Professional Documents
Culture Documents
Community Acquired Methicillin Resistant em Staph
Community Acquired Methicillin Resistant em Staph
Community Acquired Methicillin Resistant em Staph
Community-Acquired Methicillin-Resistant
Staphylococcus aureus in Surgically Treated
Hand Infections
Scott D. Imahara, MD, Jeffrey B. Friedrich, MD
RISE IN METHICILLIN-RESISTANT
Staphylococcus media.1–5 In the past, this type of drug-resistant infec-
TABLE 1. ICD-9 Procedure Codes and Diagnosis TABLE 2. Demographics, Surgical Treatment,
Codes Used to Identify Surgically Treated Hand and Comorbid Illness Among Surgically Treated
Infections Hand Infections
ICD-9 Procedure Codes Non- p
80.14 Arthrotomy—hand/finger Overall MRSA MRSA Value
82.01 Exploration tendon sheath, hand Total 159 (100) 111 48
82.03 Bursotomy of hand Male (%) 72.3 72.1 72.9 .999
82.04 Incision and drainage palmar/thenar space Mean age (y) 40.1 40.7 38.6 .311
82.09 Incision soft tissue hand NEC Mean inpatient length 4.9 4.9 5.0 .830
82.92 Aspiration bursa of hand of stay (d)
82.93 Aspiration soft tissue hand NEC No. of surgeries 1.2 1.2 1.3 .633
ICD-9 Diagnosis Codes ⬎1 surgery (%) 13.8 12.6 16.7 .617
680.30 Infection of skin and subcutaneous tissue, upper arm Second infection (%) 5.7 2.7 12.5 .023
and forearm Admit to final 707 784 541 .084
680.40 Infection of skin and subcutaneous tissue, hand follow-up (d)
681.00 Cellulitis and abscess, unspecified, finger Potential risk factors
681.01 Felon Homeless (%) 32.1 28.8 39.6 .199
681.02 Onychia and paronychia of finger Inmate (%) 6.9 5.4 10.4 .309
711.04 Pyogenic arthritis, hand Diabetes mellitus (%) 6.3 7.2 4.2 .724
727.05 Tenosynovitis, hand and wrist Human 4.4 2.7 8.3 .200
immunodeficiency
virus (%)
IVDU (%) 35.2 27.0 54.2 .002
studies describing CA-MRSA hand infections have had Any comorbidity (%) 3.8 4.5 2.1 .669
relatively short study periods and minimal description Any complication (%) 6.3 7.1 4.4 .720
of risk factors for MRSA.18 –20 The purposes of this
study are to determine the change in proportion of IVDU, intravenous drug use.
Boldface values indicate statistical significance.
surgically treated CA-MRSA hand infections over the
last decade (1997–2007) at a single urban level I trauma
center and to analyze the risk factors associated with
hand infections caused by this pathogen. During the 11-year period encompassed by this
study, 159 patients had surgical intervention in the
PATIENT POPULATION AND METHODS
operating room for a hand infection. There were 115
Demographic data male and 44 female patients, with an average age of 40
After the study was approved by the institutional review years (range, 11– 82 y; Table 2). Mean length of hos-
board, applicable patients were identified from the pital stay was 4.9 days (median, 4 days; range, 0 –22 d).
