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Multidrug-Resistant & 
Extensively-Drug Resistant 
Organisms 
G.VANITHA
Antimicrobial resistance 
Antibiotics are a class of drugs that treat bacterial 
infections by stopping growth of bacteria or killing 
the bacteria directly 
Antimicrobial resistance (AMR) is resistance of a 
microorganism to an antimicrobial drug that was 
originally effective for treatment of infections caused 
by it. 
Emergence of resistance to multiple antimicrobial 
agents in pathogenic bacteria has become a 
significant public health
Antibiotic resistance is the ability of a 
microorganism to withstand the effects of an 
antibiotic. 
It is a specific type of drug resistance. 
Antibiotic resistance evolves selective pressure, 
mutation, gene transfer, inappropriate drug use, 
inadequate diagnostics, hospital use and 
agricultural use of drugs. 
Once such a gene is generated, bacteria can then 
transfer the genetic information in a horizontal 
fashion (between individuals) by plasmid 
exchange.
How do bacteria become 
resistant to an antibiotic 
Resistance happen when an infection is treated with 
antibiotics but all the bacteria are not killed the ones 
that remain learn how to outlive that antibiotic and are 
now resistant 
Not finishing the whole prescription 
Not taking the proper dosage or at the proper times 
Taking someone else’s prescription 
Taking antibiotics when not needed
MDR 
MDR is defined as non-susceptibility to at least one 
agent in three or more antimicrobial categories. 
Bacteria that resist treatment with more than one 
antibiotic are called multidrug-resistant organisms 
Multidrug-resistant organisms are found mainly in 
hospitals and long-term care facilities. 
They often affect people who are older or very ill and 
can cause bad infections 
Penicillin resistance in Staphylococcus aureus, a 
common type of bacteria, was first found in the 1940s. 
The more often the antibiotics are used, the more 
likely it is that resistant bacteria will develop.
Hey kid wana be a MDR…? Stick some of this 
into your genome… 
Even Penicillin won’t be able to harm you….
Common multi-drug-resistant 
organisms (MDROs) 
MDROs are microorganisms, predominantly bacteria, that are 
resistant to one or more classes of antimicrobial agents 
Methicillin-resistant Staphylococcus aureus (MRSA) 
Vancomycin-intermediate Staphylococcus aureus (VISA) 
Vancomycin-resistant Staphylococcus aureus (VRSA) 
Vancomycin-resistant enterococcus (VRE) 
Streptococcus pneumoniae resistant to penicillin and 
other broad-spectrum agents 
MDR-TB 
(ESBLs) producing Gram-negative bacteria
VRE 
MRSA 
Gram-negative bacilli
Every year, over 2 million people in the United States 
become infected with bacteria that are resistant to 
antibiotics, and around 23,000 people die as a result of 
these infections (CDC, 2013a). 
Multidrug-resistant organisms, are bacteria that are 
resistant to current antibiotic therapy and, therefore, 
difficult to treat. 
MDROs can cause serious local and systemic 
infections that can be severely debilitating and even 
life-threatening. 
In the past, these infections were usually controlled by 
penicillin.
The most serious concern with antibiotic resistance 
is that some bacteria have become resistant to 
almost all of the easily available antibiotics. 
For example, Staphylococcus aureus (‘golden 
staph’) and Neisseria gonorrhoeae (the cause of 
gonorrhoea) are now almost always resistant to 
benzyl penicillin. 
These bacteria are able to cause serious disease 
and this is a major public health problem.
Methicillin-Resistant Staphylococcus 
aureus 
 Resistant to Methicillin, Oxacillin and nafcillin 
Transmitted by direct and indirect contact 
more virulent than MSSA 
Susceptible to common disinfectants
Staphylococcus aureus is very common, but also 
very deadly if it gets into the blood stream. 
It was formerly a major cause of death following 
surgery. 
Penicillin proved to be very effective. 
When penicillin began to fail in 1950s, methicillin 
proved effective. 
Methicillin resistant strains were identified in 1961 
but did not become common until the 1990s 
(MRSA). 
Vancomycin was an effective drug of last resort, but 
VRSA was reported in the late 1990s. 
About 2 billion people worldwide carry Staph A. and 
about 50 million carry MRSA.
MRSA now accounts for more than 50% of hospital-acquired 
staph infections. 
According to the CDC, almost 1,00,000 cases of 
invasive MRSA occurred in 2005, with 18% of these 
individuals dying during their hospitalization. 
