• It's Not a Spider Bite, It's Community-Acquired Methicillin-Resista

    From marijuni71@aol.com@21:1/5 to georgia on Tue Dec 22 19:34:32 2015
    On Wednesday, August 4, 2004 at 10:14:30 PM UTC-4, georgia wrote:
    It's Not a Spider Bite, It's Community-Acquired Methicillin-Resistant Staphylococcus Aureus


    Tamara J. Dominguez, MD
    J Am Board Fam Pract 17(3):220-226, 2004. (c) 2004 American Board of Family Practice

    Posted 07/23/2004


    Skin and soft tissue infections caused by hospital-acquired methicillin-resistant Staphylococcus aureus, or HA-MRSA, have been a problem in
    hospital and
    nursing home settings for several years.[1] In recent years, infections caused
    by a new isolate termed community-acquired MRSA (CA-MRSA) have been increasing
    in incidence,[2-4] and outbreaks of CA-MRSA have been identified in other settings, including athletic teams and prisons.[5-7] Community-acquired MRSA differs from HA-MRSA in that CA-MRSA is not multidrug-resistant and can usually
    be
    treated with clindamycin, trimethoprim/ sulfamethoxazole, or linezolid.[8,9] Both organisms carry the staphylococcal cassette chromosome mecA (SCCmecA) gene

    that encodes resistance to the ß-lactams[10,11]--the class of antibiotics most
    commonly used in treating skin and soft tissue infections. At this time, it is not known whether CAMRSA is the result of HA-MRSA that escaped the hospital
    setting and mutated to its present form or is community-generated in origin.[12] Several studies are currently being conducted in molecular genetics
    to
    identify the source of CA-MRSA and effectively treat it.[13] This article presents
    a case review of several CA-MRSA infections identified in a community clinic setting, identifies clues that might lead the clinician to suspect a CA-MRSA infection, recommends questions to consider in making this diagnosis, and discusses options for treatment. It may be that contact with prisons or prisoners
    needs to be placed on the list of known risk factors associated with CA-MRSA.

    Case Review
    From July 2002 to September 2003, 10 patients were identified as having CA-MRSA skin and soft tissue infections at an indigent health care clinic in San
    Antonio, Texas. These infections were classified as community-acquired MRSA based on several factors: (1) none of the patients had risk factors for nosocomially acquired MRSA (ie, recent hospitalization or surgery[1]) or those
    risk
    factors previously associated with acquisition of MRSA outside a short-term care

    setting: residence in a long-term care facility, current intravenous drug abuse, or underlying illnesses such as cardiovascular or pulmonary disease, diabetes mellitus, malignancy, or chronic skin disease such as eczema,[14] and
    (2)
    antimicrobial resistance patterns were consistent with CA-MRSA--ie, they showed
    susceptibility to several classes of antimicrobial agents other than ß-lactams.

    Patients were identified through a positive wound culture using an aerobic/anaerobic Culturette. Many had been diagnosed and treated for other causes of
    their infection, including spider bites, impetigo, and varicella zoster. Four of
    the patients had been incarcerated and reported they had been treated for recurring skin infections several times while in prison. One of these 4 patients
    had a positive nasal culture for CA-MRSA. The other 6 patients had contact with either a prison facility or someone recently released from prison. One patient also played on his high school football team. Several patients were treated
    by other providers for what were thought to be spider bites. All CA-MRSA infections treated at the community clinic responded well to clindamycin, mupirocin, and drainage of the abscess, if present. The sensitivity pattern was

    similar in the positive MRSA cultures in that all were sensitive to clindamycin,
    rifampin, trimethoprim/sulfamethoxazole, and vancomycin (Table 1). All the isolates were resistant to amoxicillin/clavulanic acid, cefazolin, erythromycin,
    oxacillin, and penicillin. A brief detail of the patients' histories is outlined
    below (Table 2):

    Case A
    A 10-year-old girl was brought to the clinic by her mother for a lesion to her left lower extremity that the family thought was caused by a spider bite.
    She had been treated for impetigo at her pediatrician's office 2 weeks before,
    but her condition did not improve after treatment with amoxicillin/clavulanic
    acid. The patient was then seen at this community clinic, and her wound culture

    was positive for CAMRSA. Both the patient and her mother had recently visited
    the patient's father in prison. Her mother had been treated 2 weeks earlier for a similar infection and was told by the emergency department physician that

    her infection was the result of a spider bite. The patient's infection cleared after treatment with oral clindamycin and topical mupirocin applied to
    the
    wound.