records of a level I trauma center. Using a discharge Mean follow-up was 21 months (range 0 days–10 y);
database from 1997 to 2007, patients were identified however, because the study was focused on pathogens
using the International Classification of Diseases, 9th and risk factors, the length of follow-up was not an
Edition/Revision (ICD-9) procedure codes for surgical inclusion criterion. Many patients had potential risk
drainage of an infection of the hand in the operating factors for community-acquired drug-resistant infec-
room (Table 1). Patients identified by ICD-9 procedure tion, including homelessness (51), incarceration (11),
codes were confirmed to have an infection by indepen- intravenous drug use (IVDU) (57), history of diabetes
dent chart review. Current procedural terminology mellitus (10), and documented history of human immu-
codes were not available for use in identifying patients. nodeficiency virus (5). Because of the retrospective
Bacterial pathogens were identified by microbiologic nature of the data, the authors were unable to determine
culture and susceptibility data obtained from each sur- whether patients lived in communal living quarters such
gery. In addition, patients were coded by specific diag- as barracks or dormitories. Patients who had drainage of
noses using ICD-9 diagnosis codes, which included a hand infection in the emergency department were
suppurative tenosynovitis, abscess, septic arthritis, excluded, chiefly because the fluid from these infections
felon, and paronychia. was not routinely sent for gram stain and culture. Pa-
n 159 111 48
Infection type
Tenosynovitis (%) 67.3 69.4 62.5 .462
Abscess (%) 17.0 13.5 25.0 .106
Septic arthritis (%) 11.9 15.3 4.2 .061
Felon (%) 1.9 0.0 6.3 .026
Paronychia (%) 0.6 0.0 2.1 .302
FIGURE 1: Proportion of patients with surgically treated hand
Cellulitis/osteomyelitis 0.6 0.9 0.0 .999
infections due to CA-MRSA over time. Values above each bar
(%)
represent the percentage of patients with CA-MRSA among
Infected laceration (%) 0.6 0.9 0.0 .999
the total number of patients each year.
Anatomic location
Finger and thumb (%) 2.5 2.7 2.1 .999
Hand (%) 13.8 13.5 14.6 .999
RESULTS
Forearm (%) 0.6 0.9 0.0 .999
During the 11-year period between 1997 and 2007, 48
Multiple sites (%) 11.3 11.7 10.4 .999
of 159 patients had cultures positive for CA-MRSA.
Wrist (%) 2.5 1.3 4.2 .585
The number of patients admitted with CA-MRSA in-
Finger joint (%) 6.9 7.2 6.3 .999
fections requiring surgical drainage rose significantly
Finger, no thumb (%) 73.0 74.8 68.8 .442
between 1997 and 2007. In contrast, the number of
Thumb only (%) 13.2 11.7 16.7 .447
patients admitted who required surgical drainage of
Non-MRSA microbiology
non-MRSA infections, although varying from year to
year, did not steadily increase (Fig. 1). Logistic regres- AHS (%) 3.8 5.4 0.0 .179
sion was used to compare the odds of being treated for GABHS (%) 29.6 36.9 12.5 .002
a CA-MRSA hand infection in each subsequent study MSSA (%) 31.4 45.0 0.0 ⬍.001
year during the period of study. The risk of having an N gonorrhea (%) 17.6 25.0 0.0 ⬍.001
MRSA infection was found to be 41% higher each Atypical (%) 6.3 9.0 0.0 .033
progressive calendar year during the study period rela- AHS, alpha-hemolytic Streptococcus; GABHS, group A beta-hemo-
tive to the risk of having a non-MRSA infection (odds lytic; MSSA, methicillin-sensitive Staphylococcus aureus; N gonor-
rhea, Neisseria gonorrhea.
ratio [OR], 1.41; 95% confidence interval [CI], 1.21– Boldface values indicate statistical significance.
1.64; p ⬍ .001).
Variables found by univariate analysis to be associ-
ated with CA-MRSA were IVDU (p ⫽ .002); a second
distinct, temporally unrelated hand infection (p ⫽ .01); p ⫽ .003) was independently associated with a higher
and felon-type hand infection (p ⫽ .026) (Tables 2 and risk of CA-MRSA hand infections (Table 5).
4). Factors not associated with CA-MRSA were age,
gender, other types of infection (tenosynovitis, abscess, DISCUSSION
etc.), location of infection on the hand, number of The proportion of methicillin-resistant Staphylococcus
surgeries, homelessness, incarceration, and other co- aureus infections continues to grow in hospital-
morbidities. Of the 143 patients for whom follow-up associated settings and, more recently, in community
data were available, there was no significant difference settings in the United States.4,22,23 Infection due to
in complication rates among the CA-MRSA and non- Staphylococcus aureus imposes a high and increasing
CA-MRSA groups (p ⫽ .72) (Table 2). Variables found burden on health care resources.4 A growing concern is
to be associated with CA-MRSA were analyzed by the emergence of MRSA infections among patient pop-
logistic regression to determine risk factors for CA- ulations with no apparent risk factors.21 Outbreaks of
MRSA. Only IVDU (OR, 3.58; 95% CI, 1.55– 8.29; CA-MRSA infections have emerged among healthy
tance, but this finding has not been corroborated by and in better elucidating the characteristics of multi-
others.1,18 With surgically treated infections, multidrug drug-resistant bacterial infections.
