MRSA otorrhea: a case series and review of the literature.
Methicillin-resistant Staphylococcus aureus methicillin-resistant Staphylococcus aureus Methicillin-aminoglycoside resistant Staphylococcus aureus, MRSA An organism with multiple antibiotic resistances–eg, aminoglycosides, chloramphenicol, clindamycin, erythromycin, rifampin, tetracycline, (MRSA MRSA Methicillin-resistant Staphylococcus aureus. See MARSA. ) has become an increasingly common cause of difficult-to-treat head and neck infections. We report a retrospective analysis of 3 cases of MRSA otorrhea treated in our clinic between 2007 and 2009. Culture analysis of otorrhea isolates revealed MRSA infections with identical drug sensitivities. Treatment success was achieved using combinations of linezolid with gentamicin gentamicin /gen·ta·mi·cin/ (jen?tah-mi´sin) an aminoglycoside antibiotic complex isolated from bacteria of the genus Micromonospora, ear drops for 3 to 4 weeks or trimethoprim/sulfamethoxazole (TMP/SMX) with gentamicin drops for 6 weeks. This study illustrates the importance of determining individual drug sensitivities for optimal treatment and maintaining current knowledge of the local MRSA strains. Empiric em·pir·ic
1. One who is guided by practical experience rather than precepts or theory.
2. An unqualified or dishonest practitioner; a charlatan.
2. combination therapy of TMP/SMX with gentamicin is an effective first-line treatment for MRSA otorrhea. Regional differences in clindamycin sensitivities warrant clinical discretion. Fluoroquinolones should be avoided because of high rates of resistance unless culture sensitivity determines that they are appropriate. First-line agents for severe infections include combination therapy with vancomycin or linezolid.
Methicillin-resistant Staphylococcus aureus (MRSA) presents a host of clinical problems, including identification (commonly after initial treatment failure), increasing incidence, broadening drug resistance, and colonization resulting in its spread and recurrence. As the number of MRSA infections rises, the incidence of head and neck MRSA infections is also rising, as evidenced by a 16.3% increase in pediatric pediatric /pe·di·at·ric/ (pe?de-at´rik) pertaining to the health of children.
Of or relating to pediatrics. head and neck MRSA infections from 2001 to 2006. (1) Otologic infections were found most frequently (34%), with smaller percentages of sinonasal (28.3%) and oropharynx/neck (14.2%) infections. (1)
A range of monotherapy and combination therapies has been employed by physicians for the treatment of MRSA, some of which are often no longer effective. This study of three patients with MRSA otorrhea treated between 2007 and 2009, along with a literature review of the current treatment options and recommendations for MRSA otorrhea, highlights concepts that are of practical importance for anyone caring for patients with otorrhea.
Patient 1. A 56-year-old man presented with left otalgia otalgia /otal·gia/ (o-tal´jah) pain in the ear; earache.
Pain in the ear; earache.
o·tal and otorrhea 5 weeks after right (contralateral) total stapedectomy Stapedectomy Definition
Stapedectomy is a surgical procedure in which the innermost bone (stapes) of the three bones (the stapes, the incus, and the malleus) of the middle ear is removed, and replaced with a small plastic tube of stainless-steel wire (a with oval window graft, tympanoplasty tympanoplasty /tym·pa·no·plas·ty/ (tim´pah-no-plas?te) surgical reconstruction of the tympanic membrane and establishment of ossicular continuity from the tympanic membrane to the oval window. , and myringotomy myringotomy /my·rin·got·o·my/ (mi-ring-got´ah-me) tympanotomy; creation of a hole in the tympanic membrane, as for tympanocentesis.
n. tube placement. An old myringotomy tube was present on the left and had not been changed during the recent surgery. The patient had a history of chronic bilateral ear infections, cholesteatoma and mastoidectomy Mastoidectomy Definition
Mastoidectomy is a surgical procedure to remove an infected portion of the bone behind the ear when medical treatment is not effective. This surgery is rarely needed today because of the widespread use of antibiotics. as a teenager, multiple myringotomy and tube placements, and ossicular os·si·cle
A small bone, especially one of the three bones of the middle ear.
[Latin ossiculum, diminutive of os, bone; see ost- in Indo-European roots. reconstruction surgery 8 years previously. He had been free of infection in either ear at the time of his surgery.