    Case B
    A 24-year-old man presented to the clinic with a 4-day history of painful raised pustules to his left hip that the patient attributed to spider bites. A
    culture of these lesions proved positive for CAMRSA. The lesions cleared after
    treatment with oral clindamycin and topical mupirocin. His girlfriend had been
    treated at our clinic for a similar infection 4 months earlier but a culture was not done at that time. His girlfriend's sister had been hospitalized for an

    abscess on her abdomen caused by a "spider bite" during that same period. His
    girlfriend's other roommate was released from prison and had moved in with the patient's girlfriend and her sister 2 weeks before their infections began.

    Case C
    A 43-year-old man recently released from prison was treated at the clinic for
    multiple pustules over his legs, arms, and inguinal area. An aerobic/anaerobic wound culture was taken and was positive for CA-MRSA. This patient had been
    treated several times while in prison for similar lesions and was told they were the result of spider bites. His last intravenous drug use was 4 years before. This infection resolved after treatment with oral clindamycin and topical
    mupirocin.

    Case D
    A 25-year-old woman was first treated in the emergency department for varicella zoster then at the clinic for impetigo that did not respond to amoxicillin/clavulanic acid or gatifloxacin. The patient developed an abscess on her right
    gluteal area with a central eschar. An aerobic/anaerobic culture was positive
    for CA-MRSA. The patient's boyfriend had recently been released from prison. The patient responded well to drainage of the abscess and was treated with oral clindamycin and topical mupirocin.

    Case E
    Case D's 45-year-old mother presented at the clinic 1 week after her daughter's treatment for a left gluteal abscess. The wound culture proved positive for
    CA-MRSA. This infection cleared with incision and drainage of the abscess and
    antimicrobial treatment with clindamycin and mupirocin.

    Case F
    A 41-year-old man recently released from prison presented to the clinic with a history of recurring skin infections thought to be impetigo. He had been treated several times while in prison for similar lesions. The wound culture and
    nasal swab done at clinic were positive for CA-MRSA. The patient's lesions cleared after treatment with oral clindamycin. Mupirocin was applied intranasally
    and topically to his wounds.

    Case G
    A 50-year-old man presented to the clinic with multiple furuncles on his legs
    and arms. He had been recently released from prison and had a history of recurring "staph" infections while in prison. This patient failed treatment with
    ciprofloxacin for what was thought to be impetigo. His wound culture done at clinic was positive for CA-MRSA. The lesions resolved after treatment with clindamycin and mupirocin.

    Case H
    A 36-year-old woman was treated at the clinic for multiple furuncles to the left knee, nape of the neck, and scalp. This patient also had an abscess on her

    left gluteus that was incised and drained. Wound cultures done on all areas proved positive for CA-MRSA. The patient had been visiting her pregnant daughter in prison for several weeks before her outbreak. This infection cleared
    after drainage of her abscess and treatment with clindamycin and mupirocin.

    Case I
    A 16-year-old boy presented to the clinic with a 4-day history of a "boil" to
    his right axilla. The patient stated he had a similar infection on his neck a
    year before and was told it was from a "spider bite" when he sought medical attention. Cultures taken from his axilla grew CA-MRSA and a Gram stain showed
    many Gram-positive cocci. It is notable that the patient's father had been recently released from prison and returned home 1 week before the patient's most
    recent infection. The father reported being treated twice while incarcerated for similar lesions. The patient participated in high school football and was
    not aware that anyone else on the team had experienced a similar infection.

    Case J
    A 42-year-old man presented to the clinic with a 3-day history of a "spider bite" to his left inguinal area. (Figures 1-3). He had been treated several times over an 8-year period for similar lesions and was told each time it was the
    result of a spider bite. His first episode occurred when he was incarcerated in the county jail. The patient stated that his sister and niece were both treated for similar "spider bites." The patient's wound culture was positive for
    MRSA and responded well to treatment with clindamycin.




    Figure 1. CA-MRSA lesion of patient J. Location: left groin.


    Figure 2. Lesion of patient J.


