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The Increasing Prevalence of MRSA Skin Infections in the General Population - Case Study Example

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This paper 'The Increasing Prevalence of MRSA Skin Infections in the General Population" focuses on the fact that the upward trends in the prevalence of methicillin-resistant Staphylococcus aureus infections in the community are highlighted from the literature. …
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The Increasing Prevalence of MRSA Skin Infections in the General Population
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The Increasing Prevalence of MRSA Skin Infections in the General Population and Current Treatment Strategies ABSTRACT In this review, the upward trends in the prevalence of methicillin-resistant Staphylococcus aureus infections in the community are highlighted from the literature. Community-associated MRSA skin infections are coming into their own as a distinct therapeutic challenge, complicated by their ubiquitous occurrence in a variety of institutional environments. Treatment strategies consist of both drug and non-drug options. There is a wide variety of pharmacological agents available for management, but extensive studies are still required to put in place evidence-based consensus treatment guidelines. INTRODUCTION This review addresses issues concerning the increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) skin infections in the general population and current treatment strategies. MRSA diseases have constituted a formidable clinical challenge for several years. Although the pathogen has been typically associated with health care environments and patients who have been exposed to some form of hospitalization-related treatment (i.e. health care-associated MRSA), an emerging development has been the increasing occurrence of community-associated or community-acquired MRSA types, resulting in a new challenge to the medical community. The classical mechanism of resistance of MRSA to beta-lactam antibiotics is alteration of target penicillin-binding proteins which makes them have a low affinity for the penicillins. This is mediated by the mecA gene, carried on the staphylococcal cassette chromosome (SCC). However, several MRSA strains now possess resistance to multiple classes of antibiotics via alternative mechanisms. Community-acquired MRSA differs from health care-associated MRSA in a few respects (Rybak & LaPlante, 2005). Isolates of community MRSA are generally susceptible to non-beta-lactam antibiotics, while the hospital-acquired MRSA isolates typically show resistance to multiple antibiotics. Also, community isolates are genotypically distinct from health care-derived types, with a novel methicillin resistance gene element previously unreported among the health care-derived isolates. Moreover, community isolates typically occur in patients who do not have any of those risk factors associated with MRSA. Community-associated MRSA isolates have a greater likelihood of encoding virulence factors, such as enterotoxins, and the bicomponent cytotoxin Panton-Valentine leucocidin, which was previously reported to be produced by less than 5% of Staphylococcus aureus isolates. It is believed that the genetic patterns observed in community-associated MRSA isolates suggest that they must have resulted from methicillin-sensitive strains that successfully incorporated the SCCmec IV element which is uniquely characteristic of community-acquired MRSA. According to guidelines from the Centers for /Disease Control and Prevention, the criteria for distinguishing between community-associated and health care-associated MRSA are as follows (Rybak & LaPlante, 2005): The diagnosis must be made in an outpatient setting or by culture showing MRSA within 48 hours after admission to the hospital The patient must not have experienced any of the following during the years before an infection: hospitalization; admission to a nursing home, skilled nursing facility, or hospice; dialysis; or surgery. The patient must be without permanent indwelling catheters or medical devices that pass through the skin into the body. The increasing prevalence of community-associated MRSA skin infections is of additional concern because owing to their high virulence, such skin infections can lead to severe necrotizing pneumonia with a high mortality rate. REVIEW OF THE LITERATURE Prevalence in Health Care-Related Settings In a prospective observational study in California, Frazee and co-workers (Frazee et al., 2005) attempted to determine the prevalence of MRSA among emergency department patients with skin and soft tissue infections, identify demographic and clinical variables associated with MRSA, and characterize MRSA by antimicrobial susceptibility and genotype. Over 51% of the 119 patients studied had MRSA infections, which constituted 75% of the S. aureus cultures isolated. 