These infections account for more than 5,000 deaths 
each year which are directly attributable to MRSA. 
Specifically, MRSA has an attributable mortality rate 
of 6.9% at 30 days and 16.7% at 1 year. 
The additional cost of MRSA alone is 39,000 per 
case in patients with a MRSA surgical-site infection 
Mortality rates were 13% higher in patients with 
MRSA infection, regardless of mechanism of death.
Extended spectrum beta-lactamase 
producers (ESBLs) 
Gram negative organisms - Enterobacteriaceae 
Excrete the enzyme beta-lactamase 
Inactivates β-lactam (penicillin) type antibiotics 
Resistance to β-lactams emerged several years ago 
and has continued to rise ESBLs 
Klebsiella 
E. coli 
Serratia 
others
Beta-lactam resistance
Drug resistance facts 
 MRSA and VRE are terms that describe specific types 
of antibacterial resistance; MRSA describes Methicillin- 
Resistant Staphylococcus aureus bacteria while VRE 
describes Vancomycin-Resistant Enterococi. 
 Drug resistance occurs when microbes survive and 
grow in the presence of a drug that normally kills or 
inhibits the microbe's growth. 
 The history of drug resistance began with the 
development of antimicrobial drugs, and the 
subsequent ability of microbes to adapt and develop 
ways to survive in the presence of antimicrobials.
Diagnosis of antimicrobial drug resistance is 
performed by lab tests that challenge the isolated 
microbes to grow and survive in the presence of the 
drug. 
Treatment of antimicrobial drug resistance depends 
on the type of infection and what the patient and 
their doctor decide. 
Prevention of antimicrobial drug resistance is aided 
by preventing the overuse and misuse of 
antimicrobials; infections can be reduced by a 
healthy lifestyle, hand washing, and other good 
hygiene methods 
Antimicrobial resistance is a growing health issue 
because more resistant microbes are being 
detected and societal pressures often result in 
overuse.
XDR 
XDR is defined as non-susceptibility to at least one 
agent in all but two or fewer antimicrobial categories 
(i.e. bacterial isolates remain susceptible to only one 
or two categories). 
Multidrug-resistant tuberculosis (MDRTB) 
Resistance to Isoniazid and Rifampicin 
Extensively (extremely) drug-resistant (XDR-TB) 
MDR-TB plus resistance to a second line injectable 
drug such as amykacin plus a quinolone.
MDR & XDR TB 
The term XDR TB appears to have been used for the 
first time in March 2006. 
WHO describing strains of TB, referred to as XDR TB, 
that were resistant not only to isoniazid and rifampicin 
(that is they were MRD TB) but they were also resistant 
to at least three of the six classes of second line anti TB 
drugs. 
In 1980 50% of TB bacilli were resistant to 1 drug. 
Multi-drug resistant TB (MDR-TB) began to emerge. 
There are now an estimated 1.5million MDR cases 
worldwide. 
Extreme drug resistance (XDR-TB) was reported in 
2006.
The first completely drug resistant (CDR-TB) case was 
reported in Italy in 2007. 
MDR-TB has emerged and spread due to the 
inadequacy of treatment. Today, treatment for drug-resistant 
TB can take up to two years, and is so 
complex, expensive, and toxic that a third of all MDR-TB 
patients die. 
WHO treatment standards require that at least four 
drugs be used to treat TB in order to avoid the 
development of further resistance. 
According to the WHO, Eastern Europe's rates of MDR-TB 
are the highest, where MDR-TB makes up 20% of 
all new TB cases. 
In some parts of the former Soviet Union, up to 28% of 
new TB cases are multidrug-resistant.
Among previously treated cases in the same region, 
reported rates of drug resistance are commonly 
above 50% and as high as 61%. 
During the late 1980s and early 1990s, outbreaks of 
MDR-TB in North America and Europe killed more 
than 80% of those who contracted the disease. 
During a major TB outbreak in New York City in the 
early 1990s, one in 10 cases proved to be drug-resistant. 
Today, drug-resistant TB is also quite common in India 
and China —the two countries with the highest MDR-TB 
burdens. 
Treatment for MDR-TB consists of what are called 
second-line drugs. These drugs are administered 
when first-line drugs fail.
 Treatment for MDR-TB is commonly administered for 
2 years or longer and involves daily injections 
for six months. Many second-line drugs are toxic and 
have severe side effects. 
