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M.R.S.A also
known as STAPH infection!

What is MRSA?
MRSA is a type of Staphylococcus aureus (S. aureus).
Staphylococcus aureus, often referred to simply as “staph,” are
bacteria commonly carried on the skin or in the nose of healthy people.
Some S. aureus are resistant to the class of antibiotics that are
frequently used to treat staph such as methicillin—and thus are called
methicillin-resistant S. aureus(MRSA).
Who gets MRSA?
S. aureus (staph) including MRSA can be spread among people
having close contact with infected people. MRSA is almost always spread
by direct physical contact and not through the air. Spread may also
occur through indirect contact by touching objects (e.g., towels,
sheets, wound dressings, clothes, workout areas, or sports equipment)
contaminated by the infected skin of a person with staph bacteria or
MRSA.
Just as S. aureus can be carried on the skin or in the nose
without causing any disease, MRSA can be carried in this way also. This
is known as colonization.
MRSA infections are usually mild, superficial infections of the skin
that can be treated successfully with proper skin care and antibiotics.
MRSA, however, can be difficult to treat and can progress to
life-threatening blood or bone infections because there are fewer
effective antibiotics available for treatment.
MRSA infections occur commonly among persons in hospitals and healthcare
facilities. However, MRSA can cause illness in persons outside of
hospitals and healthcare facilities as well. Cases of MRSA infection in
the community have been associated with recent antibiotic use, sharing
contaminated items, having recurrent skin diseases, and living in
crowded settings. Clusters of skin infections caused by MRSA have been
described among injecting drug-users (1,2); aboriginals in Canada (3),
New Zealand (4) and Australia (5,6); Native Americans in the United
States (7); incarcerated persons (8); players of close-contact sports
(9,10); men who have sex with men (MSM); and other populations (11-17).
Most of the transmission in these settings appeared to be from people
with active MRSA skin infections.
How do I know if I got MRSA from the community or from a healthcare
setting?
Persons with MRSA infections that meet all of the following criteria
likely have community-associated MRSA (CA-MRSA) infections:Diagnosis of
MRSA was made in the outpatient setting or by a culture positive for
MRSA within 48 hours after admission to the hospital. The patient has no
medical history of MRSA infection or colonization The patient has no
medical history in the past year of: Hospitalization Admission to a
nursing home, skilled nursing facility, or hospice Dialysis Surgery The
patient has no permanent indwelling catheters or medical devices that
pass through the skin into the body.
If my doctor or healthcare provider has told me that I have an MRSA
skin infection, what can I do to prevent others from getting infected?
You can prevent spreading an MRSA infection to those you live with or
others around you by following these steps:Keep infections, particularly
those that continue to produce pus or to drain material, covered with
clean, dry bandages. Follow your healthcare provider’s instructions on
proper care of the wound. Pus from infected wounds can contain MRSA and
spread the bacteria to others. Advise your family and other close
contacts to wash their hands frequently with soap and warm water,
especially if they change your bandages or touch the infected wound or
potentially infectious materials. Avoid sharing personal items (e.g.,
towels, washcloth, razor, clothing, or uniforms) that may have had
contact with the infected wound and potentially infectious material.
Wash linens and clothes that become soiled with hot water and laundry
detergent. Drying clothes in a hot dryer, rather than air-drying, also
helps kill bacteria in clothes. Tell any healthcare providers who treat
you that you have an antibiotic-resistant staph skin infection.
How is MRSA diagnosed?
A sample of the infected wound (either a small biopsy of skin or pus
taken with a swab) must be obtained to grow the bacteria in the
microbiology laboratory. Once the staph is growing, the organism is
tested to determine which antibiotics will be effective for treating the
infection. A culture of skin lesions is especially useful in recurrent
or persistent cases of skin infection, in cases of antibiotic failure,
and in cases that present with advanced or aggressive infections.

What is the mortality rate of CA-MRSA?
CA-MRSA infections are typically limited to the skin and do not result
in severe disease (such as infection of the bloodstream) or death.
However, on rare occasion, CA-MRSA can cause severe illness even when
treated quickly, as in the cases of four children who died from CA-MRSA
(18).
Does CDC think CA-MRSA should be reportable?
