Department of Medicine, McGill University, Montreal, QC, Canada.
Division of Infectious Diseases, McGill University Health Centre, Montreal, QC, Canada.
BMC Infect Dis. 2024 Sep 27;24(1):1032. doi: 10.1186/s12879-024-09957-y.
The performance and availability of invasive and non-invasive investigations for the diagnosis of Pneumocystis jirovecii pneumonia (PCP) vary across clinical settings. Estimating the pre-test probability of PCP is essential to the optimal selection and interpretation of diagnostic tests, such as the 1,3-β-D-glucan assay (BDG), for the prioritization of bronchoscopy, and to guide empiric treatment decisions. We aimed to develop a multivariable risk score to estimate the pre-test probability of PCP.
The score was developed from a cohort of 626 individuals who underwent bronchoscopy for the purposes of identifying PCP in a Canadian tertiary-care centre, between 2015 and 2018. We conducted a nested case-control study of 57 cases and 228 unmatched controls. Demographic, clinical, laboratory, and radiological data were included in a multivariable logistic regression model to estimate adjusted odds ratios for PCP diagnosis. A clinical risk score was derived from the multivariable model and discrimination was assessed by estimating the score's receiver operating characteristic curve.
Participants had a median age of 60 years (interquartile range [IQR] 49-68) and 115 (40%) were female; 40 (14%) had HIV and 49 (17%) had a solid organ transplant (SOT). The risk score included prior SOT or HIV with CD4 ≤ 200/µL (+ 2), serum lactate dehydrogenase ≥ 265.5 IU/mL (+ 2), radiological pattern typical of PCP on chest x-ray (+ 2) or CT scan (+ 2.5), and PCP prophylaxis with trimethoprim-sulfamethoxazole (-3) or other antimicrobials (-2). The median score was 4 points (IQR, 2-4.5) corresponding to a 28% probability of PCP. The risk prediction model had good discrimination with a c-statistic of 0.79 (0.71-0.84). Given the operating characteristics of the BDG assay, scores ≤ 3 in patients without HIV, and ≤ 5.5 in those with HIV, paired with a negative BDG, would be expected to rule out PCP with 95% certainty.
We propose the PCP Score to estimate pre-test probability of PCP. Once validated, it should help clinicians determine which patients to refer for invasive investigations, when to rely on serological testing, and in whom to consider pre-emptive treatment.
侵袭性和非侵袭性检查在诊断卡氏肺孢子菌肺炎(PCP)中的表现和可用性因临床环境而异。估计 PCP 的术前概率对于最佳选择和解释诊断测试至关重要,例如 1,3-β-D-葡聚糖检测(BDG),以便优先进行支气管镜检查,并指导经验性治疗决策。我们旨在开发一个多变量风险评分来估计 PCP 的术前概率。
该评分是从 2015 年至 2018 年期间在加拿大一家三级保健中心接受支气管镜检查以确定 PCP 的 626 名个体的队列中开发的。我们对 57 例病例和 228 例未匹配的对照进行了嵌套病例对照研究。将人口统计学、临床、实验室和影像学数据纳入多变量逻辑回归模型,以估计 PCP 诊断的调整比值比。从多变量模型中得出临床风险评分,并通过估计评分的接收者操作特征曲线来评估其区分度。
参与者的中位年龄为 60 岁(四分位距 [IQR] 49-68),115 人(40%)为女性;40 人(14%)患有 HIV,49 人(17%)有实体器官移植(SOT)。风险评分包括先前的 SOT 或 HIV 合并 CD4≤200/µL(+2)、血清乳酸脱氢酶≥265.5IU/mL(+2)、胸部 X 线或 CT 扫描上具有典型的 PCP 放射学模式(+2.5)、以及使用甲氧苄啶-磺胺甲恶唑(-3)或其他抗生素(-2)进行 PCP 预防。中位数评分为 4 分(IQR,2-4.5),对应 PCP 的概率为 28%。风险预测模型具有良好的区分度,C 统计量为 0.79(0.71-0.84)。鉴于 BDG 检测的操作特征,如果没有 HIV 的患者评分≤3,而 HIV 患者评分≤5.5,并与阴性 BDG 配对,则预计可 95%确定排除 PCP。
我们提出了 PCP 评分来估计 PCP 的术前概率。一旦得到验证,它应该有助于临床医生确定哪些患者需要进行侵袭性检查,何时依赖血清学检测,以及在哪些患者中考虑预防性治疗。