» Articles » PMID: 3415205

Ciprofloxacin Activity in Cyst Fluid from Polycystic Kidneys

Overview
Specialty Pharmacology
Date 1988 Jun 1
PMID 3415205
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Renal cyst infection in patients with polycystic kidney disease (PKD) is often unresponsive to standard antimicrobial therapy, in part because of the failure of most antibiotics to adequately penetrate cyst fluid. Ciprofloxacin, a new quinolone antibiotic, possesses in vitro activity against most pathogens likely to be encountered in renal cyst infection. To study the potential usefulness of ciprofloxacin for the treatment of cyst infection, fluid from 70 cysts was obtained from seven patients with polycystic kidney disease who were receiving the drug. Cysts were categorized as nongradient or gradient by the sodium concentration in the fluid. The ciprofloxacin concentration within cysts was measured, and the cyst fluid bactericidal activity against likely cyst fluid pathogens was determined. The mean (+/- standard error) ciprofloxacin concentration was 12.7 +/- 2.9 micrograms/ml. Preferential accumulation of ciprofloxacin occurred in gradient cysts; these levels exceeded levels in serum by more than fourfold. Cyst fluid bactericidal activity titers were uniformly high against Escherichia coli and Proteus mirabilis, while less activity was observed against Streptococcus faecalis, Pseudomonas aeruginosa, Staphylococcus aureus, and Staphylococcus epidermidis.

Citing Articles

Cyst infection in autosomal dominant polycystic kidney disease: our experience at Toranomon Hospital and future issues.

Suwabe T Clin Exp Nephrol. 2020; 24(9):748-761.

PMID: 32700112 PMC: 7474715. DOI: 10.1007/s10157-020-01928-2.


Multiple urinary tract infections are associated with genotype and phenotype in adult polycystic kidney disease.

Eroglu E, Kocyigit I, Cetin M, Zararsiz G, Imamoglu H, Bayramov R Clin Exp Nephrol. 2019; 23(10):1188-1195.

PMID: 31165946 DOI: 10.1007/s10157-019-01752-3.


Bacteremic kidney cyst infection caused by Helicobacter cinaedi.

Ito K, Yamamoto T, Nishio H, Sawaya A, Murakami M, Kitagawa A CEN Case Rep. 2017; 5(2):121-124.

PMID: 28508961 PMC: 5413748. DOI: 10.1007/s13730-015-0207-9.


Diagnostic Algorithm in the Management of Acute Febrile Abdomen in Patients with Autosomal Dominant Polycystic Kidney Disease.

Neuville M, Hustinx R, Jacques J, Krzesinski J, Jouret F PLoS One. 2016; 11(8):e0161277.

PMID: 27529555 PMC: 4987061. DOI: 10.1371/journal.pone.0161277.


Cyst infection in autosomal dominant polycystic kidney disease: causative microorganisms and susceptibility to lipid-soluble antibiotics.

Suwabe T, Araoka H, Ubara Y, Kikuchi K, Hazue R, Mise K Eur J Clin Microbiol Infect Dis. 2015; 34(7):1369-79.

PMID: 25851811 DOI: 10.1007/s10096-015-2361-6.


References
1.
DALGAARD O . Bilateral polycystic disease of the kidneys; a follow-up of two hundred and eighty-four patients and their families. Acta Med Scand Suppl. 1957; 328:1-255. View

2.
Crump B, Wise R, Dent J . Pharmacokinetics and tissue penetration of ciprofloxacin. Antimicrob Agents Chemother. 1983; 24(5):784-6. PMC: 185942. DOI: 10.1128/AAC.24.5.784. View

3.
Huseman R, Grady A, Welling D, Grantham J . Macropuncture study of polycystic disease in adult human kidneys. Kidney Int. 1980; 18(3):375-85. DOI: 10.1038/ki.1980.148. View

4.
Bricker N, Patton J . Cystic disease of the kidneys; a study of dynamics and chemical composition of cyst fluid. Am J Med. 1955; 18(2):207-19. DOI: 10.1016/0002-9343(55)90236-9. View

5.
Wise R, Andrews J, Edwards L . In vitro activity of Bay 09867, a new quinoline derivative, compared with those of other antimicrobial agents. Antimicrob Agents Chemother. 1983; 23(4):559-64. PMC: 184701. DOI: 10.1128/AAC.23.4.559. View