Graduate Program in Infectious Diseases and Tropical Medicine, School of Medicine, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, 190, Santa Efigênia, Belo Horizonte MG, CEP: 30130-100, Brazil.
Hospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
BMC Infect Dis. 2024 Sep 13;24(1):974. doi: 10.1186/s12879-024-09544-1.
The greater predisposition to infections, as well as the possibility of a worse response to treatment, can lead to the excessive use of antimicrobials among cancer patients. C-reactive protein (CRP) has gained prominence as a tool for monitoring therapeutic responses and reducing the duration of antibiotic therapy; however, few studies have analyzed this protein in cancer patient populations. We hypothesize that cancer patients with a good response to antibiotic therapy show a faster decline in serum CRP levels, which would allow us to identify candidates for short-course treatments.
To evaluate the behavior of serum CRP levels among adult cancer patients using antibiotic therapy, and its association with the duration of this treatment, therapeutic response, and clinical recurrence.
This work consisted of a retrospective study with cancer patients admitted to a university hospital between September 2018 and December 2019. Adults (age ≥ 18 years) who underwent at least one course of antibiotic therapy were included. CRP behavior over the first 7 days of treatment was classified as: i) good response: when the CRP value on the fifth day of therapy reached 50% or less of the peak value detected in the first 48 h of treatment, and ii) poor response: Maintenance, within the same interval, of a CRP value > 50% of the peak value in the first 48 h. The duration of antibiotic therapy was categorized as up to seven full days or more. Outcomes were assessed by events that occurred during the 30 days of hospitalization or until hospital discharge.
Clinical recurrence of the index infection.
i) Death from any cause; ii) microbiological recurrence; iii) therapeutic response; iv) colitis associated with Clostridioides difficile; and v) isolation of multi-resistant bacteria, whether in clinical or surveillance samples.
The final analysis consisted of 212 patients, with a median age (IQ) of 59.2 (48 - 67) years old and a predominance of females (65%), who were hypertensive (35%), smokers (21%), and diabetics (17.8%). There was no difference in clinical recurrence between the two groups (8.1% vs. 12.2%; p = 0.364), with a lower 30-day mortality in the good CRP response group (32.2% vs. 14.5%; p = 0.002). Despite the tendency towards a lower occurrence of other secondary outcomes in the good response group, these differences were not statistically significant. In the poor CRP response group, outcomes like clinical recurrence, mortality, and therapeutic response were significantly worse, regardless of the duration of antibiotic treatment.
In this study, cancer patients with a good CRP response during antibiotic therapy presented lower mortality and a higher proportion of satisfactory therapeutic responses. CRP can be a useful tool when combined with other clinical information in optimizing the duration of antimicrobial treatment in a hospitalized cancer population.
癌症患者更容易感染,并且对治疗的反应可能更差,这可能导致他们过度使用抗生素。C 反应蛋白(CRP)作为监测治疗反应和缩短抗生素治疗时间的工具已经得到了广泛的关注;然而,很少有研究分析 CRP 在癌症患者人群中的作用。我们假设对抗生素治疗有良好反应的癌症患者 CRP 血清水平下降更快,这将使我们能够识别适合短期治疗的患者。
评估使用抗生素治疗的成年癌症患者的 CRP 血清水平的变化,并分析其与抗生素治疗持续时间、治疗反应和临床复发的关系。
这是一项回顾性研究,纳入了 2018 年 9 月至 2019 年 12 月期间在一所大学医院接受治疗的癌症患者。纳入至少接受过一次抗生素治疗的成年人(年龄≥18 岁)。将 CRP 治疗前 7 天的变化分为:i)良好反应:治疗第 5 天 CRP 值达到治疗前 48 小时内最高值的 50%或以下;ii)不良反应:治疗前 48 小时内最高值的 CRP 值在同一时间内仍维持在 50%以上。抗生素治疗的持续时间分为 7 天及以下和 7 天以上。住院期间或直至出院后 30 天内发生的事件评估结局。
指数感染的临床复发。
i)任何原因导致的死亡;ii)微生物学复发;iii)治疗反应;iv)与艰难梭菌相关的结肠炎;v)临床或监测样本中分离出多重耐药菌。
最终分析纳入了 212 例患者,中位年龄(IQR)为 59.2(48-67)岁,女性占多数(65%),高血压(35%)、吸烟者(21%)和糖尿病患者(17.8%)。两组之间的临床复发率没有差异(8.1% vs. 12.2%;p=0.364),但良好 CRP 反应组的 30 天死亡率较低(32.2% vs. 14.5%;p=0.002)。尽管良好 CRP 反应组其他次要结局的发生率较低,但差异无统计学意义。在 CRP 反应不良的患者中,临床复发、死亡率和治疗反应等结局明显较差,而与抗生素治疗的持续时间无关。
在这项研究中,抗生素治疗期间 CRP 反应良好的癌症患者死亡率较低,治疗反应良好的比例较高。CRP 可以与其他临床信息结合使用,优化住院癌症患者抗菌药物治疗的持续时间。