Pentamidine: a review. Rev Infect Dis 1985;7(5):625-34
Date
09/01/1985Pubmed ID
3903942DOI
10.1093/clinids/7.5.625Scopus ID
2-s2.0-0022121314 (requires institutional sign-in at Scopus site) 331 CitationsAbstract
Pentamidine, recently released for clinical use, is effective in therapy for the hemolymphatic stage of Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia. The mechanism of action is unclear and may differ for different organisms. Trypanosomes actively transport pentamidine intracellularly, and the drug may then interfere with DNA biosynthetics. However, pentamidine appears to kill nonreplicating P. carinii. The mechanism of killing is unexplained. The pharmacokinetics of pentamidine has been incompletely studied in humans. The estimated volume of distribution is 3 liters/kg. Levels in plasma of pentamidine range from 0.3-1.4 microgram/ml after standard 4 mg/kg dosing, with no appreciable increase in drug levels on successive dosing and no correlation between levels and creatinine clearance or adverse reactions. The drug appears to be concentrated in the kidney and excreted in the urine, with levels detectable six to eight weeks after cessation of therapy. Immediate adverse reactions have included hypotension, nausea, and vomiting. Local pain or abscess formation at an injection site, mild azotemia, leukopenia, abnormal findings from liver function tests, and hypoglycemia may also occur.
Author List
Sands M, Kron MA, Brown RBAuthor
Michael Kron MD Director, Professor in the Medicine department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
AmidinesAnimals
Babesiosis
Clinical Trials as Topic
Disease Models, Animal
Drug Resistance, Microbial
Humans
In Vitro Techniques
Kidney
Kinetics
Leishmaniasis
Pentamidine
Pneumonia, Pneumocystis
Trypanosoma brucei gambiense
Trypanosomiasis, African