The decision to make a particular disease reportable to public health
authorities is made by each state based on the needs of that individual
state. CDC supports the resolutions passed by the Council of State and
Territorial Epidemiologists (CSTE) in May 2003. For more information on
CSTE resolutions regarding MRSA go to:
www.cste.org
I have heard this bacterium is attacking healthy people and healthy
skin. Is this what CDC is seeing?
Yes, staph infections commonly affect healthy people and healthy skin.
Usually, these infections are easily treated. Any activity that promotes
breakdown in skin integrity (e.g., chronic skin infections, physical
trauma, poor health) can promote staph skin infections including those
caused by MRSA.

Are people who are positive for the human immune deficiency virus
(HIV) at increased risk for MRSA? Should they be taking special
precautions?
People with increased exposure to antibiotics and the healthcare setting
may be at increased risk for antibiotic-resistant infections of various
kinds, including MRSA. People with compromised immune systems, which
include some patients with HIV, may be at risk for more severe illness
if they get infected with MRSA.
Why does CDC think so many cases of MRSA are being recognized across
the country?
MRSA has been recognized as a problem in the healthcare setting for over
20 years. CDC believes that MRSA has been emerging in the community over
the last several years. It is difficult to determine whether there is an
increase in MRSA disease in the community or an increased awareness and
recognition of MRSA disease. However, it is clear that some of the
recently recognized outbreaks of CA-MRSA are associated with strains
that have some unique properties compared to the traditional
hospital-based MRSA strains, suggesting some biologic properties (like
virulence factors) may allow the CA-MRSA strains to spread more or cause
more disease; however, these hypothesis need testing and confirmation.
Are all the cases of CA-MRSA in the U.S caused by the same strain of
staph? Are these cases all related?
At present, there appears to be at least three different strains of
staphylococci that can cause CA-MRSA infections in the United States.
CDC continues to work with state health departments to gather both the
organisms and epidemiologic data from all the cases reported in the
medical media to determine why certain groups of people get infections
with these organisms. Efforts to evaluate staphylococci from around the
U.S. are ongoing.
What is CDC doing about CA-MRSA?
Public Health Response
· CDC is providing technical assistance to various professional
organizations and state health departments to develop guidance for
control of MRSA.
· CDC is beginning a national program of surveillance for
serious infections with MRSA.

Prevention Activities
Outbreaks among correctional facilities
· CDC and the Federal Bureau of Prisons are sharing information
about risk factors in correctional facilities that potentially lead to
increase MRSA spread among incarcerated persons. The Federal Bureau of
Prisons has developed specific recommendations for infection control of
MRSA in correctional facilities (URL
www.nicic.org).
· LINK TO MMWR for more information
www.cdc.gov/mmwr/preview/mmwrhtml/mm5042a2.htm
www.cdc.gov/mmwr/preview/mmwrhtml/mm5205a4.htm
Outbreaks among athletic Teams
· CDC plans to review existing disease prevention guidelines
developed by sporting organizations (e.g. The National Collegiate
Athletic Association).
· LINK TO MMWR for more information
www.cdc.gov/mmwr/preview/mmwrhtml/mm5233a4.htm
Surveillance and epidemiologic studies in community populations
· In 2000, CDC began working closely with four states, with a
combined population of about 12 million persons, to study the
epidemiology of CA-MRSA infections. The information from these studies
is helping CDC understand the nature of the disease, why people get
infected, and to develop future studies designed to improve our ability
to prevent these infections. These data are being collected in
Connecticut, Minnesota, Georgia, and Maryland as part of CDC's Emerging
Infections Program,
Active Bacterial Core surveillance (ABCs). This program is being
expanded to six states in 2004.
· In addition to enhancing our detection of MRSA cases in
healthcare settings by adding a module to CDC's National Healthcare
Safety Network, we are working with representatives of state health
departments to augment a national surveillance program for invasive MRSA,
including CA-MRSA infections.CDC is using data collected in outbreak
investigations in correctional facilities, in athletic teams, in
children, in MSM and from sporadic cases to learn about strain
characteristics, risk factors for disease, and prevention measures and
to provide clinical education about CA-MRSA. Some of this information
has been published in the MMWR. Findings from investigations in various
settings will be published in peer-reviewed literature and the MMWR over
the next year.
