Walsh F W, Rolfe M W, Rumbak M J
Division of Pulmonary and Critical Care Medicine, University of South Florida College of Medicine, Tampa, USA.
Chest Surg Clin N Am. 1999 Feb;9(1):19-38.
Practical approaches to the initial evaluation of solid organ transplant patients, BMT patients, and HIV-infected patients with pulmonary disease are summarized in Figures 2, 3, and 4. These algorithms are meant to be used as guidelines for the clinician. The clinical setting will ultimately determine the extent and speed of the evaluation. Patients who are recipients of solid organ transplants and have pulmonary symptoms may have focal or diffuse changes or may have normal chest radiographs. In all these groups, sputum is obtained by expectation. If a pathogen is found in any of the groups, it is treated. When no pathogen is found on sputum examination in patients with focal disease, empiric antibiotic therapy is given. If the patients do not improve on the empiric antibiotics, then bronchoscopy is performed. Some centers proceed directly to bronchoscopy before antibiotics are started in the hope of directing antibiotic therapy. Patients who have a normal CXR or diffuse infiltrates and no identified pathogen on examination of sputum undergo bronchoscopy, and the protocol is followed until a diagnosis is made (see Fig. 2). Patients who have received a BMT and who present with pulmonary symptoms are treated as shown in Figure 3. The CXR will reveal if the infiltrate is focal or diffuse. Those with focal infiltrates are treated with broad-spectrum antibiotics for 48 to 72 hours. If the symptoms and signs do not show some resolution, then bronchoscopy is usually performed. The effect of diffuse infiltrates in BMT patients depends to a large extent how far along in recovery from the transplant the patient is when they develop the infiltrates. During the first 30 days posttransplant, pulmonary edema commonly occurs, and the infiltrates may resolve with diuresis. If the patient is not clinically fluid overloaded or they do not respond to the diuretic therapy, then bronchoscopy with BAL is indicated. Finally, many HIV-infected patients may present with pulmonary symptoms. They may have a normal CXR or a diffuse or focal pattern (Fig. 4). All patients are subjected to sputum induction to identify a pathogen. If one is identified, it is treated. Should the patient not respond to treatment adequately or a pulmonary pathogen is not found, then bronchoscopy with BAL, protected specimen brush, or a transbronchial biopsy is attempted. The above schema is a general guideline to the initial evaluation of pulmonary disorders in the ICP. The respiratory abnormality is found in most of the cases if these algorithms are closely followed. If the patient does not improve or deteriorates further, additional diagnostic procedures such as video-assisted thorascopic lung biopsy or CT-directed transthoracic needle biopsy may be needed.
图2、图3和图4总结了对实体器官移植患者、骨髓移植患者以及患有肺部疾病的HIV感染患者进行初步评估的实用方法。这些算法旨在作为临床医生的指导方针。临床情况最终将决定评估的范围和速度。实体器官移植受者出现肺部症状时,可能有局灶性或弥漫性改变,也可能胸部X线片正常。在所有这些组中,通过咳痰获取痰液。如果在任何一组中发现病原体,就进行治疗。当局灶性疾病患者痰液检查未发现病原体时,给予经验性抗生素治疗。如果患者在使用经验性抗生素后没有改善,那么就进行支气管镜检查。一些中心在开始使用抗生素之前直接进行支气管镜检查,希望能指导抗生素治疗。胸部X线片正常或有弥漫性浸润且痰液检查未发现病原体的患者接受支气管镜检查,并按照方案进行检查,直到做出诊断(见图2)。接受骨髓移植并出现肺部症状的患者按图3所示进行治疗。胸部X线片将显示浸润是局灶性还是弥漫性。局灶性浸润患者用广谱抗生素治疗48至72小时。如果症状和体征没有得到一定程度的缓解,那么通常进行支气管镜检查。骨髓移植患者弥漫性浸润的影响在很大程度上取决于患者在出现浸润时距离移植恢复有多远。在移植后的前30天内,常发生肺水肿,通过利尿浸润可能会消退。如果患者临床上没有液体过载或对利尿治疗无反应,那么就需要进行支气管肺泡灌洗的支气管镜检查。最后,许多HIV感染患者可能出现肺部症状。他们的胸部X线片可能正常,也可能呈现弥漫性或局灶性模式(图4)。所有患者都进行痰液诱导以确定病原体。如果发现病原体,就进行治疗。如果患者对治疗反应不佳或未发现肺部病原体,那么尝试进行支气管肺泡灌洗、保护样本刷检或经支气管活检的支气管镜检查。上述方案是对免疫受损患者肺部疾病进行初步评估的一般指导方针。如果严格遵循这些算法,大多数情况下能发现呼吸异常。如果患者没有改善或进一步恶化,可能需要额外的诊断程序,如电视辅助胸腔镜肺活检或CT引导下经胸针吸活检。