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Multiple drug resistance ( MDR), multidrug resistance or multiresistance is antimicrobial resistance shown by a species of to at least one drug in three or more antimicrobial categories. Antimicrobial categories are classifications of antimicrobial agents based on their mode of action and specific to target organisms. The MDR types most threatening to are MDR that resist multiple ; other types include MDR , (resistant to multiple , , and drugs of a wide chemical variety).

Recognizing different degrees of MDR in bacteria, the terms extensively drug-resistant ( XDR) and pandrug-resistant ( PDR) have been introduced. Extensively drug-resistant (XDR) is the non-susceptibility of one bacteria species to all antimicrobial agents except in two or less antimicrobial categories. Within XDR, pandrug-resistant (PDR) is the non-susceptibility of bacteria to all antimicrobial agents in all antimicrobial categories. The definitions were published in 2011 in the journal Clinical Microbiology and Infection and are openly accessible.A.-P. Magiorakos, A. Srinivasan, R. B. Carey, Y. Carmeli, M. E. Falagas, C. G. Giske, S. Harbarth, J. F. Hinndler et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria... . Clinical Microbiology and Infection, Vol 8, Iss. 3 first published 27 July 2011 via. Retrieved 16 August 2014.


Common multidrug-resistant organisms (MDROs)
Common multidrug-resistant organisms, typically bacteria, include:
  • Vancomycin-Resistant Enterococci (VRE)
  • Methicillin-resistant Staphylococcus aureus (MRSA)
  • Extended-spectrum β-lactamase (ESBLs) producing Gram-negative bacteria
  • Klebsiella pneumoniae carbapenemase (KPC) producing Gram-negatives
  • Multidrug-resistant Gram negative rods (MDR GNR) such as species, E.coli, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa
  • Multi-drug-resistant tuberculosis

Overlapping with MDRGN, a group of and bacteria of particular recent importance have been dubbed as the ESKAPE group ( Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and species).


Bacterial resistance to antibiotics
Various microorganisms have survived for thousands of years by their ability to adapt to antimicrobial agents. They do so via spontaneous mutation or by . This process enables some bacteria to oppose the action of certain antibiotics, rendering the antibiotics ineffective. These microorganisms employ several mechanisms in attaining multi-drug resistance:
  • No longer relying on a
  • Enzymatic deactivation of antibiotics
  • Decreased cell wall permeability to antibiotics
  • Altered target sites of antibiotic
  • Efflux mechanisms to remove antibiotics
  • Increased as a stress response

Many different bacteria now exhibit multi-drug resistance, including , , , , , as well as numerous other Gram-negative bacteria and Mycobacterium tuberculosis. Antibiotic resistant bacteria are able to transfer copies of that code for a mechanism of resistance to other bacteria even distantly related to them, which then are also able to pass on the resistance genes, resulting in generations of antibiotics resistant bacteria.Hussain, T. Pakistan at the verge of potential epidemics by multi-drug resistant pathogenic bacteria (2015). Adv. Life Sci. 2(2). pp: 46-47 This initial transfer of DNA is called horizontal gene transfer.


Bacterial resistance to bacteriophages
Phage-resistant bacteria variants have been observed in human studies. As for antibiotics, horizontal transfer of resistance can be acquired by acquisition.


Antifungal resistance
Yeasts such as Candida species can become resistant under long-term treatment with preparations, requiring treatment with a different drug class. Lomentospora prolificans infections are often fatal because of their resistance to multiple antifungal agents.


Antiviral resistance
is the prime example of MDR against antivirals, as it mutates rapidly under monotherapy. has become increasingly MDR; first to amantadines, then to neuraminidase inhibitors such as , (2008-2009: 98.5% of Influenza A tested resistant), also more commonly in people with weak immune systems. can become resistant to and under treatment, especially in immunosuppressed patients. Herpes simplex virus rarely becomes resistant to preparations, mostly in the form of cross-resistance to and , usually in immunosuppressed patients.


Antiparasitic resistance
The prime example for MDR against antiparasitic drugs is . has become and sulfadoxine-pyrimethamine resistant a few decades ago, and as of 2012 -resistant Plasmodium falciparum has emerged in western Cambodia and western Thailand.Dondorp, A., Nosten, F., Yi, P., Das, D., Phyo, A., & Tarning, J. et al. (2009). Artemisinin Resistance in Plasmodium falciparum Malaria. New England Journal Of Medicine, 361, 455-467. Toxoplasma gondii can also become resistant to , as well as and , but is not usually MDRDoliwa C, Escotte-Binet S, Aubert D, Velard F, Schmid A, Geers R, Villena I. Induction of sulfadiazine resistance in vitro in Toxoplasma gondii.Exp Parasitol. 2013 Feb;133(2):131-6. resistance is mainly reported in the veterinary literature, for example in connection with the practice of livestock drenchingLaurenson YC, Bishop SC, Forbes AB, Kyriazakis I.Modelling the short- and long-term impacts of drenching frequency and targeted selective treatment on the performance of grazing lambs and the emergence of antihelmintic resistance.Parasitology. 2013 Feb 1:1-12. and has been recent focus of FDA regulation.


Preventing the emergence of antimicrobial resistance
To limit the development of antimicrobial resistance, it has been suggested to:
  • Use the appropriate antimicrobial for an infection; e.g. no antibiotics for viral infections
  • Identify the causative organism whenever possible
  • Select an antimicrobial which targets the specific organism, rather than relying on a broad-spectrum antimicrobial
  • Complete an appropriate duration of antimicrobial treatment (not too short and not too long)
  • Use the correct dose for eradication; subtherapeutic dosing is associated with resistance, as demonstrated in food animals.
  • More thorough education of and by prescribers on their actions' implications globally.
  • Vaccination to prevent drug resistance for instance pneumococcus vaccine or flu vaccine

The medical community relies on education of its prescribers, and self-regulation in the form of appeals to voluntary antimicrobial stewardship, which at hospitals may take the form of an antimicrobial stewardship program. It has been argued that depending on the cultural context government can aid in educating the public on the importance of restrictive use of antibiotics for human clinical use, but unlike , there is no regulation of its use anywhere in the world at this time. Antibiotic use has been restricted or regulated for treating animals raised for human consumption with success, in Denmark for example.

Infection prevention is the most efficient strategy of prevention of an infection with a MDR organism within a hospital, because there are few alternatives to antibiotics in the case of an extensively resistant or panresistant infection; if an infection is localized, removal or can be attempted (with MDR-TB the lung for example), but in the case of a systemic infection only generic measures like boosting the immune system with immunoglobulins may be possible. The (viruses which kill bacteria) is a developing area of possible therapeutic treatments.

It is necessary to develop new antibiotics over time since the selection of resistant bacteria cannot be prevented completely. This means with every application of a specific antibiotic, the survival of a few bacteria which already have a resistance gene against the substance is promoted, and the concerning bacterial population amplifies. Therefore, the resistance gene is farther distributed in the organism and the environment, and a higher percentage of bacteria means they no longer respond to a therapy with this specific antibiotic. In addition to developing new antibiotics, new strategies entirely must be implemented in order to keep the public safe from the event of total resistance. New strategies are being tested such as treatments and bacteriophage utilization, however more resources must be dedicated to this cause.


See also


Further reading


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