Sixth Plague of Egypt. Community MRSA. Epidemiology. Basic Features of Community MRSA. Populations with CA-MRSA

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Community MRSA Henry F. Chambers, M.D. University of California San Francisco San Francisco General Hospital Sixth Plague of Egypt (~ 1200 BCE) So they took soot from a kiln, and stood before Pharaoh; and Moses threw it toward the sky, and it became boils breaking out with sores on man and beast. Exodus 9:10 Epidemiology INCREASING BURDEN OF RESISTANCE 1 Penicillin introduced Penicillin resistance Methicillin introduced Φ80/81 2 MRSA-I 3 MRSA-II & III 4 CA-MRSA VRSA VISA MRSA-IV 1940 1960 1980 2000 Basic Features of Community MRSA Populations with CA-MRSA First occurrences mid 1990s in US and Australia Novel methicillin-resistant gene cassette: SCCmec type IV or V Specific clones, not hospital clones USA300 (ST8) USA400 (ST1) Toxin production (Panton-Valentine leukocidin, PVL) Children, infants Jail and prison inmates Military recruits Native populations MSM HIV+ patients Homeless populations Football teams Wrestlers Gymnasts Fencing teams Injection drug users Tattoo recipients Individuals with no risk factors at all

Household Transmission of CA-MRSA Number 80 Total number of positive MRSA cultures among household members 70 MRSA infections among household members Households with >1 person with a positive * 60 MRSA isolate 50 40 30 USA300 20 10 Clonal Distribution of MRSA in San Francisco Hospitals 2004-2005 Community- Onset other (4.2%) CC5 (15.7%) other CC8 (4.2%) USA300 (75.9%) Community- Onset Hospital- Onset other (6.7%) Hospital- Onset CC5 (41.2%) other CC8 (6.7%) USA300 (45.4%) 0 1998 1999 2000 2001 2002 2003 2004 Crum, et al. Am J Med 119:943, 2006 Liu, CID 46:1637, 2008 Types of CA-MRSA Infections Potentially Toxin-Mediated Manifestations of CA-MRSA Infections Other Other Bone & Joint Necrotizing fasciitis SSTI All CA-MRSA Infections Resp Urine Blood Other CA-MRSA Infections Furunculosis, abscesses Fridkin, NEJM 352:1436, 2005; Kaplan, CID 40:1785, 2005; Liu, CID 46:1637, 2008; Purcell, Arch Ped Adolesc Med 159:980, 2005 Necrotizing pneumonia Waterhouse-Friderichsen Overwhelming sepsis Outcomes of CA-MRSA vs CA- MSSA ~ 4-fold higher rates of similar infections in household contacts of CA-MRSA patients (49% USA300) CA-MRSA infections more likely to be hospitalized Recurrence/relapse more common in CA-MRSA patients Agent Resistance Profiles SFGH Isolates (% R) USA300, MDR USA300, non-mdr Other MRSA Clinda 100 23 31 Mupirocin 100 0 0 Cipro 77 73 80 Tet 63 29 15 TMP-SMX 0 0 0 Davis, et al J Clin Micro 2007;45:1795

Impact of MRSA Emergence as an important pathogen in out-patients Empirical antibiotics used in the therapy of SSTIs must cover MRSA Predilection for more serious disease Enhanced transmissibility Tendency for recurrence Treatment Prevalence of MRSA among S. aureus isolates Grundmann et al. Lancet 2006;368:874-85 Audience Interactive A healthy 20-year-old college basketball player Abscess: area of erythema was 5 x 3 cm and a firm central area 2 cm in diameter. No direct trauma to the area. Subjective low-grade fevers the night before presentation, T= 37.7 C Hammand and Baden, NEJM 359:e20 (Oct 9, 2008) What is the most appropriate management option? 1. I&D alone 2. I&D + MRSA agent 3. I&D + MSSA agent Rank of Management Options by Readers of NEJM 1. I&D + MRSA agent (41% of the 11,205 votes ) 2. I&D alone: (31% of the votes cast) 3. I&D + MSSA agent (28% of the votes cast) Hammand and Baden, NEJM 359:e20 (Oct 9, 2008) Hammand and Baden, NEJM 359:e20 (Oct 9, 2008)

