Imipenem: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Howard C. Berkowitz
(New page: '''Impipenem''' is a synthetic broad-spectrum antibiotic, which contains a beta-lactam ring structure but is not considered a member of the penicillin or cephalosporin clas...)
 
imported>Howard C. Berkowitz
No edit summary
 
(4 intermediate revisions by the same user not shown)
Line 1: Line 1:
'''Impipenem''' is a synthetic broad-spectrum [[antibiotic]], which contains a [[beta-lactam]] ring structure but is not considered a member of the [[penicillin]] or [[cephalosporin]] class. It is a frequent choice for treatment of infections involving multidrug-resistant bacteria, or multiple types of bacteria.
{{subpages}}
{{TOC|right}}
'''Imipenem''' is a synthetic broad-spectrum [[antibiotic]] of the [[carbepenem]] class, which contains a [[beta-lactam]] ring structure but is not considered a member of the [[penicillin]] or [[cephalosporin]] class, and is not affected by [[beta-lactamase]]s. It is a frequent choice for treatment of infections involving multidrug-resistant bacteria, or multiple types of bacteria. Imipenem is derived from the naturally occurring antibiotic thienamycin, which is too unstable for clinical use. 
 
Imipenem is administered with cilistatin to reduce the rate of its renal excretion; cilistatin does not have a direct antibacterial effect but keeps imipenem levels high.
==Indications==
==Pharmacology==
"Its effectiveness is enhanced when it is administered in combination with [[cilistatin]], a renal dipeptidase inhibitor,"<ref>{{MeSH}}</ref> especially when the patient's kidney function is diminished. <ref>{{citation
| title = The pharmacokinetics of imipenem (thienamycin-formamidine) and the renal dehydropeptidase inhibitor cilastatin sodium in normal subjects and patients with renal failure.
| author = G A Verpooten, L Verbist, A P Buntinx, L A Entwistle, K H Jones,  M E De Broe
| journal = Br J Clin Pharmacol
| date = 1984 August | volume = 18 | issue = 2 | pages = 183–193
| url = http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1463530/}}</ref>
==Administration==
Imipenem must be injected. It has FDA-approved [[intramuscular]] and [[intravenous]] forms.
 
In veterinary medicine, it also can be administered [[subcutaneous|subcutaneously]] to [[cat]]s, as well as intravenously.
==References==
{{reflist}}

Latest revision as of 21:11, 20 July 2010

This article is developing and not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

Imipenem is a synthetic broad-spectrum antibiotic of the carbepenem class, which contains a beta-lactam ring structure but is not considered a member of the penicillin or cephalosporin class, and is not affected by beta-lactamases. It is a frequent choice for treatment of infections involving multidrug-resistant bacteria, or multiple types of bacteria. Imipenem is derived from the naturally occurring antibiotic thienamycin, which is too unstable for clinical use.

Imipenem is administered with cilistatin to reduce the rate of its renal excretion; cilistatin does not have a direct antibacterial effect but keeps imipenem levels high.

Indications

Pharmacology

"Its effectiveness is enhanced when it is administered in combination with cilistatin, a renal dipeptidase inhibitor,"[1] especially when the patient's kidney function is diminished. [2]

Administration

Imipenem must be injected. It has FDA-approved intramuscular and intravenous forms.

In veterinary medicine, it also can be administered subcutaneously to cats, as well as intravenously.

References

  1. Anonymous (2024), Imipenem (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. G A Verpooten, L Verbist, A P Buntinx, L A Entwistle, K H Jones, M E De Broe (1984 August), "The pharmacokinetics of imipenem (thienamycin-formamidine) and the renal dehydropeptidase inhibitor cilastatin sodium in normal subjects and patients with renal failure.", Br J Clin Pharmacol 18 (2): 183–193