When this patient presented with infection, his left tympanic membrane had a myringotomy tube in place, and the infection originated in his middle ear. Culture and sensitivity of the left ear fluid was obtained, and the patient was empirically started on ofloxacin drops. The fluid was suctioned from the ear canal and from the middle ear through the tube. Suction was repeated frequently until the otorrhea resolved. The culture revealed MRSA with drug sensitivities (table 1). Linezolid 600 mg twice daily for 10 days was prescribed, and his previous medication was discontinued.
Approximately 3 months later, the patient returned with bilateral otorrhea. Cultures and sensitivities were obtained with bilateral MRSA results identical to those from the previous culture. He was treated with linezolid 600 mg twice a day for 3 weeks and gentamicin drops three times a day. A weeklater the right ear was dry, while the left ear had a wet discharge. The linezolid course was continued for a total of 3 weeks, and gentamicin application to the left ear was continued for 1 more week. Follow-up cultures did not reveal MRSA. He has been free of MRSA infection for 22 months.
Patient 2. In 2007, a 67-year-old man underwent right tympanomastoidectomy. Two weeks after surgery, he complained of right otorrhea. His history included multiple ear surgeries and infections beginning in the 1980s, a mastoidectomy for cholesteatoma in 2001, and ossicular chain reconstruction ossicular chain reconstruction ENT A procedure for tympanoplasty–see there, using malleus strut, peg-top, and hydroxyapatite cap prostheses, and revision stapedectomy using stapedial tendon reconstruction in 2002.
The external auditory canal external auditory canal
See ear canal. wall and eardrum ear·drum
The thin, semitransparent, oval-shaped membrane that separates the middle ear from the external ear. Also called drum, drumhead, drum membrane, myringa, myrinx, tympanic membrane, were intact, but the infection involved the middle ear and ear canal. The mastoid mastoid /mas·toid/ (mas´toid)
2. mastoid process.
3. pertaining to the mastoid process.
The mastoid process. was not tender, erythematous erythematous
characterized by erythema. , or bulging. Culture revealed MRSA with the same sensitivities as Patient 1 and Patient 3 (table 1), and he began a 4-week course of vancomycin. Fluid was suctioned at 1- to 2-week intervals. A week after the completion of the vancomycin treatment, the patient's right ear was improved but not completely dry. He was started empirically on acetic acid drops. A second culture yielded MRSA along with Klebsiella pneumoniae.
Following the culture results, acetic acid was discontinued and a 4-week course of gentamicin drops three times daily was prescribed. At a 2-week follow-up visit, a prescription of trimethoprim/sulfamethoxazole (TMP/SMX) 160mg/800 mg twice daily for 6 weeks was added, which was later reduced to once daily because of constipation. The infection resolved following completion of the combination treatment. There has been no recurrence in the subsequent 22 months.
Patient 3. A 55-year-old woman was referred with right otorrhea and sensorineural hearing loss Sensorineural hearing loss
Hearing loss caused by damage to the nerves or parts of the inner ear governing the sense of hearing.
Mentioned in: Tinnitus
sensorineural hearing loss . She also complained of light-headedness and intermittent clicking noises in her right ear. Eight months previously, she had been hospitalized for streptococcal streptococcal /strep·to·coc·cal/ (-kok´al) pertaining to or caused by a streptococcus.
Pertaining to any of the Streptococcus bacteria. meningitis secondary to suppurative suppurative
pertaining to or emanating from suppuration; pus in e.g. suppurative arthritis, bronchopneumonia. otitis media complicated by a cerebrovascular accident. Prior to her hospitalization, she had denied any history of ear infections, hearing loss, tinnitus, or vertigo. Computed tomography of this patient's temporal bones revealed right mastoiditis mastoiditis
Inflammation of the mastoid process, a bony projection just behind the ear, almost always due to otitis media. It may spread into small cavities in the bone, blocking their drainage. Very severe cases infect the whole middle ear cleft. , and magnetic resonance imaging magnetic resonance imaging (MRI), noninvasive diagnostic technique that uses nuclear magnetic resonance to produce cross-sectional images of organs and other internal body structures. revealed a "mass" in her right internal auditory canal, along with mastoiditis. Previous treatment for her otorrhea had included 2 weeks of tobramycin/dexmethasone and a combination of ofloxacin drops and cefuroxime.
