School of Health and Related Research (ScHARR), University of Sheffield, Regent Court, 30 Regent Street, Sheffield, S1 4DA, UK.
Sheffield Adult Cystic Fibrosis Centre, Brearley Outpatient, Northern General Hospital, Herries Road, S5 7AU, Sheffield, UK.
Eur J Clin Microbiol Infect Dis. 2018 Apr;37(4):735-743. doi: 10.1007/s10096-017-3168-4. Epub 2018 Jan 6.
Pseudomonas aeruginosa status influences cystic fibrosis (CF) clinical management but no 'gold standard' definition exists. The Leeds criteria are commonly used but may lack sensitivity for chronic P. aeruginosa. We compared clinicians' decision with the Leeds criteria in three adult CF centres. Two independent prospective datasets (Sheffield dataset, n = 185 adults; ACtiF pilot dataset, n = 62 adults from two different centres) were analysed. Clinicians involved in deciding P. aeruginosa status were blinded to the study objectives. Clinicians considered more adults with CF to have chronic P. aeruginosa infection compared to the Leeds criteria. This was more so for the Sheffield dataset (106/185, 57.3% with clinicians' decision vs. 80/185, 43.2% with the Leeds criteria; kappa coefficient between these two methods 0.72) compared to the ACtiF pilot dataset (34/62, 54.8% with clinicians' decision vs. 30/62, 48.4% with the Leeds criteria; kappa coefficient between these two methods 0.82). However, clinicians across different centres were relatively consistent once age and severity of lung disease, as indicated by the type of respiratory samples provided, were taken into account. Agreement in P. aeruginosa status was similar for both datasets among adults who predominantly provided sputum samples (kappa coefficient 0.78) or adults > 25 years old (kappa coefficient 0.82). Across three different centres, clinicians did not always agree with the Leeds criteria and tended to consider the Leeds criteria to lack sensitivity. Where disagreement occurred, clinicians tended to diagnose chronic P. aeruginosa infection because other relevant information was considered. These results suggest that a better definition for chronic P. aeruginosa might be developed by using consensus methods to move beyond a definition wholly dependent on standard microbiological results.
铜绿假单胞菌状态影响囊性纤维化(CF)的临床管理,但目前尚不存在“金标准”定义。利兹标准被广泛应用,但可能对慢性铜绿假单胞菌感染缺乏敏感性。我们在三个成人 CF 中心比较了临床医生的决策与利兹标准。分析了两个独立的前瞻性数据集(谢菲尔德数据集,n=185 名成人;ACtiF 试点数据集,n=来自两个不同中心的 62 名成人)。参与决定铜绿假单胞菌状态的临床医生对研究目标不知情。与利兹标准相比,临床医生认为更多的 CF 患者存在慢性铜绿假单胞菌感染。谢菲尔德数据集更为明显(106/185,临床医生决策为 57.3%,而利兹标准为 80/185,43.2%;这两种方法之间的kappa 系数为 0.72),而 ACtiF 试点数据集则不太明显(34/62,临床医生决策为 54.8%,而利兹标准为 30/62,48.4%;这两种方法之间的kappa 系数为 0.82)。然而,一旦考虑到年龄和肺部疾病的严重程度(由提供的呼吸道样本类型指示),不同中心的临床医生就相对一致。在主要提供痰样本的成年人(kappa 系数 0.78)或年龄大于 25 岁的成年人(kappa 系数 0.82)中,两个数据集的铜绿假单胞菌状态的一致性相似。在三个不同的中心,临床医生并不总是同意利兹标准,而且往往认为利兹标准缺乏敏感性。在出现分歧的情况下,临床医生往往会诊断为慢性铜绿假单胞菌感染,因为考虑到了其他相关信息。这些结果表明,可以通过使用共识方法来制定更好的慢性铜绿假单胞菌定义,从而超越完全依赖标准微生物学结果的定义。