Sackler Faculty of Medicine, School of Public Health, Tel-Aviv University, Tel-Aviv, Israel.
Clin Microbiol Infect. 2013 Apr;19(4):E190-6. doi: 10.1111/1469-0691.12099. Epub 2013 Jan 17.
The natural history of KPC-producing Klebsiella pneumoniae (KPC KP) carriage is unknown. We aimed to examine the duration of KPC KP carriage following hospital discharge and to study the risk factors for persistent carriage. A cohort of 125 KPC KP carriers was followed monthly for between 3 and 6 months after discharge from an acute-care hospital. Rectal swabs and data were collected at baseline and at each visit. KPC KP was detected by culture and direct blaKPC PCR. Acquisition time was regarded as the earliest date of KPC KP isolation. Resolution of carriage was defined as a negative KPC KP test in at least two consecutive samples. Analyses were separated for recent (<4 months) (REC, 75 patients) and remote (≥4 months) (REM, 50 patients) acquisition groups. Risk factors for persistent carriage were examined by survival analyses for the REC group and by prevalence methods for the REM group. The mean age of patients was 67.5 years and 49.6% were male. Forty-six (61%) patients in the REC group and 14 (28%) in the REM group were persistent carriers (p < 0.001). A significant risk factor for persistent carriage identified in both the REC and REM groups was the presence of any catheter (p < 0.05). Unique risk factor groups included long-term care facility (LTCF) residence (p < 0.01) and a low functional status as measured by the Barthel's index (p < 0.05) in the REC group and high Charlson's score in the REM group (p < 0.05). Out of the entire 100 patients who had at least one negative sample, only 65 remained negative on subsequent cultures. In conclusion, persistent carriage of KPC KP is associated with catheter use and a low functional status; it is more common in patients with recent acquisition and is related to LTCF stay. A single negative KPC KP test is insufficient to exclude persistent carriage.
携带产 KPC 肺炎克雷伯菌(KPC KP)的自然史尚不清楚。我们旨在研究患者出院后携带 KPC KP 的持续时间,并研究持续性携带的危险因素。对 125 名 KPC KP 携带者进行了队列研究,这些患者在急性护理医院出院后,每月进行一次随访,随访时间为 3 至 6 个月。在基线和每次就诊时采集直肠拭子和数据。通过培养和直接 blaKPC PCR 检测 KPC KP。获得时间被视为最早分离出 KPC KP 的日期。携带的解决定义为至少两个连续样本的 KPC KP 检测均为阴性。分析分为近期(<4 个月)(REC,75 例)和远程(≥4 个月)(REM,50 例)两组。通过 REC 组的生存分析和 REM 组的患病率方法,研究了持续性携带的危险因素。患者的平均年龄为 67.5 岁,49.6%为男性。在 REC 组中,46(61%)例患者和 REM 组中 14(28%)例患者为持续性携带者(p<0.001)。在 REC 和 REM 组中,持续性携带的一个显著危险因素是存在任何导管(p<0.05)。REC 组的独特危险因素组包括长期护理机构(LTCF)居住(p<0.01)和 Barthel 指数(p<0.05)测量的功能状态较低,而 REM 组的危险因素组包括高 Charlson 评分(p<0.05)。在至少有一个阴性样本的 100 例患者中,只有 65 例随后的培养仍为阴性。总之,KPC KP 的持续性携带与导管使用和功能状态低下有关;在近期获得的患者中更为常见,与长期护理机构的停留有关。单次阴性 KPC KP 检测不足以排除持续性携带。