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Published on: September 1, 2015
Cyst infections in patients with autosomal dominant polycystic kidney disease
Marion Sallée1, Cédric Rafat, Jean-Ralph Zahar
1Department of Nephrology, Hôpital Necker, Paris, France.
Insights
Diagnosing and treating cyst infections in autosomal dominant polycystic kidney disease (ADPKD) is challenging. Positron emission tomography (PET) scans improve diagnosis, while combination antibiotics and drainage of large cysts are key treatments.
Area of Science:
- Nephrology
- Infectious Diseases
- Radiology
Background:
- Cyst infection presents diagnostic and therapeutic challenges in autosomal dominant polycystic kidney disease (ADPKD).
- Published data on diagnosing and managing ADPKD cyst infections are limited.
Purpose of the Study:
- To evaluate diagnostic methods and treatment strategies for cyst infections in ADPKD patients.
- To analyze the incidence, microbiology, and outcomes of cyst infections in a cohort of ADPKD patients.
Main Methods:
- Retrospective study of ADPKD patients with suspected renal/hepatic cyst infection at a referral center (Paris, France).
- Inclusion of patients admitted between January 1998 and August 2008.
- Review of medical files and analysis of diagnostic imaging (ultrasound, CT, MRI, PET) and treatment outcomes.
Main Results:
- 33 out of 389 ADPKD patients (8.4%) experienced 41 cyst infection episodes.
- Escherichia coli was the predominant pathogen (74% of documented cases).
- Positron emission tomography (PET) scan demonstrated superior diagnostic accuracy compared to other imaging modalities. Initial antibiotic therapy was effective in 71% of cases, with combination therapy showing better outcomes than monotherapy. Large cysts (>5 cm) often required drainage.
Conclusions:
- PET scans are likely to enhance the accuracy and ease of diagnosing ADPKD cyst infections.
- Combined antibiotic therapy, particularly with a fluoroquinolone, and drainage of large cysts are the primary treatment approaches for ADPKD cyst infections.
Background And Objectives:
Cyst infection is a complex diagnostic and therapeutic issue in patients with autosomal dominant polycystic kidney disease (ADPKD); however, published data regarding the diagnosis and the management of cyst infections in patients with ADPKD are sparse.
Design, Setting, Participants, & Measurements:
A retrospective study was conducted in a referral center for patients with ADPKD in Paris, France. We identified using a computerized database all patients who had ADPKD and were admitted in the nephrology department of Hôpital Necker between January 1998 and August 2008 with likely or definite renal and/or hepatic cyst infection. Medical files of all included patients were reviewed.
Results:
Among 389 identified patients with ADPKD, 33 (8.4%) had 41 episodes of cyst infection, including eight definite and 33 likely cases. The incidence of cyst infections in patients with ADPKD was 0.01 episode per patient per year. Microbiological documentation was available for 31 episodes (75%), Escherichia coli accounting for 74% of all retrieved bacterial strains. Positron emission tomography scan proved superior to ultrasound, Computed tomography scan, and magnetic resonance imaging for the detection of infected cysts. Clinical efficacy of initial antibiotic treatment was noted in 71% of episodes. Antibiotic treatment modification was more frequently required for patients who were receiving initial monotherapy compared with those who were receiving bitherapy. Large (diameter >5 cm) infected cysts frequently required drainage.
Conclusions:
Positron emission tomography scan will probably make the diagnosis of cyst infections easier and more accurate. Antibiotic association, including a fluoroquinolone, and the drainage of large infected cysts remain the main treatment for cyst infections.
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