76% of the cases fit the clinical definition of community acquired MRSA. 99% of MRSA isolates possessed the SCC mec IV allele (typical of community-associated MRSA), 94.1% possessed Panton-Valentine leukocidin genes, and 87.1% belonged to a single clonal group (ST8:S). A limitation of the study lay in the use of a patient population which was essentially a convenience sample. In a 2005 report (Moran et al., 2005), Community-associated MRSA was found to be the most common pathogen among patients with skin and soft tissue infections seeking treatment at a Los Angeles (USA) area emergency department. The proportion caused by MRSA increased from 29% in 2001 to 2002 to 64% in 2003 to 2004. Interestingly, the study found that no clinical or historical features reliably predict MRSA etiology. Roesch and co-workers reported on the elimination of a community-acquired MRSA infection in a nurse with atopic dermatitis (Roesch et al., 2005). Johnston and co-workers described an investigation of soft-tissue infections caused by community-acquired MRSA strains in two healthcare workers employed in an outpatient clinic for patients with human immunodeficiency virus infection (Johnston et al., 2006). Cultures of environmental samples from multiple surfaces in the clinic grew toxin-producing CA-MRSA strains, suggesting that fomites may play a role in the transmission of these strains of MRSA. Prevalence in Military Facilities In a study at the Norfolk naval base, Zinderman and co-workers reported an outbreak of 235 community-acquired MRSA infections among military recruits (Zinderman et al., 2004). In this unique environment, the close contact between recruits and the physical demands of training may have contributed to the spread of MRSA. Control measures included improved hygiene and aggressive clinical treatment. In an interesting report from the military environment (Pagac et al., 2006), recent outbreaks of mysterious skin lesions on multiple personnel at several military facilities were initially blamed on spiders. Requests were made for pest inspection and control to remedy the situation. Greater scrutiny of the situation led to a hypothesis that instead of spiders, an infectious outbreak of community-acquired CA-MRSA should be investigated as the etiology. Subsequent culturing of the lesions on personnel at one facility confirmed this bacterial etiology. The authors noted that barracks, as well as other close quarter military living conditions, are ripe environments for the establishment, persistence, and spread of community-acquired MRSA, and recommended that military medical personnel should consider CA-MRSA as a more likely etiologic agent than spider bites for cutaneous eruptions in which there are multiple lesions on one person or multiple patients with similar lesions. In a review by Cloran, MRSA was noted as being a pathogen of growing concern among community-based practices in medicine, particularly those in the military (Cloran, 2006). The risk of colonization and infection by community-acquired MRSA is significantly higher among military members than that of the general population. The unique environment of the deployed, military aviator (impaired hygiene practices, close contact in warm, space-limited cockpits, and shared life support equipment) may increase risks of colonization, infection, and transmission of CA-MRSA and hence warrants the clinical attention of the flight surgeon. Prevalence in Correctional Facilities A retrospective investigation of skin and soft tissue infections caused by community-associated MRSA strains among inmates in a Wisconsin correctional facility suggested a shift in MRSA genotype (Stemper et al., 2006). The case timeline indicated a displacement of USA400 clone by USA300 clone. From the results of the investigation, the USA300 index case was associated with an infected new tattoo. In a review of MRSA skin infection prevalence, Lu and Holtom (Lu & Holtom, 2005)noted that young and healthy persons in crowded conditions are at risk, including athletes, military personnel, jail inmates, and children in daycare. Prevalence among Athletes and in Sports Facilities Saben reported on a case of community-acquired MRSA skin infection in a football player (Saben, 2004). Using a retrospective cohort study and nasal-swab survey of players and staff members during the 2003 football season, Kazakova and co-workers reported an investigation of an outbreak of abscesses due to MRSA among members of a professional football team (St. Louis Rams) and examined the transmission and microbiologic characteristics of the outbreak strain (Kazakova et al., 2005). S. aureus recovered from wound, nasal, and environmental cultures was analyzed by means of pulsed-field gel electrophoresis (PFGE) and typing for resistance and toxin genes. MRSA from the team was compared with other community isolates and hospital isolates. During the football season, there was an incidence of 9% of MRSA skin and soft tissue infections. All of the infections developed at turf-abrasion sites. MRSA infection was significantly associated with the lineman or linebacker position and a higher body-mass index. No MRSA was found in nasal or environmental samples; however, methicillin-susceptible S. aureus was recovered from whirlpools and taping gel and from 35 of the 84 nasal swabs from players and staff members (42 percent). MRSA from a competing football team and from other community clusters and sporadic cases had PFGE patterns that