#2898 Treatment outcomes of liver cyst infection in patients with autosomal dominant polycystic kidney disease

Abstract Background and Aims Liver cyst infection (LCI) is a rare and severe complication of autosomal dominant polycystic kidney disease (ADPKD), and evidence-based data for optimal management is lacking. Method We conducted a multicentric retrospective study (from 2012 to 2024) to investigate the treatment and outcomes of LCI. LCI was either defined by (i) C-reactive protein levels ≥50 mg/L and suspicion at computed tomography scan, 18Fluorodeoxyglucose (18FDG) positron-emission tomography computed tomography (PET/CT), magnetic resonance imaging, or (ii) proven by cyst puncture. We studied the determinants of treatment failure (persistent infection with requirement for antibiotic therapy (ATBT) change, cyst drainage, hepatectomy), relapse (<2 months) and recurrence (>2 months) of LCI after ATBT discontinuation, using multivariate analysis. Results Sixty-two patients and 112 episodes were included. At least one microorganism was identified in 70/112 (63%) episodes, mainly Escherichia coli in 36/70 (51%) of cases. E. coli was resistant to 3rd generation cephalosporin, fluoroquinolone or cotrimoxazole in 13%, 16% and 34%, respectively. Treatment failure and relapse occurred in 30/112 (27%) episodes, including 5 episodes requiring cyst drainage and 1 episode requiring partial hepatectomy. Risk factors for treatment failure/relapses included an ATBT duration <14 days (OR = 39, IC 95% [3.56;427], P = 0.002) and a WBC count >15.000/mm3 (OR =13, IC 95% [2.27; 74.50], P = 0.003). When treatment failure and relapses were analyzed separately, WBC >15.000/mm3 was a risk factor for treatment failure (OR = 9.2, IC 95% [1.68; 50.42], P = 0.009) and ATBT duration <14 days was a risk factor for relapses (OR = 25, IC 95% [3.38; 192.33], P = 0.001). Recurrence occurred in 24/62 (38%) patients, within 1 year for 15 (24%) after the 1st episode. ATBT duration <28 days (OR = 9.22, IC 95% [2.19; 50.08], P = 0.04) and history of renal cyst infection (OR = 5.90, IC 95% [1.11; 37.74], P = 0.04) increased the risk of recurrence <1 year. Follow-up 18FDG-PET/CT was performed in 19 episodes within 64 [54–95] days post LCI diagnosis. Among them, 17 were followed at least 1 year after follow-up 18FDG-PET/CT: 6/8 (75%) and 3/9 (33%) patients with and without persistent liver cyst uptake, respectively, had relapse or recurrent LCI <1 year (P = 0.15). Neither fluoroquinolone nor dual ATBT reduced the risk of treatment failure/relapse or recurrence. No death was attributed to LCI. Conclusion Treatment failure/relapse or recurrence of LCI both occurred in one-third of cases, and are associated with a shorter ATBT duration <28 days.

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Journal
Nephrology Dialysis Transplantation
Published
2025-10-01
DOI
https://doi.org/10.1093/ndt/gfaf116.1002
Primary Topic
Genetic and Kidney Cyst Diseases
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article
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article

#2898 Treatment outcomes of liver cyst infection in patients with autosomal dominant polycystic kidney disease

Bertrand Knebelmann, Julien Dang, Charles Ronsin, François Jouret et al.
Nephrology Dialysis Transplantation
Genetic and Kidney Cyst Diseases
article

#2898 Treatment outcomes of liver cyst infection in patients with autosomal dominant polycystic kidney disease

Bertrand Knebelmann, Julien Dang, Charles Ronsin, François Jouret, Simon Ville
article en

Abstract

Abstract Background and Aims Liver cyst infection (LCI) is a rare and severe complication of autosomal dominant polycystic kidney disease (ADPKD), and evidence-based data for optimal management is lacking. Method We conducted a multicentric retrospective study (from 2012 to 2024) to investigate the treatment and outcomes of LCI. LCI was either defined by (i) C-reactive protein levels ≥50 mg/L and suspicion at computed tomography scan, 18Fluorodeoxyglucose (18FDG) positron-emission tomography computed tomography (PET/CT), magnetic resonance imaging, or (ii) proven by cyst puncture. We studied the determinants of treatment failure (persistent infection with requirement for antibiotic therapy (ATBT) change, cyst drainage, hepatectomy), relapse (<2 months) and recurrence (>2 months) of LCI after ATBT discontinuation, using multivariate analysis. Results Sixty-two patients and 112 episodes were included. At least one microorganism was identified in 70/112 (63%) episodes, mainly Escherichia coli in 36/70 (51%) of cases. E. coli was resistant to 3rd generation cephalosporin, fluoroquinolone or cotrimoxazole in 13%, 16% and 34%, respectively. Treatment failure and relapse occurred in 30/112 (27%) episodes, including 5 episodes requiring cyst drainage and 1 episode requiring partial hepatectomy. Risk factors for treatment failure/relapses included an ATBT duration <14 days (OR = 39, IC 95% [3.56;427], P = 0.002) and a WBC count >15.000/mm3 (OR =13, IC 95% [2.27; 74.50], P = 0.003). When treatment failure and relapses were analyzed separately, WBC >15.000/mm3 was a risk factor for treatment failure (OR = 9.2, IC 95% [1.68; 50.42], P = 0.009) and ATBT duration <14 days was a risk factor for relapses (OR = 25, IC 95% [3.38; 192.33], P = 0.001). Recurrence occurred in 24/62 (38%) patients, within 1 year for 15 (24%) after the 1st episode. ATBT duration <28 days (OR = 9.22, IC 95% [2.19; 50.08], P = 0.04) and history of renal cyst infection (OR = 5.90, IC 95% [1.11; 37.74], P = 0.04) increased the risk of recurrence <1 year. Follow-up 18FDG-PET/CT was performed in 19 episodes within 64 [54–95] days post LCI diagnosis. Among them, 17 were followed at least 1 year after follow-up 18FDG-PET/CT: 6/8 (75%) and 3/9 (33%) patients with and without persistent liver cyst uptake, respectively, had relapse or recurrent LCI <1 year (P = 0.15). Neither fluoroquinolone nor dual ATBT reduced the risk of treatment failure/relapse or recurrence. No death was attributed to LCI. Conclusion Treatment failure/relapse or recurrence of LCI both occurred in one-third of cases, and are associated with a shorter ATBT duration <28 days.

Nephrology Dialysis TransplantationVol. 40(Supplement_3)
University of Liège (BE), Centre Hospitalier Universitaire de Nantes (FR), Institut Necker Enfants Malades (FR), Roche (France) (FR), Hôpital Ambroise-Paré (FR), Centre Hospitalier Départemental Vendée (FR)
Openalex Percentile: Top 68%
Genetic and Kidney Cyst Diseases
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