    Figure 3. CA-MRSA lesion of patient J. Location: left groin.


    Discussion
    These cases demonstrate the ease with which patients and clinicians can confuse CA-MRSA infections with other soft tissue infections. The diagnosis of
    spider bites has been noted in other investigations of CA-MRSA outbreaks.[5] It
    is
    not known why CA-MRSA infections are commonly misdiagnosed as spider bites. In several of the above cases, a spider bite was a common diagnosis for those
    CA-MRSA infections that presented as solitary lesions. One of the patients at
    the clinic (case D) developed an abscess with a central eschar, similar in appearance to the bite of a brown recluse spider (Loxosceles reclusa). Both the

    patient and her physician (the author) had at first attributed her infection to

    a brown recluse spider bite, based solely on the appearance of her lesion. This was not the first time this misdiagnosis has been made as other skin lesions
    have been wrongly attributed to the brown recluse spider in other disease processes such as Lyme disease,[15] at times in areas outside the endemic range

    of the brown recluse.[16] It was not until the patient's wound culture showed
    CAMRSA that the correct diagnosis was made.

    During the interviewing process several other points were noted. First, those
    patients who were incarcerated (cases C, F, G, J) and former prisoners who had contact with the case study patients (cases A, B, D, E, H, I) had been incarcerated at different correctional facilities. This leads us to question the
    prevalence of CA-MRSA infections in prisons. Skin and soft tissue infections have been recognized problems in correctional facilities[6]; until recently, however, CA-MRSA outbreaks have been reported in only 2 prisons-- one in Los Angeles County, California,[5] and the other in Mississippi.[6] Second, all patients
    who had been incarcerated reported that their first outbreak of skin infections started after being sent to prison. Finally, some patients at the clinic
    reported or were noted to have large, firm pustules with a central hard white
    core, similar to furunculosis. Several patients stated that self-removal of this
    core resulted in clearing of their infection.

    Obtaining the proper diagnosis of a CA-MRSA infection is important because misdiagnosis and delay of proper treatment can have serious consequences for both the patient and the medical community. An improperly treated CA-MRSA infection results in increased medical costs for the patient and community resulting
    from multiple office and emergency department visits and possibility of hospitalization. In addition, the risk of transferring the infection increases
    as
    the number of contacts, especially familial, increases. Commu-nity-acquired MRSA
    infections with secondary familial transmission have been described in other reports.[17] Although skin and soft tissues is the most common reported site of infection, CA-MRSA has been noted in invasive diseases such as bacteremia,
    endocarditis, osteomyelitis, and pneumonia.[5,9] In 1999, 4 pediatric deaths in

    Minnesota and North Dakota were attributed to CA-MRSA.[18] None of the 4 children had established risk factors for MRSA infection (ie, prolonged hospitalization, invasive or surgical procedures, indwelling catheters, endotracheal
    tubes, and prolonged or recurrent exposure to antibiotics).[2] All 4 pediatric
    cases described above were initially treated with a cephalosporin antibiotic to

    which the organism was resistant. The delayed use of the correct antibiotic may have contributed to their deaths. At this time, it is unclear how common CA-MRSA infections occur within the adult or pediatric community, although they

    are being reported in increasing numbers.[3] The CDC is currently conducting surveillance for CA-MRSA in selected regions of the country to determine the incidence and risk factors for MRSA in the community.[4] In this case review, 2

    patients were of pediatric age (cases A and I), and neither had any of the known risk factors associated with MRSA infections. Both patients had prior contact with a prisoner, prison facility, or athletic facility.

    Antimicrobial sensitivity patterns are helpful when treating CA-MRSA infections because they can help the clinician choose the correct antibiotic. In the
    cases described above, 3 (30%) showed resistance or intermediate resistance to
    the macrolides, whereas 6 (60%) were sensitive (one was not recorded by the laboratory). The clinician needs to know that treatment of some clindamycin-susceptible CA-MRSA strains carrying the erm (erythromycin ribosome
    methylase)
    gene can be induced to become clindamycin-resistant during clindamycin treatment.[15] The possibility for clindamycin resistance developing in a clindamycin-susceptible, erythromycin-resistant organism can be checked by the
    D test. This
    laboratory test is done by a double-disk diffusion method in which the clindamycin zone becomes "D" shaped when a nearby erythromycin disk is used to
    induce
    the erm gene effect. In the United States, the prevalence of this inducible clindamycin-resistant strain seems to vary by geographic location. In Chicago
    and Minnesota, 94% and 84% of CA-MRSA isolates, respectively, tested positive
    for inducible clindamycin resistance by the D test. In Houston, only 8% of all
    CA-MRSA isolates had a positive D test and thus were less likely to become clindamycin resistant.[9]