were indistinguishable from those of the Rams' MRSA; all carried the gene for Panton-Valentine leukocidin and the gene complex for staphylococcal-cassette-chromosome mec type IVa resistance (clone USA300-0114). Prevalence: Other Data It has been suggested that sexual habits could also be a contributory factor to the spread of community acquired MRSA. Lee and co-workers investigated community-associated MRSA skin infections among HIV-positive men who have sex with men, by performing a matched case-control study of 35 case patients and 76 control subjects (N. E. Lee et al., 2005). They found that community-associated MRSA skin infections were associated with high-risk sex and drug-using behaviors and with environmental exposures but not with immune status. In a Switzerland study (Aramburu et al., 2006), the incidence of MRSA skin infections in Geneva was monitored over a three-year period from 2002 to 2004 using a voluntary reporting system. Of the 58 cases reported, most were family related, and the prevalence was commonest in people under 40 years. 71% of the cases were infected and 29% were colonized. Most infected cases presented with skin lesions such as furunculosis, impetigo or abscess, and most cases had no underlying disease. It was interesting that 65% of the cases had traveled abroad, which underlines the challenge posed by virulence in a global setting. It was also noted that 69% of the isolates carried the Panton-Valentine leukocidin (PVL) toxin. The study concluded there was a need for continued surveillance to adequately describe transmission patterns and the spread of the pathogen. A recent epidemiological study conducted in Atlanta, Georgia examined the proportion of infections caused by community-acquired MRSA, associated clinical characteristics, and the molecular epidemiology of community-acquired MRSA among persons with community-onset S. aureus skin and soft-tissue infection, using an active, prospective laboratory surveillance to identify Staphylococcus aureus from skin and soft-tissue sources (King et al., 2006). It was found that MRSA accounted for 72% of community-onset skin and soft-tissue infection due to Staphylococcus aureus. Of these, 99% were found to be of the MRSA USA 300 clone type (using pulsed-field gel electrophoresis and antimicrobial susceptibility patterns). Factors found to be significantly associated with community-acquired MRSA included African-American race, female sex, and hospitalization within the past twelve months. Inadequate initial antibiotic therapy was statistically significantly more common among those with community-acquired MRSA (65%) than among those with methicillin-susceptible Staphylococcus aureus skin and soft-tissue infection (1%). An important limitation of the study lay in the non-availability of some MRSA isolates for molecular typing, leading to the use of antimicrobial susceptibility testing as a parameter for their epidemiological classification. Treatment Strategies: Pharmacologic measures In a retrospective cohort study at two tertiary medical centers involving 492 adult patients with 531 independent episodes of community-acquired MSRA (Ruhe et al., 2007), the impact of active antimicrobial treatment and other potential risk factors on the outcome for patients with uncomplicated community acquired MRSA skin and soft tissue infections was examined, using treatment failure as the primary outcome of interest. The results showed that treatment failure occurred in 45 (8%) of 531 episodes of community-onset MRSA skin and soft tissue infections. Therapy was successful for 296 (95%) of 312 patients who received an active antibiotic, compared with 190 (87%) of 219 of those who did not (P=.001 in bivariate analysis). In contrast, the use of an inactive antimicrobial agent was an independent predictor of treatment failure. The study’s conclusions weighed in on the benefit of empirical treatment of patients with skin infections likely due to MRSA using antimicrobial agents with activity against the organism. A randomized open-label study compared oral linezolid and intravenous vancomycin for management of complicated skin and soft-tissue infections caused by MRSA (Sharpe et al., 2005). Linezolid was associated with greater rates of clinical cure and improvement, a 3-day shorter median length of stay, and reduced outpatient charges, all at acceptable significance levels. Vancomycin therapy was associated with more treatment failures and subsequent lower-extremity amputations (P=.011). Additionally, linezolid was associated with reduced length of stay and outpatient charges. However, the results of the study may not necessarily apply to MRSA infections that do not involve the lower extremities. In a randomized pharmacoeconomic study of linezolid versus vancomycin (McKinnon et al., 2006), 717 patients were enrolled in a multinational, open-label, clinical trial of skin and soft tissue infections caused by suspected or proven methicillin-resistant Staphylococcus aureus. It was found that linezolid therapy was associated with improved clinical outcomes and significantly lower treatment costs than was vancomycin. The largest cost advantage was demonstrated in patients with documented MRSA infections. In