移植受者的肺炎:诊断与管理的全面回顾。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL Cureus Pub Date : 2024-11-14 eCollection Date: 2024-11-01 DOI:10.7759/cureus.73669
Ramakanth Pata, Joanna Kristeva, Bhanu Kosuru
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引用次数: 0

摘要

移植受者出现并发症的风险增加,包括移植物功能障碍和感染,如果不能及早发现,可能会危及生命。肺炎是实体器官移植和造血干细胞移植中最常见的并发症之一。在免疫力低下的患者感染期间,临床症状表现较晚。以早期确诊和低门槛经验疗法为中心的积极方法往往是最有效的策略。在上气道样本中分离出病原体并不一定意味着肺炎是由同一病原体引起的。CMV(巨细胞病毒)等病毒除了引起自身的原发性感染综合征外,还可能成为移植受者机会性感染的共同病原体。此外,有些病毒还具有免疫调节作用,会影响移植物的功能。鉴于肺炎的致病病原体种类繁多,最佳的诊断方法是建立一个概念框架,其中包括详细的病史,如移植类型、免疫抑制程度、抗菌药物预防、风险因素、移植后的发病时间以及胸部 CT(胸部计算机断层扫描)的影像模式。处理方法主要取决于抗菌药耐药程度、药物间相互作用以及免疫抑制的调整。
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Pneumonia in Transplant Recipients: A Comprehensive Review of Diagnosis and Management.

Transplant recipients have an increased risk of complications, including graft dysfunction and infections, which can be life-threatening if not recognized early. Pneumonia ranks as one of the most frequent complications in both solid organ and hematopoietic stem cell transplants. Clinical symptoms manifest late during infections in immunocompromised patients. An aggressive approach centered on early confirmatory diagnosis and a low threshold for empiric therapy is often the most effective strategy. The isolation of a pathogen in an upper airway sample does not necessarily mean the same organism is responsible for pneumonia. Viruses such as CMV (cytomegalovirus virus) may function as co-pathogens for opportunistic infections in transplant recipients in addition to causing their own primary infectious syndrome. Furthermore, some viruses exhibit immunomodulatory effects that can affect the graft function. Given the exhaustive list of causative pathogens responsible for pneumonia, the best approach to the diagnosis is to have a conceptual framework that includes a detailed history, such as the type of transplant, degree of immunosuppression, antimicrobial prophylaxis, risk factors, time of presentation since transplantation and the radiographic pattern on the CT chest (computer tomography of the chest). Management depends predominantly on the degree of antimicrobial resistance, drug-to-drug interaction, and adjustments to the immunosuppression.

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