematemesis in December 2004. Based on the diagnosis of gastric cancer with lymph node metastases, surgery was performed. On the 15th postoperative day, the patient was treated with chemotherapy using paclitaxel. Paclitaxel was administered at a dose of 60 mg/m2 as a 1 h iv infusion in 250 mL of saline. Hemodialysis was started 1 h after the completion of the paclitaxel infusion and was performed for 3 h. Paclitaxel was administered weekly on d 1, 8, and 15 on a 28-d cycle. The maximum plasma concentration of paclitaxel was 1390 microg/L. The area under the curve of paclitaxel was 4398.6 microg x h/L. Grade 2 leukopenia was encountered during the first cycle. The plasma concentrations of paclitaxel from 6 to over 24 h after the infusion were 0.01 to 0.1 micromol/L in our patient, and these concentrations have been shown to be effective on inhibiting the growth of gastric cancer cells without producing adverse side effects in the patient. The plasma concentration of paclitaxel was not influenced by hemodialysis. We conclude that the pharmacokinetics of paclitaxel is not altered in a patient with renal failure, and that weekly paclitaxel is a suitable treatment regimen for hemodialysis patients with advanced gastric cancer.
    背景与目标: :我们首次报告了接受血液透析的晚期,不可切除胃癌患者每周紫杉醇化疗的可能性。一名因双侧多囊肾而导致慢性肾功能衰竭的50岁男子于5周内每周进行了3次血液透析,并于2004年12月发生了呕血。根据诊断为具有淋巴结转移的胃癌,我们进行了手术。执行。术后第15天,使用紫杉醇对患者进行化疗。紫杉醇以60 mg / m2的剂量在250 mL盐水中静脉滴注1 h。紫杉醇输注完成后1 h开始进行血液透析,并进行3 h。紫杉醇在第28天的第1、8和15天每周给药一次。紫杉醇的最大血浆浓度为1390 microg / L。紫杉醇曲线下的面积为4398.6微克×h / L。在第一个周期中遇到了2级白细胞减少症。输注后6至24小时内紫杉醇的血浆浓度在我们的患者中为0.01至0.1 micromol / L,并且这些浓度已被证明可有效抑制胃癌细胞的生长而不会对患者产生不良副作用。紫杉醇的血浆浓度不受血液透析的影响。我们得出的结论是,紫杉醇在肾衰竭患者中的​​药代动力学没有改变,并且每周紫杉醇是晚期胃癌血液透析患者的合适治疗方案。
  • 【用于透皮药物递送的颗粒加速性能研究。】 复制标题 收藏 收藏
    DOI:10.1007/s11517-006-0050-4 复制DOI
    作者列表:Liu Y
    BACKGROUND & AIMS: :We have proposed a transdermal biolistic method to accelerate a powder formulation of drugs to penetrate human skin for the treatment of a range of diseases. One of the key issues for designing and evaluating transdermal biolistic system is ensuing that the powder drugs are delivered into the skin with a controllable velocity range and spatial distribution. The aerodynamics of supersonic nozzles and performance of the delivery system were initially studied, mainly analytically and experimentally. In this paper, computational fluid dynamics is utilized to characterize two existing prototype devices, in order to further investigate the transient gas and particle dynamics in their supersonic nozzles. To validate the implemented numerical approach, calculated pressure histories, two-dimensional flow structures and particle velocity distributions are made and compared with the reported experimental measurements. The key features of gas dynamics, gas-particle interaction and performance of the prototype transdermal biolistics are discussed and interpreted.
    背景与目标: :我们提出了一种透皮生物弹射法,以加速药物粉末制剂渗透人体皮肤,从而治疗多种疾病。设计和评估透皮生物弹药系统的关键问题之一是确保将粉末药物以可控制的速度范围和空间分布传递到皮肤中。最初主要是通过分析和实验研究超音速喷嘴的空气动力学和输送系统的性能。在本文中,利用计算流体动力学来表征两个现有的原型设备,以进一步研究其超音速喷嘴中的瞬态气体和粒子动力学。为了验证已实施的数值方法,计算了压力历史,二维流动结构和颗粒速度分布,并将其与报告的实验测量结果进行了比较。讨论并解释了气体动力学,气体-颗粒相互作用和原型透皮生物弹性能的关键特征。
  • 【局部神经节神经母细胞瘤后生长激素缺乏症:一例报告。】 复制标题 收藏 收藏
    DOI:10.1097/01.mph.0000212984.51867.88 复制DOI
    作者列表:Schiavetti A,Ingrosso A,Picone S,Boscherini B
    BACKGROUND & AIMS: :Growth hormone deficiency (GHD) related to standard dose chemotherapy has rarely been described. We report on a case of localized ganglioneuroblastoma treated by carboplatin/etoposide for 2 courses and surgery, which developed a serious GHD after 56 months. At present, the child is growing on by GH replacement therapy. We discuss about the hypothesis that GHD may be related to chemotherapy and we report a review of previous published cases.
