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Organ Transplant Infection Prevention and Detection Project

2012年8月14日 更新者:University of Pittsburgh

Organ Transplant Infection Prevention and Detection Project 1.0; Cohort Study of Transplant Recipients at "Ultra-High" Risk for Invasive Fungal Infections

Fungal infections are leading causes of morbidity and mortality in transplant recipients, yet comprehensive epidemiologic studies in this area are lacking. For this reason, the Centers for Disease Control and Prevention have provided a grant to the University of Pittsburgh to study this subject.

The study has four specific aims:

1. To determine the risk of fungal infections in a center where "tolerogenic" immunosuppressive protocols are currently in place, and to determine whether there are any measures of immune system function which correlate with risk of fungal infection.

2: To create a repository of serum, urine and bronchoalveolar lavage specimens for the purpose of determining the effectiveness of novel diagnostic tests for invasive fungal infections. Such a repository could also be utilized for the purpose of determining the effectiveness of novel diagnostic tests for viral infections such as West Nile Virus, cytomegalovirus, HHV-6 and HHV-8.

Specific aim 1 will be investigated by creating a prospective database of solid organ transplant recipients at the University of Pittsburgh Medical Center, including demographic factors as well as subsequent development of infection. The immune function of patients will be assessed by measuring T cell subsets and assessing T cell function using the Cylex assay. Specific aim 2 involves collection of serum, urine and bronchoalveolar lavage fluid. These specimens will be stored and later tested at the Centers for Disease Control and Prevention in the assessment of novel tests developed for the diagnosis of invasive fungal infections.

研究概览

地位

完全的

条件

详细说明

This is a longitudinal cohort study. Participation in the research database is limited to placement of the subjects' identifiable medical information related to their organ transplantation and immunosuppression use. Participants can consent to allow only medical information collected and/or provide blood and tissue samples.

Patients seen by the Infectious Disease/Transplant team will be asked to provide their written informed consent to allow their past, current and future identifiable medical record information related to their condition placed in the research database. The medical record information that will be placed in the database will be related directly to the patients'-participants' disease process. However, since concurrent medical conditions and treatments (i.e., not related directly to transplantation) may impact substantially the patients'-participants' condition, it is likely that all of the patients'-participants' past, current and future identifiable medical record information will be placed in the research database. Consent will be obtained in the pre-transplant period. The advantage of this system is that consent is obtained directly from the patient (rather than from a proxy, as would be necessary in situations where consent is obtained post-transplant). Secondly, since the timing transplantation can not be predicted with certainty and may occur at hours during which research coordinators are not working, consent prior to transplantation ensures that the entire post-transplant period is covered by consent. This would ensure that early post-transplant infections are not missed, thereby eliminating a form of systematic bias. The disadvantage of this system is that some patients undergo informed consent who do not subsequently undergo transplantation. Additionally, occasional patients who present with acute organ system failure (for example, patients with fulminant hepatic failure) will not undergo pre-transplant consent. We will attempt to minimize this risk by pre-study and subsequent meetings with transplant surgeons to ensure the study team is informed about such patients on a timely basis.

Participant medical information will be stored electronically within the research data base.

The names, social security numbers, and medical record numbers of the participants will be deleted from their stored medical information and replaced with a linkage code. Access to participant medical information contained within the research database will be restricted to the research investigator and research staff..

Information linking the linkage codes to the participants' names, social security numbers and medical record numbers will be stored in a secure location separate from the medical information. Access to the information linking the linkage codes with participant names, social security numbers and medical record numbers will be granted only to the Principal Investigator and research coordinator of this research database.

Participant medical record information will be stored in the research database for an indefinite period of time.

The participant will be followed for up to four years after transplantation.

Epidemiologic information to be collected

At baseline (upon signing informed consent), the following information will be collected: Demographic data - age, sex, state of birth, prior travel to an area endemic for histoplasmosis, coccidioidomycosis or blastomycosis, indication for listing for transplantation, other prior medical problems, prior chemotherapy/immunosuppressive therapies and prior fungal infections.

During the first week post transplant, the following information will be collected: Type and date of transplant, UNOS status, pre-transplant conditioning with thymoglobulin or alemtuzumab, ongoing immunosuppressive regimen. At the time of fungal infection, the following information will be collected - symptoms and signs of infection and their duration, receipt of antifungal prophylaxis, presence of indwelling vascular devices, duration of neutropenia, presence of graft versus host disease (GVHD) and its severity and treatment, history of graft rejection and its treatment

Six weeks following the fungal infection, the following information will be collected - treatment of the infection, outcome (including duration of hospitalization, fate of organ graft and mortality)

Blood work to be collected

A separate consent form will be presented for blood work. This is to ensure that the patients who decline blood work specifically for the study still have the opportunity to have their epidemiologic information collected. The following tests will be collected specifically for the study.

  • CD4 lymphocyte count pre-transplant and then every three months post-transplant
  • Blood for Cylex assay pre-transplant then once per month X18 months
  • Blood for storage (see below)* Additionally, bronchoalveolar lavage fluid will be collected (see below for schedule)

    *Blood for storage will be collected on those patients at highest risk for invasive fungal infections (4, 11, 42, 43). These patients will be:

  • Lung transplant recipients
  • Intestinal transplant recipients
  • Kidney/pancreas transplant recipients
  • Liver transplant recipients on renal replacement therapy or requiring re-transplantation in the first week post-transplantation

The BAL samples will be collected only if the subject undergoes a clinically indicated bronchoscopy and only the excess BAL fluid will be collected for the study.

Mycologic samples

All fungi grown from routine clinical specimens from patients in the study will be saved by the clinical microbiology laboratory. They will be made available to the Centers for Disease Control and Prevention (CDC) - other researchers working in conjunction with the CDC may also examine these isolates for mechanisms of antifungal resistance or mechanisms of pathogenicity. No patient identifiers would be provided to either the CDC or to other researchers. Only relevant "de-identified" clinical information (eg, prior use of specific antifungal agents) would be provided.

研究类型

观察性的

注册 (实际的)

200

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Pennsylvania
      • Pittsburgh、Pennsylvania、美国、15213
        • University of Pittsburgh Medical Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

非概率样本

研究人群

lung transplant recepients

描述

Inclusion Criteria:

  • will to sign consent
  • speak English
  • On lung transplant list awaiting lung transplantation

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:David L Paterson, MD、University of Pitttsburgh

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2006年5月1日

初级完成 (实际的)

2012年8月1日

研究完成 (实际的)

2012年8月1日

研究注册日期

首次提交

2005年9月13日

首先提交符合 QC 标准的

2005年9月13日

首次发布 (估计)

2005年9月15日

研究记录更新

最后更新发布 (估计)

2012年8月16日

上次提交的符合 QC 标准的更新

2012年8月14日

最后验证

2012年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • IRB# 0408132
  • CDC (CDC)

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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