a valuable prospective cohort study of 201 patients discharged after hospitalization for both community-acquired methicillin-resistant as well as methicillin-sensitive Staphylococcus aureus infections, outcomes based on clinical response and re-infection were studied (Miller et al., 2007). Contrary to the widespread belief that patients with CA-MRSA skin infection may have more serious outcomes than those with CA-MSSA skin infection, the study found similar outcomes in these two groups after hospital discharge. Clinical nonresponse at day 30 was associated with a lack of receipt of incision and drainage. The data also suggested that close contacts of persons with CA-MRSA skin infection may have a higher likelihood of acquiring an infection. A retrospective analysis of clinical presentation and treatment 2004 outbreak in Los Angeles (Iyer & Jones, 2004) concluded that the first line treatment is incision and drainage in combination with linezolid, vancomycin, or combination trimethoprim/sulfamethoxazole and rifampin. Another study conducted simultaneously in two pediatric emergency departments in the southeastern United States and southern California showed that all community-associated MRSA isolates tested were sensitive to vancomycin, trimethoprim-sulfamethoxazole, rifampin, and gentamicin (Hasty et al., 2007). One isolate at each center was resistant to clindamycin. The sensitivities at both institutions were similar despite their geographical distance, suggesting that optimal diagnostic and management strategies for CA-MRSA will likely be widely applicable if results from a larger, more collaborative study yield similar findings. Linezolid also inhibits toxin production, which may prove to be of significant benefit since the gene encoding for the production of Panton–Valentine leukocidin toxin (which promotes inflammation and tissue necrosis) is almost always found in community-acquired MRSA strains (de Almeida & Bush, 2006). Although the empirical use of trimethoprim–sulfamethoxazole, minocycline, doxycycline, and clindamycin is often recommended, few published clinical data are available to substantiate their use, and most data precede the recent emergence of MRSA as a common pathogen in community-acquired skin and soft-tissue infections. It has also been noted that the lipopeptide daptomycin and the tetracycline tigecycline are additional treatment options, although they are hampered by their parenteral-only route of administration; in addition, few patients with MRSA infection were enrolled in trials that studied these drugs (de Almeida & Bush, 2006). It was suggested that linezolid should be considered as one of the antimicrobial agents of choice for empirical treatment of skin and soft-tissue infections in areas with a high prevalence of community-acquired MRSA, especially with its 100% oral bioavailability, which potentially eliminates the need for hospital admission in many cases. Barnes and co-workers reported on the successful utilization of alternative oral antibiotic therapy to patients with community-acquired MRSA soft tissue infections, using both retrospective and concurrent review methodologies (Barnes, Dooley, Hepburn, & Baum, 2006). The following antibiotics were successful in effecting remission: clindamycin, trimethoprim/sulfamethoxazole, doxycycline/minocycline, fluoroquinolones, and a beta-lactam antibiotic (with abscess drainage). They concluded that community-acquired MRSA skin and soft tissue infections can be successfully treated with orally administered antibiotics to which the organism has demonstrable in vitro susceptibility. In Frazee’s study discussed earlier on, the antimicrobial susceptibility among MRSA isolates was reported to be trimethoprim/sulfamethoxazole 100%, clindamycin 94%, tetracycline 86%, and levofloxacin 57% (Frazee et al., 2005). Johnson argued for the merits of the tetracyclines, of which minocycline is the most potent against staphylococci and with which there is the most clinical experience in treating MRSA infections (Johnson, 2006). Tetracyclines are highly orally bioavailable, inexpensive, and well tolerated, and remain active against nearly 100% of S. aureus isolates (whether methicillin-resistant or methicillin-susceptible) in many U.S. locales. These agents represent an economical option that avoids certain problems associated with clindamycin and trimethoprim–sulfamethoxazole. He advocated that these agents deserve more attention in commentaries and should be studied in clinical trials to establish their comparative efficacy for treatment of MRSA infections. A recent report described the successful use of doxycycline in treating patients with community-associated MRSA skin infections that have earlier failed treatment or experienced infection recurrence with other antimicrobial agents (Carter, Ebers, Younes, & Lacy, 2006). The results were all the more promising as no doxycycline adverse effects were noted in the patients’ medical records and no patient discontinued therapy before resolution of infection. The potential merits of using cephalosporins were advocated in a recent review (Hedrick, 2006). Cephalosporins are an effective broad-spectrum empirical treatment for uncomplicated