 The World Health Organization has issued a target of 
treating 80% of MDR-TB cases by 2015. 
 The cost of curing MDR-TB can be literally thousands 
of times as expensive as that of regular treatment in 
some regions.
Top MDR-TB High-Burden 
Countries 
1. China 
2. India 
3. Russian Federation 
4. Pakistan 
5. South Africa 
6. Philippines 
7. Nigeria 
8. Bangladesh 
9. Indonesia 
10.Myanmar 
11.Ukraine 
12.Uzbekistan 
13.Kazakhstan 
14.Viet Nam 
15. Democratic Republic of Congo 
16. Ethiopia 
17. Azerbaijan 
18. Tajikistan 
19. Republic of Moldova 
20. Kyrgistan 
21. Belarus 
22. Georgia 
23. Armenia 
24. Bulgari 
25. Lithuania 
26. Latvia 
27. Estonia
Extensively drug-resistant TB (XDR-TB), also known 
as Extremely Drug-Resistant TB, is emerging as an 
even more ominous threat. 
This makes XDR-TB treatment extremely complicated, 
if not impossible, in resource-limited settings. 
In a 2006 XDR-TB outbreak in South Africa, 52 of 53 
people who contracted the disease died within months. 
It is estimated that 70% of XDR-TB patients die within a 
month of diagnosis. 
The most recent drug-resistance surveillance data 
issued by the WHO estimates that an average of 
roughly 5 % of MDR-TB cases are XDR-TB. 
Estimating the incidence of XDR-TB is extremely 
difficult because most laboratories are ill-equipped to 
detect and diagnose it; it is thought that the majority of 
XDR-TB cases go undocumented.
MDR & XDR TB is not 
spread by 
 Shaking someone’s hand 
 Sharing food or drink 
 Touching bed linens or toilet 
seats 
 Sharing toothbrushes 
 Kissing 
Smoking or sharing cigarettes
Relationship of MDR, XDR and 
PDR to each other
Prevent of MDR & XDR? 
Hand Hygiene – The Most Important Way to Prevent 
Transmission of Microorganisms and Infection 
 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. 
Minimize unnecessary 
prescribing and overprescribing 
of antibiotics.
REFERANCE 
Centers for Disease Control www.cdc.gov 
www.hain-lifescience.de 
http://www.micro-blog.info/2014/04/considering-the-burden- 
of-enhanced-cre-screening/ 
http://www.cdc.gov/drugresistance/threat-report-2013/. 
http://whqlibdoc.who.int/publications/2010/97892415991 
91_eng.pdf 
Multidrug-Resistant Organisms Ann Bailey, Joanne 
Dixon
MDR , XDR

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MDR , XDR

  • 1. Multidrug-Resistant & Extensively-Drug Resistant Organisms G.VANITHA
  • 2. Antimicrobial resistance Antibiotics are a class of drugs that treat bacterial infections by stopping growth of bacteria or killing the bacteria directly Antimicrobial resistance (AMR) is resistance of a microorganism to an antimicrobial drug that was originally effective for treatment of infections caused by it. Emergence of resistance to multiple antimicrobial agents in pathogenic bacteria has become a significant public health
  • 3. Antibiotic resistance is the ability of a microorganism to withstand the effects of an antibiotic. It is a specific type of drug resistance. Antibiotic resistance evolves selective pressure, mutation, gene transfer, inappropriate drug use, inadequate diagnostics, hospital use and agricultural use of drugs. Once such a gene is generated, bacteria can then transfer the genetic information in a horizontal fashion (between individuals) by plasmid exchange.
  • 4. How do bacteria become resistant to an antibiotic Resistance happen when an infection is treated with antibiotics but all the bacteria are not killed the ones that remain learn how to outlive that antibiotic and are now resistant Not finishing the whole prescription Not taking the proper dosage or at the proper times Taking someone else’s prescription Taking antibiotics when not needed
  • 5. MDR MDR is defined as non-susceptibility to at least one agent in three or more antimicrobial categories. Bacteria that resist treatment with more than one antibiotic are called multidrug-resistant organisms Multidrug-resistant organisms are found mainly in hospitals and long-term care facilities. They often affect people who are older or very ill and can cause bad infections Penicillin resistance in Staphylococcus aureus, a common type of bacteria, was first found in the 1940s. The more often the antibiotics are used, the more likely it is that resistant bacteria will develop.