MD Use of I&D + Antibiotics for Abscess as a Function MRSA Rate Effect of Initial Therapy on Outcome of SSTIs % MDs 100 80 60 40 20 0 P = 0.0015 Neth US <5% 25-50% MRSA Rate 2 1.75 1.5 1.25 1 0.75 0.5 0.25 0 Inactive Rx > 1 F/u I&D @ F/u New Rx @ F/u Hammand and Baden, NEJM 359:e20 (Oct 9, 2008) Fridkin, NEJM. 2005; 352:1436 Treatment of MRSA SSTI 406 of 422 (96%) patients with complete information 85% had I&D performed + antibiotics 198/311 (64%) patients given antibiotics received a beta-lactam 57% of MRSA infections treated with wrong antibiotic MRSA infections no different in outcome and no adverse effect of wrong antibiotic on outcome. Moran, NEJM. 2006; 355:666 Cefdinir vs. Cephalexin for usstis Cure Rates MSSA (n=72) MRSA (n=79) MSSA 66 (92%) 72 (91%) Cellulitis: 2 Impetigo: 2 Other: 2 Failures MRSA Abscess: 2 Cellulitis: 3 Other: 2 Giordano, Curr Med Res Opin. 2006; 22: 2419 Impact of Antibiotics on Outcome of Community-Onset MRSA SSTI Retrospective cohort study 531 episodes of abscess, furuncles, carbuncles, or cellulitis in 492 patients All culture-positive for MRSA (71% CA-MRSA) Clinical specimen obtained as OP or w/in 48h hospital admission Failure defined as any one of the following I&D after 48h of therapy Subsequent hospital admission New lesion or microbiological failure Ruhe, et al. Clin Infect Dis. 2007;44:777 Impact of Antibiotics on Outcome of Community MRSA SSTI Types of infections Abscess in 361 (68%) Cellulitis, all with a focal lesion, in 116 (22%) Furuncle or carbuncle in 54 (10%) Antimicrobial therapy Active in 312 episodes (59%) Inactive in 219 episodes (41%) Successful outcomes 296 active (95%) vs. 190 inactive (87%): p =0.001 Only inactive therapy associated with failure (OR 2.82, 95% CI 1.49-5.34) 24 (83%) of 29 inactive failures received a β-lactam Ruhe, et al. Clin Infect Dis. 2007;44:777

Randomized, double-blind, placebo controlled trial of cephalexin for SSTI Rajendran P, et al. Antimicrob Agents Chemother. 2007;51:4044 N=82 Cure Rates N=80 Bar indicates upper 95% confidence interval Summary Spider Bite Lesion..Not! Incision and drainage is probably sufficient in most cases, especially in OP therapy Use of an antibiotics to which the isolate is susceptible may provide a marginal benefit in a minority of cases Beta-lactams may not only be ineffective, but could worsen outcome* *Stevens, JID. 2007;195:202 Oral Antistaphylococcal Agents Trimethoprim-sulfamethoxazole Minocycline > doxycycline > tetracycline Clindamycin Fluoroquinolones (levo, gati, moxi) Linezolid IDSA Practice Guidelines: Stevens et al, CID 2005;41:1373 CDC Guidelines: Gorwitz et al. http://www.cdc.gov/ncidod/dhqp/ar_mrsa_ca.html. Trimethoprim-sulfamethoxazole Most MRSA are susceptible (~95%) Beta-hemolytic strep (GAS) coverage? Bactericidal, mostly Less efficacious than vancomycin in one comparative clinical trial (Markowitz) Dose? 1 DS (160/800) or 2 DS bid? Off-label use, not much published, most experience in minor to mod SSTI Markowitz et al, \Ann Intern Med. 1992;117:390 Szumowski et al, Antimicrob Agents Chemother. 2007;51:423 Cenizal et al, Antimicrobial Agents Chemother. 2007;51:2628 Proctor, Clin Infect Dis. 2008; 46:584