skin and soft tissue infections, with considerable activity against methicillin-susceptible S. aureus. In addition, the use of antimicrobial agents in infective strains that may be resistant does not appear to be associated with adverse patient-reported outcomes, suggesting that cephalosporins may still be effective in treating community-acquired MRSA-associated skin infections. Treatment Strategies: Non-Pharmacologic Measures From the results of a recent study (Fleming, Brown, & Tice, 2006), it was recommended that clinicians have an awareness of high-risk patients, perform routine culturing of soft tissue infections, and prescribe antibiotics based on culture and sensitivities. Awareness, prevention, early diagnosis, and implementation of effective antibiotic management by nurse practitioners were also advocated to help limit an epidemic of community-acquired MRSA. It has been recommended that in order to prevent MRSA infections from spreading in health-care settings, health-care providers should use standard precautions and appropriate hand hygiene between treating patients, clean surfaces of examination rooms with commercial disinfectant or diluted bleach (1 tablespoon bleach in 1 quart water), and carefully dispose of dressings and other materials that come into contact with pus, nasal discharge, blood, and urine (Centers for Disease Control and Prevention, 2003). In a controversial study, a team at the University of Texas Southwestern Medical Center reported on the management and outcome of children with skin and soft tissue abscesses caused by community-acquired MRSA (M. C. Lee et al., 2004). A total of sixty-nine children presenting to for management of skin and soft tissue abscesses caused by culture-proved CA-MRSA were prospectively followed and retrospective chart review was performed 2-6 months after the initial visit. From their results, they concluded that incision and drainage without adjunctive antibiotic therapy was effective management of community-acquired MRSA skin and soft tissue abscesses with an initial diameter of less than 5 cm in immunocompetent children. In a rejoinder to the Lee publication, Miller and Spellberg challenged the notion that withholding antibiotics in community acquired MRSA skin and soft-tissue infections is beneficial. They pointed out that that the study was limited by a small sample size, which biased the significance of the treatment failures recorded, and that there was not enough investigation of uncommon but very serious outcomes with the treatment failures. They drew from their own experience to buttress the latter point. They concluded that nothing short of large, randomized, prospective studies will be required to definitively clarify whether short antibiotic courses or no antibiotics in conjunction with surgical drainage results in different outcomes of patients with skin/soft tissue infections caused by S. aureus. DISCUSSION Prevalence Although health care-associated MRSA infections have been known for many years, an emerging problem is that of MRSA infections that originate outside the hospital setting. Since the first report of community-associated MRSA in 1982 (Centers for Disease Control and Prevention, 2001), onward march of the pathogen has been steady. Outbreaks of community-associated MRSA skin infections have occurred in sports facilities, child care centers, correctional facilities, military barracks, and hospital emergency departments. Outbreaks have been reported at several locations in the United States, as well as in countries in Europe and Asia. Risk factors have been found to include routine exposure to hospital facilities, high-risk sexual conduct, and drug use. It has been identified as a growing problem for health care management because of its virulence and propensity for developing into life-threatening infections. It is also a challenge in the sense that treatment strategies have not been fine-tuned in the medical community, as collection of evidence in clinical trials is still ongoing. Treatment Strategies It is important that an early accurate diagnosis be made, considering the commonality of occurrences in which community-associated MRSA skin infections have been misdiagnosed as spider bites or some other kind of skin/soft tissue infection. This may be facilitated by paying attention to the following hints: history of contact with a prison facility or sports facility, previous treatment of the patient or a close contact for a spider bite, recurrent impetigo- or furunculosis-like skin diseases (Rybak & LaPlante, 2005). Current consensus in the literature is that the first step in treatment is incision and drainage of abscesses, if any, followed by microbial culture and antibiotic sensitivity tests. If the patient has a recurrent infection, nasal swabs for determining carrier status are recommended. Intranasal mupirocin is recommended for patients testing positive for carrier status (Rybak & LaPlante, 2005). Patients should be instructed on techniques for limiting the spread of the infection by avoiding contact with personal items and shared objects. Similarly, the spread can be controlled in health care settings by having practitioner implement appropriate infection