Examination revealed a right anterior tympanic membrane perforation tympanic membrane perforation Perforated, punctured, ruptured ear drum ENT A disruption of the tympanic membrane due to acoustic trauma, direct injury, barotrauma, introduction of Q-tips or small objects, or infection with fluid buildup in the middle ear. See Tympanoplasty. with mild otorrhea. The ear was totally deaf. The patient was started empirically on a 10-day course oftobramycin/dexmethasone drops and levofloxacin 750 mg daily. The levofloxacin was stopped when culture results identifying MRSA were received, and she began TMP/SMX 160 mg/800 mg twice daffy for 2 weeks. Sensitivities are listed in table 1. Two weeks from the initial referral, the patient underwent a right tympanomastoidectomy with planned staged reconstruction and myringotomy.
Two months after the surgery, the patient developed right otorrhea and initially was started on a 10-day course of tobramycin/dexmethasone drops, and levofloxacin 750 mg daffy for 1 week, while awaiting her culture results. The graft was intact. Frequent suction was used to keep the ear as free of purulence purulence /pu·ru·lence/ (pur´ah-lins) suppuration.pur´ulent
1. The condition of containing or discharging pus.
2. Pus. as possible. The results demonstrated MRSA with the aforementioned susceptibilities. Her previous medications were discontinued, and she was started on 2 weeks of linezolid 600 mg twice daffy and gentamicin drops, three times a day. Her otorrhea resolved, but 3 days after completing the course of antibiotics she developed otorrhea, otalagia, and imbalance. Linezolid 600 mg twice a day and gentamicin drops three times daily for 1 month were prescribed.
Three months later she developed thick, clear otorrhea and a new anteroinferior perforation. Cultures and sensitivities were identical to previous cultures. The therapy initially included sulfacetamide drops three times a day for 3 weeks, and linezolid 600 mg twice a day for 1 month. She continued the course of prescribed sulfacetamide drops, and the otorrhea resolved.
Two months later, this patient's right ear began to drain again, and she noted mild imbalance. She was started on linezolid 600 mg twice daffy for the next month along with gentamicin, three drops three times daily, for presumed MRSA otorrhea, but the culture was negative for MRSA and grew only normal skin flora.
Approximately I year after she underwent tympanomastoidectomy, she presented to the office with right mastoiditis. A culture revealed no organisms other than normal skin flora. She was started on ciprofloxacin 500 mg twice daily and ofloxacin drops. A week later, she was taken to the operating room, where she underwent a right revision mastoidectomy, drainage of purulence, and removal of a right mastoid titanium plate. MRSA was not present at the time, and the patient has remained free of MRSA infection and otorrhea from any other cause for 21 months.
In light of the increasing incidence of MRSA otorrhea and the rising resistance to common MRSA treatments, familiarity with current and anticipated treatment options is vital for expedient otolaryngologic treatment.
The current nomenclature divides MRSA into two types: healthcare-associated (HA-MRSA) and community-acquired (CA-MRSA). Initially, MRSA was responsible for nosocomial infections and referred to as HA-MRSA. (2) Risk factors for nosocomial nosocomial /noso·co·mi·al/ (nos?o-ko´me-il) pertaining to or originating in a hospital.
1. Of or relating to a hospital.
2. MRSA include prolonged hospitalization, care in an intensive care unit, prolonged antimicrobial therapy, surgical procedures, and close proximity to a patient infected or colonized with MRSA. (3) In the past decade, CA-MRSA has been isolated in the outpatient setting, in young, healthy individuals without any healthcare association. (4) CAMRSA has been associated with soft-tissue infections and necrotizing pneumonia, (4) as well as less multidrug resistance than HA-MRSA (2) but higher growth rates,s The Centers for Disease Control and Prevention Centers for Disease Control and Prevention (CDC), agency of the U.S. Public Health Service since 1973, with headquarters in Atlanta; it was established in 1946 as the Communicable Disease Center. (CDC See Control Data, century date change and Back Orifice.