    背景与目标: :很少有人描述与标准剂量化疗有关的生长激素缺乏症(GHD)。我们报告了一例通过卡铂/依托泊苷治疗的局部神经节神经母细胞瘤的疗程为2个疗程和手术,该病例在56个月后出现了严重的GHD。目前,孩子正在通过GH替代疗法长大。我们讨论了GHD可能与化学疗法有关的假说,并且我们报告了以前发表过的病例的综述。
  • 【艾滋病患者的更昔洛韦耐药性巨细胞病毒(CMV)视网膜炎一例:CMV病毒载量和血室中病毒突变的纵向分子分析。】 复制标题 收藏 收藏
    影响因子 :
    发表时间:1997-06-01
    来源期刊:AIDS
    DOI:10.1097/00002030-199707000-00005 复制DOI
    作者列表:Boivin G,Gilbert C,Morissette M,Handfield J,Goyette N,Bergeron MG
    BACKGROUND & AIMS: OBJECTIVE:To study the temporal relationships between cytomegalovirus (CMV) viral load and specific UL97 mutations in polymorphonuclear leukocytes (PMNL) and plasma samples from a patient with AIDS who developed ganciclovir-resistant CMV retinitis.

    METHODS:Sequential PMNL and plasma samples were analysed for determination of the CMV viral load using non-molecular methods and a quantitative polymerase chain reaction (PCR) assay. Screening of the same samples for the most common mutations conferring ganciclovir resistance was performed using nested PCR and restriction enzyme analysis.

    RESULTS:At the time of progression of CMV retinitis (after 6 months of ganciclovir), a rapid increase in the CMV DNA load was found in both PMNL and plasma samples. This increase paralleled the emergence of a specific mutation (V594) in the same samples and recovery of ganciclovir-resistant blood isolates. In this patient, however, the only tests that substantially predicted the progression of CMV disease were the quantitative PCR assay using PMNL and to a lesser extent the pp65 antigenemia assay.

    CONCLUSIONS:Quantitative evaluation of the CMV viral load in PMNL using sensitive assays such as PCR appears to be a promising approach for monitoring antiviral therapy in subjects with AIDS. In addition, common mutations conferring ganciclovir resistance can be detected directly in PMNL and plasma samples.