control measures. There are limited trials to demonstrate unequivocally the efficacy of therapeutic agents used in management of community-associated MRSA. However, current drugs being used include the tetracyclines (especially minocycline and doxycycline), clindamycin, the fluoroquinolones, and trimethoprim/sulfamethoxazole alone or in combination with rifampicin. Clindamycin has been reported to be susceptible to inducible resistance. This can be pre-determined by the disk diffusion method (D-test), and current recommendations advise that this test must be carried out on the isolate if clindamycin is to be used. The fluoroquinolones are associated with development of resistance, and caution is advised in their utilization. Expectedly, the cephalosporins are not a popular choice, although some limited studies indicate their potential utility. For severe infections, the mainstay of treatment has been vancomycin, but recent studies show the development of glycopeptide resistance, as well as the efficacy of new alternatives. One such is linezolid. Linezolid is orally active and has good target penetration. Other alternatives are the streptogramin combination drug quinupristin-dalfopristin and the lipopeptide daptomycin, which has been found useful in the treatment of multidrug-resistant strains. It is important to note that more research is needed to definitively recommend therapeutic choices for community-acquired MRSA treatment because the number of randomized clinical trials done so far is limited, the patient groups investigated have been relatively small and limited in scope, and there is not much done to map the toxin-producing variants of the pathogen with current antibiotics available. CONCLUSION Community-associated MRSA skin infections are a recent and advancing menace in the society. The prevalence cuts across a wide variety of institutional settings, including hospital emergency departments, child care centers, sports facilities, military locations and prisons. The pathogen, while sharing a common origin with the health care-associated MRSA, has unique virulence and molecular properties which make it constitute a different kind of challenge. Treatment strategies used comprise proper wound management including incision and drainage, microbial culture and sensitivity tests, and aggressive treatment with appropriate antibiotics. The evidence in favor of using particular drugs still requires further wide-ranging clinical trials in order to arrive at streamlined therapeutic guidelines. Implementation of measures for controlling the spread of infection through contact is also a crucial element of the management strategy. REFERENCES Aramburu, C., Harbarth, S., Liassine, N., Girard, M., Gervaix, A., Scherenzel, J., et al. (2006). Community-acquired methicillin-resistant Staphylococcus aureus in Switzerland: first surveillance report. Euro Surveillance: Bulletin Europeen sur les Maladies Transmissibles = European Communicable Disease Bulletin, 11(1), 42-43. Barnes, E. V., 2nd, Dooley, D. P., Hepburn, M. J., & Baum, S. E. (2006). Outcomes of community-acquired, methicillin-resistant Staphylococcus aureus, soft tissue infections treated with antibiotics other than vancomycin. Military Medicine, 171(6), 504-507. Carter, M. K., Ebers, V. A., Younes, B. K., & Lacy, M. K. (2006). Doxycycline for Community-Associated Methicillin-Resistant Staphylococcus aureus Skin and Soft-Tissue Infections. Annals of Pharmacotherapy, 40(9), 1693-1695. Centers for Disease Control and Prevention. (2001). Methicillin-resistant Staphylococcus aureus skin or soft tissue infections in a state prison-Mississippi, 2000. MMWR - Morbidity & Mortality Weekly Report, 50, 919-922. Centers for Disease Control and Prevention. (2003). Outbreaks of community-associated methicillin-resistant Staphylococcus aureus skin infections--Los Angeles County, California, 2002-2003. MMWR - Morbidity & Mortality Weekly Report, 52(5), 88. Cloran, F. J. (2006). Cutaneous infections with community-acquired MRSA in aviators. Aviation Space & Environmental Medicine, 77(12), 1271-1274. de Almeida, K. N. F., & Bush, L. M. (2006). Treatment of community-acquired methicillin-resistant Staphylococcus aureus infection.[comment]. Annals of Internal Medicine, 145(3), 231-232; author reply 232-233. Fleming, S. W., Brown, L. H., & Tice, S. E. (2006). Community-acquired methicillin-resistant Staphylococcus aureus skin infections: report of a local outbreak and implications for emergency department care. Journal of the American Academy of Nurse Practitioners, 18(6), 297-300. Frazee, B. W., Lynn, J., Charlebois, E. D., Lambert, L., Lowery, D., Perdreau-Remington, F., et al. (2005). High prevalence of methicillin-resistant Staphylococcus aureus in emergency department skin and soft tissue infections.[see comment]. Annals of Emergency Medicine, 45(3), 311-320. Hasty, M. B., Klasner, A., Kness, S., Denmark, T. K., Ellis, D., Herman, M. I., et al. (2007). Cutaneous community-associated methicillin-resistant staphylococcus aureus among all skin and soft-tissue infections in two geographically distant pediatric emergency departments. Academic Emergency Medicine, 14(1), 35-40. Hedrick, J. (2006). Cephalosporins for uncomplicated skin and skin structure infections in emerging community-acquired MRSA. Expert Opinion on Pharmacotherapy, 7(15), 2019-2024. Iyer, S., & Jones, D. H. (2004). Community-acquired methicillin-resistant Staphylococcus aureus skin infection: a retrospective analysis of clinical presentation and treatment of a local outbreak.