CDC - Control Data Corporation ) requires all of the following to establish a diagnosis of CA-MRSA (6):
1. A culture obtained either outpatient or within 48 hours of hospital admission;
2. No history of MRSA infection or colonization;
3. No history of hospitalization, dialysis, surgery, or admittance to a nursing home, skilled nursing facility, or hospice within one year; and
4. No permanent catheter or other device that passes through the skin and into the body.
The antibiotic profile is also commonly referred to for MRSA designation, typically indicating clindamycin susceptibility as CA-MRSA. (7) Distinguishing between CA-MRSA and HA-MRSA is not always straightforward, since colonization might have been present over a period of time, thus obscuring the source. (2,4)
Common MRSA algorithms categorize separate treatment options for mild to moderate or severe infections, along with consideration of whether a patient has healthcare risk factors. (4) An algorithm by the American Academy of Pediatrics for CA-MRSA infections qualifies patients with mild infection as afebrile afebrile /afe·brile/ (a-feb´ril) without fever.
afebrile adjective Feverless and previously healthy, those with moderate infections as febrile and previously healthy, and those with severe infections as toxic-appearance, immunocompromised immunocompromised /im·mu·no·com·pro·mised/ (-kom´pro-mizd) having the immune response attenuated by administration of immunosuppressive drugs, by irradiation, by malnutrition, or by certain disease processes (e.g., cancer). , or limb-threatening and requiring hospitalization. The treatment of moderate infections can follow the recommendations for mild or severe infections at the discretion of the clinician,s
Mild to moderate infections
TMP/SMX and clindamycin are the most commonly used first-line agents for mild to moderate CA-MRSA otorrhea. (9) TMP/SMX remains an effective monotherapy and maintains high susceptibility rates, (10-13) although combination therapy has been recommended. (14) Combinations of TMP/SMX with gentamicin, polymyxin polymyxin /poly·myx·in/ (-mik´sin) generic term for antibiotics derived from Bacillus polymyxa; they are differentiated by affixing different letters of the alphabet. B/neomycin/hydrocortisone, or ofloxacin have proven effective in MRSA otorrhea treatment. (12) However, the high incidence of resistance to aminoglycosides and quinolones may cause such combinations to be unpredictable. (15) Additionally, higher rates of TMP/SMX resistance have been found in patients infected with HIV HIV (Human Immunodeficiency Virus), either of two closely related retroviruses that invade T-helper lymphocytes and are responsible for AIDS. There are two types of HIV: HIV-1 and HIV-2. HIV-1 is responsible for the vast majority of AIDS in the United States. , not surprisingly, due to the use of TMP/SMX for Pneumocystitis prophylaxis. (16)
Given the low resistance rates to rifampin rifampin (rĭfăm`pĭn), antibiotic used in the treatment of tuberculosis. It is also used to eliminate the meningococcus microorganism from carriers and to treat leprosy, or Hansen's disease. and its successful use in combination therapy, (11,15,17) a study of TMP/SMX and rifampin might be useful for acute otitis media Acute otitis media
Inflammation of the middle ear with signs of infection lasting less than three months.
Mentioned in: Myringotomy and Ear Tubes
acute otitis media with otorrhea. (12) TMP-SMX has been recommended as a first-line treatment for MRSA after tympanostomy-tube placement along with tobramycin/ dexmethasone and chloramphenicol chloramphenicol (klōr'ămfĕn`əkŏl'), antibiotic effective against a wide range of gram-negative and gram-positive bacteria (see Gram's stain). It was originally isolated from a species of Streptomyces bacteria. drops. (18) However, we remain cautious about using ototoxic ototoxic /oto·tox·ic/ (o´to-tok?sik) having a deleterious effect upon the eighth nerve or on the organs of hearing and balance.
adj. drops when the eardrum is not intact.
Literature reports indicate increasing clindamycin resistance in the United States (1,12,19) and even higher resistance in Korea and Taiwan, where the highest rates of CA-MRSA are reported (table 2). (15,20-22) The SENTRY Antimicrobial Surveillance Program determined that only 20.8% of all MRSA isolates in the United States (1997-1999) were susceptible to clindamycin. (13) Geographical regions in which CA-MRSA isolates demonstrate > 10 to 15% resistance to clindamycin necessitate replacing empiric clindamycin treatment with TMP/ SMX SMX Search Marketing Expo
SMX Server Macro Expansion
SMX Santa Maria, CA, USA - Santa Maria Public Airport (Airport Code)
SMX Smithway Motor Xpress, Inc. (8,14) or another antibiotic. Because of the rising resistance, clinical trials of clindamycin and rifampin combination therapy for otorrhea may be a worthwhile consideration. Infections that have failed treatment with clindamycin or TMP/SMX can be treated with vancomycin or linezolid. (14,23)
A global, multicenter study in 2004 reviewed susceptibilities of MRSA isolates to fluoroquinolone fluoroquinolone /flu·o·ro·quin·o·lone/ (-kwin´o-lon) any of a subgroup of fluorine-substituted quinolones, having a broader spectrum of activity than nalidixic acid.
