Patients admitted to 32 Swedish hospitals between 2011 and 2014 were retrospectively included from the Swedish National Quality Register of CAP. Using propensity score matched data, stratified by CRB-65 score, we studied the effect of performing UAT and of positive test results on treatment with broad-spectrum β-lactam monotherapy (BSBM) and antibiotics with coverage for atypical bacteria compared to narrow-spectrum β-lactam monotherapy (NSBM).
UAT was performed for 4,995/14,590 (34.2%) patients, 603/4,995 (12.1%) of whom had positive test results. At day three, performing UAT was not associated with decreased use of BSBM (OR 1.07, 95% CI 0.94-1.23) but was associated with increased atypical coverage among patients with CRB-65 score 2 (OR 1.47, 95% CI 1.06-2.02). A positive UAT was associated with decreased BSBM use (OR 0.39, 95% CI 0.25-0.60) and decreased atypical coverage (OR 0.25, 95% CI 0.16-0.37), predominantly in non-severe CAP. At day one, performing UAT was associated with atypical coverage among patients with CRB-65 scores 2 (OR 2.60, 95% CI 1.69-3.98) and 3-4 (OR 3.69, 95% CI 1.55-8.79), and a positive test reduced the odds of BSBM treatment among CRB-65 score 3-4 patients (OR 3.49, 95% CI 1.02-12.0).
Performing UAT had no overall effect on decreasing the use of BSBM treatment by day three of hospitalization, yet non-severely ill patients with positive UAT results were less likely to be treated with BSBM and antibiotics with atypical coverage.
2011年至2014年期间,32家瑞典医院收治的患者被回顾性纳入了瑞典国家CAP质量登记册。使用倾向得分匹配的数据,按CRB-65评分分层,与窄谱β-内酰胺单药治疗(NSBM)相比,我们研究了使用广谱β-内酰胺单药治疗(BSBM)和具有非典型细菌覆盖率的抗生素进行UAT和阳性检测结果的效果.
对4,995/14,590(34.2%)患者进行了UAT,603/4,995(12.1%)的测试结果为阳性。第三天,在CRB-65评分为2分的患者中,进行UAT与BSBM使用减少无关(OR1.07,95%CI0.94~1.23),但与非典型覆盖率增加相关(OR1.47,95%CI1.06~2.02).UAT阳性与BSBM使用减少(OR0.39,95%CI0.25-0.60)和非典型覆盖率降低(OR0.25,95%CI0.16-0.37)相关,主要发生在非重度CAP中。第一天,在CRB-65评分为2(OR2.60,95%CI1.69-3.98)和3-4(OR3.69,95%CI1.55-8.79)的患者中,执行UAT与非典型覆盖率相关,在CRB-65评分为3~4分的患者中,阳性检测降低了BSBM治疗的几率(OR3.49,95%CI1.02~12.0).
进行UAT对减少住院第三天使用BSBM治疗没有总体影响,然而,UAT结果为阳性的非重症患者接受BSBM和非典型覆盖抗生素治疗的可能性较小.