Toxicity of polymyxins: a systematic review of the evidence from old and recent studies

被引:721
作者
Falagas, Matthew E. [1 ]
Kasiakou, Sofia K.
机构
[1] Alfa Inst Biomed Sci, Athens, Greece
[2] Henry Dunant Hosp, Dept Med, Athens, Greece
[3] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
来源
CRITICAL CARE | 2006年 / 10卷 / 01期
关键词
D O I
10.1186/cc3995
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
Background The increasing problem of multidrug-resistant Gram-negative bacteria causing severe infections and the shortage of new antibiotics to combat them has led to the reevaluation of polymyxins. These antibiotics were discovered from different species of Bacillus polymyxa in 1947; only two of them, polymyxin B and E ( colistin), have been used in clinical practice. Their effectiveness in the treatment of infections due to susceptible Gram-negative bacteria, including Pseudomonas aeruginosa and Acinetobacter baumannii, has not been generally questioned. However, their use was abandoned, except in patients with cystic fibrosis, because of concerns related to toxicity. Methods We reviewed old and recent evidence regarding polymyxin-induced toxicity by searching Pubmed ( from 1950 until May 2005). Results It was reported in the old literature that the use of polymyxins was associated with considerable toxicity, mainly nephrotoxicity and neurotoxicity, including neuromuscular blockade. However, recent studies showed that the incidence of nephrotoxicity is less common and severe compared to the old studies. In addition, neurotoxic effects of polymyxins are usually mild and resolve after prompt discontinuation of the antibiotics. Furthermore, cases of neuromuscular blockade and apnea have not been reported in the recent literature. Conclusion New evidence shows that polymyxins have less toxicity than previously reported. The avoidance of concurrent administration of nephrotoxic and/or neurotoxic drugs, careful dosing, as well as more meticulous management of fluid and electrolyte abnormalities and use of critical care services may be some of the reasons for the discrepancy between data reported in the old and recent literature.
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页数:13
相关论文
共 85 条
[1]
Bronchial constriction and inhaled colistin in cystic fibrosis [J].
Alothman, GA ;
Ho, B ;
Alsaadi, MM ;
Ho, SL ;
O'Drowsky, L ;
Louca, E ;
Coates, AL .
CHEST, 2005, 127 (02) :522-529
[2]
Anthony M A, 1966, Ohio State Med J, V62, P336
[3]
BAINES RD, 1964, JAMA-J AM MED ASSOC, V190, P278
[4]
SODIUM SULPHOMETHYL DERIVATIVES OF POLYMYXINS [J].
BARNETT, M ;
BUSHBY, SRM ;
WILKINSON, S .
BRITISH JOURNAL OF PHARMACOLOGY AND CHEMOTHERAPY, 1964, 23 (03) :552-+
[5]
*BEDF LAB, 1999, POL B INJ PACK INS
[6]
Effects of polymyxin B on mammalian urinary bladder [J].
Berg, JR ;
Spilker, CM ;
Lewis, SA .
JOURNAL OF MEMBRANE BIOLOGY, 1996, 154 (02) :119-130
[7]
Modulation of polymyxin B effects on mammalian urinary bladder [J].
Berg, JR ;
Spilker, CM ;
Lewis, SA .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 275 (02) :F204-F215
[8]
Use of colistin in the treatment of multiple-drug-resistant gram-negative infections [J].
Berlana, D ;
Llop, JM ;
Fort, E ;
Badia, AB ;
Jódar, R .
AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2005, 62 (01) :39-47
[9]
ACUTE RENAL FAILURE DUE TO OVERDOSAGE OF COLISTIN [J].
BROWN, JM ;
DORMAN, DC ;
ROY, LP .
MEDICAL JOURNAL OF AUSTRALIA, 1970, 2 (20) :923-&
[10]
Brumfitt W, 1966, Br J Urol, V38, P495, DOI 10.1111/j.1464-410X.1966.tb09743.x