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肾脏病与透析肾移植杂志 ›› 2012, Vol. 21 ›› Issue (6): 501-506.

• 论文 •    下一篇

激素治疗并发重症肺部感染患者的临床分析

  

  • 出版日期:2012-12-28 发布日期:2012-12-31

Severe pulmonary infection as a complication of glucocorticosteroids therapy in patients with podocytopathy

  • Online:2012-12-28 Published:2012-12-31

摘要:

摘  要    目的:探讨足细胞病患者糖皮质激素(GC)治疗后并发重症肺部感染的临床特点。 方法:回顾性分析2011年4月~2012年4月南京军区南京总医院全军肾脏病研究所肾脏病ICU收治的11例足细胞病患者,均在GC治疗后并发重症肺部感染和ARDS。收集患者足细胞病的临床特点,GC治疗剂量及疗效,肺部感染的临床表现,免疫功能、病原学特点、治疗经过和预后。  结果:11例患者(男7例,女4例)年龄28.5±12.7岁(16~50岁)均经肾活检诊断为足细胞病,给予足量GC诱导治疗,其中甲泼尼龙8例(48mg/d),泼尼松3例(50~60mg/d)。GC治疗8周内均达到完全缓解予减量,但在GC治疗13±2周时并发重症肺部感染,以发热和胸闷为首发症状,最高体温39.9±0.76℃(38.9~41.2℃),伴有咳嗽、少痰。病情进展急剧,突出表现为呼吸困难,氧合指数均低于200,平均117.7±42.1(57.5~200)。病初肺部体征少,无明显干湿啰音,胸部CT或胸片提示双肺弥漫性间质性炎症。体液免疫检查示血清IgG、IgM正常,而细胞免疫功能低下,外周血淋巴细胞总数偏低(538.8±165.5/µl),其中CD4+T淋巴细胞计数明显减低,为133.3±45.43个/µl。病原学检查阳性率低,影像学检查提示间质性肺炎,临床疑诊为耶氏肺孢子虫肺炎(Pneumocystis carinii pneumonia, PCP)。患者均给予辅助机械通气、复方磺胺甲噁唑联合米卡芬净、甲强龙及抗感染、对症支持治疗,6例行连续性肾脏替代治疗(CRRT),1例联合体外膜肺氧合(ECMO)治疗,最终8例(72.7%)痊愈,3例(27.3%)死亡或放弃;平均ICU住院时间为18±7d(11~33d),总住院时间平均24±14d(13~55d)。  结论:激素治疗敏感的足细胞病患者,在肾脏病完全缓解、激素减量过程中仍可继发严重细胞免疫缺陷和重症肺部感染,病情进展快,病死率高,需要引起临床医生重视。

关键词: 关键词 , 重症肺部感染 糖皮质激素 足细胞病

Abstract:

ABSTRACT  Objective: To investigate the clinical features of severe pulmonary infection in patients treated with glucocorticosteroids for their podocyte injury.  Methodology : Eleven patients with podocytopathy who admitted to ICU because of severe pulmonary infection as well as ARDS was retrospectively reviewed. The clinical features of podocytopathy, time and efficacy of GC therapy, the clinical manifestations of pulmonary infection, immune function, pathogenic characteristics, treatment through and prognosis were investigated. Results: They were 7 males and 4 females with an average age of 28.5±12.7 years old ranged from16 to 50. All patients with biopsy-proved podocytopathy, Among them, 8 cases used full-dose methylprednisolone (48mg/day), and 3 cases used prednisone (50 to 60mg/day). At the 8th week, 11 patients (100%) had total remission. However, all of them developed pulmonary infection after taking glucocorticosteroids within 9~16weeks, with an average time of 13±2 weeks. They complained of progressive dyspnea and fever, cough and a little white sputum. Their temperature was higher at 39.9±0.76°C (38.9 to 41.2°C). Rapid progression was observed in the patients, with difficulty breathing and severe hypoxemia as the significant symptoms. The oxygenation indices were below 200 with an average of 118±42.1 (57.5 to 200). Coarse breath sounds was heard initially and a few wet and dry rales later on lung auscultation. Chest CT or chest radiography was suggestive of bilateral diffuse interstitial inflammation. Laboratory examination revealed a lower level of cellular immune function and reduced count of peripheral blood lymphocytes(539±166/µl), as well as significantly decreased CD4+ T lymphocyte count at 133±45.4/µl . On the contrary, IgG and IgM levels were with the normal range. All patients were given suspected diagnosis of pneumocystis carinii pneumonia and need ventilatory support therapy. The triple therapy of antiinfection drugs was SMZ, micafungin and methylprednisolone. 6 patients required continuous renal replacement therapy (CRRT), one of them given extracorporeal membrane oxygenation therapy (ECMO). After therapy, 8(72.7%) patients recovered and 3 (27.3%) died or gave up treatment. The average ICU stay was 18±7.0 days (11 to 33), and the overall average length of stay 24±14 days (13 to 55). Conclusion: steroid-sensitive patients who were treat with glucocorticosteroids for their podocyte injury may appears severe pulmonary infections even though they had complete remission. Regard to immunodeficiency, the disease can rapidly progress and mortality is high.

Key words: Key words:Severe pulmonary infection , glucocorticosteroid , podocytopathy