  • 6. Hey kid wana be a MDR…? Stick some of this into your genome… Even Penicillin won’t be able to harm you….
  • 7. Common multi-drug-resistant organisms (MDROs) MDROs are microorganisms, predominantly bacteria, that are resistant to one or more classes of antimicrobial agents Methicillin-resistant Staphylococcus aureus (MRSA) Vancomycin-intermediate Staphylococcus aureus (VISA) Vancomycin-resistant Staphylococcus aureus (VRSA) Vancomycin-resistant enterococcus (VRE) Streptococcus pneumoniae resistant to penicillin and other broad-spectrum agents MDR-TB (ESBLs) producing Gram-negative bacteria
  • 9. Every year, over 2 million people in the United States become infected with bacteria that are resistant to antibiotics, and around 23,000 people die as a result of these infections (CDC, 2013a). Multidrug-resistant organisms, are bacteria that are resistant to current antibiotic therapy and, therefore, difficult to treat. MDROs can cause serious local and systemic infections that can be severely debilitating and even life-threatening. In the past, these infections were usually controlled by penicillin.
  • 10. The most serious concern with antibiotic resistance is that some bacteria have become resistant to almost all of the easily available antibiotics. For example, Staphylococcus aureus (‘golden staph’) and Neisseria gonorrhoeae (the cause of gonorrhoea) are now almost always resistant to benzyl penicillin. These bacteria are able to cause serious disease and this is a major public health problem.
  • 11. Methicillin-Resistant Staphylococcus aureus  Resistant to Methicillin, Oxacillin and nafcillin Transmitted by direct and indirect contact more virulent than MSSA Susceptible to common disinfectants
  • 12. Staphylococcus aureus is very common, but also very deadly if it gets into the blood stream. It was formerly a major cause of death following surgery. Penicillin proved to be very effective. When penicillin began to fail in 1950s, methicillin proved effective. Methicillin resistant strains were identified in 1961 but did not become common until the 1990s (MRSA). Vancomycin was an effective drug of last resort, but VRSA was reported in the late 1990s. About 2 billion people worldwide carry Staph A. and about 50 million carry MRSA.
  • 13. MRSA now accounts for more than 50% of hospital-acquired staph infections. According to the CDC, almost 1,00,000 cases of invasive MRSA occurred in 2005, with 18% of these individuals dying during their hospitalization. These infections account for more than 5,000 deaths each year which are directly attributable to MRSA. Specifically, MRSA has an attributable mortality rate of 6.9% at 30 days and 16.7% at 1 year. The additional cost of MRSA alone is 39,000 per case in patients with a MRSA surgical-site infection Mortality rates were 13% higher in patients with MRSA infection, regardless of mechanism of death.
  • 14.
  • 15. Extended spectrum beta-lactamase producers (ESBLs) Gram negative organisms - Enterobacteriaceae Excrete the enzyme beta-lactamase Inactivates β-lactam (penicillin) type antibiotics Resistance to β-lactams emerged several years ago and has continued to rise ESBLs Klebsiella E. coli Serratia others
  • 17. Drug resistance facts  MRSA and VRE are terms that describe specific types of antibacterial resistance; MRSA describes Methicillin- Resistant Staphylococcus aureus bacteria while VRE describes Vancomycin-Resistant Enterococi.  Drug resistance occurs when microbes survive and grow in the presence of a drug that normally kills or inhibits the microbe's growth.  The history of drug resistance began with the development of antimicrobial drugs, and the subsequent ability of microbes to adapt and develop ways to survive in the presence of antimicrobials.
  • 18. Diagnosis of antimicrobial drug resistance is performed by lab tests that challenge the isolated microbes to grow and survive in the presence of the drug. Treatment of antimicrobial drug resistance depends on the type of infection and what the patient and their doctor decide. Prevention of antimicrobial drug resistance is aided by preventing the overuse and misuse of antimicrobials; infections can be reduced by a healthy lifestyle, hand washing, and other good hygiene methods Antimicrobial resistance is a growing health issue because more resistant microbes are being detected and societal pressures often result in overuse.
  • 19. XDR XDR is defined as non-susceptibility to at least one agent in all but two or fewer antimicrobial categories (i.e. bacterial isolates remain susceptible to only one or two categories). Multidrug-resistant tuberculosis (MDRTB) Resistance to Isoniazid and Rifampicin Extensively (extremely) drug-resistant (XDR-TB) MDR-TB plus resistance to a second line injectable drug such as amykacin plus a quinolone.