· Representatives from 40 states and territories participated in
a March 2003 meeting on enhancing state-based reporting of MRSA. CDC is
working with states that are interested in initiating or expanding
surveillance of MRSA (both CA- and healthcare-associated MRSA) in their
states.
References:
1. Saravolatz LD, Markowitz N, Arking L, Pohloh D, Fisher E. Methicillin-resistant
Staphylococcus aureus. Epidemiologic oberservations during a
community-acquired outbreak. Ann Intern Med. 1982;96:11-16.
2. Centers for Disease Contorl and Prevention. Community-acquired
methicillin-resistant Staphylococcus aureus infections—Michigan.
MMWR. 1981;30:185-7.
3. Embil J, Ramotar K, Romance L, et al. Methicillin-resistant
Staphylococcus aureus in tertiary care institutions on the Canadian
prairies 1990-1992. Infect Control Hosp Epidemiol 1994;15:646-51.
4. Rings T, Findlay R, Lang S. Ethnicity and methicillin-resistant S.
aureus in South Auckland. N Zeal Medica Journal 1998; 111:151.
5. Maguire GP, Arthur AD, Boustead PJ, Dwyer B, Currie BJ. Emerging
epidemic of community-acquired methicillin-resistant Staphylococcus
aureus infection in the Northern Territory. Medical Journal of
Australia 1996; 1996; 164:721-3.
6. Collignon P, Gosbell I, Vickery A, Nimmo G, Stylianopoulos T,
Gottlieb T. Community-acquired methicillin-resistant Staphylococcus
aureus in Australia. Australian Group on Antimicrobial Resistance.
Lancet 1998; 352:145-6.
7. Groos A, Naimi T, Wolset D, Smith-Johnson K, Moore K, Cheek J.
Emergence of community-acquired methicillin-resistant Staphylococcus
aureus in a rural American Indian community (Abstract 1230), 39th
Annual Interscience Conference on Antimicrobial Agents and Chemotherapy,
San Francisco, CA, 1999.
8. Centers for Disease Control and Prevention. Methicillin-resistant
Staphylococcus aureus skin or soft tissue infections in a state
prison—Mississippi, 2000. MMWR 2001; 50 (42): 919-22.
9. Lindenmayer JM, Schoenfeld S, O’Grady R, Carney JK. Methicillin-resistant
Staphylococcus aureus in a high school wrestling team and the
surrounding community. Arch Int Med 1998;158:895-9.
10. Stacey AR, Endersby KE, Chan PC, Marples RR. An outbreak of
methicillin- resistant Staphylococcus aureus infection in a rugby
football team. Br J Sports Med 1998; 332: 153-4.
11. Kallen AJ, Driscoll TJ, Thornton S, Olson PE, Wallace MR. Increase
in community-acquired methicillin-resistant Staphylococcus aureus
at a Naval Medical Center. Infect Control Hosp Epidemiol 2000;21:223-6.
12. Hussain FM, Boyle-Vavra S, Bethel CD, Daum RS. Current trends in
community-acquired methicillin-resistant Staphylococcus aureus at
a tertiary care pediatric facility. Pediatr Infect Dis J 2000; 19:
1163-6.
13. Feder HM, Jr. Methicillin-resistant Staphylococcus aureus
infections in 2 pediatric outpatients. Arch Fam Med 2000; 1163-6.
14. Goetz A, Posey K, Fleming J, et al. Methicillin-resistant
Staphylococcus aureus in the community: a hospital-based study.
Infect Control Hosp Epidemiol 1999 20:689-91.
15. Frank AL, Marcinak JK, Mangat PD, Schreckenberger PC.
Community-acquired and clindamycin-susceptible methicillin-resistant
Staphylococcus aureus in children. Pediatr Infect Dis J
1999;18:993-1000.
16. Price MF, McBride ME, Wolf JE, Jr., Prevalence of methicillin-resistant
Staphylococcus aureus in a dermatology outpatient population.
South Med J 1998:91:369-71.
17. Herold BC, Immergluck LC, Maranan MC, et al. Community-acquired
methicillin-resistant Staphylococcus aureus in children with no
identified predisposing risk. JAMA 1998;279:593-8.
18. Centers for Disease Control and Prevention. Four pediatric deaths
from community-acquired methicillin-resistant Staphylococcus aureus
—Minnesota and North Dakota, 1997-1999. JAMA 1999;282:1123-5.
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