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Updated: Aug 28, 2026

Isolation And Dendritic Cell-Uptake of Small Extracellular Vesicles from Echinococcus granulosus
Published on: March 28, 2025
Postoperative Prophylaxis of Cystic Echinococcosis with Albendazole and Praziquantel: A Retrospective Cohort Study
Galya Popova-Daskalova1,2, Kostadin Kostadinov3,4, Krasimira Eneva1,2
1Department of Infectious Diseases, Parasitology and Tropical Medicine, Section of Parasitology, Medical University of Plovdiv, 4002 Plovdiv, Bulgaria.
Abstract:
Background/Objectives: Cystic echinococcosis is primarily managed surgically, yet postoperative recurrence affects 2-22% of patients despite albendazole prophylaxis. This study describes the tolerability of adding praziquantel to postoperative albendazole and reports recurrence signals where efficacy cannot be inferred. Methods: In this single-centre, retrospective, two-arm cohort, 60 patients undergoing hydatid cyst surgery (2024-2026) received albendazole and 30 additionally received praziquantel. The follow-up was substantially shorter in the combination arm (median 10 versus 24 months), and recurrence was first ascertainable only from 12 months, the central limitation. Analyses used standardized mean differences, person time incidence, propensity score and inverse probability weighting, a DAG-based hepatotoxicity model, and a Bayesian Beta-Binomial re-analysis. Results: Baseline covariates were markedly imbalanced (14/15 with |SMD| > 0.10). Two recurrences occurred, both in the albendazole arm (3.73/100 person-years) and none in the combination arm's shorter window. Adverse events were similar (43.3% vs. 50.0%), with no added hepatotoxicity after adjustment (odds ratio 1.45, 95% CI 0.49-4.37). The Bayesian posterior probability of benefit (0.88-0.93) remained below 0.95, a descriptive signal only. Conclusions: Albendazole plus praziquantel was well tolerated, but severe baseline imbalance, differential follow-up, and only two events mean efficacy cannot be assessed. The results of our study are hypothesis-generating. Further confirmation requires a prospective, multicentre randomized trial with balanced long-term follow-up.