体重减轻和糖尿病是侵袭性曲霉感染在非免疫功能低下人群中发展的新危险因素。

Farhad Ghanaat, John A Tayek
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引用次数: 24

摘要

公认的曲霉病危险因素包括艾滋病毒、癌症、最近的皮质类固醇(强的松)治疗、化疗或胸外科手术。未确定的危险因素可能包括体重减轻和糖尿病史。回顾性分析了20年间(1992-2012)在Harbor UCLA医学中心通过出院诊断确定的23例无典型IA危险因素的患者。没有一种已知的危险因素与侵袭性糙皮病(IA)有关。66%的IA患者(15 / 23)有体重减轻史。体重减少从3.3磅到43磅不等。体重减轻的患者平均减轻22±3磅(平均值±SEM)。在这一小组IA患者中,23例患者中有8例(34%)患有糖尿病,这明显高于100例严重脓毒症患者中19%的糖尿病发病率(结论:糖尿病的发病率高于免疫功能低下患者,可能被认为是曲霉菌感染发展的另一个危险因素。此外,对于非免疫功能低下的患者,体重减轻史应增加对IA诊断的怀疑。非免疫功能低下患者早期识别和治疗曲霉病可能改善预后。对于侵袭性曲霉病及其高死亡率,应将体重减轻和糖尿病列入众所周知的危险因素清单。
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Weight loss and diabetes are new risk factors for the development of invasive aspergillosis infection in non-immunocompromized humans.

Well-established risk factors for aspergillosis include HIV, cancer, recent corticosteroid (prednisone) therapy, chemotherapy, or thoracic surgery. Non-established risk factors may include weight loss and a history of diabetes. Twenty-three patients without the classical risk factors for IA were identified retrospectively at Harbor UCLA Medical Center by discharge diagnosis over a 20 year period (1992-2012). None of the well-known risk factors are for Invasive Apergillious (IA). A history of weight loss was seen in 66% of the patients with IA (15 of 23). The weight loss ranged from 3.3 lbs to 43 lbs. In patients with weight loss the average loss was 22±3 lbs (mean±SEM). In this small group of patients with IA, diabetes was seen in 8 of the 23 (34%), which is significantly higher than the 19% incidence of diabetes seen in 100 patients with severe sepsis (p<0.05). Likewise, the 34% incidence of diabetes was higher than the 21% incidence reported in immunocompromised patients with invasive aspergillus (IA) infection (p<0.05). A reduced serum albumin concentration was seen in 33% of the study patients, which was less common than the 87% incidence seen in patients with severe sepsis or candidaemia (54%). Seventeen of the 23 patients had pulmonary involvement. While no one had a well-established risk factor for aspergillious, four patients had alcoholism as a potential risk factor. Eleven of the 23 (48%) died during the hospital stay despite antifungal therapy. Immunocompromised patients are known to have a mortality rate of approximately 45% for pulmonary or disseminated disease.

Conclusion: The incidence of diabetes was greater than seen in immunocompromised patients and may be considered an additional risk factor for the development of aspergillois infection. In addition, a history of weight loss should increase the suspicion for the diagnosis of IA in otherwise a non-immunocompromised patient. Early recognition and treatment of aspergillosis in the non-immunocompromised patient may improve outcome. Weight loss and diabetes should be added to the list of well-known risk factors for invasive aspergillosis and its high mortality rate.

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