5/2/2012

Eric Bosley, MD Laura Stadler, MD JhJohn Draus, MD MRSA: A TEAM APPROACH

PART I: OUTPATIENT ISSUES AND MANAGEMENT NOT REQUIRING I&D OR HOSPITALIZATION

Eric L. Bosley, MD, FAAP Pediatric Associates, PSC Crestview Hills, KY President, Kentucky Chapter of the AAP

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MRSA HISTORICAL PERSPECTIVE

 Methicillin-resistant strains of (MRSA) were first recognized in 1961, one year after the methicillin was introduced for treating S. aureus  The first documented MRSA outbreak in the United States occurred at a Boston hospital in 1968.  For the next two decades most MRSA infections occurred in persons who had contact with hospitals or other healthcare settings  Beginning in the 1990s community associated MRSA (CA MRSA) infections emerged in persons having none of the risk factors associated with MRSA in the past. Genetic and epidemiologic evidence shows that CA MRSA is caused by strains of S. aureus different from those associated with HA MRSA.

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HOSPITAL VS. COMMUNITY ASSOCIATED MRSA

HA-MRSA CA-MRSA Heal th care contact Yes No Mean age at Older Younger Skin and soft tissue infections 35% 75% Antibiotic resistance Many agents Some agents Resistance gene SCCmec Types I, II,III SCCmec Type IV, V Strain type USA 100 and 200 USA 300 and 400 PVL toxin gen Rare (5%) Frequent (almost 100%)

RISK FACTORS FOR CA-MRSA INFECTIONS

 • History of MRSA infection or colonization in patient or close contact  • High prevalence of CA MRSA in local community or patient population  • Recurrent skin disease such as eczema  • Crowded living conditions (e.g. homeless shelters, military barracks)  • History of incarceration  • Participation in contact sports  • Skin or soft tissue infection with poor response to B-lactam  • Recent and/or frequent antibiotic use  • Injection drug use  • Member of Native American, Pacific Island, Alaskan Native populations  • Child under 2 years of age  • Male with history of having sex with men  • Shaving of body hair

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PRESENTATIONS OF MRSA IN OUTPATIENT SETTING THAT DO NOT WARRANT I&D

/Furuncle

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CELLULITIS

CELLULITIS

 Nonpurulent cellulitis is characterized by area of erythema, edema,,, warmth, tenderness to p pp,alpation, but no fluctuance , drainage, or central area of pus  While MRSA is an emerging cause of cases of cellulitis overall, many nonpurulent cases of cellulitis are still caused by spp. or MSSA  Treatment of nonpurulent cellulitis consists of antibiotic coverage for Streptococcus spp. and/or other suspected pathogens, followed by close follow-up, and possible addition of coverage for MRSA if patient does not respond.

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IMPETIGO

BULLOUS IMPETIGO

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IMPETIGO

 Impetigo is common infection of discrete lesions that are nearly always caused by β-hemolytic streptococci and/or S. aureus. Nonbullous impetigo is a superficial that manifests as clusters of vesicles or pppustules that rupture and develo pyp a honey-colored crust. is a superficial skin infection that manifests as clusters of vesicles or pustules that enlarge rapidly to form bullae. The bullae burst and expose larger bases, which become covered with honey-colored varnish or crust.  Peak incidence in amongst children ages 2-5, although other ages are affected.  Nonbullous impetiggyyo was traditionally caused by streptococcus spp., but now are more commonly caused by Staphylococcus spp. alone or mixed Staph and Strep spp. Bullous Impetigo is caused by toxin producing Staph Aureus strains with MRSA strains increasing in frequency.  Treatment involves Gentle cleansing, removal of the honey-colored crusts of nonbullous impetigo using antibacterial soap and a washcloth as well as topical antibiotics.

 Treatment involves Gentle cleansing, removal of the honey- colored crusts of nonbullous impetigo using antibacterial soap and a washcloth as well as topical antibiotics.  Topical antibiotics alone are often adequate for mild cases while combination topical and systemic antibiotics are used in cases of bullous impetigo, more significant, or poorly responding cases.  with a penicillinase-resistant penicillin or first- generation cephalosporin is considered adequate in most cases where both topical and systemic treatment is required but systemic coverage for MRSA may be needed in some refractory cases.

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FOLLICULITIS

8 5/2/2012

FOLLICULITIS

 Infection in the hair follicles  It usually is caused by bacteriabacteria. It also can be caused by yeast or another type of fungus.  most common on the face and scalp and areas rubbed by clothing, such as the thighs and groin  "" most often appears about 72 hours after you've been in a hot tub or spa. Many small appear on your stomach and sometimes on your arms and legs. You might have a mild fever and have an upset stomach. Most of the time, this kind of folliculitis goes away on its own in 7 to 10 days.

RISK FACTORS FOR FOLLICULITIS

 Use a hot tub, whirlpool, or swimming pool that is not properly treated with chlorine.  Wear tight clothes.  Use antibiotics or steroid creams for long periods.  Use or work with substances that can irritate or block the follicles. Examples include makeup, cocoa butter, motor oil, tar, and creosote.  Have an infected cut, scrape, or surgical wound. The or fungi can spread to nearby hair follicles.  Have a disease such as diabetes or HIV that lowers your ability to fight infection  Shaving

9 5/2/2012

FOLLICULITIS

 Treatment can often be accomplished at home and includes such measures as warm compresses made with white vinegar or Burow's solution. These may ease itching and help healing. Medicated shampoo. It can be used to treat folliculitis on the scalp or beard.  Failures of these measures may indicate presence of MRSA ((gor Fungal infection ) and use of to pical mupirocin can be tried with addition of systemic anti-MRSA antibiotics added if poor response to topical treatment.

BOIL/FURUNCLE

10 5/2/2012

STYE

BOIL/FURUNCLE

 For small furuncles, moist heat, which helps to promote drainage, may be sufficient treatment  It remains controversial whether antibiotics provide any clinically significant additional benefit, but incision and drainage is likely adequate for most simple . Multiple, mostly observational studies indicate high cure rates (85%–90%) whether or not an active antibiotic is used. Two recently published randomized clinical trials involvinggpp adult and pediatric patients showed no significant difference in cure rates when TMP-SMX was compared with placebo; however, there was a suggestion that antibiotics may prevent the short-term development of new lesions.

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