    背景与目标: 目的:研究巨细胞病毒耐药性巨细胞病毒性视网膜炎的艾滋病患者的巨细胞病毒(CMV)病毒载量与多形核白细胞(PMNL)和血浆样品中特定UL97突变之间的时间关系。

    方法:使用非分子方法和定量聚合酶链反应(PCR)分析了连续的PMNL和血浆样品,以测定CMV病毒载量。使用巢式PCR和限制性内切酶分析对相同样品中最引起更昔洛韦耐药的突变进行筛查。

    结果:在CMV视网膜炎进展时(6个月后) (更昔洛韦)的检测,在PMNL和血浆样品中均发现CMV DNA载量迅速增加。这种增加与相同样品中特异突变(V594)的出现和更昔洛韦耐药血分离株的回收率平行。然而,在该患者中,唯一可以预测CMV疾病进展的检测方法是使用PMNL进行定量PCR检测,并在较小程度上使用pp65抗原血症检测。使用敏感的检测方法(如PCR)评估PMNL中CMV病毒载量似乎是监测艾滋病患者抗病毒治疗的一种有前途的方法。此外,可以在PMNL和血浆样品中直接检测到更昔洛韦耐药的常见突变。

  • 【病例报告:爱泼斯坦-巴尔病毒相关的舌基未分化癌。】 复制标题 收藏 收藏
    DOI:10.1016/j.anl.2006.05.009 复制DOI
    作者列表:Wakisaka N,Murono S,Minato H,Furukawa M,Yoshizaki T
    BACKGROUND & AIMS: :Outside the nasopharynx, undifferentiated carcinomas occur only rarely at other head and neck locations. Although the association between undifferentiated nasopharyngeal carcinoma and Epstein-Barr virus (EBV) is consistent, there is conflicting evidence as to the association of EBV with undifferentiated carcinomas outside the nasopharynx. Here, we report on a case of undifferentiated carcinoma of the tongue base. A 71-year-old male, who had been treated with irradiation for primary unknown right neck metastatic EBV-positive undifferentiated carcinoma 9 years previously, was referred to our clinic with masses at the tongue base and right neck. The lesion at the tongue base was revealed to be an EBV-positive undifferentiated carcinoma. He was treated with resection of tongue base tumor and bilateral-neck dissection, and the defect at the tongue base was reconstructed with a free rectus abdominis myocutaneous flap. Re-irradiation was added post-operatively because of a positive surgical margin at the tongue base. The patient is presently alive without recurrence or distant metastasis 20 months after treatment. Although it is unclear whether our case is recurrent or newly developed EBV-latently infected undifferentiated carcinoma, we propose that EBV-associated tumors should be carefully observed after treatment at least for more than 10 years.
    背景与目标: :在鼻咽以外,未分化癌仅在其他头颈部位置很少发生。尽管未分化的鼻咽癌和爱泼斯坦-巴尔病毒(EBV)之间的关联是一致的,但关于EBV与鼻咽外未分化癌的关联有相互矛盾的证据。在这里,我们报道一例未分化舌基癌。一位71岁的男性在9年前接受过放射治疗,原发性右颈部转移性EBV阳性原发性未分化癌已经接受过放射治疗,现被转诊至我们的诊所,舌根和右颈部有肿块。舌根处的病变显示为EBV阳性未分化癌。对他进行了舌根肿瘤切除术和双侧颈淋巴结清扫术,并用游离的腹直肌肌皮瓣修复了舌根缺损。由于舌根的手术切缘阳性,因此在术后增加了再次照射。治疗后20个月,该患者目前尚无复发或远处转移。尽管尚不清楚我们的病例是复发的还是新发的EBV潜伏感染的未分化癌,但我们建议治疗至少10年后应仔细观察与EBV相关的肿瘤。
  • 【罗非昔布是一种有效的细胞色素P450 1A2抑制剂:在健康受试者中使用替扎尼定和咖啡因进行的研究。】 复制标题 收藏 收藏
    DOI:10.1111/j.1365-2125.2006.02653.x 复制DOI
    作者列表:Backman JT,Karjalainen MJ,Neuvonen M,Laitila J,Neuvonen PJ
    BACKGROUND & AIMS: AIMS:Case reports suggest an interaction between rofecoxib and the CYP1A2 substrate tizanidine. Our objectives were to explore the extent and mechanism of this possible interaction and to determine the CYP1A2 inhibitory potency of rofecoxib. METHODS:In a randomized, double-blind, two-phase cross-over study, nine healthy subjects took 25 mg rofecoxib or placebo daily for 4 days and, on day 4, each ingested 4 mg tizanidine. Plasma concentrations and the urinary excretion of tizanidine, its metabolites (M) and rofecoxib, and pharmacodynamic variables were measured up to 24 h. On day 3, a caffeine test was performed to estimate CYP1A2 activity. RESULTS:Rofecoxib increased the area under the plasma concentration-time curve (AUC(0-infinity)) of tizanidine by 13.6-fold [95% confidence interval (CI) 8.0, 15.6; P < 0.001), peak plasma concentration (C(max)) by 6.1-fold (4.8, 7.3; P < 0.001) and elimination half-life (t(1/2)) from 1.6 to 3.0 h (P < 0.001). Consequently, rofecoxib markedly increased the blood pressure-lowering and sedative effects of tizanidine (P < 0.05). Rofecoxib increased several fold the tizanidine/M-3 and tizanidine/M-4 ratios in plasma and urine and the tizanidine/M-5, tizanidine/M-9 and tizanidine/M-10 ratios in urine (P < 0.05). In addition, it increased the plasma caffeine/paraxanthine ratio by 2.4-fold (95% CI 1.4, 3.4; P = 0.008) and this ratio correlated with the tizanidine/metabolite ratios. Finally, the AUC(0-25) of rofecoxib correlated with the placebo phase caffeine/paraxanthine ratio (r = 0.80, P = 0.01). CONCLUSIONS:Rofecoxib is a potent inhibitor of CYP1A2 and it greatly increases the plasma concentrations and adverse effects of tizanidine. The findings suggest that rofecoxib itself is also metabolized by CYP1A2, raising concerns about interactions between rofecoxib and other CYP1A2 substrate and inhibitor drugs.