Tetracyclines Minocycline > doxycycline > tetracycline Off-label use (except tigecycline) One observational study (*), and one clinical trial (**) indicate efficacy of ~90+% Cross-resistance occurs, but if tet resistance is due to efflux, doxy and mino, (not efflux substrates) are still active in vitro 90+% of MRSA are susceptible Activity against GAS unknown Contraindicated in children < 8 years old *Ruhe and Menon, Antimicrob Agents Chemother 2007;51:3298 **Cenizal et al. Antimicrobi Agents Chemother 2007;51:2628 Clindamycin FDA approved for treatment of staphylococcal infections Oral dose at 300-450 mg tid Excellent coverage against GAS Major issue is cross-resistance with macrolides ribosomal methylase producers are or can become resistant macrolide efflux pump producers not cross-resistant My personal favorite D-Test for Inducible Clindamycin Resistance _ Is There a Role for Decolonization? + Erm Cln Case 42 y/o hospitalist First episode of abscess on face 3 months prior: drained Three weeks later, abscess of arm, back: CA-MRSA, treated with T/S Four weeks later, recurrence of facial abscess: treated with clinda and mupirocin Now comes in with new abscess L cheek What would you recommend for this patient? 1. Retirement 2. Decolonization regimen of intranasal mupirocin for 5-7 days 3. Intranasal mupirocin + chlorhexidine baths for 5-7 days 4. Rifampin + TMP/SMX for 5-7 days 5. All of the above

Rationale for S. aureus Decolonization Nasal carriage is present in about of third of humans 20% of persons are persistent carriers 60% are intermittent carriers 20% almost never carrier S. aureus Carriers can be a source of S. aureus transmission Colonization predisposes to infection Eradication of carriage could Prevent transmission of S. aureus to others Prevent occurrence of infection Prevent recurrent infection Strategies for Decolonization Targeted (i.e., known carrier) vs. untargeted Chlorhexidine or bleach (1/2 c in bathtub) baths: largely ineffective. Mupirocin-based topical application to anterior nares Systemic (i.e., rifampin-based) therapy Kitchen sink approach Review of Mupirocin Decolonizationg for S. aureus Decolonization 9 prospective trials of eradication of nasal carriage Mupirocin highly effective in the short term Less effective in achieving long-term eradication 7 prospective trials to prevent infection The body of literature currently does not support routine administration of prophylactic intranasal mupirocin to patients in an attempt to decrease the rate of clinical infection. Antimicrob Agents Chemother. 2007;51:3591 Clin Infect Dis. 2003;37:933 Study Design Randomized, double-blind placebo controlled US army personnel enrolled in a 16-week medic training course Screened for S. aureus by swab culture of anterior nares Mupirocin bid in each nostril for 5 days for those culture positive for CA-MRSA Primary outcome: infections occurring within 16 weeks Results 3447 soldiers screened and randomized 1669 to placebo group 1778 to mupirocin group Colonization 134 (3.9%) with CA-MRSA (54% USA300 and 40% ST5/USA800) 1316 (38.2%) with MSSA 65 placebo-treated and 66 mupirocin-treated subjects completed follow-up Placebo treated Colonization decreased from 4.0% to 3.2% 5 (7.7%) infections Mupirocin treated Colonization decreased from 3.8% to 1.9% 7 (10.6%) infections

