Jagannathan Megha
Internal medicine, Wayne State University School of Medicine, Detroit, USA.
Cureus. 2019 Oct 9;11(10):e5874. doi: 10.7759/cureus.5874.
Pneumocystis jirovecii pneumonia (PJP), historically regarded as an AIDS-defining illness, has been increasingly reported in non-HIV patients due to a myriad of risk factors resulting in immunosuppression. One of the more salient risk factors is corticosteroid use, including both low and high doses in prolonged, short-course, and intermittent-course regimens. The stance on PJP prophylaxis with trimethoprim-sulfamethoxazole (TMP-SMX) for non-HIV patients on corticosteroids alone (e.g., for inflammatory conditions) is unclear, with no official guidelines classifying patients by dosage, length of treatment, or preexisting conditions. Additionally, clinicians often prescribe significant dosages of corticosteroids without proper consideration of the immunosuppressive risk. Here, we describe a case of a non-HIV patient with suspected dermatomyositis who was initially prescribed prednisone 15 mg daily with no prophylaxis for one month, then increased prednisone 80 mg daily with added TMP-SMX prophylaxis. Three days following increase, the patient developed significant PJP-associated pneumomediastinum and expired within one week despite mechanical ventilation and aggressive TMP-SMX treatment. This deterioration within days following corticosteroid increase with appropriately prescribed prophylaxis is an unusual presentation of PJP pneumonia and emphasizes the fulminant progression of the disease. The unnecessary over-prescription of steroids in unconfirmed autoimmune conditions has led to an unfortunate increase in devastating infections such as PJP. Clinicians should maintain high clinical suspicion concerning the development of PJP pneumonia in corticosteroid patients as well as consider prophylaxis even before a significant steroid dose increase is prescribed.
耶氏肺孢子菌肺炎(PJP),历史上被视为艾滋病定义性疾病,由于多种导致免疫抑制的危险因素,在非HIV患者中的报道越来越多。其中一个较为突出的危险因素是使用皮质类固醇,包括长期、短疗程和间歇疗程方案中的低剂量和高剂量。对于仅使用皮质类固醇的非HIV患者(例如,用于炎症性疾病),使用甲氧苄啶-磺胺甲恶唑(TMP-SMX)进行PJP预防的立场尚不清楚,没有官方指南根据剂量、治疗时长或既有病症对患者进行分类。此外,临床医生经常在未适当考虑免疫抑制风险的情况下开具大剂量的皮质类固醇。在此,我们描述一例疑似皮肌炎的非HIV患者,最初每天服用15毫克泼尼松,未进行预防,持续一个月,然后将泼尼松剂量增加至每天80毫克,并添加TMP-SMX进行预防。剂量增加三天后,患者出现严重的与PJP相关的纵隔气肿,尽管进行了机械通气和积极的TMP-SMX治疗,但仍在一周内死亡。在适当开具预防药物的情况下,皮质类固醇剂量增加后数天内病情恶化是PJP肺炎的一种不寻常表现,强调了该疾病的暴发性进展。在未确诊的自身免疫性疾病中不必要地过度开具类固醇药物导致了诸如PJP等毁灭性感染的不幸增加。临床医生应高度怀疑皮质类固醇患者发生PJP肺炎的可能性,并在大幅增加类固醇剂量之前就考虑进行预防。