    背景与目标: 目的:病例报告表明罗非考昔与CYP1A2底物替扎尼定之间存在相互作用。我们的目标是探索这种可能的相互作用的程度和机制,并确定罗非昔布对CYP1A2的抑制作用。
    方法:在一项随机,双盲,两阶段交叉研究中,九名健康受试者每天服用25毫克罗非考昔或安慰剂,持续4天,并在第4天,每人摄入4毫克替扎尼定。在长达24小时内测量替扎尼定,其代谢产物(M)和罗非考昔的血浆浓度和尿排泄,以及药效学变量。在第3天,进行了咖啡因测试以评估CYP1A2的活性。
    结果:罗非昔布将替扎尼定的血浆浓度-时间曲线下面积(AUC(0-无穷大))增加了13.6倍[95%置信区间(CI)8.0、15.6; P <0.001),峰值血药浓度(C(max))从1.6到3.0 h的6.1倍(4.8,7.3; P <0.001)和消除半衰期(t(1/2))(P <0.001) 。因此,罗非昔布显着增强了替扎尼定的降压和镇静作用(P <0.05)。罗非昔布将血浆和尿液中替扎尼定/ M-3和替扎尼定/ M-4的比例提高了几倍,尿液中替扎尼定/ M-5,替扎尼定/ M-9和替扎尼定/ M-10的比例提高了几倍(P <0.05)。此外,它使血浆咖啡因/对黄嘌呤比率增加了2.4倍(95%CI 1.4、3.4; P = 0.008),并且该比率与替扎尼定/代谢产物比率相关。最后,罗非昔布的AUC(0-25)与安慰剂相咖啡因/对黄嘌呤的比​​例相关(r = 0.80,P = 0.01)。
    结论:罗非昔布是一种有效的CYP1A2抑制剂,它大大提高了血浆浓度和替扎尼定的不良反应。研究结果表明罗非考昔本身也被CYP1A2代谢,引起对罗非考昔与其他CYP1A2底物和抑制剂药物之间相互作用的担忧。
  • 【铜绿假单胞菌的广泛基因组可塑性通过临床分离株中新基因的鉴定和分布研究揭示。】 复制标题 收藏 收藏
    DOI:10.1128/IAI.00546-06 复制DOI
    作者列表:Shen K,Sayeed S,Antalis P,Gladitz J,Ahmed A,Dice B,Janto B,Dopico R,Keefe R,Hayes J,Johnson S,Yu S,Ehrlich N,Jocz J,Kropp L,Wong R,Wadowsky RM,Slifkin M,Preston RA,Erdos G,Post JC,Ehrlich GD,Hu FZ
    BACKGROUND & AIMS: :The distributed genome hypothesis (DGH) states that each strain within a bacterial species receives a unique distribution of genes from a population-based supragenome that is many times larger than the genome of any given strain. The observations that natural infecting populations are often polyclonal and that most chronic bacterial pathogens have highly developed mechanisms for horizontal gene transfer suggested the DGH and provided the means and the mechanisms to explain how chronic infections persist in the face of a mammalian host's adaptive defense mechanisms. Having previously established the validity of the DGH for obligate pathogens, we wished to evaluate its applicability to an opportunistic bacterial pathogen. This was accomplished by construction and analysis of a highly redundant pooled genomic library containing approximately 216,000 functional clones that was constructed from 12 low-passage clinical isolates of Pseudomonas aeruginosa, 6 otorrheic isolates and 6 from other body sites. Sequence analysis of 3,214 randomly picked clones (mean insert size, approximately 1.4 kb) from this library demonstrated that 348 (10.8%) of the clones were unique with respect to all genomic sequences of the P. aeruginosa prototype strain, PAO1. Hypothetical translations of the open reading frames within these unique sequences demonstrated protein homologies to a number of bacterial virulence factors and other proteins not previously identified in P. aeruginosa. PCR and reverse transcription-PCR-based assays were performed to analyze the distribution and expression patterns of a 70-open reading frame subset of these sequences among 11 of the clinical strains. These sequences were unevenly distributed among the clinical isolates, with nearly half (34/70) of the novel sequences being present in only one or two of the individual strains. Expression profiling revealed that a vast majority of these sequences are expressed, strongly suggesting they encode functional proteins.
