• Retrospective identification of ADPKD patients presenting with abdominal pain and/or fever between January 2005 and June 2015 in a prospective computerized database
• Stepwise and systematic review of all medical files • Diagnostic criteria:
CyH: intracystic density above 50 Hounsfield units on CT CyI:
~ “definite” by cyst fluid analysis showing bacteria or neutrophils ~ “probable” in case of concomitant presence of:
1. temperature >38°C for 3 days 2. loin or liver tenderness
3. CRP plasma level >50 mg/L 4. no CT evidence for CyH
IUO: episodes out of criteria for CyH or CyI
Diagnostic Management of Suspected Acute Cyst Complication
in Patients with Autosomal Dominant Polycystic Kidney Disease
Marie Neuville
1, Roland Hustinx
2, Jessica Jacques
3, Jean-Marie Krzesinski
1and François Jouret
1Divisions of (1) Nephrology, (2) Nuclear Medicine and (3) Medico-Economic Information, University of Liège Hospital (ULg CHU), Liège, Belgium
• Two main types of acute cyst complication in patients with autosomal dominant polycystic kidney disease (ADPKD): cyst infection (CyI)
cyst hemorrhage (CyH) • Double diagnostic challenge :
differentiating acute cystic from non-cystic diseases distinguishing CyI from CyH
• Prominence of an accurate diagnosis to target the treatment: CyI: 6-week antibiotic therapy (and cyst puncture)
CyH: antalgics and watchful waiting
• Recent suggestion of diagnostic criteria, with unknown sensibility and specificity
This monocentric 10-year retrospective study aims at challenging clinical, biological and imaging criteria in order to propose a diagnostic algorithm in the management of suspected acute cyst complication
Background and Objectives
Background and Objectives
Demographics of the Cohort
Demographics of the Cohort
Bacteriological Documentation
Bacteriological Documentation
Diagnostic Algorithm
Diagnostic Algorithm
Discussion
Discussion
This monocentric 10-year retrospective study including 88 episodes of suspected acute cyst complication in 53 ADPKD patients highlights:
• the usefulness of clinical, i.e. fever, and biological, i.e. CRP levels, criteria to distinguish CyI from CyH; • the limitations of bacteriological and conventional radiological investigations;
• the yield of 18FDG-PET/CT imaging in the diagnosis of CyI.
Table 1. Clinical and biological characteristics of the cohort
KTR, kidney transplant recipients; eGFR, estimated glomerular filtration rate; WBC, white blood cells at admission; CRP, C-reactive protein level at admission; ID, identification; IUO, inflammation of unknown origin. Mean +/- Standard Deviation.
n Age Gender Dialysis KTR eGFR* T°>38°C Pain WBC CRP Hematuria Leucocyturia Germ ID PET/CT
(years) (male, %) (%) (%) (ml/min) (%) (%) (106/mm³) (mg/L) (%) (%) Urine
(%) Blood (%) (+, %)
Hemorrhage 30 46 ± 13 50 0 17 77 ± 49 7 97 9.7 ± 3.3 13 ± 14 23 10 10 7 0/1, 0
Renal cyst infection
Definite 7 52 ± 11 70 15 43 39 ± 16 100 86 11.3 ± 3.9 163 ± 98 29 43 15 57 3/3, 100
Probable 10 48 ± 14 30 20 30 61 ± 43 100 100 10.8 ± 3.1 252 ± 204 40 40 40 20 3/4, 75
Liver cyst infection
Definite 4 63 ± 5 50 25 75 29 ± 14 100 100 12.1 ± 2.6 230 ± 87 50 1/1, 100
Probable 2 [66 ; 66] 50 50 50 38 100 100 [4.2 ; 6.5] [51 ; 342] 50 1/2, 50
IUO 35 55 ± 15 50 6 66 49 ± 31 66 66 11.8 ± 5.6 98 ± 92 37 60 48 23 7/17, 42
Diagnostic yields of conventional imaging techniques in CyI were:
Ultrasounds: 10% (1/10)
Computed tomography: 26.1% (6/23) Magnetic resonance imaging: 25% (1/4)