Medical Department, Sunpasitthiprasong Hospital, Ubon Ratchthani, Thailand.
Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
PLoS One. 2019 Oct 9;14(10):e0223457. doi: 10.1371/journal.pone.0223457. eCollection 2019.
Sepsis can be caused by malaria infection, but little is known about the utility of the quick Sequential (Sepsis-Related) Organ Failure Assessment (qSOFA) and SOFA score in malaria. We conducted a prospective observational study from March 2013 to February 2017 to examine adults admitted with community-acquired infection in a tertiary-care hospital in Ubon Ratchathani, Northeast Thailand (Ubon-sepsis). Subjects were classified as having sepsis if they had a modified SOFA score ≥2 within 24 hours of admission. Serum was stored and later tested for malaria parasites using a nested PCR assay. Presence of severe malaria was defined using modified World Health Organization criteria. Of 4,989 patients enrolled, 153 patients (3%) were PCR positive for either Plasmodium falciparum (74 [48%]), P. vivax (69 [45%]), or both organisms (10 [7%]). Of 153 malaria patients, 80 were severe malaria patients presenting with sepsis, 70 were non-severe malaria patients presenting with sepsis, and three were non-severe malaria patients presenting without sepsis. The modified SOFA score (median 5; IQR 4-6; range 1-18) was strongly correlated with malaria severity determined by the number of World Health Organization severity criteria satisfied by the patient (Spearman's rho = 0.61, p<0.001). Of 80 severe malaria patients, 2 (2.5%), 11 (14%), 62 (77.5%) and 5 (6%), presented with qSOFA scores of 0, 1, 2 and 3, respectively. Twenty eight-day mortality was 1.3% (2/153). In conclusion, qSOFA and SOFA can serve as markers of disease severity in adults with malarial sepsis. Patients presenting with a qSOFA score of 1 may also require careful evaluation for sepsis; including diagnosis of cause of infection, initiation of medical intervention, and consideration for referral as appropriate.
疟疾感染可引发脓毒症,但目前对于快速序贯器官衰竭评估(qSOFA)和 SOFA 评分在疟疾中的应用知之甚少。我们进行了一项前瞻性观察研究,对象为 2013 年 3 月至 2017 年 2 月期间在泰国东北部乌汶叻差他尼府的一家三级保健医院因社区获得性感染而入院的成年人(乌汶脓毒症)。如果患者在入院后 24 小时内改良 SOFA 评分≥2,则将其归类为脓毒症。采集血清并使用巢式 PCR 检测疟疾寄生虫。根据改良世界卫生组织标准定义严重疟疾的存在。在纳入的 4989 例患者中,有 153 例(3%)PCR 检测疟原虫阳性,其中恶性疟原虫(恶性疟)74 例(48%)、间日疟原虫(间日疟)69 例(45%)或两种疟原虫均阳性 10 例(7%)。在 153 例疟疾患者中,80 例为出现脓毒症的严重疟疾患者,70 例为出现脓毒症的非严重疟疾患者,3 例为无脓毒症的非严重疟疾患者。改良 SOFA 评分(中位数 5;四分位距 4-6;范围 1-18)与根据患者满足的世界卫生组织严重程度标准数量确定的疟疾严重程度密切相关(Spearman's rho=0.61,p<0.001)。在 80 例严重疟疾患者中,qSOFA 评分为 0、1、2 和 3 的患者分别为 2(2.5%)、11(14%)、62(77.5%)和 5(6%)。28 天死亡率为 1.3%(2/153)。总之,qSOFA 和 SOFA 可作为疟疾脓毒症成人疾病严重程度的标志物。qSOFA 评分为 1 的患者可能也需要仔细评估脓毒症;包括感染原因诊断、开始医疗干预以及是否需要转诊。