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肝移植患者潜伏性结核的检测和管理。

Detection and management of latent tuberculosis in liver transplant patients.

机构信息

Division of Gastroenterology, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Liver Transpl. 2011 Mar;17(3):306-14. doi: 10.1002/lt.22203.

Abstract

The optimal means for detecting and managing liver transplantation (LT) patients with latent tuberculosis (TB) are not well defined. Our study aims were to (1) determine the frequency and risk factors of latent TB in a large cohort of consecutive adult LT candidates and (2) determine the safety and efficacy of isoniazid treatment in LT recipients with latent TB. A review of patients assessed for latent TB by skin testing using purified protein derivative (PPD; January 2004 to September 2008) or with the interferon-γ release assay QuantiFERON-TB Gold (QFT; March 2008 to October 2009) was undertaken. The baseline clinical features and outcomes of subjects with latent TB and subjects without latent TB were compared. Twenty-five of 420 subjects (6.0%) were positive for PPD. In comparison, 11 of 119 subjects (9.2%) had a positive QFT assay, and 15 others (13%) had indeterminate results. Both PPD-positive and QFT-positive subjects were less likely to be Caucasian than subjects without latent TB (p < 0.001). The 3-year survival rate of the 25 LT recipients with latent TB was similar to that of the 296 LT recipients without latent TB (78.7% versus 74.6%, P = 0.58). Fifteen of the 25 latent TB patients received isoniazid at a mean of 0.67 months after LT. Although isoniazid was discontinued in 8 subjects because of possible side effects, none of the 25 latent TB patients developed TB reactivation after transplantation with a mean follow-up of 33 months. In conclusion, both QFT testing and PPD testing demonstrate similar rates of detecting latent TB infection in American LT candidates, but QFT testing also leads to a moderate rate of indeterminate test results. Early isoniazid chemoprophylaxis after LT is poorly tolerated and is frequently discontinued.

摘要

检测和管理潜伏性结核病(TB)的肝移植(LT)患者的最佳方法尚未明确。我们的研究目的是:(1)确定大批次连续成年 LT 候选者中潜伏性 TB 的频率和危险因素;(2)确定 LT 受者中潜伏性 TB 的异烟肼治疗的安全性和有效性。对接受纯化蛋白衍生物(PPD)皮肤试验(2004 年 1 月至 2008 年 9 月)或干扰素 -γ 释放试验 QuantiFERON-TB Gold(QFT;2008 年 3 月至 2009 年 10 月)评估潜伏性 TB 的患者进行了回顾性研究。比较了潜伏性 TB 患者和无潜伏性 TB 患者的基线临床特征和结局。在 420 例患者中,有 25 例(6.0%)PPD 阳性。相比之下,119 例患者中有 11 例(9.2%)QFT 检测阳性,另有 15 例(13%)结果不确定。PPD 阳性和 QFT 阳性患者比无潜伏性 TB 的患者更不可能为白人(p<0.001)。25 例 LT 接受者中潜伏性 TB 的 3 年生存率与 296 例无潜伏性 TB 的 LT 接受者相似(78.7%比 74.6%,p=0.58)。在 LT 后平均 0.67 个月,25 例潜伏性 TB 患者中有 15 例接受了异烟肼治疗。尽管由于可能的副作用,有 8 例患者停用了异烟肼,但在平均 33 个月的随访中,25 例潜伏性 TB 患者无一例在移植后发生 TB 再激活。总之,QFT 检测和 PPD 检测均能检测出美国 LT 候选者中的潜伏性 TB 感染,但 QFT 检测也会导致一定比例的不确定检测结果。LT 后早期异烟肼化学预防耐受性差,且经常被停用。

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