resistance is probably less important to the final out-
come than adequate drainage. However, multidrug re- REFERENCES
sistance does have far-reaching implications for the 1. Eady EA, Cove JH. Staphylococcal resistance revisited: community-
acquired methicillin resistant Staphylococcus aureus—an emerging
treatment of infections in general. Finally, we found problem for the management of skin and soft tissue infections. Curr
that fully two-thirds of all patients in our series had Opin Infect Dis Apr 2003;16:103–124.
infections of the flexor tendon sheath. This observation 2. Frazee BW, Lynn J, Charlebois ED, Lambert L, Lowery D, Perd-
reau-Remington F. High prevalence of methicillin-resistant Staphy-
was different from Kiran’s findings in which most CA- lococcus aureus in emergency department skin and soft tissue infec-
MRSA hand infections were in the form of abscesses.20 tions. Ann Emerg Med 2005;45:311–320.
This may also reflect the fact that the current study 3. Berens M, Armstrong K. Culture of resistance. Seattle Times, Nov
16 –18, 2008.
concentrates on surgically treated infections, and sup- 4. National Nosocomial Infections Surveillance (NNIS) System Re-
purative flexor tenosynovitis is not amenable to emer- port, data summary from January 1992 through June 2004, issued
gency room treatment. October 2004. Am J Infect Control 2004;32:470 – 485.
5. Graham J. Study paints picture of rampant “superbug”. Chicago
Our study has a number of important limitations. Tribune, June 25, 2007:1.
Retrospective medical record reviews are subject to 6. Skiest DJ, Brown K, Cooper TW, Hoffman-Roberts H, Mussa HR,
incomplete or incorrect information. In particular, we Elliott AC. Prospective comparison of methicillin-susceptible and
methicillin-resistant community-associated Staphylococcus aureus
found that many records lacked antibiotic susceptibility
infections in hospitalized patients. J Infect 2007;54:427– 434.
results for all cultures, which removed a potentially 7. Olesevich M, Kennedy A. Emergence of community-acquired me-
valuable source of information for this study. Although thicillin-resistant Staphylococcus aureus soft tissue infections. J Pe-
the inclusion of surgically treated infections alone al- diatr Surg 2007;42:765–768.
8. Herold BC, Immergluck LC, Maranan MC, Lauderdale DS, Gaskin
lowed some uniformity of the patient population, the RE, Boyle-Vavra S, et al. Community-acquired methicillin-resistant
lack of culture data from most of the patients treated in Staphylococcus aureus in children with no identified predisposing
our emergency department greatly reduced the avail- risk. JAMA 1998;279:593–598.
9. Archibald LK, Shapiro J, Pass A, Rand K, Southwick F. Methicillin-
able population of the study. Further, the need for resistant Staphylococcus aureus infection in a college football team:
surgical (versus bedside) drainage was entirely at the risk factors outside the locker room and playing field. Infect Control
discretion of the treating physician, thereby introducing Hosp Epidemiol 2008;29:450 – 453.
10. Begier EM, Frenette K, Barrett NL, Mshar P, Petit S, Boxrud DJ, et
another source of selection bias. Finally, CA-MRSA al. A high-morbidity outbreak of methicillin-resistant Staphylococ-
was defined among those patients without prior hospi- cus aureus among players on a college football team, facilitated by
talizations or hospital-acquired infections. Microbio- cosmetic body shaving and turf burns. Clin Infect Dis 2004;39:
1446 –1453.
logic identification of clonal strains associated with 11. Centers for Disease Control and Prevention (CDC). Methicillin-
CA-MRSA was not performed in this study, so the resistant Staphylococcus aureus among players on a high school
designation of CA-MRSA depends solely on social and football team—New York City, 2007. MMWR Morb Mortal Wkly
clinical criteria. Defining CA-MRSA by the absence of Rep. 2009;58:52–55.