n. treatment, showing the lowest susceptibility in North America, where ciprofloxacin and levofloxacin demonstrated <6% susceptibility. (24) Interestingly, the use of ciprofloxacin and levofloxacin has been associated with MRSA infection occurrence, and studies propose that their use increases the risk of infection or colonization with MRSA via an undetermined mechanism. (25) The usefulness of fluoroquinolone treatment now seems to be very limited because of the prevalence of resistant strains. (12,14,15,18,23)
Recent publications reveal the usefulness of acetic acid and other cleansing agents for use as monotherapy or combination therapy for MRSA otitis. (26) Aural cleansing with diluted acetic acid was shown to be a more desirable choice for the treatment of chronic MRSA suppurative otitis media than intravenous vancomycin or teicoplanin, having similar efficacy and treatment duration. (27) Burow's solution was found to be effective for treatment of MRSA and intractable chronic ear infections, (26,28) as well as reducing granulation tissue. (26) Fusidic acid (widely used in Europe but not available in the United States) was reportedly a very effective topical and parenteral therapy, (20,21,29) with currently reduced usefulness in Europe due to high levels of resistance from its widespread use as a monotherapy. (29) Fusidic acid susceptibility remains very high in other parts of the world. (15) Typically, fusidic acid is combined with rifampin to help avoid resistance. (30)
Moderate to severe infections
Treatment options for moderate to severe MRSA infections, including otorrhea, encompass a group of highly effective anti-MRSA agents. Vancomycin is recommended as the first-line agent for severe MRSA, as culture sensitivities remain extremely high (table 2). (15,20-22) However, as evidenced by the current study, vancomycin is not an infallible agent even if culture sensitivities indicate susceptibility. Along with the standard parenteral administration, vancomycin can be used successfully as a topical preparation or in combination with naficillin, rifampin, or gentamicin, which are recommended when vancomycin monotherapy is unsuccessful. (14,31-33) The combinations of rifampin or gentamicin with vancomycin are synergistic and useful in treatment of severe infections. (15,34)
Although vancomycin has been the gold standard for severe MRSA infections, resistance to vancomycin has been growing. (30) This rise has been attributed to the transfer of vancomycin resistance from vancomycin-resistant enterococci. (34-36)
For vancomycin-resistant infections, a group of highly effective drugs are used sparingly to retain high susceptibility for severe infections. Linezolid is considered equivalent to vancomycin, (15,22) has an oral formulation, (23) and is the only antibiotic in this group approved for children. (14) An in vitro study examining linezolid combination therapy found that the addition of rifampin was additive in rifampin-sensitive MRSA strains, whereas gentamicin and vancomycin caused decreases in efficacy. (37)
Although linezolid is generally well tolerated, with the most common side effect being diarrhea, (8) there have been reports of peripheral neuropathy, thus limiting its use in most cases to no more than 4 weeks in adults and 2 weeks in children. (14,34) Vitamin B6 can be used to prevent and treat linezolid-induced thrombocytopenia Thrombocytopenia Definition
Thrombocytopenia is an abnormal drop in the number of blood cells involved in forming blood clots. These cells are called platelets. , anemia, and leukopenias associated with extended administration. (8,38)
In vitro studies have shown extremely promising results for daptomycin, which allows for a shorter treatment duration than vancomycin. (15,39,40) The efficacy of quinupristin/dalfopristin is also comparable to vancomycin in treating skin and soft-tissue infections. (41) However, it is not as successful in complete eradication and has a high rate of adverse drug reactions, such as infusion site pain, which can occur in as many as 68% of patients. (42)
Other agents useful for vancomycin failure include teicoplanin and tigecycline. (15,43) Teicoplanin is not available in the United States and has a mechanism of action similar to that of vancomycin. (36) Its advantages are that it is generally well tolerated, lacks the renal monitoring required for the potential nephrotoxic nephrotoxic /neph·ro·tox·ic/ (nef´ro-tok?sik) destructive to kidney cells.