    背景与目标: :分布式基因组假设(DGH)指出,细菌物种中的每个菌株都从基于种群的超基因组中获得独特的基因分布,其比任何给定菌株的基因组都要大很多倍。自然感染种群通常是多克隆的,大多数慢性细菌病原体具有水平基因转移的高度发达的机制的观点提出了DGH,并提供了解释哺乳动物宿主面对适应性防御机制时慢性感染如何持续存在的手段和机制。先前已确定DGH对专性病原体的有效性,我们希望评估其对机会细菌病原体的适用性。这是通过构建和分析包含约216,000个功能性克隆的高度冗余的集合基因组文库实现的,该文库由铜绿假单胞菌的12种低通道临床分离株,6种耳泻分离株和6个其他身体部位构建而成。对来自该文库的3,214个随机挑选的克隆(平均插入片段大小,约1.4 kb)进行序列分析,结果表明,对于铜绿假单胞菌原型菌株PAO1的所有基因组序列,其中348个(10.8%)克隆是唯一的。在这些独特序列内的开放阅读框的假想翻译证明了与许多细菌毒力因子和以前在铜绿假单胞菌中未鉴定出的其他蛋白质的蛋白质同源性。进行了基于PCR和逆转录PCR的分析,以分析这些序列的70个开放阅读框子集在11种临床菌株中的分布和表达模式。这些序列在临床分离株中分布不均,只有一半或34个新序列出现在一个或两个单独的菌株中。表达谱分析表明这些序列中的绝大多数都被表达,强烈暗示它们编码功能蛋白。
  • 【内窥镜经膀胱-经尿道瘘管修复阴道阴道瘘:初次病例报告。】 复制标题 收藏 收藏
    DOI:10.1089/end.1997.11.203 复制DOI
    作者列表:Okamura K,Kanai S,Kurokawa T,Kondo A
    BACKGROUND & AIMS: :Through an endoscopic transvesico-transurethral approach, we closed a vesicovaginal fistula that occurred after hysterectomy in a patient with uterine leiomyoma. The 3-mm fistula, located in the midportion of retrotrigone, was resected transurethrally and sutured in two layers through two 5-mm suprapubic trocars placed into the bladder and the urethral route under pneumobladder. The patient had no urine leakage from the vagina after surgery.
    背景与目标: :通过内窥镜经膀胱-经尿道入路,我们关闭了子宫平滑肌瘤患者子宫切除术后发生的膀胱阴道瘘。将3毫米的瘘管位于后三角骨的中部,经尿道切除,并通过两根5毫米的耻骨上耻骨套管针将其缝合在两层中,然后将其插入膀胱和在气囊下的尿道。病人术后没有尿液从阴道漏出。
  • 【使用口译员进行跨文化访谈研究:系统的文献综述。】 复制标题 收藏 收藏
    DOI:10.1111/j.1365-2648.2006.03963.x 复制DOI
    作者列表:Wallin AM,Ahlström G
    BACKGROUND & AIMS: AIM:This paper reviews how the interpreter's role is described in empirically based, qualitative cross-cultural interview studies and how trustworthiness is determined. BACKGROUND:Increased immigration during the past decades has created a multiethnic society in many countries. This development poses a challenge to healthcare staff, in that they need to understand how people from different cultures experience health and illness. One way to assess immigrants' experiences is through cross-cultural interview studies, involving an interpreter. Thorough knowledge of the interpreter's role is needed in order to increase the trustworthiness of this kind of nursing research. METHOD:Literature searches were conducted from October to November 2004 using PubMed, CINAHL, Psycinfo, Sociological abstract, Your Journals@ovid, and Eric databases. Qualitative interview studies written in English and performed with an interpreter were included. The Matrix Method was used to review the literature. FINDINGS:In almost all of the 13 relevant papers found, the role of the interpreter(s) in the research process was only sparsely described. In addition, all studies except one employed different techniques to established trustworthiness. The most common techniques were prolonged engagement, member check or triangulation, the latter performed either on the data, investigators or methods. CONCLUSION:Methodological issues with respect to interpreters have received only limited attention in cross-cultural interview studies. Researchers in the field of nursing need to consider (1) the interpreter's role/involvement in the research process; (2) the interpreter's competence and the style of interpreting; (3) the interpreter's impact on the findings. This information is a prerequisite when trying to determine the trustworthiness of a cross-cultural study.
