Nomogram for Pneumocystis jirovecii Pneumonia in Non-HIV-Infected Pneumonia Patients Undergoing Oral Glucocorticoid Treatment

被引:5
作者
Lang, Qin [1 ,2 ]
Li, Lijuan [3 ]
Zhang, Yue [4 ]
He, Xing [5 ]
Liu, Yafeng [6 ,7 ]
Liu, Zhen [8 ]
Yan, Haiying [1 ,9 ,10 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Pulm & Crit Care Med, Chengdu 610000, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Pulm & Crit Care Med, Chengdu 610000, Peoples R China
[3] Capital Med Univ, China Japan Friendship Hosp, Natl Clin Res Ctr Resp Dis, Beijing 100000, Peoples R China
[4] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Nephrol, Chengdu 610000, Peoples R China
[5] Chengdu Med Coll, Sch Clin Med, Chengdu 610000, Peoples R China
[6] Anhui Univ Sci & Technol, Sch Med, Huainan 232000, Peoples R China
[7] Anhui Prov Engn Lab Occupat Hlth & Safety, Huainan 232000, Peoples R China
[8] First Hosp Liangshan Prefecture, Xichang 615000, Peoples R China
[9] Chengdu Qing Cheng Mt Hosp, Dept Pulm & Crit Care Med, Chengdu 610000, Peoples R China
[10] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Pulm & Crit Care Med, 32 Sec 2,1st Ring Rd, Chengdu 610000, Sichuan, Peoples R China
来源
INFECTION AND DRUG RESISTANCE | 2023年 / 16卷
关键词
Pneumocystis jirovecii pneumonia; pneumonia; nomogram; glucocorticoid; PROGNOSTIC-FACTORS; CARINII-PNEUMONIA; DIAGNOSIS; AIDS;
D O I
10.2147/IDR.S398850
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose: Pneumocystis jirovecii pneumonia (PJP) is an opportunistic but potentially fatal infection with increasing prevalence in HIV-free patients. Glucocorticoid therapy is one of the most important risk factors for PJP. The delay in diagnosis contributes to poor outcomes. Hence, the aim of this study was to develop and validate a nomogram for the diagnosis of PJP in patients with non-HIVinfected pneumonia who are undergoing oral glucocorticoid treatment. Patients and Methods: This study was a retrospective, cross-sectional research. The development group included 434 patients who were admitted with pneumonia from 6 hospitals. Demographics, symptomatic features, laboratory and computed tomography data were analyzed using the least absolute shrinkage and selection operator (LASSO) to select potential diagnostic indicators. Binary logistic regression was used to develop a diagnostic nomogram. Another 119 patients with pneumonia admitted at Sichuan Provincial People's Hospital was used as the validation group. The diagnostic performance of the nomogram was measured by area under the receiver-operating-characteristics curve (AUC), calibration curves, and the net benefit by decision curve. Results: PJP prevalence was 25.3% in the development group. LASSO regression revealed that age, lymphocyte count, fever, dry cough, respiratory failure, ground-glass opacity in lungs, glucocorticoid therapy duration, and immunosuppressive therapy were indicators of PJP. The nomogram showed robust discrimination, with an AUC of 0.82 (95% CI 0.77-0.86) in the development group and an AUC of 0.87 (95% CI 0.80-0.94) in the validation group, both showing acceptable calibration. In the decision curve analysis, our model consistently achieved a greater net benefit across almost all ranges of clinical thresholds. Conclusion: We developed a nomogram with good diagnostic power for PJP diagnosis in pneumonia patients receiving oral glucocorticoids. This nomogram may help promote timely treatment of PJP and thus reduce the mortality rate in these patients.
引用
收藏
页码:755 / 767
页数:13
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