Toxic, or damaging, to the kidney. effects of vancomycin, and may be administered intramuscularly. (34,36) A phase III randomized, double-blinded study comparing tigecycline and vancomycin for the treatment of complicated MRSA skin and soft-tissue infections found clinical cure to be similar, but with almost double the incidence of nausea and vomiting Nausea and Vomiting Definition
Nausea is the sensation of being about to vomit. Vomiting, or emesis, is the expelling of undigested food through the mouth. with tigecycline versus vancomycin. (44)
Interesting MRSA treatments are in various stages of animal or clinical testing. The first cephalosporins effective against MRSA, ceftobiprole and ceftaroline, look very promising, with ceftobiprole showing effectiveness similar to that of vancomycin and linezolid. Dalbavancin, iclaprim, oritavancin, and telavancin have all done well in trials, with success rates similar to those of the comparator. Several antibody therapies are also in clinical trials that might provide immunity to MRSA infections in the future. (34) With new drug options, trials of various types of combination therapies are ongoing and should continue in an effort to protect the efficacy of important drugs.
In summary, MRSA otorrhea can be treated successfully using combination therapy based on individual culture sensitivities and/or a current knowledge of local strains. Recommended first-line treatments are combination therapies, including TMP/SMX for mild to moderate infections and vancomycin or linezolid for more severe infections. High rates of resistance to fluoroquinolones and clindamycin make them inferior choices as empiric treatment for suspected MRSA. Cost-effective treatments, including acetic acid and fusidic acid, can be used effectively in combination therapy. There is a group of highly effective drugs recommended for use in the most severe cases, including vancomycin-resistant infections. Otolaryngologists should be familiar not only with current options but also emerging advances for the treatment of this potentially serious infection.
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Inflammation of the middle ear with signs of infection lasting three months or longer.
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a derivative of rifamycin; an antibacterial and antifungal agent used in the treatment of mycobacterial infections, actinomycosis and histoplasmosis. against methicillin-resistant Staphylococcus aureus by time-kill curve methods. J Antimicrob Chemother 2003;51(4): 857-64.
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(46.) Jung H, Lee SK, Cha SH, et al. Current bacteriology of chronic otitis media with effusion effusion /ef·fu·sion/ (e-fu´zhun)
1. escape of a fluid into a part; exudation or transudation.
2. effused material; an exudate or transudate. : High rate of nosocomial infection and decreased antibiotic sensitivity. J Infect 2009;59(5):308-16.
Katherine M. Baugher, MS; Troy Sommers Hemme, DO; Mary Hawkshaw Hawkshaw
implacable detective with photographic memory. [Br. Lit.: The Ticket-of-Leave Man, Barnhart, 546]
See : Sleuthing , RN, BSN BSN
Bachelor of Science in Nursing , CORLN; Robert T. Sataloff, MD, DMA, FACS FACS Fellow of the American College of Surgeons.
Fellow of the American College of Surgeons
fluorescence-activated cell sorter.
From the Department of Otolaryngology-Head and Neck Surgery, Philadelphia College of Osteopathic Medicine (Ms. Baugher and Dr. Hemme), and the Department of Otolaryngology-Head and Neck Surgery, Drexel University College of Medicine Drexel University College of Medicine is the medical school of Drexel University. It represents the consolidation of two venerable medical schools: the nation's first medical school for women and the first U.S. college of homeopathy. Residency Locations
St. (Ms. Hawkshaw and Dr. Sataloff), Philadelphia.