    背景与目标: 目的:本文回顾了如何在基于经验的定性跨文化访谈研究中描述口译员的角色,以及如何确定信任度。
    背景:过去几十年来移民的增加在许多国家创建了一个多种族的社会。这种发展对医护人员提出了挑战,因为他们需要了解来自不同文化背景的人们如何经历健康和疾病。评估移民经验的一种方法是通过跨文化访谈研究,其中包括一名口译员。为了增加这种护理研究的可信度,需要对口译员的作用有透彻的了解。
    方法:从2004年10月至2004年11月使用PubMed,CINAHL,Psycinfo,Sociological abstract,Your Journals @ ovid和Eric数据库进行文献检索。包括用英语撰写并由口译员进行的定性访谈研究。矩阵法用于回顾文献。
    结果:在发现的所有13篇相关论文中,几乎都很少描述口译员在研究过程中的作用。此外,除一项研究外,所有研究均采用不同的技术来建立可信度。最常见的技术是长时间的接触,成员检查或三角剖分,后者根据数据,研究人员或方法进行。
    结论:关于口译员的方法论问题在跨文化访谈研究中仅受到了有限的关注。护理领域的研究人员需要考虑(1)口译员在研究过程中的角色/参与程度; (二)口译人员的能力和口译风格; (3)口译员对调查结果的影响。在尝试确定跨文化研究的可信赖性时,此信息是前提条件。
  • 【[睑结膜形式的睑板腺癌。适当的案例]。】 复制标题 收藏 收藏
    DOI: 复制DOI
    作者列表:Cherif N,D'Hermies F,Barraco P,Elmaleh C,Renard G,Pouliquen Y
    BACKGROUND & AIMS: :A case of Meibomian carcinoma of the left eyelid was observed in a 53-year-old-female patient. SHe had been previously treated for chronic unilateral blepharoconjunctivitis; an excisional biopsy disclosed a Meibomian carcinoma. First a total resection of both left eyelids was performed with plastic reconstructive surgery, three months later a recurrence required an orbital exenteration. This case underlines the interest of an early diagnosis which allows a more conservative treatment. The diagnosis must be kept in mind in any case of chronic unilateral blepharoconjunctivitis; histopathology has a key role in the diagnosis of Meibomian carcinoma.