[see comment]. Journal of the American Academy of Dermatology, 50(6), 854-858. Johnson, J. R. (2006). Treatment of community-acquired methicillin-resistant Staphylococcus aureus infection.[comment]. Annals of Internal Medicine, 145(3), 232; author reply 232-233. Johnston, C. P., Cooper, L., Ruby, W., Carroll, K. C., Cosgrove, S. E., Perl, T. M., et al. (2006). Epidemiology of community-acquired methicillin-resistant Staphylococcus aureus skin infections among healthcare workers in an outpatient clinic. Infection Control & Hospital Epidemiology, 27(10), 1133-1136. Kazakova, S. V., Hageman, J. C., Matava, M., Srinivasan, A., Phelan, L., Garfinkel, B., et al. (2005). A clone of methicillin-resistant Staphylococcus aureus among professional football players. New England Journal of Medicine, 352(5), 468-475. King, M. D., Humphrey, B. J., Wang, Y. F., Kourbatova, E. V., Ray, S. M., Blumberg, H. M., et al. (2006). Emergence of community-acquired methicillin-resistant Staphylococcus aureus USA 300 clone as the predominant cause of skin and soft-tissue infections.[see comment][summary for patients in Ann Intern Med. 2006 Mar 7;144(5):I11; PMID: 16520467]. Annals of Internal Medicine, 144(5), 309-317. Lee, M. C., Rios, A. M., Aten, M. F., Mejias, A., Cavuoti, D., McCracken, G. H., Jr., et al. (2004). Management and outcome of children with skin and soft tissue abscesses caused by community-acquired methicillin-resistant Staphylococcus aureus.[see comment]. Pediatric Infectious Disease Journal, 23(2), 123-127. Lee, N. E., Taylor, M. M., Bancroft, E., Ruane, P. J., Morgan, M., McCoy, L., et al. (2005). Risk factors for community-associated methicillin-resistant Staphylococcus aureus skin infections among HIV-positive men who have sex with men.[erratum appears in Clin Infect Dis. 2005 Jul 1;41(1):135]. Clinical Infectious Diseases, 40(10), 1529-1534. Lu, D., & Holtom, P. (2005). Community-acquired methicillin-resistant Staphylococcus aureus, a new player in sports medicine. Current Sports Medicine Reports, 4(5), 265-270. McKinnon, P. S., Sorensen, S. V., Liu, L. Z., Itani, K. M., McKinnon, P. S., Sorensen, S. V., et al. (2006). Impact of linezolid on economic outcomes and determinants of cost in a clinical trial evaluating patients with MRSA complicated skin and soft-tissue infections. Annals of Pharmacotherapy, 40(6), 1017-1023. Miller, L. G., Quan, C., Shay, A., Mostafaie, K., Bharadwa, K., Tan, N., et al. (2007). A prospective investigation of outcomes after hospital discharge for endemic, community-acquired methicillin-resistant and -susceptible Staphylococcus aureus skin infection. Clinical Infectious Diseases, 44(4), 483-492. Moran, G. J., Amii, R. N., Abrahamian, F. M., Talan, D. A., Moran, G. J., Amii, R. N., et al. (2005). Methicillin-resistant Staphylococcus aureus in community-acquired skin infections.[see comment]. Emerging Infectious Diseases, 11(6), 928-930. Pagac, B. B., Reiland, R. W., Bolesh, D. T., Swanson, D. L., Pagac, B. B., Reiland, R. W., et al. (2006). Skin lesions in barracks: consider community-acquired methicillin-resistant Staphylococcus aureus infection instead of spider bites. Military Medicine, 171(9), 830-832. Roesch, A., Linde, H. J., Landthaler, M., Vogt, T., Roesch, A., Linde, H.-J., et al. (2005). Elimination of a community-acquired methicillin-resistant Staphylococcus aureus infection in a nurse with atopic dermatitis. Archives of Dermatology, 141(12), 1520-1522. Ruhe, J. J., Smith, N., Bradsher, R. W., Menon, A., Ruhe, J. J., Smith, N., et al. (2007). Community-onset methicillin-resistant Staphylococcus aureus skin and soft-tissue infections: impact of antimicrobial therapy on outcome.[see comment]. Clinical Infectious Diseases, 44(6), 777-784. Rybak, M. J., & LaPlante, K. L. (2005). Community-Associated Methicillin-Resistant Staphylococcus aureus: A Review. Pharmacotherapy, 25(1), 74-85. Saben, B. (2004). Community-acquired methicillin-resistant Staphylococcus aureus skin infection in a football player. Current Sports Medicine Reports, 3(5), 269-271. Sharpe, J. N., Shively, E. H., Polk, H. C., Jr., Sharpe, J. N., Shively, E. H., & Polk, H. C., Jr. (2005). Clinical and economic outcomes of oral linezolid versus intravenous vancomycin in the treatment of MRSA-complicated, lower-extremity skin and soft-tissue infections caused by methicillin-resistant Staphylococcus aureus. American Journal of Surgery, 189(4), 425-428. Stemper, M. E., Brady, J. M., Qutaishat, S. S., Borlaug, G., Reed, J., Reed, K. D., et al. (2006). Shift in Staphylococcus aureus clone linked to an infected tattoo. Emerging Infectious Diseases, 12(9), 1444-1446. Zinderman, C. E., Conner, B., Malakooti, M. A., LaMar, J. E., Armstrong, A., Bohnker, B. K., et al. (2004). Community-acquired methicillin-resistant Staphylococcus aureus among military recruits. 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MRSA-Caused Mortality Levels

