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Epidemiology, drug resistance, and clinical risk factors of peritoneal dialysis-associated peritonitis: a five-year
Min Zhang1,2, Xiang Li1,3, Yun Zhang1,4
1Department of Clinical Laboratory, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Background:
Peritoneal dialysis-associated peritonitis (PDAP) remains a major complication in long-term dialysis patients, leading to significant morbidity and healthcare burden. This study aimed to investigate the microbial spectrum, antimicrobial resistance patterns, and clinical risk factors associated with PDAP in hospitalized patients in Anhui, China, over the past five years.
Methods:
A retrospective analysis was conducted on 438 peritoneal dialysis (PD) patients from three PD centers in Anhui from 2020 to early 2025. Of these, 238 patients were diagnosed with PDAP and 200 served as controls without peritonitis. Peritoneal effluents were cultured and microbiologically identified using MALDI-TOF MS and VITEK 2 systems. Antimicrobial susceptibility testing followed CLSI M100 standards. Clinical and laboratory data were statistically analyzed using SPSS v26.0, and multivariate logistic regression model was used to determine independent risk factors.
Results:
Significant differences were observed between the PDAP and control cohorts in sex, age, hospitalization time, PD duration, red blood cell count, total protein, albumin, blood glucose, and concomitant conditions (e.g., hepatitis B, autoimmune diseases, and hyperthyroidism) (p < 0.05). Laboratory infectious markers including peripheral blood white blood cell (WBC) count, neutrophil percentage, procalcitonin (PCT), C-reactive protein, peritoneal dialysate WBC and multinucleated cell counts, were significantly elevated in the PDAP population compared to controls, with serum PCT and dialysate WBCs presented as significant predictors after multivariate adjustment. Staphylococcus species showed predominant methicillin resistance (47.22% oxacillin-susceptible) with moxifloxacin outperforming other fluoroquinolones, while carbapenems demonstrated near-universal efficacy against Enterobacterales (esp., for ertapenem). Candida species mounted variable antifungal responses, with optimal activities of amphotericin B/flucytosine except fluconazole, underscoring both therapeutic opportunities and emerging resistance threats across bacterial and fungal pathogens.
Conclusion:
The multicenter study confirmed elevated serum PCT and peritoneal dialysate leukocytes as robust independent clinical predictors for PDAP, with other risk factors significantly increasing disease susceptibility. The diverse microbial spectrum and antimicrobial resistance features shed light on the importance of updated local microbial surveillance to guide empirical treatment and clinical management strategies on PDAP.
Insights
Peritoneal dialysis-associated peritonitis (PDAP) is a major complication. Elevated serum procalcitonin (PCT) and peritoneal dialysate white blood cells (WBCs) are key predictors, guiding better management of PDAP.
Area of Science:
- Nephrology
- Infectious Diseases
- Clinical Microbiology
Background:
- Peritoneal dialysis-associated peritonitis (PDAP) is a significant complication for long-term dialysis patients, causing morbidity and high healthcare costs.
- Understanding the microbial landscape, resistance patterns, and risk factors for PDAP is crucial for effective patient management.
Purpose of the Study:
- To investigate the microbial spectrum, antimicrobial resistance, and clinical risk factors of PDAP in hospitalized patients in Anhui, China.
- To identify predictive markers for PDAP to improve early diagnosis and treatment.
Main Methods:
- A retrospective analysis of 438 peritoneal dialysis (PD) patients (238 with PDAP, 200 controls) from 2020 to early 2025.
- Microbial identification using MALDI-TOF MS and VITEK 2, antimicrobial susceptibility testing following CLSI standards.
- Statistical analysis including multivariate logistic regression to identify independent risk factors.
Main Results:
- PDAP patients showed significant differences in demographics, PD duration, and comorbidities compared to controls.
- Elevated serum procalcitonin (PCT) and peritoneal dialysate WBC counts were significant predictors of PDAP.
- Staphylococcus species exhibited high methicillin resistance; carbapenems were effective against Enterobacterales; Candida species showed variable antifungal responses.
Conclusions:
- Elevated serum PCT and peritoneal dialysate leukocytes are robust independent predictors for PDAP.
- Updated local microbial surveillance is essential for guiding empirical treatment and clinical management strategies for PDAP.
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