    背景与目标: :在一名53岁的女性患者中观察到左眼睑睑肌癌的病例。他曾接受过慢性单侧睑结膜炎的治疗;切除活检揭示了睑板癌。首先用整形外科手术对两个左眼皮进行全切,三个月后复发,需要眼眶切除。该病例强调了允许更保守治疗的早期诊断的兴趣。在任何情况下,慢性单侧睑结膜炎都必须牢记诊断;组织病理学在睑板癌的诊断中具有关键作用。
  • 【田纳西州东部怀孕少女的生殖道沙眼衣原体感染:一项为期7年的病例对照研究。】 复制标题 收藏 收藏
    DOI:10.1016/s1083-3188(97)70060-3 复制DOI
    作者列表:Chokephaibulkit K,Patamasucon P,List M,Moore B,Rodriguez H
    BACKGROUND & AIMS: STUDY OBJECTIVE:To examine the prevalence, symptomatology, risk factors, and other infections associated with urogenital chlamydial infection in pregnant teenagers. DESIGN:Retrospective case-control study by medical record review. SETTING:Prenatal care clinic for adolescents at University of Tennessee Medical Center, Knoxville, Tennessee. PARTICIPANTS:Pregnant adolescents younger than 19 years of age who were diagnosed with chlamydial infection on the first prenatal visit from 1988 to 1994 were studied. Pregnant adolescents of similar age and socioeconomic background who came in the same day for the first prenatal visit, but were not infected, made up the control group. INTERVENTION:Routine prenatal questionnaires regarding personal and medical histories, and routine prenatal screening, including pelvic examination with Papanicolaou (PAP) smear and laboratory investigations for common genital infections and sexual transmitted disease (STDs), were obtained. MAIN OUTCOME MEASURES:Analyzed the prevalence of chlamydial infection and compared the infected group to the control group with regard to race, behavioral factors, symptoms, prenatal screening results, other concurrent genital infections, and histories of STDs. RESULTS:Of a total population of 596 pregnant teenagers, 67 (11.24%) were infected with Chlamydia trachomatis. In multivariate analysis, black race (odds ratio [OR] = 4.01; 95% confidence interval [CI] = 1.74-9.23; p = 0.001) and greater gestational age at first prenatal visit (OR = 1.11; 95% CI = 1.04-1.18; p = 0.001) were independently associated with chlamydial infection. Age, marital status, number of pregnancies, smoking, alcohol abuse, drug abuse, age at first intercourse, and multiple sex partners were not associated with the infection. Likewise, the symptom of vaginal discharge (a complaint of > 70% in each group), other genital co-infections (found > 50% in each group, mainly candidiasis and bacterial vaginosis), abnormal PAP smears (found > 60% in each group) and histories of STDs or previous chlamydial infection were not significantly different between case and control groups. Human papillomavirus infection, trichomonal infection, and dysplasia or atypia were found more often in patients infected with chlamydia, but were not statistically significant. CONCLUSION:Pregnant adolescents in east Tennessee were at risk for chlamydial infection as well as for other genital infections and abnormal PAP smears. Routine prenatal chlamydial screening is warranted because of a lack of specific symptoms.
    背景与目标: 目的:研究孕妇青少年泌尿生殖道衣原体感染的患病率,症状,危险因素和其他感染情况。
    设计:回顾性病例对照研究,病历审查。
    地点:田纳西州诺克斯维尔市田纳西大学医学中心的青少年产前保健诊所。
    研究对象:1988年至1994年第一次产前检查时被诊断患有衣原体感染的19岁以下的青少年。年龄相同,社会经济背景相似的怀孕青少年在同一天进行第一次产前检查,但未感染,组成了对照组。
    干预措施:获得有关个人和医学史的常规产前问卷,以及常规的产前筛查,包括用帕潘尼古拉(PAP)涂片进行盆腔检查以及常见生殖器感染和性传播疾病(STD)的实验室检查。
    主要观察指标:分析衣原体感染的发生率,并比较种族,行为因素,症状,产前筛查结果,其他并发生殖器感染和性病史,比较感染者与对照组。
    结果:在596名怀孕的青少年总数中,有67名(11.24%)感染了沙眼衣原体。在多变量分析中,黑人种族(赔率[OR] = 4.01; 95%置信区间[CI] = 1.74-9.23; p = 0.001)和第一次产前检查时的胎龄较高(OR = 1.11; 95%CI = 1.04- 1.18; p = 0.001)与衣原体感染独立相关。年龄,婚姻状况,怀孕次数,吸烟,酗酒,药物滥用,初次性交年龄和多性伴侣均与感染无关。同样,白带的症状(每组投诉> 70%),其他生殖器合并感染(每组发现> 50%,主要是念珠菌病和细菌性阴道病),PAP涂片异常(每发现> 60%)病例组和对照组之间的性病史或以前的衣原体感染史无显着差异。感染衣原体的患者更常发现人乳头瘤病毒感染,滴虫感染和异型增生或异型性,但无统计学意义。
    结论:田纳西州东部的怀孕青少年有衣原体感染以及其他生殖器感染和PAP涂片异常的危险。由于缺乏特定症状,需要常规的产前衣原体筛查。
  • 【CROPPER:用于跨平台和跨物种纲要研究的元基因创建者资源。】 复制标题 收藏 收藏
    DOI:10.1186/1471-2105-7-418 复制DOI
    作者列表:Paananen J,Storvik M,Wong G
    BACKGROUND & AIMS: BACKGROUND:Current genomic research methods provide researchers with enormous amounts of data. Combining data from different high-throughput research technologies commonly available in biological databases can lead to novel findings and increase research efficiency. However, combining data from different heterogeneous sources is often a very arduous task. These sources can be different microarray technology platforms, genomic databases, or experiments performed on various species. Our aim was to develop a software program that could facilitate the combining of data from heterogeneous sources, and thus allow researchers to perform genomic cross-platform/cross-species studies and to use existing experimental data for compendium studies. RESULTS:We have developed a web-based software resource, called CROPPER that uses the latest genomic information concerning different data identifiers and orthologous genes from the Ensembl database. CROPPER can be used to combine genomic data from different heterogeneous sources, allowing researchers to perform cross-platform/cross-species compendium studies without the need for complex computational tools or the requirement of setting up one's own in-house database. We also present an example of a simple cross-platform/cross-species compendium study based on publicly available Parkinson's disease data derived from different sources. CONCLUSION:CROPPER is a user-friendly and freely available web-based software resource that can be successfully used for cross-species/cross-platform compendium studies.