Detection of MRSA Carriage in ICU Patients Site sampled Sensitivity (%) Nose only 69 Throat only 71 Groin only 67 Nose and throat 82 Throat and groin 91 Nose and groin 88 Nose, throat, groin 94 Marshall and Spelman, J Clin Micrbiol. 2007;45:3855 Effect of Mupirocin on Nasal, Pharyngeal, Perineal Carriage of S. aureus Healthy adults 16 persistent carriers 26 intermittent carriers 20 noncarriers Cultured 1 day before and 5 weeks after a 5d course of intranasal mupirocin Nasal carriage eliminated in 69% of persistent carriers, 58% of intermittent carriers; similar efficacy in throat carriers Perineal carriage did not change significantly Wertheim, et al. Antimicrob Agents Chemother. 2005; 49:1465 Study Design Infect Control Hops Epidemiol 28:1036, 2007 Randomized, double-blind trial in hospitalized patients colonized with MRSA Whole-body washing with 4% chlorhexidine for 5 days versus placebo All subjects also received mupirocin intranasally and chlorhexidine mouth wash Sites sampled: nares, throat, groin area, perineal region, skin defects, and any previously colonized site Sampled taken before treatment and on days 3, 4, 5, 9, and 30 after the end of treatment 58 placebo subjects, 56 chlorhexidine-treated Primary outcome: eradication of carriage @ 30 days Results Any benefit gone by 5 days Eradication @ 30 days 7 (13%) placebo recipients 4 (8%) chlorhexidine recipients Adverse events: all more common with chlorhexidine Discontinuation of daily washing: 4 chlor vs 1 placebo Skin Fissures (17.7% chlor vs. 1.8% placebo) Itching (41.5% vs 10.9% or burning of skin (50.0% vs 10.9%) Failure associated with Colonization of groin Colonization of perineum Colonization > 1 site Success associated with single site of colonization Clin Infect Dis. 2007;44:e88

Setting German village, 144 persons (30 children), 58 households Presence of a shooting club, local voluntary fire brigade, a local citizen s group, and a soccer club One bar Case finding: retrospective, self-report Epidemiology 98% participation rate Case rates: 8/30 children and 28/111 adults 23 cases (64%) had experienced at least 1 relapse. Overall attack rate of 26% (95% CI, 19%-34%). In persons colonized with PVL-positive S. aureus attack rate of 78% (95% CI, 40% 97%) In persons colonized with PVL-negative S. aureus, attack rate of 19% (95% CI, 8%-33%) Microbiological findings 36% (51 of 140 tested) with nasal colonization 9 PVL-positive (7 ST121, 2 ST-30) Mo MRSA Multivariate Analysis of Risk Factors Associated with Furunculosis Exposure Odds Ratio (95% CI) PVL-positive strain 9.2 (1.2 73.1) Contact with a case 4.7 (1.3 17.3) Voluntary fireman 5.5 (1.6 19.0) Sharing objects 3.6 (1.1 12.2) Chronic skin disease 12.3 (1.5 100.2) Owning live chickens 0.3 (0.1 0.7) Treatment Regimen Mupirocin 3x daily for 5 days Alcohol-based hand sanitizer after mupirocin Octenidin-based wash of skin and hair daily 0.1% chlorhexidine solution gargle 3x daily Disinfection of personal items, bathtub/shower floor with an alcohol-based antimicrobial cleanser daily Towels, bedclothes, underwear, clothing changed and washed daily (water temperature > 60 o C) Increased hand hygiene and minimized contact with other villagers during decolonization Cleaning and disinfection of fire-protective suits Mupirocin for a Year 34 patients with recurrent MSSA infections treated with mupirocin for 5 days 17 randomized to placebo 17 randomized to mupirocin 5d treatment monthly for a year 8 mupirocin and 2 placebo patients remained free of nasal colonization (p < 0.01) 26 infections in mupirocin recipents vs 62 in placebo recipients (p < 0.002) Raz, et al, Arch Intern Med. 1996;156:1109 Eradication Rate 80 70 60 50 40 30 20 10 Regimens for Eradication of S. aureus carriage 0 0-2 days 1 wk 1 mo 3 mo 6 mo Falagas et al. Am J Infect Control 2007; 35:106 No Rx Mup Non-rif Rif

Decolonization Chlorhexidine: Not effective alone, Transient effect at best Mupirocin: Effective short-term eradication of nasal and pharyngeal colonization Little evidence that it prevents infection (with some exceptions?) Rifampin (with another active agent to prevent resistance) Side-effects & drug interactions Best agent for eradication of colonization Little evidence at best that it prevents infection MRSA: no evidence supporting use of any regimen for prevention of infection Cochrane Review of Mupirocin for Staph. aureus Nasal Colonization Hospitalized patients + positive nasal culture AND Surgical patients Cardiothoracic surgery Orthopedic surgery General surgery Dialysis patients (CAPD General medicine patients???? (only one study, no benefit) General medicine patients???? (only one study, no benefit) The Cochrane Library 2009, Issue 1