Best Practice of Peritoneal Dialysis-Associated Gram-Negative Peritonitis in Children: Insights From the International Pediatric Peritoneal Dialysis Network Registry

医学 腹膜透析 头孢唑林 经验性治疗 腹膜炎 内科学 腹痛 抗生素 透析 外科 生物 替代医学 病理 微生物学
作者
Dagmara Borzych–Dużałka,Rebeca Same,Alicia M. Neu,Hui‐Kim Yap,Enrico Verrina,Sevcan A. Bakkaloğlu,Francisco Cano,Hiren P. Patel,Maria Szczepańska,Łukasz Obrycki,Ana Paula Spizzirri,Lisa Sartz,Karel Vondrák,Anabella Rébori,Gordana Miloševski‐Lomić,Eugene Chan,Biswanath Basu,Andrea Lazcano Pezo,Ariane Zaloszyc,Vimal Chadha
出处
期刊:Kidney International Reports [Elsevier BV]
卷期号:9 (6): 1654-1663 被引量:5
标识
DOI:10.1016/j.ekir.2024.03.031
摘要

IntroductionGram-negative peritonitis (GNP) is associated with significant morbidity in children receiving long-term peritoneal dialysis (PD) and current treatment recommendations are based on limited data. Methods: Analysis of 379 GNP episodes in 308 children (median age 6.9 years, IQR 3.0-13.6) from 45 centers in 28 countries reported to the International Pediatric Peritoneal Dialysis Network (IPPN) registry between 2011–2023. Results: Overall, 74% of episodes responded well to empiric therapy and full functional recovery (FFR) was achieved in 82% of cases. In vitro bacterial susceptibility to empiric antibiotics and lack of severe abdominal pain at onset were associated with a good initial response. Risk factors for failure to achieve FFR included severe abdominal pain at onset and at 60-72 hours from treatment initiation (OR, 3.81 [95%CI,2.01-7.2] and OR, 3.94 [95%CI,1.06-14.67], respectively), Pseudomonas spp. etiology (OR, 1.73 [95% CI, 1.71-4.21]) and in vitro bacterial resistance to empiric antibiotics (OR, 2.40 [95%CI, 1.21-4.79]); the risk was lower with the use of monotherapy as definitive treatment (OR, 0.40 [95%CI, 0.21-0.77]). Multivariate analysis showed no benefit of dual antibiotic therapy for treatment of Pseudomonas peritonitis after adjustment for age, presenting symptomatology, 60–72-hour treatment response and treatment duration. Monotherapy with cefazolin in susceptible Enterobacterales peritonitis resulted in a similar FFR rate (91 vs. 93%) as treatment with ceftazidime or cefepime monotherapy. Conclusions: Detailed microbiological assessment, consisting of patient- and center- specific antimicrobial susceptibility data, should guide empiric treatment. Treatment "de-escalation" with use of monotherapy and narrow spectrum antibiotics according to susceptibility data is not associated with inferior outcomes and should be advocated in the context of emerging bacterial resistance.
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