    What then would lead the clinician to suspect a CA-MRSA infection? In this case review, several factors seemed common. First, the propensity for this infection to be misdiagnosed as either a spider bite or some type of skin or soft
    tissue infection (impetigo or furunculosis) based on appearance; second, the connection of CA-MRSA infections to correctional facilities--whether as a prisoner, a visitor, or someone having close contact with a former prisoner; third,
    the link to sports facilities; and fourth, the recurring nature of the infection. Thus, some clues to consider when dealing with a possible CA-MRSA skin or
    soft tissue infection are summarized below:

    Has the patient had any form of contact with a prisoner or prison facility?

    Has the patient or a close contact been treated for a "spider bite?"

    Has the patient experienced recurring skin infections such as "impetigo" or "furunculosis?"

    Does the patient play contact sports or have some other form of contact with a sports facility?


    If a CA-MRSA infection is suspected, any abscess should be incised and drained and a microbiologic culture of wounds performed to determine appropriate
    antimicrobial agents.[5] Swab specimens of the anterior nares could be obtained

    to check for carrier status[6] if a patient has a history of recurring infection
    s. If the patient is found to be a carrier of CA-MRSA, intranasal mupirocin may be considered, although the use of intranasal mupirocin is not advocated for use with every CA-MRSA infection because of the concern for future resistance.[19] If a dermonecrotic lesion is identified, it is important to think not
    only of CA-MRSA but other infections as well-- cutaneous anthrax, Lyme disease,
    cancerous lesions, and necrotizing fasciitis. A diagnosis of a brown recluse spider bite should be made after careful consideration is given to other possible diagnoses, especially if the patient is not within the region endemic
    to
    the brown recluse (southeastern Nebraska through Texas, east to Georgia and southernmost Ohio).[16]

    Because transmission of CA-MRSA is primarily a problem with hygiene, it is important to instruct the patient and family on methods to prevent its spread.
    Patients should keep cuts and abrasions clean by washing with soap and water and to limit contact with common objects (eg, athletic equipment, towels, benches) and personal items (linen, pillows, clothing).[5] Health care providers
    should use standard precautions to prevent transmission of MRSA infections in
    health care settings.[20]




    Conclusion
    In summary, it is probable that CA-MRSA infections are more common in the medical community and correctional facilities than clinicians are currently aware. At this time, the Centers for Disease Control and Prevention (CDC) are
    performing surveillance in several areas across the country to determine the prevalence and risk factors associated with this organism. A careful, thorough
    history will help identify those patients who may have had contact with CA-MRSA.
    Questions to ask the patient should include:

    Has the patient had contact with a correctional facility, prisoner or former prisoner?

    Have they or any of their close contacts been recently treated or told they had an infection from a spider bite?

    Have they been treated for recurring skin infections such as impetigo or furunculosis?

    Do they play any type of contact sports or work or work out at a gym or other
    sports facility?


    These questions should help the clinician to quickly identify and properly treat infections caused by CA-MRSA. Ongoing studies by the CDC should provide
    more information on the recognition and treatment of this growing problem in health care.[21]