12. Coronado F, Nicholas JA, Wallace BJ, Kohlerschmidt DJ, Musser K,
risk factors for health care exposure might underesti- Schoonmaker-Bopp DJ, et al. Community-associated methicillin-
mate the true number of CA-MRSA cases.26 resistant Staphylococcus aureus skin infections in a religious com-
This study presents a longitudinal analysis of the munity. Epidemiol Infect 2007;135:492–501.
13. Hall AJ, Bixler D, Haddy LE. Multiclonal outbreak of methicillin-
changing proportion of CA-MRSA hand infections and resistant Staphylococcus aureus infections on a collegiate football
the potential risk factors that are associated with this team. Epidemiol Infect 2009;137:85–93.
problem. Multivariable analysis demonstrated that 14. Lee MC, Rios AM, Aten MF, et al. Management and outcome of
children with skin and soft tissue abscesses caused by community-
more recent years of infection and admitted IVDU were acquired methicillin-resistant Staphylococcus aureus. Pediatr Infect
associated with increased odds of having MRSA as a Dis J 2004;23:123–127.
pathogen in the hand infection. Although we did not 15. Nguyen DM, Bancroft E, Mascola L, Guevara R, Yasuda L. Risk
factors for neonatal methicillin-resistant Staphylococcus aureus in-
find other risk factors such as homelessness and incar- fection in a well-infant nursery. Infect Control Hosp Epidemiol
ceration to be associated with a higher risk of CA- 2007;28:406 – 411.
MRSA, these factors should be taken into consideration 16. Cohen PR. Cutaneous community-acquired methicillin-resistant
Staphylococcus aureus infection in participants of athletic activities.
when initially providing empiric antibiotic treatment for
South Med J 2005;98:596 – 602.
hand infections. Fortunately, in cases of hand infections 17. Nguyen DM, Mascola L, Brancoft E. Recurring methicillin-resistant
involving fluid collection, drainage of the infected ma- Staphylococcus aureus infections in a football team. Emerg Infect
terial is usually adequate treatment. Future prospective Dis 2005;11:526 –532.
18. LeBlanc DM, Reece EM, Horton JB, Janis JE. Increasing incidence of
multi-institutional studies will be valuable in further methicillin-resistant Staphylococcus aureus in hand infections: a 3-year
refining the risk profile of CA-MRSA hand infections county hospital experience. Plast Reconstr Surg 2007;119:935–940.
19. Bach HG, Steffin B, Chhadia AM, Kovachevich R, Gonzalez MH. 23. Grundmann H, Aires-de-Sousa M, Boyce J, Tiemersma E. Emer-
Community-associated methicillin-resistant Staphylococcus aureus gence and resurgence of meticillin-resistant Staphylococcus aureus
hand infections in an urban setting. J Hand Surg 2007;32A:380 –383. as a public-health threat. Lancet 2006;368:874 – 885.
20. Kiran RV, McCampbell B, Angeles AP, Montilla RD, Medina C, 24. Moran G, Krishnadasan A, Gorwitz R, Fosheim GE, McDougal LK,
Mitra A, et al. Increased prevalence of community-acquired methi- Carey RB, et al. Methicillin-resistant S. aureus infections among
cillin-resistant Staphylococcus aureus in hand infections at an urban patients in the emergency department. N Engl J Med 2006;355:
medical center. Plast Reconstr Surg 2006;118:161–166; discussion 666 – 674.
167–169. 25. Davis SL, Perri MB, Donabedian SM, Manierski C, Singh A, Vager
21. Boucher H, Corey G. Epidemiology of methicillin-resistant Staphy- D, et al. Epidemiology and outcomes of community-associated me-
lococcus aureus. Clin Infect Dis 2008;46 Suppl 5:S344 –349. thicillin-resistant Staphylococcus aureus infection. J Clin Microbiol
22. Laupland K, Church D, Mucenski M, Sutherland L, Davies H. 2007;45:1705–1711.
Population-based study of the epidemiology of and the risk factors 26. David MZ, Glikman D, Crawford SE, Peng J, King KJ, Hostetler MA,
for invasive Staphylococcus aureus infections. J Infect Dis 2003; et al. What is community-associated methicillin-resistant Staphylococ-
187:1452–1459. cus aureus? J Infect Dis 2008;197:1235–1243.