Corresponding author: Robert T. Sataloff, MD, DMA, FACS, 1721 Pine St., Philadelphia, PA 19103. E-mail: firstname.lastname@example.org
Table 1. Common MRSA otorrhea culture results from all three patients in this series Resistance Sensitivity amoxicillin/clavulanate gentamicin cefazolin linezolid ciprofloxacin * tetracycline clindamycin TMP/SMX erythromycin vancomycin levofloxacin oxacillin penicillin * Not reported for Patient 3. Table 2. Literature reports of drug susceptibilities of MRSA isolates from ear and other head and neck infections * Baugher Saunders Naseri (1) Klein ([dagger]) (19) (45) Year of publication 2009 2009 2010 Type of MRSA infection Oto SOM Ped HN Ped MEF Location US - PA US - OK US - National US - DE n ([double dagger]) 3 15 4534 25(31) Clindamycin 0 40 53 14-67 Fusidic Acid Linezolid 100 100 Quinupristin/ dalfopristin Rifampin Teicoplanin TMP/SMX 100 67 100 Vancomycin 100 Chloramphenicol Ofloxacin Ciprofloxacin 0 Levofloxacin 0 Cefazolin 0 Cefalotin Cefprozil Cefpodixime Cefotaxime Gentamicin 100 Tobramycin Tetracycline 100 Minocycline Penicillin 0 Amoxicillin/ 0 clavulanate Oxacillin 0 Erythromycin 0 Imipenem Al-Shawwa Hartnick Jung (46) (12) (46) Year of publication 2005 2000 2009 Type of MRSA infection Ped AOM+Oto Ped PTTO Ped MEF, PTTO Location US - rural US-OH S Korea n ([double dagger]) 6 8 (12,9) Clindamycin 67 83,56 Fusidic Acid Linezolid 75,67 Quinupristin/ 75,67 dalfopristin 100,100 Rifampin 100 100 Teicoplanin 100 83,78 TMP/SMX 100 88 100,100 Vancomycin 100 14 58,56 Chloramphenicol Ofloxacin Ciprofloxacin 0,0 Levofloxacin 0 100 Cefazolin 0,0 Cefalotin Cefprozil 0,0 Cefpodixime Cefotaxime 92,33 Gentamicin 100 0,0 Tobramycin Tetracycline Minocycline Penicillin Amoxicillin/ clavulanate Oxacillin 0 Erythromycin 0 Imipenem Park DC Park MK (10) (11) Year of publication 2008 2008 Type of MRSA infection CSOM CA, HA-CSOM Location Korea - National S Korea n ([double dagger]) 288 118,19 Clindamycin 12 25,0 Fusidic Acid Linezolid Quinupristin/ 90,10 dalfopristin 100 Rifampin Teicoplanin 88 100,0 TMP/SMX 100 Vancomycin 7 Chloramphenicol 14,5 Ofloxacin 12 Ciprofloxacin 1 Levofloxacin 4 Cefazolin 9 Cefalotin Cefprozil 0 Cefpodixime 0 Cefotaxime 4 Gentamicin Tobramycin Tetracycline Minocycline Penicillin Amoxicillin/ clavulanate Oxacillin Erythromycin Imipenem Yeo Hwang Hwang (22) (20) (21) Year of publication 2007 2002 2002 Type of MRSA infection CSOM CA-Ear CA-Ear Location Korea - National Taiwan Taiwan n ([double dagger]) 225 (224) 22 27 Clindamycin 12 14 15 Fusidic Acid 96 96 Linezolid Quinupristin/ dalfopristin 100 100 100 Rifampin Teicoplanin 85 TMP/SMX 100 100 100 Vancomycin Chloramphenicol Ofloxacin 17 Ciprofloxacin Levofloxacin 32 37 Cefazolin Cefalotin 96 96 Cefprozil 1 Cefpodixime 0 Cefotaxime 5 9 11 Gentamicin Tobramycin Tetracycline Minocycline Penicillin Amoxicillin/ clavulanate Oxacillin Erythromycin Imipenem * Results are presented as the rounded percentages of isolates susceptible in vitro to a given drug; ([dagger]) Present series; ([double dagger]) Number of patients or events. Key: Oto = otorrhea; SOM = suppurative otitis media; Ped = pediatric; HN= head and neck; MEF = middle ear effusion fluid; AOM = acute otitis media; PTTO = post- tympanotomy tube otorrhea; CSOM = chronic SOM; CA = community-acquired MRSA; HA = hospital-acquired MRSA
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|Title Annotation:||ORIGINAL ARTICLE; Methicillin-resistant Staphylococcus aureus|
|Author:||Baugher, Katherine M.; Hemme, Troy Sommers; Hawkshaw, Mary; Sataloff, Robert T.|
|Publication:||Ear, Nose and Throat Journal|
|Date:||Feb 1, 2011|
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