    背景与目标: 背景:目前的基因组研究方法为研究人员提供了大量数据。结合生物学数据库中常用的不同高通量研究技术的数据,可以得出新颖的发现并提高研究效率。但是,合并来自不同异构源的数据通常是一项艰巨的任务。这些来源可以是不同的微阵列技术平台,基因组数据库或对各种物种进行的实验。我们的目标是开发一个软件程序,以方便来自不同来源的数据的合并,从而使研究人员能够进行基因组跨平台/跨物种研究,并将现有的实验数据用于纲要研究。
    结果:我们开发了一个基于Web的软件资源,称为CROPPER,该资源使用有关Ensembl数据库中不同数据标识符和直系同源基因的最新基因组信息。 CROPPER可用于组合来自不同异构来源的基因组数据,从而使研究人员无需复杂的计算工具或建立自己的内部数据库即可进行跨平台/跨物种纲要研究。我们还提供了一个简单的跨平台/跨物种纲要研究的例子,该研究基于从不同来源获得的公开可用的帕金森氏病数据。
    结论:CROPPER是一种用户友好且免费提供的基于Web的软件资源,可以成功地用于跨物种/跨平台纲要研究。
  • 【恶性室管膜瘤的颅外转移-病例报告。】 复制标题 收藏 收藏
    DOI:10.2176/nmc.30.339 复制DOI
    作者列表:Itoh J,Usui K,Itoh M,Hashizume Y
    BACKGROUND & AIMS: :A case of malignant ependymoma with extracranial metastases is reported. A 59-year-old male was admitted to our hospital with vomiting and ataxia. Following computed tomographic (CT) scanning indicating a ring-like enhanced mass in the cerebellum, the tumor was subtotally removed in December, 1985. Histological diagnosis was malignant ependymoma. A second operation was performed in February, 1987, due to recurrence of the tumor in the fourth ventricle. Postoperative radiation therapy at a total dose of 7780 rads was given over 2 years. Eleven months after radiation therapy was completed, he reported cough and multiple skin metastases. Chest x-rays showed metastases at the right hilus. Repeated CT scans revealed separate frontal cerebral metastatic tumors. He died of respiratory insufficiency. Extracranial metastases of infratentorial ependymoma to the skin and lung are rare pathological entities.
    背景与目标: :一例恶性室间隔膜瘤伴颅外转移的报道。一名59岁的男性因呕吐和共济失调入院。在计算机断层扫描(CT)扫描显示小脑环状肿块后,于1985年12月将肿瘤小块切除。组织学诊断为恶性室间隔膜瘤。由于第四脑室肿瘤的复发,于1987年2月进行了第二次手术。术后2年进行了总剂量为7780 rads的术后放射治疗。放疗结束11个月后,他报告出现了咳嗽和多处皮肤转移。胸部X光片显示右肺门有转移。重复的CT扫描显示单独的额叶脑转移瘤。他死于呼吸功能不全。颅下膜上室间隔瘤向皮肤和肺的颅外转移是罕见的病理学实体。

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