Introduction Staphylococcus aureus and Methicillin-resistant Staphylococcus aureus (MRSA) colonization, results in severe infections in humans.... The article considered evidence based research to highlight allocated resources to deal with MRSA and emphasize on the decision of policy makers to adopt control measures, but the article does not state the control measures to be adopted in different hospital settings to check spread of nosocomial spread of mrsa.... The screening method that is suggested by Hardy et al, (2007) directly implicate the molecular methods for detection of mrsa such as multiplexed PCR primers to detect the presence of gene (mecA)....
3 Pages (750 words) Research Paper

Opportunistic Microbial Infections

They then become virulent when the general immune resistance of the organism drops.... They then become virulent when the general immune resistance of the organism drops.... They then become virulent when the general immune resistance of the organism drops.... Some types of opportunistic infections are contagious and they spear easily in the human population.... Microbacterium avium complex- this is a bacterial infection that causes fevers that are recurring, digestion problems and general sickness accompanied by the loss of weight....
3 Pages (750 words) Essay

Prevention of Infection in Home Health Care

For instance, studies on home care have typically indicated that the most common types of infections are concentric upon urinary tract infections, followed by an array of different types of skin infections, with staphylococcus aureus, and enterococcus rounding out the least... For this very reason, the prevalence of disease and the severity with which it affects patients within the given context is almost invariably higher than a similarly community of patients within a traditional medical facility....
5 Pages (1250 words) Essay

Central line associated bloodstream infections

The rates of central line-associated bloodstream infections in the ICUs of United States have been observed to decline dramatically in a few years as reported to the National Healthcare Safety Network (NHSN).... A meta-analysis conducted recently affirms the exercise of CHG, or chlorhexidine gluconate bathing, within the population of ICU in order to prevent CLABSI (Miller & Maragakis, 2012).... Central Line Associated Bloodstream infections [Institution Name] Central Line Associated Bloodstream infections Central line-associated bloodstream infections (CLABSIs) cause thousands of deaths annually and billions dollars of costs to the United States healthcare system, although these infections can be prevented....
3 Pages (750 words) Research Paper

Infection and Immunity

threadworms or pinworms, commonly comprise weight loss, skin infections, vomiting, appetite loss and intense itching among others (NHS, n.... hellip; Various environmental changes that are largely linked with population intensification, development in water resources and population movements, has day after day contributed towards the increasing rate of parasitic burden in the current environmental setting.... Additionally, with the increasing mortality rates and the simultaneous growth in the ageing population rate, the healthcare sector of the UK has been witnessing significant pressure (Nature Cures, 2010)....
3 Pages (750 words) Essay

Chlamydia Trachomatis in a Woman of Childbearing Age

Chlamydia Trachomatis causes this disease and has an estimated prevalence of 4 million infections annually.... Chlamydia Trachomatis causes this disease and has an estimated prevalence of 4 million infections annually.... Treponema Pallidum and Neisseria Gonorrhoeae are both infections caused by a bacterium.... Both infections may be passed from mother to baby.... Both infections make the sufferer more susceptible to acquire HIV and if not treated, both may lead to death....
3 Pages (750 words) Essay

MRSA and the risks associated with AIDS patients

Methicillin-resistant Staphylococcus aureus (MRSA) has come out as a common cause of infections in community and hospital settings (Hidron, 2005).... Studies carried out in past also revealed distinct risk factor patterns for MRSA infections in patients with HIV including low CD4 cell count, high HIV-RNA viral load, and absence of cotrimoxazole prophylaxis (Tumbarello , 2002, Mathews, 2005).... Most studies of mrsa infection in HIV-infected patients have primarily evaluated skin and soft tissue infections with only a small number of bloodstream infections (Nguyen, 1999, Mathews, 2005)....
5 Pages (1250 words) Research Paper

Staphylococcus

The strain was seen to cause infections in children who were not at risk.... Surveillance studies from 1990s indicated an increase in the incidence of mrsa infections.... Studies indicate that the organism is present in the nasal colonization of the adult population.... The organism causes nosocomial or hospital acquired infections.... This trait makes it hard to treat these infections....
5 Pages (1250 words) Research Paper
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