  • 20. MDR & XDR TB The term XDR TB appears to have been used for the first time in March 2006. WHO describing strains of TB, referred to as XDR TB, that were resistant not only to isoniazid and rifampicin (that is they were MRD TB) but they were also resistant to at least three of the six classes of second line anti TB drugs. In 1980 50% of TB bacilli were resistant to 1 drug. Multi-drug resistant TB (MDR-TB) began to emerge. There are now an estimated 1.5million MDR cases worldwide. Extreme drug resistance (XDR-TB) was reported in 2006.
  • 21. The first completely drug resistant (CDR-TB) case was reported in Italy in 2007. MDR-TB has emerged and spread due to the inadequacy of treatment. Today, treatment for drug-resistant TB can take up to two years, and is so complex, expensive, and toxic that a third of all MDR-TB patients die. WHO treatment standards require that at least four drugs be used to treat TB in order to avoid the development of further resistance. According to the WHO, Eastern Europe's rates of MDR-TB are the highest, where MDR-TB makes up 20% of all new TB cases. In some parts of the former Soviet Union, up to 28% of new TB cases are multidrug-resistant.
  • 22. Among previously treated cases in the same region, reported rates of drug resistance are commonly above 50% and as high as 61%. During the late 1980s and early 1990s, outbreaks of MDR-TB in North America and Europe killed more than 80% of those who contracted the disease. During a major TB outbreak in New York City in the early 1990s, one in 10 cases proved to be drug-resistant. Today, drug-resistant TB is also quite common in India and China —the two countries with the highest MDR-TB burdens. Treatment for MDR-TB consists of what are called second-line drugs. These drugs are administered when first-line drugs fail.
  • 23.  Treatment for MDR-TB is commonly administered for 2 years or longer and involves daily injections for six months. Many second-line drugs are toxic and have severe side effects.  The World Health Organization has issued a target of treating 80% of MDR-TB cases by 2015.  The cost of curing MDR-TB can be literally thousands of times as expensive as that of regular treatment in some regions.
  • 24. Top MDR-TB High-Burden Countries 1. China 2. India 3. Russian Federation 4. Pakistan 5. South Africa 6. Philippines 7. Nigeria 8. Bangladesh 9. Indonesia 10.Myanmar 11.Ukraine 12.Uzbekistan 13.Kazakhstan 14.Viet Nam 15. Democratic Republic of Congo 16. Ethiopia 17. Azerbaijan 18. Tajikistan 19. Republic of Moldova 20. Kyrgistan 21. Belarus 22. Georgia 23. Armenia 24. Bulgari 25. Lithuania 26. Latvia 27. Estonia
  • 25. Extensively drug-resistant TB (XDR-TB), also known as Extremely Drug-Resistant TB, is emerging as an even more ominous threat. This makes XDR-TB treatment extremely complicated, if not impossible, in resource-limited settings. In a 2006 XDR-TB outbreak in South Africa, 52 of 53 people who contracted the disease died within months. It is estimated that 70% of XDR-TB patients die within a month of diagnosis. The most recent drug-resistance surveillance data issued by the WHO estimates that an average of roughly 5 % of MDR-TB cases are XDR-TB. Estimating the incidence of XDR-TB is extremely difficult because most laboratories are ill-equipped to detect and diagnose it; it is thought that the majority of XDR-TB cases go undocumented.
  • 26.
  • 27. MDR & XDR TB is not spread by  Shaking someone’s hand  Sharing food or drink  Touching bed linens or toilet seats  Sharing toothbrushes  Kissing Smoking or sharing cigarettes
  • 28.
  • 29. Relationship of MDR, XDR and PDR to each other
  • 30. Prevent of MDR & XDR? Hand Hygiene – The Most Important Way to Prevent Transmission of Microorganisms and Infection  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
  • 31. 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. Minimize unnecessary prescribing and overprescribing of antibiotics.
  • 32. REFERANCE Centers for Disease Control www.cdc.gov www.hain-lifescience.de http://www.micro-blog.info/2014/04/considering-the-burden- of-enhanced-cre-screening/ http://www.cdc.gov/drugresistance/threat-report-2013/. http://whqlibdoc.who.int/publications/2010/97892415991 91_eng.pdf Multidrug-Resistant Organisms Ann Bailey, Joanne Dixon