    Tables
    Table 1. Sensitivity Patterns for Patients Diagnosed with CA-MRSA





    Table 2. Presenting Patients Diagnosed with CA-MRSA





    References
    Groom AV, Wolsey DH, Naimi TS, et al. Community-acquired methicillin-resistant Staphylococcus aureus in a rural American Indian community. JAMA
    2001;286:1201-5.
    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.
    Purcell K, Fergie E. Exponential increase in community-acquired methicillin-resistant Staphylococcus aureus infections in south Texas children
    [letter].
    Pediatr Infect Dis J 2002;21:988-9.
    Lowy FD. Medical progress: Staphylococcus aureus infections. N Engl J Med 1998;339:520-32.
    Outbreaks of community-associated methicillinresistant Staphylococcus aureus skin infections--Los Angeles County, California, 2002-2003. MMWR Morb Mortal Wkly Rep 2003;52:88.
    Methicillin-resistant Staphylococcus aureus skin or soft tissue infections in
    a state prison--Mississippi, 2000. MMWR Morb Mortal Wkly Rep 2001;50:919-22. Lindemayer JM, Schoenfeld S, O´Grady R, Carney JK. Methicillin-resistant Staphylococcus aureus in a high school wrestling team and the surrounding community. Arch Intern Med 1998;158:895-9.
    Frank AL, Marcinak JF, Mangat PD, Tjhio JT, Kelkar S, Schreckenberger PC. Clindamycin treatment of methicillin-resistant Staphylococcus aureus infections

    in children. Pediatric Infect Dis J 2002;21: 530-4.
    Marcinak JF, Frank AL. Treatment of community acquired methicillin-resistant Staphylococcus aureus in children. Curr Opin Infect Dis 2003;16:265-9.
    Ma XX, Ito T, Tiensasitorn C, et al. Novel type of staphylococcal cassette chromosome mec identified in community-acquired methicillin-resistant Staphylococcus aureus strains. Antimicrob Agents Chemother 2002;46:1147-52. Daum RS, Ito T, Hiramatsu K, et al. A novel methicillin-resistant cassette in
    community-acquired methicillin-resistant Staphylococcus aureus isolates of diverse genetic backgrounds. J Infect Dis 2002;186: 1344-7.
    Eady E, Cove JH. Staphylococcal resistance revisited: community-acquired methicillin-resistant Staphylococcus aureus--an emerging problem for the management
    of skin and soft tissue infections. Curr Opin Infect Dis 2003;16:103-24.
    Fey PD, Said-Salim B, Rupp ME, et al. Comparative molecular analysis of community- or hospitalacquired methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother 2003;47:196-203.
    Bukharic HA, Abdelhadi MS, Saeed IA, Rubaish AM, Larbi EB. Emergence of methicillin-resistant Staphylococcus aureus as a community pathogen. Diag Micro

    Infect Dis 2001;40:1-4.
    Osterhoudt KC, Zaoutis T, Zorc J. Lyme Disease masquerading as a Brown Recluse spider bite. Ann Emerg Med 2002;39:558-61.
    Vetter RS, Bush SP. The diagnosis of brown recluse spider bite is overused for dermonecrotic wounds of uncertain etiology. Ann Emerg Med 2002;39:544-6. Gross-Schulman S, Dassey D, Mascola L, Anaya C. Community-acquired methicillin-resistant Staphylococcus aureus [letter]. JAMA 1998;280:421-2. Four pediatric deaths from community-acquired methicillin-resistant Staphylococcus aureus--Minnesota and North Dakota 1997-1999. MMWR Morb Mortal Wkly Rep
    1999;48:707-10.
    Hollis RJ, Barr JL, Doebbeling BN, Pfaller MA, Wenzel RP. Familial carriage of methicillin-resistant Staphylococcus aureus and subsequent infection in a premature neonate. Clin Infect Dis 1995;21:328-32.
    CDC DHQP guidelines. MRSA--Information for healthcare personnel [updated 1999
    Aug]. Available from: http://www.cdc.gov/ncidod/hip/aresist/ mrsahcw.htm
    CDC DHQP information. Community-associated MRSA frequently asked questions [updated 2003 Aug]. Available from: http://www.cdc.gov/ncidod/ hip/aresist/mrsa_comm_faq.htm
    Acknowledgements

    Many thanks to Michael Parchman, MD, and Abraham Verghese, MD, for their time, advice, and help writing this article. Thanks also to Joe Babb and Methodist
    Health Care Ministries for their support of this article and for allowing time for research and writing.

    Funding Information

    This work was supported by Methodist Healthcare Ministries of South Texas, Inc., which operates the Dixon Clinic.




    Tamara J. Dominguez, MD, Bishop Ernest T. Dixon Clinic, Methodist Healthcare Ministries of South Texas, Inc., San Antonio

    ------------------------------------------------------------------------------
    --

    THANKS FOR POSTING THIS GEORGIA

    --- SoupGate-Win32 v1.05
    * Origin: fsxNet Usenet Gateway (21:1/5)