JWissmille
2004-08-05 02:14:30 UTC
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. © 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
Staphylococcus Aureus
Tamara J. Dominguez, MD
J Am Board Fam Pract 17(3):220-226, 2004. © 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
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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